entry
stringlengths 6
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| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
Q8D2B6
|
SDHE_WIGBR
|
FAD assembly factor SdhE
|
MKIKNKSMVYWSCRRGMLELDIIINNFFKKEFDFLSNKEKIFFVNMLSYDDIYLYKCLIFNYEPKNKKIKKIIKLIKRSSFSFS
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q8D3C5
|
FETP_WIGBR
|
Probable Fe(2+)-trafficking protein
|
MKRNIFCHFMKNFHERLDFPPYPGSIGKKIYKNISKKAWEIWKNHQTILINEKQLNMLNKKDRKTIEIEMINFLFKNK
|
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}.
|
Q8DC84
|
SDHE_VIBVU
|
FAD assembly factor SdhE
|
MYTTEEKARIRWACRRGMLELDVVVMPFFEECFEKLSEQEQRDFVSLLECDDPDLFTWVMGHGRSENLGHASMVDKIVAHNLSKVR
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q8DCC5
|
FETP_VIBVU
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCARLNKEADGLDFQLYPGELGKRIFDNISKEAWGQWQHKQTMLINEKKLNMMDPEHRKLLETEMVNFLFEGKEVHIEGYTPPSK
|
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}.
|
Q8DCR2
|
TUSC_VIBVU
|
Protein TusC homolog
|
MSQLTYLFRTAPHSHSSGREGVDALLAASAYCEAISVVFIGDGVYQLLAGQQTASILCKDYAPMFKLFDLYDIEHVYVCQQSLQQRGLTSEDLLIEVEVVDTAQLQGVLHNSAQLLSF
|
Could be part of a sulfur-relay system.
|
Q8DFB9
|
SYDP_VIBVU
|
Protein Syd
|
MSSPVSLALADFSQRFQAAWQAQHNALPSSEELADLPSPCVVESKGDEVLWRSVSLSAPVDFANVEQAIELTLHDDIKAFYGSQLSADMTATWEGNELTLLQVWNDDDFTRLQENILGHLVTQRRLKLKPTVFIAATDAELDVLSICNITGNVVLERLGTSQRDVLAENVTEFLTKLQPMV
|
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}.
|
Q8DKU4
|
HRCA_THEVB
|
Heat-inducible transcription repressor HrcA
|
MTIELSDRQKQILGATINHYIATAEPVASKAIATEYNLNVSPATVRNTMLLLEKSGLLYQPHTSAGRVPSDSGYRVYVDELIQPIPDIARKAESLLSERFIWRQQRLEVILRQAAQLLSDLSGYITLITLPNALERQIRVIQLVALDSQQVMVILVLDTYETQSALIQLEQGEEDPELRERTLQVLTNFLNHQLQGRSLVELSAIDWQKLDLEFQTYSQQLQALLRQLRDRYSHQGTAFVISGLADLLQQPEFSQVEQVQMLLHLLEDQQDQLAPLITTDSQAPSQVQIRIGSENTLAPMQCCTLVYSCYCYGDSPVGSIGILGPTRMPYARIIPLVATAADYLTEQVSCRR
|
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}.
|
Q8DLD1
|
YIDD_THEVB
|
Putative membrane protein insertion efficiency factor
|
MGNGLSKALIVLIRIYQRWISPLFLPTCRYTPSCSAYAVEAIARYGAVKGTYLAIRRILRCHPFAVGGYDPVPTTCPDPCNESSPPNPPC
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8DNJ1
|
YIDD_STRR6
|
Putative membrane protein insertion efficiency factor
|
MKRILIALVRFYQRFISPVFPPSCRFELTCSNYMIQAIEKHGFKGVLMGLARILRCHPWSKTGKDPVPDHFSLKRNQEGE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8DPH0
|
Y1167_STRR6
|
UPF0122 protein spr1167
|
MEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFGVSRQAVYDNIKRTEKILEDYEMKLHMYSDYIVRSQIFDQILERYPKDNFLQEQIEILTSIDNRE
|
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}.
|
Q8DSR1
|
YIDD_STRMU
|
Putative membrane protein insertion efficiency factor
|
MKKVLIAPIKFYQKFISPIFPASCRYRPTCSAYMIEAIEKHGLKGFLMGIARILRCHPFVEGGEDPVPNHFTLRRNKKEKPSKS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8DSU9
|
YABA_STRMU
|
Initiation-control protein YabA
|
MDKKDLFDVFDGFSQNLMETLAEAEALKKQVQDLVEQNASLRLENDKLRDRLSHFSQMEESDPSSKAISSRKENLENIYEDGFHICTFFYGQRRENNEDCAFCMELLYRE
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q8DYB5
|
YABA_STRA5
|
Initiation-control protein YabA
|
MDKKDLFDAFDDFSQNLLVGLSEIETMKKQIQKLLEENTVLRIENGKLRERLSVIEAETETAVKNSKQGRELLEGIYNDGFHICNTFYGQRRENDEECAFCIELLYRD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q8E3Y0
|
YABA_STRA3
|
Initiation-control protein YabA
|
MDKKDLFDAFDDFSQNLLVGLSEIETMKKQIQKLLEENTVLRIENGKLRERLSVIEAETETAVKNSKQGRELLEGIYNDGFHICNTFYGQRRENDEECAFCIELLYRD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q8E7Q9
|
HRCA_STRA3
|
Heat-inducible transcription repressor HrcA
|
MITQRQNDILNLIVELFTQTHEPVGSKALQRTIESSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYHVIKAFDFEAFKLEDMLQKASHILSEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDGSVMDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQGLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLAAKLGDYYRYLNSNHYEVH
|
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}.
|
Q8EKT5
|
YIDD_SHEON
|
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}.
|
Q8EQL0
|
YIDD_OCEIH
|
Putative membrane protein insertion efficiency factor
|
MKFIFIGLIKFYRSAISPFTPSSCRFYPTCSEYGLEAIKRFGAFKGGILTIKRISKCHPFHPGGVDVVPDKVKNINNEKHLEKGVIRNED
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8ER03
|
Y1530_OCEIH
|
UPF0122 protein OB1530
|
MLDKTTRINYLFDFYQELLTPKQRNYMEMYYLEDYSLGEISELFQVSRQAVYDNIKRTEAMLESYEEKLHLYSKFEQRVKLLEKLKLMTTDKHVHEHIQKLKDLD
|
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}.
