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
|
|---|---|---|---|---|
A8AI79
|
CBPM_CITK8
|
Chaperone modulatory protein CbpM
|
MVNVTVTFTITEFCLHTGVSEEELNEIVGLGVIEPCENETASWLFDDHAAIVVQRALRLRQELALDWPGIAMTLTLLEENDRLRQENRLLIQRLSRFIKHP
|
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}.
|
A8AL48
|
FDHE_CITK8
|
Protein FdhE homolog
|
MSIRIIPQDELEKSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEANAQGKPPLDIHVLPRDKHWQKLLHSLIAELKPEMSGPALAVIENLEKASEQELEQMASALFESNFASVSSDKAPFIWAALSLYWAQMASLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSRDLHYWSLDNEQASIKAESCGDCGTYLKILYQEKDPKVEAVADDLASLVLDARMEQEGFARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A8AP01
|
SYDP_CITK8
|
Protein Syd
|
MDELTSQALTAFTTRYCDAWHEKHNSWPLSEELYGVPSPCIISSTSDAVYWQPQPFEGEANVNAVESAFDIVIQSAVHAFYTTQFAGDMYAQFADEKLTLLQTWSADDFRRVQENLIGHLVTQKRLKLPPTLFIATLENELEVISVCNLSGEVCKETLGTRNRTVLAASLAEFLTQLKPLL
|
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}.
|
A8API1
|
FETP_CITK8
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLQREAEGQDFQLYPGELGKRIYNEISKEAWAQWQHKQTMLINEKKLNMMNVEHRKLLEQEMINFLFEGKDVHIEGYTPEEKK
|
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}.
|
A8AVA6
|
HRCA_STRGC
|
Heat-inducible transcription repressor HrcA
|
MVTERQNEILNLIIDIFTKTHEPVGSKALQDSINSSSATIRNDMAALEKQGLLEKAHTSSGRKPSVAGFQYFVKHSLSFDRLAENELYEVIKAFDHEFFNLEDILQQAADLLAKLSGCTVVALDVEPSRQRLTAFDIVVLSQHTALAVFTLDESNTITSQFMIPRNFLREDLDRLKALVQERFLGQTVLDIHYKIRTEIPQIIQRYFTTTDNVIHLFEHIFGDIFKENVIVSGKVGLLNFSDLKAYQFFDDSQKVAFEIRDSLAEDQMQSVRVADSRESCLSDLTIISSKFLIPYRGFGILAVIGPVNLDYQRVVSQVNVINRVLTMKLTDFYRYLSSNHYEVH
|
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}.
|
A8AXA1
|
Y1122_STRGC
|
UPF0122 protein SGO_1122
|
MEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFGVSRQAVYDNIKRTEKILEDYEMKLHMYSDYIVRSQILEEIAEKYPKDSFLQEQIATLSSIDNRD
|
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}.
|
A8AYF6
|
YABA_STRGC
|
Initiation-control protein YabA
|
MDKREIFDALDDFSQNLMLTLAEVEAIKKNLKSVIEENTVLRLENDKLRERLGEVEKTGPSKGGGQGRENLERIYLDGFHICTDFYGQRRDNDEEECAFCNELLFRE
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
A8E7D3
|
COX14_DANRE
|
Cytochrome c oxidase assembly protein COX14 homolog
|
MVSGKRIADVGYRLFSGSMMLLTVYGGYLCVVRAQRYMQRKKQLELAAQSENTASEIIKE
|
Plays a role in the assembly or stability of the cytochrome c oxidase complex (COX).
|
A8EV98
|
YIDD_ALIB4
|
Putative membrane protein insertion efficiency factor
|
MKWLFKYLIRFYQKYLTILSFGSCRYYPTCSQYALWQLDNNTFFKAIYFTILRILKCNQLFDGGFDYPIIKLKKNQNINYNKIKIVYWYVPLKNGKYLVVKNREWKKNNE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8EZ89
|
YIDD_RICCK
|
Putative membrane protein insertion efficiency factor
|
MSKILLLLIRFYQYFISPLLGNNCRFHPTCSEYAKESITLYGSLKGLWRAFKRIIKCQPFYNGTVLYDTEVRCHARKSGNPVKNKEPK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8F1C3
|
YIDD_RICM5
|
Putative membrane protein insertion efficiency factor
|
MTRILLLLLRFYQYFISPLLSNNCRFHPTCSEYAKEAISMHGSIKGLWLTFKRIIKCQPFCDGGYDTVPISIKNSKPLNKKI
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8FD61
|
Y1495_BACP2
|
UPF0122 protein BPUM_1495
|
MTLEKTTRMNYLFDFYQSLLTAKQKSYMSLYYLDDFSLGEIADEYEVSRQAVYDNIKRTEAMLEQYEEKLLLFKKFKERKELLKKMRELVADSAQTEEAEALIESLEKLD
|
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}.
