entry
stringlengths 6
10
| entry_name
stringlengths 5
11
| protein_name
stringlengths 3
2.44k
| sequence
stringlengths 2
35.2k
| function
stringlengths 7
11k
|
|---|---|---|---|---|
C1CTA3
|
YIDD_STRZT
|
Putative membrane protein insertion efficiency factor
|
MKRILIALVRFYQRFISPVFPPSCRFELTCSNYMIQAIEKHGFKGVLMGLARILRCHPWSKTGKDPVPDHFSLKRNQEGE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C1CZW1
|
YIDD_DEIDV
|
Putative membrane protein insertion efficiency factor
|
MSLASRGLVRVIRAYQRELSPRKPSPTCRFIPTCSQYAVEAIERHGALKGGWLATWRIMRCNPLVPGGVDPVPERFPQGRKTHP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C1D6H9
|
YIDD_LARHH
|
Putative membrane protein insertion efficiency factor
|
MSRIVLALIRFYQLAISPWLPPRCRYQPTCSQYAIEAVQKHGALKGGWLALRRIGRCHPWGSSGYDPVP
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C1DD12
|
FETP_LARHH
|
Probable Fe(2+)-trafficking protein
|
MARMVQCIKLGREAEGLDFPPLPGELGKKVYENVSKEAWQAWLRHQTMLINENRLNLADSRARQYLTQQLQNYFFGTGADMPAGFVPPSV
|
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}.
|
C1DIY8
|
COWN_AZOVD
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MSTTTYRSICGEESLPYIDCDRCIRALYARLQHYVQQDRGDCPICAYFREKIGSRDGSESDARLLLHAQVNVVYELFARHADQEALALLERIEDDCC
|
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}.
|
C1DJC2
|
FETP_AZOVD
|
Probable Fe(2+)-trafficking protein
|
MTRTVHCRKYKEELPGLDRPPYPGPKGEDIYNNVSRQAWDEWQKHQTMLINERRLNMMNAEDRKFLQAEMEKFLSGEEYAQAEGYVQPKE
|
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}.
|
C1DNF8
|
YIDD_AZOVD
|
Putative membrane protein insertion efficiency factor
|
MRKLALAAIQFYRYAISPLMANHCRFHPSCSCYAHEAISTHGLLRGGWLSLRRLGRCHPWNPGGYDPVPPIKTSRSSSMAE
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C1EKT5
|
LUTA2_BACC3
|
Lactate utilization protein A 2
|
MKVSLFITCLSDVFFPQVGKSVVEIMNQCGVELDFPEGQTCCGQPAYNSGYQEDAKLAAKQMIKAFEHSEYIVTPSGSCASMVHHYYKEMFKGDSEWYEKAVHLADRTYELTDFLVNVLGKNDWKSKLVEKAVFHQSCHMSRALGIKEEPLKLLSQVEGLDIKELPYCQDCCGFGGTFAVKMSSISETMVDEKIKHIEATEANLLIGADMGCLMNIGGRLRRKNKNIQVLHVAEVLAKGLNK
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C1EM10
|
LUTA1_BACC3
|
Lactate utilization protein A 1
|
MKVTLFVTCLVDMFETNVGKATVEVLERLGCEIEFPEAQVCCGQPAYNSGHVEAAKEAMKHMIETFEDAEYIVTPSGSCATMFHEYPHVFKDDPKWAKRAQKVADKTYEFTQFIVDVLKVTDVGASLPGIATIHKSCHMTRMLGVTEAPGILLSNVKGLTVRELPNVQNCCGFGGTFSVKMTPISEQMVDEKVDSAMETGADYLIGADCGCLLNIGGRIERLGKEIKVMHIAEVLNSRS
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C1EM12
|
LUTC_BACC3
|
Lactate utilization protein C
|
MTGLIQNRDSFLDNIAKELGRTRKTDGVERPVWKNNVNKETLKDYSQEELLEVFKNQCTNIHTTVVETTNDRLREDIQKVIVENGGGPIMLSADERFDSYGLTSLFKEELPKQNVEVNVWDPEKKEENMRIAERANIGIAFSDYTLAESGTIVVQSHKGQGRSLHFLPTVYFAIIPRETLVPRITQAVQDMNTRVENGEEVASCINFITGPSNSADIEMNLVVGVHGPLKAVYFIV
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
C1EP70
|
Y3946_BACC3
|
UPF0122 protein BCA_3946
|
MLEKTTRMNYLFDFYQSLLTQKQRSYMSLYYLDDLSLGEIAEEFDVSRQAVYDNIKRTEAMLEEYEDKLVLLQKFQERQRLVAKLKQLISEEEHVNEEMKQVVEAIEKLD
|
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}.
|
C1ES35
|
YABA_BACC3
|
Initiation-control protein YabA
|
MEKKDIFASVSSMEEQIGHLYKQLGELKQHLAELLEENQHIKMENENLRHRFEEVQIKEKQKTQKRKEVKPKTDIGEGYDNLARLYQEGFHICNLHYGSVRKEGDCLFCLSFLNKK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
C1ESL0
|
HRCA_BACC3
|
Heat-inducible transcription repressor HrcA
|
MLTERQLLILQTIIDDFIGSAQPVGSRTLAKKDAITFSSATIRNEMADLEELGFIEKTHSSSGRVPSEKGYRFYVDHLLAPQNLPKDEIVQIKDLFAERIFEAEKIAQQSAQILSELTNYTAIVLGPKLSTNKLKNVQIVPLDRQTAVAIIVTDTGHVQSKTITVPESVDLSDLEKMVNILNEKLSGVPMSELHNKIFKEIVTVLRGYVHNYDSAIKMLDGTFQVPLSEKIYFGGKANMLSQPEFHDIHKVRSLLTMIDNEAEFYDILRHKQVGIQVKIGRENSATAMEDCSLISATYSIGEEQLGTIAILGPTRMQYSRVISLLQLFTRQFTDGLKK
|
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}.