|
Q8ET90
|
LUTC_OCEIH
|
Lactate utilization protein C
|
MAIHNRDKFLSNLAANLGRPRKTEGVERPEYSVQPQYEVLKGASQDELIDVLEKHCEVIHTDFVRTSKQELPHVVRQTIERYEAKSIIASNDKRNAEYGMDQAYNQFAEELDMHIWDASIGKENQVIAEKADVGISFSDITLAESGTVTLKNDKDNGRSISLMPKSYIAIIPKETLVPRMTQAAKQIHDDHMNGIQTPSSVCFVTGPSNSADIEMNLIVGVHGPVNVTYIVVD
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
Q8ET92
|
LUTA_OCEIH
|
Lactate utilization protein A
|
MKVSLFITCVSDIVFADVGKHTVEILERVGCEVDFPAAQTCCGQPAYNSGYLQEAKKSMKQMIKAFKNSEYVVGPSGSCVGMLKEYPHIFKGDPDWEQPAIDLANKSYEITQFLVDVLGVTDLGSTFKGRVTYHPSCHMTRVLGVKDAPQKLLQSVKGIDFVELPVKEDCCGFGGTFSIKNPEISREMVKEKSQHVSETKAEYLVGGDMGCLMNIGGRMRREGKDVKVVHITEILNTHREGGIA
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
Q8EU35
|
SP5G_OCEIH
|
Putative septation protein SpoVG
|
MEVTDVRLRRVNTEGRMRAIASITLDQEFVVHDIRVIDGNNGLFVAMPSKRTPDGEFRDIAHPINSGTRSKIQEAVLAEYQKAGEDEVNYEEAGAS
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q8EVS4
|
Y485_MALP2
|
UPF0122 protein MYPE4850
|
MKELDLSQISLLIDFYGNLLTDKQLQNLIDYYFNDLSLSEIAANNNVSRTAIHDSIKKSKNELEQFENKLKFIYRFNLRKEIYKQIKDNNLLDQLLETEVEQLWKTK
|
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}.
|
Q8FBE8
|
FDHE_ECOL6
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTTRIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q8FGN7
|
USPC_ECOL6
|
Universal stress protein C
|
MSYSNILVAVAVTPESQQLLAKAVSIARPVKGHISLITLASDPEMYNQLAAPMLEDLRNVMQEETQSFLDKLIQDAGYPVDKTFIAYGELSEHILEVCRKHHFDLVICGNHNHSFFSRASCSAKRVITSSEVDVLLVPLTGD
|
Required for resistance to DNA-damaging agents.
|
Q8FJ51
|
CBPM_ECOL6
|
Chaperone modulatory protein CbpM
|
MANVTVTFTITEFCLHTGISEEELNEIVGLGVVEPSEIQETTWVFDDHAAIVVQRAVRLRHELALDWPGIAVALTLMDDIAHLKQENRLLRQRLSRFVAHP
|
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}.
|
Q8FSU9
|
YIDD_COREF
|
Putative membrane protein insertion efficiency factor
|
MCEPISDDPQVIPQPKGPAAKALAGAVRFYQKYLSGLKMGSTCRFDPVCSTYALKSVSVHGAVKGTVLAAVRLAKCGPWHPGGFDPVPNPGYWSTETVR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8FUM7
|
LIVB5_BRUSU
|
Leu/Ile/Val-binding protein homolog 5
|
MIGTRLPAWTRVLACGVAGLSLMTISAKAEDVITLGASVQLSGPVANTGRYYQDAYNITIDKINAAGGVKVDGKPYKLALKIYDNQSNVNLSVRQYTQLVTTDKVNFLLGPFASNFALADSVISEKYRIPMVQGGGASDEIYSRNFKYIFGTLAPASNYFGSTVEMLKGLDPKVTNVALVYADDSFDISVADGTRKLLKDAGFTIAADEKFATNSTDFTSLISQIKSKNVDAVLVAGHETEVLNFVRQSKSLAFDPKLYSFTVGVPTEDFRKALGKDANYAFGMTAWLPSADLKDRWFGDAAKFETEYKARFNYEPDYHAASGASDVEAFAEAIEKANSLDPQKVRDALASIKFDSLYGPIAFDKQGQINLPQIVVQVQDGKLVEIRGPAGQVNPPQYPMPAWNAR
|
Component of an amino-acid transport system.
|
Q8FW17
|
LIVB6_BRUSU
|
Leu/Ile/Val-binding protein homolog 6
|
MKKIALTALAVFSLAASAAYADVVKVGVIGPFSGPFALQGKNFKAGIDAYMAEHGNKVGDDTVEVVYRDVPQADPAQSKALAQELVVKEGVQYLAGFYFTPDAMAVTPILKQGNVPMVVMNAATSSIVTKSPYVVRTSFTTWQTSTPIARVALDKGVKKVISVVSDYGPGVDAENAFKAAFTDAGGEVVEAIRMPLATNDFSPIMQRIKDSGAQGVFAFLPSDPTTLGFMKAYVDNGLKSSGIQLFAPGDLTQESDLPALGENALGVLTTFHYAVSHDSPENRKFVEEARKAIGNPAELSFPSVGAYDGMHVIYKMIEATGGKKDAAKAVEAVKGMEWVSPRGPVSIDPESRHITQNIYLREVAKADDGTYYNKEIQTFEKQGDPGLKAQ
|
Component of an amino-acid transport system.
|
Q8FWQ3
|
LIVB8_BRUSU
|
Leu/Ile/Val-binding protein homolog 8
|
MRLSRLLIGASLGVALSSTAFTAALADVKFGSLYPISGSLALLGEESARGLELAVDEVNAAGGIKGEKVVLERGDAVDNNQATGEARRLISLVGVKAIFGTYSSARVIAASQVSELAGIPYFEMGAVADEVTGRGLQYLFRTNPTAENMAKDSVDMLIKGIAPGLGKDPKDMKIGIIYEDSSYGTSVAGHQEDNAKAAGLTVVLKSGYPSNTVDMSSLVLELREKGADVVMQTSYQNDSVLFLQQANEAGYKPLAIIGGGGGYSMQPTADAVGHDLIDGVFDADYTQYAVNTSATPGLTEFVEAYKAKYGSQPRSGHSLTNYVGAKAIFQALNAGEGFEPDQIVSAVKALDIPDGQTAAGYGVKFGKNNQNERATMMGMQWQDGKLVTVYPENAAIAKMRFKK
|
Component of an amino-acid transport system.
|
Q8FYS6
|
LIVB1_BRUSU
|
Leu/Ile/Val-binding protein homolog 1
|
MRKTLFSGVALAAVIAFGGSAWADVLVGIGIPVTGPNAVYGAQIQKGAEAAIKEVNDAGGINGEKIAITIGDDVSDPKQGISVANKFAADGVKFVIGHFNSGVTIPASQVYAENGILEISPGATNPQYTEQGLWNTFRTCGRDDQQGTVAGQYIFDHFKDAKIAVIHDKTPYGQGLADETKKKLNELGTKETLYEGVNVGEKDFSALIAKLKQAGVNVVYWGGLHPEAGLIIRQMADQGLKAQFISGDGIVSNELASIAGPAVEGTLNTFGPDPRNNPDNAELVKKFRDAGFEPEAYTLYSYAAVQSLAQAAKAAGSNDPQEVAKAMKEKGPFKTVLGDLSYDEKGDPKLPGYVMYKWEKGADGKYNYIQQ
|
Component of an amino-acid transport system.