|
A8FDN4
|
LUTA_BACP2
|
Lactate utilization protein A
|
MKVHLFVTCLIDTMQPNVGKATVEVLERLGVEVEFPESQVCCGQPAFNSGYTKETIKAAKNMIKAFETAEYVVTPSGSCKAMFLEYPQLLKEDPVWSTQAEALAEKTYELTEFIVDILHVTDVGASLKGNATYHTSCHMTRLLRIKEAPFTLLSNVKDLSMTPLPRAENCCGFGGTFSVKMTPISEQMVDEKVQSIEETGAQYIIGADCGCLLNIGGRLNRLDKPIQVMHIAEVLNSR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
A8FDN6
|
LUTC_BACP2
|
Lactate utilization protein C
|
MKGTISHRESFLTHIRQQLGKDSSSSASIQRPAWKHQVQWETNGLLSKEELVEQLKMQCQRIHTRVVETTPEEAPSALRSLMTEYGEGSVMTSGDHRFEQYGFYPMFDSLQHEGFAVTSWNAEASREENIRLAEQAAYSVVFSDYTLAESGTIVLSSHQGQGRALHFLPMMYIVCIEKSTVVPRMIQAVSTLNRLVEEGEQAKGAIHFISGPSNSADIEMNLVVGVHGPVRAVYLLIDDE
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
A8FGJ7
|
YIDD_BACP2
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKCISPLTPPSCRFYPTCSNYGLEAIKTHGALKGGWLTIKRILKCHPLHPGGIDPVPPKKEK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8FP43
|
YIDD_SHESH
|
Putative membrane protein insertion efficiency factor
|
MAKTQSPLQWLATTLIRGYQVFISPFLGANKCRFHPTCSTYAIEAIRLHGFAKGSWLAARRILKCHPLHPGGIDPVPPKKHRCNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8FSK6
|
FETP_SHESH
|
Probable Fe(2+)-trafficking protein
|
MARTVNCVYLKKESEGLGFQLYPGELGKRIFDNVSKEAWALWQSKQTMLINEKKLNMMNVDDRKFLEEQMMNFLFEGKEVEIEGYVPQKDDE
|
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}.
|
A8G7P9
|
YIDD_SERP5
|
Putative membrane protein insertion efficiency factor
|
MASPLSPGSRILIGLVRAYQLVISPLLGPRCRFQPTCSHYAIEALSRFGMIKGSWLALKRVLKCHPLNPGGDDPVPPKPDDNREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8G7V7
|
FDHE_SERP5
|
Protein FdhE homolog
|
MSIRIVPKEQLGAQREKSTTAETIPPLLFANLKSLYSRRAERLRKLATDNPLGDYLNFAAQLAEAQHHALHDNPLTLDLTEELQQGAASGKPPLDLSVFPRSEHWHKLLVSLIAELRPQAPEHILAVLDNLEKASSHELELLADALLNQDFGKIGSEKAPFIWAALSLYWAQMAGLIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTVSGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLATLVLDAKMEDEGFARSSINPFLFPGS
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A8GI78
|
NRDI_SERP5
|
Protein NrdI
|
MNPLVYFSSSSENTHRFVEKLSLPAMRIPIAGARSKLLMETPYILIVPSYGGGSAVGAVPIQVIRFLNDPQNRAFLRGVIAAGNTNFGAAYGIAGDIIAKKCQVPFLYRFELLGTTQDVANVRQGVTAFWQRQN
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A8GJ49
|
FETP_SERP5
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLQRDAEGQDFQLYPGEVGKRIYNEISKEAWAEWMKKQTMLINEKKLNMMNVDDRKLLEGEMIKFLFEGHDVHIEGYTPPSE
|
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}.
|
A8GN48
|
YIDD_RICAH
|
Putative membrane protein insertion efficiency factor
|
MSKILLLIVKFYQYFISPLLGNNCRFHPSCSEYAKEAITIYGSTKGLWITFKRIIKCQPFCNGGYDNVPISIKNYKSLNKKI
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8GX83
|
YIDD_RICB8
|
Putative membrane protein insertion efficiency factor
|
MTRILLLLLTFYRYFISPLLGGNNCRFYPTCSKYAKEALNTHGGIKGLWLIFKRIIKCQPLCDGGYDPVPPTK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8H1J7
|
FETP_SHEPA
|
Probable Fe(2+)-trafficking protein
|
MARTVNCVYLNKEAEGLGFQLYPGDLGKRIFDNVSKEAWALWQSKQTMLINEKKLNMMNVEDRKFLEEQMVNFLFEGKDVEIEGYVPQKDDE
|
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}.
|
A8H6N2
|
SYDP_SHEPA
|
Protein Syd
|
MSSLPALDLFLSKYQQAYVDQLGEQPRYYAQEQESDCVVGEMDSDGAVFWQGVVRDNPGQFENVESALELTLCPEINTFYGRHFSAPLFFDSKWGSGELIQVWNQTDFEYLQQNIIGHLMMKKKLKQEPTWFIGVLDDEDKMLTVNNADGSVWVEIPGELQSTKLAESLDEFISLLTPRVMPPVKPIEESMPELDHPGIWQRMKLMWNNLRGK
|
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}.
|
A8HAI1
|
YIDD_SHEPA
|
Putative membrane protein insertion efficiency factor
|
MAKTQSPLQWLATTIIRGYQLLISPMMGPRCRFNPTCSHYAIEAIRLHGVVKGCWFAGKRILRCHPLHPGGEDPVPNKKHRCDK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8HV62
|
COWN_AZOC5
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MRASPTPWLSRAEPYCQRESPMNLLTTTPAGDRYVTFNGIDFEGNMARVLAHLRRYIDDPRTGNAFWDRFKARLAAAESGGNAFQDKLLLLHSHVYYMGDLFEDQEDEAALADLRKLEEECF
|
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}.