|
C1EW67
|
YIDD_BACC3
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQKHGAFKGFWLTCKRILKCHPFHPGGFDPVPDKKDDKVNS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C1F8R9
|
FETP_ACIC5
|
Probable Fe(2+)-trafficking protein
|
MAHNVFCARYKQEMEGLDEPPFDSDFGHKIYNNVSKRAWGEWIEHQKMLLNEYRLQPWTPQAQEFLVEQMNQYFFGEGAQLPKEYVPPSPR
|
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}.
|
C1FNF2
|
SP5G_CLOBJ
|
Putative septation protein SpoVG
|
MQITDVRVRKIAAEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPDGEYKDIAHPINTETREKIQKSIIEEYERAKMEEESSEKVQE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
C1FP34
|
YIDD_CLOBJ
|
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}.
|
C1FSM0
|
Y2743_CLOBJ
|
UPF0122 protein CLM_2743
|
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}.
|
C1KVC2
|
HRCA_LISMC
|
Heat-inducible transcription repressor HrcA
|
MLTERQLLIFRAIIDHFTWTIQPVGSKNLLKEKGLPYSSATIRNEMGVLEEYGFIEKTHSSSGRVPSEKGYRFYVDYLLQPKKLDKSDRQMIRSFFSENYYEMEGLIQNSALMLSDLTNYTSILLGPEATKNHLSGFRFVPINNFQAMLILITDQGHVDNHLVTIPEGTTLSDIERMVNILNERLVGLSLDDLKVQIPMEVKELLGKHVRNYESFMHVFSDSFAQASQQKVYFGGKTNILNQPEFHDINKVREMLHLMEEEQDVYELFRDIPDGLQVKIGRENNNSLMEDCSIITATYNIAGERVGGIVLLGPTRMEYSRMMGLVDVMSRDLTDVLTKLYRDNQN
|
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}.
|
C1KWA1
|
Y1818_LISMC
|
UPF0122 protein Lm4b_01818
|
MFEKTNRMNLLFDFYQELLTTKQKAYVSFYYLDDYSLGEIAEEFEVSRQAIYDNIKRTEESLEKYEEKLGMLKKYQQREKLFSQLEAQLTKKNFLDEQVKDTLEQLKNID
|
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}.
|
C1KXY3
|
YABA_LISMC
|
Initiation-control protein YabA
|
MDKKAIFDSVSNMEEQIGELYQQLGDLKTNLGEMLEENNRLNLENEHLRRRLSLTDEATPEPKAEIEAEHGVMAPNRKEAMQQMIELGEGYDNLVQLYKEGFHVCNVHFGSPRGNDEDCLFCLSLLNKK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
C3K6U5
|
FETP_PSEFS
|
Probable Fe(2+)-trafficking protein
|
MTRTIICRKYKEELPGLERPPYPGAKGQDIFDHVSAKAWGDWLKHQTLLINEKRLNMMNAEDRKYLAGEMDKFFSGEEYAKADGYVPPAQ
|
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}.
|
C3KWA2
|
SP5G_CLOB6
|
Putative septation protein SpoVG
|
MQITDVRVRKIAAEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPDGEYKDIAHPINTETREKIQKSIIEEYERAKMEEESSEKVQE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
C3KWJ8
|
YIDD_CLOB6
|
Putative membrane protein insertion efficiency factor
|
MKNLLICIIKMYRKYISSLKRPSCRFYPTCSQYSIEAIEKYGALKGTLISIKRILKCHPFNEGGYDPVK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C3L0E8
|
Y2675_CLOB6
|
UPF0122 protein CLJ_B2675
|
MEEIVEMSLLLDFYGSLLTEKQNKIMDLYYNNDYSLKEISELTNTSRQAVHDIVKRCHKALIQYEEKLHMMERFINLENSKEKLLNMLNKVTKENIKEIDHIKKYIIDNI
|
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}.
|
C3L5R9
|
HRCA_BACAC
|
Heat-inducible transcription repressor HrcA
|
MLTERQLLILQTIIDDFIGSAQPVGSRTLAKKDEITYSSATIRNEMADLEELGFIEKTHSSSGRVPSEKGYRFYVDHLLAPQNLPNDEIVQIKDLFVERIFEAEKIAQQSAQILSELTNYTAIVLGPKLSTNKLKNVQIVPLDRQTAVAIIVTDTGHVQSKTITVPESVDLSDLEKMVNILNEKLSGVPMSELHNKIFKEIVTVLRGYVHNYDSAIKMLDGTFQVPLSEKIYFGGKANMLSQPEFHDIHKVRSLLTMIDNEAEFYDILRHKQVGIQVKIGRENSATAMEDCSLISATYSIGEEQLGTIAILGPTRMQYSRVISLLQLFTRQFTDGLKK
|
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}.
|
C3L781
|
Y647_BACAC
|
UPF0122 protein BAMEG_0647
|
MLEKTTRMNYLFDFYQSLLTQKQRSYMSLYYLDDLSLGEIAEEFDVSRQAVYDNIKRTEAMLEEYEEKLVLLQKFQERQRLVAKLKQLISEEEHVNEEMKQVVEAIEKLD
|
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}.
