entry stringlengths 6 10 | entry_name stringlengths 5 11 | protein_name stringlengths 3 2.44k | sequence stringlengths 2 35.2k | function stringlengths 7 11k |
|---|---|---|---|---|
B1YQJ8 | YIDD_BURA4 | 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}. |
B1YT59 | FETP_BURA4 | Probable Fe(2+)-trafficking protein | MARMIQCAKLGKEAEGLDFPPLPGELGKRIYESVSKEAWQGWLKQQTMLINENRLNMADPRARQYLMKQTEKYFFGDGADQASGFVPPTEG | 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}. |
B1YTJ4 | HRCA_BURA4 | Heat-inducible transcription repressor HrcA | MLDPRARTLLKTLIERYIADGQPVGSRTLSRYSGLELSPATIRNVMSDLEELGLVSSPHTSAGRVPTPRGYRLFVDTMLTVETPIDAEAVARQVQHTLQAGEPQQRVVAAAASVLSNLSQFAGVVLTPRRSHVFKQIEFMRLSDKRILLIIVTPEGDVQNRMLATPRDYSPSQLTEASNYINAHFAGLSFDEVRRRLRDEIDQLRGDMTTLMHAAVTASTEVPDTEDTVLISGERNLLEVADLSSDMARLRKLFDVFDQKTGLLQLLDVSSHAQGVQIFIGGESTLVPIEEMSVVTAPYEVNGQIVGTLGVIGPTRMAYN... | 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}. |
B2FL93 | FETP_STRMK | Probable Fe(2+)-trafficking protein | MPRTVFCQYEQRDAEGLDFVPYPGELGQRIFNNIGKQAWAAWLAHQTMLINENRLSPRTPEHRAFLEGELVKFLFEKDAQKPAGFTPEA | 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}. |
B2G6W1 | HRCA_LIMRJ | Heat-inducible transcription repressor HrcA | MLTQRQKKILQAIVRQYTSTGQPVGSKHLAEKLPFKVSSATVRNEMAVLEDNDLILKEHSSSGRIPSKRGYRYYVDNLLDPQAVTDNDLVVIQNSLGNGFQKIDEIISHSADILSNLTSYTAFTLKPEQESVRLSGFRVVPLGNHKVIAILVTDSGEVENQSFTLPPDIDTDAMQAVIRMINDQLVGLPLSEVVKRLKDDIPLQVLHYMHSPDGFLDIFDNVLSQAARERFFVGGRLNLLDFASTHDPHAIQSLYGLLDKNDNLSNILDSTLTSDNGVNVKIGQEISKNKLLDDYSLITASYNVEQYGRGIIAVLGPTRM... | 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}. |
B2G823 | Y1089_LIMRJ | UPF0122 protein LAR_1089 | MEIEKNYRINSLFEFYQPLLTKKQNDYLELYYGDDYSLGEIAENFHVSRQAVYDNIKRTESILEDYEAKLHLYAEFQVRNQQADRIQRYVRENYPDDATLNHLVNHLESLEEE | 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}. |
B2GAV0 | YIDD_LIMF3 | Putative membrane protein insertion efficiency factor | MTRLVKALVIAYQRFFSARRPYRVCRFEPTCSEYMLQAIDRYHSRGILMGLARILRCQPFARGGYDPLPDHFTLKRNQPK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2GD39 | Y1235_LIMF3 | UPF0122 protein LAF_1235 | MELEKNERINALFAFYQPLLTAKQNDYLQLYYADDYSLGEIATEFSVSRQAVYDNIKRTEKILEGYEQKLHLYAEFEARNQQADRIRDYVLSHYPTDQTLRDLIDGMENLEAK | 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}. |
B2HZX4 | YIDD_ACIBC | Putative membrane protein insertion efficiency factor | MVRILRWFIRLYQIAISPLLGPRCRYIPTCSQYALEALQTHGAIKGVWLSSKRICRCHPWGGSGYDPVPPKAIRFISFHQIDSQTHHVAVPFRDRLMKQNLSNHLG | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2I1W8 | FETP_ACIBC | Probable Fe(2+)-trafficking protein | MSRQVFCRKYQKEMEGLDFAPFPGAKGQEFFENVSKQAWQEWLQHQTTLINEKRLNVFEPEAKKFLEEQREKFFNNDESVEKAEGWKPE | 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}. |
B2I4S5 | FETP_XYLF2 | Probable Fe(2+)-trafficking protein | MQRIIFCEYEKRDTEGLDFVPYPGELGQKIFACIGKVGWAAWLAHQTMLINENRLSPRNPSHRAFLEEELNKFLFERSAAKPEGYIEPDA | 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}. |
B2I6F8 | HRCA_XYLF2 | Heat-inducible transcription repressor HrcA | MCASFSPTLDSRSRQLLRTLISCYIQNGEPIGSKTLAQQAGLDISPATIRNILADLEELGLLNSPHTSAGRVPTAHGYRMFVDSLVQMQPPSEDDIRRLRVEMTGGGTQTLLGSASEILSAMTHFVGVVSAPRREQFVFRHIDFVPLDARQIMAILIFADNEVQNRVIEPRRVYEPGELERVSNYLNAHFIGRTLADIRTTVLCELRKAKDEMEQLLAHSLDLASQMLVPNDSEDIVVTGQTRLMALQDLSDMDRLRELFEIFASKREILQLLERTIDAPGVRIFIGEETGMVSMEDISLVTAPYAAHGQVLGVLGVIGP... | 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}. |
