entry stringlengths 6 10 | entry_name stringlengths 5 11 | protein_name stringlengths 3 2.44k | sequence stringlengths 2 35.2k | function stringlengths 7 11k |
|---|---|---|---|---|
A3QJT2 | YIDD_SHELP | Putative membrane protein insertion efficiency factor | MAQAQSPLQWLATKLIRGYQIFISPILGPKCRFHPTCSNYALEAIRLHGFVKGSWFAGKRVLKCHPLHPGGEDPVPPKNNRCNK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A4G419 | FETP_HERAR | Probable Fe(2+)-trafficking protein | MTRMVHCIKLDKEAEALDFPPYPGELGKRIYESVSKEAWAAWLKHQTMLVNENRLNLADVRARKYLATQMEKHFFGEGADAAQGYVPPTE | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4GZ97 | CAPSD_TTVG1 | Capsid protein | MPFWWGRRNKFWYGRNYRRKKRRFPKRRKRRFYRRTKYRRPARRRRRRRRKVRRKKKTLIVRQWQPDSIVLCKIKGYDSIIWGAEGTQFQCSTHEMYEYTRQKYPGGGGFGVQLYSLEYLYDQWKLRNNIWTKTNQLKDLCRYLKCVMTFYRHQHIDFVIVYERQPPFEIDKLTYMKYHPYMLLQRKHKIILPSQTTNPRGKLKKKKTIKPPKQMLSKWFFQQQFAKYDLLLIAAAACSLRYPRIGCCNENRMITLYCLNTKFYQDTEWGTTKQAPHYFKPYATINKSMIFVSNYGGKKTEYNIGQWIETDIPGEGNLAR... | Self-assembles to form an icosahedral capsid with a T=1 symmetry, about 30 nm in diameter, and consisting of 60 capsid proteins. The capsid encapsulates the genomic DNA. Capsid protein is involved in attachment and entry into the host cell (By similarity). |
A4HH79 | EFTS_LEIBR | Elongation factor Ts, mitochondrial (EF-Ts) (EF-TsMt) | MLHRSFFRFAALADKKAFMELVKALRYRTEAPISDCSAALTEAAGDMDAAMQLLRKRGVARAMKKGDCVTEHGFVVSCVGSTPASGAAIITMCSETDFAARNEHFQRTCVQARDQLRKLMDATNGAVLANPEEAAKQLSDIMGEELRAAIAVLGENMRIRSIAPLVPAPHMSERLLVGSYTHGVLNVDGVGRIVGLVAVSQVRENEVISKDVLTSIGRHFVATSGAEGNYAHQNFFGSETETVGKWLKHHGLTFSSSLVQEFGKEPVVHTAAEPHQ | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF-Tu.GTP complex up to the GTP hydrolysis stage on the ribosome. {ECO:0000255|HAMAP-Rule:MF_03135}. |
A4IFN2 | MEDAG_BOVIN | Mesenteric estrogen-dependent adipogenesis protein | MAGLESAPAARPSLTSISSGELRSLWTCDCELALLPLGQLLRLQPGAFQLRGDQLVVPAPAEPASARGGFNVFGDGFVRLDGQLYRLSSYMRRYVELTNYCDYKDYRETILSKPMLFFVHVQTKKDSLKERTYAFLVNTRHPKIRRQIEQGMDMVISSVIGESYRLQFDFQEVVKNFFPPGNKVVNGEDLSFAYEFKADALFDFFYWFGLSNSTVKVNGKVLNLSSTSPEKKETIKLFLEKMSEPLIRRSSFSDRKFSVTSRGSIDEVFNCNLSPRSSLMEPLVAELPFPCVLESEETPNPFI | Involved in processes that promote adipocyte differentiation, lipid accumulation, and glucose uptake in mature adipocytes. |
A4IJC5 | SP5G_GEOTN | Putative septation protein SpoVG | MEVTDVRLRRVNTEGRMKAIASITLDNEFVVHDIRVIDGNNGLFVAMPSKRTPDGEFRDIAHPINSATRGKIQEAILAEYHRLGKLEEELEEAGAS | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
A4IK94 | LUTC_GEOTN | Lactate utilization protein C | MTRGTIQNRDAFLQNIAKRLGRSPRLSGVSQPQWDYAPQWTVFAGYSQDDLLSALREQCKLIHTDYIETTSSELAGALKQQVAAYGGGPVIVPDDPRFAEYGLSALLHDEWPAEQTAVHVWNSSLGRQNIDAAEQANVGIAFSEITLAESGTVVLFSRNEQGRTIHFLPKTYIAIVPKSSVVPRMTQAAAYIHEQIEKGAVVPSCINFITGPSNSADIEMNLVVGVHGPMKAAYIVVTDR | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}. |
A4IK96 | LUTA_GEOTN | Lactate utilization protein A | MKVSLFVTCLIDLFYTNVGKATVELLERLGCEIDFPEAQTCCGQPAYNSGYIKDAKEAMKQMMRAFADADYVVTPSGSCAAMLKEYPHIFRGDPEWEEEAKRLAAKTYELTQFLVNVLRVEDVGASLPGRATYHTSCHMTRLLGEKEVPLRLLEHVKGLELVPLPNAHQCCGFGGTFSVKMGPISEQMVDEKIEHIEEVKADYLIGADCGCLMNIGGRIGRVGKPIRVMHIAEVLNHRN | Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}. |