|
C3LAQ2
|
LUTC_BACAC
|
Lactate utilization protein C
|
MTGLIQNRDSFLDNIAKELGRTRKTDGVERPVWKNNVNKETLKDYSQEELLEVFKNQCTNIHTTVVETTNDRLREDIQKVIVENGGGPIMLSADERFDSYGLTSLFKEELPKQNVEVNVWDPEKKEENMRIAERANIGIAFSDYTLAESGTIVVQSHKGQGRSLHFLPTVYFAIIPRETLVPRITQAVQDMNTRVENGEEVASCINFITGPSNSADIEMNLVVGVHGPLKAVYFIV
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
C3LAQ4
|
LUTA2_BACAC
|
Lactate utilization protein A 2
|
MKVTLFVTCLVDMFETNVGKATVEVLERLGCEIEFPEAQVCCGQPAYNSGHVEAAKEAMKHMIETFEDAEYIVTPSGSCATMFHEYPHVFKDDPKWAKRAQKVADKTYEFTQFIVDVLKVTDVGASLPGIATIHKSCHMTRMLGVTEAPGILLSNVKGLTVRELPNVQNCCGFGGTFSVKMTPISEQMVDEKVDSAMETGADYLIGADCGCLLNIGGRIERLGKEIKVMHIAEVLNSRS
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C3LB28
|
YIDD_BACAC
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQKHGAFKGFWLTCKRILKCHPFHPGGFDPVPDKKDDKVNS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C3LCL5
|
LUTA1_BACAC
|
Lactate utilization protein A 1
|
MKVSLFITCLSDVFFPQVGKSVVEIMNQCGVELDFPEGQTCCGQPAYNSGYQEDAKLAAKQMIKAFEHSEYIVTPSGSCASMVHHYYKEMFKGDSEWYEKAVHLADRTYELTDFVVNILGKNDWKSKLVEKAVFHQSCHMSRALGIKEEPLKLLSQVEGLDIKELPYCQDCCGFGGTFAVKMSSISETMVDEKIKHIEATEANLLIGADMGCLMNIGGRLRRENKNIQVLHVAEVLAKGLNK
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C3LJ05
|
YABA_BACAC
|
Initiation-control protein YabA
|
MEKKDIFASVSSMEEQIGHLYKQLGELKQHLAELLEENQHIKMENENLRHRFEEVQIKEKQKTQKRKEVKPKTDIGEGYDNLARLYQEGFHICNLHYGSVRKEGDCLFCLSFLNKK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
C3LP78
|
YIDD_VIBCM
|
Putative membrane protein insertion efficiency factor
|
MATPLSPFSWLAIGIVKLYQWFISPLIGPRCRFTPTCSTYAIEALRAHGFIKGCWLSTKRLLKCHPLNEGGFDPVPPVQKQDRDK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C3LRW8
|
FETP_VIBCM
|
Probable Fe(2+)-trafficking protein
|
MARTVFCTRLQKEADGLDFQLYPGELGKRIFDNICKEAWAQWQTKQTMLINEKKLNMMDPEHRKLLEQEMVNFLFEGKEVHIEGYTPPAK
|
Could be a mediator in iron transactions between iron acquisition and iron-requiring processes, such as synthesis and/or repair of Fe-S clusters in biosynthetic enzymes. {ECO:0000255|HAMAP-Rule:MF_00686}.
|
C3N1X1
|
Y365_SULIA
|
Putative antitoxin M1627_0365
|
MAKTITISEEAYKLLLKEKRDGESFSDVIVRLIKGNRREVMDYAGIWSDMNDEESNKLFKDLEKMWERWNVNA
|
Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. {ECO:0000255|HAMAP-Rule:MF_00794}.
|
C3P1X2
|
LUTA2_BACAA
|
Lactate utilization protein A 2
|
MKVSLFITCLSDVFFPQVGKSVVEIMNQCGVELDFPEGQTCCGQPAYNSGYQEDAKLAAKQMIKAFEHSEYIVTPSGSCASMVHHYYKEMFKGDSEWYEKAVHLADRTYELTDFVVNILGKNDWKSKLVEKAVFHQSCHMSRALGIKEEPLKLLSQVEGLDIKELPYCQDCCGFGGTFAVKMSSISETMVDEKIKHIEATEANLLIGADMGCLMNIGGRLRRENKNIQVLHVAEVLAKGLNK
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C3P4C3
|
LUTA1_BACAA
|
Lactate utilization protein A 1
|
MKVTLFVTCLVDMFETNVGKATVEVLERLGCEIEFPEAQVCCGQPAYNSGHVEAAKEAMKHMIETFEDAEYIVTPSGSCATMFHEYPHVFKDDPKWAKRAQKVADKTYEFTQFIVDVLKVTDVGASLPGIATIHKSCHMTRMLGVTEAPGILLSNVKGLTVRELPNVQNCCGFGGTFSVKMTPISEQMVDEKVDSAMETGADYLIGADCGCLLNIGGRIERLGKEIKVMHIAEVLNSRS
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C3P4C5
|
LUTC_BACAA
|
Lactate utilization protein C
|
MTGLIQNRDSFLDNIAKELGRTRKTDGVERPVWKNNVNKETLKDYSQEELLEVFKNQCTNIHTTVVETTNDRLREDIQKVIVENGGGPIMLSADERFDSYGLTSLFKEELPKQNVEVNVWDPEKKEENMRIAERANIGIAFSDYTLAESGTIVVQSHKGQGRSLHFLPTVYFAIIPRETLVPRITQAVQDMNTRVENGEEVASCINFITGPSNSADIEMNLVVGVHGPLKAVYFIV
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
C3P5P7
|
Y4008_BACAA
|
UPF0122 protein BAA_4008
|
MLEKTTRMNYLFDFYQSLLTQKQRSYMSLYYLDDLSLGEIAEEFDVSRQAVYDNIKRTEAMLEEYEEKLVLLQKFQERQRLVAKLKQLISEEEHVNEEMKQVVEAIEKLD
|
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}.
