jonghyunlee/UniProt_function_text_descriptions

entry stringlengths 6 10	entry_name stringlengths 5 11	protein_name stringlengths 3 2.44k	sequence stringlengths 2 35.2k	function stringlengths 7 11k
C6DAH5	SYDP_PECCP	Protein Syd	MEHEVVSALAAFTQRYVDCWQQEKGHLPASEALYGIPSPCIVENHEDTVYWSPQPFAPAAALDGVERALEISLHPDVHAFYTAQYAGDMAAQFDSLSCQLLQVWSEDDFTRMQENLIGHLLTQKRLKLTPTLFLATTDSEMTMVSLCNISGEIILEEFGTKKRQILAPTLAAFLFGLNPLAV	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}.
C6DYS2	YIDD_GEOSM	Putative membrane protein insertion efficiency factor	MLKQIFIGLVVFYQRFISPLKAPSCRFYPTCSHYSLQALEKYGPVKGLWLTAARVLKCHPFHPGGYDPVK	Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255\|HAMAP-Rule:MF_00386}.
C6HEL8	LCL2_AJECH	Long chronological lifespan protein 2	MVHIFTGILLGLLLLATGTQAQFQFFEQMFGGGQQQQHDSREQNVPSDSDWYQRTYDNARCSNYLCPGTLACVAVPHHCPCQHPAVEDKFELGDGSAICVSKGGFKFGEAARKVELARKGLL	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
C6UP45	LPMG_ECO5T	mgtA leader peptide (Regulatory leader peptide for mgtA)	MEPDPTPLPRRRLKLFR	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).
C7GLG0	CRS5_YEAS2	Metallothionein-like protein CRS5	MTVKICDCEGECCKDSCHCGSTCLPSCSGGEKCKCDHSTGSPQCKSCGEKCKCETTCTCEKSKCNCEKC	Critical role in copper (specific) homeostasis and detoxification. May protect by directly chelating and sequestering copper ions (By similarity).
C7GQE4	IRC19_YEAS2	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).
C7GQS7	LCL2_YEAS2	Long chronological lifespan protein 2	MSQSRWSIVLIFALFIFGSTGVNAFFNFGHHQQQQQQQQQSYEDQVLNNPCDGYLCPDTLTCVAQQKDCPCPFPKSQLKCVLPDNKFVCISKPATHNEKFRAIYDDPVKGPKAKNKGFRDCGWVSDAYKNH	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
C7GVL2	MTC2_YEAS2	Maintenance of telomere capping protein 2	MGDHNLPDFQTCLKFSVTAKKSFLCMYRDSVSKEKLASSMPSTCDIQLKRAINDAYPGGGIKVTVLNSTTASLDSLATTHVKEFEIVIIPDINSLLQPDQAKLVKIMRDCTVAIEKAQSTRIFIGVVHWNNPVQPSGAAKDGDEAGKPAPKTRIFLPTSLRMGAWLKHKFWFACAPPYLDFESSTESSINTRANNSIGMAEEEKQEPESKRSIILNEEANLNDVFVGSTVRRYILDIMVHLRTHRLTYNAKAGGVYTNSLDDVVLLSRLIGLHSGKMFVSPSHVKEASRWYFPMHLELVQRSSMDSSLLYGSDPNLVDEMLEKLAKIKCEEVNEFENPLFLESLVVKNVLSKVVPPV	May be involved in telomere capping.
C7GVS1	RRG1_YEAS2	Required for respiratory growth protein 1, mitochondrial	MAQNFGKIPSHKSYVLSLYRTVLRNIPKCCHSYAFQYEIKKTLSKQLFKHKHDKSSWSVYTLLNEFSLLNNCLLEGKLQEIKNLMKPLKKMKKQLETTKILNSLTSLGDVKTNDPEEVRRFHVLSAYIKRKQDLGLLPAYIPKTYQHKLLLPLALNEHACLKLFHIQQKLKNGPPSAGLSYTKEGRNQIWFVRSPINKGRQQSKKLGILIRKERKDSQKNIDNLNFCEINAAWALHEAIWEEYLESKKIIKVNLPKYLEYAANIPKSTKCNPSSQYQKIKEWVDPVREIMFELHSKSFQRVEYFNKYKEKLLKNGGQLAYFDKKSKEMYAKRLTLFRKMSKETLPYVTLFIEGRDLPSVLAKYGF	Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).
C7GVY4	RGI2_YEAS2	Respiratory growth induced protein 2	MTKKDKKAKGPKMSTITTKSGESLKVFEDLHDFETYLKGETEDQEFDHVHCQLKYYPPFVLHDAHDDPEKIKETANSHSKKFVRHLHQHVEKHLLKDIKTAINKPELKFHDKKKQESFDRIVWNYGEETELNAKKFKVSVEVVCKHDGAMVDVDYKTEPLQPLI	Involved in the control of energetic metabolism and significantly contribute to cell fitness, especially under respiratory growth conditions.
C7GWA2	SPG4_YEAS2	Stationary phase protein 4	MGSFWDAFAVYDKKKHADPSVYGGNHNNTGDSKTQVMFSKEYRQPRTHQQENLQSMRRSSIGSQDSSDVEDVKEGRLPAEVEIPKNVDISNMSQGEFLRLYESLRRGEPDNKVNR	Stationary phase-essential protein not required for growth on nonfermentable carbon sources.
C7GXS8	RRG8_YEAS2	Required for respiratory growth protein 8, mitochondrial	MGLPKSAYKKLLIDCPTRVINKNCAQRVKDVSPLITNFEKWSDKRKKLYFKDEEEMVGHFHLENFNLKNNLYGRLLASPMRAEKISKLKSCRELLIPLKVVPSTGKDQHADKDKLKLVPTLDYSKSYKSSYVLNSASIVQDNLAAATSWFPISVLQTSTPKSLEVDSSTFITEYNANLHAFIKARLSVIPNVGPSSINRVLLICDKRKTPPIEIQVVSHGKGLPITQSVFNLGYLHEPTLEAIVSKDAVTKGIYLDADNDKDLIKHLYSTLLFQSVN	Required for respiratory activity and maintenance and expression of the mitochondrial genome.
C7GYE7	IRC6_YEAS2	Increased recombination centers protein 6	MVLQYPQNKILVLSDHPHNFSKTQFLQDLFHCSSTGISIVKDQTWENRYYKVHFDLYIDSCKDIPVWVEEFITPECEPLRNVMAGIILITDIRQTKPQELLHQFMIAAHRNTFVVLVNVNEEVEQDEIDELNEIWSNAFTNVIEFVNWKRSKPTVNHNDYGEKLGLDRIQEIIDTHDWLNCEVLPATKIREEIPNEMPLEQIIRNLQSARLKYKSIENSSEADAFANEMADELSRYL	Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
C7ZKL5	PEP2L_FUSV7	PEP2-like protein NECHADRAFT_97050	MVDLHSLPIGSRPSAAIRNNGPDRLVLERLKLRELAEGWPSYRDSCEWENFESIFHPGAHVYTTWSGRVPYQDFITASKAGMDKGAFIMHRCHGTSTDINAEGTRAVTKLKAIITQRFEVDGAEFDVEADCRFCFFFEKVGSRWGAQLVRHWYEKDKMIPANPARFPAVDEERLKGYPPGYRYLAYWQEATMGVKVLLDMPGHRRHVGTPNLEKHDLLYRQAKQWLEGEQIEI	May contribute to the ability of the fungus to cause disease on pea plants.
