entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
Q2YWL4
|
EMP_STAAB
|
Extracellular matrix protein-binding protein emp
|
MKKKLFVLTMSTLFATQLINSNHANASTESVDKNFVVPESGINKIIPTYDEFKKAPKVNVGSLADNKNFVASEDKLSKIADPSAASKIVDKNFVVPESKLGNIVPEYKEINNRVNVATNNPASQQVDKHFVAKGPEVNRFITQNKVNHPFITTQTHYKKVITSYKSTHVHKHVNHATGSINKHFIVKPSEAPRYTQPSQSLMINHYFAVPGYHAHKFVTPGHASIKINHFCVVPQINSFKVIPPYGHNSHRMHVPSFQNNTTATHQNAKVKKAYDYKYFYSYKVVKGVKKYFSFSQSNGYKIGEPSLNIKNVNYQYAVPSYSPTHYVPEFKGSIPAPRV
|
Adhesin that binds to the host cell extracellular matrix proteins fibronectin, fibrinogen, collagen, and vitronectin.
|
Q2YXI0
|
Y1100_STAAB
|
UPF0122 protein SAB1100
|
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}.
|
Q2YXX8
|
CVFB_STAAB
|
Conserved virulence factor B
|
MALDKDIVGSIEFLEVVGLQGSTYLLKGPNGENVKLNQSEMNDDDELEVGEEYSFFIYPNRSGELFATQNMPDITKDKYDFAKVLKTDRDGARIDVGLPREVLVPWEDLPKVKSLWPQPGDHLLVTLRIDRENHMYGRLASESVVENMFTPVHDDNLKNEVIEAKPYRVLRIGSFLLSESGYKIFVHESERKAEPRLGESVQVRIIGHNDKGELNGSFLPLAHERLDDDGQVIFDLLVEYDGELPFWDKSSPEAIKEVFNMSKGSFKRAIGHLYKQKIINIETGKITLTKKGWSRIDSKE
|
Contributes to the expression of virulence factors and to pathogenicity. Involved in the production of hemolysin, DNase, protease and protein A (By similarity).
|
Q2YY17
|
MSA_STAAB
|
Protein msa (Modulator of SarA)
|
MKYLILSLVANLLVFGVLSAIGLNINILAAMMMILVIPITISGILFFKTNLDKTYIFFNILFIDFYYYIYNVHLMALPRFNSYIKAEMMELEDIDVLITSKDFGFDEILFFTLYLLLILIILYYLKKQVKTKS
|
Accessory element involved in the expression of sarA and several virulence factors. Modulates SarA production and/or function in a strain-dependent manner. Affects the transcription of the accessory gene regulator (agr) and genes encoding virulence factors including alpha toxin (hla) and protein A (spa) (By similarity).
|
Q2YY38
|
CVFC_STAAB
|
Conserved virulence factor C
|
MEILRIEPTPSPNTMKVVLSYTREDKLSNTYKKVEETQPEFINQLLSIDGITSIFHVMNFLAVDKSPKADWEVILPDIKAAFSDANKVLESVNEPQIDNHFGEIKAELLTFKGIPYQIKLTSADQELREQLPQTYVDQMTQAQTAHDNIVFMRKWLDLGNRYGNIEEVMDGVLEEVLATYPESQLPVLVKHALEENHATNNYHFYRHVSLDEYHATDNWKTRLRTLNHFPKPTFEDIPLLDLALSDEKVPVRRQAIVLLGMIESKEILPYLYKGLRDKSPAVRRTAGDCISDLGYPEALPEMVLLLDDPQKIVRWRAAMFIFDEGNAEQLPALKAHINDNAFEVKLQIEMAISRIENGDEALGSVWKQMANRTI
|
Required for hemolysin production.
|
Q30YQ4
|
YIDD_OLEA2
|
Putative membrane protein insertion efficiency factor
|
MTIELRKIAILPIRFYQRFISPLFPPSCRFVPTCSAYAAEAVLRHGIIKGGFLALRRILRCNPLCAGGYDPVPESRHQDAKRVRSC
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q31CC8
|
YIDD_PROM9
|
Putative membrane protein insertion efficiency factor
|
MFKTINKSITSILLFMISFYQKWFSPFFGPRCRFIPSCSSYGYEAITRHGPWKGGWLTLRRLSRCHPLTPCGCDPVPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q31EE3
|
YIDD_HYDCU
|
Putative membrane protein insertion efficiency factor
|
MNPFKWLIILPVRFYQLFISPILGPRCRFYPTCSHYTIEAVQQHGVFCGLWLAIKRIAKCHPGNPGGVDPVPSCGCHSDKETTPKEKSDNA
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q31JF6
|
FETP_HYDCU
|
Probable Fe(2+)-trafficking protein
|
MTRMVNCVKMEQELEGLDFPPFPGDLGQKIYENVSKEAWKQWLAQQTILINEYRLSSLDPKAQNFLKEEMQKFLFGGEDLEMPEEFQAID
|
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}.