|
C3P8M2
|
HRCA_BACAA
|
Heat-inducible transcription repressor HrcA
|
MLTERQLLILQTIIDDFIGSAQPVGSRTLAKKDEITYSSATIRNEMADLEELGFIEKTHSSSGRVPSEKGYRFYVDHLLAPQNLPNDEIVQIKDLFVERIFEAEKIAQQSAQILSELTNYTAIVLGPKLSTNKLKNVQIVPLDRQTAVAIIVTDTGHVQSKTITVPESVDLSDLEKMVNILNEKLSGVPMSELHNKIFKEIVTVLRGYVHNYDSAIKMLDGTFQVPLSEKIYFGGKANMLSQPEFHDIHKVRSLLTMIDNEAEFYDILRHKQVGIQVKIGRENSATAMEDCSLISATYSIGEEQLGTIAILGPTRMQYSRVISLLQLFTRQFTDGLKK
|
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}.
|
C3P9H8
|
YABA_BACAA
|
Initiation-control protein YabA
|
MEKKDIFASVSSMEEQIGHLYKQLGELKQHLAELLEENQHIKMENENLRHRFEEVQIKEKQKTQKRKEVKPKTDIGEGYDNLARLYQEGFHICNLHYGSVRKEGDCLFCLSFLNKK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
C3PCE8
|
YIDD_BACAA
|
Putative membrane protein insertion efficiency factor
|
MKQIFIGIIRFYQKFISPMTPPTCRFYPTCSHYGLEAFQKHGAFKGFWLTCKRILKCHPFHPGGFDPVPDKKDDKVNS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C3PN67
|
YIDD_RICAE
|
Putative membrane protein insertion efficiency factor
|
MTRILLLLLGFYQYFISPLLGNNCRFHPTCSEYAKEAISMHGSIKGLWFTFKRIIKCQPFCNGGYDTVPISIKNSKPLNKKI
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C4K2P7
|
YIDD_RICPU
|
Putative membrane protein insertion efficiency factor
|
MTRILLLLLRFYQYFISPLLGNNCRFHLTCSEYAKEAISMHGSIKGLWFTFKRIIKCQPFCDGGYDTVPISIKNSKPLNKKI
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C4K3H3
|
FETP_HAMD5
|
Probable Fe(2+)-trafficking protein
|
MSRTIFCTFLKKEAIGQDFQIYPGDIGRRIYDDISQEAWSLWLNKQTMLINEKKLSMIHHEDRALLEREMIQFLFEGKDVHVSGYIPPKD
|
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}.
|
C4KZV2
|
SP5G_EXISA
|
Putative septation protein SpoVG
|
MQITDVKIRKVATEGRMKALASITLDHEFVVHDLRIIEGSSGLFVAMPSKRTPEGIFRDIAHPINGEMRQKVEAAVLETYSNMDVEILDPQHVSYGTHE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
C4L0S0
|
LUTC_EXISA
|
Lactate utilization protein C
|
MNPGTITNREDFLQRIAKQLGREVKLTPPKREYTHRPQDEVLKGASEEELLETFRMVATRIHTDLVECESAKLDDTLRLLIERYHGARILAENDERISAWAPTTSETFDWWDSSQPEASRELAIRADIGITIADAAFAESATIVQYAMPGRSRTISLLPQDHIAIIPKSVLVPRMTQTAQQLATLDRDGLHSPNGVNFISGPSNSADIEMNLIVGVHGPVRVSYVLVHDL
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
C4L0S2
|
LUTA_EXISA
|
Lactate utilization protein A
|
MPNVALFVTCLSDTLFPSVGQATVELLEHLGCEVTFPFEQTCCGQPAYNSGYHEETKKIAKHMIETFEQADAEYIVGPSGSCVMMMRDYPHLFQDDPVWRPRAEAHAAKTFELTQFIVDVLEVTDVGAKFPAKATYHASCHMTRLLGIEAAPGKLLGNVDGLTMVPLANVHNCCGFGGTFSVKMPDVSVQMVDEKVDSILQSGAEVLIGADASCLMNIGGRLHKQGHPIKVMHIAEVLNEGVKQA
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C4L2G6
|
YIDD_EXISA
|
Putative membrane protein insertion efficiency factor
|
MKRVLVKGIQGYQRFISPLKPPTCRFYPSCSHYGIEAIEKHGAVKGSYLTARRLIRCQPFHPGGLDYVPDTFDWKAPLQREKPESQRDD
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C4L5Z9
|
Y2891_EXISA
|
UPF0122 protein EAT1b_2891
|
MTLEKTNRMNYLIDFYQALLTPKQRNYMSLYYLDDYSLGEIAEEFEVSRQAVYDNIKRTETMLEQYEEKLALFEKFEQRQQLLQTLKRQVELTDDVSATISALENLE
|
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}.
|
C4L9Z4
|
SYDP_TOLAT
|
Protein Syd
|
MADQVICALSDVFARWFAYQQQRGIQVCCPEDELRPSPCRYDAQHPERWKPWSRPEMSDLQNIASALECVFHPAIHAYYGHGYAGQITASFKGLAVTLVQPWNEEDFERLQQNLVAHVLMLRRLKLPITLFLATVSDESRVISLDNETGEVVLEQLGKKKRWVLADSLPAFLQRLSPLAQTAVTPAVPVNLPA
|
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}.
|
C4LBG4
|
COWN_TOLAT
|
N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)
|
MPCSCKQKKATPSDITTDRYITFDGIDCDGNARILMSYIHKHIDDPQKTNKFWDYFRKKAEGGNGPKPDDLFLIHSNLNQIRELFELYEDSEALALLDVVEIECC
|
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}.