A4J671 | Y2057_DESRM | UPF0122 protein Dred_2057 | MKEFHKINLLNDYYGSLLTERQQNFIELYYGEDLSLGEIAEQYNVTRQAVHDTLKRAEQTLTNYEEKLGLVSKFSQESKSLVEVINLLDGYESGEAPEGLEKSKGILKKILEKRQDL | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A4JBR5 | HRCA_BURVG | Heat-inducible transcription repressor HrcA | MLDPRARTLLKTLIERYIADGQPVGSRTLSRYSGLELSPATIRNVMSDLEELGLVSSPHTSAGRVPTPRGYRLFVDTMLTVEAPIDAEAVARQVQNTLQAGEPQQRVVAAAASVLSNLSQFAGVVLTPRRSHVFKQIEFMRLSDKRILLIIVTPEGDVQNRMLATPRDYTPSQLTEASNYINAHFAGLSFDEVRRRLRDEIDQLRGDMTTLMHAAVTASTEVPDTEDTVLISGERNLLEVADLSSDMARLRKLFDVFDQKTGLLQLLDVSSHAQGVQIFIGGESTLVPIEEMSVVTAPYEVNGKIVGTLGVIGPTRMAYN... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A4JG35 | FETP_BURVG | Probable Fe(2+)-trafficking protein | MARMIQCAKLGKEAEGLDFPPLPGELGKRIYESVSKEAWQGWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGDGADQASGYVPPTEG | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4JJ47 | YIDD_BURVG | Putative membrane protein insertion efficiency factor | MKTVLIALLRFYKVAVSPMLGDRCRFYPSCSDYAREAIQYHGAARGTYLAVRRVCRCHPFSAGGIDLVPPPNSDIRARGEADARSHRL | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A4PBP9 | MVP_RGDV | Movement protein (Non-structural protein 7) (Pns7) | MVKLRDISTIAVSESTHNFEVFSGLEGVSDTVANLKSENVEINVLGHNPGSLNILIDASPHFRDEKALSDCFGPQMGGVVYDSYDRMVMKNGRIENYPDTEIPTLDVTPLNVDRSLTPKQKENRNKCKKLFDHLLLEIQRGKITAGCVDDYFAFMHAAYCVLSKVYLPRFKYKHFEISSRLVTIHECNNNTKPSLFWSNRDDESHDYMTIIQMMVQVFSNAMTKYATSHLINEYHNDLDSPTSDILTKVVDELKDIDIEPATYATIVYLWLTGEDEIEDLDVLAVIFDECRSDGFVDNLLVRMLPPCEGASLTSEAIDTG... | Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier (By similarity). |
A4QFZ9 | HRCA_CORGB | Heat-inducible transcription repressor HrcA | MVSATEKRRYEVLRAIVADYIASQEPVGSKSLLERHKLNVSSATIRNDMSVLESDGFIVQEHASSGRVPTERGYRLFVDSIHDIKPLSLAERRAILGFLEGGVDLEDVLRRSVQLLSQLTHQAAVVQLPTLKTARVKHCEVVPLSPMRLLLVLITDTGRVDQRNVELEEPLAAEEVNVLRDLLNGALGEKTLTAASDALEELAQQAPTDIRDAMRRCCDVLVNTLVDQPSDRLILAGTSNLTRLSRETSASLPMVLEALEEQVVMLKLLSNVTDLDQVRVHIGGENEDIELRSATVITTGYGSQGSALGGLGVVGPTYMD... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A4QGT2 | NRDI_CORGB | Protein NrdI | MLIVYFSSATDNTHRFVQKLDLPNVRIPLTRVEEPLKINEPYVLITPTYGGGVSMTGENSRPVPPQVIRFLNDEHNRSFIRAVVAGGNSNFGSDFGLAGEIISKKCKVPYVYRFELMGNEEDVSILRGGLTQNAQALGLEPQEPVTSR | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
A4QUA4 | LCL2_MAGO7 | Long chronological lifespan protein 2 | MQSPVLLQLLLLALMGTVSAQFGGFFDQMFGGGGGGGGGQQQRQEQNVPSDSAWYRSNVDAAVCSNYLCPDTLACVHFPHHCPCPFPDHEDKFELAEGQRICVSRGGFKAGEAARKVELARKGLL | Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway. |
A4SFR7 | HRCA_CHLPM | Heat-inducible transcription repressor HrcA | MGSRELSLRERQVLGIIIQSYVVTAAPVGSRYIARNYSLGLSDATIRNVMADLEDEGYIHQPHTSAGRIPTDLGYRYYVDLIMKVQRIDEDEKRRMETDYGQIAMEHPGTSRDVLLSAAKVLGCISRQLSVVLSPTLSDAVFERLDMVLLSSTRMMVILSIHSLFVKTIVMELPLEVSRKMIEEVSNVINERLAGLTLSEIRRSIAHRLAGSHGDGALKDLIVRSAGSLFDESPIFERLYISGTEYIVDQPEFKQPERVRELITMIEDKFSVARLVEKSGHMSEALRPSDMDVTISIGSENSTREAEDLTIVSTPYYAGN... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A4SIF7 | FETP_AERS4 | Probable Fe(2+)-trafficking protein | MSRTVFCQRLKKEGPGLDFQLYPGELGKRIFDNISKEAWTEWQKKQVMLINEKKLNMMNLEHRQLLEKEMVSYLFEAGEVAIDGYTPPSQ | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4SQJ8 | SYDP_AERS4 | Protein Syd | MSDQVLSALEHFFLRWQRDGEARRGLPLCEWEADWRSPCELDEPREGRVAWRPHQRQQAADFAAMANALELVLHPAAQALFGHWFSRPIPCSYKGLRLEIILPWNEADLNLLRENLIGHLLMLRKLKRTPSLFIATTRNEMTLVSLDNESGQVWLEWLDSGRRLTLAPSLPAFLERLETLPH | Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}. |
A4STS6 | YIDD_AERS4 | Putative membrane protein insertion efficiency factor | MAHSVTPLQWVAVKLIRLYQLIISPLLGQRCRFTPTCSQFAIEAIRLHGFIKGVWLASKRLLKCHPLSEGGYDPVPQPKRRN | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A4SYB3 | FETP_POLAQ | Probable Fe(2+)-trafficking protein | MARMVQCIKLNKEAEGMDFAPLPGELGKKIWNQVSKEAWAAWLKQQTMLINENRLNMADPRARQYLLKQVEKYFFEGGADMAQGYVPEAE | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4T2C4 | HRCA_MYCGI | Heat-inducible transcription repressor HrcA | MGSAEDRRFEVLRAIVADFVATKEPIGSKTLVDRHNLGVSSATVRNDMAVLEAEGYITQPHTSSGRVPTEKGYREFVDRLDDVKPMSSAERRAILSFLESGVDLDDVLRRAVRLLAQLTRQVAVVQYPMLSTSTVRRLEVVALTPARLLLIVITDSGRIDQRIVELGDAIDEDELTQLRDLLGQALEGKPLTTASIAVSDLASHLGGQGRLANAVGRSATVLVESLVEHREERLLLGGTANLTRNTADFGGSLRSLLEALEEQVVVLRLLAKQQEAGKVTVRIGHETEAEEMAGASVVTTAYGSAGKVFGGMGVLGPTRM... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A4TDU4 | NRDI_MYCGI | Protein NrdI | MANIVYFSSVSENTHRFVQKLELPAIRIPLKDRIRVEEPYVLILPTYGGGHANGPDPDRGGYVPKQVIAFLNDEHNRSLIRGVIAAGNTNFGAEFGYAGVVVSRKCDVPFLYRFELMGTTDDVFAVRAGLQDFWKDQSCPQPSQLQNR | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