|
Q31N53
|
YIDD_SYNE7
|
Putative membrane protein insertion efficiency factor
|
MKLLLLALIQFYRRWISPLTPASCRFYPTCSQYGLEAIDRFGPLKGSWLTLCRILRCHPFHPGGYDPVPPLPSCSCGKSPCD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q31UA2
|
FDHE_SHIBS
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLDDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q31UV8
|
YIDD_SHIBS
|
Putative membrane protein insertion efficiency factor
|
MAPPLSPGSRVLIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFDTREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q31X44
|
NRDI_SHIBS
|
Protein NrdI
|
MSQLVYFSSSSENTQRFIERLGMPAVRIPLNERERIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIARKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q31XJ7
|
SYDP_SHIBS
|
Protein Syd
|
MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQPTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLASNLAEFLNQLKPLL
|
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}.
|
Q31YR0
|
CBPM_SHIBS
|
Chaperone modulatory protein CbpM
|
MANVTVTFTITEFCLHTGISEEELNEIVGLGVVEPREIQETTWVFDDHAAIVVQRAVRLRHELALDWPGIAVALTLMDDIAHLKQENRLLRQRLSRFVAHP
|
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}.
|
Q329B3
|
YIDD_SHIDS
|
Putative membrane protein insertion efficiency factor
|
MAPPLSPGSRVLIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFDTREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q32A61
|
FDHE_SHIDS
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q32BR9
|
GLGS_SHIDS
|
Surface composition regulator
|
MEHSLNSLNNFDFLARSFARMHAEGRPVDILAVTGNMDEEHRTWFCARYAWYCQQMMQTRELELEH
|
Major determinant of cell surface composition. Negatively regulates motility, adhesion and synthesis of biofilm exopolysaccharides. {ECO:0000255|HAMAP-Rule:MF_00525}.
|
Q32CC5
|
SYDP_SHIDS
|
Protein Syd
|
MDDLTAQALKEFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQSAIHTFYTTQFAGDIHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLASNLAEFLNQLKPLL
|
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}.
|
Q32CQ1
|
NRDI_SHIDS
|
Protein NrdI
|
MSQLVYFSSSSENTQRFIERLGLPAVRIPLNERKQIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIARKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
Q32KT7
|
CJ120_BOVIN
|
Uncharacterized protein C10orf120 homolog
|
MIREWENGCPKIGKQRARDSRAQERMTTEGKLNKNGIPARVFNISDSFLNKESLSSQGDVCPASPLGIWTKFYKSDPRIALGKYSPLEKEILRLGGVHTVAARRFLTYKQEEERKMLKELQTLSADYKRVVDCRRQHTSPCATCGSLGKMWTAKVIVSPEEFRMPRRERLNVSKHIERMQLARALRSKQLLPYIERFRGSSLLPSGGLGPMARARAGEGQDDGNTDDGNDVHQKGRGEVESKTSKRQEIKMNVIFKSEEPQKCITSHPNDLKPFFPAKKAERSITGLTNRSLLHVSEFPGDLMLMNQDFLSRGIYPSYASQATRLEEENAWKEYMCKVAPHHY
|
Dispensable for normal development and fertility.
|
Q37898
|
VG17_BPB03
|
Early protein GP17
|
MNNYQLTIKEVLYIIKTSRNYGKKSSAKLHTITVKELITDVLNLKYTIDIILTELNSVDRVKMNNYMLAILEAVEYIEDTQEIISSLSNKDTSAKGLSKLPKPRLVEIFLRLENLMYRIEDILEVTNND
|
This protein is involved in the replication of the phage DNA.
|
Q37907
|
RCRO_BPD3
|
Regulatory protein cro (Antirepressor)
|
MTTIYKELVAHFGTQDETAAKLGVDQSTVSGWVRGKHGMSPVVAKRAQVLTDGKFKKEDLCPAFPWEVLSAVA
|
Cro represses genes normally expressed in early phage development and is necessary for the late stage of lytic growth. It does this by binding to the OL and OR operators regions normally used by the repressor protein for lysogenic maintenance (By similarity).
|
Q38038
|
VGK_BPPHK
|
K protein
|
MKHVNTLLMQELRLLICELKRLKLSAVSDPDFSQEKIHAELDSLLCKLSRHFD
|
No function has yet been ascribed to K protein.
|
Q38278
|
GP19_BPLC2
|
Gene product 19 (gp19) (AbiQ resistance protein) (E19)
|
MINLQNKKLDIKEFLQELGFTVSLDYEREPMGVMFAEIHPIVSQVSNNSAIYQSFRTLEIELMVICTEETENSLYRAVQLLSDEHYIYANTITDNTNIIKLRGNYYD
|
Seems to be involved in escape from killing mediated by the bacterial type III toxin-antitoxin module AbiQ toxin protein upon infection of L.lactis subsp. lactis strain IL1403. A single variant independently isolated from 5 different phage confers on the virus the ability to partially escape killing (i.e. the virus grows in the bacteria).
|
Q38563
|
P14_BPPH6
|
Protein P14
|
MATLQDVHLRVNDRVTPVYFTARSFLLVSPKRAGQATFLAREEGTDNPVVTCHVSDFYKDGV
|
Needed for optimal phage development.
|
Q38WL1
|
YIDD_LATSS
|
Putative membrane protein insertion efficiency factor
|
MRKILIALVRFYQTGISPFLPPSCRYYPTCSSYMIQAIQKHGAIKGLAMGIGRILRCHPFIKGGYDPVPDHFTVFRNKSVDH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q38XR2
|
Y713_LATSS
|
UPF0122 protein LCA_0713
|
MELAQNARMNSLFEFYGALLTAKQHSYLSLYYGDDFSLGEIAEEYQVSRQAVYDNIRRTEKILEGYEAKLHLFQNYEQQNASADALQKYIQAQYPNDQQLAKLLADLLNLTEQ
|
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}.