|
C4LCM1
|
FETP_TOLAT
|
Probable Fe(2+)-trafficking protein
|
MTRMVFCQRLKKEAPGMAFQLVPGELGKRIFDNICQEAWAEWQKKQTMLINEKKLNMMNAEHRALLQTEMEKYLFEDGDVQIEGYVPPSEK
|
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}.
|
C4LDZ5
|
YIDD_TOLAT
|
Putative membrane protein insertion efficiency factor
|
MAHPRTPQQRLAVALIRVYQWVISPLLGPRCRFTPTCSQYMINAICLHGLIKGIWLGGKRLLKCHPLHSGGHDPVPQPQQSKRRK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C4QVR9
|
IRC19_KOMPG
|
Increased recombination centers protein 19
|
MSNGPAKYTIINRLVQPILPIKKQLLEENPNHSLRLLSLYRRHLRLRPFISPRADIKQFYTDLVRLRFKEDIELRRKHFTTPYTPLDKDSIIERVIRTLEIVNNGCVDSPNSIERQIIRNILDVEYANKNIKMVPLMSVEYFKEELWKGRELDVVSEPKLYDWVNKIDISNKSKKKNEQLNLLTALRNHYRSVASFNEVQKTLL
|
Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).
|
C4R2P5
|
LCL2_KOMPG
|
Long chronological lifespan protein 2
|
MRGFVVATIIVGAANCVMAFDFEQFFGGQNRQQQRTQQNNQPQDYEQQQLNSDCQKYLCPETFACVAKPVDCPCPFPQSQIKCVFPDKQNFVCISSPVDNVNGVPVRDCKWVEKAWKGLL
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C4Y2M6
|
RRT14_CLAL4
|
Regulator of rDNA transcription 14
|
MAFSSASSKARSKASVNKLFESMLPGTSLLPSSSGKSSATEKFAAQVNKKKLTKHEIQKAHKVEKAKKNKLINQKLEKEKKFKKLVKFNVIKAHKEEKDLTPEEQKYLKKLIKKNANAVVRASEVDDPFVKDEIDALRSEILALTNEKYDKSRDRKLDAKLQSFNDKIKKGVLAYPGLTPGLAPVGYDDESDEE
|
Involved in ribosome biogenesis, probably through modulation of rDNA transcription.
|
C4Y6U0
|
IRC6_CLAL4
|
Increased recombination centers protein 6
|
MDRNNVLVLGPPKSGKIRFAQFISGDYETETISDDSHSGLMYKCNLKTKYFSVDVNLLIEEFPESRKEPEEKWISSLQTWFGEFESDTMADLREVIEGVVFTVCVNEWDDNVIKQQLDILSNMKDLLKDNDPFFIVMGVSEHDIEQDTMADLEDLVLLNGFEFVYFNDSGMNEFRDKMGKDRLLEVLETHEWTQKHLTHVSNEDYMAYKKEKMTSMTQGLLQEDDCNIPTLDVLLQKLQIEKSKVEEMKENERKGYVDGLVDEFLEYF
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
C4YAT5
|
LCL2_CLAL4
|
Long chronological lifespan protein 2
|
MFRILYLFVLCGAVSASIFNFMHDQYQHQEPRHEVSFEQRVLESNCDKYLCPGTLECVARPQDCPCPYPSSQMRCVLPNGDPLCISKPTGDYNGKYDDPAKNWKVDAKDDNVRDCGWVKRAWEGRV
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C4YH38
|
IRC6_CANAW
|
Increased recombination centers protein 6
|
MIPNHILILGSPNSGKLRIANLISKNEEIPNLEDVELHSGLIVKASLRTKYYFLKLNILIDEYSESKGATDEKKLSELHKWYQEFKSEEFGELREVLDGLMFTINMKTDSISFIRDALEIIEQIKISLGDEENLHDWGGFIAVVGSCPENQIVEDDLILEIEDMVLSQGLEFINLSTEGENEYKEKQGKDRIVELIESHDWTNLEMLKVDSKQYETNKLAKMESMKQKLINEKEELDLDDIFSKLNLARDHAQSLTQDERDKYANKVIEEIIDFL
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
C4YM26
|
LCL2_CANAW
|
Long chronological lifespan protein 2
|
MFQKLIVITFAIALASANIFDFLNNFNTGGRQQQNQGVRTPQEYESVVLNSQCDKYLCPDTGLCVEAPKFCPCPYPSSQIRCFLPDGRFVCISKPAGEGISEKYNDPKTNWKIDAKDDNIRDCGWVNRAWRGLV
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C4Z4L6
|
SP5G_LACE2
|
Putative septation protein SpoVG
|
MNITDVRVRKIAKEGKMRAVVSITIDDEFVVHDIKVIEGEKGLFIAMPSRKSSDGEYRDIAHPINTQTRDKLQKIVLEAYEKAEYVEE
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
C4Z927
|
Y1504_AGARV
|
UPF0122 protein EUBREC_1504
|
MEEKLEQAYLYDFYGELLNEHQRQVYEDFVFNDLSLGEIASEEGISRQGVADLIKRCNKKLLDYEAKLHLVEKFMSIKSDIRRIHELTNDFKKSHNELLMNEIEAISNQILEEL
|
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}.
|
C4ZBV4
|
SP5G_AGARV
|
Putative septation protein SpoVG
|
MQITDIRIRKVEKEGKMKAVVSITIDDEFVVHDIKVIEGEKGLFIAMPSRKANDGEYRDIAHPINSATRENIQNMILEKYKTEIENV
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
C4ZQC7
|
CBPM_ECOBW
|
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}.
|
C4ZQW6
|
GLGS_ECOBW
|
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}.