|
Q8FYS9
|
LIVB2_BRUSU
|
Leu/Ile/Val-binding protein homolog 2
|
MKKSLFCGVCLCALVAMGGTSFADIMVGVGAPLTGSQAAFGEQIKRGVEAAVAEANAKGGMNGEQITLVYGDDAADPKQGISVANKFVGDGVKFVIGHFNSGVSIPTSDIYAENGVLMIAPGTTNPTFTERELWNTFRTCRRDDKQGIVAGKYMADNYKDGKVAILHDKTPYGQGLADETKKSLNENGMKETLYEGVNQGDKDFSALISKMKAAGITAVYWGGMHPEAGLLIRQMADQGLKAQFISGDGIVSNELASIAGDAVAGVMNTFGPDPRDDKANAELIKAFRDKGFEPEAYTFYAYAGVQSLVNAANAAGSNDPMEVATAMKEKGPFKTVLGDISFDAKGDPSLSPYVMFEWRKGEDGKYNYFQK
|
Component of an amino-acid transport system.
|
Q8G0L6
|
YIDD_BRUSU
|
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}.
|
Q8G3D4
|
LIVB3_BRUSU
|
Leu/Ile/Val-binding protein homolog 3
|
MNLKLLSSLAFAATIGFASAAYADITIGVIAPLTGPVAAFGDQVKKGAETAVEVINKAGGIKGEKVVLKFADDAGEPKQGVSAANQIVGDGIKFVVGPVTTGVAVPVSDVLSENGVLMVTPTATGPDLTARGLENVFRTCGRDDQQAEVMADYVLKNMKDKKVAVIHDKGAYGKGLADAFKAAINKGGITEVHYDSVTPGDKDFSALVTKLKSAGAEVVYFGGYHAEGGLLSRQLHDAGMQALVLGGEGLSNTEYWAIGGTNAQGTLFTNAKDATKNPAAKDAIQALKAKNIPAEAFTMNAYAAVEVIKAGIERAGSTDDSAAVAKALHDGKPIETAIGTLTYSETGDLSSPSFDIFKWDDGKIVGLE
|
Component of an amino-acid transport system.
|
Q8G6J7
|
YIDD_BIFLO
|
Putative membrane protein insertion efficiency factor
|
MTASFKAVMIGGVRWYQQHISANTPPCCKYYPTCSNYAIEALERYGAFKGGVLAVLRLLRCRPWSRGGIDDVPQRYSVFYRFSWSKAHEEPRLTPLATTQREAQR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8GED8
|
ALBB_STRNR
|
Protein AlbB (Albonoursin synthase protein B)
|
MNPGETVLPPQLREEIALLAVYLLSSGRGLLEEPADYGIYRCTDGARRALQLLDEHGGSTARLTAVRERLDEVMFAPMGEDRDMGAILDDLCRQMADALPEIETP
|
Involved in the biosynthesis of albonoursin (cyclo[(alpha,beta-dehydro-Phe)-(alpha,beta-dehydro-Leu)]), an antibacterial peptide. AlbB is essential for cyclic dipeptide oxidase AlbA (CDO) activity.
|
Q8GH81
|
HRCA_CHLAB
|
Heat-inducible transcription repressor HrcA
|
MSKSWISKRESKLLYILLTTTELYLKTGQPVGSKTLKEYECSNLSTATIRNYFAELEAEGFLKKNHVSGGRIPTDLAFRYYVDHRADFLQDDLPETTIHLLNQLPKESQNIVKDLQKASELLGEALQLPTCFSSPRFENDSVTNIQLSLVDEQRVVVILSTEFGQIFTDTLWLAETSNYASLKRIETFLQNYLRKQPPSETLSQKEEDLGMTLYNEVVVRYLTRYCNFSEEDLYQTGLSKLLKYDAFKDPDMLALGLSFFESRCHMCKLLDIGMHRDRPTAFIGSELSDIFGTPNPHCAVITTPYYMNRTPLGAFGVLGPINLPYREIYKTLTIFADKVKESLTQSFYKFKLSFRRPCPSDPKLSKEPTLLARYSSIKLLPPKETS
|
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}.
|
Q8GWL2
|
LOR7_ARATH
|
Protein LURP-one-related 7
|
MADSETPYHPDPEDLRRIPVDLFASKKLPGLSSGDLGFADSSEHLVFILRKSSSSLKSLLDSSGVPLFSISRLHNGVWELHKGDVEKRKDLVLTVKRTSKRFSKTESEVSFAGESSENLVIKGVPFQKSCTIYSQDSIVAQTSLMYKLRQIYVGRSKFRLTIFPGSIDHSLVVAMVAIFLQG
|
Might be related to the phospholipid scramblase and tubby-like superfamily of membrane tethered transcription factors.
|
Q8HAD9
|
VG07_BPST6
|
DNA transfer protein gp7
|
MLYAFKLGRKLRGEEPLYPEKGGKGGSSSSGAKEAARATQYAADLQNQQFNRVMEQLAPYAAAGLPALQQIQQLSTLEGQNSALNQYYNSDQYKQLADQARYQSLNAAEATGGLGSTATSNQIASIAPTLGQNWLSGQMQNYGNLLNVGQSAAAGQASAGQNYANNAGNLAQQMAAIRSQGSGQSTLGSAISGGTSGALAGAGLAGMLGASTPWGAGIGAGIGLLGSLF
|
Component of the phage injection machinery. Required for injection of the phage DNA into the host (By similarity).
|
Q8JL91
|
VTF3L_ECTVM
|
Intermediate transcription factor 3 large subunit (VITF-3 45 kDa subunit)
|
MDNLFTFLHEIEDRYARTIFNFHLISCDEIGDIYGLMKERISSEDMFDNIVYNKDIHPAIKKLVYCDIQLTKHIINQNTYPVFNDSSQVKCCHYFDINSDNSNISSRTVEIFEREKSSLVSYIKTTNKKRKVNYGEIKKTVHGGTNANYFSGKKSDEYLSTTVRSNINQPWIKTISKRMRVDIINHSIVTRGKSSILQTIEIIFTNRTCVKIFKDSTMHIILSKDKDEKGCIHMIDKLFYVYYNLFLLFEDIIQNKYFNEVANIVNHVLTVTALDEKLFLIKKMAEHDVYGVSNFKIGMFNLTFIKSLDHTVFPSLLDEDSKIKFFKGKKLNIVALRSLDDCINYVTKSENMIEMMKERSTILNSIDIETESVDRLKELLLK
|
Acts with RNA polymerase to initiate transcription from intermediate gene promoters.
|
Q8K925
|
FETP_BUCAP
|
Probable Fe(2+)-trafficking protein
|
MNRIIFCTFLQKKSEGQDYPPYPGKLGEKIYNQISKIAWKEWKLQQTKLINEEKLNMFNQNDRKKIEKYMKLFLFNNE
|
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}.