|
Q38YT3
|
YABA_LATSS
|
Initiation-control protein YabA
|
MSKTDLYEQLLTIEQQAKLTFDGITEMKAVLSKVLEENAELEIENKHLREHLQELQQTTEETDTKDLSQGLSKSKQNLQNLYEEGFHICPYFYGSRRENDEPCAFCNDVIYGERTAD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q39BQ1
|
YIDD_BURL3
|
Putative membrane protein insertion efficiency factor
|
METVLIALLRFYKVAVSPMLGNRCRFYPSCSDYAREAIQYHGAARGTYLAVRRVCRCHPFSAGGIDLVPPPNSDTRARGEADARSHRL
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q39EQ6
|
FETP_BURL3
|
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}.
|
Q39PQ7
|
YIDD_GEOMG
|
Putative membrane protein insertion efficiency factor
|
MLKILIKIIGIYQRYLSPLTGPTCRFYPSCSTYAKESLMRHGLLKGLWYSAVRIMKCHPYHPGGYDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q39ZS8
|
YIDD_SYNC1
|
Putative membrane protein insertion efficiency factor
|
MIRKFLIVLIIAYQRYISPFTAPSCRFYPSCSEYARQSLIKYGLIKGVVKTCGRLCRCHPFHPGGYDPV
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3AG59
|
YIDD_CARHZ
|
Putative membrane protein insertion efficiency factor
|
MRKIILLLIRFYQKFVSPILGSNCRFYPSCSQYTYEAIERYGVIYGSYLGIKRILRCHPFTPGGYDPVPEKKLRR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3ALH6
|
YIDD_SYNSC
|
Putative membrane protein insertion efficiency factor
|
MHESNTLYGGPMTKLRQAINQVLAAVLLAGIGFYRRFISPMIGPRCRFTPTCSAYGLEAIQKHGPWKGGWLTVKRLLRCHPFTPCGCDPVPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3ANZ6
|
YIDD_CHLCH
|
Putative membrane protein insertion efficiency factor
|
MSIWKIINAIPIVLIRLYRTFLSPLLGPSCKYVPTCSSYALEAFERHNFFYALWLTIWRILRCNPFSKGGYDPVPPLQGTQQSSSHHQESSHHG
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3AQP3
|
HRCA_CHLCH
|
Heat-inducible transcription repressor HrcA
|
MDYRELTARERQILGIIIQSYVVSAAPVGSKYIARHYNLGLSDATIRNVMAELEELGFISQPHTSAGRVPTDKGYRYYVDLIMTVKTLDEQEKQRFEQHITPLERKGTSADVLLSAVKVLGTISRQLSVVLSPTLSNALFEKLDMVLLSSTRMMVIISIQSLFVKTIVMELHMQVSRQMLDEVVDVLNERLSGLTLSEIRRSINQRLADCSCDNELKNLIVRSAGTLFDEMPVFERLYISGTEYLVEQPEFQQPEKVRDLITMLEDKFSVATLVEQHHANNPDVTITIGKEHGKRQAEDLTVLSAPYYVGDMVGTVGILGPKRMDYEHAVRILHYMAGSLSSTLSIQN
|
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}.
|
Q3AWW6
|
YIDD_SYNS9
|
Putative membrane protein insertion efficiency factor
|
MHESPILSNGDQPNRWAGLNRRVAALLLALIGFYRTFISPLLGPRCRFTPTCSAYGLEAIQRHGPWRGGWLTLKRVLRCHPFTPCGCDPVPD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3B109
|
YIDD_CHLL3
|
Putative membrane protein insertion efficiency factor
|
MVIWKVVNKAPLALIKFYRAILSPMFPPSCRFYPTCSAYALEAFETHNFFKASWLSLWRILRCNPFSKGGFDPVPPHDGVPGKKED
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3BRX9
|
FETP_XANC5
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCHYQQSDAEGLDFVPYPGELGQRIFVQIGKTAWQAWLAHQTMLINENRLSPRDPKHRAFLEAELQKFLFERNADKPEGYVAPVRD
|
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}.
|
Q3BSH4
|
YIDD_XANC5
|
Putative membrane protein insertion efficiency factor
|
MQVAYHWQVISRLLIALLRVYKLVISPLLGPRCRFAPSCSDYAMTAIGRFGPLRGSWLAARRLGRCHPFHPGGFDPVPDAPASPSPSSSCSCKGPHP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3BVC0
|
HRCA_XANC5
|
Heat-inducible transcription repressor HrcA
|
MRASQSPMLDPRARQLLRTLIARYIRDGEPVGSKTLAQHAGLDVSPATIRNILADLEDVGLLSSPHTSAGRVPTAHGYRVFVDSLVQMQPPGEEEVRRLRAELASGNGTQSLLGSASQMLSAMSHFVGVVSAPRREQFAFRHIDFVALDARRVLAILVFADNEVQNRVIEPRRAYEPAELERVANYLNAQFAGRALADIRACLLRELRMAKSEMEQLLAHSVDLASEALVPADAEDMVMAGQTRLMGVQDLSDLDRLRELFEAFASKREILQLLERTIQAPGVRIFIGEETGMVSLEDVSLVTAPYAANGQVLGVLGVIGPKRMAYDRLIPLVQTAADVLGAAMESPGTR
|
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}.