|
A8LMA3
|
YIDD_DINSH
|
Putative membrane protein insertion efficiency factor
|
MSPLAWLLSLPVRAYRLIFSPWVGFNCRYDPTCSAYAMEALRKHGGVKGGWLTLRRILRCHPWGGTGVDDVPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8MK46
|
SP5G_ALKOO
|
Putative septation protein SpoVG
|
MQVTDVRIRRVTAEGKMKAIVSVTFDDEFVVHDIKIIEGQNGLFIAMPSRKMGEGDFRDIAHPINSSTRTKLQDAIFAEYEKMSDMEEEAANE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A8MKS2
|
YIDD_ALKOO
|
Putative membrane protein insertion efficiency factor
|
MSRLCIFLIQIYRKYISPLKRPSCRFHPTCSAYSMAAYERYGFFKGTYLTLKRILKCHPFHPGGYDPLR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8Q2R5
|
WDR48_BRUMA
|
WD repeat-containing protein 48 homolog
|
MTAIPVKKKVQVSFVIRDEKEPMHRSGVNCLQYDAQTGRLFSGGSDTIIRIWKSPDRKDDSGSSYSVGGKTRVRRDLHLQSMEHHTDWVNDIVLCCGVISASSDTTVKVWNAQKGFCMSTLRTHRDYVRALAYARDVEMVASGGFDQLIYLWDIATLTKLTALNNTVTTSSLTGNKDSIYSLATNPSGTVVISGSTEKVLRVFDPRACQKLMKLRGHTDNVKAVVVNRDGTQCISASSDGTIKLWSIGQQCCISSLKCHSESVWALQVDSNFSCVYSGGRDKRIFRTAINDFKTAQLMFIEDAPVQRLQLIDSESRFIWTATWNSSIKRWPLPSDAQISVEIKSDQYGETIPSIHEPDLTIPGAASIRQHVVLNDKRHIVTKDTDDNVAMWDVLKGRKVCDHGKRPMEEVIKDHFKKVFVPSWFTVDLKSGMLQITLDESDFFSAWVSAKDAGFPNIQNDTKINYGGMLLRALFEHWSRSFSDVDEESPTHRFNSVPGHTPLILCESTGRPIFRLMIRDAAHETESQMLSDFVPPWVLDVVERNQLPKFNKMPFFLLPHLSLGIKTPKKDRLSATEMLQVRKVMEHVYEKILNVNDASYSENGIPSAAQMLSPSLQANIEERVELYCQDQKLDPEMDLRTVKHFIWKQGGDLMLYYKPIR
|
Regulator of deubiquitinating complexes. Activates deubiquitination by increasing the catalytic turnover without increasing the affinity of deubiquitinating enzymes for the substrate (By similarity).
|
A8X7Z3
|
DCT6_CAEBR
|
Protein dct-6 (Daf-16/foxo controlled, germline tumor-affecting protein 6)
|
MIESTTSHQDFQQRSMTGYALEHPSYRVRGALFRHQDDGRLLSGTSSNFFHVRSSSKITGCGGDLEVIHALELERSQHTGLPVRVTNVVVFGSNDVVRLIQPIEGTEDVIVNGDYHVSIVQSVELFESSTVSKSRILKLPGKIVAVNAEKHSNTELLLVFLLETGLYHYSFCAQTSDHFQCIQAFRCNRPITSGLLWRDSGLLHVAYYDGFVRVGVVHEQYDDMLLVKRVAVNRNNLSVLLDVVFEEIGRIQKFEDTEKQRREDMLTTSKCLSDKLVSEEEVVEGDTATEDFAKLKVDFKNQSIRCERVSQRLISLRKLITIIKSYMDMNDQIEQMIALLVDQLEELEKLEQLCDEVQKTGNQNLIGKSWIAVEEKRMVVDELIAKVNSDQIKKHSAEWGNKIDQIIDQLNGCSESAKDMRMIISQNIFEHRGDKKDVYTHFVLDSQSRDITLYCLSGLTTLAIYPRKGKRHTSKTTNIRKSQIFRVASISLDASFATCLTAACAMKSAEGVYVADQNAVFPIYFYSEKRYLDAGNQLQIPAFDSISSILIEPHQMILGSVTGGLLHLSFDFASNYEHFVVASSMLAHPISSGAVNCIKLLATGESLLALHCTDAEVVVSEKDQDRWHRVTHHTGGAHSIAVTPFSVDERGSFAVVASDTFVRLKALQYAEESLIGLHDLGESRAEDENGHPIEVLNVSLDPSMQYRQLPCKLRYAVGFSDKAIRTYVALLTGQHDFTVTEKFIAQIEPLFSVQNMICFHGRPMGCYVSCAKTLQIWNDLDRHQQKKLKSERMQLLKLSSSVTSMERTEGFLLVGFADDRLSIYEEKGNGAVDLVGTIENWHTGLNDRSVLGLRTRISKTSCGTRLFIHSLTAHHIVIHTVLVTSSKIEQHDFIVAHEHSMSQPIGFEFVSYKYFEFLVYGRGISNEKLSIEDRKRMDCFRDFEFN
|
May have a role in tumor suppression.
|
A8YUK5
|
YIDD_LACH4
|
Putative membrane protein insertion efficiency factor
|
MRKILIFIVRIYQTLISPLFPPSCRYYPTCSNYMIDALKKHGPILGLIMGISRTLRCNPFVRGGVDPVPDNFTVFRNPHPERYEDEIIASKFHSNSK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A8Z002
|
NRDI_STAAT
|
Protein NrdI
|
MKIIYFSFTGNVRRFIKRTELENTLEITAENCMEPVHEPFIIVTGTIGFGEVPEPVQSFLEVNHQYIRGVAASGNRNWGLNFAKAGRTISEEYNVPLLMKFELHGKNKDVIEFKNKVGNFNENHGREKVQSY
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A8Z0V0
|
PSMA2_STAAT
|
Phenol-soluble modulin alpha 2 peptide
|
MGIIAGIIKFIKGLIEKFTGK
|
Peptide which can recruit, activate and subsequently lyse human neutrophils, thus eliminating the main cellular defense against infection.
|
A8Z0V1
|
PSMA1_STAAT
|
Phenol-soluble modulin alpha 1 peptide
|
MGIIAGIIKVIKSLIEQFTGK
|
Peptide which can recruit, activate and subsequently lyse human neutrophils, thus eliminating the main cellular defense against infection.
|
A8Z4C1
|
HRCA_STAAT
|
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}.
|
A8Z4L7
|
YIDD_STAAT
|
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}.