B2IBC1 | YIDD_BEII9 | Putative membrane protein insertion efficiency factor | MRRFVRSLSSTGRSQTGSLPVRGLRKLLRFYQLTFSSLVGTQCRHLPTCSAYMDEALARHGVWAGLFIGLARLSRCHPWGTAGYDPVPDQLDANVPRLQPWRHGRWRGPLEITWKPEHKDQNL | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2IFA4 | COWN_BEII9 | N(2)-fixation sustaining protein CowN (CO weal-nitrogenase) | MTAQVDRYVSFKGIDWVGRSREIFARLQSHIDQANSPFWPYFTRQRKLAHSQGLDDLRVLHNYLPTLRELLENMGDLKTLGMLEELEQICM | 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}. |
B2IQ79 | Y1251_STRPS | UPF0122 protein SPCG_1251 | MEIEKTNRMNALFEFYAALLTDKQMNYIELYYADDYSLAEIAEEFGVSRQAVYDNIKRTEKILEDYEMKLHMYSDYIVRSQIFDQILERYPKDNFLQEQIEILTSIDNRE | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY/ffh. May be a regulatory protein. {ECO:0000255|HAMAP-Rule:MF_00245}. |
B2ISX1 | YIDD_STRPS | Putative membrane protein insertion efficiency factor | MKRILIALVRFYQRFISPVFPPSCRFELTCSNYMIQAIEKHGFKGVLMGLARILRCHPWSKTGKDPIPDHFSLKRNQEGE | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2IY41 | YIDD_NOSP7 | Putative membrane protein insertion efficiency factor | MKLLFIWLIRGYRMFISPLFLPTCRFQPTCSMYAIEAIERFGVLRGSWMATRRILRCHPFHPGGYDPVPEVVEKVKEE | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2JJC9 | FETP_PARP8 | Probable Fe(2+)-trafficking protein | MTRMVQCTKLGKEAEGLDFPPLPGELGKRIYESISKEAWQQWLKQQTMLINENRLNMADPRARQYLMKQTEKFFFGEGADQASGYVPPAQG | 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}. |
B2JJR9 | YIDD_PARP8 | Putative membrane protein insertion efficiency factor | MQTVLFALLRFYKIAVSPMLGNRCRFYPSCSDYAREAIQYHGAARGTYLAARRLCRCHPFSAGGIDLVPPPTPKKR | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2JZ43 | SYDP_YERPB | Protein Syd | MDLNISTALRSFTQRYIDLWQQQTGHLPASKELYGVPSPCIVETGEDQVFWQPQAFLPEATLTNIERALEIQLHPDIHDFYTQQYAGDMMADLGNHRFTLLQVWSEDDFIRLQENLIGHLVTQKRLKLSPTLFLATTSSEMTMASLCNVSGNVVLEQFGSDKRTLLASTLSHFLDALRPVLPE | Interacts with the SecY protein in vivo. May bind preferentially to an uncomplexed state of SecY, thus functioning either as a chelating agent for excess SecY in the cell or as a regulatory factor that negatively controls the translocase function. {ECO:0000255|HAMAP-Rule:MF_01104}. |
B2K0V1 | FETP_YERPB | 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}. |
B2K7H7 | FDHE_YERPB | Protein FdhE homolog | MSIRIVPKDQLGKQREKGTTAGNIPPLLFANLKSLYTRRTERLQQLALDNPLADYLDFAAKITEAQQKALHDHPLVLDMQAELVQSAASGKPPLDGSVFPRTEHWRKLLSALIAELRHDAPDHILAVLDNLDKASVHELELYADALLNRDFSQVGSEKAPFIWAALSLYWAQMASQIPGKARAEYGEHRQFCPVCGSIPVSSVVHIGTHNGLRYLHCNLCESEWHVVRIKCSNCEQTRDLNYWSLDSELAAVKAESCGDCGTYLKILYQEKDPQVEAVADDLASLILDAKMEGEGFARSSINPFLFPGE | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
B2K870 | YIDD_YERPB | Putative membrane protein insertion efficiency factor | MASPLSPGSRILIGLIRGYQLVISPLLGPRCRFHPTCSHYGIEALRRFGMIKGSWLTLKRVLKCHPLNSGGDDPVPPKLDDNREH | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2KAB9 | NRDI_YERPB | Protein NrdI | MNPLVYFSSSSENSHRFVEKLQLPAIRIPIAGAREKLRVEQPYILLVPSYGGGSPVGAVPIQVIRFLNDVHNRSLIRGVIAAGNTNFGDAYCLAGDIISHKCQVPYLYRFELLGTAEDVANVRKGVTEFWQRQN | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
B2KI57 | TP8L2_RHIFE | Tumor necrosis factor alpha-induced protein 8-like protein 2 (TIPE2) (TNF alpha-induced protein 8-like protein 2) (TNFAIP8-like protein 2) | MEPFSSKSLALQAEKKLLSKMAGRSVAHLFIDETSSAVLDELYRVSKEYTHSRPQAQRVIKDLIKVAVKVAVLHRSGCFGPSELALAARFRQKLQQGAMTALSFGEVDFTFEAAVLAGLLTECRDMLLELVEHHLTPKSHNRIRHVFDHFSDPGLLTALYGPDFTQHLGKICDGLRKMLDEGKL | Acts as a negative regulator of innate and adaptive immunity by maintaining immune homeostasis. Negative regulator of Toll-like receptor and T-cell receptor function. Prevents hyperresponsiveness of the immune system and maintains immune homeostasis. Inhibits JUN/AP1 and NF-kappa-B activation. Promotes Fas-induced apop... |