|
Q3IIT1
|
SYDP_PSET1
|
Protein Syd
|
MSVVLQLTQLHQRFNDKTLKNTQKHPLMVHDEQWPSPCEIGNVDQQGNIQWQAVLQQPAGSLNDLAKALDVTFPSGLNALYGHMYGGNIQASIDGHQVELLQVWNSDDFDLLQQNITGHVLMKRKLKQPETVFIGLTAQDDLLVCVLLHSGEVCLEYVGKKTHHVLAANIEEFLQALEV
|
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}.
|
Q3IK54
|
YIDD_PSET1
|
Putative membrane protein insertion efficiency factor
|
MRLLKPLVALPTYCLVLFIRGYQKWISPLLGPHCRFNPTCSSYAIQAINLHGSVKGSWLAVKRILKCHPLHSGGNDPVPEKLTHINHQHEK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3ILI9
|
FETP_PSET1
|
Probable Fe(2+)-trafficking protein
|
MARTVFCQKLQKEAEGLGFQLYPGEIGEKIFNNISKEAWAQWQHKQTMLINEKHLNMMDPEHRSFLEQQMVGFLFENKEVEIEGYKPPEK
|
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}.
|
Q3IYY9
|
YIDD_CERS4
|
Putative membrane protein insertion efficiency factor
|
MSPLAQVLALPVRAYRLLLSPWVGHGCRYQPTCSVYALDALERHGALKGGWLAARRILSCHPWGGSGYDPVPGADPEHDRRPRG
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3J8F4
|
YIDD_NITOC
|
Putative membrane protein insertion efficiency factor
|
MKNILLSLIIFYRYALSPFMGNHCRYYPSCSVYTQEAIQRYGGFRGGWLGLRRLLRCHPFCPGGIDQVPEIAKWRSKS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3J8X0
|
FETP_NITOC
|
Probable Fe(2+)-trafficking protein
|
MSRTVHCVKLDHEAEGLDFPPYPGELGKRLYEQVSKEAWQMWMKHQTILINEYRLTLVDPKARQFLEQEMEKFFFGEGSTPPQEYTPPEQ
|
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}.
|
Q3JP05
|
HRCA_BURP1
|
Heat-inducible transcription repressor HrcA
|
MLDPRARTLLKTLIERYIADGQPVGSRTLSRYSGLELSPATIRNVMSDLEELGLVSSPHTSAGRVPTPRGYRLFVDTMLTVESPIDSDAVTRLVQTTLQAGEPQQRVVAAAASVLSNLSQFAGVVLTPRRSHVFKQIEFLRLSDKRILLIIVTPEGDVQNRMIATQRDYAPAQLTEASNYINAHFAGLSFDEVRRRLREEIDQLRGDMTALMHAAVTASTEEPDDEETVLISGERNLLEVADLSSDMARLRKLFDVFDQKTSLLQLLDVSSHAQGVQIFIGGESTLVPIDEMSVVTAPYEVNGKIVGTLGVIGPTRMAYNRVIPIVDITARLLSLTLSQQ
|
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}.
|
Q3JQJ0
|
FETP_BURP1
|
Probable Fe(2+)-trafficking protein
|
MARMIHCAKLGKEAEGLDFPPLPGELGKRLYESVSKQAWQDWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGEGADQASGYVPPAQG
|
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}.
|
Q3JXI4
|
YIDD_BURP1
|
Putative membrane protein insertion efficiency factor
|
MQTVLIALLRFYKLAVSPLLGSRCRFYPSCSDYAREAIQYHGAARGTYLAARRLCRCHPFSAGGVDLVPPPNSDARNAPHEAEASSHRL
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3JZW0
|
YABA_STRA1
|
Initiation-control protein YabA
|
MDKKDLFDAFDDFSQNLLVGLSEIETMKKQIQKLLEENTVLRIENGKLRERLSVIEAETETAVKNSKQGRELLEGIYNDGFHICNTFYGQRRENDEECAFCIELLYRD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
Q3K3T4
|
HRCA_STRA1
|
Heat-inducible transcription repressor HrcA
|
MITQRQNDILNLIVELFTQTHEPVGSKALQRTIDSSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYYVIKAFDFEAFKLEDMLQKASHILSEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDGSVMDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQSLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLATKLGDYYRYLNSNHYEVH
|
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}.
|
Q3K427
|
YIDD_PSEPF
|
Putative membrane protein insertion efficiency factor
|
MRKLALVPIRFYRYAISPLMASHCRFYPSCSCYAYEAIENHGLLRGGWLTFRRLGRCHPWNPGGYDPVPPIPTSRSSSMAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3KJJ3
|
FETP_PSEPF
|
Probable Fe(2+)-trafficking protein
|
MTRTVMCRKYKEQLEGLERPPYPGAKGQDIFEHVSAKAWADWQKHQTLLINEKRLNMMNAEDRKFLQGEMDKYFSGEEYAQAEGYVPPAE
|
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}.
|
Q3KLM5
|
YIDD_CHLTA
|
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}.