A4TGQ2 | FDHE_YERPP | Protein FdhE homolog | MSIRIVPKDQLGKQREKGTTAGNIPPLLFANLKSLYTRRTERLQQLALDNPLADYLDFAAKITEAQQKALHDHPLVLDMQAELVQSAASGKPPLDGSVFPRTEHWRKLLSALIAELRHDAPDHILAVLDNLDKASVHELELYADALLNRDFSQVGSEKAPFIWAALSLYWAQMASQIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTHNGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLASLILDAKMEGEGFARSSINPFLFPGE | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
A4TI59 | FETP_YERPP | Probable Fe(2+)-trafficking protein | MSRTIFCTFLKKDAEGQDFQLYPGEIGKRIYNEISKEAWSQWITKQTMLINEKKLSMMNIEDRKLLEQEMVNFLFEGQDVHIAGYTPPSK | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4TLA1 | SYDP_YERPP | Protein Syd | MDLNISTALRSFTQRYIDLWQQQTGHLPASKELYGVPSPCIVETGEDQVFWQPQAFLPEATLTNIERALEIQLHPDIHDFYTQQYAGDMMADLGNHRFTLLQVWSEDDFIRLQENLIGHLVTQKRLKLSPTLFLATTSSEMTMASLCNVSGNVVLEQFGSDKRTLLASTLSHFLDALRPVLPE | Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}. |
A4TSL2 | YIDD_YERPP | Putative membrane protein insertion efficiency factor | MASPLSPGSRILIGLIRGYQLVISPLLGPRCRFHPTCSHYGIEALRRFGMIKGSWLTLKRVLKCHPLNSGGDDPVPPKLDDNREH | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A4TSQ1 | LCRV_YERPP | Virulence-associated V antigen (Low calcium response locus protein V) | MIRAYEQNPQHFIEDLEKVRVEQLTGHGSSVLEELVQLVKDKNIDISIKYDPRKDSEVFANRVITDDIELLKKILAYFLPEDAILKGGHYDNQLQNGIKRVKEFLESSPNTQWELRAFMAVMHFSLTADRIDDDILKVIVDSMNHHGDARSKLREELAELTAELKIYSVIQAEINKHLSSSGTINIHDKSINLMDKNLYGYTDEEIFKASAEYKILEKMPQTTIQVDGSEKKIVSIKDFLGSENKRTGALGNLKNSYSYNKDNNELSHFATTCSDKSRPLNDLVSQKTTQLSDITSRFNSAIEALNRFIQKYDSVMQRLL... | Possibly involved in calcium regulation of YOP expression, which includes the export process. |
A4VFW9 | FDHE_STUS1 | Protein FdhE homolog | MAGTILEPGQIEAAASKPPFTNLPPRDLFALRSARLAKLAEDHPLADYLRLLAGVCQAQQQVLDNPPASAPLDPARTRECFKHAMPPLAADTLVREGAWLPLLDAWLDAFAVPDNLSVIAAVDQLRRADSGQRKAWAVALVSGQYDSLPPALVPFLGAALQLAWTHWLLQLDLSDLREREDQTLCPCCGAPPMAGVIRHRGQLNGLRYLVCSLCACEWHYVRLKCSHCRSTKKLDYLHFEGSPQGIKAEACPECNGYLKQLYLELAPDGESLSADLATLDLDLLLADQGYNRQAPNLLLAPGHEA | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
A4VRX0 | FETP_STUS1 | Probable Fe(2+)-trafficking protein | MTRTVNCRKYNQELPGLERPPFPGQKGEDIYNNISRQAWDDWQKHQTMLINERRLNMMNAEDRKFLQGEMDKFFSGEDYAKAEGYVPPSE | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4VU40 | YABA_STRSY | Initiation-control protein YabA | MDKKEIFDALDDFSQNLLTTLAEVDAIKKHLQGVIDENTTLRLENSKLRERLEKEDKTGHKSSNFGKENLENIYEDGFHICTFSYGQRRDNDEPCMFCVELLNRD | Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}. |
A4VUQ2 | Y875_STRSY | UPF0122 protein SSU05_0875 | MKFMEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFQVSRQAVYDNIKRTEKLLEDYEMKLHMYSDYVVRSQIFDEILNKYPEDAYLKEKIAILTSIDNRE | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A4W0D2 | YABA_STRS2 | Initiation-control protein YabA | MDKKEIFDALDDFSQNLLTTLAEVDAIKKHLQGVIDENTTLRLENSKLRERLEKEDKTGHKSSNFGKENLENIYEDGFHICTFSYGQRRDNDEPCMFCVELLNRD | Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}. |
A4W0Z7 | Y878_STRS2 | UPF0122 protein SSU98_0878 | MKFMEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFQVSRQAVYDNIKRTEKLLEDYEMKLHMYSDYVVRSQIFDEILNKYPEDAYLKEKIAILTSIDNRE | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A4WDN8 | NRDI_ENT38 | Protein NrdI | MSVLVYFSSSSENTLRFIERVGLPAVRIPLNERERIQVDEPYILVVPSYGGGGTAGAVPRQVIRFLNDPHNRALIRGVIAAGNRNFGDAFCRAGDLISQKCGVPYLYRFELMGTQQDVENVRKGVNEFWQRQPQNA | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