|
A9A9R2
|
EF1B_METM6
|
Elongation factor 1-beta (EF-1-beta) (aEF-1beta)
|
MATVIAKVKVMPTSPEVEKEALKETLKELVEKNDAKCRGVSDEPLAFGLYTVFVMVEMEEKEGGMDPIEEAMNALENVESAEVVELSLV
|
Promotes the exchange of GDP for GTP in EF-1-alpha/GDP, thus allowing the regeneration of EF-1-alpha/GTP that could then be used to form the ternary complex EF-1-alpha/GTP/AAtRNA. {ECO:0000255|HAMAP-Rule:MF_00043}.
|
A9AGR3
|
FETP_BURM1
|
Probable Fe(2+)-trafficking protein
|
MARMIQCAKLGKEAEGLDFPPLPGELGKRIYENVSKEAWQGWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGEGADQASGYVPPTEG
|
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}.
|
A9AUH0
|
HRCA_HERA2
|
Heat-inducible transcription repressor HrcA
|
MHLELNERRRRVLKAVIQQYIDTATPVASQDLARSLGVSSATVRNEMAALEDAGLLTHLHTSAGRLPTDAGYRFFVENLMDRAALSTQEQRMIQHQFYQIRSELNQWIHLAAAVLARTAQTAAVVTPPRAYESRFKHIELISINDALVLLVLVLHEGSVKQQTLPADPNTTQEQLSRIAGRINELCHEASAKAIANIAHNQSTNQPPLSSFEVLVIESVARAMQQFEEHVNELIHHDGLLEMLHQPEFGQVTRVREVLSILEGGTMLESLIPQALASDGVQVIIGGEHSRDELRDYSVILSRYGVNGDVAGVVGVLGPRRMAYPRSISSVRYIAGVMSDLMGDLYGERKIEPSE
|
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}.
|
A9AXJ9
|
YIDD_HERA2
|
Putative membrane protein insertion efficiency factor
|
MGKILLALIRLYQRFSRYTPPSCIYTPTCSHYGYQAIAKYGAFKGTWLTLKRIARCHPWAQGGEDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9BJC5
|
YIDD_PETMO
|
Putative membrane protein insertion efficiency factor
|
MKKLVLKSIDFYRKHISPATPPKCIYLPTCSSYTYEAVEKFGVFKGLYLGFRRFIRCNPLHKGGYDPVPEKFSFFVHKQGKNKQHRRSV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9C3G0
|
FETP_DELAS
|
Probable Fe(2+)-trafficking protein
|
MARTVHCIKLGVDAEGLDFPPYPGELGKRIFEGVSKQAWADWLKHQTMLVNENRLNLADARARQYLARQMENHFFGGGADAAAGYVPPTA
|
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}.
|
A9G6D9
|
YIDD_SORC5
|
Putative membrane protein insertion efficiency factor
|
MLATLLLALIRAYQMTLSRLIVALMGPVCRFEPSCSRYAAACIVDHGALRGSLLSLKRLCRCHPFHPGGFDPPPPPRLHRAAAARMPRQRDADPRDTTRCSSTGAELASHASSPCRAGFSGRVTLMD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9H4F6
|
COWN_GLUDA
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MTEQIDRYVSFRNVEWERRTAEVFALLQPHFDGSTSPFWDYFLRQRVIAHAQGLDDLRVLHNFLPTLKDLLEELDDERTLSRLEELEVLCM
|
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}.
|
A9ILE7
|
HRCA_BART1
|
Heat-inducible transcription repressor HrcA
|
MKHKPIDNELKYLDERSRDIFRHIVEAYLNDGEPVGSRNLSRLLQQTLSPATIRNVMSDLEHLGLIYAPHVSAGRMPTQSGLRFFVDAFMEAGDLPNEERENIEMQVKEAGHAQSVEHFLVQASRVLSDLSRGAGLVLATKQEGTLKHIEFVRLDREHALAVLVTQQGEVENRIVHLPEGVTHAQLTEATNFLNAHIQGRTLSEAKEEIACLCAETRAALDDLSHHLVETGLALLGGEGADHKIHLIVRGRSNLLEDVKAEEDLERLRHLFDDLETRESMAQLLDLTDEGSGVRIFIGSENKLFSLSGSSLVVAPYRDSQQRVIGALGVIGPTRLNYARIVPMVDYTAQLVSQLLR
|
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}.
|
A9IML0
|
NRDI_BART1
|
Protein NrdI
|
MGLIVYYSSATGNTEHFVSQLGQRLFKIDKRKPSAFVGEPYVLVVPTYADGEGRGAVPKAVIHFLNEAENRKLIRGVIGSGNRNFGRYYSLASKIIAEKCGVPCLYRFELRGTDEDVICVKKGLERFWKQLG
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A9IVA8
|
YIDD_BART1
|
Putative membrane protein insertion efficiency factor
|
MLKSQFQQKKMTRNYTGAWQKTPGRLLGIFLIRFYQITLSSLIGNQCRHAPTCSEYIYEAIARHGLWAGAWMGLFRIMRCGPFGTDGFDPVPPSLGHSCCFYKPWRYWKISDKHNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9KBT2
|
YIDD_COXBN
|
Putative membrane protein insertion efficiency factor
|
MYKQIVHAIGKAIQTLLLGLIKSYRYLISPVLMSSCRFYPSCSCYAETALKRFGVIKGSGLTVWRLLRCHPFHPGGVDFVPEKSNEMV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9KCK3
|
FETP_COXBN
|
Probable Fe(2+)-trafficking protein
|
MTRRIICQKLGKEADALNYSPYPGELGERIYNHISEQAWQAWLSHQTMLINEYRLSLIDPKARQFLEQEMINFLFGTGSEKPAGYTSEKE
|
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}.
|
A9KE66
|
CBPM_COXBN
|
Chaperone modulatory protein CbpM
|
MTKQIIKGIIIERSSPLKIDELSQAVHLRREIIIEMVEHRLIEPEGSSPTSWKFDNVCLKRAKIAASFYRDLEINMPGIAIALDLLDKIEHLEQRLRTLERFENQE
|
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}.