B2RHI2 | YIDD_PORG3 | Putative membrane protein insertion efficiency factor | MRLIKAFLVQLLLLPIFFYKRFISPLTPPSCRFTPSCSSYAIEALRKYGPGKGLLLSIKRILRCHPWGGSGYDPVP | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2RYU8 | LYRM1_RAT | LYR motif-containing protein 1 | MTAASRQEVLGLYRSFFRLARKWQAASGQMEDTIKEKQYILNEARTLFQKNKNLTDPDLIKQCIDECTARIEIGLHYQIPYPRPIHLPPMGLTPRRGRGLQTQEKLRKFSKPLYLKSHDEVS | May promote cell proliferation and inhibition of apoptosis of preadipocytes. |
B2S1C7 | SP5G_BORHD | Putative septation protein SpoVG | MNITDVRIRRVDNKNPGSKLLAYVTVTFDDCLVLHNIRVIRGQKGVFIVMPNRRTKVGEYKDIVHPINQSFREILQSAIFKEYVKENPSSLELEIG | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
B2S8G3 | HRCA_BRUA1 | Heat-inducible transcription repressor HrcA | MMRPPEHQLLSSLDQRSRDIFRLIVETYLNDGDPVGSRNLSRLLPHTLSPATIRNVMSDLEHLGLIYAPHISAGRLPTQIGLRFFVDAFLEVGDLPPEERSSIEAQVRAAGTSNSVESVLTEASQVLSGLSRGAGLVLTNKTDVALKHIEFVRLEPMRALAVLVMQNGDVENRVIDLPAGISTSQLIEASNFLNAHIHGHTLSEAKSELRKLSEETRRELDQLSQELVAKGLAVWSGAGADQPARLIVRGRANLLENVHAQEDIERLRHLFDDLETKDGMVQLLDLAEAGSGVRIFIGSENKLFSLSGSSLVVAPYRDSE... | 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}. |
B2SBS5 | NRDI_BRUA1 | Protein NrdI | MSLIVYFSSRSGNTHRFVERLGVRSSRIPLEASGALQVREPFVLVTPTYGGGSTKGAVPNPVIRFLNDADNRALIRGVIAAGNSNFGEAFCIAGNIISAKCGVPYLYRFELLGTAEDVGNVRNGMEQFWTRQTQA | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
B2SDR3 | FETP_FRATM | Probable Fe(2+)-trafficking protein | MTKVFCKKYHQELDAIPFQPLPGELGKKIHNEISNKAWQAWLAHQTILINEYRLNLIETKAKEFLKEEMHKFLFEGKEEKPEQFSEI | 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}. |
B2SE59 | YIDD_FRATM | Putative membrane protein insertion efficiency factor | MFFKKITLIPFVMLINLYRYCISPFIPARCRYYPTCSEYALEALKTHGILKGLYLTTRRLLRCHPLSKRDYYDLVPCKNKKG | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2SXB7 | HRCA_PARPJ | Heat-inducible transcription repressor HrcA | MLDPRAQTLLKTLIERYIAEGQPVGSRTLSRYSGLELSPATIRNVMSDLEDLGLVISPHTSAGRIPTPRGYRLFVDTMLTVESAADEEAVTRTVKTTLQAGEPQKIVAAAASVLSNLSQFAGVVLTPRRSHVFKQIEFMRLSDKRILLIIVTPEGDVQNRIMATQRDFSPSQLVEASNYINAHFAGLSFDDVRRRLREEIDALRGDMTTLMHAAVTASTDESDTGETVLISGERNLLEVADLSSDMARLRKLFDVFDQKTSLLQLLDVSSHAAGVQIFIGGESNLVPIEEMSVVTAPYEVNGKIVGTLGVIGPTRMAYNR... | 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}. |
B2T5R7 | FETP_PARPJ | Probable Fe(2+)-trafficking protein | MTRMVQCAKLGKEAEGLDFPPLPGELGKRIYEGISKEAWQAWLKQQTMLINENRLNMADPRARQYLMKQTEKFFFGEGADTAQGYVPPSAE | 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}. |
B2T7U2 | YIDD_PARPJ | Putative membrane protein insertion efficiency factor | MQTVLIALLRFYKVAVSPMLGNRCRFYPSCSDYAREAIQYHGAARGTYLAARRICRCHPFSAGGIDLVPPPTSEKR | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2TI06 | SP5G_CLOBB | Putative septation protein SpoVG | MQITDVRIRKISSEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPTGEFKDIAHPIVMDSREKIQNEILSAYAKAIEEQDVEEE | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
B2TJ26 | Y1244_CLOBB | UPF0122 protein CLL_A1244 | MEDRVEISMLMDFYSSLLTEKQRSVMALYYDDDLSLAEIAELNKTSRQAIHDLIKRCDKQLLSYESKLNLLQKSMRKEKYIMNFLEELKEKYSVSDKDYLMFKEKLENL | 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}. |
