accession
stringlengths 6
10
| name
stringlengths 6
11
| Full Name
stringlengths 1
147
⌀ | taxon
stringlengths 3
46
⌀ | sequence
stringlengths 16
2.75k
| function
stringlengths 6
5.51k
| AlphaFoldDB
stringlengths 6
10
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B7LNJ1 | LPLT_ESCF3 | Lysophospholipid transporter LplT | Escherichia | MSESVHTNTSLWSKGMKAVIVAQFLSAFGDNALLFATLALLKAQFYPEWSQPVLQMVFVGAYILFAPFVGQVADSFAKGRVMMFANGLKLLGAASICFGFNPFVGYTLVGIGAAAYSPAKYGILGELTTGDKLVKANGLMEASTIAAILLGSVAGGVLADLHVLVALAACALAYAGAVAANIYIPKLAAARPGQSWNVLKMTCSFKSACTSLWQNGETRFSLVGTSLFWGAGVTLRFLLVLWVPVALGITDNATPTYLNAMVAIGIVLGAGAAAKLVTLETVSRCMPAGILIGVVVLFFSLQHELLPAYALLMLIGVLGGFFVVPLNALLQERGKKSVGAGNAIAVQNLGENSAMLLMLGIYSLAVLVGIPVVPIGIGFGTLFALAITALWIWQRRH | Catalyzes the facilitated diffusion of 2-acyl-glycero-3-phosphoethanolamine (2-acyl-GPE) into the cell. | B7LNJ1 |
Q6LG09 | OTC_PHOPR | Ornithine carbamoyltransferase | Photobacterium | MSFNLRNRNFLKLLDFTGKEIEHLIALAQDLKHAKYAGTEQQKLKGKNIALIFEKTSTRTRCAFEVAAHDQGAHVTYIGGGSQMGHKESTKDTARVLGRFYDGIEYRGFGQDVVETLGEHAGVPVWNGLTDEWHPTQIIADWMTMLEHGNGKRLNQMKLAYMGDAKNNMGNSLMVGAAKVGMEIRLVGPKAYWPDPALVAECNELCKISGGKIVITDNVQEGVDSVDFIYGDVWVSMGEPEELWATRINDLAPYQVNMSVITATQNPAVKYMHCLPAFHNDETRVGKKIEEKFNMKGLEVTEDVFESSYTICFDEAENRMHSIKAIMVATLGD | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline. | Q6LG09 |
Q01345 | NHEB_ONCMY | Na(+)/H(+) antiporter | Oncorhynchus | MPAFSCAFPGCRRDLLVIVLVVFVGIGLPIEASAPAYQSHGTEGSHLTNITNTKKAFPVLAVNYEHVRKPFEIALWILLALLMKLGFHLIPRLSAVVPESCLLIVVGLLVGGLIKVIGEEPPVLDSQLFFLCLLPPIILDAGYFLPIRPFTENVGTILVFAVIGTLWNAFFMGGLLYALCQIESVGLSGVDLLACLLFGSIVSAVDPVAVLAVFEEIHINELVHILVFGESLLNDAVTVVLYNLFEEFSKVGTVTVLDVFLGVVCFFVVSLGGVLVGAIYGFLAAFTSRFTSHTRVIEPLFVFLYSYMAYLSSEMFHLSGIMALIACGVVMRPYVEANISHKSYTTIKYFLKMWSSVSETLIFIFLGVSTVAGPHAWNWTFVITTVILCLVSRVLGVIGLTFIINKFRIVKLTKKDQFIVAYGGLRGAIAFSLGYLLSNSHQMRNLFLTAIITVIFFTVFVQGMTIRPLVELLAVKKKKESKPSINEEIHTEFLDHLLTGVEGVCGHYGHYHWKEKLNRFNKTYVKRWLIAGENFKEPELIAFYRKMELKQAIMMVESGQLPSVLPSTISMQNIQPRAIPRVSKKREEEIRRILRANLQNNKQKMRSRSYSRHTLFDADEEDNVSEVRLRKTKMEMERRVSVMERRMSHYLTVPANRESPRPGVRRVRFESDNQVFSADSFPTVHFEQPSPPSTPDAVSLEEEEEEVPKRPSLKADIEGPRGNASDNHQGELDYQRLARCLSDPGPNKDKEDDDPFMSC | Involved in pH regulation to eliminate acids generated by active metabolism or to counter adverse environmental conditions. Major proton extruding system driven by the inward sodium ion chemical gradient. | Q01345 |
Q54ME1 | GMSA_DICDI | Gamete and mating-type specific protein A | Dictyostelium | MKLILVLLCLISTLFVVKGGLSPTEQQIIVSYHNKWRSSPIGPTPSTTIPALKWNATIAAALQSSLDKCDGKFSTMSQYGTNSEWQSWWTPNTYFNLNATLDNIQKGASFYDWNAKGCNSSANYNCQLWTYAVWSKSTSYGCAKTICPDKSEVSCSYYPAGGFKGVLPYTPKTTTPAPTTPAPTTPKPTTPAPTTPKPTTPAPTTPKPTTPAPTTPKPTTPAPTTPKPTTPAPTTPAPTSTLTVDWTSYQTPIRDQGQCGSCWAFASSAALESRYLIKYGTAQKSTLQLSNQNAVNCIASGCNGGWSGNYFNFFKTPGIAYEKDDPYKAVTGTSCITTSSVARFKYTNYGYTEKTKAALLAELKKGPVTIAVYVDSAFQNYKSGIYNSATKYTGINHLVLLVGYDQATDAYKIKNSWGSWWGESGYMRITASNDNLAIFAYNSYYPTF | Thiol protease that seems to be involved in the sexual development. | Q54ME1 |
Q8UIE8 | SYW_AGRFC | Tryptophanyl-tRNA synthetase | Agrobacterium tumefaciens complex | MNAFKPLVFSGVQPTGNLHLGNYLGAIRKFVALQEDNDCIYCVVDMHAITAQLVHSDLKAQTRSIAAAFIAAGIDPVKHIVFNQSAVPQHAELAWVFNCVARIGWMERMTQFKDKSGKNAEQVSLGLLAYPSLMAADILVYRATHVPVGDDQKQHLELARDIAQKFNIDFGGHIRNAGLGVNITVGDEPVHAYFPMVEPLIGGPAPRVMSLKDGTKKMSKSDPSDLSRINLMDDVDAISKKIKKAKTDPDALPSEVEGLKGRPEAENLVGIYAALSDKTKADVLAEFGGQQFSTFKPALVELAVNVLAPVNNEMRRLLDDPTHIDAILSQGGERARTIAEKTMNEVRDIIGFLR | Catalyzes the attachment of tryptophan to tRNA(Trp). | Q8UIE8 |
A6UYL3 | PYRR_PSEA7 | Uracil phosphoribosyltransferase | Pseudomonas | MSLPNPAELLPRMASDLRAHLAERGIERPRYVGIHTGGIWVAEALLKALGNEEPLGTLDVSFYRDDFTRNGLHPQVRPSALPFEIDGQHLVLVDDVLMSGRTIRAALNELFDYGRPASVTLVCLLDLNARELPIRPDVVGQTLSLGRDERVKLVGPAPLALERKVLSPAS | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant. | A6UYL3 |
B7GFF3 | RECR_ANOFW | Recombination protein RecR | Anoxybacillus | MYYPEPISKLIDSFMKLPGIGPKTAVRLAFFVLNMKEDVVLDFAKALVNAKRNLTYCSSCGHITDKDPCYICEDDKRDRSIICVVQDPKDVIAMEKMKEYNGLYHVLHGAISPMEGIGPEDIKIAELLRRLQDETVQEVILATNPNIEGEATAMYISRLLKPTGVKITRIAHGLPVGGDLEYADEVTLSKALEGRREL | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO. | B7GFF3 |
O42807 | FAEA_ASPNG | Ferulic acid esterase A | Aspergillus subgen. Circumdati | MKQFSAKYALILLATAGQALAASTQGISEDLYNRLVEMATISQAAYADLCNIPSTIIKGEKIYNAQTDINGWILRDDTSKEIITVFRGTGSDTNLQLDTNYTLTPFDTLPQCNDCEVHGGYYIGWISVQDQVESLVKQQASQYPDYALTVTGHSLGASMAALTAAQLSATYDNVRLYTFGEPRSGNQAFASYMNDAFQVSSPETTQYFRVTHSNDGIPNLPPADEGYAHGGVEYWSVDPYSAQNTFVCTGDEVQCCEAQGGQGVNDAHTTYFGMTSGACTW | Involved in degradation of plant cell walls. Hydrolyzes the feruloyl-arabinose ester bond in arabinoxylans, and the feruloyl-galactose ester bond in pectin. Binds to cellulose. | O42807 |
B1IA76 | RIMP_STRPI | Ribosome maturation factor RimP | Streptococcus | MDAIATIVELVREVVEPVIEAPFELVDIEYGKIGSDMILSIFVDKPEGITLNDTADLTEIISPVLDTIKPDPFPEQYFLEITSPGLERPLKTKDAVAGAVGKYIHVGLYQAIDKQKVFEGTLLAFEEDELTMEYMDKTRKKTVRIPYSLVSKARLAVKL | Required for maturation of 30S ribosomal subunits. | B1IA76 |
P40283 | H2B11_ARATH | HTB4 | Arabidopsis | MAPKAEKKPAEKKPASEKPVEEKSKAEKAPAEKKPKAGKKLPKEAGAGGDKKKKMKKKSVETYKIYIFKVLKQVHPDIGISSKAMGIMNSFINDIFEKLAQEASKLARYNKKPTITSREIQTAVRLVLPGELAKHAVSEGTKAVTKFTSS | Core component of nucleosome. Nucleosomes wrap and compact DNA into chromatin, limiting DNA accessibility to the cellular machineries which require DNA as a template. Histones thereby play a central role in transcription regulation, DNA repair, DNA replication and chromosomal stability. DNA accessibility is regulated via a complex set of post-translational modifications of histones, also called histone code, and nucleosome remodeling. | P40283 |
Q5L3D3 | PURQ_GEOKA | Phosphoribosylformylglycinamidine synthase subunit I | Geobacillus thermoleovorans group | MKFAVVVFPGSNCDVDMYHAIADELGEEVEYVWHDEDNLDRFDAVLLPGGFSYGDYLRSGAIARFSKVMAAVKKAAEAGKPVLGVCNGFQILLEAGLLPGAMRRNQGLKFICRPVQLTVENHETMFTSAYEKGEVITIPIAHGEGNYYCDEQTLERLVENRQIVFRYHGENPNGSLADIAGIVNEQGNVLGMMPHPERAVDALLGSADGLKLFRSIVNYWRETHVVTA | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL. | Q5L3D3 |
Q90WG1 | SPINZ_CHICK | Spindlin-Z | Gallus | MKTPFGKSPGQRSRADAGHAGVSASMMKKRTSHKKHRNNVGPSKPISQPRRNIVGCRIQHGWKEGSGPVTQWKGTVLDQVPVNPSLYLIKYDGFDCVYGLELHKDERVSALEVLPDRVASSRISDAHLADTMIGKAVEHMFETEDGSKDEWRGMVLARAPIMNTWFYITYEKDPVLYMYQLLDDYKEGDLRIMPDSNDSPPAEREPGEVVDSLVGKQVEYAKEDGSKRTGMVIHQVEAKPSVYFIKFDDDFHIYVYDLVKTS | May play a role in mitosis. | Q90WG1 |
A4WVP0 | PCKA_CERS5 | Phosphoenolpyruvate carboxykinase (ATP) | Cereibacter | MNFGRVNPAQTLDAQGITGLGEVHYNLIEPALVEAAVKRGEGRLGRGGAFLCSTGAFTGRSPKDKFVVRTPSVEDTIWWENNAPMDPEAFDRLHADMLEHMKGRTYFVQDLFAGADPELRLDVRMVTELAWHGLFIRHMLRRPERTELDSFVPEWTVINCPSFKADPARHGCRTDTVITLNFDKKLILIANTEYAGENKKSVFTLLNYILPGKGVMAMHCSANHAIGNTDDAAVFFGLSGTGKTTLSADPSRTLIGDDEHGWSDKGTFNFEGGCYAKTINLSPEAEPEIYATTSKFATVVENMVYNEETLELDFDDDSLTANTRCAYPLEYISNASATGMGGHPKNVIMLTCDAFGVLPPIARLTPAQAMYHFLSGFTSKVAGTERGVTEPQPTFSTCFGAPFMPRRPEVYGKLLQEKITSLGATCWLVNTGWTGGAYGTGKRMPIKATRALLTAALDGSLANVTFRKDPNFGFEVPTELHGVDSSLLDPRSTWADPAAYDAQAKKLVEMFANNFAQYVPYIDADVKAAAIG | Involved in the gluconeogenesis. Catalyzes the conversion of oxaloacetate (OAA) to phosphoenolpyruvate (PEP) through direct phosphoryl transfer between the nucleoside triphosphate and OAA. | A4WVP0 |
Q9CY34 | UB2FA_MOUSE | Ubiquitin-conjugating enzyme E2 F | Mus | MLTLASKLKRDDGLKGSRTSASTSDSTRRVSVRDKLLVKEVAELEANLPCTCKVHFPDPNKLHCFQLTVSPDEGYYQGGKFQFETEVPDAYNMVPPKVKCLTKIWHPNITETGEICLSLLREHSIDGTGWAPTRTLKDVVWGLNSLFTDLLNFDDPLNIEAAEHHLRDKEDFRDKVDEYIKRYAR | Accepts the ubiquitin-like protein NEDD8 from the UBA3-NAE1 E1 complex and catalyzes its covalent attachment to other proteins. The specific interaction with the E3 ubiquitin ligase RBX2, but not RBX1, suggests that the RBX2-UBE2F complex neddylates specific target proteins, such as CUL5. | Q9CY34 |