A4WDY0 | SYDP_ENT38 | Protein Syd | MDIETANALTAFTARYCDAWHEMNGTWPQSEELYGVPSPCIITTMDDKILWQPQPFSLEQTVNAVERAMDIVVQPAVHAFYTTQFAGDMQARFANETMTLLQTWSENDFQRVQENLIGHLVTQKRLKLAPTLFIATLDSELDVIAVCNLNGEVIKETLGTRKRDVLAPSLADFLNQLEPVL | Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}. |
A4WE99 | FETP_ENT38 | Probable Fe(2+)-trafficking protein | MARTIFCTYLQRDAEGQDFQLYPGDLGKRIFNEISKEAWAQWQQKQTMLINEKKLTMMNPDHRKLLEAEMVNFLFEGKEVHIEGYTPPEK | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4WGB3 | FDHE_ENT38 | Protein FdhE homolog | MSIRIIPQDELGSSEKRTADYIPPLLFPRLKNLYNRRAERLRELAENNPLGDFLRFAALIAHAQEVVLYDHPLQIDLTARIKEANDQGKPPLDIHVLPRDKHWHTLLQSLIAELKPEMSGPALAVIENLEKASALELEEMASALFAADFALVSSDKAPFIWAALSLYWAQMASLIPGKARAEYGEARQFCPVCGSMPVTSMVQIGTTQGLRYLHCNLCETEWHVVRIKCSNCEQTRDLNYWSLENENAAVKAESCGDCGTYLKILYQEKDPKVEAVADDLATLVLDAHMEQEGFARSSINPFLFPGEGE | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
A4WGH3 | YIDD_ENT38 | Putative membrane protein insertion efficiency factor | MAPPLSPGSRVLIGLIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFDTREH | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A4WNL6 | YIDD_CERS5 | Putative membrane protein insertion efficiency factor | MSPLAQIFALPVRAYRLLLSPWVGHGCRYQPTCSVYALEALERHGALKGGWLAARRILRCHPWGGSGYDPVPGADPEHDRRPRG | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A4WXK6 | COWN_CERS5 | N(2)-fixation sustaining protein CowN (CO weal-nitrogenase) | MNDHTPDRYVTFLGIDCDAKADRMMEMLSARLASTDSPWVRYFEQKLAEKARMATDNLHFVGSQINSLYSFFEEAEDEEGLDLLWHLEHNCC | Is required to sustain N(2)-dependent growth in the presence of low levels of carbon monoxide (CO). Probably acts by protecting the N(2) fixation ability of the nitrogenase complex, which is inactivated in the presence of CO. {ECO:0000255|HAMAP-Rule:MF_02117}. |
A4XGE7 | SP5G_CALS8 | Putative septation protein SpoVG | MQVTDVRIRKITNEGRMKAIVSVTFDNCFVVHDIKIIEGQNGLFIAMPSRKTPEGEFKDIAHPINQEMRDMVQKAVIEKYEAVISAGE | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
A4Y091 | FETP_PSEMY | Probable Fe(2+)-trafficking protein | MTRTVLCRKYKQELPGLDRAPYPGPKGEDIFANVSKQAWDEWQKHQTMLINERRLNMMNAEDRKFLQTEMDKFLSGEEYAQAEGYVPPSE | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4Y525 | SYDP_SHEPC | Protein Syd | MSCLPALDKFLQNYHQAYLTTLGELPRYYPQGEPSVCIQGEFFADSDKPIAWQPVKRDEVGSFTNVEHALDLPLWPDIHLFYGQYFSAPLLFDSKWGTGELLQVWNDDDFKCLQQNVIGHLMMKKKLKQPPTWFIGLLDEGDKMLTINNSDGSVWIEIPGEEQSEQLSTSLTAFIEALSPRIAPPVKHEELPMPALDHPGIFANIKRMWQNLFGKS | Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}. |
A4Y8Y7 | FETP_SHEPC | Probable Fe(2+)-trafficking protein | MARTVNCVYLNKEADGLDFQLYPGDLGKRIFDNISKEAWGLWQKKQTMLINEKKLNMMNVDDRKFLEEQMTSFLFEGKEVEIEGFVPEKDQD | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A4YCM3 | YIDD_SHEPC | Putative membrane protein insertion efficiency factor | MAQTQSPLQWLATTLIRGYQIFISPILGPRCRFNPTCSHYAIEAIKVHGTAKGCWFALKRILKCHPLHPGGSDPVPPKNDRCNK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5CVC4 | YIDD_CLAM3 | Putative membrane protein insertion efficiency factor | MKRALTSVVLAPRNAAIAVISLYRRVVSPIYGDVCRYYPSCSAYGLEAVQEHGLVHGGVLAAWRVCRCHPWAEGGIDDVPARRVQQYRRTRLGFVVAPSHGKG | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5D3X8 | HRCA_PELTS | Heat-inducible transcription repressor HrcA | MKLDDRKQKVLLAIVHDYIATAEPVGSRTIAKKYKLGVSPATIRNEMADLEEMGYIEQPHTSAGRIPSERGYRYYVDYLMKRQELSREEEELIRREYEAKVRDVGQVIQKTGQLLSQLTNYTAVVLSPQIESSRFKYIQLVSMHPSQAMVIVVMDNGIVHNRMIEVPESITCADMETISRVLNAKLRGLTMESIRLTLMKEIYFELARHKHILDLAMELIQDSLLHKVEDKIYLGGVFNMLNQPEFHDVEKVKTLLGILEQEKLLRDLITSGGSEEGVTVRIGGEIMHEDIRECSMVTAPYSVCGRKIGSLGVLGPTRME... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A5DMM1 | IRC6_PICGU | Increased recombination centers protein 6 | MAQNNVLVLGAPHSGKLRASAIIGAGFSGDGDFSGSHSGLIFKIKRQTKYFKHDLSIMVDEYPEKRTITPSWEHLNAWSDEFMSEDMEELRRALDGIVFCLNLDDKATMKDLEPTIGVLEKIYESLGGAEWAGFFAIVGVSSSEDNENHAIVEDAATIRGFEYINLEEEGQNEFRDKLGIDRLVELFDTHDWSDIETSEDDGFAARKRKMAESMCQRLLDDDEKDMSSENGVNDVNVEEFENVIEKLKQARIKAESMEGAERNEYAQQVMEDVLSYL | Involved in gross chromosomal rearrangements (GCRs) and telomere healing. |