C8Z4Y4	RRG1_YEAS8	Required for respiratory growth protein 1, mitochondrial	MAQNFGKIPSHKSYVLSLYRTVLRNIPKCCHSYAFQYEIKKTLSKQLFKHKHDKSSWSVYTLLNEFSLLNNCLLEGKLQEIKNLMKPLKKMKKQLETTKILNSLTSLGDVKTNDPEEVRRFHVLSAYIKRKQDLGLLPAYIPKTYQHKLLLPLALNEHACLKLFHIQQKLKNGPPSAGLSYTKEGRNQIWFVRSPINKGRQQSKKLGILIRKERKDSQKNIDNLNFCEINAAWALHEAIWEEYLESKKIIKVNLPKYLEYAANIPKSTKCNPSSQYQKVKEWVDPVREIMFELHSKSFQRVEYFNKYKEKLLKNGGQLAYFDKKSKEMYAKRLTLFRKMSKETLPYVTLFIEGRDLPSVLAKYGF	Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).
C8Z7X8	IRC6_YEAS8	Increased recombination centers protein 6	MVLQYPQNKILVLSDHPHNFSKTQFLQDLFHCSSTGISIVKDQTWENRYYKVHFDLYIDSCKDIPVWVEEFITPECEPLRNVMAGIILITDIRQTKPQELLHQFMIAAHRNTFVVLVNVNEEVEQDEIDELNEIWSNAFTNVIEFVNWKRSKPTVNHNDYGEKLGLDRIQEIIDTHDWLNCEVLPATKIREEIPNEMPLEQIIRNLQSARLKYKSIENSSEADAFANEMADELSRYL	Involved in gross chromosomal rearrangements (GCRs) and telomere healing.
C8ZAJ0	RGI2_YEAS8	Respiratory growth induced protein 2	MTKKDKKAKGPKMSTITTKSGESLKVFEDLHDFETYLKGETEDQEFDHVHCQLKYYPPFVLHDAHDDPEKIKETANSHSKKFVRHLHQHVEKHLLKDIKTAINKPELKFHDKKKQESFDRIVWNYGEETELNAKKFKVSVEVVCKHDGAMVDVDYRTEPLQPLI	Involved in the control of energetic metabolism and significantly contribute to cell fitness, especially under respiratory growth conditions.
C8ZC77	MTC2_YEAS8	Maintenance of telomere capping protein 2	MGDHNLPDFQTCLKFSVTAKKSFLCMYRDSVSKEKLASSMPSTCDIQLKRAINDAYPGGGIKVTVLNSTTASLDSLATTHVKEFEIVIIPDINSLLQPDQAKLVKIMRDCTVAIEKAQSTRIFIGVVHWNNPVQPSGAAKDGDEAGKPAPKTRIFLPTSLRMGAWLKHKFWFACAPPYLDFESSTESSINTRANNSIGMAEEEKQEPESKRSIILNEEANLNDVFVGSTVRRYILDIMVHLRTHRLTYNAKAGGVYTNSLDDVVLLSRLIGLHSGKMFVSPSHVKEASRWYFPMHLELVQRSSMDSSLLYGSDPNLVDEMLEKLAKIKCEEVNEFENPLFLESLVVKNVLSKVVPPV	May be involved in telomere capping.
C8ZCU0	IRC19_YEAS8	Increased recombination centers protein 19	MRKPSITITTAKAIITPDYTLIKSHSKYQLPSRFQKLDADSPERSTVVKLFYRRFMRLKPFISNVKMVKDTYRDYVRYKFMKENYELKRYLVFNPDGLRSKIKLELLSNTKCCERIVPVTEMQRTLEFVLKSCSYLPETKVQKWDIARDNTYCRQILKNLLTMQYEKYRSILHRGIGHDELDVKFSHLKTTSSPLTKLNKTEKKKIPLFKVFSDFDTTLIYLNETLGTRL	Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).
C8ZD75	LCL2_YEAS8	Long chronological lifespan protein 2	MSQSRWSIVLIFALFIFGSTGVNAFFNFGHHQQQQQQQQQSYEDQVLNNPCDGYLCPDTLTCVAQQKDCPCPFPKSQLKCVLPDNKFVCISKPATHNEKFRAIYDDPVKGPKAKNKGFRDCGWVSDAYKNH	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
C8ZEW0	SPG4_YEAS8	Stationary phase protein 4	MGSFWDAFAVYDKKKHADPSVYGGNHNNTGDSKTQVMFSKEYRQPRTHQQENLQSMRRSSIGSQDSSDVEDVKEGRLPAEVEIPKNVDISNMSQGEFLRLYESLRRGEPDNKVNR	Stationary phase-essential protein not required for growth on nonfermentable carbon sources.
C8ZHZ1	CRS5_YEAS8	Metallothionein-like protein CRS5	MTVKICDCEGECCKDSCHCGSTCLPSCSGGEKCKCDHSTGSPQCKSCGEKCKCETTCTCEKSKCNCEKC	Critical role in copper (specific) homeostasis and detoxification. May protect by directly chelating and sequestering copper ions (By similarity).
C8ZJD8	RRG8_YEAS8	Required for respiratory growth protein 8, mitochondrial	MGLPKSAYKKLLIDCPTRVINKNCAQRVKDVSPLITNFEKWSDKRKKLYFKDEEEMVGHFHLENFNLKNNLYGRLLASPMRAEKISKLKSCRELLIPLKVVPSTGKDQHADKDKLKLVPTLDYSKSYKSSYVLNSASIVQDNLAAATSWFPISVLQTSTPKSLEVDSSTFITEYNANLHAFIKARLSVIPNVGPSSINRVLLICDKRKTPPIEIQVVSHGKGLPITQSVFNLGYLHEPTLEAIVSKDAVTKGIYLDADNDKDLIKHLYSTLLFQSVN	Required for respiratory activity and maintenance and expression of the mitochondrial genome.