Q8EGW8 | SSRP_SHEON | Small protein B | Shewanella | MVKKNSKKAAPATIARNKRATFEYRFEEKMEAGLSLMGWEVKSIRMGKVNLSDCYVFLKNGEAFMHGCTIIPLNTASTHVVCDPIRLKKLLLSRKELDKLAGLVERQGYSIIPISMYWRKGAWVKVEIGLGKGKKDHDKREDTKAREWEVEKARVMKKEKTRG | Required for rescue of stalled ribosomes mediated by trans-translation. Binds to transfer-messenger RNA (tmRNA), required for stable association of tmRNA with ribosomes. tmRNA and SmpB together mimic tRNA shape, replacing the anticodon stem-loop with SmpB. tmRNA is encoded by the ssrA gene; the 2 termini fold to resemble tRNA(Ala) and it encodes a 'tag peptide', a short internal open reading frame. During trans-translation Ala-aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA; the nascent peptide is terminated with the 'tag peptide' encoded by the tmRNA and targeted for degradation. The ribosome is freed to recommence translation, which seems to be the essential function of trans-translation. | Q8EGW8 |
Q5WH37 | DEOB_ALKCK | Phosphodeoxyribomutase | Alkalihalobacillus | MKKRFERIFLIVMDSVGIGEAPDAKEFGDEGANTLGSIAEAFNGLHVPELEKLGLGKIAPLKGVKNVPTPLASYGIMQEASLGKDTMTGHWEIMGLHITKPFQVFPDGFPTELLEQLKSETGRGIIGNKVASGTEILDELGEEHVKTGDLIVYTSADSVLQIAAHEEVVPLEELYDICEKARKLTLAPEYMVGRVIARPFVGEPGKWKRTANRHDYALKPFGRTVMNTLEDAGLASIALGKISDIYDGEGVTKAVRTTSNEDGMDKLAEQINTSFEGLCFLNLVDFDALYGHRRDVIGYGEAIMAFDQRLGEILPQLGDEDLLIVTADHGNDPTHTGTDHTREYVPLLVYNKGIKPVNLGKRRTFADIGATVADNFQVERPSNGTSFLTELKPE | Phosphotransfer between the C1 and C5 carbon atoms of pentose. | Q5WH37 |
Q5QYV0 | RUVC_IDILO | Holliday junction resolvase RuvC | Idiomarina | MAIILGIDPGSRLTGYGVIEQRGRQLNYLGSGCIKVIGTTKEPLTLAEKLRRIHDSVSELITQFKPNEFAIEQVFMAKNPDSALKLGQARGAAIVAAACAELPVAEYSARQIKQSVVGNGGAEKSQVQHMVMALLNLQRCPQEDAADALAVALCHAHSSQNLIKMAGAARKTVRGRLR | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group. | Q5QYV0 |
P0AE71 | MAZF_ECO57 | mRNA interferase MazF | Escherichia | MVSRYVPDMGDLIWVDFDPTKGSEQAGHRPAVVLSPFMYNNKTGMCLCVPCTTQSKGYPFEVVLSGQERDGVALADQVKSIAWRARGATKKGTVAPEELQLIKAKINVLIG | Toxic component of a type II toxin-antitoxin (TA) system. MazF is a sequence-specific endoribonuclease that inhibits protein synthesis and induces bacterial stasis. It is very stable, single-strand specific and cleavage is independent of the ribosome. The endoribonuclease activity (a toxin) is inhibited by the labile cognate antitoxin MazE. Toxicity results when the levels of MazE decrease in the cell, leading to mRNA degradation. Both MazE and MazE-MazF bind to the promoter region of the mazE-mazF operon to inhibit their transcription. | P0AE71 |
A0A1W2PPG7 | GBG14_HUMAN | Putative guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-14 | Homo | MSSKVAINSDIGQALWAVEQLQMEAGIDQVKMAADLLKFCTEQAKNDPFLVGIPAATNSFKEKKPYAIL | Guanine nucleotide-binding proteins (G proteins) are involved as a modulator or transducer in various transmembrane signaling systems. The beta and gamma chains are required for the GTPase activity, for replacement of GDP by GTP, and for G protein-effector interaction. | A0A1W2PPG7 |
Q8XXL5 | ADE_RALSO | Adenine aminohydrolase | Ralstonia | MPISPALAERIATSPKAELHIHIEGSLEPELMFALAERNGVKLPYASVDEVRAAYAFNDLQSFLDLYYAGASVLLTEQDFYDMTAAYVARAVADNVRHAEIFFDPQTHTARDVPMHVVIGGIVRALDDAERAHGFSSRLILCFLRHLSEADAFDTLEAALPYIQDPANRIIGVGLDSSERGNPPEKFARVFARCKALGLRLVAHAGEEGPAQYVIDALDILQVERIDHGVRAIDDAALVKRLAASRVALTVCPLSNEKLKVYPDLRDHSLKQLLDAGCAVTLHSDDPAYFGGYMNTNWLATFNALGLSAADAHTLARNSFEASFLPEQDKALWLNAVDIHWRAHT | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism. | Q8XXL5 |
A7ZSM0 | TUSD_ECO24 | tRNA 2-thiouridine synthesizing protein D | Escherichia | MRFAIVVTGPAYGTQQASSAFQFAQALIVEGHELSSVFFYREGVYNANQLTSPASDEFDLVRGWQQLNAQHGVALNICVAAALRRGIVDETEAGRLGLASSNLQPGFTLSGLGALAEASLTCDRVVQF | Part of a sulfur-relay system required for 2-thiolation of 5-methylaminomethyl-2-thiouridine (mnm(5)s(2)U) at tRNA wobble positions. Accepts sulfur from TusA and transfers it in turn to TusE. | A7ZSM0 |
B4S433 | DER_PROA2 | GTP-binding protein EngA | Prosthecochloris | MKPLVALVGRPNVGKSTLFNRITHQKSAIVDSTPGVTRDRHIMPAEWIGKEFLVMDTGGYCHDSDGISKAMLEQTLTAIGEADVIIFLVDVRSGLTYLDLDMAKLLKRDFNDKPVYFAVNKVESPQLAYEGESFRKTGFTEPWFISARDGSGVADLLDAVVDSFEEKSGQEEEDDSIRLAIIGRPNVGKSSFVNALLGTNRNIVSNKPGTTRDAIDTRFKRNGREIVLIDTAGLRKRARIDAGIEFYSSLRTERAIERCDVALVLIDAEQGLEKQDMKIIEMAAERKKGVLLLVNKWDLIEKDSKTSKLYSDRMYDDMGNLGWIPIQFISAMTKKNLYRAIDAALDIQEQRSQQITTSDLNRFLQDTLLQAPPSSKSGKELKIKYMTQIRAPWPVFAFFCNDPKLLQNNYKRFLEKRIRQNYNLSGVPFSLRFMQK | GTPase that plays an essential role in the late steps of ribosome biogenesis. | B4S433 |
J7FK10 | IDTM_CLAPA | Indole-diterpene biosynthesis cluster protein M | Claviceps | MADDFKVVIVGGSVAGLSLAHCLERLGVSYVVLEKGSQIAPQLGASIGILPNGGRILDQLGIFRDVEDEIEPLNFAVIRYADGFSFRSQYPKALHSSYGYPVSFLERQKFIQILYDKLRGKNHVHTRKRVVSIVDGPGKALIRTDDGDEYDADMVVGADGVHSVVRSEIWRHAKEAAGTAVTEEEPNADIKYDYACVYGISVNVPHADTGVQLSSLSDGVSIHLFAGKGSKFFWFIMVRTSRDEFLELKKDSAHMARRTCEGLGSKRLSDAVYFRDVWSRCTVYQMTPLEEGVFRQWNRGRLVCIGDAIRKMAPNIGQGANMAIEDAAQLSNLIREMLASPRKASATTVEKMLRDFAAMQKARTKSMCGQSEFLVRMHANEGFGRRLLGRYLIPSLQDAPAGLAGLSIRGAVKLECAGVPSRTLGKAWEGSWGSSLRNLMYLRPRLGILSLVYVVAGLAMMYMSIYLVVPARLAAQAFDVSRDGTEGKGGG | FAD-dependent monooxygenase; part of the gene cluster that mediates the biosynthesis of paspalitrems, indole-diterpene (IDT) mycotoxins that are potent tremorgens in mammals . The geranylgeranyl diphosphate (GGPP) synthase idtG is proposed to catalyze the first step in IDT biosynthesis via catalysis of a series of iterative condensations of isopentenyl diphosphate (IPP) with dimethylallyl diphosphate (DMAPP), geranyl diphosphate (GPP), and farnesyl diphosphate (FPP), to form GGPP (Probable). Condensation of indole-3-glycerol phosphate with GGPP by the prenyltransferase idtC then forms 3-geranylgeranylindole (3-GGI) (Probable). Epoxidation of the two terminal alkenes of the geranylgeranyl moiety by the FAD-dependent monooxygenase idtM, and cyclization by the terpene cyclase idtB then leads to the production of paspaline (Probable). The cytochrome P450 monooxygenase idtP then catalyzes oxidative elimination of the pendant methyl group at C-12 of paspaline and generates the C-10 ketone to yield 13-desoxypaxilline . The cytochrome P450 monooxygenase idtQ may catalyze the C-13 oxidation of 13-desoxypaxilline to afford paxilline (Probable). Considering that both paspalicine and paxilline were detected in C.paspali, idtQ also catalyzes the formation of paspalinine from 13-desoxypaxilline via paspalicine as an intermediate (Probable). Finally, the alpha-prenyltransferase idtF prenylates paspalinine at the C-20 or the C-21 positions to yield paspalitrems A and C, respectively . The hydroxylation of paspalitrem A at C-32 by a still unknown oxidase affords paspalitrem B (Probable). | J7FK10 |
Q98LX2 | GLMU_RHILO | Glucosamine-1-phosphate N-acetyltransferase | Mesorhizobium | MSQRSCLSVILAAGEGTRMKSALPKVLHQIAGLPMVAHVVKAADAAGASSDAIVIGHGAEEMRKAVTKFSPKAETFVQEERLGTAHAVLAAREAISRGYDDILVMFGDTPLIDAEALNLARLKLAEGAAVAVIGFRPPLPNGYGRLVEKGGKLIAIREEKDCSEAEKKIGFCNAGMMAVAGAHALKLLDAVGNKNAKGEYYLTDIVEIAGAQGLDVVATEASFENALGINNRAELAQAEGIWQARRRQEAMLSGVTLIAPETVYFSHDTEIGADTVVEPNVWFGPGVKIAGGAKIHAFSHIEGATIAANCDVGPFARLRPGADLRNKAKVGNFCEVKQAVIEEGAKVNHLTYIGDARVGAGANIGAGTITCNYDGFSKFFTDIGEGAFVGSNSSLVAPVSIGKGGYIASGSVITESVPDDALAFGRARQKTIPGKGKELRERFASAAAAKKKAAGADH | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP-GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5-monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain. | Q98LX2 |
B1ZND9 | RS17_OPITP | 30S ribosomal protein S17 | Opitutus | MSSSPAQRHTRKTQIGFVSSRSGDKSIKVTVPYKSPHPLYHKIVNRQTVLHVHDEKNEAKLGDTVEVMETRPMSRLKRWRIVSIVQRAVTTDAVAISETDVAAQVPTKTTASNTPAPAEQPAPQA | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA. | B1ZND9 |
B0TUD3 | TRMN6_SHEHH | tRNA m6A37 methyltransferase | Shewanella | MPFTFKLFHVDDSRCGMPVSTDGVLLGAWAPLVQAKTILDIGAGSGLLSLMAAQRSQAKITAIELDNDAALDCQQNFDASHWSERLEIICCDIQAYCQREQARQFDHIICNPPYFANGPQSSKFSRATARHTDSLSFDALLQAIKQLLAPEGQASLILPTESVSLLEAILSTYNLRLCHKLLAASVEGKAPNRQILVLGHDLKAKKIHNFGTELQAVAQQQLYIREKTGHYSLAFTLLSQDFYLKL | Specifically methylates the adenine in position 37 of tRNA(1)(Val) (anticodon cmo5UAC). | B0TUD3 |
