entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
A6QTA3
|
LCL2_AJECN
|
Long chronological lifespan protein 2
|
MVRIFTSILLGLLLLVTGTRSQFQFFEQMFGGGQQQQHDSREQNVPSDSDWYQRTYDNARCSNYLCPGTLACVAVPHHCPCQHPAVEDKFELGDGSAICVSKGGFKFGEAARKVELARKGLL
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
A6RPX6
|
LCL2_BOTFB
|
Long chronological lifespan protein 2
|
MAKVLFSLFSFLFLIIGVSAQFQFFEQMFNGQQQQHQRQPQDVPSDSQWYQDNYDRAHCTSYLCPGTLSCVAFPHHCPCAHPTYEEKFELADGNAICISKGGFKAGEAARKVELARKGLI
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
A6SX71
|
FETP_JANMA
|
Probable Fe(2+)-trafficking protein
|
MTRMIHCIKLDKEAEGLDFPPYPGELGKRIYETVSKEAWAAWLKHQTMLVNENRLNLADVRARKYLATQMEKHFFGDGADAAQGYVPPTY
|
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}.
|
A6TCU0
|
NRDI_KLEP7
|
Protein NrdI
|
MSLIVYFSSRSENTHRFVQRLGLPAVRIPLNEREHLRVDEPYILIVPSYGGGGTAGAVPRQAIRFLNDVHNRQLIRGVIAAGNRNFGDGWGRAGDVIAQKCAVPYLYRFELMGTPDDINTVRKGVSEFWQRQPQNV
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A6TD66
|
SYDP_KLEP7
|
Protein Syd
|
MDHQTAEALRAFTQRYCAVWQQQRHSLPRSEELYGVPSPCVVDTQGEAVFWQPQPFSLAQNISAVERALDIVVQQPLHSYYTTQFAGDMSGRFAGETLTLLQTWSEEDFQRVQENLIGHLVVQKRLKLSPTLFIATLESELDVISVCNLSGEVVKETLGTAKRITLSPSLAGFLNHLEPVL
|
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}.
|
A6TDX0
|
FETP_KLEP7
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLQREADGQDFQLYPGELGKRIYNEISKEAWAQWQHKQTMLINEKKLSMMNPEHRKLLEQEMVQFLFEGKDVHIEGYTPPEKQ
|
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}.
|
A6TG82
|
FDHE_KLEP7
|
Protein FdhE homolog
|
MSIRIIPQDELGSSEKRTAEAIPPLLFPRLKNLYNRRAERLRELAANNPLGDYLRFAALIAHAQEVVLYDHPLQMDLTARIKAASEQGKPPLDIHVLPRDKHWHKLLHSLIAELKPEMSGPALAVIENLEKASEQELEQMASALFVSDFASVSSDKAPFIWAALSLYWAQMASLIPGKARAEYGEQRQFCPVCGSMPVSSIVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSRDLHYWSLDNEQAAVKAESCGDCGTYLKIMYQEKDPKVEAVADDLASLVLDARMEQEGFARSSINPFMFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A6TJM4
|
SP5G_ALKMQ
|
Putative septation protein SpoVG
|
MKVTDVRIRKVAAEGKMKAIVSVTFDEEFVVHDIKIIEGQNGLFIAMPSRKMGEGDFRDIAHPINSDTRSKIQDAIFAEYAIMNEEVQVQVQVTEEAL
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A6TSM2
|
HRCA_ALKMQ
|
Heat-inducible transcription repressor HrcA
|
MQLNERKLKILQAIIQDYIYTAEPVGSRSLSKKYDLQVSPATIRNEMADLEDMGYLIQPYTSAGRIPSDKGYRLYVDHLLQLEKNMVIQRDQIRSDLLNRFGEIEQLLQYSSKILSQLTNYTTIALAPQIKEVRLKHIQLIPMDEHHLLGIIITDTGLIKKTVLQVPEGLDAEAISKISEVINGRLQGVAIKGIPGEFTEEFTHELEQLSHGFDSVIPKMFQTLEELDKIELFLHGTTNIFNFPEFNDIFKAKSFLSMLEEKELISQLILSSSHKGMNATIGSENIYKEAKEYSLVTATYKIDEDVIGFVSIIGPTRMDYSNVMSTMGQVNKYINEVLKGKYK
|
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}.
|
A6TXE8
|
YIDD_ALKMQ
|
Putative membrane protein insertion efficiency factor
|
MSKFLIKLITLYQKWISPLKGQTCRFYPTCSSYSISAYNTYGFFRGTYLTIRRLLKCHPFHPGGFDPLK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A6TYW0
|
YABA_STAA2
|
Initiation-control protein YabA
|
MDRNEIFEKIMRLEMNVNQLSKETSELKAHAVELVEENVALQLENDNLKKVLGNDEPTTIDTANSKPAKAVKKPLPSKDNLAILYGEGFHICKGELFGKHRHGEDCLFCLEVLSD
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
A6TYX2
|
SP5G_STAA2
|
Putative septation protein SpoVG
|
MKVTDVRLRKIQTDGRMKALVSITLDEAFVIHDLRVIEGNSGLFVAMPSKRTPDGEFRDIAHPINSDMRQEIQDAVMKVYDETDEVVPDKNATSEDSEEA
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A6TZK9
|
NRDI_STAA2
|
Protein NrdI
|
MKIIYFSFTGNVRRFIKRTELENTLEITAENCMEPVHEPFIIVTGTIGFGEVPEPVQSFLEVNHQYIRGVAASGNRNWGLNFAKAGRTISEEYNVPLLMKFELHGKNKDVIEFKNKVGNFNENHGREKVQSY
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A6U155
|
Y1320_STAA2
|
UPF0122 protein SaurJH1_1320
|
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}.