C9SNH6	LCL2_VERA1	Long chronological lifespan protein 2	MRALTSLSVVLLALISTVSAQFGFFEQMFGGQQQGQQQRPQNVPSDSAAYRQQYDRSYCEHYLCPDTLACVHYPHHCPCPWPMNEDKFELSEGQRICVSKGGFAANEAARKVELARKGLL	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
D0UFC9	M1_QRFVE	Probable matrix protein	MACHTGNRRFPSVEELSLGMAQMTLLGTPVSSGTFDSVETLADRMGELKINDKSKVAGLTSVWVASRYNPFQGGALFKSHLRCNSLKKIIYRTDRNKCVKTAKVYLDRGGPPQAEDWEKLFECAIGLLAKQDWGDSQFREETALRLVVAAGGGVKRDACSAGTGGTEEGDSDTEEEPLEKVMERATKRIIEETARLSKRRRPEALEAALELRDSFKILSAQGGPFSKLSKDEKTRWVTAFSKCLQPILDLNEGRLLYDYVKQVGSK	May play a role in virion budding and release by binding the ribonucleocapsid and the host membrane.
D0ZV07	ORGA_SALT1	Oxygen-regulated invasion protein OrgA	MIRRNRQMNRQPLPIIWQRIIFDPLSYIHPQRLQIAPEMIVRPAARAAANELILAAWRLKNGEKECIQNSLTQLWLRQWRRLPQVAYLLGCHKLRADLARQGALLGLPDWAQAFLAMHQGTSLSVCNKAPNHRFLLSVGYAQLNALNEFLPESLAQRFPLLFPPFIEEALKQDAVEMSILLLALQYAQKYPNTVPAFAC	Oxygen-regulated protein required for bacterial internalization.
D3NXD9	COWN_AZOS1	N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)	MDSFDAPDRYVSFKGIDCEGNSRRIIDRLHMHIDDPAKTNAFWERFRAKLAIAEDPLKRQADGLCLLCANIYYIADLFEEHDDEDGLAMLRQLEDECC	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}.
D3QLG0	LPMG_ECOCB	mgtA leader peptide (Regulatory leader peptide for mgtA)	MEPDPTPLPRRRLKLFR	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).
D3RQU0	COWN_ALLVD	N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)	MSQAAVKIDRYITFEGIECDEQARRVLDCIRDCIEAPEASSWSAYFERKLDEITRMGQDELFVVGSQVNYIRALFEHHGHREGLDLLDRIEDECC	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}.
D3WAC0	TERS_BPLP2	Terminase small subunit (Gene product 1) (gp1)	MQTQKGGRPTILPKMYEEPLFSQIIDKIESGCNDREIYTSLHCSAKTFRKWRDDNIKAYDEAKSIARGNLLELAESALASKLTVRTLKETETIYDADGNVEKVKVKEKELDKDSLVAMMVAKAGNPELYNPTEWRRLQQEESSAHDLKAKIEELDDYKLSKYKTPEIEVPEGFE	Probable terminase small subunit. The terminase lies at a unique vertex of the procapsid and is composed of two subunits, a small terminase subunit and a large terminase subunit. Both terminase subunits heterooligomerize and are docked on the portal protein to form the packaging machine. Once the capsid is packaged with the DNA, the terminase complex is substituted by the connector proteins gp15.
D4G3R3	WAPI_BACNB	Immunity protein WapI	MKFFKRYNIDQKTLDEFKKYYVLLHGPFPNDMYDFEEETNTSLDEFYEFFALITGSLNYIIEDKKIPRYQREMLKKTFYEHYPHFRNYKSDILKYQELSECLEFHEKIRILINKLITGG	Immunity protein component of a toxin-immunity protein module, which functions as a cellular contact-dependent growth inhibition (CDI) system. Neutralizes the tRNase activity of cognate toxin WapA upon expression in E.coli. Does not inhibit WapA from other strains of B.subtilis. The WapA C-terminus cannot be expressed on its own in E.coli, however it can be cloned in the presence of its cognate immunity protein gene. Cell contact is probably necessary for growth inhibition.
D4H539	COWN_DENA2	N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)	MCNCKKNIKVDESYVSFKDIDCFENACLVIDNLLRILKEPKNTNAYWEKFIEKIPEAYYTRDSKKDPSEALLYLVCSCTSNIMELFEEIDDEEAIDAMSKCEQECC	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}.
D5ANI6	COWN_RHOCB	N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)	MNDQTPDRYVTFMGIACDTNADRLCEMLAARMAGNDSRWVAYFEKKLAENAQMGHDRLRFIGAQVNALMSFFEEEDDEAALALLWHIEHHCL	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}.
D5V2I8	COWN_ARCNC	N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)	MSNFEIRVNESYESFKNIDCFENACVVIDNMLRVLENPKNMNIYWKKIVPMIPKAYYDRDPKSDTKEELLYLVCSNSFYLDELFEKAEDEQAINALSKCEQECC	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}.
D6RMH5	LCL2_COPC7	Long chronological lifespan protein 2	MSRSSLLLVFFTLFGLAAAQFQFFNDFFGGQQHHQQQQRTGASQYAAFSENVPCSHYLCPGTMDCVERPRDCPCPDVQDVKCLIPDMDSDDDEATVVCVRGGTDCSTVEKLMKRGS	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
E1B9R1	SMIP4_BOVIN	Sperm-associated microtubule inner protein 4	MIPISLPEEHRPKCEPPRVMGKGHQHYGFGGEIWPRLPKPPNSTVGEICSPYPIEHPYHTHISRGAMFPTFTSPKDLYTGIKARTQQPFPPTVPTKPYDTTVLKTRGNPYRYELLDFPMDSKKKALVWPGQRVYFDLPKCVEKNKPVFYPKPPKTFAPNTSLNSWDPITSLKEVNIQRNLEKSHWITSYNHDFTGLGPMNPLELDDYHEKEVAELTGQIGFDPEPQEKVHPALKPTRPLEGRIARLIQNQRPLEAILEQRPSSCPDCTPRVLCTFHTFVPSSTEMMALSDNIPADVTHKNQEIEEKIKEEQSLLSTYALPSCYPTKDLANTYDIKPFPKITDTKKTEDLYWRQLSLKPQLIPYCNPDHYIPYEHLNQYNVYQNPVSLSKPGILQSKPDLKTFDFEHFLSKPEQLTLNMEDDEETKPILGWIPRAGVAKPQTDLLELKNAFSKTGAQKRFHKSVLEDYKDLRDKEHLGKKHQFYGHNSYYFYN	Microtubule inner protein (MIP) part of the dynein-decorated doublet microtubules (DMTs) in flagellum axoneme. May serve to reinforce and thus stabilize the microtubule structure in the sperm flagella.