Q8UVQ4 | KAISO_XENLA | Zinc finger and BTB domain-containing protein 33 | Xenopus | METKKLITATDTQYSGILLNALNDQRIQGLYCDVTVIVEDRKFRAHRNILSACSTYFHQLFSVAGQVVELNFVKADIFAEILNYIYSSKIVRVRCDMLEELIKSGKLLGVPFIAELGIPLSQVKSISGAGGKDGGTDAPSNPDHKAPEPQKSSDSPLPCTVKIKADVKTEMPVITESFSLSSDDYKDKKASGSQDHNSEKEDDDDDVIFCSEIVSSKQAPAERKEAAQTQIPPDNEQVPEVKKVTPSSQVQLTQNSLPTNQQSSKNTSSTTQKFTPPVNANISKNPTPAANGFLSPTAQKQGTPNAVQNQHSQNITSGNALPQQKPVVNFSSIKPQQISAIKPKTEVIIHGNGLSPPSSSVIPLGQQPVTPKHISFDGVQKKQVVTFTQGSPSKPGEFKIKIADVVSGSSLDSFKDSEPRRIIDGKKIITLDTASEIEGLSTGCKVYANIGEDTYDIVIPIKEDPEEGEAKLDLDGLPNRKRMKLKHDDHYELIVDGRVYYICIVCKRSYVCLTSLRRHFNVHSWEKKYPCRYCERVFPLAEYRTKHEIHHTGERRYQCLTCGSSFINYQVMASHIRSVHSLDPSGDSKLYRLNPCKTLQIRQYAYVNNSTNGTVINDGAINVPVITDGGINVPVINDGGIVYDIDPDEPQQPASEGNHANSATKPVNWDNIFIQQSNQNMFKLNTSEGGTEFEFVIPESY | Transcriptional regulator with bimodal DNA-binding specificity. Binds to methylated CpG dinucleotides in the consensus sequence 5'-CGCG-3' and also binds to the non-methylated consensus sequence 5'-CTGCNA-3'. May recruit the N-CoR repressor complex to promote histone deacetylation and the formation of repressive chromatin structures in target gene promoters. Contributes to the repression of target genes of the Wnt signaling pathway and to the methylation-dependent repression of zygotic transcription prior to the mid-blastula transition (MBT). Also required for gastrulation movements. | Q8UVQ4 |
B0BAF4 | PSD_CHLTB | Phosphatidylserine decarboxylase beta chain | Chlamydia | MAAREMLYVNRETGKVEQERIICSSLVKFFIETRIGRALYSVLCKNSLFSRIVGWCQRLRVTRYFIKPFVTKYRICIEESASPLHDYASFNDFFVRKLKPDARPICQGEDICVTPADGAYLVFPSMADLSLFTIKNKPFSLESFLGDPQLAHQYAQGSMAIARLAPFDYHRFHFPIAGIAEAPRRINGHLFSIHPLMLKRNFEVFTENKREITIITSKEFGEVAYVEVGALNVGSIHQTFSPGSYVKKGAEKGFFAFGGSTVVLLFQPQRIIFDADLVGYSAQGLETRCRMGQSLGKHFSS | Catalyzes the formation of phosphatidylethanolamine (PtdEtn) from phosphatidylserine (PtdSer). | B0BAF4 |
Q8Y4B6 | ATP6_LISMO | F-ATPase subunit 6 | Listeria | MEEEFPTISLLGIDFNLSNILMITVTCVIVLLIAIICTRNLQRRPTGKQNFIEWVMDFVRGIINSNMDWKTGGRFHVLGITILMFVFVANMLGLPLQIAVNDEVWWRSPTADPIVTLTLAIMVLGLTHYYGIKMRGFKHYFVGTYLSPMKFLFPLKLVEEFANTLTLGLRLYGNIFAGEVLLTIIATQLAHINIFVGVLAIIPAIIWQAFSLFIGAIQAYIFTMLTMVYMSHKVSDEH | Key component of the proton channel; it plays a direct role in the translocation of protons across the membrane. | Q8Y4B6 |
A2DZE8 | ALG5A_TRIVA | Dolichyl-phosphate beta-glucosyltransferase ALG5A | Trichomonas | MKFWRFVQILFFLGVAAVGLVVAVMIANADDTTLFDRMQLPDGDPNKLNYYIQPAPNGNEKVPFPTIFDPASVYLSLVVPAYNEEKRLPKMLDETLNYLKSREEKDKSFTWEIVIVNDGSKDKTKEVVLNYAKEYPNIFLLNQPVNMGKGAAIQAGCLHVRGELVLMLDADGATKIDDFEVLEKEIKSLMKTTNQAIVIGSRAQNEKAKRTPLRKFLSIGMHTLIVLSGVHGIRDTQCGFKLFTRESCKMIFMNQHVQRWCCDPEILVIARRLGMKISELPVEWNEIDGSKMKISGMIKMATDLIKIAIFHRVGAWKIRDRRH | Dolichyl-phosphate beta-glucosyltransferase involved in the glycosylation of glycoproteins through the synthesis of dolichyl beta-D-glucosyl phosphate which serves as a sugar donor for transfer of three glucose residues to the Man-9-GlcNAc-2-PP-dolichol precursor to N-glycans. | A2DZE8 |
O46392 | CO1A2_CANLF | Alpha-2 type I collagen | Canis | MLSFVDTRTLLLLAVTSCLATCQSLQEATARKGPTGDRGPRGERGPPGPPGRDGDDGIPGPPGPPGPPGPPGLGGNFAAQYDGKGVGLGPGPMGLMGPRGPPGASGAPGPQGFQGPAGEPGEPGQTGPAGARGPPGPPGKAGEDGHPGKPGRPGERGVVGPQGARGFPGTPGLPGFKGIRGHNGLDGLKGQPGAPGVKGEPGAPGENGTPGQTGARGLPGERGRVGAPGPAGARGSDGSVGPVGPAGPIGSAGPPGFPGAPGPKGEIGPVGNPGPAGPAGPRGEVGLPGVSGPVGPPGNPGANGLTGAKGAAGLPGVAGAPGLPGPRGIPGPVGAAGATGARGIVGEPGPAGSKGESGNKGEPGSAGAQGPPGPSGEEGKRGPNGEAGSAGPSGPPGLRGSPGSRGLPGADGPAGVMGPPGPRGATGPAGVRGPNGDSGRPGEPGLMGPRGFPGAPGNVGPAGKEGPMGLPGIDGRPGPIGPAGARGEPGNIGFPGPKGPTGDPGKNGDKGHAGLAGARGAPGPDGNNGAQGPPGPQGVQGGKGEQGPAGPPGFQGLPGPAGTAGEVGKPGERGLPGEFGLPGPAGPRGERGPPGESGAAGPSGPIGSRGPSGPPGPDGNKGEPGVLGAPGTAGASGPGGLPGERGAAGIPGGKGEKGETGLRGEIGNPGRDGARGAPGAMGAPGPAGATGDRGEAGPAGPAGPAGPRGTPGERGEVGPAGPNGFAGPAGAAGQPGAKGERGTKGPKGENGPVGPTGPIGSAGPSGPNGPPGPAGSRGDGGPPGATGFPGAAGRTGPPGPSGITGPPGPPGAAGKEGLRGPRGDQGPVGRTGETGASGPPGFTGEKGPSGEPGTAGPPGTPGPQGLLGAPGILGLPGSRGERGLPGVAGSVGEPGPLGIAGPPGARGPPGAVGAPGVNGAPGEAGRDGNPGNDGPPGRDGQAGHKGERGYPGNIGPVGAVGAPGPHGPVGPTGKHGNRGEPGPAGSVGPVGAVGPRGPSGPQGIRGDKGEPGEKGPRGLPGLKGHNGLQGLPGLAGQHGDQGAPGSVGPAGPRGPAGPSGPAGKDGRTGQPGTVGPAGIRGSQGSQGPAGPPGPPGPPGPPGPSGGGYDFGYEGDFYRADQPRSPPSLRPKDYEVDATLKSLNNQIETLLTPEGSRKNPARTCRDLRLSHPEWSSGYYWIDPNQGCTMDAIKVYCDFSTGETCIRAQPENIPAKNWYRNSKVKKHIWLGETINGGTQFEYNVEGVTTKEMATQLAFMRLLANHASQNITYHCKNSIAYMDEETGNLKKAVILQGSNDVELVAEGNSRFTYTVLVDGCSKKTNEWRKTIIEYKTNKPSRLPILDIAPLDIGDADQEFRVDVGPVCFK | Type I collagen is a member of group I collagen (fibrillar forming collagen). | O46392 |
C5CFW2 | MURA_KOSOT | UDP-N-acetylglucosamine enolpyruvyl transferase | Kosmotoga | MSEIVVEGGRKLIGEVPISGSKNAALPILAAAVMIDEPVVLDNVPELKDVFTMLTILQRIGKKVSFRDNRVVVEPGNVLMGDVPYELVRMMRASFNVLGPLTMVCGWAKVGKPGGCNIGQRPVDFHIEGLKALGFLIKEEHGDVIAKKPSSFKEELYYKLPFPSVGATEQLMTVAALMSESKTIIENVAREPEIQDLQNFLNKAGAKIKGAGTDRIEIEGVEKLHGIEYHIIPDRIEAGTYLLAGVSTRGRVKVSNVIPEHLEALLKVLDELGVSITCDKNSIEVSVSGELKPIRVSTAPYPGFPTDLQPMLTAVLCTVPGESIIEEKVFENRFGYVDEMNRMSANIKVMNRVAHIVGVEKLSGAQIYAPDIRATAGMLIAALSAEGQTVIKNAAHIFRGYEKLKEKFTTIGAQIEVYPEE | Cell wall formation. Adds enolpyruvyl to UDP-N-acetylglucosamine. | C5CFW2 |
Q31G53 | FABZ_HYDCU | Beta-hydroxyacyl-ACP dehydratase | Hydrogenovibrio | MLNVKEIFEYLPHRYPFLLVDRVTEFKSGESLKAYKNVTYNEPQFTGHFPDNPIMPGVMIIEAMAQCTGILAFKTQDVKPDGTSMYYLAAVDNCRFRKPAIPGDKLEFEVKTVNNKKGIWKFECTTSVDGKLIASCDMLCAERKV | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs. | Q31G53 |
B9ME46 | PTH_ACIET | Peptidyl-tRNA hydrolase | Diaphorobacter | MIKLFVGLGNPGPEYEATRHNAGFWWIDALARELKVTLVPERSYHGLVARASVAGHSVWLLQPQTFMNLSGKSVAALARFFKIPPEEILVAHDELDIPPGQAKLKRGGSHAGHNGLRDIHAQLGTSDYWRLRIGIGHPGVKAEVVNWVLKKPAPDQRTLIEDSILHSLKAYPALLAGDMDKATLLVHTTKPPRPKATRPAQAQAAPQAGAD | The natural substrate for this enzyme may be peptidyl-tRNAs which drop off the ribosome during protein synthesis. | B9ME46 |
B0BR79 | FTSP_ACTPJ | Cell division protein FtsP | Actinobacillus | MMNLTRRQLLTRSAVAATMFSAPKTLWAAERQPLKIPPIIDVGRGRPVRLDLRPAQTQFDKGKLVDVWGVNGQYLAPTVRVKSDDFVKLTYVNNLPQTVTMNIQGLLAPTDMIGSIHRKLEAKSSWSPIISIHQPACTCWYHADTMLNSAFQIYRGLAGMWIIEDEQSKKANLPNKYGVNDIPLILQDQQLNKQGVQVLDANQKQFFGKRLFVNGQESAYHQVARGWVRLRIVNASLSRPYQLRLDNDQPLHLIATGVGMLAEPVPLESITLAPSERVEVLVELNEGKTVSLISGQKRDIFYQAKNLFSDDNELTDNVILELRPEGMAAVFSNKPSLPPFATEDFQLKIAEERRLIIRPFDRLINQKRFDPKRIDFNVKQGNVERWYITSDEAVGFTLQGAKFLIETRNRQRLPHKQPAWHDTVWLEKNQEVTLLVRFDHQASAQLPFTFGVSDFMLRDRGAMGQFIVTE | Cell division protein that is required for growth during stress conditions. May be involved in protecting or stabilizing the divisomal assembly under conditions of stress. | B0BR79 |
A2RJS5 | RIMM_LACLM | Ribosome maturation factor RimM | Lactococcus cremoris subsp. cremoris | MENFYKVGTIVNTQGLQGEVRILPSTDFANERFSKGAVLALFDDKDNYIQDLKVKSGRLQKNFYVVKFEGFYHINDVEKYKGYVVKIAQENQEELNDGEFYYHEIIGSDVYDNDILIGQISEILQPGANDVWVVKRKGKRDLLLPYIPPVVLKVDVAQHRVDVDIMEGLDD | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes. | A2RJS5 |
B3QBR5 | GLNE_RHOPT | Adenylyl transferase | Rhodopseudomonas | MIFSAITADLDNTALAARFGAGPRLYDPVLAAERWAGWLVDLAPEQADAIAALGNAFPDLQIALQSIAEASPYLFDLIRGDPVRLLRVLRGAPEQRLAKLLEDAETFVAAASAEDEVMAALRRLKAEAALLIALCDIGGIWPVMQVTQALTDLAGRSVQMALRFLLRLEAGRGRIVPPNPDCPEQGSGLIVLAMGKMGAGELNYSSDIDLIVFYELDAPTLAPDIEPQPFFVRVTQGLSRILQQRRGDGYVFRVDLRLRPDPASTPVALSTVSALDYYEREGRTWERAAMIKARPCAGDLVAGDALLSEIAPFVWRKHLDFAALSDVHDMKRQMQTYRGQTEIAVEGHNVKVGRGGIREIEFFAQTQQLIAGGRHPELRVRPTLEALEILAARNWITIQARDELTEAYLFLRKVEHRVQMIADEQTHALPDTVEAIERFSRFLGYDSRDSFARDLLGYLERVQGHYAKLFEGDPTGTAKLPPVDYGAGPEDTRLLDHLLSLGYKKPLMIATTLQQWMTGGYRVLKVETTQRAFREFVPALIEELARAEQPDDAVNAFDRLLQALHRGGRLISLLSQNRELLTLVALVLGAAPRLGDMLARQPQILDGLIDPRFFGAMPDQAELSARLAVTLADAGSYEEFLDRLRLFGQESLFLIGTRILSGTVPTQQAAVAFADVAEGIVGTVHGLVSEQFASTYGRVKGQQTAILAMGKLGSREMTASSDLDLILIYDFDDDQPDSDGERSLHGAQYFARFTQRLISAFTTRTNYGVLYDVDMRLRPSGRAGPVASRLDAFAAYQEQEAWTWEHLALTRARVISAPPEFRSRIEQVIRAVLTRPRDAAIIANDVAEMRRAIAQEKGEDDVWDLKYAAGGMVDIDFIAQYLQLVHAHEAPDILHVNTLSALDNATRLGLLAQADAEVLRPAARLYQNLTQILRLCVSEKFNPDTAGDDLLRVMVRAGDAPDFSSLQARVKETQSDVRAIFNRLIGGEDA | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell. | B3QBR5 |