|
A9KLY2
|
YIDD_LACP7
|
Putative membrane protein insertion efficiency factor
|
MKRILIAIVKLYRKYISPMKRVPTCRFTPTCSEYALEALQRYGAIRGSYLAVRRILKCHPFHKGGFDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9KR30
|
SP5G_LACP7
|
Putative septation protein SpoVG
|
MQITDVRVRRVSKEGKMKAVVSITLDNEFVVHDIKVIEGEKGLFIAMPSRKAGDGEYRDIAHPINSITRDKIQSIILEKYELAALEGNIEEAE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A9KUI6
|
SYDP_SHEB9
|
Protein Syd
|
MSCLPALDKFLQNYHQAYLTSLGELPRYYPQGEPSVCIQGEFHADLDQAVSWQPVKREVEGSFANVEHALELTLWPEINHFYGQYFSAPLLFDSKWGTGELLQVWNEDDFTCLQQNLIGHLMMKKKLKQPPTWFIGLLDEGDKMLTINNSDGSVWIELPGEIPTQQLSPSLAEFIGALSPRIAPPVKHEELPMPALEHPGIFASFKRMWQNLFGKR
|
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}.
|
A9KV86
|
FDHE_SHEB9
|
Protein FdhE homolog
|
MSHTAEIPLVPGSESPLELKPLKAADPQIVYHRRAHRLLSLAKDSPLADYFELCRRLVSIQAKLAEGADFGQLLAWGKDEATPLSLLGSEADSYWQGLLQQLLSDLLPQVDESIARVVRLLMQQSPEQLSSWGRSLRQGHVSEVPAHFSLFIWAAMGVYWSHWAPMVIKRMDQRKVAQQSMCPVCGCHPVASVIVDQPRAGLRYLHCSLCESEWHYIRAHCTSCGQDKEMTIWSLDDAQAQVRIESCDECHGYTKMMFVENSPSMDVAADDLATLMLDSELNAKGFGATTLNPLLMAHETT
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A9KX21
|
YIDD_SHEB9
|
Putative membrane protein insertion efficiency factor
|
MAQTQSPLQWLATTLIRGYQVFISPILGPRCRFNPTCSHYAIEAIKVHGTAKGCWFALKRILKCHPLHPGGSDPVPPKNDRCNK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9KXQ7
|
FETP_SHEB9
|
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}.
|
A9M0D3
|
FETP_NEIM0
|
Probable Fe(2+)-trafficking protein
|
MARMVFCVKLNKEAEGMKFPPLPNELGKRIFENVSQEAWAAWTRHQTMLINENRLSLADPRAREYLAQQMEQYFFGDGADAVQGYVPQ
|
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}.
|
A9M153
|
YIDD_NEIM0
|
Putative membrane protein insertion efficiency factor
|
MNFLLSKLLLGLIRFYQYCISPLIPPRCRYTPTCSQYAVEAVKKYGAFKGGRLAIKRIARCHPFGGHGHDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9M7B7
|
HRCA_BRUC2
|
Heat-inducible transcription repressor HrcA
|
MMRPPEHQLLSSLDQRSRDIFRLIVETYLNDGDPVGSRNLSRLLPHTLSPATIRNVMSDLEHLGLIYAPHISAGRLPTQIGLRFFVDAFLEVGDLPPEERSSIEAQVRAAGTSNSVESVLTEASQVLSGLSRGAGLVLTNKTDVALKHIEFVRLEPMRALAVLVMQNGDVENRVIDLPAGISTSQLIEASNFLNAHIHGHTLSEAKSELRKLSEETRRELDQLSQELVAKGLAVWSGAGADQPARLIVRGRANLLENVHAQEDIERLRHLFDDLETKDGMVQLLDLAEAGSGVRIFIGSENKLFSLSGSSLVVAPYRDSEQRVIGALGVIGPTRLNYARIVPMVDYTAQIVSRLLR
|
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}.
|
A9ME65
|
NRDI_BRUC2
|
Protein NrdI
|
MSLIVYFSSRSGNTHRFVERLGVRSSRIPLEASGALQVREPFVLVTPTYGGGSTKGAVPNPVIRFLNDADNRALIRGVIAAGNSNFGEAFCIAGNIISAKCGVPYLYRFELLGTAEDVGNVRNGMEQFWTRQTQA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A9MG06
|
NRDI_SALAR
|
Protein NrdI
|
MSALVYFSSSSENTHRFMQRLGLPATRIPLNERERIRVDEPYILVVPSYGGGGMAGAVPRQVIRFLNDEHNRARIRGVIASGNRNFGDAWGCAGDVIAQKCGVPWLYRFELMGTQRDIDHVRKGVNEFWRQQTRSA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A9MH54
|
CBPM_SALAR
|
Chaperone modulatory protein CbpM
|
MANITVTFTITEFCLHTGVTEEELNEIVGLGVIEPYEDDNANWQFDDRAASVVQRALRLREELALDWPGIAVALTLLEENSRLREENRQLLLRLSRFISHP
|
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}.
|
A9MI98
|
FDHE_SALAR
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNVYNRRAERLRELAESNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEANEQGKPPLDIHVLPRDKHWQKLLHSLIAELKPEMSGPALAVIENLEKASDQELEQMASALFDSDFSYVSSDKAPFIWAALSLYWAQMASLIPGKARAEYGEARQYCPVCGSMPVSSVVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSRDLHYWSLENEQAAVKTESCGDCGTYLKILYQEKDPKVEAVADDLASLVLDARMEQEGFARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A9MSB6
|
SYDP_SALAR
|
Protein Syd
|
MDELTAQALKAFTRRYCGAWQEKHGSWPLSEELYGVPSPCIISSTRDAVYWQPQPFEGEENVNAVERAFDIVVQPALHAFYTTQFAGDMPAQFADEKLTLLQTWSQDDFRRVQENLIGHLVTQKRLRLSPTLFIATQENELEVISICNLSGEVIKETLGTRHRIVLAATLAEFLTQLNPLL
|
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}.