B2TLZ5 | HRCA_CLOBB | Heat-inducible transcription repressor HrcA | MTIDDRKIKILQAIINDYIHTGDPVGSRTIAKKYNLGVGSATIRNEMADLEDMGYLEQPHASSGRVPSNKGYRLYVDSLMENQLLTPEENLKIKQYIIDTAMLEVDKIVRQTSSLLSELTNLTCVIQTPSVNKSFIKSLQLMKVDSTTLVSVIITDAGVMKNHIIRVNSTPTIEELNKINAVINRRLVNLCIEQINLQVINQLKEDLQGYDELFNALLTPLYETLKNAADSPDLIMEGATNIFNYPEYNDIEKAKEMLSLLNDKESLRDLLKTNKDITIRIGEENYKPQAKECSIIAAEYSFGNRPIGTIGLIGPKRIDY... | 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}. |
B2TTP9 | CBPM_SHIB3 | 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}. |
B2TVN6 | FDHE_SHIB3 | Protein FdhE | MSIRIIPQDELGSSEKRTADMIPPLLFPRLKNLYNRRAERLRELAENNPLDDYLRFAALIAHAQEVVLYDHPLEMDLTARIKEASAQGKPPLDIHVLPRDKHWQKLLMALIAELKPEMSGPALAVIENLEKASTQELEDMASALFASDFSSVSSDKAPFIWAALSLYWAQMANLIPGKARAEYGEQRQYCPVCGSMPVSSMVQIGTTQGLRYLHCNLCETEWHVVRVKCSNCEQSGKLHYWSLDDEQAAIKAESCDDCGTYLKILYQEKEPKVEAVADDLASLVLDARMEQEGYARSSINPFLFPGEGE | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
B2TZE0 | SYDP_SHIB3 | Protein Syd | MDDLTAQALKDFTARYCDAWHEEHKSWPLSEELYGVPSPCIISTTEDAVYWQPQPFTGEQNVNAVERAFDIVIQSTIHTFYTTQFAGDMHAQFGDIKLTLLQTWSEDDFRRVQENLIGHLVTQKRLKLPPTLFIATLEEELEVISVCNLSGEVCKETLGTRKRTHLASNLAEFLNQLKPLL | 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}. |
B2U069 | NRDI_SHIB3 | Protein NrdI | MSQLVYFSSSSENTQRFIERLGLPAVRIPLNERERIQVDEPYILIVPSYGGGGTAGAVPRQVIRFLNDEHNRALLRGVIASGNRNFGEAYGRAGDVIARKCGVPWLYRFELMGTQSDIENVRKGVTEFWQRQPQNA | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
B2U9W7 | FETP_RALPJ | Probable Fe(2+)-trafficking protein | MARMVHCVKLNKEAEGLDFPPLPGELGKKLWQSVSKEAWAGWLKHQTMLINENRLNMADSRARQYLLKQTEKYFFGDGADEAAGYVPPPSA | 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}. |
B2UVJ4 | YIDD_HELPS | Putative membrane protein insertion efficiency factor | MRNNKTPFLSAIFTALIRGYQRFFSAFTFSSCRFYPTCSNYALWLLYFENPLSAMGKIAIRILSCNPFCSGGIAYPTTRLKRPSLLQSHKDFNRNFKTITFWLVPTTKSHATYYIIKV | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B2UXS5 | SP5G_CLOBA | Putative septation protein SpoVG | MQITDVRIRKISSEGKMKAIVSVTFDNEFVVHDIKVIEGQNGLFIAMPSRKTPTGEFKDIAHPIVMDSREKIQNEILSAYAKAIEEQDVEE | Could be involved in septation. {ECO:0000255|HAMAP-Rule:MF_00819}. |
B2V2I3 | HRCA_CLOBA | Heat-inducible transcription repressor HrcA | MTIDDRKIKILQAIINDYIHTGDPVGSRTIAKKYNLGVGSATIRNEMADLEDMGYLEQPHASSGRVPSNKGYRLYVDSLMENQLLTPEENLKIKQYIIDTAMLEVDKIVRQTSSLLSELTNLTCVIQTPSVNKSFIKSLQLMKVDSTTLVSVIITDAGVMKNHIIRVNSTPTIEELNKINAVINRRLVNLCIEQINLQVINQLKEDLQGYDELFNALLTPLYETLKNAADSPDLIMEGATNIFNYPEYNDIEKAKEMLSLLNDKESLRDLLKTNKDITIRIGEENYKPQAKDCSIIAAEYSFGDRPIGTIGLIGPKRIDY... | 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}. |
B2V4E0 | Y1195_CLOBA | UPF0122 protein CLH_1195 | MEDRVEISMLMDLYSSLLTEKQRSVMALYYDDDLSLAEIAELNKTSRQAIHDLIKRCDKQLLSYESKLNLLQKSMRKEKYIMNFLEELKEKYSVSDKDYLMFKEKLENL | 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}. |
B2VCF8 | FDHE_ERWT9 | Protein FdhE homolog | MTILIIPQDPSENGNPAVDTIPPLLFPRLKNSYSRRAARLRQLAAKNPLGDYLRFAAVIASAQEIVLYDHPLRMDPRARLEESARSGRPPLDINTLPRDAHWQRLLHSLIAELKPDMSGQALSVLENLEKSSSVELEAMAGALFSNEFSQVSSDKAPFIWAALSIYWAQMAALIPGKAYVKAGEQRQFCPVCGSVPVSSMIHVDGVRYLHCNLCESEWHVADAKCSNCEQTRDLHHWSLDSAAVKAESCGDCGTWLKRLYQEKDPAVEAVADDLATLILDARMEQEGFARSSLNPFLFPGE | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
B2VEZ9 | FETP_ERWT9 | Probable Fe(2+)-trafficking protein | MSRTIFCTFLQRDAEGQDFQLYPGDTGKRIFNEISKEAWSKWMAKQTMLINEKKLSMMNPDDRKLLEQEMIKFLFEGHEVHIEGYTPPEE | 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}. |
B2VFX0 | SYDP_ERWT9 | Protein Syd | MIDETSQALRDFSQRYCDLWQQKSGHAPASQELYGIPSPCVMATDEDEVWWQPRPFTLAPNLDAVERALDIRLQPAVTAFYTSQFAGDMTGTLDGRPLSLVQVWSEDDFIRVQENLIGHLVMKRRLKQSPTLFIATTDSELEVISVCNVSGEVILEQLGTKKRQVIASSIENLLIALQPLIINCSN | 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}. |