Q0UK52 | STHC_PHANO | Stemphyloxin II biosynthesis cluster protein C | Parastagonospora | MAPAETTGNVQRPEAGKQSMGSFWTQMFPPKPTYTEEQVPDLTGKIFIVTGSSSGVGKEAARMLYAKNAKVYMAARPGPKLPAAINSVQEAVPKSGGALIPLELDLADLAVVKKAVEKFTSLETKLHGLINNAAVQALKDTDGDARTAQGHEIHMGVNVLAPFLFTRLLTGVLTATARQEPPGTVRVVWVSSMGTETIGEKRRGLSPDYVDYWPLMSPLERYGLSKAGNWLHGVEFARRYAADGIASFPINPGHLKSDLYREGGALFKFALKPVLYPPTYGAYVELFAALSPTLTLKDSGAWSKYVEMVYFPDC | Short-chain dehydrogenase/reductase; part of the gene cluster that mediates the biosynthesis of the phytotoxin stemphyloxin II . The first step of the pathway is the synthesis of dehydroprobetaenone I by the polyketide synthase sthA and the enoyl reductase sthE via condensation of one acetyl-CoA starter unit with 7 malonyl-CoA units and 5 methylations . The C-terminal reductase (R) domain of sthA catalyzes the reductive release of the polyketide chain . Because sthA lacks a designated enoylreductase (ER) domain, the required activity is provided the enoyl reductase sthE . The short-chain dehydrogenase/reductase sthC then catalyzes reduction of dehydroprobetaenone I to probetaenone I . The cytochrome P450 monooxygenase sthF catalyzes successive epoxidation, oxidation (resulting from epoxide opening) and hydroxylation to install a tertiary alcohol in the decaline ring to yield betaenone C from dehydroprobetaenone I and betaenone B from probetaenone I . The FAD-linked oxidoreductase sthB is responsible for the conversion of betaenone C to betaenone A via an intramolecular aldol reaction between C-1 and C-17 to form the bridged tricyclic system in betaenone A . Finally, the cytochrome P450 monooxygenase sthD catalyzes the hydroxylation of C-15 to afford the final metabolite stemphyloxin II . | Q0UK52 |
P00457 | NIFH1_NOSS1 | Nitrogenase reductase | Nostoc | MTDENIRQIAFYGKGGIGKSTTSQNTLAAMAEMGQRIMIVGCDPKADSTRLMLHSKAQTTVLHLAAERGAVEDLELHEVMLTGFRGVKCVESGGPEPGVGCAGRGIITAINFLEENGAYQDLDFVSYDVLGDVVCGGFAMPIREGKAQEIYIVTSGEMMAMYAANNIARGILKYAHSGGVRLGGLICNSRKVDREDELIMNLAERLNTQMIHFVPRDNIVQHAELRRMTVNEYAPDSNQGQEYRALAKKIINNDKLTIPTPMEMDELEALLIEYGLLDDDTKHSEIIGKPAEATK | The key enzymatic reactions in nitrogen fixation are catalyzed by the nitrogenase complex, which has 2 components: the iron protein and the molybdenum-iron protein. | P00457 |
B7IE21 | PANC_THEAB | Pantoate-activating enzyme | Thermosipho | MKVIEKIEEMKKISREILESKKAIGFVPTMGFLHEGHLSLVKAAKSENDITVVSIFVNPTQFGPNEDYNNYPRDLERDLSMLKDMEVDYVFVPSVEEMYPDSFSTYVEEIKLSRFLCGASRPGHFRGVCTVVTKLFNIVKPTRAYFGQKDAQQFRVLRRMVRDLNMDVELVEMPIVREPDGLALSSRNTYLNDEERKEAVRLYKSLLKAKELIESGEKDVEIIKNEMKKILTHPLLRIDYIEIVDEENLEPVEKIDRRVIIAIAVFVGRARLIDNMII | Catalyzes the condensation of pantoate with beta-alanine in an ATP-dependent reaction via a pantoyl-adenylate intermediate. | B7IE21 |
Q9NX24 | NHP2_HUMAN | snoRNP protein NHP2 | Homo | MTKIKADPDGPEAQAEACSGERTYQELLVNQNPIAQPLASRRLTRKLYKCIKKAVKQKQIRRGVKEVQKFVNKGEKGIMVLAGDTLPIEVYCHLPVMCEDRNLPYVYIPSKTDLGAAAGSKRPTCVIMVKPHEEYQEAYDECLEEVQSLPLPL | Required for ribosome biogenesis and telomere maintenance. Part of the H/ACA small nucleolar ribonucleoprotein (H/ACA snoRNP) complex, which catalyzes pseudouridylation of rRNA. This involves the isomerization of uridine such that the ribose is subsequently attached to C5, instead of the normal N1. Each rRNA can contain up to 100 pseudouridine ('psi') residues, which may serve to stabilize the conformation of rRNAs. May also be required for correct processing or intranuclear trafficking of TERC, the RNA component of the telomerase reverse transcriptase (TERT) holoenzyme. | Q9NX24 |
B8GT00 | MINE_THISH | Cell division topological specificity factor | Thioalkalivibrio | MNFFNYFRSQKKKSAQVAKERLQVIVARERVHRDGPDYLPRLQEEILNVIRKYVQVDEDAVSIQLERDGDCEVLELNVTLPEHKA | Prevents the cell division inhibition by proteins MinC and MinD at internal division sites while permitting inhibition at polar sites. This ensures cell division at the proper site by restricting the formation of a division septum at the midpoint of the long axis of the cell. | B8GT00 |
Q6A1G2 | FUT11_XENTR | Galactoside 3-L-fucosyltransferase 11 | Silurana | MSAGCTQLVWGGRLHWGASHLLSCLLALCALWVLAAAEPTEGGSANVQGVGEAALYQGRGQHRVPSEDNVAVLSDQWEPSSFQPSSAFSGTDLGTMVADSYRGPGNSDRRSNKELPILLWWSENLFPHFPGDAERIDCPLSSCMVTKNKSVKLHKRTKSIIFYGTDFRAYEAPLPRLPHQTWALFHEESPMNNYVLSHLPGIRLFNYTATFSRESDYPLTLQWLPTIGYLHNPALSMAEKNRWRKNGYAPVLYMQSHCDVPSDRDRYVKELMKHLEIDSYGQCMKNREHPNKRLEDTSTATTEDPEFMAFTARYKFHLAMENAICADYMTEKLWRPMHLGAIPIYRGSPSVRDWMPNNHSIIMIDDFASPKELAEFIMTLDSDDEQYLKYLEYKKPGGTTNTFLLSSMEKREWGVNDMTAPNYLNGFECFVCDKENSRIKAEKTYKKSQQGGAAPEPHIADFNHMGCPMPTPGFGSAQEIPESDSWKQMWLQDYWQSFDQGEALTAMIQRNETNQDRFWDYMHETYIKRSMNH | Probable fucosyltransferase. | Q6A1G2 |
Q9CG33 | SCPA_LACLA | Segregation and condensation protein A | Lactococcus | MIKEINIKIKNFEGPLDLLLHLVSQYEMDIFEVPLVPVIEQYLIYIQTMKELELEVAGEYMLMASQLMLIKSRRLLPTVTETFIEDTEQLEYDLLAQIDEYRKYKMLSQDLDELHQERSHFYSKAKTEIITDETVLLQDKSALDLFLAFTKILELQRQHFQDENTKIAAEKFTIADKILELSTRFTEQKICKFSDLFSSSTNKDELVTTFMALLELIKNQQISFSQGELFGEIILERKETSE | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves. | Q9CG33 |
Q2JFF1 | RS13_FRACC | 30S ribosomal protein S13 | Frankia | MARLSGVDLPREKRVEIALTYIFGIGRSRSRDTLAATAVNPDTRVRDLSEEEIVRLRDWIDANYRVEGDLNREIKQDIRRKMEIGCYQGLRHRRNLPVHGQRTHTNARTRKGPRRAIAGKKKAGKK | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits; these bridges are implicated in subunit movement. Contacts the tRNAs in the A and P-sites. | Q2JFF1 |
B2HUM8 | HEM1_ACIBC | Glutamyl-tRNA reductase | Acinetobacter calcoaceticus/baumannii complex | MSFFALGVNHQTASVELREQIAFNAERLSNLLAEQRHHESLKDLVVVSTCNRTEVYAMAEDAESLLKWLADANNIDVKQLIHHVYRYENAQAITHLMRVASGLDSLMLGEPQILGQVKSALALSKEAQTVSPELNSVFEYAFYAAKRVRSETAVGSHAVSMGYAVAQLALQVFSKPEKLTVMVVAAGEMNSLVAKHLAEMGVAKMIICNRSRERADQLAQEIAHQVEVEIIDFSDLAENLYRADVVSSCTGSLHQVIAYADVKTALKKRRYQQMLMVDLAVPRDIDPKVESLDGVYLYGVDDLQSVIDENLAQRRQAAVEAEVMVNQLATQLITHQKVKEAGSTIHAYRQHSEEISQRELTQALEALHHGGNPEQVLQQFAHRLTQKLIHPTSMLLREAAKAESPDYFEWLQQHLQDVFDHERKPKR | Catalyzes the NADPH-dependent reduction of glutamyl-tRNA(Glu) to glutamate 1-semialdehyde (GSA). | B2HUM8 |
O94811 | TPPP_HUMAN | p25-alpha | Homo | MADKAKPAKAANRTPPKSPGDPSKDRAAKRLSLESEGAGEGAAASPELSALEEAFRRFAVHGDARATGREMHGKNWSKLCKDCQVIDGRNVTVTDVDIVFSKIKGKSCRTITFEQFQEALEELAKKRFKDKSSEEAVREVHRLIEGKAPIISGVTKAISSPTVSRLTDTTKFTGSHKERFDPSGKGKGKAGRVDLVDESGYVSGYKHAGTYDQKVQGGK | Regulator of microtubule dynamics that plays a key role in myelination by promoting elongation of the myelin sheath . Acts as a microtubule nucleation factor in oligodendrocytes: specifically localizes to the postsynaptic Golgi apparatus region, also named Golgi outpost, and promotes microtubule nucleation, an important step for elongation of the myelin sheath . Required for both uniform polarized growth of distal microtubules as well as directing the branching of proximal processes . Shows magnesium-dependent GTPase activity; the role of the GTPase activity is unclear . In addition to microtubule nucleation activity, also involved in microtubule bundling and stabilization of existing microtubules, thereby maintaining the integrity of the microtubule network . Regulates microtubule dynamics by promoting tubulin acetylation: acts by inhibiting the tubulin deacetylase activity of HDAC6 . Also regulates cell migration: phosphorylation by ROCK1 inhibits interaction with HDAC6, resulting in decreased acetylation of tubulin and increased cell motility . Plays a role in cell proliferation by regulating the G1/S-phase transition . Involved in astral microtubule organization and mitotic spindle orientation during early stage of mitosis; this process is regulated by phosphorylation by LIMK2 . | O94811 |