|
C4ZYS6
|
NRDI_ECOBW
|
Protein NrdI
|
MSQLVYFSSSSENTQRFIERLGLPAVRIPLNERERIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIARKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA
|
Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}.
|
C4ZYY2
|
YIDD_ECOBW
|
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}.
|
C4ZZU8
|
SYDP_ECOBW
|
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}.
|
C5A059
|
FDHE_ECOBW
|
Protein FdhE
|
MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLGDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCDTYLKILYQEKDPKIEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
C5BB03
|
FDHE_EDWI9
|
Protein FdhE homolog
|
MSIRIHPQEQIDAKSRSGALGPIAPLLLPNLQRLYSQRAERLRMLADGHPLTDYLCFAATLADAQQQALFDNPLTLDLAPVVANAAANGTPPLATQTFARTPHWQRLLLAIIAELRPQAPVHVLPVLEGLEKCAAGEREALASALLAGDYAAVGSDRALFLWAALSLYWAQMASQLPGRAQAEYGEQRHVCPVCGSMPVSSVVHIGGSNGLRYLHCSLCESEWHMVRVKCSNCEESRDLSYWSLESEQAAVKAESCGDCGSYLKILYQEKDSGVDAVADDLATLLLDAKMEEAGFARSSLNPFLFPGE
|
Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}.
|
C5BCF0
|
FETP_EDWI9
|
Probable Fe(2+)-trafficking protein
|
MSRTVFCTFLNREAEGLDFQSYPGDLGKRIYDHISKEAWGQWMAKQTMLINEKKLNMMNPDDRSLLAREMEKFLFEGHDVHIEGYTPPNQ
|
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}.
|
C5BHA8
|
SYDP_EDWI9
|
Protein Syd
|
MEHQVSAALREFTQRYVAQWQQQHGDWPSSHALYGIPSPCVVYSRDDCVFWRPEPGRGEDLEGIGRALDIRLHPALAPFFTTQYAGDMRARWNEIEMDLVQVWSVEDLHRLQENQIGHLVTQRRLKLSPTLFLASTADELSMVTLCNLSGSVLLEQFGSPQRRVLAQTLTEFLAELQPLAQEVG
|
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}.
|
C5BM93
|
FETP_TERTT
|
Probable Fe(2+)-trafficking protein
|
MTRTVHCRKYNKEMEGLAVPPLPGAKGTELFNSVSKQAWQEWLQHQTMLINEKQLNLMDLTARAYLTEQMEKFLSGADYDQADGYVPK
|
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}.
|
C5CD37
|
YIDD_KOSOT
|
Putative membrane protein insertion efficiency factor
|
MKKIVLTLINFYRKYISPSKPPTCRFTPTCSAYTFEAVQRFGVFKGLLLGTWRILRCNPFNKGGYDPVPEEFKLLRRNTK
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C5CNX5
|
FETP_VARPS
|
Probable Fe(2+)-trafficking protein
|
MARMVQCIKLGKEAEGLDFPPYPGELGKRLWENVSKEAWAAWLKQQTMLVNENRLNLADLRARQYLARQMEKHFFGEGADVAQGYVPPSN
|
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}.
|
C5CYY5
|
HRCA_VARPS
|
Heat-inducible transcription repressor HrcA
|
MLDDRAKLLLKTLVERYIAEGQPVGSRTLSRAPGLDLSPATIRNVMSDLEGLGLITSPHTSAGRIPTARGYRLFVDTMLTAQREHMNAPSHLPPDQPQKVIANAANLLSNLSQFVGVVMTPRRASVFKQIEFLRLSDRRLLVIIVSPDGDVQNRVIFPEADYTQSQLVEASNYINAHYAGLTIEQVRDRLQSEVEKLRGEIAALMQAAVKVSSEVLTEAQEDDVVISGERNLLSVTDFSSDMGQLRRAFELFEQKAQLMRLLDVSSKAEGVRIFIGGESQVVPIEELSIVSANYEVDGQVVGTLGVIGPTRMPYERMIQIVDITSRLVSNALSHRK
|
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}.
|
C5D355
|
YABA_GEOSW
|
Initiation-control protein YabA
|
MDKKEIFQSVTSMEEQLSHLYRQLVQLKEHVVQLLEENHHLQIENDHLRRRLEQVTSELAEEKQKEKDHKHGHERKLVDIGEGYDNLARLYQEGFHICHVHYGSVRKEGDCLFCLSFLNKK
|
Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}.
|
C5D370
|
SP5G_GEOSW
|
Putative septation protein SpoVG
|
MEVTDVRLRRVNTEGRMKAIASITLDNEFVVHDIRVIDGNNGLFVAMPSKRTPDGEFRDIAHPINSATRGKIQEAILAEYHRLGKLEEELEEAGAS
|
Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}.
|
C5D4U3
|
HRCA_GEOSW
|
Heat-inducible transcription repressor HrcA
|
MLTDRQLLILQVIIDDFIRSGQPVGSRTLSKKHEIALSSATIRNEMADLEELGYIEKTHVSSGRVPSEKGYRYYVDHLLSPQRLTQEDIQKIKSIFAERIYELEKVVQKSAQILSDLTNYTSIALGPAVKENKLKRIQIIPLNQQTAVAIIVTDTGHVENHVITVPASVNPSDLEKMVNILNERLIGVPLVDLKDKIYKEVADVLRTHIHNYDSMLKTIVDTLDIPQEEKMFFAGTTNMLNQPEFSDIQKVRSLMKMIEQEKDFYRLLRKHNRKGIQVTIGRENQLSGMENCSLITATYSIGNEQLGTIAILGPTRMEYSRVITILNRVASDLSTALTKWYQNN
|
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}.