A5DP59 | LCL2_PICGU | Long chronological lifespan protein 2 | MHLIYFLFLVVGCSASLFDFIQNQFGGGGQAQKSPEHYEAQVLNSNCDKYLCPGTSLCVDAPKFCPCPYPSSQLRCFLPDGRYLCISKPAGDVAANYDDPRTNWKVDAKDDNIRDCGWVSRAWKGVV | Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway. |
A5E0N1 | LCL2_LODEL | Long chronological lifespan protein 2 | MLQKFLICLSLIFTLASANLFDFLNNQFQGGNGGGGGGRHQNGGSKSPQQHEEAMLNANCNTYLCPDTGICVDAPKFCPCPYPSSQLRCFLPDGRYVCISKPAGYGIADKYNDPQTNFKIDAKDDNIRDCGWVNRAWRNEKLKK | Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway. |
A5F9I5 | FETP_VIBC3 | Probable Fe(2+)-trafficking protein | MARTVFCTRLQKEADGLDFQLYPGELGKRIFDNICKEAWAQWQTKQTMLINEKKLNMMDPEHRKLLEQEMVNFLFEGKEVHIEGYTPPAK | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A5FPT3 | HRCA_DEHMB | Heat-inducible transcription repressor HrcA | MLTSRAEIILRSIVRQYITKAVPVSSSSILEDCGLDICSATIRNEVVRLEIEGYILRPHHSAGSIPADKGYRYYVESLKDVELPTNDKFLIRHLFHQVEKEMEEWLNLTVAVLSQRVQSMAVVTMPRQTQGKVHHIELVSLQDNLVLVVLILRGAKVKQQLVNFENVVSQPELTLISNRLNDAYDGLTRFQIEQKPLGLNHDELKVKDSLVKMMRGEDEQESREPFFDGLHYMLEQPEFHQNQRAQEIMQLLEQKKLSKMIVPPMPFNRGVQVYIGQENASAEIRDYSLIVSQYGIPDEAVGTIGVIGPTRMAYERALSA... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A5G0F7 | YIDD_ACICJ | Putative membrane protein insertion efficiency factor | MNTATKLLRGGVRAYQLTLSSVLGGQCRFYPSCSAYAMEALAVHGALHGSALAARRILRCHPWNPGGVDPVPPAHHHDEMKQNG | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5G9V5 | YIDD_GEOUR | Putative membrane protein insertion efficiency factor | MLNIIATRSILFYQRYISPFKGSSCRFYPSCSHYSLQSLEKYGFLKGLLYSVRRIMKCHPFHPGGYDPVK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5GP57 | HRCA_SYNPW | Heat-inducible transcription repressor HrcA | MELLPRRQQEVLQATVHHYVDTIEPVGSKTLVQRFGLQASSATVRSAMGALEQKGLLVQPHPSAGRIPSPRGYRHYVDCLLPKPGAAVHHLEQELTQLSLRWAALDDLLQQLTRRLTDFTGLMSLITLPQPSEQRLHAIRLVPTDERLLVMLVADSSQTHHLNLRLPHGSVHQVAALERWTDDQLHQSGQISWESLPQQLQTCGQALREALHNEEGRFISPSDQSAHVHGVSRLVAQPEFSDSTKVAPLLDLMDCNPAAFIPSGPGHDDWVWIGGEHPHTALSDCSVIQSSYRDGQGGVGQVALVGPMRMAYATARAAVQ... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A5GWB6 | HRCA_SYNR3 | Heat-inducible transcription repressor HrcA | MLPLPRRQQQVLQATVQHYVDTVEPVGSRTLVRRFGLDASPATVRSAMGALEQKGLLTQPHTSAGRVPSPKGYRQFVDALLPEPGAAVVQLQRELAELSLQWAALDDLLHHLARRLADLTGLMSIITRPQRQEPRLKALRLVRSGDRLLVFLVESSAASSSLNLRLPPDSSAQLQALEHWLNDQLSKSAINWSGLPSHLQSVGAPLKQALASHNRGRNRQAEGALTTGLAGLLCQPEFQLTTSLRPLLQLVEQQPHELLNPAAATASGGVWIGQEHPHPALSGCAVVQAPYATASGGEGSVALVGPMRMAYATALAAVEA... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A5I4M8 | Y2450_CLOBH | UPF0122 protein CBO2450/CLC_2298 | MEEIVEMSLLLDFYGSLLTEKQNKIMDLYYNNDYSLKEISELTNTSRQAVHDIVKRCHKALLQYEEKLHMMERFINLENSKEKLLNMLNKVTKENIKEIDHIKKYIIDNI | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A5I7S1 | SP5G_CLOBH | Putative septation protein SpoVG | MQITDVRVRKIAAEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPDGEYKDIAHPINTETREKIQKSIIEEYERAKMEEESSEKVQE | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