|
A6U254
|
HRCA_STAA2
|
Heat-inducible transcription repressor HrcA
|
MITDRQLSILNAIVEDYVDFGQPVGSKTLIERHNLNVSPATIRNEMKQLEDLNYIEKTHSSSGRSPSQLGFRYYVNRLLEQTSHQKTNKLRRLNQLLVENQYDVSSALTYFADELSNISQYTTLVVHPNHKQDIINNVHLIRANPNLVIMVIVFSSGHVEHVHLASDIPFSNDKLNTISNFVTNKLTEFNQNLQDDIVSFVQSEQEEIFINKLINTMNNHISNQSNSIYMGGKVKLIDALNESNVSSIQPILQYIESNRIAELLQDISSPNINVKIGNEIDDSLSDISIVTSQYHFDETLKGQIAVIGPTAMHYQNVIQLLNRIW
|
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}.
|
A6U2Q5
|
YIDD_STAA2
|
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}.
|
A6VDR9
|
FETP_PSEA7
|
Probable Fe(2+)-trafficking protein
|
MSRTVMCRKYHEELPGLDRPPYPGAKGEDIYNNVSRKAWDEWQKHQTMLINERRLNMMNAEDRKFLQQEMDKFLSGEDYAKADGYVPPSA
|
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}.
|
A6VGY7
|
EF1B_METM7
|
Elongation factor 1-beta (EF-1-beta) (aEF-1beta)
|
MATVIAKVKVMPTSPEVDKESLKATLKELVENNDAKCRGVSDEPLAFGLYTVFVMVEMEEKEGGMDPIEEAMNALENVESAEVVELSLV
|
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}.
|
A6VLR9
|
FETP_ACTSZ
|
Probable Fe(2+)-trafficking protein
|
MARTVFCEHLKQEAEGLDFQLYPGELGKRIFEHISKQAWGDWLKKQTMLVNEKKLNMMNAEHRKLLEQEMVNFLFEGKDVHIEGYVPPEK
|
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}.
|
A6VNS4
|
FDHE_ACTSZ
|
Protein FdhE homolog
|
MAIRILPENEIKQVASSFQNPPLLFSSPQNLYARRAQRLRQLAENHPFSDYLLFAADVVEAQNLIFAENPLEKTEFTFNQLRPLDIKHWPRSAKWREYLSALLAEIKPRANEQMIGTIDCLEKASSEELERLADKLLVQEYAQVASDKAVFIWAALSLYWVQLTQFIPHHAIMENAEDLHTCPVCNSVPVASVVQFGSNQGLRYLHCSLCESEWNVVRAKCTVCDQSKELEYWGIDTDKETVKAETCGDCHSYLKTVYQEKDPYVDPVADDLASIFLDIEMEEKQFSRSGLNPFVFPAE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A6VR62
|
YIDD_ACTSZ
|
Putative membrane protein insertion efficiency factor
|
MAASHSLGEKILIKLIRFYQIVISPLIGPRCRFVPTCSCYGLEAIKTHGAVRGAWLTLKRILKCHPLNAGGYDPVPPKSDNHSKENKK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A6VTB4
|
FETP_MARMS
|
Probable Fe(2+)-trafficking protein
|
MANTVFCKKFQKEMEALDRAPLPGAKGQEILQNVSKQAWQEWQHLQTMLINEKQLNLMQSESRKYVMEQMDKFFNNEATDKLAGYVDPDDIKEL
|
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}.
|
A6WHI5
|
FDHE_SHEB8
|
Protein FdhE homolog
|
MSHTAEIPLVPGSESPLELKPLKAADPQAVYHRRAHRLLSLAKDSPLADYFELCRRLVSIQAKLAEEADFGQLLAWGKDEATPLSLLGSEADSYWQGLLQQLLSDLLPQVDESIARVMRLLMQQSPEQLSSWGRSLRQGHVSEVPAHFSLFIWAAMGVYWSHWAPMVIKRMDQRKVAQQSMCPVCGCHPVASVIVDQPRAGLRYLHCSLCESEWHYIRAHCTSCGQDKEMTIWSLDDAQAQVRIESCDECHGYTKMMFVENSPSMDVAADDLATLMLDSELNAKGFGATTLNPLLMAHETT
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A6WL87
|
SYDP_SHEB8
|
Protein Syd
|
MSCLPALDKFLQNYHQAYLTSLGELLRYYPQGEASVCIQGEFHADLDQAVSWQPVKREVEGSFANVEHALELTLWPEINHFYGQYFSAPLLFDSEWGTGELLQVWNEDDFTCLQQNLIGHLMMKKKLKQPPTWFIGLLDEGDKMLTINNSDGSVWIELPGEIPTQQLSPSLAEFIGALSPRIAPPVKHEELPMPALEHPGIFASFKRMWQNLFGKR
|
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}.
|
A6WQU6
|
FETP_SHEB8
|
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}.
|
A6WUK5
|
YIDD_SHEB8
|
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}.
|
A6X0W8
|
YIDD_BRUA4
|
Putative membrane protein insertion efficiency factor
|
MCSCGKNRAGEGAPKRYSRNFTDPWRKTPGRVIGTSFVRFYQVTLSSLIGNSCRHLPTCSEYAYEAIARHGLWSGGWMGLFRVVRCGPFGTHGFDPVPRALSSDLKWYLPWRYWRCSAS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A6ZMG4
|
SPG4_YEAS7
|
Stationary phase protein 4
|
MGSFWDAFAVYDKKKHADPSVYGGNHNNTGDSKTQVMFSKEYRQPRTHQQENLQSMRRSSIGSQDSSDVEDVKEGRLPAEVEIPKNVDISNMSQGEFLRLYESLRRGEPDNKVNR
|
Stationary phase-essential protein not required for growth on nonfermentable carbon sources.