|
C5D585
|
LUTC_GEOSW
|
Lactate utilization protein C
|
MMQTGTIHNRDKFLQTVANRLGRHQRTSGVSRPHWRHQPQWTVFQGYSQDELLEALKAQCPRIHTQCVETTAVELKETLKEVVAKHGGGPIVTWDDPRFDEYGLTRLLRNEWPNENVDVHIWDASAGRKNIDYAEQANVGITFSDITLAESGTVVLFSGNGKGRTVSFLPKTYIAIIAKSTIVPRMTQAAAYIHEQIEKGHLIPSCINFITGPSNSADIEMNLVVGVHGPMKATYIVVTDR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02104}.
|
C5D587
|
LUTA_GEOSW
|
Lactate utilization protein A
|
MKVSLFATCLIDLFYTNAGKATVELLERLGCEIDFPEAQTCCGQPAYNSGYVKEAKEAMKHMIRTFEHADYVVTPSGSCATMLKEYPRVFQGDREWESKAKALADKTYELTQFIVDVLKMEDVGAKLQGRATYHTSCHMTRLLGVKEAPFKLLKNVKGLELVPLPNAYQCCGFGGTFSVKMGTISEQMVDEKIEHIEEVNADYLIGADCGCLMNIGGRLKRQGKPIKVMHIAEVLNSR
|
Is involved in L-lactate degradation and allows cells to grow with lactate as the sole carbon source. {ECO:0000255|HAMAP-Rule:MF_02105}.
|
C5D6T9
|
YIDD_GEOSW
|
Putative membrane protein insertion efficiency factor
|
MKKLLISFIRFYQIFISPLKPPTCRFYPTCSHYGLEAVKRFGAIKGGWLTIKRILKCHPFHPGGFDPVPEKQENGKS
|
Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.
|
C5D8T9
|
Y1086_GEOSW
|
UPF0122 protein GWCH70_1086
|
MLEKTMRMNYLYDFYQALLTPKQRSYMSLYYLDDYSLGEIAQQYEVSRQAVYDNIKRTEAMLEEYEKKLSLFQKFQKRKQLMNQLKDYVLQKYGEDKQLFDMIKELEELE
|
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}.
|
C5DGD8
|
SPG4_LACTC
|
Stationary phase protein 4
|
MGGIFDAFEVYNKKKHSSNPHMFGNTSNTGGTKTDYVYSSEYRAPKKNKLMKDELLAPDSEHADGAKAMLTESAAQAGTPNMVDLSKLSQHELESLMKDLRKGEPNNRVNF
|
Stationary phase-essential protein not required for growth on nonfermentable carbon sources.
|
C5DGI8
|
MTC2_LACTC
|
Maintenance of telomere capping protein 2
|
MSGQEPSLPPMGPTLPAALAFRKNLVCYCEDPTVVVEFLQALHLPYALWENYDDIDARPKPEAEQVLVLPNVDRLLTLQQDKLAKFLQVMRSRDTPFFAAVATVSPGFVPYAHFTPYLKRQFWFACAEPMTGGATDFNEETLPQLRNSLRKVHVHHSIRRYVLDIIMHLRVHRFSSQASGGGCSTHSLRDILELCQTLALAEERAFVVPDIVKTASYWYFPFHLELIQNPSHEISLQYGSDPDLVAQLVNAMQQFSLQRASEIHYPLYFQYMVLRDVLNLVVPAI
|
May be involved in telomere capping.
|
C5DHP6
|
IRC19_LACTC
|
Increased recombination centers protein 19
|
MASRGITITTNKAITTSKSTLILKHDKFLPPRNMINEFPHDDVLRMCYRRHMRLKPFISQRSMIQTTYVDYVRYKYKNEDYPKKCRASGIAHKTPVQSVLQQAELSLRFCLQAVMQVKKGVSDERSVSNEIRLSRNMLKNILAIEHEKAKLIAQNPRQNYPILREAFSYISPTAHKSSLLLRFNALREFDRCLIRFNMCMGTKL
|
Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).
|
C5DLJ0
|
IRC6_LACTC
|
Increased recombination centers protein 6
|
MTTGLSLDEGKVIEGRPKALRDKVLIVFSNKVFNREEILFEVFGVEDNAGKQVHRGVDWTTKYYTVTIDVYVDSFSNLEDWTNEFCDPDFDELRDVIAGWIIVLPFSGNIEEETKALSRLVNNATSEDFFTAILATELNVGKNERAFLEYNVLAGAVELVHNELDSDGELKEVNGVDRVKEIIDTCDWHPRLLRTAHLESETGMESACTGISLAQIMGSLREARTKYMAMDPGLDREEFANEMANELSKLL
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
C5DMZ6
|
LCL2_LACTC
|
Long chronological lifespan protein 2
|
MRGSSLGLYFILPIASGFFFDFNQRNQHEGQQPQVSYEDKVLNNDCADFLCPDTLTCVKTAKDCPCPFPKSQLRCTLPNGQFVCISKPATHDKNLNAIYDDPVKGPQSKIKGLRDCGWVQDAYKGIV
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C5DVG0
|
LCL2_ZYGRC
|
Long chronological lifespan protein 2
|
MNCACRVIAVCLLLVQVSGFLFNFNQDPPTPPQPYEDKFLNSGCEGYLCPDTLECVSHVKECPCPFPKSQLKCTLPNNQYICISKPATHDEKLNAIYDDPAKGPKAKNKGIRDCGWVLEAYKDQV
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C5DZE1
|
IRC19_ZYGRC
|
Increased recombination centers protein 19
|
MAGRTILTRNAVINSTHTLIKCPEKYLLPSLEVSNLPSFVRMAYRRLFRLQSFISNRKMVRDTYGEYLRYKFKKENYDTKRSIVVGDTPKAPLREEIRNSVMFVVKAVSHLPETKDSKFAIARDNTTCRQVLKNLLTIEYEKQSLIARYRPPTKRRDMVGPYQIYRKDFTHMQELNKSAQWRVFGEFDICTVYLNEILQTRL
|
Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).