|
Q8K9K7
|
FLGD_BUCAP
|
Basal-body rod modification protein FlgD
|
MGTVNINSSINNNIIENNTNNVKNNSNALDLQKNFLSLLMAQMKNQDPTDPIKNSELTSQLAQINTATGIERLNSTVGIFSNKINQSQNIQVSSLIGHHVMIPSSQIVHTKGIETKYGIELISDATAVNIQITDKNGKIIHIQKIKNLKSGIHSLTWDGQNLDKEDMKTEKYNVTVIAKNQNREIPVQVLSEALVNSIITSSSIDPIIDLGTVGTVTLSKIRKILK
|
Required for flagellar hook formation. May act as a scaffolding protein (By similarity).
|
Q8KGG3
|
YIDD_CHLTE
|
Putative membrane protein insertion efficiency factor
|
MNIVPILLIRFYQSFISPLLGPSCKYHPTCSNYAIEAFRQHNFFYASWLTVWRVLRCNPFSKGGYDPVPPKSVKSAGNSKDSK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8KML8
|
HRCA_FRUSA
|
Heat-inducible transcription repressor HrcA
|
MLTERQSMILKYIIDDYSKTGVPIGSKALAEQLPIHVSSATIRNEMAVLSHQNFIEKLHTSSGRVPSNQGYRYYIDNLAKPAKLDTKRLEYISEMLDGSFQQIDEIVRQSADILSHLTDYTALTFSPELTTENTIKHLQLVNLGLNRMMVVIVMGNEQVESQSFLVTNQYIDSQLSLATNLLNQQLVGKTAREVKQVFQSKILTELHTYLPDTKQFVRAIQAILSKIDDDHYFISGQMNMFEQNGKQDFSKIKSLYSMFNNDNGIDALLEKSSKPISVKIGAEFDNDWLKDYSIITGSYDLGNHGIGRIALIGPMRMSYPNMLGVVDAFRHELKNRISGYYRSYDQ
|
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}.
|
Q8KQF5
|
COP_STAEP
|
Protein cop
|
MTFNKIFKYLISLLFLSILFHTIIHKNNLVFSKTMHKKVAFFSFSIFFVWIRHLKRYNSMLEKATFFVLQTSYTNELKGLYIAGNSYPYYQDKKKLVFNSFQKPFKNHQSTKIPRE
|
Putative control of replication message.
|
Q8L3A0
|
HRCA_ACHLA
|
Heat-inducible transcription repressor HrcA
|
MISSRQKLILKAIIDMYSEKGEPVGSKALMALPYLNYSSATLRYDMAVLEELGFLEKMHTSSGRVPSERGYRYYIEHLVTRDNDVTEVFPLIDEVFSKKALGREHTIKEALKLLTDLTSYTAVAVGPDILQSHIKRIEMVPLGLKDAVMLIVTDTGHVQHQQIHISDDMRMDDIKEVIHTLDDLLKNRTLEDALKVLKEEYAISELNQFMSYQSQIIDSFIEAFSKFASDSFYLSGMTNAFEQPEFNDVSHMKRFIDMMDRREIVKLIGTAEGISVRFGSDMEIKPLNQMTIISIPYQIDSKQKGTIALVGPSRMSYQKVIPLLEYIAANLAKLYKDNNKET
|
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}.
|
Q8NWA8
|
HRCA_STAAW
|
Heat-inducible transcription repressor HrcA
|
MITDRQLSILNAIVEDYVDFGQPVGSKTLIERHNLNVSPATIRNEMKQLEDLNYIEKTHSSSGRSPSQLGFRYYVNRLLEQTSHQKTNKLRRLNQLLVENQYDVSSALTYFADELSNISQYTTLVVHPNHKQDIINNVHLIRANPNLVIMVIVFSSGHVEHVHLASDIPFNNDKLNTISNFVTNKLTEFNQNLQDDIVSFVQSEQEEIFINKLLNTMNNHISNQSNSIYMGGKVKLIDALNESNVSSIQPILQYIESNRIAELLQDISSPNINVKIGNEIDDSLSDISIVTSQYHFDETLKGQIAVIGPTAMHYQNVIQLLNRIW
|
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}.
|
Q8NWR0
|
Y1315_STAAW
|
DegV domain-containing protein MW1315
|
MTKQIIVTDSTSDLSKEYLEANNIHVIPLSLTIEGASYVDQVDITSEEFINHIENDEDVKTSQPAIGEFISAYEELGKDGSEIISIHLSSGLSGTYNTAYQASQMVDANVTVIDSKSISFGLGYQIQHLVELVKEGVSTSEIVKKLNHLRENIKLFVVIGQLNQLIKGGRISKTKGLIGNLMKIKPIGTLDDGRLELVHNARTQNSSIQYLKKEIAEFIGDHEIKSIGVAHANVIEYVDKLKKVFNEAFHVNNYDINVTTPVISAHTGQGAIGLVVLKK
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q8NWS9
|
CVFB_STAAW
|
Conserved virulence factor B
|
MALDKDIVGSIEFLEVVGLQGSTYLLKGPNGENVKLNQSEMNDDDELEVGEEYSFFIYPNRSGELFATQNMPDITKDKYDFAKVLKTDRDGARIDVGLPREVLVPWEDLPKVKSLWPQPGDHLLVTLRIDRENHMYGRLASESVVENMFTPVHDDNLKNEVIEAKPYRVLRIGSFLLSESGYKIFVHESERKAEPRLGESVQVRIIGHNDKGELNGSFLPLAHERLDDDGQVIFDLLVEYDGELPFWDKSSPEAIKEVFNMSKGSFKRAIGHLYKQKIINIETGKITLTKKGWSRMDSKE
|
Contributes to the expression of virulence factors and to pathogenicity. Involved in the production of hemolysin, DNase, protease and protein A (By similarity).
|
Q8NXI8
|
EMP_STAAW
|
Extracellular matrix protein-binding protein emp
|
MKKKLLVLTMSTLFATQIMNSNHAKASVTESVDKKFVVPESGINKIIPTYNEFKKAPKVNVGNLADNKNFVASEDKLNKIVDSSAASKIVDKNFAVPESKLGNIVPEYKEINNRVNVATNNPASQQVDKHFVAKGPEVNRFITQNKVNHHFITTQTHYKKVITSYKSTHVHKHVNHAKDSINKHFIVKPSESPRYTHPSQSLIIKHHFAVPGYHAHKFVTPGHASIKINHFCVVPQINSFKVIPPYGHNSHRMHVPSFQNNTTATHQNAKVNKAYDYKYFYSYKVVKGVKKYFSFSQSNGYKIGKPSLNIKNVNYQYAVPSYSPTHYVPEFKGSLPAPRV
|
Adhesin that binds to the host cell extracellular matrix proteins fibronectin, fibrinogen, collagen, and vitronectin.