|
A6ZNN4
|
CRS5_YEAS7
|
Metallothionein-like protein CRS5
|
MTVKICDCEGECCKDSCHCGSTCLPSCSGGEKCKCDHSTGSPQCKSCGEKCKCETTCTCEKSKCNCEKC
|
Critical role in copper (specific) homeostasis and detoxification. May protect by directly chelating and sequestering copper ions (By similarity).
|
A6ZVL3
|
RGI2_YEAS7
|
Respiratory growth induced protein 2
|
MTKKDKKAKGPKMSTITTKSGESLKVFEDLHDFETYLKGETEDQEFDHVHCQLKYYPPFVLHDAHDDPEKIKETANSHSKKFVRHLHQHVEKHLLKDIKTAINKPELKFHDKKKQESFDRIVWNYGEETELNAKKFKVSVEVVCKHDGAMVDVDYKTEPLQPLI
|
Involved in the control of energetic metabolism and significantly contribute to cell fitness, especially under respiratory growth conditions.
|
A6ZWZ7
|
RRG8_YEAS7
|
Required for respiratory growth protein 8, mitochondrial
|
MGLPKSAYKKLLIDCPTRVINKNCAQRVKDVSPLITNFEKWSDKRKKLYFKDEEEMVGQFHLENFNLKNNLYGRLLASPMRAEKISKLKSCRELLIPLKVVPSTGKDQHADKDKLKLVPTLDYSKSYKSSYVLNSASIVQDNLAAATSWFPISVLQTSTPKSLEVDSSTFITEYNANLHAFIKARLSVIPNVGPSSINRVLLICDKRKTPPIEIQVVSHGKGLPITQSVFNLGYLHEPTLEAIVSKDAVTKGIYLDADNDKDLIKHLYSTLLFHSVN
|
Required for respiratory activity and maintenance and expression of the mitochondrial genome.
|
A6ZY30
|
RRG1_YEAS7
|
Required for respiratory growth protein 1, mitochondrial
|
MAQNFGKIPSHKSYVLSLYRTVLRNIPKCCHSYAFQYEIKKTLSKQLFKHKHDKSSWSVYTLLNEFSLLNNCLLEGKLQEIKNLMKPLKKMKKQLETTKILNSLTSLGDVKTNDPEEVRRFHVLSAYIKRKQDLGLLPAYIPKTYQHKLLLPLALNEHACLKLFHIQQKLKNGPPSAGLSYTKEGRNQIWFVRSPINKGRQQSKKLGILIRKERKDSQKNIDNLNFCEINAAWALHEAIWEEYLESKKIIKVNLPKYLEYAANIPKSTKCNPSSQYQKIKEWVDPVREIMFELHSKSFQRVEYFNKYKEKLLKNGGQLAYFDKKSKEMYAKRLTLFRKMSKETLPYVTLFIEGRDLPSVLAKYGF
|
Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).
|
A6ZZL8
|
MTC2_YEAS7
|
Maintenance of telomere capping protein 2
|
MGDHNLPDFQTCLKFSVTAKKSFLCMYRDSVSKEKLASSMPSTCDIQLKRAINDAYPGGGIKVTVLNSTTASLDSLATTHVKEFEIVIIPDINSLLQPDQAKLVKIMRDCTVAIEKAQSTRIFIGVVHWNNPVQPSGAAKDGDEAGKPAPKTRIFLPTSFRMGAWLKHKFWFACAPPYLDFESSTESSINTRANNSIGMAEEEKQEPESKRSIILNEEANLNDVFVGSTVRRYILDIMVHLRTHRLTYNAKAGGVYTNSLDDVVLLSRLIGLHSGKMFVSPSHVKEASRWYFPMHLELVQRSSMDSSLLYGSDPNLVDEMLEKLAKIKCEEVNEFENPLFLESLVVKNVLSKVVPPV
|
May be involved in telomere capping.
|
A7A0M4
|
IRC19_YEAS7
|
Increased recombination centers protein 19
|
MRKPSITITTAKAIITPDYTLIKSHSKYQLPSRFQKLDADSPERSTVVKLFYRRFMRLKPFISNVKMVKDTYRDYVRYKFMKENYELKRYLVFNPDGLRSKIKLELLSNTKCCERILPVTEMQRTLEFVLKSCSYLPETKVQKWDIARDNTYCRQILKNLLTMQYEKYRSILHRGIGHDELDVKFSHLKTTSSPLTKLNKTEKKKIPLFKVFSDFDTTLIYLNETLGTRL
|
Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).