E1XTG1	CAPSD_BPSAV	Major capsid protein (Major head protein)	MTKKLVTEEMRKQWLPVLQKESEAIQPLSAENVTIRLMQNQAEWNAKNLGESDAPGSVNSTVGKWQPVLIDMAKRLAPINIAMDFFGVQPLSGPDGQIFALRARQGVGDGSTTAQARKELFMNEADSGYSGDGTVQAGDPSGFSQAEIEGSGSVVTTIGKGMPSTDAELLGTTTNPWARVGITVQKATVTAKSRGLYADYSHELRQDMMAIHGEDVDNILSDVMVTEIQAEMNREFIRTMNFSAVRFKKFGTNGVVDIAQDISGRWALEKWKFLTFMLEVEANGIGVDTRRGKGNRVLCSPNVASALAMSGMLDYAPVLQENTKLAVDPTGQTFAGVLSNGMRVYVDPYAVAEYITLAYKGATALDAGIFFAPYVPLEMYRTQGETTFSPRMAFKTRYGICANPFVQIPANQDPQVYVTADGIAQDSNPYFRKGLIKSLF	Major capsid protein that self-associates to form the icosahedral capsid.
E3I7Z1	COWN_RHOVT	N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)	MSEQIDRYVSFKNIDCNARAGQMMDALQPYIQAAENPFWAYFQQKRAEFNAKGYDDLRVLHNYLPTLKELIEDDELLAQLEDLEYTCM	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}.
E3QVL2	LCL2_COLGM	Long chronological lifespan protein 2	MRFFASLPLVILALISSAQAQFGFFDQMFGGQQQQQQQPQNVPSDPSQYQQRYDGSYCENYLCPDTLACVHFPHHCPCPWPANQDKFELTEGSSRICVSKGGFAAGEAARKVELARKGLL	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
E4UUB3	LCL2_ARTGP	Long chronological lifespan protein 2	MASILRTALLGLLLFTTAQAQFQFFEQMFGGGQQHQESSGQGGNVPSDSAWYQNTYNGAQCSNYLCPGTLACVAVPHHCPCAHPKVEEKFELGEGSAICASKGGFKAGETARKIELARKGLL	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
E5A960	LCL2_LEPMJ	Long chronological lifespan protein 2	MARPYMIFAVLTAWFFGCNAQFGFFDQMFGGGGGGGQQQQQPQNVRSDSVWYQQQYEAAQCSHYLCPGTLSCVHFPHHCPCAWEGVEEKIELGEGIAICASKGGWAEGEFAKKVELARKGML	Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.
F5HC16	UL34_HCMVM	Transcriptional regulator UL34	MNFIITTRDFSNDDSVLRAAEMRDNVAGSISKAYKGTVRAEGKKKLLLKHLPVPPGGCSRRNSNLFVFCTERDYRKFHQGIAQLKRAPAELDPHEIQQVTASIRCRLQPSLREPPTPADELQTAVSRVCALFNQLVFTAQLRHYCEHQDKVVSYARDELTKRCGEKSALGVEVHQLVALLPHERHRELCHVLIGLLHQTPHMWARSIRLIGHLRHYLQNSFLHLLMNSGLDIAQVFDGCYHSEAYRMLFQIGHTDSVSAALELSHSAAAGPPEADENNDEGEEDDDELRHSDPAPLHDSKKPRNARRPRTRVPPHEQKPEENEEEEEELFPSCKATAAFLRAEPSVSNDDGNGGERCDTLATALRHRADEEDGPLASQTSVRVAATPSPSVTSALTPVTSPITPLCI	Acts as a transcriptional repressor of the US3 gene expression through a specific DNA sequence named the transcriptional repressive element (tre).
F5HH39	UL21A_HCMVM	Uncharacterized protein UL21A	MGGSPVPQLTTVTQGLMPSVRMDFRARRPLRRLAFYAPRARRRLFQNHIHPEQRRVLVGEGDEEMLPDLPMEIDIVIDRPPQQPLPNPLVLLLDDVPPHVPGFAPYRVPRPHPMIPEEHWDQF	Required for efficient viral DNA synthesis and the late accumulation of viral IE transcripts.
G0KYB0	TRI10_TRIAR	Trichothecene biosynthesis transcription regulator TRI10 (Trichothecene biosynthesis protein 10)	MILPKRTQEKEISLLMHYLDEVFPLQFPFHERRYVGKREWLLTILASTRPVYYATLSLSLLHKEACLHEFEAELAEIWQKEKMRYYILALQESQQQLDALDTAYGIAKMKGNIHALASTLQLISFESSSLSKGDWQLHLRAGTSLIPVLIDGWAVALKSDKVASSSSLWTELDASDFNATHDEDSLSYEYVGALKFFANVLAMFGIFSCISIGPSSPFMEYRFLMDQAGLIQMDQIMGCRNWAMLAILEIGTLDKWKREEQENRRLSLKALTSRAMAIEGVLESGLREASGSALVDLITSIYATSALTYLHTVVSGLNPNLSEVQESVAATIVLLKRLPDLRAAKSLVWPLGVTGCMASRSQEDFFRGLIISAGATPRALRNCWGLMKVWEDTWKMREYMSKQPPERWEEVVSGQGPPMLLM	Transcriptional activator of all of the trichothecene biosynthesis genes. Acts upstream of the cluster-encoded transcription factor TRI6 and is necessary for full expression of both the other trichothecene genes and the genes for the primary metabolic pathway that precedes the trichothecene biosynthetic pathway.
G2K048	HRCA_LISM4	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}.
G2TRS2	STEEP_SCHPO	ER exit protein	MSNQGKDSFKAYSYFCPCGQLFLTIHVSLTRLPQRQLDKRHVVDEKLNHIAHFSTGNKYYITRSDGGYEQRIQLLCRRCTLECAYALEAAPGYIYVDPTLVNEKPVTVSVSNLKE	May stimulate membrane curvature formation and subsequent endoplasmic reticulum exit site (ERES) establishment.
G4NYJ5	WAPI_BACS4	Immunity protein WapI	MILSSFLKIERMSSMHELKFRDLNVEVNEEDTVLLSMTESEIIVLTKKEIDYGAKYINHIVLYCNTDGRFLNSFSIQTNEQVINVQKVDDSFLFLIDKEYEDSVRDVEPNIYLWNPIEGFHQSFYAGRYINSMIIDQNKNLWVGYDETGIFSCVDQEISTRGINKFVLKNGKYELYFHGVSSYVIDQYFSTFVSEDAIYLYYRSMGEDYLQKLNLLGETLERVEVGIECSSCIKNGSSIYLFSRDDDSYNIEKVFKTNDMQNYVEQKISNENNGESLCFTQVASYKDKVAGIDHNNKLFLLNNQSL	Immunity protein component of a toxin-immunity protein module, which functions as a cellular contact-dependent growth inhibition (CDI) system. Neutralizes the tRNase activity of cognate toxin WapA upon expression in E.coli. Does not inhibit WapA from other strains of B.subtilis. The WapA C-terminus cannot be expressed on its own in E.coli, however it can be cloned in the presence of its cognate immunity protein gene. Cell contact is probably necessary for growth inhibition.