|
Q8NXM4
|
Y711_STAAW
|
DegV domain-containing protein MW0711
|
MKIAVMTDSTSYLSQDLIDKYNIQIAPLSVTFDDGKNFTESNEIAIEEFYNKMASSQTIPTTSQPAIGEWITKYEMLRDQGYTDIIVICLSSGISGSYQSSYQAGEMVEGVNVHAFDSKLAAMIEGCYVLRAIEMVEEGYEPQQIIDDLTNMREHTGAYLIVDDLKNLQKSGRITGAQAWVGTLLKMKPVLKFEDGKIIPEEKVRTKKRAIQTLEKKVLDIVKDFEEVTLFVINGDHFEDGQALYKKLQDDCPSAYQVAYSEFGPVVAAHLGSGGLGLGYVGRKIRLT
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q8NXZ8
|
SP5G_STAAW
|
Putative septation protein SpoVG
|
MKVTDVRLRKIQTDGRMKALVSITLDEAFVIHDLRVIEGNSGLFVAMPSKRTPDGEFRDIAHPINSDMRQEIQDAVMKVYDETDEVVPDKNATSEDSEEA
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q8NY02
|
YABA_STAAW
|
Initiation-control protein YabA
|
MDRNEIFEKIMRLEMNVNQLSKETSELKALAVELVEENVALQLENDNLKKVLGNDEPTTIDTANSKPAKAVKKPLPSKDNLAILYGEGFHICKGELFGKHRHGEDCLFCLEVLSD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q8NZM6
|
HRCA_STRP8
|
Heat-inducible transcription repressor HrcA
|
MITQRQNDILNLIVELFTQTHEPVGSKALQRTIDSSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYHVIKTFDFEAFKLEDMLQKASHILAEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDSSVIDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQSLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLAAKLGDYYRYLNSNHYEVH
|
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}.
|
Q8NZW1
|
Y1709_STRP8
|
DegV domain-containing protein spyM18_1709
|
MTWKIVTDSGCDLRSLTRQSKELRFERVPLTLQIGTEIFRDDDGLDIDNMMTTMYQSSKATTSSCPSPEAFLQAYRGSDNVIVMTITGTLSGSHNSARLAKNELLEENPNVNIHLIDSLSAGGEMDLLVLELERLINLGLSFEEVVKQITAYQQKTRLIFVLAKVDNLVKNGRLSKLVGKVIGLLNIRMVGKASNKGTLELLQKARGQKKAVSALIEEIQKEGYVGGKVYIAHAQNPKICEQISEKIKSLYPDAVIQTGRTSGLCSFYAEDGGLLMGYEI
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q8P1E4
|
Y926_STRP8
|
DegV domain-containing protein spyM18_0926
|
MKLAVITDSTATLPIDLKQDKAIFSLDIPVIIDDETYFEGRNLSIDDFYQKMADSQNLPKTSQPSLSELDNLLGLLSSKGYTHVIGLFLAGGISGFWQNIQFLAEEHPEIEMAFPDSKITSAPLGSMVKNVLDWSRQGMTFQAILNKLQEQIDRTTAFIMVDDLNHLVKGGRLSNGSALLGNLLSIKPILRFDEEGKIVVYEKVRTEKKAMKRLVEILNDLIADGQYNVSIIHSKAQDKADYLKRLLQDSGYQYDIEEVHFGAVIATHLGEGAIAFGVTPRL
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q8P2A7
|
YABA_STRP8
|
Initiation-control protein YabA
|
MNKKELFDAFDGFSQNLMVTLAEIEAMKKQVQSLVEENTILRLENTKLRERLSHLEHETVAKNPFKQRKDHLEGIYDEGFHICNFFYGQRRENDEECMFCRELLDRK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q8P2C7
|
YIDD_STRP8
|
Putative membrane protein insertion efficiency factor
|
MMKKLLIVSVKAYQKYISPLSPPSCRYKPTCSAYMLTAIEKHGTKGILMGIARILRCHPFVAGGVDPVPEDFSLMRNKNTSKNEKF
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8P5F9
|
Y3382_XANCP
|
DegV domain-containing protein XCC3382
|
MRIGIVVDSACDLPQDFIQRNNVIVLPISVRIGEAVLADHRDEEATLSFLHAHVAERGHEAETTPFSVNQIRDLFLQRLVIDYDHVFCLTISKLRSQIFDNATQASFAILNDYKPVRQAAGHTSPFALRVIDTLNLFAGQGITAVEAVRLRAQGLGVAPIRARLEQLAEHTYGYMIPRDLYYLRARARTKGDRSVGLIGAALGSALDIKPVLRAYRGVTEPVAKLKGFEPSAEKLFAFTVRKLREGLMTPTVCVGYGGELAELHALPGYAALQAACQTQGVELFESVMSLTGMVNVGKGALAVAFAAEPHSFSA
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q8P8I5
|
YIDD_XANCP
|
Putative membrane protein insertion efficiency factor
|
MAYHWQVIGRLLIALLRFYKRFISPLLGPRCRFAPSCSEYAMTAIARFGPLRGSWLAARRLGRCHPFHPGGFDPVPDAPTSSPSSCRCKGPHP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8PGV3
|
Y3508_XANAC
|
DegV domain-containing protein XAC3508
|
MRIGIVVDSACDLPQDFIQRHNIVVLPISVRIGEAVLADHRDEEATLSFLQAHVAERGHEAETTPFSVNQIRDLFLQQLVIDYDHVFCLTISKLRSQIFDNAMQASFAILNDYKPIRQAAGHTSPFALRVIDTLNLFAGQGITAVEAARLRDQGQSVAVIRTRLEQLAEHTYGYMIPRDLYYLRARARTKGDRSVGLIGAALGSALDIKPVLRAYRGVTEPVAKLKGFEPSAEKLFGFTVRKIRDGLMTPTVCVGYGGELAELHALPGYAALQGACQTHGVELLESVMSLTGMVNVGKGALAVGFAAEPHAFSA
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q8PJH7
|
FETP_XANAC
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCHYQQSDAEGLDFVPYPGELGQRIFAQIGKNAWQAWLAHQTMLINENRLSPRDPKHRAFLEAELQKFLFERNADKPEGYVAPVGD
|
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}.
|
Q8PK18
|
YIDD_XANAC
|
Putative membrane protein insertion efficiency factor
|
MAYHWQVISRLLIALLRVYKLVISPLLGPRCRFAPSCSDYAMTAIGRFGPLRGSWLAARRLGRCHPFHPGGFDPVPDAPTSPSPSSSCSCKGPHP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8PKT3
|
SDHE_XANAC
|
FAD assembly factor SdhE
|
MWFAAAPALGSGAAVVFGPPCGAVESEMDEQTLLKKLRWRCRRGMRELDQLFGRYLDQRWAQAPDAERAVFLQLLDCEDDKLWRWFMGYEACPDAANAALIADIRALPA
|
An FAD assembly protein, which accelerates covalent attachment of the cofactor into other proteins. Plays an essential role in the assembly of succinate dehydrogenase (SDH, respiratory complex II), an enzyme complex that is a component of both the tricarboxylic acid cycle and the electron transport chain, and which couples the oxidation of succinate to fumarate with the reduction of ubiquinone (coenzyme Q) to ubiquinol. Required for flavinylation (covalent attachment of FAD) of the flavoprotein subunit SdhA of SDH and other flavinylated proteins as well.