B2WHK5 | LCL2_PYRTR | Long chronological lifespan protein 2 | MTNPTILLTTVLLTLLTTPALAQFGFFDQMFGGGGGQQQGHHHHHEQEAQNVRSDASWYQSQYEGAQCTHYLCPGTLSCVHFPHHCPCSWETVEDKVELGEGIAVCGSKGGWVEGEFGKKVEMARKGLL | Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway. |
B3A052 | FAR12_KARBO | Extended FMRFamide-12 (FMRFa-12) | SPALDDERNDNFIRL | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A070 | FAR10_KARBI | Extended FMRFamide-10 (FMRFa-10) | PAPDSSFLRDP | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A082 | FAR2_LOBRE | Extended FMRFamide-2 (FMRFa-2) | SDYLQLARG | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A089 | FAR10_LOBRE | Extended FMRFamide-10 (FMRFa-10) | PAPDSSFIRDP | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0A8 | FAR10_AUSRA | Extended FMRFamide-10 (FMRFa-10) | PAPESGFIRDP | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0A9 | FAR12_AUSRA | Extended FMRFamide-12 (FMRFa-12) | SPTLDDEHNDNFVRL | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0C8 | FAR10_HEMMO | Extended FMRFamide-10 (FMRFa-10) | PAPDSSFLRDP | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0E0 | FAR2_AUSGA | Extended FMRFamide-2 (FMRFa-2) | PDYLQLARA | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0E7 | FAR10_AUSGA | Extended FMRFamide-10 (FMRFa-10) | PAPETNYLRDP | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0F9 | FAR2_PRAMA | Extended FMRFamide-2 (FMRFa-2) | ADYLQLTRA | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0H7 | FAR2_TYRGL | Extended FMRFamide-2 (FMRFa-2) | ADYLRLARA | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0I4 | FAR10_TYRGL | Extended FMRFamide-10 (FMRFa-10) | PASDSGFLRDP | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3A0J7 | FAR2_PACBA | Extended FMRFamide-2 (FMRFa-2) | SDYLQLART | FMRFamides and FMRFamide-like peptides are neuropeptides. |
B3DUH7 | YIDD_METI4 | Putative membrane protein insertion efficiency factor | MKKVVFFLLDFYRYGLSSFRQTLGMYGVCRYYPTCSQYCREAVQKHGIIHGLYLCLRRLMRCHPWGAAGWDPVPEKSNLGIKRTKKADHPLKKKVSLMRVMHLFFK | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B3E2A4 | COWN_TRIL1 | N(2)-fixation sustaining protein CowN (CO weal-nitrogenase) | MSKPDRYVSFVGIDGDSNARKLVALLRRHIDDPARTNRFWELFKDKLEKINKPDETSGFSQDELYLVHAYINNIRELFETYDDQPALALLDRIEAESC | 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}. |
B3EPC5 | HRCA_CHLPB | Heat-inducible transcription repressor HrcA | MMFHDLSERERQVLSIIIQAYVMNASPVGSRYIARNYNLGLSDATIRNVMADLEDAGYISQPHTSAGRVPTDKGYRYYVDLIMRVQGIDDEEINRIDRNFRLLKYDPKDSADILQAAAKVLGSISQQLSVVISPRLSNALFERLDLVVLSSSRIMVVLSIQSLFVRTIVMELSLEVSRQQIDNVIDLLNQRLSGLTLREIRNSISRRLADCDKDRELLNMIVGSADNLFDDTPVLERLYIAGAEHIVNQPEFDQPQKVRDLVCMIEDKNRMVELLEKEGRVKPVTSSGMDVSISIGRENSATTAEDFTVVTTPYYVGNTI... | 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}. |
B3EUG7 | YIDD_AMOA5 | Putative membrane protein insertion efficiency factor | MWLLKRIVIFPIWVYQVALAPYLTPCCRFQPTCSAYAHEAINKHGIVKGIWLAGKRILRCHPCGKSGYDPVQ | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B3EWI5 | AMP1_CENMR | Putative antimicrobial protein 1 | VLSHNNESSYSDTSSCTSQ | May have antimicrobial activity. |
B3EWI6 | AMP2_CENMR | Putative antimicrobial protein 2 | DLPECCSATELELDSGKQTS | May have antimicrobial activity. |
B3EWI8 | AMP3_CENMR | Putative antimicrobial protein 3 (Cm-p2) | SESILIVHQQQSRSSGS | May have antimicrobial activity. |