|
Q3KLV9
|
HRCA_CHLTA
|
Heat-inducible transcription repressor HrcA
|
MENRIEMSQLRASKKDSKISYVLLMATKLYLESSQPVGSKLLKETYCSDLSSATIRNYFAQLETDGFLRKNHISGGRIPTDLAFRYYVDHNVPFLEQEEILAIQQKLTELPEYSKNIVKDLQKASEVLSDILQLPVCFSSPRFESDSVINIQLVAIDDQRVVFVLSTEFGQVFTDVLWLPEQLPENSLKRIEGFLQNYLRKQPSDGLLSQKEEDLGMVLYNEVVVRYLTRYCHFSEEDLYQTGLSRLLKYGTFKEPETLAQGLAFFENRKHMCQLLNTYLHKETPTAFIGRELADIVGNTDPSCAVITIPYYMDHTPLGAFGVLGPMNLPYQQVFGTLSLFTERLKVILTQSFYKFKLSFRRPCPTDPRCSQRPAELTRSSSIKLLPAKELS
|
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}.
|
Q3KQ10
|
CENPM_XENLA
|
Centromere protein M (CENP-M)
|
MATVRPFDKMPMLNAAALLLVGTEESHREQLASAMLKEPKTFEVKIHMAQSLPLPYEREHLRPRFDMVVFLINLHSQLSLSTILASLTQLDVNFFLGKVCFVATGGGQVKHCMVDIATVKKLADTHLSTLLFSEFASEDDVTCTAQRLLQMLKICAGLVPGISALYLGSFMSSTLQTDQF
|
Probable component of a centromeric complex involved in assembly of kinetochore proteins, mitotic progression and chromosome segregation.
|
Q3M5B5
|
YIDD_TRIV2
|
Putative membrane protein insertion efficiency factor
|
MKQIFIWLIKGYRMFISPLFPPTCRFQPTCSMYALEAIERFGVFRGGWMGIRRILRCHPFHPGGYDPVPEVGEHCCHHDSGK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3MCK2
|
HRCA_TRIV2
|
Heat-inducible transcription repressor HrcA
|
MQVQLTNRQQHILWATVRHYIATAEPVGSKALVEEYDLGVSSATIRNVMGVLEKSGLLYQPHTSAGRVPSDSGYRIYVDQLITPSLRDTTRTEVLAKEVESALQQHLQWEDWSLEILLQGAAQILASLSGCISLITMPQTNTASVRHLQLVQIETGRIMLILVTDSYETHSKLMDLPPARSETKPDPEVIDRELQIVSNFLNSHLRGRSLLEISTLDWSQLDREFQSYGEFLKNSVAELAHRSAAPAATQIMVRGLAEVLRQPEFSQLQQVKTIIQLLEEEQEQLWRLIFEEPELEDTHKSKVTVRIGAENPLEPIRTCSLISSTYRRGGVPLGSVGVLGPTRLDYESAIAVVAAAADYLSEAFS
|
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}.
|
Q3SFW8
|
YIDD_THIDA
|
Putative membrane protein insertion efficiency factor
|
MNLAQKCLVGAIRVYQLALSPWLGRQCRYLPTCSEYGKEAIEKHGALKGSWLAAKRIGRCRPGCSHGYDPVPPVDPRK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3SMR4
|
FETP_THIDA
|
Probable Fe(2+)-trafficking protein
|
MTRMVNCVKLGREAEGLAFQPVPGDLGKKIFENVSKEAWAGWQRHQTMLINENRLNLADPQARSYLMEQMERYFFGGGNVDAAAGYVPPTR
|
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}.
|
Q3ST04
|
YIDD_NITWN
|
Putative membrane protein insertion efficiency factor
|
MKTIPSEVRCSRLCPACTNAALRLPRNAGRALIWIYRHTLSPLVGFNCRHLPTCSAYGDEAIARFGLWGGGWMTLARILRCRPWGTSGIDNVPVAKPSGATWYRPWRYGRWRGVNAK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3TTL0
|
CC038_MOUSE
|
Uncharacterized protein C3orf38 homolog
|
MSGLSHLESEGCRNLLGLLDNDEIMALCDTVTNRLVQPVDRQDAIHAILVYSQNVEELLRRKKVHREVIFKYLAKQGVVVPPTAEKHNLIQYAKDYWAKQSPKLKDTAEPVTKTEDIQLFKQQAKEDKEAEKVDFRRLGEEFCHWFFELLNSQNPFLGPPQDDWGPQHFWHDAKLRFYYNTSEQNTTDYQGAEIVSLRLLSLVKEEFLFLSPNLDSQGLKCASSPHGLVMVGVAGTVHRGNSCLGIFEQIFGLIRSPFVENTWKIKFINLRIIGGSSLAPESVLKPSVTFEPSDLEAFYNVITLCNSPEVRPNVRQIIDSGTGDQVLHSGDEALLNKREMNLLTPLKH
|
May be involved in apoptosis regulation.