|
Q8PTT5
|
BRIX_METMA
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MLVTTSRKPSAKSRTLCKLLSRFTASRCISRGKMGMQELLDFTEGNTFIVVGEYHGNPGELSFHDNEGKLLFSIRFSDRYSEEIDSYWFPDVLPVLTGEGEIAEALESFFHFERVESDRVVQLPQNSLVMAIGDKEIDFMGSGKSLFKFNIKGFKKY
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
Q8PU66
|
Y2475_METMA
|
Putative antitoxin MM_2475
|
MPTRTISISEEAYERLKSLKTSEKDSFSDVILKYYPRKRKLSEVLAEIGSNPELADAIEKASRDMRKAKMRNVDLDAGA
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. {ECO:0000255|HAMAP-Rule:MF_00794}.
|
Q8QL36
|
CAPSD_SIRV1
|
Putative capsid protein
|
MAKGHTKRSYSQRYAKWQAKFNAFSNPTVASTILSNVAPVAQQNFQTNVPTFTAVNENVSAVLSQYGITGPNRAIYQGFGLKIARALNRIGSGPALVNMINGLKSYYISAFNANPQVLDAVVNIITGSPTGYVS
|
Self-assembles to form a helical, filamentous nucleocapsid. The capsid proteins wrap around the DNA and maintain it in an A-form by non-specific desolvation and specific coordination of the DNA phosphate groups by positively charged residues. This certainly protects the viral DNA under conditions such as the extreme desiccation of its host.
|
Q8QL85
|
LEF11_NPVMC
|
Late expression factor 11
|
MDEPRPEAANVDSQQNSQCCLTRSEVYALVREVINKRKHHNLVTNVCDHVFDDGFEEQLKYIRANIDKALITVGGEHKHCKRLAAHIKKINKIFKLNKSLETEYKQSIDRYGSNRFNRNN
|
Involved in late/very late gene activation.
|
Q8QVL3
|
CAPSD_TTVF1
|
Capsid protein
|
MYQSRRRRRRRWGRRILSRYKRKWGRRSRRGHGIYRRWRRWRRRPRTVVTEQHSRRVKTIIVRGWEPLGNICPTDSARAKATPYASYDSDSGQGQWHGTWGHHWFTFQSLVDRAEARLNSFSGNWESYDYLRFLGGTMYFMQPREMCFMFGNDPYLMTSDLDKTASQKNRAEETWITPGYLMHRPGTHLILSRQKVERRSMYKIRVPVPTSWRGWFPIPDCFSYVLCHWYWTWWDPDACFFDPCATGSSCEAEPWWSTAQTKQAWVDRTKLDDPPVGGTGPNQKTWAPFLPSRPCTNYYTHSASFWFKYKLKFQVTGENIWAPVPRDYSQRGTVPTAPSRQQVESEARAPYPKTNRPPTTADILPGDLDSDGILEDEAYERITRDNPCPKRPRPLGIRWWDGTPGRTLQEQQQAAVLRPKPRRQLLRRLRDVLLQL
|
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).
|
Q8R1F0
|
L10K_MOUSE
|
Leydig cell tumor 10 kDa protein homolog
|
MAQGQRKFQAQKPKSKAAAAERSRGPRKGGRVIAPKKARVVQQQKLKKSLEVGIRKKIEHDVVMKASSSLPKRLALLKGASKKSEATIPGKTPS
|
May have a potential role in hypercalcemia of malignancy.
|
Q8R6K5
|
YIDD_CALS4
|
Putative membrane protein insertion efficiency factor
|
MKNFVIFLIRLYQKYISPMKPRTCRFYPTCSQYSIEAISKYGLLKGGLMSIWRILRCNPFNPGGYDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8R751
|
SP5G_CALS4
|
Putative septation protein SpoVG
|
MKITDVRVRKLNDEGRMKAVVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPEGEFKDIAHPINSDTRNKLQKAILEEYEKAKENNSNKE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
Q8R9U5
|
Y1491_CALS4
|
DegV domain-containing protein TTE1491
|
MEKIAIVTDSLSDIPEDLIKTYGIFVVPLTINIDGKSYKDGVDIKKEEFYKLLREGKMPTTTQASPVEFMEVFEDLLKSFDYVIAIILTSKFSGTYQSAVIARDMVDKNRIEVIDSRHFTLGNGMLVLKAARMAVEGASKEEIVSTVYETIPRIRGIMVFDSLDYLYRGGRLSRTQSIIGGILNVKPILTNEDGELKVIDKVRGQKKAIRWIIDYMKNTGIDFAEREVGLIHTDKEEFLNEIEAALRSELEITRFIRSQAGCGIGTHAGPDAAGVFFEEK
|
May bind long-chain fatty acids, such as palmitate, and may play a role in lipid transport or fatty acid metabolism.
|
Q8R9W9
|
Y1463_CALS4
|
UPF0122 protein TTE1463
|
MEDDFLFMTLLYDFYGALLTDKQREIFEMYYLNDYSLGEISEILDISRQGVYDALKRAEDSLEFYEEKLGLVKKHQEMMKKIEKIKECIKLIKEREKDEEILKIIEDMARELEELNP
|
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 (By similarity).
|
Q8RDV6
|
Y1394_FUSNN
|
UPF0122 protein FN1394
|
MILDEFVEIANLLEIYSSLLSEKQKEYLEDHFENDLSLSEIAKNNNVSRQAIYDNIKRGVALLYDYEDKLKFYQMKKNIRKELVDLKEDFTKENLEKIIENLL
|
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 (By similarity).
|
Q8RHA5
|
YIDD_FUSNN
|
Putative membrane protein insertion efficiency factor
|
MKKILILLIRFYQKFISPMFPAKCRFYPTCSQYTLEAIKEHGTIKGTYLAIRRILKCHPFHEGGYDPVPKRKNKNSEGKREE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q8RKH1
|
ALBG_BACIU
|
Antilisterial bacteriocin subtilosin biosynthesis protein AlbG
|
MSKSTVFTVLLLLLGMAAYSFGWVQAVAEAAAQYVQIFNNDALRLGLLACIAAVLMLPAFLYLHYVTQSVKNMTAAFQKLTQSHQSCCDFQHHRLCSRYAEEVKSLRDRYKNVRQTYVMAAVLCQVIIFGCMFEIVKAVPFRLHTPPIVSTGMALLLILYLLFYMRMYLLKLFQHGTLFKKILACVLTGAGIGWMLSFTISELLFLIILAAIQQIGSFIYKRFSNRGFTSLDL
|
Involved in the production of the bacteriocin subtilosin.