B3EWP9 | NLTP_FOEVU | Non-specific lipid-transfer protein (LTP) (allergen Foe v 3) | AITXGQVTSKLG | Plant non-specific lipid-transfer proteins transfer phospholipids as well as galactolipids across membranes. May play a role in wax or cutin deposition in the cell walls of expanding epidermal cells and certain secretory tissues (By similarity). |
B3GXP2 | FDHE_ACTP7 | Protein FdhE homolog | MSIRILPENEIKQAASSFQNPPLLFANPKNLYFRRAKRLRQLAENNPFGDYLEFAANLSEVQLDLLENHPIANYAEKLTACIEESNGQKPLNAKTFKRSSEWRELLLLLTEKFKPYANDTMLATIELLEKSSTSELEALADDLLNERYEAVGADKAVFLWAALSLYWTQLAQQLPRNTQTEVGERHTCPVCDSAPIVSVVHFGDTQGLRYLHCSLCESEWNMVRSQCSVCDQSGKLDYWSIDSVDAPVKAESCGDCESYLKVLYQEKDPHVEPVADDLGTLFLDAEMEQKGFARSGLNPFLFQVE | Necessary for formate dehydrogenase activity. {ECO:0000255|HAMAP-Rule:MF_00611}. |
B3GYW7 | FETP_ACTP7 | Probable Fe(2+)-trafficking protein | MARTVFCEYLKQEAEGLDFQLYPGELGKRIFDSISKQAWSEWIKKQTMLVNEKKLSMMNAEHRKLLETEMVNFLFEGKEVQIEGYVPVEQK | 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}. |
B3H5L1 | LOR9_ARATH | Protein LURP-one-related 9 | MVSVVGEMFCNPYTTELVVRRRRESLKRERYDVFDLSNNLIFTVDGGIWNIRRKRVLRDAAGIPLLSMRTKGLVPMRYNWEVYKGDSTESDNLLFSAREPNLLSFKTSLDVTLPPDQSSTDISSVEPDFQTFGRYIGSSFKLFEPIHNTLLAEVVHDFTWGGLIKGSYSFKVRVNPYVDFAFVVALLVITDDTSNLR | Might be related to the phospholipid scramblase and tubby-like superfamily of membrane tethered transcription factors. |
B3LGK5 | RRG1_YEAS1 | Required for respiratory growth protein 1, mitochondrial | MAQNFGKIPSHKSYVLSLYRTVLRNIPKCCHSYAFQYEIKKTLSKQLFKHKHDKSSWSVYTLLNEFSLLNNCLLEGKLQEIKNLMKPLKKMKKQLETTKILNSLTSLGDVKTNDPEEVRRFHVLSAYIKRKQDLGLLPAYIPKTYQHKLLLPLALNEHACLKLFHIQQKLKNGPPSAGLSYTKEGRNQIWFVRSPINKGRQQSKKLGILIRKERKDSQKNIDNLNFCEINAAWALHEAIWEEYLESKKIIKVNLPKYLEYAANIPKSTKCNPSSQYQKIKEWVDPVREIMFELHSKSFQRVEYFNKYKEKLLKNGGQLAY... | Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity). |
B3LJ84 | CRS5_YEAS1 | Metallothionein-like protein CRS5 | MTVKICDCEGECCKDSCHCGSTCLPSCSGGEKCKCDHSTGSPQCKSCGEKCKCETTCTCEKSKCNCEKC | Critical role in copper (specific) homeostasis and detoxification. May protect by directly chelating and sequestering copper ions (By similarity). |
B3LK80 | RRG8_YEAS1 | Required for respiratory growth protein 8, mitochondrial | MGLPKSAYKKLLIDCPTRVINKNCAQRVKDVSPLITNFEKWSDKRKKLYFKDEEEMVGHFHLENFNLKNNLYGRLLASPMRAEKISKLKSCRELLIPLKVVPSTGKDQHADKDKLKLVPTLDYSKSYKSSYVLNSASIVQDNLAAATSWFPISVLQTSTPKSLEVDSSTFITEYNANLHAFIKARLSVIPNVGPSSINRVLLICDKRKTPPIEIQVVSHGKGLPITQSVFNLGYLHEPTLEAIVSKDAVTKGIYLDADNDKDLIKHLYSTLLFQSVN | Required for respiratory activity and maintenance and expression of the mitochondrial genome. |
B3LLZ8 | SPG4_YEAS1 | Stationary phase protein 4 | MGSFWDAFAVYDKKKHADPSVYGGNHNNTGDSKTQVMFSKEYRQPRTHQQENLQSMRRSSIGSQDSSDVEDVKEGRLPAEVEIPKNVDISNMSQGEFLRLYESLRRGEPDNKVNR | Stationary phase-essential protein not required for growth on nonfermentable carbon sources. |
B3LQZ6 | MTC2_YEAS1 | Maintenance of telomere capping protein 2 | MGDHNLPDFQTCLKFSVTAKKSFLCMYRDSVSKEKLASSMPSTCDIQLKRAINDAYPGGGIKVTVLNSTTASLDSLATTHVKEFEIVIIPDINSLLQPDQAKLVKIMRDCTVAIEKAQSTRIFIGVVHWNNPVQPSGAAKDGDEAGKPAPKTRIFLPTSLRMGAWLKHKFWFACAPPYLDFESSTESSINTRANNSIGMAEEEKQEPESKRSIILNEEANLNDVFVGSTVRRYILDIMVHLRTHRLTYNAKAGGVYTNSLDDVVLLSRLIGLHSGKMFVSPSHVKEASRWYFPMHLELVQRSSMDSSLLYGSDPNLVDEM... | May be involved in telomere capping. |
B3LT72 | LCL2_YEAS1 | Long chronological lifespan protein 2 | MSQSRWSIVLIFALFIFGSTGVNAFFNFGHHQQQQQQQQQSYEDQVLNNPCDGYLCPDTLTCVAQQKDCPCPFPKSQLKCVLPDNKFVCISKPATHNEKFRAIYDDPVKGPKAKNKGFRDCGWVSDAYKNH | Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway. |