|
Q3YV85
|
FDHE_SHISS
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
Q3YWA9
|
YIDD_SHISS
|
Putative membrane protein insertion efficiency factor
|
MAPPLSPGSRVLIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFDTREH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q3YXJ3
|
GLGS_SHISS
|
Surface composition regulator
|
MDHSLNSLNNFDFLARSFARMHAEGRPVDILAVTGNMDEEHRTWFCARYAWYCQQMMQARELELEH
|
Major determinant of cell surface composition. Negatively regulates motility, adhesion and synthesis of biofilm exopolysaccharides. {ECO:0000255|HAMAP-Rule:MF_00525}.
|
Q3YY63
|
SYDP_SHISS
|
Protein Syd
|
MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQPTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLASNLAEFLNQLKPLL
|
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}.
|
Q3Z3C4
|
CBPM_SHISS
|
Chaperone modulatory protein CbpM
|
MANVTVTFTITEFCLHTGISEEELNEIVGLGVVEPREIQETTWVFDDHAAIVVQRAVRLRHELALDWPGIAVALTLMDDIAHLKQENRLLRQRLSRFVAHP
|
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}.
|
Q3ZYU9
|
HRCA_DEHMC
|
Heat-inducible transcription repressor HrcA
|
MLTSRAEIILRSIVRQYITKAVPVSSSSILEDCGLDICSATIRNEVVRLEIEGYILRPHHSAGSIPADKGYRYYVESLKDVELPTNDKFLIRHLFHQVEKEMEEWLNLTVAVLSQRVQSMAVVTMPRQTQGKVHHIELVSLQDNLVLVVLILRGAKVKQQLVNFENVVSQPELTLISNRLNDAYDGLTRFQIEQKPLGLNHDELKVKDSLVKMMRGEDEQESREPFFDGLHYMLEQPEFHQNQRAQEIMQLLEQKKLSKMIVPPMPFNRGVQVYIGQENASAEIRDYSLIVSQYGIPDEAVGTIGVIGPTRMAYERALSAVSYLSLVMSTLVAELYGKAPVDKDE
|
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}.
|
Q44581
|
NCCY_ALCXX
|
Nickel-cobalt-cadmium resistance protein NccY
|
MENIDEWLVQAKKVTYEASREPGLGRIQQRLSREPSQMVLTARHDILRAVCCAALASLVAFTAIDRIAVGLYQKQQPTWVAAPSAASPFGLLIGK
|
Component of the NCC cation-efflux system that confers resistance to nickel, cobalt and cadmium. May be involved in the regulation of NCC.
|
Q45536
|
COTJA_BACSU
|
Protein CotJA
|
MKDMQPFTPVKSYTPFHSRFDPCPPIGKKYYRTPPNLYMTFQPEHMEQFSPMEALRKGTLWKDLYDFYENPYRGGDAHGKKG
|
The cotJ operon proteins affect spore coat composition. They are either required for the normal formation of the inner layers of the coat or are themselves structural components of the coat.
|
Q45811
|
CDRB_CLOAT
|
Chemical-damaging agent resistance protein B
|
MVHNDLDFIFYNNLKHSSGAIEHLGDNLTGDGDXDDEEIIIDLSLIPQNISRINFTVTIHEAGERSQNFGQVSNAYVRVVNSDNSQELLKYDLGEDFSIETAIVVAEIYRHNGEWKFNAIGSGFQGGLAALCRNFGLNV
|
Not known could confer methyl methane sulfonate (MMS), mitomycin C (MC), and UV resistance.
|
Q45812
|
CDRC_CLOAT
|
Chemical-damaging agent resistance protein C
|
MGIVLKKGQKVDLTKGNASLKKVIIGLGWDVNKYDGGHDFDLDAVAFCCGEDGKVHNEADMIFYNNLKHSSGAVEHLGDNLTGDGDGDDEQILIDLSSIPQHINKIDFTVTIHEAEERKQNFGQVSNSYVRVVNSDTKEELIKYDLGEDFSIETAIVVAELYRNGSEWKFNAIGSGFEGGLAALCKNFGLNV
|
Not known could confer methyl methane sulfonate (MMS), mitomycin C (MC), and UV resistance.
|
Q467K0
|
BRIX_METBF
|
Probable Brix domain-containing ribosomal biogenesis protein
|
MLVTSSRKPSARTRTLCKLLSRFIAGRCMTRGKMGMQELLEFAEGGPLIVIGEYHGNPGELSFYDEAGELLFSLRFTDWYSKELDSYWFSGIEPKLAGQGEIAEAFKVFFHFQRVENDKIDQLPPSSTLIVVGENDIDFMGSGKSLFKLNLRGFKKY
|
Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.
|
Q46LZ8
|
YIDD_PROMT
|
Putative membrane protein insertion efficiency factor
|
MLTKINKAIALVFVSLISFYQKWISPLFGPSCRFIPSCSAYGIEAVNKHGPWRGGWLTLKRLSKCHPLTPCGCDPVPEK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q46VL5
|
YIDD_CUPPJ
|
Putative membrane protein insertion efficiency factor
|
MKRILLALLRIYKIALSPYLGSRCRFWPTCSDYAREAVIQHGAARGSWMAACRLCRCHPFTQGGYDPVPGVETETAQTGKFAHPAAGHGPVTVRLPRP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q46ZK2
|
FETP_CUPPJ
|
Probable Fe(2+)-trafficking protein
|
MARMVQCIKLNKEAEGLDFPPLPGELGKKIWQSVSKEAWAGWLKHQTMLINENRLNMADARARQYLLKQTEKYFFGEGADEAAGYVPPQA
|
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}.