P25033 | HEMO_HYACE | Protein P4 | Hyalophora | MAFKSIAVLSACIIVGSALPVDKYPVLKDQPAEVLFRENNPTVLECIIEGNDQGVKYSWKKDGKSYNWQEHNAALRKDEGSLVFLRPQASDEGHYQCFAETPAGVASSRVISFRKTYLIASPAKTHEKTPIEGRPFQLDCVLPNAYPKPLITWKKRLSGADPNADVTDFDRRITAGPDGNLYFTIVTKEDVSDIYKYVCTAKNAAVDEEVVLVEYEIKGVTKDNSGYKGEPVPQYVSKDMMAKAGDVTMIYCMYGSNPMGYPNYFKNGKDVNGNPEDRITRHNRTSGKRLLFKTTLPEDEGVYTCEVDNGVGKPQKHSLKLTVVSAPKYEQKPEKVIVVKQGQDVTIPCKVTGLPAPNVVWSHNAKPLSGGRATVTDSGLVIKGVKNGDKGYYGCRATNEHGDKYFETLVQVN | Insect-immune protein. Forms a protein complex at the bacterial surface. Can inhibit hemocyte aggregation. | P25033 |
B2GDT7 | RL13_LIMF3 | 50S ribosomal protein L13 | Limosilactobacillus | MRTTYMAKPGQVDRKWYVVDAKGISLGRLASTVASILRGKNKPTFTPHVDTGDYVIVINAAEVKLTGKKATGKIYYRHSNHPGGLKQRTAGDFLAKDPEKMVEQTIKGMLPHTSLGRKMGMKLHVYAGESHNQAAQKPEVLDITNLI | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly. | B2GDT7 |
Q62K72 | NODI_BURMA | Nodulation ATP-binding protein I | pseudomallei group | MSVAPIDFQQVEKRYDDKLVVDGLSFHVQPGECFGLLGPNGAGKTTTLKMLLGITHPDAGSISLCGEPVPSRARHARQRVGVVPQFDNLDPDFTVRENLLVFARYFGLTAHAARALVPPLLEFAKLESKADAKVGELSGGMKRRLTLARALVNDPDVLVLDEPTTGLDPQARHLMWERLRSLLARGKTILLTTHFMEEAERLCHRLCVIEEGRKIAEGAPRMLIEAEIGCDVIEIYGPDPVQLRDELAPFAERTEISGETLFCYVDNPEPIHARLKGRAGLRYLHRPANLEDVFLRLTGREMLD | Part of the ABC transporter complex NodIJ involved in the export of the nodulation factors (Nod factors), the bacterial signal molecules that induce symbiosis and subsequent nodulation induction. Nod factors are LCO (lipo-chitin oligosaccharide), a modified beta-1,4-linked N-acetylglucosamine oligosaccharide. This subunit is responsible for energy coupling to the transport system. | Q62K72 |
Q9I7M2 | GTPBA_DROME | GTP-binding protein 10 homolog | Sophophora | MVQIFKFLLKSSKSTGRAHFRPTFLDTLRLAVRGGHGGNGLPKYGGVGGQGGCVYLVAKEGLTLRKVVQGLKDKRVAASSGEDSSKASIFGRRGADQRIEVPVGVQVYDDQQKLIADLDEHEATCIVAGGGTGGCTATNFLGRPGENRTVNLDLKLIADVGLVGFPNAGKSTLLKAVSNAKPKIAAYPFTTIRPQIGTIEYRDLRSITVADLPGLIEGAHANFGMGHKFLKHIERTRLLVFMVDIFGFQLSPKHPHRDCLANVYALNKELELYDPSLLEKPSVLLLNKMDKEGAHEIFTKVKPLVSDLASGLEQCPEELRPKQVLNFDSIVPISAMNSSKITQVKSQLRRTLVRLAEKQFLADEDQVKEKLRQRVGVVGPKIT | May be involved in the ribosome maturation process. | Q9I7M2 |
Q15NG5 | DAPF_PSEA6 | PLP-independent amino acid racemase | Pseudoalteromonas | MQVQFSKMHGLGNDFVVIDNVTQNVFFSKEKISQLADRNFGIGFDQLLVVEPPYDPEQDFHYRIFNSDGSEVSQCGNGARCFARFVKMKGLTNRNKIVVSTKAGRIVLYHERDGQITVNMGEPIFEPAKIPLKANKQENIYIIRENDHTFFCGAVSMGNPHCVLLVDDVETADVEGIGKTLVAHERFPEGANIGFMQILNSGHIKLRVYERGVGETLACGSGACAAVAVGQMQKKLNKEVTVDLPGGTLKIRWQGPGSILKMTGTAEHVFDGNITL | Catalyzes the stereoinversion of LL-2,6-diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso-DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan. | Q15NG5 |
A7H026 | FMT_CAMC5 | Methionyl-tRNA formyltransferase | Campylobacter | MNIIFMGTPAYARTILDALVRAGIGVAGVFTQPDKPVGRKQILTPSEVKIYAQQNLPHAKIFQPKTLKEGTVAAEILALKPDFIVVAAYGKILPKSVLDIAPCINLHASILPKYRGASPIQAALLNGEKNTGVTAMLMDEGLDTGDMLGFTHVSCEGKRSAEMFEILGELAGELAVKTLFDFKNLTPQKQDDALATHCKKIQKSDGLVNLSEDAEQIYNKFRAFHEWPGVFLESGLKFLELNLAEGSGAAGEILRIEKDGFVVACGTGALKILALQEAGKKALDAKAYINGKRLVAGNKIS | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus. | A7H026 |
C4L176 | HIS6_EXISA | ImGP synthase subunit HisF | unclassified Exiguobacterium | MLKRRIIPCLDVKEGRVVKGIEFVQLRDIGDPVEIAKYYDESGADELVFLDITASTERRQTMLDVVSAVARKVFIPLTVGGGIRSLEDISSLLKAGADKVSLNTLAVESPSLIREAADRFGSQCIVVAIDVKFKDGEYYVYTYGGKQKTDLLAVEWAKQVAALGAGELLVTSMNQDGKQSGYDLSILEQLREVVDIPIIASGGAGNAEHVVEALEKVDAALLASILHDRKTTVEEVKHVCKSHNLPMRFVSTKMD | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit. | C4L176 |
P0A5Y5 | MABA_MYCBO | Beta-ketoacyl-acyl carrier protein reductase | Mycobacterium tuberculosis complex | MTATATEGAKPPFVSRSVLVTGGNRGIGLAIAQRLAADGHKVAVTHRGSGAPKGLFGVECDVTDSDAVDRAFTAVEEHQGPVEVLVSNAGLSADAFLMRMTEEKFEKVINANLTGAFRVAQRASRSMQRNKFGRMIFIGSVSGSWGIGNQANYAASKAGVIGMARSIARELSKANVTANVVAPGYIDTDMTRALDERIQQGALQFIPAKRVGTPAEVAGVVSFLASEDASYISGAVIPVDGGMGMGH | Part of the mycobacterial fatty acid elongation system FAS-II, which is involved in mycolic acid biosynthesis. Catalyzes the NADPH-dependent reduction of beta-ketoacyl derivatives, the second step of the FAS-II elongation cycle. | P0A5Y5 |
P0A9G7 | ACEA_ECOL6 | Isocitratase | Escherichia | MKTRTQQIEELQKEWTQPRWEGITRPYSAEDVVKLRGSVNPECTLAQLGAAKMWRLLHGESKKGYINSLGALTGGQALQQAKAGIEAVYLSGWQVAADANLAASMYPDQSLYPANSVPAVVERINNTFRRADQIQWSAGIEPGDPRYVDYFLPIVADAEAGFGGVLNAFELMKAMIEAGAAAVHFEDQLASVKKCGHMGGKVLVPTQEAIQKLVAARLAADVTGVPTLLVARTDADAADLITSDCDPYDSEFITGERTSEGFFRTHAGIEQAISRGLAYAPYADLVWCETSTPDLELARRFAQAIHAKYPGKLLAYNCSPSFNWQKNLDDKTIASFQQQLSDMGYKFQFITLAGIHSMWFNMFDLANAYAQGEGMKHYVEKVQQPEFAAAKDGYTFVSHQQEVGTGYFDKVTTIIQGGTSSVTALTGSTEESQF | Involved in the metabolic adaptation in response to environmental changes. Catalyzes the reversible formation of succinate and glyoxylate from isocitrate, a key step of the glyoxylate cycle, which operates as an anaplerotic route for replenishing the tricarboxylic acid cycle during growth on fatty acid substrates. | P0A9G7 |
P45783 | GSPN_AERSA | General secretion pathway protein N | Aeromonas | LQANRQYLFQGSLKPGPELPEEMKQGLPFLGQPDGQGRFPLRYQGRI | Involved in a type II secretion system (T2SS, formerly general secretion pathway, GSP) for the export of proteins. | P45783 |
Q59500 | ILVC_MYCAV | Ketol-acid reductoisomerase type I | Mycobacterium avium complex (MAC) | MFYDDDADLTIIQGRKVGVIGYGSQGHAHSLSLRDSGVQVKVGLKEGSKSRAKVSEQGLDVDTPAAVAKWADVIMLLAPDTAQADIFKNDIEPNLSDGDALFFGHGLNIHFGLIKPPAEVTVAMVAPKGPGHLVRRQFVDGKGVPCLIAVDQDPTGKGEALALSYAKAIGGTRAGVIKTTFKDETETDLFGEQAVLCGGTEELVKAGFDVMVESGYPPEMAYFEVLHELKLIVDLMYEGGIARMNYSVSDTAEFGGYLSGPRVIDAGTKDRMREILRDIQNGDFVKKLVANVEGGNKQLEQLRKENVEHPIEVVGKRLRDLMSWVDRPITETA | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol-acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3-dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3-hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate. | Q59500 |
A4SDE2 | END4_CHLPM | Endonuclease IV | Chlorobium | MKRVGAHVSIAGGVENAPLNATAIGAKAFALFTRNQRQWHSPPLQKASVDAFRRHCEAGGFDARHILPHDSYLINLGNPDPDKLERSRKAFIEEMERAETLGLVLLNFHPGSHLNAIGEEECLGLIADSINLAIKATDRVTAVIENTAGQGTNLGSRFEHLRAIIDRIEDRSRIGVCLDTCHLFASGYDLGTAEAAERTFEEFDRTVGMQYLKGMHLNDALRPLGSRLDRHACIGKGMIGIEGFRYIMQSPLFEEIPLILETPDSEGWKEEIELLYSLE | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic (AP) sites, generating a 3'-hydroxyl group and a 5'-terminal sugar phosphate. | A4SDE2 |
B3R0P2 | TRMD_PHYMT | tRNA [GM37] methyltransferase | 16SrX (Apple proliferation group) | MIIEIITIFPKFFDSFFEHSIIKRAIKKNKIIFQVHDLRNYSNNKHNQVDDSPYGGGAGMLLKFPPFYECLKKIKKSFSKVILLSPQGTLLNQKMAFEYVNEIKHLIILNGNYEGIDARILNYIDAEISIGDYILTGGEIATIVLIDVLVRLLPGVINSESYLEDSHQKDLLKYPQYTKPKIYQNQKVPEILLSGNHKNIKDWRYNQSLKNTFFKRPDILKKINLTEKQQKILLEIKKKLKEG | Specifically methylates guanosine-37 in various tRNAs. | B3R0P2 |
Q9FF78 | PME46_ARATH | Pectin methylesterase 46 | Arabidopsis | MSSYGRLDEHEQAKLEASRKTKKRIAIIAISSIVLVCIVVGAVVGTTARDNSKKPPTENNGEPISVSVKALCDVTLHKEKCFETLGSAPNASRSSPEELFKYAVKVTITELSKVLDGFSNGEHMDNATSAAMGACVELIGLAVDQLNETMTSSLKNFDDLRTWLSSVGTYQETCMDALVEANKPSLTTFGENHLKNSTEMTSNALAIITWLGKIADTVKFRRRRLLETGNAKVVVADLPMMEGRRLLESGDLKKKATIVVAKDGSGKYRTIGEALAEVEEKNEKPTIIYVKKGVYLENVRVEKTKWNVVMVGDGQSKTIVSAGLNFIDGTPTFETATFAVFGKGFMARDMGFINTAGPAKHQAVALMVSADLSVFYKCTMDAFQDTMYAHAQRQFYRDCVILGTVDFIFGNAAVVFQKCEILPRRPMKGQQNTITAQGRKDPNQNTGISIHNCTIKPLDNLTDIQTFLGRPWKDFSTTVIMKSFMDKFINPKGWLPWTGDTAPDTIFYAEYLNSGPGASTKNRVKWQGLKTSLTKKEANKFTVKPFIDGNNWLPATKVPFNSDF | Acts in the modification of cell walls via demethylesterification of cell wall pectin. | Q9FF78 |
Q9LSS7 | RUBP1_ARATH | Deneddylase-1 | Arabidopsis | MGNTSDDDKILSYEDVVLRRSDLDILNGPIFLNDRVIEFYLSFLSTVHSSTTISLIPPSIAFWISNCPDTEYLKDFMKPLNLRDKDLLILPVNDNSNVEVAEGGLHWSLLVYYKEANTFVHHDSYMGVNRWSAKQLFKAVSPFVSNGDASYKECTDTPQQKNGYDCGVFLLATARVICEWFSSGGMKNRDELWFANVKETVPDLVNHLREEILALIKKLMSESVSK | Processes the pre-form of the ubiquitin-like protein NEDD8/RUB1. Has the capacity to discriminate between NEDD8/RUB1 and ubiquitin. Has no SUMO protease activity. | Q9LSS7 |