|
Q8RKH3
|
ALBE_BACIU
|
Antilisterial bacteriocin subtilosin biosynthesis protein AlbE
|
MAVNLLKTQQFSTISIAASFLKPIESAAEPEEETIYFYSAAAHLKQQIIDAFGYAAGCRFMYSANLFFDQQLKTCGTRLIHPSFNKNLHLDALMKTFADMSFPSSLSADAVEKAKDELLLKIEKKFADPFSYSAARLAEEAFGNPMYGTAMFGRKDRIQAIHPQRFLNATDFIVDLLSQHKQLNILGHVQACDIPGHASQTSAVTAGRFLVNRHVFETETRSAAGPSVLTLGFDCGEMKDASDYIKIQLIDGLLGKYGHSALFKHFREKDLAVYHVITRYDIMNNLLLVSICTNQLHEKEIPPRVLEAVSHFSADERELEQAKQFFRNEMLLQFDSPEGLLAYMGILRRFSCTKEDLLDGISAVTCRDVLQFITTINYIGAHVVRG
|
Involved in the production of the bacteriocin subtilosin.
|
Q8T6B3
|
MT1_TETTH
|
Metallothionein-1 (MT-1)
|
MDKVNNNCCCGENAKPCCTDPNSGCCCVSETNNCCKSDKKECCTGTGEGCKWTGCKCCQPAKSGCCCGDKAKACCTDPNSGCCCSSKTNKCCDSTNKTECKTCECCK
|
The metallothioneins are involved in the cellular sequestration of toxic metal ions. Binds 12 cadmium ions per molecule (By similarity).
|
Q8TQ11
|
BRIX_METAC
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MLITTSRKPSAKTRTLCKLLSRFITGRCITRGKMGMQELIGFAEGGPLIVVGEYHGNPGELGFYDDAGKLLFSLRFSDWYSEDIGSYWFPDLEPVLAGQGEIADAFESFFHFKRVESEEVDQLPPLSTVLVAGEKEIDFTGSGKSLFKLNVKGFKKY
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
Q8TQM6
|
VAPB3_METAC
|
Putative antitoxin VapB3
|
MPTRTISISEEAYEKLKSLKSSEKDSFSDVILRYYPKKRKLSEVLAEIGPNPELADAIEKVSGEMRAEKMREIDPES
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC3 (Potential). {ECO:0000255|HAMAP-Rule:MF_00794}.
|
Q8TYC5
|
BRIX_METKA
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MRPAAITTSQRPARRTRSLCRDLECALPDATYVLRGTKNLRDTVLEALESGAEVLFYVTEAKGNPARLHVIDLGEIPPRLRLSFWLGGVKLQRELFGNRVDLSGDLVITTSKRPVSGHMKVAESLSEVLGVEFVPRAGSLEDVLEEALADVLLVVEGHPRHLGTLTFYRRTEKVGPSLFYRDFRTKDERMKL
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
Q8TZD7
|
Y2058_PYRFU
|
Putative antitoxin PF2058
|
MQVIEAIYEDGVLKPLKKLKLKEHSKVIIKIIDEEELEKILDSMVIEKVEGIDYKKLKEAYYESL
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
|
Q8TZI2
|
BRIX_PYRFU
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MMLITTSHRPTRRTRSFGHDLERVFPNSLYLTRGKKTIQELLMEAYDRGYERLLILNVWKGNPLKMTFIKVHPEDWGYLGYLYLHGIKLQREMGFKGLNPIREDMPLVVTTAKRVGWDHIAFAQVFAELTTGKFVPRGDKSLTYIADKYDTDVIAVIERHPRGMVINFYRLDVTKDRPVGPLINVKIWIMEDGRRWDYKEALGIKVPRREKGEGQESSSENRD
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
Q8U1B3
|
Y1308_PYRFU
|
Putative antitoxin PF1308
|
MILKPSKPYSFCFTTYPWKKLKLKEHSKVIIKIIDEEEIEKILDSMIIEKVEGIDYKKLKETHYESL
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
|
Q8U1I5
|
Y1222_PYRFU
|
Putative antitoxin PF1222
|
MVKTITISDDVYNELLRIKGNKSFSEVLRELLKERKGNKEVLKRIFGILSEEEYQEVKKRLKELEGEFEKWEQSLTQM
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. {ECO:0000255|HAMAP-Rule:MF_00794}.
|
Q8U2Q8
|
VAPB4_PYRFU
|
Putative antitoxin VapB4
|
MVKTITVSDDVYNELLRIKGKKSFSELLRELLREKKGNSVALKHIYGILNGEEYRETRKRLKELEKEFEKWKQFLTQV
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC4 (Potential). {ECO:0000255|HAMAP-Rule:MF_00794}.
|
Q8U394
|
VAPB3_PYRFU
|
Putative antitoxin VapB3
|
MQIVEAIYEDGVLKLLKNLKLKEHSKVIIKVIDEEEIEKILDSRDY
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Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC3 (Potential).
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Q8UEL0
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YIDD_AGRFC
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Putative membrane protein insertion efficiency factor
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MCGEPGCRHEQTAVKAGRSRNWAGSFAKTPGRLFGVGFIRLYQLTLSGFVGNSCRHIPTCSEYGYEAIARHGLWAGGWMALFRVARCGPGGTSGLDPVPEELDGSKRWWTPWRYWSRHR
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Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
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Q8V2L6
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PROF_CAMPM
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Profilin
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MVEWHKIIEDISKNNKFEDAAIVDYKTTKNVLAAIPNRTFAKINPGEVIPLITNHNILKPLIGQKFCIVYTNSLMDENTYAMELLTGYAPVSPIVIARTHTALIFLMGKPTTSRRDVYRTCRDHATRVRATGN
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More likely to influence phosphoinositide metabolism than actin assembly.
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Q8V2N2
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VTF3L_CAMPM
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Intermediate transcription factor 3 large subunit (VITF-3 45 kDa subunit)
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MDNLFTFLHEIEDRYARTIFNFHLISCDEIGDIYGLMKERISSEDMFDNVVYNKDIHPAIKKLVYCDIQLTKHIINQNTYPVFNDSSQVKCCHYFDINSDNSNISSRTVEIFEREKSSLVSYIKTTNKKRKVNYGEIKKTVHGGTNANYFSGKKSDEYLSTTVRSNINQPWIKTISKRMRVDIINHSIVTRGKSSILQTIEIIFTNRTCVKIFKDSTMHIILSKDNDEKGCIHMIDKLFYVYYNLFLLFEDIIQNEYFKEVANVVNHVLTATALDEKLFLIKKMAEHDVYGVSNFKIGMFNLTFIKSLDHTVFPSLLDEDSKIKFFKGKKLNIVALRSLEDCINYVTKSENMIEMMKERSTILNSIDIETESVDRLKDLLLK
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Acts with RNA polymerase to initiate transcription from intermediate gene promoters.