|
A7A108
|
LCL2_YEAS7
|
Long chronological lifespan protein 2
|
MSQSRWSIVLIFALFIFGSTGVNAFFNFGHHQQQQQQQQQSYEDQVLNNPCDGYLCPDTLTCVAQQKDCPCPFPKSQLKCVLPDNKFVCISKPATHNEKFRAIYDDPVKGPKAKNKGFRDCGWVSDAYKNH
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
A7A283
|
IRC6_YEAS7
|
Increased recombination centers protein 6
|
MVLQYPQNKILVLSDHPHNFSKTQFLQDLFHCSSTGISIVKDQTWENRYYKVHFDLYIDSCKDIPVWVEEFITPECEPLRNVMAGIILITDIRQTKPQELLHQFMIAAHRNTFVVLVNVNEEVEQDEIDELNEIWSNAFTNVIEFVNWKRSKPTVNHNDYGEKLGLDRIQEIIDTHDWLKCEVLPATKIREEIPNEMPLEQIIRNLQSARLKYKSIENSSEADAFANEMADELSRYL
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
A7E987
|
LCL2_SCLS1
|
Long chronological lifespan protein 2
|
MSKLLFSFLLLIIGVSAQFQFFEQMFNNGGQQHHHHQQPQDVPSDSQWYQDNYDRAHCSGYLCPGTLSCVAVPHHCPCAHPVYEEKFELADGNAICISKGGFKAGEAARKVELARKGLI
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
A7FEX4
|
FETP_YERP3
|
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}.
|
A7FFG1
|
SYDP_YERP3
|
Protein Syd
|
MDLNISTALRSFTQRYIDLWQQQTGHLPASKDLYGVPSPCIVATGEDQVFWQPQAFLPEATLTNIERALEIQLHPDIHDFYTQQYAGDMMADLGNHRFTLLQVWSEDDFIRLQENLIGHLVTQKRLKLSPTLFLATTSSEMTMASLCNVSGNVVLEQFGSDKRTLLASTLSHFLDALRPVLPE
|
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}.
|
A7FFL7
|
NRDI_YERP3
|
Protein NrdI
|
MNPLVYFSSSSENSHRFVEKLQLPAIRIPIAGAREKLRVEQPYILLVPSYGGGSPVGAVPIQVIRFLNDVHNRSLIRGVIAAGNTNFGDAYCLAGDIISHKCQVPYLYRFELLGTAEDVANVRKGVTEFWQRQN
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A7FP81
|
FDHE_YERP3
|
Protein FdhE homolog
|
MSIRIVPKDQLGKQREKGTTAGNIPPLLFANLKSLYTRRTERLQQLALDNPLADYLDFAAKITEAQQKALHDHPLVLDMQAELVQSAASGKPPLDGSVFPRTEHWRKLLSALIAELRHDAPDHILAVLDNLDKASVHELELYADALLNRDFSQVGSEKAPFIWAALSLYWAQMASQIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTHNGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLASLILDAKMEGEGFARSSINPFLFPGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A7FPK3
|
SP5G_CLOB1
|
Putative septation protein SpoVG
|
MQITDVRVRKIAAEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPDGEYKDIAHPINTETREKIQKSIIEEYERAKMEEESSEKVQE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A7FPL4
|
YIDD_CLOB1
|
Putative membrane protein insertion efficiency factor
|
MKNLLICIIKMYRKYISPLKRPSCRFYPTCSQYSIEAIEKYGALKGTLISIKRILKCHPFNEGGYDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7FW14
|
Y2314_CLOB1
|
UPF0122 protein CLB_2314
|
MEEIVEMSLLLDFYGSLLTEKQNKIMDLYYNNDYSLKEISELTNTSRQAVHDIVKRCHKALLQYEEKLHMMERFINLENSKEKLLNMLNKVTKENIKEIDHIKKYIIDNI
|
Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}.
|
A7GG38
|
Y2506_CLOBL
|
UPF0122 protein CLI_2506
|
MEEIVEVSLLLDFYGSLLTEKQNKIMDLYYNNDYSLKEISELTNTSRQAVHDIVKRCHKALLQYEEKLHMMERFINLENSKEKLLNMLNKVTKENIKEIDHIKKYIIDNI
|
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}.
|
A7GJE0
|
SP5G_CLOBL
|
Putative septation protein SpoVG
|
MQITDVRVRKIAAEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPDGEYKDIAHPINTETREKIQKSIIEEYERAKMEEESSEKVQE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A7GJP2
|
YIDD_CLOBL
|
Putative membrane protein insertion efficiency factor
|
MKNLLICIIKMYRKYISPLKRPSCRFYPTCSQYSLEAIEKYGALKGTLISIKRILKCHPFNEGGYDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7GMJ2
|
LUTA_BACCN
|
Lactate utilization protein A
|
MKVTLFVTCLVDMFETNVGKATVEVLERLGCEIEFPEAQVCCGQPAYNSGHVESAKEAMKHMIETFEDAEYIVTPSGSCATMFHEYPHVFKDDPKWAARAQKVADKTYELTQFIVDVLKVTDVGASLKGTATMHKSCHMTRMLGVKEAPGILLSNVKGLTVKELPNVQNCCGFGGTFSVKMTPISEQMVDEKVDSVMETGADYLIGADCGCLLNIGGRIERLGKKVRVMHIAEVLNSRS
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
A7GMJ4
|
LUTC_BACCN
|
Lactate utilization protein C
|
MAGTIQNRDSFLDNIAKELGRARKTEGVQRPVWKNNVNLETLKDCSEEELLEVFKKQCENIHTTVIETTKDELKDAIQQMIAENGGGPILVSDDERFEKYGLTSFFREELPSQNVEVNIWDPEEKDENIRFAEKANIGIAFSDYTLAESGTIVVQSRKGQGRSLHFLPTVYFSIIPRETIVPRITQAVRDMNARVEKGEAVASCINFITGPSNSADIEMNLVVGVHGPLKAYYFVV
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
A7GRH6
|
Y2498_BACCN
|
UPF0122 protein Bcer98_2498
|
MLEKTTRMNYLFDFYQSLLTQKQRSYMSLYYLDDLSLGEIAEEFDVSRQAVYDNIKRTEAMLEEYEEKLMLLHKFQARQQLVAELKQLINEEEHVNDKMKQVVEDIEKLD
|
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}.