A5I819 | YIDD_CLOBH | Putative membrane protein insertion efficiency factor | MKNLLICIIKMYRKYISPLKRPSCRFYPTCSQYSIEAIEKYGALKGTLISIKRILKCHPFNEGGYDPVK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5ID85 | FETP_LEGPC | Probable Fe(2+)-trafficking protein | MSRTVFCCKLKQEAEGLEKQPFPGELGKKVFNEVSKQAWNMWLSHQTMLINEYRLNLIEARAREFLKEEMQKYFFGEGSEKPSGYKEIK | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A5IIT2 | HRCA_THEP1 | Heat-inducible transcription repressor HrcA | MRRLNRKNSDASKKLNDRQRKVLYCIVREYIENKKPVSSQRVLEVSNIEFSSATIRNDMKKLEYLGYIYQPHTSAGRIPTDKGLRFYYEEMLKISKETSEADLAVETFKSMPLADPEKVLFLAGNLLARLTEGYVLIERPNTRDLKILRVMLIPVSEDYLIFSILTEFGVSRVTPIKTQERLNWEEIERQLNFLLRGKTIGEVLLGRIESLKGSGFLRLIESLIGETIERYLDAGLENLLKDETLALEDIRNLLEEIKDQKFLESLVGEGISVMIGREIGRKNLEKFAVFSGRYFKGESPIGSVYFFTSKVTRYDRNHKI... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A5IMC3 | YIDD_THEP1 | Putative membrane protein insertion efficiency factor | MKKLLIMLIRFYQRYISPLKPPTCRFTPTCSNYFIQALEKHGLLKGTFLGLRRILRCNPLSKGGYDPVPEEFSFKPRRRWS | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5IQ38 | YABA_STAA9 | Initiation-control protein YabA | MDRNEIFEKIMRLEMNVNQLSKETSELKAHAVELVEENVALQLENDNLKKVLGNDEPTTIDTANSKPAKAVKKPLPSKDNLAILYGEGFHICKGELFGKHRHGEDCLFCLEVLSD | Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}. |
A5IQ50 | SP5G_STAA9 | Putative septation protein SpoVG | MKVTDVRLRKIQTDGRMKALVSITLDEAFVIHDLRVIEGNSGLFVAMPSKRTPDGEFRDIAHPINSDMRQEIQDAVMKVYDETDEVVPDKNATSEDSEEA | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
A5IQT4 | NRDI_STAA9 | Protein NrdI | MKIIYFSFTGNVRRFIKRTELENTLEITAENCMEPVHEPFIIVTGTIGFGEVPEPVQSFLEVNHQYIRGVAASGNRNWGLNFAKAGRTISEEYNVPLLMKFELHGKNKDVIEFKNKVGNFNENHGREKVQSY | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
A5ISC1 | Y1295_STAA9 | UPF0122 protein SaurJH9_1295 | MGQNDLVKTLRMNYLFDFYQSLLTNKQRNYLELFYLEDYSLSEIADTFNVSRQAVYDNIRRTGDLVEDYEKKLELYQKFEQRREIYDEMKQHLSNPEQIQRYIQQLEDLE | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A5ITB0 | HRCA_STAA9 | Heat-inducible transcription repressor HrcA | MITDRQLSILNAIVEDYVDFGQPVGSKTLIERHNLNVSPATIRNEMKQLEDLNYIEKTHSSSGRSPSQLGFRYYVNRLLEQTSHQKTNKLRRLNQLLVENQYDVSSALTYFADELSNISQYTTLVVHPNHKQDIINNVHLIRANPNLVIMVIVFSSGHVEHVHLASDIPFSNDKLNTISNFVTNKLTEFNQNLQDDIVSFVQSEQEEIFINKLINTMNNHISNQSNSIYMGGKVKLIDALNESNVSSIQPILQYIESNRIAELLQDISSPNINVKIGNEIDDSLSDISIVTSQYHFDETLKGQIAVIGPTAMHYQNVIQL... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
A5ITW0 | YIDD_STAA9 | Putative membrane protein insertion efficiency factor | MKKIFLAMIHFYQRFISPLTPPTCRFYPTCSEYTREAIQYHGAFKGLYLGIRRILKCHPLHKGGFDPVPLKKDKSASKHSHKHNH | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5KB67 | EFTS_PLAVS | Elongation factor Ts, mitochondrial (EF-Ts) (EF-TsMt) | MKLHTLVMFTLVIGSPLLPQHRCYRNSQTFQLVHTLNKFVGRRRRALKPTLHANPPSEHLQNLKYVREVTNASIQICNDALKECKGDVEKAIELVRRSAKNSSFVSTSVKVKTEGLVGSQVGGDQVVMLEVLTDSDFVARNEKFVRFVRTLLGAALAGGAAHGGAVTGEGSGATALLSLPYDEQSGGSHSGGPHIAHSTTTVGEQMNYLRNIFREDVRIGRFARYERKNANQFLHCYIHNRVEENIGTSGVLLVLTIDELSEKLKSQGECIAEVANDMALHILSAKPVSVSVSDLPEQVVKREVAIIRESLRGVKKPEGI... | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF-Tu.GTP complex up to the GTP hydrolysis stage on the ribosome. {ECO:0000255|HAMAP-Rule:MF_03135}. |
A5LFW8 | TKTI1_MACFA | Tektin bundle-interacting protein 1 | MQTLRREAARPYVPSGTLEASFPAPLYSDDYLSLEGPRWPLVIRQATRWKYTPMGRDAAGQLWYTGLTNSDTREAWYNLPLDPASPFREAYNRWHGCYQRREHTMPSAYTQHLRETAWHDPIIPAQYQVPSTRWGSTLWKDRPIRGKEYVINRNRYGVEPLWRASDYVPSLSAPQRPPGTTQNYREWGLEPYCPSTCQRPLPSSTPMPR | Microtubule inner protein (MIP) part of the dynein-decorated doublet microtubules (DMTs) in cilia axoneme, which is required for motile cilia beating. Located at the center of the tektin bundle where may function to recruit tektins or stabilize the bundle. |
A5N454 | YIDD_CLOK5 | Putative membrane protein insertion efficiency factor | MKKFLIFLIKVYRKYISPLKVPCCRFYPTCSQYVLEALQKHGIIKGGFMSIKRILRCNPFCKGGYDPVK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5N4I4 | SP5G_CLOK5 | Putative septation protein SpoVG | MQITDVRVRKIAAEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPDGEFKDIAHPINTQTREKIQKAILGEYEKVKNEETVTEEKVEE | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