G9M952	CAPSD_BPPS4	Major capsid protein (Major head protein)	MAEKSTKNETALLVAQSAKSALQDFNHTYSKSWTFGDKWDNSNTMFETFVNKFLFPKINETLLIDIALGNRFNWLAKEQDFIGQYSEEYVIMDTVPINMDLSKNEELMLKRNYPRMATKLYGSGIVKKQKFTLNNNDTRFNFQTLADATNYALGVYKKKISDINVLEEKEMRAMLVDYSLNQLSESNVRKATSKEDLASKVFEAILNLQNNSAKYNEVHRASGGAIGQYTTVSKLKDIVILTTDSLKSYLLDTKIANTFQVAGIDFTDHVISFDDLGGVFKVTKDIVVSSDESVNFLRAYGDYQTHKGDTIPVGSVFTYDVSKLSEFKDSVEEIKPKSDLYAFILDINSIKYKRYTKGMLKQPFYNGEFDEVTHWIHYYSFKAISPFFNKILITDQDVTPRTE	Assembles to form an icosahedral capsid. {ECO:0000305\|Ref.2}.
G9M973	CAPSD_BPPSP	Major capsid protein (Major head protein)	MAEKSTKNETALLVAQSAKSALQDFNHTYSKSWTFGDKWDNSNTMFETFVNKFLFPKINETLLIDIALGNRFNWLAKEQDFIGQYSEEYVIMDTVPINMDLSKNEELMLKRNYPRMATKLYGSGIVKKQKFTLNNNDTRFNFQTLADATNYALGVYKKKISDINVLEEKEMRAMLVDYSLNQLSESNVRKATSKQDLASKVFEAILNLQNNSAKYNEVHRASGGAIGQYTTVSKLKDIVILTTDSLKSYLLDTKIANTFQVAGIDFTDHVISFDDLGGVFKVTKDIVVSSDESVAFLRAYGDYQTHKGDTIPVGSVFTYDVSNLSEFKSNVEEIKPKSDLYAFILDINSIKYKRYTKGMLKQPFYNGEFDEVTHWIHYYSFKAISPFFNKILITDQDVTPRTE	Assembles to form an icosahedral capsid.
I1R9A8	GRA5_GIBZE	Gramillins biosynthetic cluster protein FGSG_00039	MHLDHKLPWKTIASHFTLARDGSSPNYNLIALGLSTQDAALGHFSRIFIATIEEFSNTETSKINLNQVDGKLFSDDVLNFPEHHFGLGPHDTNSALNNPLDAKHQELKYWKGRASTASEYGTSPEYSASYSTADGDLADAAKMLVITAAVSDNQAIRREALSALCQLSAHVPMSDLRGLSWGHGFGLSLVASEALKLYMLLNLIEAVQSRGAQQVSLLRVKILLCALGNYSLQNYDFPAQNIPHRAFWHSLGITESWADRQADGVRESDEPVVDPLGLGDDEIHQEARINLKKYLKDCFAILYVYDVFLKQIASEEERKEFWSYEINRVILYL	Part of the gene cluster that mediates the biosynthesis of gramillins A and B, bicyclic lipopeptides that induce cell death in maize leaves but not in wheat leaves. The nonribosomal peptide synthetase GRA1 incorporates respectively a glutamic adic (Glu), a leucine (Leu), a serine (Ser), a hydroxyglutamine (HOGln), a 2-amino decanoic acid, and 2 cysteins (CysB and CysA) (Probable). The biosynthesis of 2-amino decanoic acid incorporated in gramillins could be initiated by a fatty acid synthase composed of the alpha and beta subunits FGSG_00036 and FGSG_11656 (Probable). The cytochrome P450 monooxygenase FGSG_15680 could hydroxylate the fatty acid chain (Probable). Subsequent oxidation to the ketone by the oxidoreductase FGSG_00048 and transamination by aminotransferase FGSG_00049 could form 2-amino-decanoic acid (Probable). On the other hand, FGSG_15680 could also be responsible for the HO-modified glutamine at the gamma-position (Probable). Whether hydroxylation occurs on the fully assembled product or on the Gln residue prior to assembly into the gramillins requires further proof (Probable). The thioredoxin FGSG_00043 could also be required for the disulfide-bond formation between CysA and CysB (Probable). The specific involvement of the remaining proteins from the cluster is more difficult to discern, but could have broader regulatory (FGSG_00040 and FGSG_11657) or enzymatic functions (FGSG_00044 and FGSG_00045) (Probable). The final C-domain of GRA1 does not possess the expected sequence of a termination CT domain, often implicated in macrocyclization and release of a cyclopeptidein fungal NRPs and the thioesterase FGSG_00047 may act in concert with the terminal C-domain of GRA1 to catalyze the formation of the macrocyclic anhydride and release of the products (Probable).
I6WXS6	VPB51_MYCTU	Putative antitoxin VapB51	MAKHLVDIDEQALNMARTELGTTTIKDTVNAALRQATSQRVQRVAAALDTLAAAPPEDRAEAWR	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC51.
L0TGF0	VPC50_MYCTU	Putative ribonuclease VapC50 (RNase VapC50) (EC 3.1.-.-) (Toxin VapC50)	MPCCGSLTRAPIGLCGRRTSWPRLGEPWSTASTSAPNGLTTAFAFGYNDLIAAMNNHYKDRHVLAAAVRERAEVIVTTNLKHFPDDALKPYQIKALHPDDFLLDQLDLYEEATKAVILGMVDAYIDPPFTPHSLLDALGEQVPQFAAKARRLFPSGSPFGLGVLLPFDQ	Toxic component of a type II toxin-antitoxin (TA) system. An RNase. The cognate antitoxin is VapB50.
M1L9M3	PG087_MONPV	Late transcription elongation factor OPG087	MPFRDLILFNLSKFLLTEDEESLEIVSSLCRGFEISYDDLISYFPDRKYHKYISKVFEHVDLSEELSMEFHDTTLRDLVYLRLYKYSKYIRPCYKLGDNLKGIVVIKDRNIYIREANDDLIEYLLKEYTPQIYTYSNERVPIAGSKLILCGFSQVTFMAYTTSHITTNKKVDVLVSKKCIDELVDPINYQILQNLFDKGSGTINKILRKIFYSVTGGQTP	Involved in postreplicative transcription elongation on intermediate and late genes.
O05070	VGAM_HAEIN	Mu-like prophage FluMu host-nuclease inhibitor protein gam	MATKVKSQAKLRFVSVEQVQSAIKEIGDLSREHTRLATEMNDKIGATSEHYAPKLKALKEEIEPLQKAVQEYCEANRDELTEFGKTKTANFVTGEVQWRQRPPSVAIRGAEAVMEFLQRMGFDRFIRTRQEINKEALLNEPEVAKGIAGVTIKQGLEDFVIKPFEQDAR	Protects linear double-stranded DNA of Mu genome from exonuclease degradation.