|
A7GU64
|
YIDD_BACCN
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQTHGALKGFWLTLKRILKCHPFHPGGFDPVPDKKDDK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7GYZ4
|
YIDD_CAMC5
|
Putative membrane protein insertion efficiency factor
|
MKNFALSCIKFYQNYISKILPKSCRYYPTCSEYAVWEFKNNDIFSALLATLARILRCNQLFKGGIDYPVIRKRFGSFSIFKRMEFSNIDFWFVPCKNSKFYVIKVLDSLKEKR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7H369
|
YIDD_CAMJD
|
Putative membrane protein insertion efficiency factor
|
MICLKILRFYQKFLSPLKPAACRYYPSCSEYALWQFQKKNFFLAFLSTFFRILRCNPFFKGGFDYPKVSKNFYPMNLCFKPMFLAKKQLCFLYIPYKNKSFYLIKIIFKRTNQ
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7H6J8
|
SP5G_ANADF
|
Putative septation protein SpoVG
|
MEITEVRVFPVNEEKLKAYVTITLDDCFVVRDLKVIHGNTGLFIAMPAKRRKDGTFKDIAHPLNTETRERMERTILAEYDRELRKGAAPRPTGTHDD
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
A7HAA4
|
FETP_ANADF
|
Probable Fe(2+)-trafficking protein
|
MARMVMCKKLGKELPGLTFKPFPNELGQRIYDSVSQDAWKLWLEHFKMIMNEYRLSPADPRSQEILYQQAEQFFFSEGAQLPPDYRPPRSKG
|
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}.
|
A7HIY9
|
YIDD_ANADF
|
Putative membrane protein insertion efficiency factor
|
MIRRALVFLVRVYQRLVSPLLPPACRFYPSCSAYAATALERHGALKGSALAARRLLRCHPFHPGGIDPVPESER
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7HLV5
|
YIDD_FERNB
|
Putative membrane protein insertion efficiency factor
|
MRKVILKLIRFYQKYISPLKPPTCRFEPTCSTYTYQAVERFGILKGLLLGFWRVLRCNPISKGGHDPVPTEFYLFKKSNNSLRRR
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7I142
|
YIDD_CAMHC
|
Putative membrane protein insertion efficiency factor
|
MKNIFMAVIEFYQRFISPVLPNSCRYYPSCSEYSLHEFKFNSFFGAFFATVLRILRCNPLFRGGIDYPLVRLKIQHQKAIFKICRSEVKFWFVPCKSGKFYVIKSFKKEK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7IIE0
|
COWN_XANP2
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MDQPAAGFPALHFELEQPDRYLTFQGIDFEGNMRRVLAHLYRYIDDPAHGNAFWDRFKARLQAAEAGAATICDKLLLLHSHVYYMVDLFEEQEDEIALADLKTLEEECF
|
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}.
|
A7MI07
|
NRDI_CROS8
|
Protein NrdI
|
MTRLIYFSSRSENTHRFIARLGLPAARIPLEDRERLRADEPYILVVPTYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIAAGNRNFGEGFCRAGDIIAHKCQVPFLYRFELMGTGQDIDNVRKGVSEFWQRQH
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A7ML45
|
FDHE_CROS8
|
Protein FdhE homolog
|
MSIRIIPQDQLEKSDKRTAEVIPPLLFPRLKNLYNRRAARLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKAAAEQGKPPLDIHVLPRDGHWQKLLQSLIAELKPEMSGPALAVIENLEKASAQELETMASALFSADFSAVSSDKAPFIWAALSLYWAQMASLIPGKARAEYGEARQFCPVCGSIPVSSMVHIGSSQGLRYLHCNLCETEWHVVRVKCSNCEQTRDLHYWSLESEQAAIKAESCGDCGTYLKILYQEKDPNVEPVADDLASLVLDARMEQEGFARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
A7MLY0
|
FETP_CROS8
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLQRDAEGQDFQLYPGELGKRIYNEISKEAWAQWQKKQTMLINEKKLNMMNPEHRKLLEEEMVNFLFEGKEVHIEGYTPPEQQ
|
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}.
|
A7MR09
|
SYDP_CROS8
|
Protein Syd
|
MQNEVQQALAAFSARYCEAWRQQRGSLPVSEEYIGISSPCIVSTHPDAVEWEPQPFTPEDSLGAVEKALDIVIQPDVHAFYASQYAGDMAARYDDVALTLLQAWSQDDFRRVQENLIGHLVTQKRLKLSPTIFIATLDSELDVISLCNLTGEVVQETLGTRKRRVLAPSLSTFLSQLTPLV
|
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}.
|
A7MTP0
|
FETP_VIBC1
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCARLKKEGEGLDFQLYPGELGKRIFDNISKEAWAQWQHKQTMLINEKKLNMMDPEHRKQLETEMVNFLFEGKDVHIEGYTPPSE
|
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}.
|
A7MYB9
|
SYDP_VIBC1
|
Protein Syd
|
MTQTVPQALQDFSLRYQQAWQDKHNELPRSEELADLVSPCVEEKRDGAVLWKAFPREEMADFTNVENAIELTLHEDIKLFFGSQYSADMDATWQGNELTLLQVWSDDDFTRLQENILGHLVTQRRLKLKPTVFIAATDAELDVISICNLTGNVILERLGSDKRDVLAETLTEFLSKLEAAV
|
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}.
|
A7NDW6
|
FETP_FRATF
|
Probable Fe(2+)-trafficking protein
|
MTKVFCKKYHQELDAIPFQPLPGELGKKIHNEISNKAWQAWLAHQTILINEYRLNLIEPKAKEFLKEEMYKFLFEGKEEKPEQFSEI
|
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}.