|
Q47037
|
AFAF_ECOLX
|
Dr hemagglutinin AFA-III operon regulatory protein AfaF
|
MKINKLTLNERKNDILSYFSEINTPFRTSEVAEHLGVSAYQARHYLQCLEKEGKIKRSPVRRGASTLWEISAVTEPSVKTDRIAD
|
May have a possible regulatory function on the expression of the other AFA-III genes.
|
Q47132
|
DAAF_ECOLX
|
F1845 fimbrial adhesin operon regulatory protein DaaF
|
MKINKLTLNERKNDILSYFGEINAPCRTSEVAEHLGVSAYQARHYLQCLEKEGKIKRSPVRRGASTLWEISSIPP
|
May have a possible regulatory function on the expression of the other daa genes.
|
Q47133
|
DAAA_ECOLX
|
F1845 adhesin operon regulatory protein
|
MSGQVPEYQFWLLAEISPVHSEKVINALRDYLVMGYNRMEACGRHGVSPGYFSGALKRFQRVSQTVYRLVPFYFPEAGHEVHRGE
|
Regulates the transcription of genes involved in the biosynthesis of F1845 fimbrial adhesin.
|
Q477Q3
|
YIDD_DECAR
|
Putative membrane protein insertion efficiency factor
|
MKYLLIALVRGYQYAISPFLGRSCRYVPTCSEYMVDAVQKHGAFRGGWLGVKRVCRCHPWHPGGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q47836
|
ARPU_ENTHA
|
Putative autolysin regulatory protein ArpU
|
MQLLREVDFKQTRCNARDVLKNFRRLERMAGRSLIDIKSPIITDMPKAPKHGNKAEDAIIQMMDIEAERDAILAALMALSLISRQILYYSFCVPDSFSNYRISREVGYSERSIQRMKSEALIEFAEAYKHGRIIAYK
|
May be involved in the regulation of muramidase-2 export.
|
Q47A19
|
FETP_DECAR
|
Probable Fe(2+)-trafficking protein
|
MARTVNCIKLGREAEGLDFPPYPGPLGQRIFEHVSKEAWQQWIKMQTMIINENRLNLVDAKHRKYLAEQVEKHFFGEGADQIQGYVPPAA
|
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}.
|
Q47H37
|
COWN_DECAR
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MPQDCACRKTDRYVSFQDIDCTGNARRLMEHLDRQLSIPGRSTAFWEYFAKKRAGSAAAKPDDLFLIHSNINQFREFFEQWNDSDALSLLLQIEEECC
|
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}.
|
Q47HJ5
|
HRCA_DECAR
|
Heat-inducible transcription repressor HrcA
|
MLDERARTLLKTLVEHYVADGQPVGSRALSKFSGLDLSPATIRNVMADLEEAGFVASPHTSAGRIPTARGYRLFVDSLLTVQPLEARQMGEMEEALHGRPAGQIIASASQLLSSLTHFAGVVIAPRRQSSRIRQIEFLSLSEKRILLIIVTADGDVQNRIVTTDKVYSPAELVSAANYLTQNFAGLDFEQIRHRLTVEIKQLRDDIKPLMALALDAGDAAMAENTTPYVISGERNLLDVEELSSNMKRLRELFDLFEQRSSLMRLLEISNSAEGVQIFIGGESGIATLDECSVIAAPYTVDGQVVGSVGVIGPTRMAYERVIPIVDITARLLSSALSYKSDN
|
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}.
|
Q47K74
|
YIDD_THEFY
|
Putative membrane protein insertion efficiency factor
|
MTRDRPTLLARVLILPIRGYQRWISPLFPPVCRFYPSCSSYAVEALRVHGAGRGLWLTIRRLGKCHPFHPGGLDPVPPRRNESGTEISDARPGSDGEASPGAPGL
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q47RP1
|
HRCA_THEFY
|
Heat-inducible transcription repressor HrcA
|
MLDDRNVLDDRKLAVLRAIVEDYVSTNEPVGSKALAERHKLGVSPATIRNDMVALEELGYIAQPHTSAGRVPTDKGYRLFVDRLSKVKPLSKAERRAIETFLSGALDLDEIVSRTVRLLAHLTRQVAIMQYPSLTRSSVQHLELVPLGPQRLMLVLITNTGRVEQRVIDGLAEVSDDVVENLRGALNRALVGKWLTEAPKEFPTVLAQLPLEERPIAESVMSVLTESLVEKHEGKVVFGGTANLAAMGFSAGLRDVLEALEENVVLIRLLGEMGDASMLTVRIGAENNHEGLQSTSIVAAGYGIGDQTLAKLGVVGPTRMDYPGTMGAVRAVARYVGQILAGQ
|
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}.
|
Q47U34
|
YIDD_COLP3
|
Putative membrane protein insertion efficiency factor
|
MAKNNSTPQKLVITGIKGYQRFISPLLGSNCRFTPSCSAYATEAINRFGVIKGGWLASKRILRCHPLNDGGEDPVPPIKKSK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q47WL9
|
FETP_COLP3
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCQNLNKEAEGLGFQLYPGEIGKRIFDNISKEAWTIWQKKQTMLINEKKMNMMNVDDRAFLEAAMVAYLFEGKEPEIEGYVPPSK
|
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}.