O05073	VPI_HAEIN	Mu-like prophage FluMu I protein	MKAEKTSLAVLTAQLTSPDGWQQLLPKGEFRSRDGSPTDVAHWFIDGTIAQNLIHKARQLNQDLLVDYDHETILKAKKGIDAGNVVAAGWFNADEIQWFDDETRQGLYIKPRWTPKAYQQIKDGEFAFLSAVFPYDENGTPLELRMAALTNDPGITGMQRLAVLSATLNPQENVKMPESLRKLLAKLGVEIAEGVELTEEQANTALNALETLQTDKTKADEQVATLSAKNTEVDLSQYVPKATYDAVMSQVAVLSAKTDDVEIDNHISKARNEGRAVEAEVEYLKQFGKQQGVAALSAMLEKRPQIAVLSAQQTQTTKVEKPVEKGTAVLSAADKEAAKLLGISEQDYAKELEAK	Potential protease involved in virion morphogenesis.
O05290	P13_MYCMY	Probable UPF0122 protein (p13)	MKLKNNLLEKTLELSELFKIYKELLTDKQKQYFELYIDEDLSLSEIADEFNISKTAVYDSISKTSKLLFSLETKLHLKQKQDLLISLINKIETNQIDEKQFIKSLKEVIWWKY	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 (By similarity).
O06723	YISJ_BACSU	Inner spore coat protein H-like protein	MERVHLFFHREQLKRKGTAKGLFVTDRSVSPILLTQRDRAEKASYEISWEKSLLGERTLFLNAEQDDPSLMRRRLAYCFFDQIGVPAPVASYSFLTINGQPEGIYLNIKNHQPAGKRSYGVKTADPRVPLSLFNNDSSAFLHEFFILIRTAGDDELAERIKLYLDVKLFFLWLIGNTCTNQGFYYTFCLNESGRLYVSPMETRSLAVQEWYEEDPLLTKGKTLSSRLLSIPAFRSQYHTLMKNVLKRSFTIERLSPLINEWHLDICQSAADDPFIKKSPFQIEKEQTNILREIEERQDFLQAHLARL	Involved in the assembly of several proteins in the inner and outer layer of the spore coat.
O06775	VAPB8_MYCTU	Putative antitoxin VapB8	MEKSRCHAVAHGGGCAGSAKSHKSGGRCGQGRGAGDSHGTRGAGRRYRAASAPHPLAVGAHLRDELAKRSADPRLTDELNDLAGHTLDDL	Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC8.
O06777	VAPB7_MYCTU	Putative antitoxin VapB7	MSMRLAHRLQILLDDECHRRITAVARERGVPVATVVREAIDRGLVSPAGRRKSAGRRLLDAADMSVPEPRELKQELEALRARRG	Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC7.
O06779	MAZE2_MYCTU	Probable antitoxin MazE2	MLSFRADDHDVDLADAWARRLHIGRSELLRDALRRHLAALAADQDVQAYTERPLTDDENALAEIADWGPAEDWADWADAAR	Antitoxin component of a type II toxin-antitoxin (TA) system.
O10276	VE26_NPVOP	Putative early 21.8 kDa protein	METAQPPISYAPPKRGAVCAYVRTVVTTTTVSDSGGNNEDRLTQIVAQLQRTRLNFSKLSQLQRRRVRNMQKLIRKKNSVIANLAARLTTQKKTKHFAVTIRKNVIHTTSGSEQFVRQRVLELCANGGEQVFCARRADCARDRRRVAEALATALGAGVVASAANKRFEIEDEEKLVSAKLIVQQVLHDGDHSDTCAD	This protein is required for viral late gene expression.
O10277	VE18_NPVOP	Putative early 22.7 kDa protein	MEITVTLVPINLRGAEEPERNQRFRLKPLCAAAEVCLAVKCRSPFAKFKVLISVTNFDNKHLQATVCSRHAAVCVVNAPGQREVVFDGFAKPDDEGATVPLVVGPLFAARQAGRCVRAAVDAIQRQQTVLKVFINEAYLQSAWGAVRGLFFSDNNHESDLTSNVGKFISVDPTDVGARGANSSKWVPAINYVTGRQLLTILFIFKFI	This protein is required for viral late gene expression.
O10278	VE41_NPVOP	Putative early 40.3 kDa protein	MDRVASQIYSGALPYITTMDMEDRLRNRIAAKAGAKFFKACFEAVVADKSGLFVLSGGAATACHIGDDRNVLKCLDFDYYNATQEWLQLARLQQRLQACVQDNLEILSRLAQSVRMQDDLFVVKCFQNGAFCFNGPVQARLVPCVETVRTSFNGEFDLLRFALQVELKALNGVDEYVDQKVIVDRGAAVFNVFFVNIRAMKGPLTMERCVRTLAVFGDAYRVVVSPLQSVINDQIMCLLKDIFTDKPEFRVARPKALICALFAKLPREAYDECINSHHGAEPTRRRDETVTSFCRRTLHIHGPALGCRKLVYAYFKTDSFARQMPDYVANRAIYPHTDCEMKWKEFIHFFVVAKV	This protein is required for viral late gene expression.
O10300	VP47_NPVOP	Viral transcription regulator p47	MANVSMFAQSLHYTTQFLPAVCRAHDDVLLRYNLYISGAGAQLPRRVTRTVQIDADGFVRFVFDVKVFHLERLTVVERATAGDLDDYVEVTRPELSAHDAAIFKLVCRDRWCKGDAQRLRRILQQPRVDNLIKFACNVIWERGYEDHYTIGQQLSILITTKLIQSGLDFKHQPDTAAPASVRGWQDETFEKYLLSLSSVNEIIKRHVFSKKYICLEVAAAHWRSVVQALQDEGFKLAFNAHTPHVLLICVDDDKNSMVYMLKLAHLLQTRVVNLLFATDVEFYMRANHFTFYVYNSLKFYYYCLKNKFAFESNDKMLMFLLYTIVSLEWFNKGHLNSFTLEKSELYNPLELATRRLNSIKRAAQQNRVVECDSEIGVDYVRGKRVRTGTHYGQRAVQFE	It is involved in regulating viral transcription at late times postinfection.
O10311	LEF10_NPVOP	Late expression factor 10	MTHVLSAAANDLIACVLRDNLFSADGECLRYVVCKEAGHVESVYIGEIGAAQAHSGDQNAVLDASSASDVSSSASSRRVS	Involved in late/very late gene activation.