A5N811 | Y1400_CLOK5 | UPF0122 protein CKL_1400 | MEERIRLSILLDIYGELLTEKQRNVLDLYYNQDLSLAEIAEHTSTSRQAVYDIIKRCHMLLVHYEDKLNLMEEKKNIEENKKGIIDFIDSLYSDKNAEVLDKIKNYIMNNI | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A5PLI4 | LR2BP_DANRE | LRP2-binding protein | MDCSELDSTEKSKPSQLLRAINQIYEEGREESTHSETNAASVEKTMNLLKEKAETGDSQATFLLGQLHYVQGCYAEAELIFDRIKDKDPQALYQLAVIYYDGLGTKEDLGRAVEYMGRVAFWDSSEAGSVRYAALYNLGQAYLEGFGVQASSSEAERLWLLAADNGNPNASVKAQSALGMFYSRPESLDLRKAFFWHSQACGNGSLESQAALGLMYLYGHGVQRDSDSALFCLKEAAERGSVYAQGHLTACYYRRQLYSRAAALGQRVCEYKDTAAIAQQTDCLEEYVRKGIAIGMFYYARCLHLGRGVPQNRDKAKHYC... | May act as an adapter that regulates LRP2 function. |
A5UBC8 | FDHE_HAEIE | Protein FdhE homolog | MSIKILSESEIKQVANSYQAPAVLFANPKNLYQRRAKRLRDLAQNHPLSDYLLFAADIVESQLSTLEKNPLPPQQLEQLNAIEPLNAKTFKRDSIWREYLTEILDEIKPKANEQIAATIEFLEKTSSAELEEMANKLLAQEFNLVSSDKAVFIWAALSLYWLQAAQQIPHNSQVENAENLHHCPVCGSLPVASIVQIGTSQGLRYLHCNLCESEWNLVRAQCTNCNSHDKLEMWSLDEELALVRAETCGSCESYLKMMFQEKDPYVEPVADDLASIFLDIEMEEKGFARSGLNPFIFPAEEA | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
A5UDW5 | FETP_HAEIE | Probable Fe(2+)-trafficking protein | MARTVFCEYLKKEAEGLDFQLYPGELGKRIFDSVSKQAWSEWIKKQTMLVNEKKLNMMNAEHRKLLEQEMVNFLFEGKDVHIEGYVPPSN | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A5UFI3 | FDHE_HAEIG | Protein FdhE homolog | MSIKILSESEIKQVANSYQAPAVLFANPKNLYQRRAKRLRDLAQNHPLSDYLLFAADIVESQLSTLEKNPLPPQQLEQLNAIEPLNTKTFKRDSIWREYLTEILDEIKPKANEQIAATIEFLEKASFAELEEMANKLLTQEFNLVSSDKAVFIWAALSLYWLQAAQQIPHNSQVENTENLHHCPVCGSLPVASIVQIGTSQGLRYLHCNLCESEWNLVRAQCTNCNSHDKLEIWSLNEELALVRAETCGSCESYLKMMFQEKDPYVEPVADDLASIFLDIEMEEKGFARSGLNPFIFPAEEA | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
A5UHR4 | FETP_HAEIG | Probable Fe(2+)-trafficking protein | MARTVFCEYLKKEAEGLDFQLYPGELGKRIFDSVSKQAWGEWIKKQTMLVNEKKLNMMNAEHRKLLEQEMVNFLFEGKDVHIEGYVPPSN | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A5UID4 | YIDD_HAEIG | Putative membrane protein insertion efficiency factor | MAETHSLGTKILIKIIRLYQIMISPFIGARCRFVPTCSCYGIEALKTHGLLKGGWLTLKRVLKCHPLNAGGFDPVPPKTNNNDEKK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5VCE6 | YIDD_RHIWR | Putative membrane protein insertion efficiency factor | MIGRLIILLARAWQMGPSLVLPPTCRYVPSCSAYTIEAVSRYGALKGGWLGFRRICRCHPWGGSGFDPVP | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5VIR6 | YIDD_LIMRD | Putative membrane protein insertion efficiency factor | MVRILCDLIRWYQQGISAQRPFRVCRFTPSCSQYMLEALQRFGLKGILLGSWRLLRCQPFSRGGYDPVPNHFTFRRQG | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5VKN9 | Y1156_LIMRD | UPF0122 protein Lreu_1156 | MEIEKNYRINSLFEFYQPLLTKKQNDYLELYYGDDYSLGEIAENFHVSRQAVYDNIKRTESILEDYEAKLHLYAEFQVRNQQADRIQRYVRENYPDDATLNHLVNHLESLEEE | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A5VQK8 | YIDD_BRUO2 | Putative membrane protein insertion efficiency factor | MGSCGGKHTGKGAPKPYSRNFTDPWRKTPGRLFGTALIRFYQITLSSLIGNSCRHLPTCSEYAYEAIARHGLWRGGWMGFFRVVRCGPFGTHGFDPVPRELSPDLKWYMPWRYWRCSASRTGK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A5VU41 | NRDI_BRUO2 | Protein NrdI | MSLIVYFSSRSGNTHRFVERLGVRSSRIPLEASGALQVREPFVLVTPTYGGGSTKGAVPNPVIRFLNDADNRALIRGVIAAGNSNFGEAFCIAGNIISAKCGVPYLYRFELLGTAEDVGNVRNGMEQFWTRQTQA | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
A5VX68 | FETP_PSEP1 | Probable Fe(2+)-trafficking protein | MTRTVMCRKYQEELPGLERPPYPGAKGQDIFEHISQKAWADWQKHQTMLINEKRLNMMNAEDRKFLQAEMDKFFAGEEYAQAEGYVPPAE | Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}. |
A5W9N5 | CBPM_PSEP1 | Chaperone modulatory protein CbpM | MSSTLIVQLDMRTLCQEADVTAECVIEIVEHGIVEPSGRTPEDWLFDDQAPLVTKRAVKLHQELELEWEGVALALELLQEVQQLRSENNMLKQRLGRFIQM | Interacts with CbpA and inhibits both the DnaJ-like co-chaperone activity and the DNA binding activity of CbpA. Together with CbpA, modulates the activity of the DnaK chaperone system. Does not inhibit the co-chaperone activity of DnaJ. {ECO:0000255|HAMAP-Rule:MF_01155}. |