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Q8V2R6
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D3_CAMPM
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27 kDa core protein
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MDIFIVKDNKYPKVDNDDNEVFILLGNHNDFIRSKLTKLKEHVFFSEYIVTPDTYGSLCVELNGSSFQHGGRYIEVEEFIDTGRQVRWCSTSNHISEDIPEDIHTDKFVIYDIYTFDSFKNKRLVFVQVPTSLGDDSYLTNPLLSPYYRNSVARQMVNDMIFNQDSFLKYLLEHLIRSHYRVSKHITIVRYKDTEELNLTRICYNRDKFKAFAFAWFNGVLENEKVLDTYKKVSDLI
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Late protein which is part of a large complex required for early virion morphogenesis. This complex participates in the formation of virosomes and the incorporation of virosomal contents into nascent immature virions (By similarity).
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Q8V3L7
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D3_SWPV1
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27 kDa core protein
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MDIVVIRDDIYPIFNNEDKIVLLLGNHQEFISNFISKINIHALFYCKYSIIPDEIGTLNVSIIESSHKIRGRYINVEEFISLLYPIQLCSKYTYKNDIDHDTMFIHDIIFFNNTWVRILFIEFLGIIDKQYETCIINPYLVKDNYKIFKNILLASIINNIIFDKNSTLIELINKLYTRYHIDKYIMTCIVKYNDYNNIKLIYHCYNRNKFNAFIYAWFRSQITCDSIEENEKVERMFNNISKRI
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Late protein which is part of a large complex required for early virion morphogenesis. This complex participates in the formation of virosomes and the incorporation of virosomal contents into nascent immature virions (By similarity).
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Q8V4T7
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PROF_MONPZ
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Profilin
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MAEWHKIIEDISKNNKFEDAAIVDYKTTKNVLAAIPNRTFAKINPGEVIPLITNHNILKPLIGQKFCIVYTNSLMDENTYAMELLTGYAPVSPIVIARTHTALIFLMGKPTTSRRDVYRTCRDHATRVRATGN
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More likely to influence phosphoinositide metabolism than actin assembly.
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Q8V4V4
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VTF3L_MONPZ
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Intermediate transcription factor 3 large subunit (VITF-3 45 kDa subunit)
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MDNLFTFLHEIEDRYARTIFNFHLISCDEIGDIYGLMKERISSEDMFDNIVYNKDIHPAIKKLVYCDIQLTKHIINQNTYPVFNDSSQVKCCHYFDINSDNSNISSRTVEIFESEKSSLVSYIKTTNKKRKVNYGEIKKTVHGGTNANYFSGKKSDEYLSTTVRSNINQPWIKTISKRMRVDIINHSIVTRGKSSILQTIEIIFTNRTCVKIFKDSTMHIILSKDKDEKGCINMIDKLFYVYYNLFLLFEDIIQNEYFKEVANVVNHVLMATALDEKLFLIKKMAEHDVYGVSNFKIGMFNLTFIKSLDHTVFPSLLDEDSKIKFFKGKKLNIVALRSLEDCTNYVTKSENMIEMMKERSTILNSIDIETESVDRLKELLLK
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Acts with RNA polymerase to initiate transcription from intermediate gene promoters.
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Q8V566
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PG027_MONPZ
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Interferon antagonist OPG027 (Host range protein 2)
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MGIQHEFDIIINGDIALRNLQLHRGDNYGCKLKIISNDYKKLKLRFVIRPDWSEIDEVKGLTVFANNYAVKVNKVDYTLYYVIYEAVIHLYNKKTEILIYSDDENELFKHYYPYISLNMISKKYKIKEENYSSPYIEHPLIPYRDYESMD
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Plays a role for multiplication of the virus in different cell types.
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Q8V7J0
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CAPSD_TTVV6
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Capsid protein
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MAWWWGRWRRRWPRRRWRRRRRVWPRRSRFAVRRRRRGRYVSKRRRFRRRRRRRGRPRYRGRRKKRQTLVIRQWQPDVVRFCKINGWLPLIVCGSGSTQNNFIVHSEDITPRGAPYGGNLTHITWCLEAIYQEFLMHRNRWTRSNHDLDLMRYVGVRFKAYRHPTTDYIISYSKTSPFQVTELSYLSCHPLLMLLSKHHIVVKSLQTKPRGKPYVKFFCKPPKLMLNKWYFTKDFAKVPILMMWATACEPRNPWLGEGTLSPCIGFYALKPSIYTSLSNLPAKVQMFATGTQSDSLTTSSTGFYKTVHPSSITTTSKEWEYTYTGLMEKFFKQATNKPYNWENYGTPADYGSTYTTFSTHRSTRYETIKKEYQKVYPTLTTQTPTNFFLTQEFGFYSPYYLTPSKRDIDWHTPYTYTRYNPLADKGLGNMIWADWCSRDEAAYSPTQSKCMLKDLPLFILFYGYIDWVQKSIGSQTITRDMRLMVICPYTEPQLVDPQDKTKGFVLYGDTFANGNMPVLAPQIPISWFVRWYPNFAHQREVLERVVSCGPFMVRDQEKNSWDITLGYHFLFKWGGSPLPSQAIDDPSQKPTHALPEPGTLPRILQVSDPARLGPKTIFHQWDQRRGLFTKRSIKRMSEYSSDDENFSPGPSKRPALDTRPEGLAGEQRSAYAFLRALQDSQDSEESQEEAPLLEEQAHQKEKEELLLKQPQQQRQHQRVLKRGLRVLFGDVLKLRRGLHIDPLLT
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Self assemble to form an icosahedral capsid.
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Q8VMM5
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RECXP_PSEPU
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Regulatory protein RecX
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MTITAQAPAFGNWLTPGDFLNFAKKIWAPVAESNIEAMERKVDELYGAACKRYPTYDTMVQNAFCASMDAAFGTDEQAEGVAEVFAYARDAYGYMSASEREAQRQEDADNGICSHGLDSMTCPCGCFEND
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Modulates RecA activity.
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Q8X560
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USPC_ECO57
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Universal stress protein C
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MSYSNILVAVAVTPESQQLLAKAVSIARPVKGHISLITLASDPEMYNQLAAPMLEDLRSVMQEETQSFLDKLIQDAGYPVDKTFIAYGELSEHILEVCRKYHFDLVICGNHNHSFFSRASCSAKRVIASSEVDVLLVPLTGD
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Required for resistance to DNA-damaging agents.
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Q8X6T2
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SYDP_ECO57
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Protein Syd
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MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQPTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLAPNLAEFLNQLKPLL
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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}.
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Q8X8T5
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LPHI_ECO57
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his operon leader peptide (his operon attenuator peptide)
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MTRVQFKQHHHHHHPD
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This protein is involved in the attenuation mechanism for the control of the expression of the his operon structural genes.
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