O10319	LEF9_NPVOP	Late expression factor 9	MVSFLDRPPTEFDLILDPAKLNSAAFFSNDEFRAVLKSLIGDLKKNQRPNYFNSLVDQMINVYAHISAGEHADALVRIIDATCVVVTNLPSNVFLKKLKTNKFTDSIDYLILPHFILWDYNFVVFLNNTFNSKHENSLVDISGALQKIKLTHGVIKDQLQSKNGYAVQYSYSTFLNTASFYANVQCLNGVNEVMPPLHSVRRYFGRDVPHARAWTTRHPNISQLSTQVSDVRVNDRDTDWNVKVGLGIFPGANTDCDGDKKIITYLPRPNSLIDLECLLYGDPRYSFICFDKNRLTFVSQQIFYLHKNVEAVERLLKTMPLAFALWRIHANVKFSARLELLLRDFCLVASSNASYLLFKQLTELIKDEEMVCADEELFGLSGQFTDMVNSGAKGSAALIESTRQYARTRATDIDIVSTRATTSLNSYISSHNKVQVCGADIYHNTAVLQNLYIKNNYICYKNDDRRIASICALPSEYLFPEHLLDLFIE	Involved in late/very late gene activation.
O10340	LEF4_NPVOP	Late expression factor 4	MGADVLIEQEISYTINFSQDLLYLILDSYIKKRCAAPAERYTDLYDANNVRTRQTADSAVSVHKTNLRDERFVHWLRSSNALVPLVRRENRETAVPHDRVSRHIASLIETTVYKLDGVDVKFEHVYMQSGPADRYESTAAHKIAALKTALLGVDCARPSQNLQLGSDAVLARVRLELEFEGAAPAAASLDAFCELVVQMETLADHHNIAPCLPYTTLLDSATPRRFTREQRIAYGAQAPDSTGVKKWAFKLDGVRGRGAFRRGYCLVQTDDMQLHAACISSPFGLNNVVTFQCEVVADKIFVTDLLQVFRYKYNNRTQYECNLHDAYPINADVAVECLNRLHCAVGSVPWPGLGELRFQQFFDPPLAPTHYTTIPIDGYIVLDEQLQYAKYKWLPTVELEYDAPSGALHSIDGPLLGKTVVADLQLKHGAVYECAITDNAINVLKCRPDRIVPSKVC	Required for late and very late gene expression.
O10344	LEF5_NPVOP	Late expression factor 5	MALVKGVAQSQTRPLAFHGEQWTPRALFTVFGAFRASKDYAKLIEFLTNNFACYVKNKTFNFAGTGHLFHSLYAFVPNVSELVKERKQIRLQIDCVMRLFKNTTNDFKMYVELFAFIDAHGGAECPCLLLQQSKLNAVSFVENLNCKLFDIKPPKFKKEPFDSILSKYSLNYKALCFKKKEKCTVGCVTKRQKKMKRRQLLSDRVIYLHNKNDVLDERTLLHGPSGTSLAPCLHRYATVERQTRAGDEMVSFIRYCELCQMRA	Required for late and very late gene expression.
O10362	LEF7_NPVOP	Late expression factor 7	MEPPLKRCRLCHQALPKLPQLPFEMIDKILSHLPFDLHVDVVGASAATRLRALRRPDRLTRYHEYDLAADELFAAHWNIEAADPARPYVGQLCRSTCASAAQKFFNERVPRAAAMCMLNAPRAESDSVLTRRWNWWGLTRTLLIHEANSGRGRRPARVRVDADEACIGYHAPFCDASVFEFNAQPDHVVFVLLDDDKIELNMYGKRVYRIV	Involved in late/very late gene activation.
O10365	VP74_NPVOP	Protein p74	MAVLTAVDLTNASRYAGHMHRLEFINRWRERLPHILIDYTLRPASSDDDYYVPPNLRNRALAVKLAFSRRGCDSMSCFPFHETGVVSSQTPFAYTQTSETSVAYAQPACYHLDRAAAMREGAENEVQSAEFTYTPNNQCVLVDSTSKMYFNSPYLRTEEHTIMGVDDVPAFNVRPDPDPLFPERFKGEFNEAYCRRFGRDLINGGCSFRWWESLIGFVLGDTIYVTFKMLANNIFSELRDFDYAAPSPLLPPRPAADSNAVLAQWRAVRDRAVDWDFEKQFSEAPTLQQLGMDANGVLMQLSYTAETGFTKTPIAYSARGAVRVARESRAADRAMSDDDLEAIVASFLEEYALVFGIATDIGFDMLLTAFKAMLKKINTALIPALKRMLVGTSQRVTVRLLGETYKAALVHSMNRIAIKTLTTAAKALTRVAIKASSVVGIVLILFTLADLVLALWDPFGYNNMFPREFPDDLSRTFLTAYFETLDSNTSREIIEFLPEFFADIVETDDDATFQSLFHLLDYVAALEVNSDGQMLALDESDEIKDFDEATLVGQALASSSLYTRLEFMQYTYRQNTLLAMNKNNNKLNGVIAGLFLTNTAVALAAFIAHKELTFFVYFAIFLMLAFYYLVKEPYEYFKTVDLLF	Essential for virulence of baculovirus occlusion bodies for insect larvae.
O15602	ACTO_ENTHI	Actobindin homolog	DAKALAGIADAKLKHTETGDKSAPVIENVEIKKGDRNELLSGIKEGKELKKAETNDRSAPVIPADAKVQEDNRGALLADIQATAK	Is able to bind two actin monomers at high concentrations of G-actin.
O15926	CAPSD_CPVKS	Capsid protein (CP) (Coat protein)	MITSFESIEKKNAVYYPVDLKFVTDLSSDLSNTADGLGQAWYKISQVAVEHIILTALKINYVLNHRTLLLIYNKKVPDMDLINIIQSSIMVPRFVRDLIREILRPMHHSGITYIPDLDLSTRPTPHLLDTFYPIAEHLTRWNNVCQKLGFEMVPILPEAVQSVSLTFYSYETDELLSFDNLINLDWRIEAFGWTKHLVHNPTSEVDELGKSQTATSRKRVQEKDYECDDFRKVYERPLQNRRILGMIVYRYTCAPYTMRLGHLSPNCRFPTEKNHSETPPTSNRVLLSEQTMVHSIQKNRSKPKKVKIVTTECSADRSH	The capsid protein self-assembles to form an icosahedral capsid with a T=2 symmetry made of 120 subunits.
O18638	OAF_DROVI	Out at first protein	MAYGAPQCAQHLPPIGTPTLRQRSVSCYHFFRHSRGFLWFVLCNLLLTPNISDAQLLINVQNQGGEVIQESITSNIGEDLITLEFQKTDGTLITQLIDFRNEVQILKALVLGEEERGQSQYQVMCFATKFNKGDFISSDAMAKLRQKNPHTIRTPEEDKGRETYTMSSWVQLNRSLPITRHLQSLCAEATDATYVRDVDLKAWAELPGSSISSLEAATEKFPDALSTRCNEVSSLWAPCLCTLETCIGWYPCGLKYCKGKSVGGDTSGTQQQQQQTNYRCGIKTCRKCTQFTYYVRQKQQCLWDE	Vital for proper neuronal development and hatching.