|
A9MZB0
|
FDHE_SALPB
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNVYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEANDQGKPPLDIHVLPRDKHWQKLLHSLIAELKPEMSGPALAVIENLEKASEQELEQMASALFASDFASVSSDKAPFIWAALSLYWAQMASLIPGKARAEYGEARQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSRDLHYWSLENEQAAVKAESCGDCGTYLKILYQEKDPKVEAVADDLASLVLDARMEQEGFARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A9N099
|
NRDI_SALPB
|
Protein NrdI
|
MSALVYFSSSSENTHRFMQRLGLPATRIPLNERERIQVDEPYILVVPSYGGGGMAGAVPRQVIRFLNDEHNRARIRGVIASGNRNFGDAWGCAGDVIAQKCGVPWLYRFELMGTQRDIDNVRKGVNEFWQQLSRSA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A9N2H6
|
SYDP_SALPB
|
Protein Syd
|
MDELTAQALKAFTTRYCDAWQEKHGSWPLSEELYGVPSPCIISSTRDAVYWQPQPFEGEENVNAVERAFDIMVQPALHAFYTTQFAGDMPAQFADEKLTLLQTWSQDDFRRVQENLIGHLVTQKRLKLPPTLFIATQENELEVISVCNLSGEVIKETLGTRNRTVLAATLAEFLTQLNPLL
|
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}.
|
A9N6S3
|
CBPM_SALPB
|
Chaperone modulatory protein CbpM
|
MANITVTFTITEFCLHTGVTEEELNEIVGLGVIEPYEDDNADWQFDDRAASVVQRALRLREELALDWPGIAVALTLLEENSRLREENRLLLQRLSRFISHP
|
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}.
|
A9NBA4
|
YIDD_COXBR
|
Putative membrane protein insertion efficiency factor
|
MYKQIVHAIGKAIQTLLLGLIKSYRYLISPVLMSSCRFYPSCSCYAETALKRFGVIKGSGLTVWRLLRCHPFHPGGVDFVPEKSNEMV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9NCX7
|
FETP_COXBR
|
Probable Fe(2+)-trafficking protein
|
MTRRIICQKLGKEADALNYSPYPGELGERIYNHISEQAWQAWLSHQTMLINEYRLSLIDPKARQFLEQEMINFLFGIGSEKPAGYTSEKE
|
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}.
|
A9NDK7
|
CBPM_COXBR
|
Chaperone modulatory protein CbpM
|
MTKQIIKGIIIERSSPLKIDELSQAVHLRREIIIEMVEHRLIEPEGSSPTSWKFDNVCLKRAKIAASFYRDLEINMPGIAIALDLLDKIEHLEQRLRTLERFENQE
|
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}.
|
A9NE80
|
SP5G_ACHLI
|
Putative septation protein SpoVG
|
MKITDVRVRHVSSDSRLKGVVTITFEDAFVVHDIRVIEGENGLFVAMPSKKMPNGGFRDIAHPIHADMRKQIEDSIIKAYKETLDAEATASVEE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A9R2J4
|
SYDP_YERPG
|
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}.
|
A9R4E5
|
FDHE_YERPG
|
Protein FdhE homolog
|
MSIRIVPKDQLGKQREKGTTAGNIPPLLFANLKSLYTRRTERLQQLALDNPLADYLDFAAKITEAQQKALHDHPLVLDMQAELVQSAASGKPPLDGSVFPRTEHWRKLLSALIAELRHDAPDHILAVLDNLDKASVHELELYADALLNRDFSQVGSEKAPFIWAALSLYWAQMASQIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTHNGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLASLILDAKMEGEGFARSSINPFLFPGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A9R6R1
|
FETP_YERPG
|
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}.
|
A9R9H4
|
LCRV_YERPG
|
Virulence-associated V antigen (Low calcium response locus protein V)
|
MIRAYEQNPQHFIEDLENVRVEQLTGHGSSVLEELVQLVKDKNIDISIKYDPRKDSEVFANRVITDDIELLRKILAYFLPEDAILKGGHYDNQLQNGIKRVKEFLESSPNTQWELRAFMAVMHFSLTADRIDDDILKVIVDSMNHHGDARSKLREELAELTAELKIYSVIQAEINKHLSSSGTINIHDKSINLMDKNLYGYTDEEIFKASAEYKILEKMPQTTIQVDGSEKKIVSIKDFLGSENKRTGALGNLKNSYSYNKDNNELSHFATTSSDKSRPLNDLVSQKTTQLSDITSRFNSAIEALNRFIQKYDSVMQRLLDDTSGK
|
Possibly involved in calcium regulation of YOP expression, which includes the export process.
|
A9VHU3
|
HRCA_BACMK
|
Heat-inducible transcription repressor HrcA
|
MLTERQLLILQTIVDDFIGSAQPVGSRTLAKKDEITFSPATIRNEMADLEELGFIEKTHSSSGRVPSEKGYRFYVDHLLAPQNLPTDEIVQIKDLFAERIFEAEKIAQQSAQILSELTNYTAIVLGPKLSTNKLKNVQIVPLDRQTAVAIIVTDTGHVQSKTITVPESVDLSDLEKMVNILNEKLSGIPMAELHNKIFKEIVTVLRGYVHNYDSAIKMLDGTFQVPLSEKIYFGGKANMLSQPEFHDIHKVRSLLTMIDNEAAFYDILRHKQVGIQVKIGRENSSTAMEDCSLISATYSIGEEQLGTIAILGPTRMQYSRVISLLQLFTRQFTDGLKK
|
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}.