|
A7SP74
|
PSMG3_NEMVE
|
Proteasome assembly chaperone 3
|
MAAAIDGSLPVCRQSAALIDGVHTDFLASWYSDRILVLVTQFQKFGTLVSVTRDQPVARPDQAQGGTDSHTFTTKVLMGDDLPIWHVYGQQIFKAINGEDGCKPVLVAIALQNHSPEILKCILGQLESIRQVQTP
|
Chaperone protein which promotes assembly of the 20S proteasome. May cooperate with psmg1-psmg2 heterodimers to orchestrate the correct assembly of proteasomes (By similarity).
|
A7TJ20
|
LCL2_VANPO
|
Long chronological lifespan protein 2
|
MIAGFFTRFLFAILLLLPYSQGFFNFQGNQRQQQQQHHQNANPAEGFLSPHEERALSNQCPGYLCPDTEECVDSPSSCPCPFPGSQLKCSLPDGTFVCISKPATDNEDINRKYDDLSGNSKIKFNGVRDCGWVYEMAVKGFST
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
A7TN63
|
RRG1_VANPO
|
Required for respiratory growth protein 1, mitochondrial
|
MTSHFSSLPAHRSYIFSLYRDVLRNIHRCCYSVELQNILTSKLNLTMKQQKGTMSSWKAHSKIKELEELNDRLINRDLPYLKELINNLSGNKINSTQPNQYVQDLKEATNLINEYHSNNSQSIETIKKMDILNRYIKTKQSKHLLPKEISNVYKESLLLPFAIHEDSIYKLNKLHNQLIRGPPRVRLTNTKAGKITIWFLRSALNKKDRQSKKLKLRIAKEKQKHQQRIDNIKTCEKYAYWALLEASWESLLNTGKLPTININKTINNLSTLDNEDININRKNNHHIKDIHVKEWIEPITYSIKQLVDKEFERKCHYENYKKIILYGKNNGLIDFFENKTKVMYARRVSRYKTVVNGLPFIIPTIPRRDLRTALLDNKVLLP
|
Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).
|
A7TQB2
|
MTC2_VANPO
|
Maintenance of telomere capping protein 2
|
MKYNEELMDFEMALRFSVVTNKSFICFVNKEIEVTPQVVVKQAVERILSDLDGLEIEVLDSFLDTKCNNKTKSEDCKIKITIVPNLNNLTAEKQNVLSKYLRDNSNDIQGPRVKRNPKFQTTDLTNDKTEKNNTKYIVIGIVLYENKNEDENEDEEERLDKKSNVLTINDWLRNKFWLGCMAPVDESIEIVESIIYSMKDLEKYDTVVIKPVIKRYIEDIIVHLRMHNITYKPKGGGIQPDALHDIVALSQLISIMSSKYNKQLWFVTPDYIKIASMFYFPSHLRIVSDSSMDVSVAYGSKSHLVDEFLEKLNKVKFLARSQNPLFIESLVVKDVLTKIIPAI
|
May be involved in telomere capping.
|
A7TQS6
|
IRC6_VANPO
|
Increased recombination centers protein 6
|
MNEDGSVCNKILIAFQDNDQIANLKESVLGEVFRLDKANTNHDENIIKGLTWSTKYYEVRYDLYVDTFDDFEEWCKDLISSEYDDLREVLSGIIVIDSYTMEKDKIDQNKLLGQLGSVLQDKFFVFMNTNKDISQDVIDELNDDNSMQLTSDSGNSVEIINYHNVSNLKLNQYNEKIGFERVREIIDTCEWSGGHRVQTVEAKADSTDVDLESVFNRLKEARLKYLEIEDEDEREQFALEISNEFAEFLQ
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
A7TRZ8
|
IRC19_VANPO
|
Increased recombination centers protein 19
|
MDSVPSIRILTKNAVITSKYTLLKNHSKYYMPNHNLKDIDEDTVVKMYYRRFIRLRPLISRTRMVKETYTSYIRYKFKIENYQLKRKLVTGIEEQRPLIPTLQKSLEFIIKSVSFIPETKTIKFKIARDNTICRQVLKNLLTVEYQKENFIEKRSKGSELYQLLRVDFNHLVNSNNNLKFTSQLKVFNDFDMCLILMNETIGTRL
|
Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).
|
A7U6E7
|
MCP_CEV01
|
Major capsid protein (MCP)
|
MGGGLMQLVAYGAQDVYLTGNPQITFWKVTYRRYTNFAMESIEQTFNGQADFGRRVTCTISRNGDLAYRTYLQVTLPEINQQMLPAGVGQNLASNVLGSTTPGANNKGLEYGVFARWLDFPGEQMISMVEVEIGGQRIDRQYGDWMHIWNQLTLTAEQQRGYYKMVGNTTQLTFITDPSFAAVDGPCATTAPTQVCAPRNALPETTLYVPFQFWYCRNPGLALPLIALQYHEIKINLDLRPIDECLWAVSSLHNVCDSAATPTKVATAYQQSLVAASLYVDYVFLDTDERRRMAQNPHEYLIEQLQFTGDESVGSSSNKIKLNFNHPCKELIWVVQPDQNVDYCASLICGTTLFQVLGAQPFNYTDAIDVLPNGVHAFRWTRICXKDLMHSSPQLVFLIRLAQLMQSLSLVGEYDEPNFEHVSLGSASAGGGFFPPASAASSRANGGAVDFQSAVSDAGTFVLTETSLDMHCWGENPVVTAKLQLNGQDRFSEREGTYFDLVQPYQHHTRSPDTGINLYSFALRPEEHQPSGTCNFSRIDNATLQLVLSNATVGGTNTAKVRVYATNYNVLRIMSGMGGLAYSN
|
Major protein of the capsid.