B3LTD9 | IRC19_YEAS1 | Increased recombination centers protein 19 | MRKPSITITTAKAIITPDYTLIKSHSKYQLPSRFQKLDADSPERSTVVKLFYRRFMRLKPFISNVKMVKDTYRDYVRYKFMKENYELKRYLVFNPDGLRSKIKLELLSNTKCCERILPVTEMQRTLEFVLKSCSYLPETKAQKWDIARDNTYCRQILKNLLTMQYEKYRSILHRGIGHDELDVKFSHLKTTSSPLTKLNKTEKKKIPLFKVFSDFDTTLIYLNETLGTRL | Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity). |
B3LTR3 | RGI2_YEAS1 | Respiratory growth induced protein 2 | MTKKDKKAKGPKMSTITTKSGESLKVFEDLHDFETYLKGETEDQEFDHVHCQLKYYPPFVLHDAHDDPEKIKETANSHSKKFVRHLHQHVEKHLLKDIKTAINKPELKFHDKKKQESFDRIVWNYGEETELNAKKFKVSVEVVCKHDGAMVDVDYRTEPLQPLI | Involved in the control of energetic metabolism and significantly contribute to cell fitness, especially under respiratory growth conditions. |
B3LUQ4 | IRC6_YEAS1 | Increased recombination centers protein 6 | MVLQYPQNKILVLSDHPHNFSKTQFLQDLFHCSSTGISIVKDQTWENRYYKVHFDLYIDSCKDIPVWVEEFITPECEPLRNVMAGIILITDIRQTKPQELLHQFMIAAHRNTFVVLVNVNEEVEQDEIDELNEIWSNAFTNVIEFVNWKRSKPTVNHNDYGEKLGLDRIQEIIDTHDWLNCEVLPATKIREEIPNEMPLEQIIRNLQSARLKYKSIENSSEADAFANEMADELSRYL | Involved in gross chromosomal rearrangements (GCRs) and telomere healing. |
B3MET8 | WDR48_DROAN | WD repeat-containing protein 48 homolog | MLTHKTCQARKKMQVSFVIRDAEEKQHRNGVNALQLDANNGKLYSAGRDAIIRVWNTRTESNEKYIQSMEHHNDWVNDIVLCCNGRNLISASCDTTVKVWNAQKGFCMSTLRTHRDYVQALAYAKDREQVASAGLDKAIFLWDVNTLTALTASNNTVTTSSLTGSKDSIYSLAMNPSGTVIVSGSTENILRIWDPRTCMRSMKLRGHTENVRCLVVSPDGNQVVSGSSDGTIKVWNLGQQRCVQTIHVHKEGVWSLLMSENFQYIISGSRDRNIIVTEMRNPSNKMLVCEEQAPVLSLGYNIDKTGVWATTWNSDIRCWK... | Regulator of deubiquitinating complexes. Activates deubiquitination by increasing the catalytic turnover without increasing the affinity of deubiquitinating enzymes for the substrate (By similarity). |
B3NSK1 | WDR48_DROER | WD repeat-containing protein 48 homolog | MLTHKTCQARKKMQVSFVIRDAEEKQHRNGVNALQLDANNGKLYSAGRDAIIRVWNTRTDSSEKYIQSMEHHNDWVNDIVLCCNGRNLISASCDTTVKVWNAQKGFCMSTLRTHRDYVQALAYAKDREQVASAGLDKAIFLWDVNTLTALTASNNTVTTSSLTGSKDSIYSLAMNPSGTVIVSGSTENILRIWDPRTCMRSMKLRGHTENVRCLVVSPDGNQVVSGSSDGTIKVWNLGQQRCVQTIHVHKEGVWSLLMSENFQYIISGSRDRNIIVTEMRNPSNKTLVCEEQAPVLSLGYNIDKTGVWATTWNSDIRCWK... | Regulator of deubiquitinating complexes. Activates deubiquitination by increasing the catalytic turnover without increasing the affinity of deubiquitinating enzymes for the substrate (By similarity). |
B3PIU2 | YIDD_CELJU | Putative membrane protein insertion efficiency factor | MVWAGVKLLHGYRYLLSPWIGNQCRFYPSCSHYAEEALKTHGFLAGIYLTARRLIKCHPWHPGGIDPVPEHEATCCSHTHPTHGKH | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B3PJ20 | FETP_CELJU | Probable Fe(2+)-trafficking protein | MARMVFCRKYKQQLEGLDFPPYPGAKGQDLFDNVSKKAWQEWMAHQTMLINEKRLNVMDMGTKVYLTEQMHKFLSGEGYDQADGYVPPSNQ | 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}. |
B3PN01 | HRCA_META1 | Heat-inducible transcription repressor HrcA | MEKRTNYPQLTEKQNHFFKLIVDTYIKTGASVASKELVKRCNLKCSSATIRNVMASLEQIGFLEKYHISSGRVPSTLGLEYYAKFLVYNPKKYFDQKLEDLLAKRRIKIDATLEEAAAIVSEVAGVTVVATSNNAAETMKSIQLTTLSELSAIVVIVTSSGRVESKIFNFENSDISLEDLRVAIRLFKERLVDTPLIHLANKARALTPIFGQQLKNYELILQKFIKNIFVFEEETTNKTFNKGAIVLSRNISREEIANVLDLIEKHSVWESIDNDLDEDNNIKLDVSRPNLSIISKKIDFSNEKNIKEITVIGPNNLDYG... | 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}. |
B3PZA3 | HRCA_RHIE6 | Heat-inducible transcription repressor HrcA | MGTRSTSVSDAVAVLDERSREIFRRIVEGYLESGEPLGSRNLSRLLPMSLSPASVRNVMSDLEELGLIYSPHISAGRLPTQIGLRFFVDAFMQVGDLSAEDRANIDRQVRAESGGNPVESMMNEASRMLSGISRGAGLVITSKSDPVLKHVEFIRLEPTKALAVLVGDHDQVENRIIELPAGVTSSQLTEAANFLNAHMSGQTLPELRKQLSQLKDDVRHELDALSRDLVERGIAVWAGSPDEGKPAQLIIRGRANLLEGLGGAEDLDRLRMLFDDLEKKDSLIEILSLAESGSGVRIFIGSENKLFSLSGSSLIVAPYR... | 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}. |