|
A9VI76
|
LUTA1_BACMK
|
Lactate utilization protein A 1
|
MKVSIFITCVADVFYPEVGKDVVEILEDLGCEVDFPKTQTCCGQPAYNSGYVKETKTAAKHMIEAFASSEYVVAPSGSCAMMVHEFSSLFSESEADWKKKATELGNKTYEFTQFLVEVLGKEDLGAELHKKATVHTSCHMSRLMGIKEPPQKLLKCVKGLEVVSLPHNYDCCGFGGTFSVKMPEISEQMVEEKVKHIMETGAELLIGMDCSCLMNIKGRLTRNGYPIDVKHIAQVLNEDRKQGGI
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
A9VI78
|
LUTC1_BACMK
|
Lactate utilization protein C 1
|
MMAIQNREEFLLQLSEKLGRKRPEAVEKPKWSFSPQWNVFDGLAQDELVLQLMEHCEVIHTEVKRTTKENLVETLGSLIKEWNIKSAMYSNDERFNEYGLTSCFNNEGTTHFRAWGLGDKEEDIKFAKAADLGITFSDMTLAESGTVVLFNDGLKGRHVSLLPESYIAIVPKSTIVPRLTQATKLIHNQSKAGENLPACVNFVSGPSNSADIEMNLVVGVHGPIRTAYIIVDDQ
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
A9VKN0
|
LUTA2_BACMK
|
Lactate utilization protein A 2
|
MKVTLFVTCLVDMFETNVGKATVEVLERLGCEIEFPEAQVCCGQPAYNSGHVEAAKEAMKHMIETFEDAEYIVTPSGSCATMFHEYPHVFKDDPKWAKRAQKVADKTYEFTQFIVDVLKVTDVGASLPGIATIHKSCHMTRLLGVKEAPGILLSSVKGLIVRELPNVQNCCGFGGTFSVKMTPISEQMVDEKVDSVMETGADYLIGADCGCLLNIGGRIERLGKEVKVMHIAEVLNSRS
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
A9VKN2
|
LUTC2_BACMK
|
Lactate utilization protein C 2
|
MTGLIQNRESFLDNIAKELGRARKTEGVERPAWKSNVNVETLKDYSQEELLEVFKKQCTNIHTTVVETTNDRLREDIQKVIVENGGGPIILSADERFDSYGLTSLFKEELPKQNVEVNVWDPEKKEENMRIAEKANIGIAFSDYTLAESGTIVVQSHKGQGRSLHFLPTVYFAIIPRETLVPRITQAVQDMNSRVEKGEAVASCINFITGPSNSADIEMNLVVGVHGPLKAVYFIV
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
A9VLF7
|
YIDD_BACMK
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQKHGTFKGFWLTCKRILKCHPFHPGGFDPVPDKKDDKVNS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9VN46
|
YABA_BACMK
|
Initiation-control protein YabA
|
MEKKDIFASVSSMEEQIGHLYKQLGELKQHLAELLEENQHIKMENENLRHRFEEVQNKEKQKTQKRKEMKAKTDIGEGYDNLARLYQEGFHICNLHYGSVRKEGDCLFCLSFLNKK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
A9VT84
|
Y3669_BACMK
|
UPF0122 protein BcerKBAB4_3669
|
MLEKTTRMNYLFDFYQSLLTQKQRSYMSLYYLDDLSLGEIAEEFDVSRQAVYDNIKRTEAMLEEYEDKLVLLQKFQERQRLVAKLKQLLSEEEHVNEEMKQVVEAIEKLD
|
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}.
|
A9WDP2
|
YIDD_CHLAA
|
Putative membrane protein insertion efficiency factor
|
MLRWLLLKLIRFYQVAISPWTPPSCIYTPTCSHYGYEAIKKYGALRGGWMTVKRIARCHPFARGGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A9WY13
|
NRDI_BRUSI
|
Protein NrdI
|
MSLIVYFSSRSGNTHRFVERLGVRSSRIPLEASGALQVREPFVLVTPTYGGGSTKGAVPNPVIRFLNDADNRALIRGVIAAGNSNFGEAFCIAGNIISAKCGVPYLYRFELLGTAEDVGNVRNGMEQFWTRQTQA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
B0B7W4
|
HRCA_CHLT2
|
Heat-inducible transcription repressor HrcA
|
MENRIEMSQLRASKKDSKISYVLLMATKLYLESGQPVGSKLLEETYCSDLSSATIRNYFAQLETNGFLRKNHISGGRIPTDLAFRYYADHNAPFLEQEEILAIQQKLTELPEYSKNIVKDLQKASEVLSDILQLPVCFSSPRFESDSVINIQLVAIDDQRVVFVLSTEFGQVFTDVLWLPEQLPENSLKRIEGFLQNYLRKQPSDSLLSQKEEDLGMVLYNEVVVRYLTRYCHFSEEDLYQTGLSRLLKYETFKDPETLAQGLAFFENRKHMCQLLNTYLHKETPTAFIGRELTDIVGNTDPSCAVITIPYYMDRTPLGAFGVLGPMNLPYQQVFGTLSLFTERLKVILTQSFYKFKLSFRRPCPTDPRCSQRPAELTRSSSIKLLPAKELS
|
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}.