|
A7U6E9
|
MCP_POV01
|
Major capsid protein (MCP)
|
MGGGLMQLVAYGAQDIYLSGNPQITFFKVVYRRHTNFSMESIEQTFNGFPNFGKKVTCPISRNGDLIHRIYLQATVTDSIASPGLTKWAGHKLIKSVEVEIGGQRIDKHYADWLHIWNELTQTAGHWDGYKLMVNGTTASQTVAPGATTVSKTMFIPLQFWFCRNPGLALPLIALQYHEVKINLEFGDSADVMGASGASLDSAALYVDYIYLDTDERRRFAQVSHEYLIEQLQFTGDESASSKIKLNFNHPVKELIWVEKASGDGVGEYDTTYDSAKLQLNGHERFTQRTPQYFQLVQPYQHHERVPTTCVLTVDASSIETDEAVMETCTTGGINVYSFALKPEEHQPSGTCNMSRIDNATLNLQGVDTDNTVKVFAVNYNVLRVMSGMGGLAYSN
|
Major protein of the capsid.
|
A7U6F0
|
MCP_PPV01
|
Major capsid protein (MCP)
|
MAGGLMQLVAYGAQDVYLTGNPQITFWKVTYRRHTNFAMESIEQTFNGQADFGRRVTCTISRNGDLAYRTYLQITLPEIGQSLSSGAVYARWLDFPGEQLISQVEVEIGGQRIDRQYGDWMHIWNQLTLSKEQERGYFKMVGNTTQLTYVCDPNFAAIDGPCSANGVRQVCAPRDALPETTLYVPLQFWYCRNPGLALPLIALQYHEVKINLDIRNIEECLWAVSAIDGTGTKITDAYKQSLAAASLFVDYIFLDTDERRRMAQNPHEYLIEQLQFTGDESVGSSSNKIKLNLNHPCKELIWVVQPDANVDYCSSLTASTHLNNLLGAQPFNYTDAFDALPNAVHAFGGQASASGANAVINASGLFEDPFSNDIQSSVLDSGAATGADSGVSDAGTFVLAETALDMHCWGENPVIVAKLQLNGQDRFSEREGTYFDLVQPYQHHTRAPDSGINVYSFALHPEEHQPSGTCNFSRIDNATLQLVLSNATVQGVNTAKVRVYAVNYNVLRIMSGMGGLAYSN
|
Major protein of the capsid.
|
A7WZL9
|
NRDI_STAA1
|
Protein NrdI
|
MKIIYFSFTGNVRRFIKRTELENTLEITAENCMEPVHEPFIIVTGTIGFGEVPEPVQSFLEVNHQYIRGVAASGNRNWGLNFAKAGRTISEEYNVPLLMKFELHGKNKDVIEFKNKVGNFNENHGREKVQSY
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A7X1K4
|
Y1226_STAA1
|
UPF0122 protein SAHV_1226
|
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}.
|
A7X2Y4
|
HRCA_STAA1
|
Heat-inducible transcription repressor HrcA
|
MITDRQLSILNAIVEDYVDFGQPVGSKTLIERHNLNVSPATIRNEMKQLEDLNYIEKTHSSSGRSPSQLGFRYYVNRLLEQTSHQKTNKLRRLNQLLVENQYDVSSALTYFADELSNISQYTTLVVHPNHKQDIINNVHLIRANPNLVIMVIVFSSGHVEHVHLASDIPFSNDKLNTISNFVTNKLTEFNQNLQDDIVSFVQSEQEEIFINKLINTMNNHISNQSNSIYMGGKVKLIDALNESNVSSIQPILQYIESNRIAELLQDISSPNINVKIGNEIDDSLSDISIVTSQYHFDETLKGQIAVIGPTAMHYQNVIQLLNRIW
|
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}.
|
A7X3N8
|
YIDD_STAA1
|
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}.
|
A7X4P6
|
MAZE_STAA1
|
Antitoxin MazE
|
MLSFSQNRSHSLEQSLKEGYSQMADLNLSLANEAFPIECEACDCNETYLSSNSTNE
|
Antitoxin component of a type II toxin-antitoxin (TA) system. Labile antitoxin that binds to cognate MazF toxin and counteracts its endoribonuclease activity.
|
A7Z0F6
|
YABA_BACVZ
|
Initiation-control protein YabA
|
MDKKELFDTVINLEEQIGSLYRQLGDLKQHIGEMIEENHHLQLENKHLRKRLDDTTEQIEKFKADQKETKTQKAEQSDIGEGYDNLARLYQEGFHICNVHYGSVRKGDCLFCLSFLNKK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
A7Z4L7
|
Y1580_BACVZ
|
UPF0122 protein RBAM_015800
|
MSLEKTTRMNYLFDFYQSLLTSKQKSYMSLYYLDDFSLGEIAEEYDVSRQAVYDNIKRTEAMLEQYEEKLLLFKKFQERKEMFTKLKELASGLQEEEKMTALIEALEKLD
|
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}.