B3Q0Y6 | NRDI_RHIE6 | Protein NrdI | MGLIVYYSSRSENTHRFVARLGLRAARIPASGADAFHIREPFVLVVPTYSSGDGKGAVPKQVIRCLNDAENRKHIRGVIAAGNSNFGETYGLAGDVISRKCQVPYLYRFELMGTEEDVANVKHGMERFWTREQL | Probably involved in ribonucleotide reductase function. {ECO:0000255|HAMAP-Rule:MF_00128}. |
B3Q969 | HRCA_RHOPT | Heat-inducible transcription repressor HrcA | MAQHDPIGLIAPNAGLAQLNERSREIFRQIVESYLATGEPVGSRNISRLISVPLSPASVRNVMADLEQLGLIYAPHTSAGRLPTELGLRFFVDALMQIGDLTEPERQSIQAQLSSVGRAHTVEAALGEALTRLSGLTRAAAVVLTAKANVRLKHIEFVRLEPERALVILVAEDGQVENRVLTLPPGVPSSALIEAANYLNARIRGRTLAEARLELESLMVQNKAELDQLTQKVIAAGIASWSGGDGEDRQLIVRGHANLLEDLHALDDLERVRLLFDDLETKRGVIDLLGRAESADGVRIFIGSENKLFSLSGSSTIIAP... | 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}. |
B3QE28 | YIDD_RHOPT | Putative membrane protein insertion efficiency factor | MQLPSRGTDWIAPVLRLPRNAGRGLIWLYRHTLSPLVGYNCRHYPTCSMYGDEAIRKFGLWAGGWMTLARLLRCQPWGTSGIDLVPQTAPSRARWYLPWRYARWRGVNAPPPDVAEPCGCGSHSQLTPH | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B3QEP7 | COWN_RHOPT | N(2)-fixation sustaining protein CowN (CO weal-nitrogenase) | MSASFDRYVSFQHCDWEGRSERVMQRLQRHVEAAENPFWAYFAQKRAELRDKQGLDDLRILHNYLPTLRELLEDNGDLETLEMLEDLEANLM | 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}. |
B3R1I2 | FETP_CUPTR | Probable Fe(2+)-trafficking protein | MARTVHCIKLNKEAEGLDFPPLPGELGKKIWQSVSKEAWAGWLKHQTMLINENRLNMADARARQYLLKQTEKYFFGEGADQAQGYVPPQS | 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}. |
B3R884 | YIDD_CUPTR | Putative membrane protein insertion efficiency factor | MKRILLALLRVYKIALSPYLGSQCRFLPTCSDYARDAIVHHGAARGSWMAACRLCRCHPFAQGGYDPVPGTEADTPVHAATGHAPVAIRLPRP | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
B3VML2 | MVP_OUMVV | Putative movement protein (Cell-to-cell transport protein) | MGDNALDLATASSTPIPMPNTGQLVISPQDIGYSDPPKLRGRLKLEFVHDISLDANVEDPIALIPHGIWSIFKSKLAQMRCPKGYITYDKVILSWKPHVATGLARGQIAVVDTRVNHTSIEDLMHKALWKTAPVDLGCTYTIQGTVPYCLPFHPKEGGDVKSDLESQNPIRGIVYITDSRYQEAARHGALTMTLKLSIGTMPTDALTGPRATLSQPHLRDNLRSRSQRISRPPIGITQRPRRSLAEPPLEKEEEQESTLSSEASGSEQGLIIPVQGPSTSSRSRRVRG | Transports viral genome to neighboring plant cells directly through plasmosdesmata, without any budding. The movement protein allows efficient cell to cell propagation, by bypassing the host cell wall barrier (Potential). |
B3VML3 | CAPSD_OUMVV | Capsid protein (CP) (Coat protein) | MARLPKRKNRRNEKKKNANASRVQNVPRTFGLWKSTERIKYTTELKYLNSKCRAIRLHPDLVANNSFPTYCSAWKIDQVEFEFVSYMSPLAGHVGCVFFVVIPAKGLNSRISADEAESLQSAILWDEKGRLKITPISGPISRHPWTNLSQVVTPPQIPKGSTDGERQDLQSGYYLIFDSRKLFGKDLVDKQSVLGELSLTITATYWTSLS | Capsid protein self-assembles to form a baciliform capsid with a T=1 symmetry, about 18 nm in diameter. The capsid encapsulates three genomic RNAs (Potential). |
B3W9Y5 | YABA_LACCB | Initiation-control protein YabA | MEKKELYDGFLTLEKHAQQMLREIAAMKDDMAETLERNAELEIENKHLRQHLAELEKDDNKTSDGGVELSKSKQNLESLYNEGFHVCPMFYGQRRVNDEPCAFCTEIIYGEN | Involved in initiation control of chromosome replication. {ECO:0000255|HAMAP-Rule:MF_01159}. |
B3WDM3 | YIDD_LACCB | Putative membrane protein insertion efficiency factor | MKQVLTWLVRGYQRFISPLLPPSCRYYPTCSTYMIQALQKHGAIKGSLMGIARILRCNPFVKGGLDPVPAFFTLRRNPHPENDLDLSDIQNLNHKLGGRHG | Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}. |
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