|
B0B846
|
YIDD_CHLT2
|
Putative membrane protein insertion efficiency factor
|
MQTSRISSFFRGLVHLYRWAISPFLGAPCRFFPTCSEYALVALKKHPLRKSLFLIAKRLLKCGPWCIGGIDLVPRTSVEEYLSSPTPLAESPDDRTVPHTQETS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
B0BC29
|
HRCA_CHLTB
|
Heat-inducible transcription repressor HrcA
|
MENRIEMSQLRASKKDSKISYVLLMATKLYLESGQPVGSKLLEETYCSDLSSATIRNYFAQLETNGFLRKNHISGGRIPTDLAFRYYADHNAPFLEQEEILAIQQKLTELPEYSKNIVKDLQKASEVLSDILQLPVCFSSPRFESDSVINIQLVAIDDQRVVFVLSTEFGQVFTDVLWLPEQLPENSLKRIEGFLQNYLRKQPSDSLLSQKEEDLGMVLYNEVVVRYLTRYCHFSEEDLYQTGLSRLLKYETFKDPETLAQGLAFFENRKHMCQLLNTYLHKETPTAFIGRELTDIVGNTDPSCAVITIPYYMDRTPLGAFGVLGPMNLPYQQVFGTLSLFTERLKVILTQSFYKFKLSFRRPCPTDPRCSQRPAELTRSSSIKLLPAKELS
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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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B0BCB1
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YIDD_CHLTB
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Putative membrane protein insertion efficiency factor
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MQTSRISSFFRGLVHLYRWAISPFLGAPCRFFPTCSEYALVALKKHPLRKSLFLIAKRLLKCGPWCIGGIDLVPRTSVEEYLSSPTPLAESPDDRTVPHTQETS
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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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B0BPI1
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FDHE_ACTPJ
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Protein FdhE homolog
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MSIRILPENEIKQAASSFQNPPLLFANPKNLYFRRAKRLRQLAENNPFGDYLEFAANLSEVQLDLLENHPIANYAEKLTACIEESNGQKPLNAKTFKRSSEWRELLLLLTEKFKPYANDTMLATIELLEKSSTSELEALADDLLNERYEAVGADKAVFLWAALSLYWTQLAQQLPRNTQTEVGERHTCPVCDSAPIVSVVHFGDTQGLRYLHCSLCESEWNMVRSQCSVCDQSGKLDYWSIDSVDAPVKAESCGDCESYLKVLYQEKDPHVEPVADDLGTLFLDAEMEQKGFARSGLNPFLFQVE
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Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
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B0BSG9
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FETP_ACTPJ
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Probable Fe(2+)-trafficking protein
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MARTVFCEYLKQEAEGLDFQLYPGELGKRIFDSISKQAWSEWIKKQTMLVNEKKLSMMNAEHRKLLETEMVNFLFEGKEVQIEGYVPVEQK
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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}.
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B0BX69
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YIDD_RICRO
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Putative membrane protein insertion efficiency factor
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MTRILLLLLRFYQYFISPLLGNNCRFHPTCSEYAKEAISMHGSIKGLWFTFKRIIKCQPFCDGGYDTVPISIKNSKPLNKKI
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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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B0CJ31
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HRCA_BRUSI
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Heat-inducible transcription repressor HrcA
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MMRPPEHQLLSSLDQRSRDIFRLIVETYLNDGDPVGSRNLSRLLPHTLSPATIRNVMSDLEHLGLIYAPHISAGRLPTQIGLRFFVDAFLEVGDLPPEERSSIEAQVRAAGTSNSVESVLTEASQVLSGLSRGAGLVLTNKTDVALKHIEFVRLEPMRALAVLVMQNGDVENRVIDLPAGISTSQLIEASNFLNAHIHGHTLSEAKSELRKLSEETRRELDQLSQELVAKGLAVWSGAGADQPARLIVRGRANLLENVHAQEDIERLRHLFDDLETKDGMVQLLDLAEAGSGVRIFIGSENKLFSLSGSSLVVAPYRDSEQRVIGALGVIGPTRLNYARIVPMVDYTAQIVSRLLR
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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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B0FIH3
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CAPSD_BPE32
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Major capsid protein (Gene product 11) (gp11) (Major head protein)
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MANPTLFVSYDQNGKKLSFANWISVLSPQDTPFVSMTGKESINQTIFSWQTDALASVDGNNAHVEGSRAEDGEMKPTVIKSNVTQILRKVVRVSDTANTTANYGRGRELMYQLEKKGKEIKRDLEKILLSGQARTDVLADQYLTNSATDPAVVGLNDTHAARKTGAFQFLCAHGGLAGGVVDKTKNGPADPDTGAVTVKVAQNASNPTTNIGFDEADIFDMTLQLYTAGSEADIIMINPAHAKIFAGLQENTQGSRKRIFENTKQFIYEVNSITDPLGQSYKIIVNRWMPTDAVYFFRSADWTQMVLRAPKRTELAKDGSYEKWMIEMEVGLRHRNPYASGVLFTAAGKVAA
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Assembles to form a prolate capsid of about 145 nm x 44 nm.
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B0FII2
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FIB20_BPE32
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Putative tail tip fiber protein (Gene product 20) (gp20)
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MGAGGFRKNTGRNNTTLPYNVGFLNNVQDTETYNVAVYDELQKVSTATNQMFQAIDEIHEEIDVRIKALNAMNLQFDELENRITTEIETAIADIQTQMGNLSTEDIWDNSVQPPVKLESTVSGFKTSIEGNTTKIQTVEGIVNDQGQEIALVQTELQNINGSLSQYMKLSEYEATWGVNSTVNGRYAGVKLTNNGTNSQFQVTANKFIVGDGSSGNTPFVFEGGRARMEFADIKNVNITTAQIANARIQWAQIDNVSISNAQIQNLSADKITAGSMWGSNWRLTVGGDFVMGGTGGAQLWMNGNRIDFYDGSGALRIRIGSW
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Putative tail tip fiber protein.
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B0JMD9
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YIDD_MICAN
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Putative membrane protein insertion efficiency factor
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MKGIFIGLIEGYRRFISPLFPPSCRFQPTCSQYAMEAIDRFGVLRGSWLAIKRILRCHPFHPGGYDPVPPCHHKHD
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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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B0K1V2
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Y1714_THEPX
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UPF0122 protein Teth514_1714
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MDDDFLFMTLLYDFYGALLTDKQREIFEMYYLNDYSLGEISELLDISRQGVYDTLKRAESSLEFFEEKLGLVKRHQEIMNKLDKIKKGIEIIRERERDPEILKIIEEIAREIEELNL
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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}.
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