|
A7Z504
|
NRDI_BACVZ
|
Protein NrdI
|
MVQIIFDSKTGNVQRFVNKTDFQLIRKVDETDHVDTPFVLVTYTTNFGQVPASTQSFLEKYAHLLLGVAASGNKVWGDNFAKSADTISRQYQVPILHKFELSGTSKDVELFTQEVERVVTKSSAKMDPVK
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A7Z6W3
|
HRCA_BACVZ
|
Heat-inducible transcription repressor HrcA
|
MLTNRQLLILQVIINDFIQSAQPVGSRTLSKKDEITFSSATIRNEMADLEELGFIEKTHSSSGRIPSEKGYRYYVDHLLSPVKLTKTDLDLIHSIFKEKIFELEKTVQKSAQILSDLTNYTSIVLGPTLSENYLKQIQIVPIQPDKAVAILVTNTGHVENRTINFPAKVDLADIEKLVNILNDRLAGVPMDELNERIFKEVVTYLRQHIANYDSILESLRSTFHPAAHVEKLFFGGKINMLNQPEFHDIERVRSLLSLIEKEQDVLKLFQSSKAGISIKIGKENDYEEMENCSLITATYTVDTKQIGSIAIIGPTRMNYSRVVSLLQHVTSDLSKAFTSLYDE
|
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}.
|
A7Z801
|
YIDD_BACVZ
|
Putative membrane protein insertion efficiency factor
|
MKTIMIAFIRGYQKFISPLTPPSCRFYPTCSQYGIEAVKTHGALKGGWLTLKRILKCHPFHPGGVDPVPDKKQKH
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7Z900
|
LUTC_BACVZ
|
Lactate utilization protein C
|
MMMKGTVTHQESFLNRIAESLGRERRKSGVSLPEWKYQPQYQTHAGCTEDDLVTMLKDHCVNIHTELIETDAAGLYDALRTQVNRFEGGPVIIPKDSRFETYGLQTLMTEEWPDEGIPVWEWDAEQGAKNIEKAEQANVGITFSEITLAESATVVLYASEHAGRSVSLLPTTYIAIIPKSSIVPRMTQASDILKQQIRDGVTVPSCINYITGPSNSADIEMDLVVGVHGPVKAAYILVNDR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
A7Z902
|
LUTA_BACVZ
|
Lactate utilization protein A
|
MKVSLFVTCLVDMFQTNVGKATVEVLERLGCEVDFPEGQICCGQPAYNSGYVTDAKKAMKRMIAAFEEAEYVVSPSGSCTTMFREYPHLFQDDPKWAAKAQQLADKTYELTDFIVNVLGVEDVGAVLHKKATVHTSCHMTRLLGVSEEPMKLLRHVKGLELTALPGKHQCCGFGGTFSVKMAQISEQMVDEKVACVEDTEAEVLIGADCGCLMNIGGRLDRKDKNVRVMHIAEVLNSR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
A7ZCY8
|
YIDD_CAMC1
|
Putative membrane protein insertion efficiency factor
|
MKKFAIKFIAFYQKYISILLPKSCRYYPTCSQYAIWEFQTNSFFSAFFATFMRILRCNQLFKGGINYPIIRKKFNSCFIFQKSDTKNVNFWFIPCQNSKFYVVKVLDKLKEKN
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
A7ZKA4
|
CBPM_ECO24
|
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}.
|
A7ZQA5
|
NRDI_ECO24
|
Protein NrdI
|
MSQLVYFSSSSENTQRFIERLGLPAVRIPLNERERIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIAQKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
A7ZQN6
|
SYDP_ECO24
|
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}.
|
A7ZRT0
|
GLGS_ECO24
|
Surface composition regulator
|
MDHSLNSLNNFDFLARSFARMHAEGRPVDILAVTGNMDEEHRTWFCARYAWYCQQMMQARELELEH
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Major determinant of cell surface composition. Negatively regulates motility, adhesion and synthesis of biofilm exopolysaccharides. {ECO:0000255|HAMAP-Rule:MF_00525}.
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A7ZUA1
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FDHE_ECO24
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Protein FdhE
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MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
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Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
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A7ZYV1
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CBPM_ECOHS
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Chaperone modulatory protein CbpM
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MANVTVTFTITEFCLHTGISEEELNEIVGLGVVEPREIQETTWVFDDHAAIVVQRAVRLRHELALDWPGIAVALTLMDDIAHLKQENRLLRQRLSRFVAHP
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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}.
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A8A3F6
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NRDI_ECOHS
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Protein NrdI
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MSQLVYFSSSSENTQRFIERLGLPAVRIPLNERERIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIARKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA
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Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
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A8A3S8
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SYDP_ECOHS
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Protein Syd
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MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQPTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLASNLAEFLNQLKPLL
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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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A8A4K4
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GLGS_ECOHS
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Surface composition regulator
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MDHSLNSLNNFDFLARSFARMHAEGRPVDILAVTGNMDEEHRTWFCARYAWYCQQMMQARELELEH
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Major determinant of cell surface composition. Negatively regulates motility, adhesion and synthesis of biofilm exopolysaccharides. {ECO:0000255|HAMAP-Rule:MF_00525}.
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A8A6G6
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YIDD_ECOHS
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Putative membrane protein insertion efficiency factor
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MAPPLSPGSRVLIALIRVYQRLISPLLGPHCRFTPTCSSYGIEALRRFGVIKGSWLTVKRVLKCHPLHPGGDDPVPPGPFDTREH
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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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A8A6Z4
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FDHE_ECOHS
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Protein FdhE
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MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKDPKIEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
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Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
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A8A7Z8
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LPMG_ECOHS
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mgtA leader peptide (Regulatory leader peptide for mgtA)
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MEPDPTPLPRRRLKLFR
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Makes mgtA transcription sensitive to intracellular proline levels. Under low levels of proline this protein cannot be fully translated, and a stem loop forms which permits transcription of the downstream mgtA gene (By similarity).
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