A1S212 | RPOC_SHEAM | Transcriptase subunit beta' | Shewanella | MKDLLKFLKQQGKTEEFEGIKIGLASPDLIRSWSFGEVKKPETINYRTFKPEREGLFCARIFGPVKDYECLCGKYKRLKHRGVICEKCGVEVTQTKVRRERMGHIELASPVAHIWFLKSLPSRIGLMLDMTLRDIERVLYFESYVVIEPGMTSLERGQMLTEENYLDALEEYGDEFEAKMGAEAVLDLLRAIDLEKEIEQMREELPSINSETRRKKVTKRLKLIEAFYTSGNKPEWMILKVLPVLPPDLRPLVPLDGGRFATSDLNDLYRRVINRNNRLKRLLDLAAPDIIVRNEKRMLQESVDALLDNGRRGRAITGSNKRPLKSLADMIKGKQGRFRQNLLGKRVDYSGRSVITVGPTLRLHQCGLPKKMALELFKPFIYGKLEGRGLATTIKAAKKMVEREVAEVWDVLDEVIREHPVMLNRAPTLHRLGIQAFEPVLIEGKAIQLHPLVCAAYNADFDGDQMAVHVPLTLEAQLEARALMMSTNNILSPANGEPIIVPSQDVVLGLYYISRERVNGRGEAMAFESVAEAEKAYRVGAAELHARVKVRITETIIGENGERTKQRRIVDTTVGRAILSQILPAGLSFDLVNQDMGKKQISKLLNTCYRQLGLKDTVIFADQLMYTGFQYATISGASVGINDMVIPEEKYSLVADAEAEVIEIQEQFQSGLVTAGERYNKVIDIWASANEKVSKAMMENLSSETVINRHGEEEKQKSFNSIYMMADSGARGSAAQIRQLAGMRGLMAKPDGSIIETPIVANFREGLNVLQYFISTHGARKGLADTALKTANSGYLTRRLVDVAQDLVIIEDDCGATEGLSMKPLIEGGDVVEPLRERVLGRVVAEDVMYPGTDEVLAPRNTLLDEAWCDKLEQHSVDEVQVRSVITCETDFGVCAKCYGRDLARGHIINMGEAIGVVAAQSIGEPGTQLTMRTFHIGGAASRASAENSVQVKNAGTLKLHNAKYVTNSDGKLVIVSRSSELAIIDELGREKERYKVPYGTVLDTKEGAEVNAGQIIANWDPHTHPIITEVAGSIKFVDMIDGVTITRQTDELTGLSSIVVLDVGQRTSAGKEMRPAVRLVDDNGNDLTIPGTDVPAQYFLPGNAIVNLDDNAKISVGDALARIPQESSKTRDITGGLPRVADLFEARRPKEPAILAEISGTISFGKETKGKRRLVITPNDGGDAYEEMIPKWRNLNVFEGEKVERGEVIADGPESAHDILRLRGIHNVANYIVNEVQDVYRLQGVKINDKHIEVIIRQMLRKCIITQAGDSEFLEGEQVEVARVKIANRDLEAAGKQPAKFERELLGITKASLATESFISAASFQETTRVLTEAAVGGKSDNLRGLKENVIVGRLIPAGTGFAYHKNRAKARASGEETAAPTITASEAEQNLADLLNLAGSQE | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates. | A1S212 |
Q86W10 | CP4Z1_HUMAN | Laurate 7-monooxygenase | Homo | MEPSWLQELMAHPFLLLILLCMSLLLFQVIRLYQRRRWMIRALHLFPAPPAHWFYGHKEFYPVKEFEVYHKLMEKYPCAVPLWVGPFTMFFSVHDPDYAKILLKRQDPKSAVSHKILESWVGRGLVTLDGSKWKKHRQIVKPGFNISILKIFITMMSESVRMMLNKWEEHIAQNSRLELFQHVSLMTLDSIMKCAFSHQGSIQLDSTLDSYLKAVFNLSKISNQRMNNFLHHNDLVFKFSSQGQIFSKFNQELHQFTEKVIQDRKESLKDKLKQDTTQKRRWDFLDILLSAKSENTKDFSEADLQAEVKTFMFAGHDTTSSAISWILYCLAKYPEHQQRCRDEIRELLGDGSSITWEHLSQMPYTTMCIKECLRLYAPVVNISRLLDKPITFPDGRSLPAGITVFINIWALHHNPYFWEDPQVFNPLRFSRENSEKIHPYAFIPFSAGLRNCIGQHFAIIECKVAVALTLLRFKLAPDHSRPPQPVRQVVLKSKNGIHVFAKKVC | A cytochrome P450 monooxygenase that catalyzes the in-chain oxidation of fatty acids . Catalyzes the hydroxylation of carbon-hydrogen bonds. Hydroxylates lauric and myristic acids predominantly at the omega-4 and omega-2 positions, respectively . Catalyzes the epoxidation of double bonds of polyunsaturated fatty acids (PUFA). Displays an absolute stereoselectivity in the epoxidation of arachidonic acid producing the 14(S),15(R)-epoxyeicosatrienoic acid (EET) enantiomer . Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase) . | Q86W10 |
P54045 | RS5_METJA | 30S ribosomal protein S5 | Methanocaldococcus | MRFNIDEWEPKTTIGRMVKEGQITDIDYILDNNLPILEPEIVDALLPDLEEKVLDVKLVQRMHKSGRRARFRATVVVGNRNGYVGVGKGKAKEVGPAIRKAIAQAKKNIIRVKRGCGSWECGCGTPHSIPYKGYGKCGSTAIEILPAPKGVGLVAGDVAKAVLGLAGIKDVWTKTFGETRTTYNFAMATFEALKSLNFTRTMEKHKEKLGIVEGRVL | With S4 and S12 plays an important role in translational accuracy. | P54045 |
A4QJM2 | RK20_AETGR | 50S ribosomal protein L20, chloroplastic | Aethionema | MTRIKRGYIARRRRTKIRLFASSFRGAHSRLTRTMTQQRIRALVSAHRDRGRRKRDFRRLWITRINAVIQEMEVFNSYNRFIHNLYKKQVLLNRKILAQIALLNRSCLYTISNEIIK | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit. | A4QJM2 |
Q8CDT7 | CBCO1_MOUSE | Ciliary-associated calcium-binding coiled-coil protein 1 | Mus | MNFSIEQYSKFMTLLDMLLHNLQTLHMSLEDSIKWLGEVMAEIGPNHSQKSEDFHVFEVKEANAIIDYLKISLFQHYRLYEFLFYSTREEIVIGTEQTIEVVKPADYPFPAPLEEGISLDTYSTFIEPLPTPDMEQKVLDQEQGTQEALLESEMREEDPLGGFTIDDVKSALERVTDEVLISMQKEISEKLQVQEEAFNARIEKLKKA | Calcium-binding protein . May be involved in the control of sperm flagellar movement . | Q8CDT7 |
Q9VE04 | RM55_DROME | 39S ribosomal protein L55, mitochondrial | Sophophora | MLLKQLPQAVQQIRCISSATTAVTRLHRSVYCRLYPTVVVQPDGSTINIRYHEPRKIIKLPLDLSTLTDAERRARLEARKPRKKVKIMEEVEDNFNAKKYMKYIKKK | Involved in mitochondrial biogenesis and G2/M phase cell cycle progression. | Q9VE04 |
A1V9E1 | ILVD_DESVV | Dihydroxy-acid dehydratase | Desulfovibrio | MRSKKMTHGLEKAPHRSLLHALGLTREELARPLVGVVNAANEVVPGHIHLDDIAEAVKAGVRAAGGTPLEFPAIAVCDGLAMNHEGMRFSLPSRELIADSIEIMATAHPFDALVFIPNCDKSVPGMLMAMLRLDVPSVMVSGGPMLAGATLAGRADLITVFEGVGRVQRGDMTEAELDELVEGACPGCGSCAGMFTANSMNCLAETIGLALPGNGTTPAVTAARIRLAKHAGMKVMEMLERNIRPRDIVTEKAVANAVAVDMALGCSTNTVLHLPAVFAEAGLDLTLDIFDKVSRKTPNLCKLSPAGHHHIQDLHAAGGIPAVMAELDSIGLIDRSAMTVTGRTVGENLDALGAKVRDADVIRSVDAPYSPQGGIAILKGSLAPGGAVVKQSAVAPEMMVREAVARVFDSEEAACEAIMGGRIKAGDAIVIRYEGPKGGPGMREMLTPTSAIAGMGLGADVALITDGRFSGGTRGAAIGHVSPEAAEGGPIGLVQEGDRIRIDIPARALDLLVDEDELARRRAVFVPVEKEITSPLLRRYARMVSSAATGARQR | Functions in the biosynthesis of branched-chain amino acids. Catalyzes the dehydration of (2R,3R)-2,3-dihydroxy-3-methylpentanoate (2,3-dihydroxy-3-methylvalerate) into 2-oxo-3-methylpentanoate (2-oxo-3-methylvalerate) and of (2R)-2,3-dihydroxy-3-methylbutanoate (2,3-dihydroxyisovalerate) into 2-oxo-3-methylbutanoate (2-oxoisovalerate), the penultimate precursor to L-isoleucine and L-valine, respectively. | A1V9E1 |
B2UQL7 | G1092_AKKM8 | Glycosyl hydrolase family 109 protein 2 | Akkermansia | MSIFSSRRQFLKSLGLAAGAAAAGNALPGKAVEIPAGDHLWKSASPAAPRPSGSTYMGGFKAPRLGRIRLAFIGVGGRGFSHLAQMCVMDGVEIVGICDLKEELTKRGVDRVLSRMGKSPLGYSGGDMEYLTMLKELKPDAVIISTDWSSHARIACDSMKHGAHAFVEVPLAVSLEELWSLVDTSEATRKHCMMMENVNYGRDELMFLNMVRQGVIGDLLHGEAAYIHCLVTQLGDTRGEGAWRPEYHTRINGNLYPTHGLGPVAQYMNLERGEDRFCRVAAFASPALGRNAYAKKHLPADHRWNNTPFICGDMNTAVVKTQLGRTILVQLDETSPRPYSRANLIQGTEGTLAGFPTRVAGEKLGNGNYHEWIEGREKLAAIYEKYDHPLWKRIGELATKMGGHGGMDFVMLSRIVECLRNGEPMDQNVYEGASWSSLLPLTARSIAQGGMPVEFPDFTRGDWKTTMPLAVVS | Glycosidase. | B2UQL7 |
B0VNK1 | ATPD_ACIBS | F-type ATPase subunit delta | Acinetobacter calcoaceticus/baumannii complex | MAELLTLARPYAKAAFAYASEQGATDNWSNALQVLSAAVQDEAFSAYLNRPEHTPAEQVKLFAKVLGEDQSQAVSNFLTLLADNDRLVLLPEIAAEYEQLKSQNNNNVDVVIESAFPLTAEQEQLLKSALEKRFNSTVTVSVEVKPELIAGVVIRAGDQVIDDSALNKLEKMRTRLLA | This protein is part of the stalk that links CF(0) to CF(1). It either transmits conformational changes from CF(0) to CF(1) or is implicated in proton conduction. | B0VNK1 |
B9DUP5 | RNZ_STRU0 | tRNase Z | Streptococcus | MELQFLGTGAGQPAKQRNVSSLVLKLLDEINEVWMFDCGEGTQRQILETSIKPRKIQKIFITHLHGDHIFGLPGFLSSRAFQASEEQTDIEIFGPLGIKSFVQNSLAISGTRLPYKIHFHEFTDKDMGKIMETDKFLVYAEKLAHTIFCMGYRVVQKDLEGTLDAEALKKAGVPFGPLFGKIKNGQDIVLDDGRQILAKDYISEPKKGKVITILGDTRKTPASQRLALNADVLVHESTYGKGDDRIARNHGHSTNMQAAQIAKDANVKRLLLNHVSARFLSRDCRQMEKDAASLFENVKIVKDLEEVTI | Zinc phosphodiesterase, which displays some tRNA 3'-processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA. | B9DUP5 |
C6E7L6 | RLMH_GEOSM | rRNA (pseudouridine-N3-)-methyltransferase RlmH | unclassified Geobacter | MRLKLLWVGKTQESWVRTGIEEYAGRIRRYAPLEILEAREEKGAQAAAMRERECERLAKLIPKGGRLVLLDERGEAMTSPELASFLSKNRDQGTQDLVFAIGGAYGFTDAFRSQAFKSISLSRMTLTHQMVRVFLLEQIYRGFTIINGEPYHHE | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA. | C6E7L6 |
A8YXL4 | RS17_LACH4 | 30S ribosomal protein S17 | Lactobacillus | MSETNERNRRHVYQGRVVSDKMDKTIVVVVDTYKNHPVYSKRIRYSKKYYAQDENNEAKVGDTVRIMETRPLSRKKRFRLVKIVKKSV | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA. | A8YXL4 |
P48145 | NPBW1_HUMAN | G-protein coupled receptor 7 | Homo | MDNASFSEPWPANASGPDPALSCSNASTLAPLPAPLAVAVPVVYAVICAVGLAGNSAVLYVLLRAPRMKTVTNLFILNLAIADELFTLVLPINIADFLLRQWPFGELMCKLIVAIDQYNTFSSLYFLTVMSADRYLVVLATAESRRVAGRTYSAARAVSLAVWGIVTLVVLPFAVFARLDDEQGRRQCVLVFPQPEAFWWRASRLYTLVLGFAIPVSTICVLYTTLLCRLHAMRLDSHAKALERAKKRVTFLVVAILAVCLLCWTPYHLSTVVALTTDLPQTPLVIAISYFITSLSYANSCLNPFLYAFLDASFRRNLRQLITCRAAA | Interacts specifically with a number of opioid ligands. Receptor for neuropeptides B and W, which may be involved in neuroendocrine system regulation, food intake and the organization of other signals. Has a higher affinity for neuropeptide B. | P48145 |
B2VFA0 | YIHI_ERWT9 | Der GTPase-activating protein YihI | Erwinia | MKQPARTSQVKKPAARVKRKTREEINQEARDRKREKKHSGHASGSRANPATVSQKGDKSQSVKDPRIGSKKAIALGTDAPVRQPANPVKAAKPAVEKKPRLTPEEELAKLENDERLDALLDRLENGEALSAEDQAWLDQSLDRIDVLMEQLGIALDDDAEDEKAEEDMYRLLKGSHRTPE | A GTPase-activating protein (GAP) that modifies Der/EngA GTPase function. May play a role in ribosome biogenesis. | B2VFA0 |