|
Q47WN6
|
SDHE_COLP3
|
FAD assembly factor SdhE
|
MTNNENSTNLLKVNKARLKWACRRGMLELDVLFIPFVDEAYDELSTKDQFTFERLLTGQDPELFAWFMGHEVCEDTELNAMVQLILKRVKV
|
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.
|
Q47YB4
|
SYDP_COLP3
|
Protein Syd
|
MTSTNKTLTQAILNFSKSYSQQHVEQFGHLPTVEHDEQWPSPCDLGSHDTSHHYWQAVAMESVQLADNKEEALSFENVESALNIELHPDIKIYFTTIFSGDIEAQSDDGELSLLFAWNKDDFERLQENIIGHILMKQKLKQVETVFFAVTDEEDMIISVDNSSGEVWVEQVGCKPHKKLSDSLAEFISQLTHKNVVSEKS
|
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}.
|
Q48439
|
LPHI_KLEPN
|
his operon leader peptide (his operon attenuator peptide)
|
MNSVQFKNHHHHHHPD
|
This protein is involved in the attenuation mechanism for the control of the expression of the his operon structural genes.
|
Q48725
|
ABIG1_LACLC
|
Abortive phage resistance protein AbiGi
|
MAFLPRYYPENIEYLKISKENTPLKEWYIPMTCFCDIPLHQMSYHAEGKAQTGYGKFSIALHKKFGINNGIQPVQYLNSNSIPTEELRNAISILLSDNGQIYSDEALISLSNHLFEYMRRIKPLDGSMKKWDKEGKKYVEIKKNFHDEHEWRYIPDFESDELPFLLYRQDDIIAESSSQFYTKSITETKNGLLNFSVSDIRYIFVDSILSREKLISFIKRKQKGKRIPRAEKDILISKILVYDEIKEDW
|
Confers resistance to phages by a mechanism of abortive infection. Seems to act by interfering with phage RNA synthesis. Does not act at the level of phage DNA synthesis.
|
Q48726
|
ABIG2_LACLC
|
Abortive phage resistance protein AbiGii
|
MAKSKFKTTFSNDKATTSSTALLKYINKKAPKGYKYEILYKGSDIYSLKKDNTDEKISFLVRFKFPLNFEGIKVTNPQDLLELSYRTQKEIVLDETLQNGSDGQPPTLVSLKGEVGKQSIFPIPFPKLDPIKLEWFGGALEIPIKRIPYASLSEIKLESESDNILHVSFLFNETNNKVHLNTNINFEYLRTIDDYFKFRDFLKNYSEGRVKILSKNITLRSEDNNDKIKIFEKNDKLYNALRLIQSKIDTKIPFPQNLSIKDVNIIKILFESYINDRVVKFKSEPSLKFTFDDSSNFKESFPITGKKNMGIFVPFQRNIKFLSVSIPIIENQLYTDTTVKTADLQDRVLILETNKNNESFVFYQNSEEYKEISINEMLEKKKAAIELDDIDFSVLKK
|
Confers resistance to phages by a mechanism of abortive infection. Seems to act by interfering with phage RNA synthesis. Does not act at the level of phage DNA synthesis.
|
Q48BF1
|
YIDD_PSE14
|
Putative membrane protein insertion efficiency factor
|
MRKLALVPIQFYRYAMSPLMASHCRFYPSCSCYAYEAIENHGLLRGGWLSIRRLGRCHPWNPGGYDPVPAVPTSRSSSMAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
Q48C72
|
FETP_PSE14
|
Probable Fe(2+)-trafficking protein
|
MTRTVMCRKYKEELPGLERAPYPGAKGEDIFNHVSQKAWADWQKHQTLLINERRLNMMNAEDRKFLQTEMDKFLSGEEYAQAEGYVPPEK
|
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}.
|
Q48EU3
|
SDHE_PSE14
|
FAD assembly factor SdhE
|
MVEDVELNRLYWHSRRGMLELDVLLVPFVREVYPHLNDVDRDLYRRLLTCEDQDMFGWFMQRAESEDAELQRMVRMILDRVQPK
|
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.
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Q48RR1
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HRCA_STRPM
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Heat-inducible transcription repressor HrcA
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MITQRQNDILNLIVELFTQTHEPVGSKALQRTIDSSSATIRNDMAKLEKLGLLEKAHTSSGRMPSPAGFKYFVEHSLRLDSIDEQDIYHVIKTFDFEAFKLEDMLQKASHILAEMTGYTSVILDVEPARQRLTGFDVVQLSNHDALAVMTLDESKPVTVQFAIPRNFLTRDLIAFKAIVEERLLDSSVIDIHYKLRTEIPQIVQKYFVTTDNVLQLFDYVFSELFLETVFVAGKVNSLTYSDLSTYQFLDNEQQVAISLRQSLKEGEMASVQVADSQEAALADVSVLTHKFLIPYRGFGLLSLIGPIDMDYRRSVSLVNIIGKVLAAKLGDYYRYLNSNHYEVH
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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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Q48TF9
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Y888_STRPM
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UPF0122 protein M28_Spy0888
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MNIMEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIADEFGVSRQAVYDNIKRTEKILETYEMKLHMYSDYVVRSEIFDDMIAHYPHDEYLQEKISILTSIDNRE
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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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