A5WBB8 | YIDD_PSEP1 | Putative membrane protein insertion efficiency factor | MRKLALVPIQFYRYAISPLMANHCRFFPSCSCYAYEAIENHGIWRGGWLAVRRLGRCHPWNDGGFDPVPPAPSSRTSSIAE | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A6H6Q4 | TKTI1_MOUSE | Tektin bundle-interacting protein 1 | MENVRREATRPSVPSGTLELYFPDHLYRNDYVSLEGPRWAPAIKQAVRWKFTPMGRDAAGQVWFTGLTNSEPGDAWYKLPRALDTPYREAHTRWHGCFQSRQRGLPPAYTQHLREMAFWDPAITAQYLNSGPRWGCMQWRDRQIRGKEFVVTRNQFGAKLPWRSDYVPLLSLPQRPRFTAQDFRQRGLQRPCPAIGQPPPAFTPAL | Microtubule inner protein (MIP) part of the dynein-decorated doublet microtubules (DMTs) in cilia axoneme, which is required for motile cilia beating. Located at the center of the tektin bundle where may function to recruit tektins or stabilize the bundle. |
A6KZL6 | YIDD_PHOV8 | Putative membrane protein insertion efficiency factor | MKKILSYLLLLPVYFYRGYISPMTPPSCRFVPTCSEYAIEAIKKHGPFKGLYLAVRRILRCHPWGGSGYDPVP | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A6LGE9 | YIDD_PARD8 | Putative membrane protein insertion efficiency factor | MRRFFTTLLLLPVYFYKYCISLMTPASCRYTPTCSEYAVQALKKYGPVKGLYLAVKRILRCHPWGGSGYDPVP | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A6LNH3 | YIDD_THEM4 | Putative membrane protein insertion efficiency factor | MKKIILALIRFYQKFISPLKPPTCIYTPTCSEYTYQAVKKFGVFKGLFLGFKRILRCNPLHEGGEDPVPDKFYIIKGRRLD | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A6LPJ0 | SP5G_CLOB8 | Putative septation protein SpoVG | MQITDVRIRKIASEGKMKGIVSVTFDNEFVVHDIKVIEGQMGLFIAMPSRKTPDGEFKDIAHPINTEAREKIQTAILEAYEKAVSEEVVEG | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
A6LSM6 | Y1174_CLOB8 | UPF0122 protein Cbei_1174 | MEDRVEISLLMDFYGPLLTEKQSEIMQWYYNDDLSLAEIAELNQTSRQAIHDLIKRCYKQLLSYESKLNLLQKSINRKKEIMNFLEHLKNKYSIDDEDIIKYKEKLENL | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A6M3M8 | YIDD_CLOB8 | Putative membrane protein insertion efficiency factor | MKKLLIRLIKFYRKYISPGRSSCCRFVPTCSQYAIDAINKYGAFKGSALAVYRILRCNPFCKGGYDPVR | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
A6QEE0 | YABA_STAAE | Initiation-control protein YabA | MDRNEIFEKIMRLEMNVNQLSKETSELKALAVELVEENVALQLENDNLKKVLGNDEPTTIDTANSKPAKAVKKPLPSKDNLAILYGEGFHICKGELFGKHRHGEDCLFCLEVLSD | Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}. |
A6QEF1 | SP5G_STAAE | Putative septation protein SpoVG | MKVTDVRLRKIQTDGRMKALVSITLDEAFVIHDLRVIEGNSGLFVAMPSKRTPDGEFRDIAHPINSDMRQEIQDAVMKVYDETDEVVPDKNATSEDSEEA | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
A6QF39 | NRDI_STAAE | Protein NrdI | MKIIYFSFTGNVRRFIKRTELENTLEITAENCMEPVHEPFIIVTGTIGFGEVPEPVQSFLEVNHQYIRGVAASGNRNWGLNFAKAGRTISEEYNVPLLMKFELHGKNKDVIEFKNKVGNFNENHGREKVQSY | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
A6QGD6 | Y1146_STAAE | UPF0122 protein NWMN_1146 | MGQNDLVKTLRMNYLFDFYQSLLTNKQRNYLELFYLEDYSLSEIADTFNVSRQAVYDNIRRTGDLVEDYEKKLELYQKFEQRREIYDEMKQHLSNPEQIQRYIQQLEDLE | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
A6QHC5 | HRCA_STAAE | Heat-inducible transcription repressor HrcA | MITDRQLSILNAIVEDYVDFGQPVGSKTLIERHNLNVSPATIRNEMKQLEDLNYIEKTHSSSGRSPSQLGFRYYVNRLLEQTSHQKTNKLRRLNQLLVENQYDVSSALTYFADELSNISQYTTLVVHPNHKQDIINNVHLIRANPNLVIMVIVFSSGHVEHVHLASDIPFNNDKLNTISNFVTNKLTEFNQNLQDDIVSFVQSEQEEIFINKLLNTMNNHISNQSNSIYMGGKVKLIDALNESNVSSIQPILQYIESNRIAELLQDISSPNINVKIGNEIDDSLSDISIVTSQYHFDETLKGQIAVIGPTAMHYQNVIQL... | Negative regulator of class I heat shock genes (grpE-dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons. {ECO:0000255|HAMAP-Rule:MF_00081}. |
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