A6TBX4 | NUOA_KLEP7 | NUO1 | Klebsiella | MRMSTSTEVIAHHWAFAIFLIIAIGLCCLMLVGGWYLGGRARARSKNTPFESGIDSVGSARLRLSAKFYLVAMFFVIFDVEALYLYAWSTSIRESGWVGFVEAAIFILVLLAGLVYLVRIGALDWTPARSRRTLVNPETDSPTNRHMQ | NDH-1 shuttles electrons from NADH, via FMN and iron-sulfur (Fe-S) centers, to quinones in the respiratory chain. The immediate electron acceptor for the enzyme in this species is believed to be ubiquinone. Couples the redox reaction to proton translocation (for every two electrons transferred, four hydrogen ions are translocated across the cytoplasmic membrane), and thus conserves the redox energy in a proton gradient. | A6TBX4 |
Q8GSM3 | LOX22_HORVU | LOX2:Hv:2 | Hordeum | MQTATKPLVGARAVPLSRRASFLVAEARRKPSTNARRTRVGSTSTTTTTTTILTDVNGPALTTVAKPGHQYDLKQTVEMKATVSVHMKSFWWSDEKKERARDWAYDLILGSWLTLELVSSELDPKTGQEHDVISGKLKHSRETEKDYDLYEAIFTCRHRLAPSGAVRLVNYHHTEMLLGEVKIFPAGEDPTKSSAVTLFHCQSWIDPSHCSPDKRTFFPVEKSYIPSQTPKGVEKLRKSELEALRGNGCGERKKHDRIYDYDVYNDLGKPESKRPVLGGKEHPYPRRCRTGRPRSKTDPSSEEESHKKGEMYVPRDETFTERKEQAFLTKQLLSQLHGLCTGLKVNKDILPSFPTLASIDALYDDDFRNQPVQPEGGKVRLILDLLAKELVHLVKLEGAEFVEGIRRVFKFETPEIHDMDKLAWFRDEEFARQTLAGMNPLSIQLVTELPIVSKLDELKYGPADSLITKELIEKQINRIMTAEEAVAQKKLFMLDYHDLLLPYVHRVRKLDNKTMYGSRTLFFLADDGTLRPIAIELTRPKSPHKQQWRKVFTPGSGYSGSVTGSWEWQLAKIHVLSHDTGYHQLVSHWLRTHCCVEPYVIAANRQLSQMHPIYRLLHPHFRFTMEINAQARGMLICADGIIEKTFSPGEFSMEISSAAYDKQWRFDMEALPEDLIRRGMAVRGEDGKLELAIEDYPYANDGLLVWDAIKQWASDYVAHYYPCAVDIVDDEELQDWWTEVRTKGHPDKQDEPWWPELDCHESLVQVLATIMWVTSAHHAAVNFGQYPMAGYVPNHPSIARRNMPCEMGPEEMLAFKAAPEKVWLDTLPSQLQTVMVMATLDLLSSHASDEEYMGTHQEPAWQRDGEVDKAFQVFQKKMRDIAEQVEEWNKDDSRRNRHGAGVVPYVLLRPLNGNPMDAKTVMEMGIPNSISI | Plant lipoxygenase may be involved in a number of diverse aspects of plant physiology including growth and development, pest resistance, and senescence or responses to wounding. This enzyme exhibits linoleate 13-lipoxygenase activity. | Q8GSM3 |
Q9Y597 | KCTD3_HUMAN | Renal carcinoma antigen NY-REN-45 | Homo | MAGGHCGSFPAAAAGSGEIVQLNVGGTRFSTSRQTLMWIPDSFFSSLLSGRISTLRDETGAIFIDRDPAAFAPILNFLRTKELDLRGVSINVLRHEAEFYGITPLVRRLLLCEELERSSCGSVLFHGYLPPPGIPSRKINNTVRSADSRNGLNSTEGEARGNGTQPVLSGTGEETVRLGFPVDPRKVLIVAGHHNWIVAAYAHFAVCYRIKESSGWQQVFTSPYLDWTIERVALNAKVVGGPHGDKDKMVAVASESSIILWSVQDGGSGSEIGVFSLGVPVDALFFIGNQLVATSHTGKVGVWNAVTQHWQVQDVVPITSYDTAGSFLLLGCNNGSIYYIDMQKFPLRMKDNDLLVTELYHDPSNDAITALSVYLTPKTSVSGNWIEIAYGTSSGAVRVIVQHPETVGSGPQLFQTFTVHRSPVTKIMLSEKHLVSVCADNNHVRTWTVTRFRGMISTQPGSTPLASFKILSLEETESHGSYSSGNDIGPFGERDDQQVFIQKVVPITNKLFVRLSSTGKRICEIQAVDCTTISSFTVRECEGSSRMGSRPRRYLFTGHTNGSIQMWDLTTAMDMVNKSEDKDVGGPTEEELLKLLDQCDLSTSRCATPNISPATSVVQHSHLRESNSSLQLQHHDTTHEAATYGSMRPYRESPLLARARRTESFHSYRDFQTINLNRNVERAVPENGNLGPIQAEVKGATGECNISERKSPGVEIKSLRELDSGLEVHKIAEGFSESKKRSSEDENENKIEFRKKGGFEGGGFLGRKKVPYLASSPSTSDGGTDSPGTASPSPTKTTPSPRHKKSDSSGQEYSL | Accessory subunit of potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 3 (HCN3) up-regulating its cell-surface expression and current density without affecting its voltage dependence and kinetics. | Q9Y597 |
Q72HM3 | FABZ_THET2 | Beta-hydroxyacyl-ACP dehydratase | Thermus | MDIREILKVLPHRYPFLLVDRVLEADERRFKALKNVTFNEPHFQGHFPGHPVMPGVLILEAMAQAAVGALVRQPGFPQGGLAFLAGVEGARFRRPVYPGDTLILEGELLAFRRGVGKVAVRALVEGEERASATLTFVLQGAS | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs. | Q72HM3 |
Q8JI40 | CRVP_GLOBL | Cysteine-rich venom protein ablomin | Gloydius | MIVFIVLPILAAVLQQSSGNVDFDSESPRKPEIQNEIVDLHNSLRRSVNPTASNMLKMEWYPEAAANAERWAYRCIEDHSSPDSRVLEGIKCGENIYMSPIPMKWTDIIHIWHDEYKNFKYGIGADPPNAVSGHFTQIVWYKSYRAGCAAAYCPSSEYSYFYVCQYCPAGNMRGKTATPYTSGPPCGDCPSACDNGLCTNPCTQEDVFTNCNSLVQQSNCQHNYIKTNCPASCFCHNEIK | Blocks contraction of smooth muscle elicited by high potassium-induced depolarization, but does not block caffeine-stimulated contraction. Since high potassium-treatment activates voltage-gated channels and caffeine exposure activates ryanodine receptors, this toxin may target L-type voltage-gated calcium channels (Cav) (and not ryanodine receptors) on smooth muscle . This toxin also shows a little inhibition on cyclic nucleotide-gated CNGA1 channel . | Q8JI40 |
A0KF26 | RL22_AERHH | 50S ribosomal protein L22 | Aeromonas | MEAIAKHRYARTSAQKARLVADQVRGLSVDKALNILTFSPKKAAALVKKVLESAIANAEHNEGADIDALRVATIMVDEGPSMKRIRPRAKGRADRILKRTAHITVVVSDAKAGR | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome. | A0KF26 |
Q635G3 | BIOD_BACCZ | Dethiobiotin synthase | Bacillus cereus group | MSGFFITATDTEVGKTVVAGALAGVFRELGYNIGVYKPLQSGHVASNPEGDAARLKALSGVPTKEDEICPYSIEEPLAPRLAMKRAGRTVTLKDIIHHYNERLKEFNSLFVEGAGGLAVPYTEDALVIDFAKELQLPLIVVARPTLGTVNHTVLTIAYAKAHGLTVAGVILSGCKECEMERVQENKVMIEELSGVPVLGLLPFFEGEFTKKEVLESAKEYIMISKLEECIRNESTVAHTSSN | Catalyzes a mechanistically unusual reaction, the ATP-dependent insertion of CO2 between the N7 and N8 nitrogen atoms of 7,8-diaminopelargonic acid (DAPA, also called 7,8-diammoniononanoate) to form a ureido ring. | Q635G3 |
Q04KR9 | DAPA_STRP2 | 4-hydroxy-tetrahydrodipicolinate synthase | Streptococcus | MSYQDLKECKIITAFITPFHEDGSINFDAIPALIEHLLDHHTDGILLAGTTAESPTLTHDEELELFAAVQKIVNGRVPLIAGVGTNDTRDSIEFVKEVAEFGGFAAGLAIVPYYNKPSQEGMYQHFKAIADASDLPIIIYNIPGRVVVELTPETMLRLADHPNIIGVKECTSLANMAYLIEHKPEEFLVYTGEDGDAFHAMNLGADGVISVASHTNGDEMHEMFIAIAESDVKKAAAIQRKFIPKVNALFSYPSPAPVKAVLNYMGFEAGPTRLPLVPAPEEDAKRIIKVVVDGDYEATKATVTGVLRPDY | Catalyzes the condensation of (S)-aspartate-beta-semialdehyde [(S)-ASA] and pyruvate to 4-hydroxy-tetrahydrodipicolinate (HTPA). | Q04KR9 |
B7IGQ4 | PLSX_THEAB | Phosphate-acyl-ACP acyltransferase | Thermosipho | MKKIAIDLMGGDYAPEEILAGALSFAKENEDVELYLVGIEENFKDVQLPKNCVKVVTDDFLPMDVKPTEAVRRRKSTMYVSCQLAREKKVDAVVSAGNTGALLACATFVVGRIKGIERPTLAVPIPTKNDFCVLADAGANIDVKPSNLLQFAIMGVEYAKLLGKDNPTIGLLNVGTEENKGTQKEKEAFQILKERFGNQFVGNVEGNDLNAGKVDVVVADGFHGNIAMKTMEGAAKMITELIKSEVKKNIISALGALLMKPVFSSLKNKLDPKKYGGTFFIGVEGVVVKAHGNSNRTAIFNALKVAKKGVEEKLPLKIKEALLKCAE | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl-[acyl-carrier-protein] (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA. | B7IGQ4 |
A2C6X2 | ATPF2_PROM3 | F-type ATPase subunit b' | Prochlorococcus | MTSLLLFGAGGLFDFDATLPLMALQVVLLTFILNALFFRPVGRVVEEREVYVTTSRAEAKQKLAEAEKLELELKEQLKSARIAAQQLIQEAEKDSEQLYREALAIANADANAAREKARREIDAQRDSALTQLKGDAEKLGDLIVNRLLAAK | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0). The b'-subunit is a diverged and duplicated form of b found in plants and photosynthetic bacteria. | A2C6X2 |
Q4KLT6 | FL2D_XENLA | Wilms tumor 1-associating protein | Xenopus | MTNEEPLPKKVRLNESDFKVLPREDLLQRWKQYEAYVQALENKYTDLNSNDVTGLRESEEKLKQQQQESARRENILVMRLATKEQEMQECTNQIQHLKQVQQPSVAQLRATMVDPAINLFFIKMKAELEQTKDKLEQAQNELSAWKFTPDSQTGKKLMAKCRMLIQENQELGRQLSQGRIAQLEAELALQKKYSEELKSSQDELNDFIIQLDEEVEGMQSTILVLQQQLKDSRQQLSQFQQQIQISGNRTPSSEPKDEGETSGKDCGRILNGPSNGGSSLQRTHSSAGLYREGSSTEDDFSASPINEGKLSNHSQERTSRDGSSYINPLSTGYESVDSPTGSENSLTHQSNDTDSNHDSQEEKPVSGKGNRTVSSRHLQNGLDSSVNVQGSVL | Associated component of the WMM complex, a complex that mediates N6-methyladenosine (m6A) methylation of RNAs, a modification that plays a role in the efficiency of mRNA splicing and RNA processing. | Q4KLT6 |
Q1GVN5 | RS11_SPHAL | 30S ribosomal protein S11 | Sphingopyxis | MAREPQRLRRRERKNISSGVAHVNATFNNTMITITDAQGNAIAWSSAGMMGFKGSRKSTPYAAQVCAEDAGKKAAEHGVRTLEVEVKGPGAGRESALRALQAVGFHITSIRDVTPIPHNGVRPAKRRRV | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome. | Q1GVN5 |
C0K3N1 | TXVE_BITAR | VEGF-F | Bitis | MAAYLLAVAILFCIQGWPSGTVQGEVRPFMEVYQRSVCQPRETLVSILEEYPDKISKIFRPSCVAVLRCGGCCSDESLTCTSVGERTVELQVMQVTPKTLSSKIKVMKFREHTACECRPRSGSRVNIGKHKRSPEEGEREPSSPLTPGSL | Snake venom VEGFs that may contribute to venom dispersion and prey subjugation by inducing vascular permeability and hypotension. This protein induces an increase in capillary permeability after intradermal injection, as well as a drastic hypotensive effect after intravenous injection. The hypotension is mediated by nitric oxide (NO), which is produced by VEGF-activated endothelium NO synthase. Also induces angiogenesis in vitro, probably through VEGF receptor (KDR/VEGFR-2) signaling. | C0K3N1 |