|
C5DZT2
|
RRG1_ZYGRC
|
Required for respiratory growth protein 1, mitochondrial
|
MVQNFIHLPEHRQCVLHLYRHTLRNSKQCCHSQHLINRIKKITRQTIVKHRYDKSSWSVHFYLQKLYELNHLLIQRDVKTVWNLLTDVSKSKSKSKSKKSSTRSSRILKALQDIHQLKQDKGLQDPQIVREKLILNNYIKREQARNHLPRFIPEEYKTKLLLPLALHTVAMARLNSIHGKLVEGPPKVFLTHTTPMGHRIWFVRSAFNKKKRQSKTLGILIRREKNEGHKRWDYLRQCKSNAYWAQQEANWEQLIENKIVPQFDLNRYLDSQSIGKKKIECPPQLAHWLEPIGYSIQKLNQINADKAAYFRNYKNRVLLNGGQALYFENKSITMYQRRVKRFQQMVQNDLPYVVPFFPGRDLLSTLTKYRF
|
Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).
|
C5E1C0
|
MTC2_ZYGRC
|
Maintenance of telomere capping protein 2
|
MAVDKLPDFISGLRFMVAAKKHLVYFYSMKESGSPTSEQIEIERQTSLLKNIVERSYLQERVSCYVLKNIPQEGLPTYNDQTHTGIEIIIIPQVHTLTKGDQNVLVRMMMASQVSRPVRLFIGMIPWDTTKESAMSGDIELALSSRITSEDWLKHKFWFACYEPDENEVFSPLIGALPESLEKAQYTDVHANRSIHRYILDVMIHLRMHKLLDTTKGGGIHTSALRDVLALSQLLALYRFNKAFVTPEHVKLACIWYFPLHVEFLKGSAMDTSVLYGSRPELVDGLLKCIADVKLSNTVETENPLFLETIVVQDVLNKVVPPV
|
May be involved in telomere capping.
|
C5E4V9
|
IRC6_ZYGRC
|
Increased recombination centers protein 6
|
MIMDSVSSPEQPKNKILVTFGDGDSIHQRELISQLFGIDIGIGDRIVKGLVWKTKYYRVEFDLYIDDYNDFSSWFQEFASEEFAALREAMAGLVVVDQYEPTKPLNPLGLQDTFVVWVNTDSKVGQDQVDEINDKLFQTEESTVELVNLHSNEDTNEYGEKIGIPRFKEIVDTCSWKNCDMDYLTSTSSTTNPEVSLELIVQRMQHARLKHANSEMDNDEALQIAQEIAEELTGKED
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Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
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C5FVJ9
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LCL2_ARTOC
|
Long chronological lifespan protein 2
|
MLRTALLGLLFITTAKAQFQFFEQMFGGGQQHQESSSQGGNVPSDSAWYQNTYNGAQCSNYLCPGTLACVAVPHHCPCAHPQVEDKFEFGEGSAICASKGGFKAGETARKIELARKGLL
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C5GHR3
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LCL2_AJEDR
|
Long chronological lifespan protein 2
|
MIHIITGTLLGLLFLATGARAQFQFFEQMFGGGQQQQESQEHNVPSDSSWYQRTYDNARCSDYLCPGTLACVSVPHHCPCQHPGVEDKFELGDGSAICVSKGGFKPGEAARKVELARKGLL
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Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C5M2I3
|
IRC6_CANTT
|
Increased recombination centers protein 6
|
MIPNHILILGSPNSGKLRVSKLISNDKDFPEIKENESHSGIIIKTSLSTKYYHIKLNILIDEYPEERNKSVTDEEKLLELEKWFNEFKSEEFGELREVLDGLVFTVNMKADSLEFIEKALETVSEIRTSLGDEESQWDGFISIIGSTTQGESVDDDTVEEIEDLVITHGFEFINLNTQGINEFKEKQGKDRVVELIESHEWTNMELLKVNPDQYEKNKMNKVEQMKQNLLEEKESMDLDVVFSKLSVAKERAEDMTQEQKEKYANEIIEEIIDFI
|
Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
|
C5M3K2
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LCL2_CANTT
|
Long chronological lifespan protein 2
|
MQYLLVALSLFISLSSANLFDFLNNFNHGGGGRQQQQGARNPQEYENRILNSQCDQYLCPDTGLCVESPKFCPCPYPSSQIRCFLPDGRFVCISKPAGEGISDKYNDPKTNWKIDAKDDNIRDCGWVNRAWRGLV
|
Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
|
C5M9K8
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RRT14_CANTT
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Regulator of rDNA transcription 14
|
MSSSFSSDASQYQAENTVNKLFSNILHTNISTTKSTTNANQLFAQHGSSVKKNKKNEAKRIKKNEERTKAFNKFVKYNYIKNKENKNESDKKYLSKLVRKNVNKLNSSSKIDDFEINEEFNIVSSELLDQIKPKNGKRLRKKLFRVNENDERAKEFNEKLQKGVISYPGLTPGLAPVDYNESDSE
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Involved in ribosome biogenesis, probably through modulation of rDNA transcription.
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C6DAC3
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FETP_PECCP
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Probable Fe(2+)-trafficking protein
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MSRTIFCTFLQRDAEGQDFQLYPGDLGKRIYNEISKEAWAQWQTKQTMLINEKKLSMMNVDDRKLLEQEMIKFLFEGKDVHIEGYTPPSH
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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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