Q8DSD7 | RS6_STRMU | 30S ribosomal protein S6 | Streptococcus | MAKYEILYIIRPNIEEEAKNALVARFDAVLTDNGATIVESKDWEKRRLAYEIQDFREGLYHVINVETEDAHALNEFDRLSKINNDILRHMIVKLDA | Binds together with S18 to 16S ribosomal RNA. | Q8DSD7 |
C3P8M5 | LEPA_BACAA | Ribosomal back-translocase LepA | Bacillus cereus group | MNKEERAKRQSKIRNFSIIAHIDHGKSTLADRILEKTNALTQREMKAQLLDSMDLERERGITIKLNAIQLNYKAKDGEEYILHLIDTPGHVDFTYEVSRSLAACEGAILVVDAAQGIEAQTLANVYLALDNNLEILPVINKIDLPSADPERVRQEVEDVIGLDASEAVLASAKAGIGIEEILEQIVEKVPAPTGDSEEPLQCMIFDSLYDPYRGVIAYIRVVNGTVKVGDKVRMMATGKEFEVTEVGVFTPKTTQRDELTVGDVGFLAASIKNVGDTRVGDTITHAKRPAAEPLAGYRKLNPMVFCGLYPIDSARYNDLRDALEKLELNDSALEFEPETSQALGFGFRCGFLGLLHMEILQERIEREFKIDLITTAPSVIYKVFLTNGEDMIVDNPSNMPDPQTIDRVEEPFVKAAIMVPNDYVGAVMEICQGKRGTFIDMQYLDETRVTLTYEIPLSEIVYDFFDQLKSNTKGYASFDYELIGYKPSKLVKMDILLNSEQVDALSFIVHRDSAYDRGKVIVEKLKELIPRQQFEVPIQATIGNKVVARSTIKAMRKNVLAKCYGGDISRKRKLLDKQKEGKKRMKSVGSVEVPQEAFMAVLKMDDN | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back-translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner. | C3P8M5 |
O35652 | LHX8_MOUSE | LIM/homeobox protein Lhx7 | Mus | MYWKSDQMFVCKLEGKEVPELAVPREKCPGLMSEECGRPAALAAGRTRKGAGEEGLVNPEGAGDEDSCSSSAPLSPSSSPQSMASGSVCPPGKCVCSSCGLEIVDKYLLKVNDLCWHVRCLSCSVCRTSLGRHTSCYIKDKDIFCKLDYFRRYGTRCSRCGRHIHSTDWVRRAKGNVYHLACFACFSCKRQLSTGEEFALVEEKVLCRVHFDCMLDNLKREVENGNGISVEGALLTEQDVNHPKPAKRARTSFTADQLQVMQAQFAQDNNPDAQTLQKLAERTGLSRRVIQVWFQNCRARHKKHVSPNHSSSAPVTAVPSSRLSPPMLEEMAYSAYVPQDGTMLTALHSYMDAHQQLLDSSPCYPIQ | Transcription factor involved in differentiation of certain neurons and mesenchymal cells. | O35652 |
B4U741 | EFG_HYDS0 | Elongation factor G | unclassified Hydrogenobaculum | MPRTVPIQDLRNIGIVAHIDAGKTTTTERILYYTGKTYKIGEVHEGAATMDWMPQEKERGITITAATTACYWAGKQINIIDTPGHVDFSVEVVRSMRVLDGIIFIFSAVEGVQPQSEANWRWADKFNVARIAFINKLDRLGADFYRVYDEIVKKLTIKPVAIQIPIGTEDNFVGVVDLMNMNAIIWLEETLGAKYEIRDIPEEYKAKAQEWREKMVESIAETDDTLMEKYLEGQEISTDELKQALRKATINKQLVPVLCGSSFKNKGVQPLLDAVVDYLPSPLDVPSVVGINPKTVQEETRLPEDDQPFCAYIFKVVSDPYAGQLSYFRVFSGKVQAGSYVLNSTKDKKERVGRLLLMHANTREDITEVAAGEIAAAVGVDAATGDTICDEKSPIILEKLEFPEPVISMAIEPKTKKDQEKLSQVLNKFMKEDPTFKASMDPETGQTLIHGMGELHLEIMVDRMKREYNIEVNVGKPQVAYKEAIKGKAVAEGKFIRQTGGRGQYGHVVIEVEPLERGSGFVFENAIVGGVIPKEFIPPVEEGIKEAMENGVLAGYPVVDVKVKLFDGSYHEVDSSEIAFKIAGSMAFKEAAKKASVVLLEPIMEVEVETPDDYVGDVIGDLNSRRGKIMGMENKGIITSIKAHVPLSEMFGYATNLRSLTQGRGTFIMKFSHYSEAPQSITEKVVGERTHT | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post-translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome. | B4U741 |
B9DN91 | RS4_STACT | 30S ribosomal protein S4 | Staphylococcus | MARFRGSNWKKSRRLGISLSGTGKELEKRPYAPGQHGPNQRKKLSEYAIQLREKQKLRYLYGITERQFHNTFIEAGKQSGVHGENFMRLLARRLDAVVYALGLARTRRQARQLVGHGHIEVDGKRVNIPSYTLKPGQVVSVREKSQKLDIIQESVEINNFVPEYLDFDEEKLSGTFVRVPERSELPAEINEQLIVEYYSGK | With S5 and S12 plays an important role in translational accuracy. | B9DN91 |
A4X491 | GATB_SALTO | Aspartyl/glutamyl-tRNA(Asn/Gln) amidotransferase subunit B | Salinispora | MTTTLPAYDEVVARYEPVIGLETHVELGTNTKMFCGCPTDFGGAPNTRVCPVCLGLPGSLPVANRAAVEATIRIGLALNCSIAEWCRFARKNYYYPDMPKNYQISQYDEPLCVDGYLDVEVDGEPVRISIERVHMEEDTGKTLHVGGATGRIHGATESLVDYNRAGIPLVEIVTKPIPGAGAMAPEVARAYVTELRDVLRSLGVSDVRMEEGSLRCDVNTSLNLPGEQWGTRTETKNVNSLRSVERAVRSEMIRQASVLEGGGRITQETRHFHEDTGDTTSGRSKETATDYRYFPEPDLVPVAPDPTWVAELKAALPELPRLHRRRLQQEWGLSDLDMQSILNAGAVELIEATIAAGATPTAARKWWLGELSRRANEAGVELADIGATPEQVAELQGLVDAGKLTDKLARTVLEHVVAGEGSPAKIMADRNLEVVSDTGALTAAVDEAIAANPAIADKVRGGKVAAAGALVGAVMKTTRGQADAKTVRELILERLGVQG | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp-tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln). | A4X491 |
B4SBU6 | RS10_PELPB | 30S ribosomal protein S10 | Pelodictyon | MAVQQKIRIKLKSYDHSLVDKWALRIIDVVKQTDAIIFGPIPLPTKSHVYTVNRSPHVDKKSREQFSFSSHKRLIEIINPTSRTIDMLMKLELPSGVDVEIKS | Involved in the binding of tRNA to the ribosomes. | B4SBU6 |
B6JN80 | NTPP_HELP2 | Nucleotide pyrophosphatase | Helicobacter | MELILGSQSSARANLLKEHGIKFEQKALYFDEESLKTTDPREFVYLACKGKLEKAKELLANNCVIVVADSVVSVDNRMQRKAQSKREALEFLKRQNGNEIEVLTCSALISPKLEWLDLSVFRARLKAFDPSEIEKYLESGLWQESAGCVRLEDFHRPYIKSSSKNLSVGLGLNVEGLLGALKLGAKIASL | Nucleoside triphosphate pyrophosphatase. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. | B6JN80 |
A6UC30 | UREF_SINMW | Urease accessory protein UreF | Sinorhizobium | MAEHADTQALLRLVTWLSPAFPVGSFSYSGGLEQAIHQGLVTSADDLRLWCETLLERGNTWNDALLLSESYRAYGDAQRLIAVSELAEALAGSRERHMETMLLGEAFLAAAGHWPHPSLAVLGTKAAYPVSVGAVAGAHRTGLKPALAAFLNATVSNAVSVAIRCGITGQRDGVGVLARVEDTIGAVVARAAAASLEDLGGATFIAEIASLKHENLHSRLFRS | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter. | A6UC30 |
P0CW31 | VPB16_MYCTU | Putative antitoxin VapB16 | Mycobacterium tuberculosis complex | MALWYQAMIAKFGEQVVDAKVWAPAKRVGVHEAKTRLSELLRLVYGGQRLRLPAAASR | Putative antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC16. | P0CW31 |
A0ZZ18 | PSBK_GOSBA | Photosystem II reaction center protein K | Gossypium | MLNIFNLICICFNSALFSSSFLFAKLPEAYAFLNPIVDFMPVIPVLFFLLAFVWQAAVSFR | One of the components of the core complex of photosystem II (PSII). PSII is a light-driven water:plastoquinone oxidoreductase that uses light energy to abstract electrons from H(2)O, generating O(2) and a proton gradient subsequently used for ATP formation. It consists of a core antenna complex that captures photons, and an electron transfer chain that converts photonic excitation into a charge separation. | A0ZZ18 |
Dataset Card for Prot2Text-Data
Page: Prot2Text
Paper: https://arxiv.org/abs/2307.14367
Github: https://github.com/hadi-abdine/Prot2Text
Authors: Hadi Abdine(1), Michail Chatzianastasis(1), Costas Bouyioukos(2, 3), Michalis Vazirgiannis(1)
(1)DaSciM, LIX, École Polytechnique, Institut Polytechnique de Paris, France.
(2)Epigenetics and Cell Fate, CNRS UMR7216, Université Paris Cité, Paris, France.
(3)Bioinformatics Research Laboratory, Department of Biological Sciences, University of Cyprus, Nicosia, Cyprus.
Prot2Text paper is published in AAAI 2024. Preliminary versions of the paper were accepted as a spotlight at DGM4H@NeurIPS 2023 and AI4Science@NeurIPS 2023.
Dataset Description
This dataset is designed for training the Prot2Text framework. It contains information for 256,690 proteins and is comprised of three modalities:
- Protein sequence (amino acid sequence).
- Protein structure using its AlphaFold accession ID.
- Textual description of the protein
The dataset is built from the SwissProt database, a component of UniProtKB Release 2022_04.
Dataset Structure
Data Fields:
- name: (string) codename of the protein.
- Full Name: (string) Full name of the protein.
- sequence: (string) Amino acid sequence of the protein.
- AlphaFoldDB: (string) Accession ID of the protein in AlphaFold database.
- taxon: (string) Species information for the protein.
- function: (string) Textual description of the protein.
Data Splits:
The dataset is split into training, validation, and test sets with a maximum sequence similarity threshold of 40% within each set using the CD-HIT clustering algorithm.
- Train: 248,315 proteins
- Validation: 4,172 proteins
- Test: 4,203 proteins
Considerations for Using the Data
The dataset is built from a single source (SwissProt). Consider incorporating data from other sources to increase diversity. The textual descriptions may contain biases present in the original database. Be mindful of these biases when using the data for downstream tasks.
License
We are releasing this dataset under the terms of CC-BY-NC-4.0.
Citation
Please cite this dataset and the original sources if you use this dataset in your work
@inproceedings{abdine2024prot2text,
title={Prot2Text: Multimodal Protein's Function Generation with GNNs and Transformers},
author={Abdine, Hadi and Chatzianastasis, Michail and Bouyioukos, Costas and Vazirgiannis, Michalis},
booktitle={Proceedings of the AAAI Conference on Artificial Intelligence},
volume={38},
pages={10757--10765},
year={2024}
}
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