O21869	TERS_BPLSK	Terminase small subunit (Gene product 1) (gp1)	MQTQKGGRPTILPKMYEEPLFSQIIDKIESGCNDREIYTSLHCSAKTFRKWRDDNIKAYDEAKGIARGNLLELAESALASKLTVRTLKETETIYDADGNVEKVKVKEKELDKDSLVAMMVAKAGNPELYNPTEWRRLQQEESSAHDLKAKIEELDDYKLSKYKTPEIEVPEGFE	Probable terminase small subunit. The terminase lies at a unique vertex of the procapsid and is composed of two subunits, a small terminase subunit and a large terminase subunit. Both terminase subunits heterooligomerize and are docked on the portal protein to form the packaging machine. Once the capsid is packaged with the DNA, the terminase complex is substituted by the connector proteins gp15.
O21894	SAV_BPLSK	SaV protein (Gene product 26) (Gp26)	MNYGTNNHYANEYGMELNEYFKHHFNYEELAGWYTMQVLKYLVRAGKKEGESYDKDRNKALDYAGELANLSNENELTEYTTDDIMGFAQDIADDFKQWKDERNNFKSEFTKEEIKAIDERYLEFIEEV	Involved in the sensitivity of the virus to the host AbiV system.
O22005	TFA_BPSF5	Probable tail fiber assembly protein (P37)	MSRTLDLILLCRLVQDTAHLLMRITLQWDINEMSYFYSASTNGFYSTEFHGTNIPDDAVEISESEWETLINSQGVTKMITCGENGHPVIVDRPSPTPERLALINDEKKSALIAEATNVIAPLQDAVDLGMATDDETKLLLAWEKYRVLLMRVDIKNTEWPKKPEGNK	Chaperone involved in tail fiber assembly.
O22010	VXIS_BPSF5	Excisionase	MHGMGYDSRLDRLAATSWYPFFNNVTARGEIMEPYSLTLDEACDFLKISRPTAINWIRTGRLQATRKDPTKSKSPYLTTRQACIAALQSPLHTVQVSAGDGITEERKCHSSAEVKYGTPVSHCRTVKDLNSLLEQRTKGRRQNSMTS	Excisionase and integrase are necessary for the excision of prophage from the host genome by site-specific recombination.
O22426	NO40_LOTJA	Early nodulin-40	MRFCWQKSIHGS	Modulates the action of auxin, and may function as plant growth regulator that alters phytohormone responses.
O24369	NO40_SESRO	Early nodulin-40	MKLCWQKSIHGS	Modulates the action of auxin, and may function as plant growth regulator that alters phytohormone responses.
O25156	PLPHP_HELPY	Pyridoxal phosphate homeostasis protein (PLP homeostasis protein)	MLDYRQKIDALITKIEKARTAYSRHHIVKIVAVSKNASPEAIQHYYNCSQRAFGENKVQDLKTKMHSLEHLPLEWHMIGSLQENKINALLSLKPALLHSLDSLKLALKIEKRCEILGVNLNALLQVNSAYEESKSGVVPEEALEIYSQISETCKHLKLKGLMCIGAHTDDEKEIEKSFITTKKLFDQIKNASVLSMGMSDDFELAIACGANLLRIGSFLFKE	Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis. {ECO:0000255\|HAMAP-Rule:MF_02087}.
O25988	YIDD_HELPY	Putative membrane protein insertion efficiency factor	MRNNKTPFLSAIFTASIRGYQRFFSAFTPSSCRFYPTCSNYALWLLCFESPLSAMGKIAIRILSCNPFCSGGIAYPTTRLKRPSLIQSHKDSNRNFKTITFWLVPTKSHATYYIIKV	Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255\|HAMAP-Rule:MF_00386}.
O26776	BRIX_METTH	Probable Brix domain-containing ribosomal biogenesis protein	MLLTTSRKPSQRTRSFSQRLSRIMGWRYINRGKMSLRDVLIEARGPVAVVSERHGNPARITFLDERGGERGYILFNPSFEMKKPELADKAVRVSSCPPGSEGLCNLMGLEVDESSSRDAWSIRTDEEYAWVMELMDARGTPAGFKLLIRDFRVGE	Probably involved in the biogenesis of the ribosome. {ECO:0000255\|HAMAP-Rule:MF_00699}.
O28071	VPB21_ARCFU	Putative antitoxin VapB21	MPKIIEAVYENGVFKPLQKVDLKEGERVKIKLELKVEPIDLGEPVSVEEIKKIRDGTWMSS	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC21 (Potential).
O28282	VPB18_ARCFU	Putative antitoxin VapB18	MTKTISISDDVYEMLVKIKGKRSFSEVIRELVKKEGNFDLLMVAFGTRSEEEVEKLKREMKEVEEWMQSLCNH	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC18 (Potential). {ECO:0000255\|HAMAP-Rule:MF_00794}.
O28301	CUTA_ARCFU	Divalent-cation tolerance protein CutA	MHNFIYITAPSLEEAERIAKRLLEKKLAACVNIFPIKSFFWWEGKIEAATEFAMIVKTRSEKFAEVRDEVKAMHSYTTPCICAIPIERGLKEFLDWIDETVE	Involved in resistance toward heavy metals.
O28561	VPB17_ARCFU	Putative antitoxin VapB13	MGEIIEAVYQKGVLKPLRKVSLREGEIVKVEIRETKKVTGRFYAKLRELEKRIERVEGAHRELEEIRDDRY	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC17 (Potential).
O28584	VPB16_ARCFU	Putative antitoxin VapB16	MKNIMVRDEVYEKLQKMKKGRESFSDVILRLIEGRKKRGIEILERYAGSLSDSELEKIVMEERRKFRVRSFDS	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC16 (Potential). {ECO:0000255\|HAMAP-Rule:MF_00794}.
O28791	Y1481_ARCFU	Putative antitoxin AF_1481	MKTISIRDDVYRKLLEMKDEEDSFSDVIEKLLKRKKTDIRRYFGVLKDSEVLDEIEKSLNARKSARFRV	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. {ECO:0000255\|HAMAP-Rule:MF_00794}.
O28794	VPB15_ARCFU	Putative antitoxin VapB15	MPTKTITITLEAYERLKREKREGESFSDVIIRLTEKRRDLLEFAGKWKDSGEEIEKIILEGRKEFDKHVLS	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC15 (Potential). {ECO:0000255\|HAMAP-Rule:MF_00794}.
O29159	BRIX_ARCFU	Probable Brix domain-containing ribosomal biogenesis protein	MQVLTTSRKPGRKTRRFAKVLARFFNWKYVNRGKLSLEDLAGIAERFWIISEVKGNPAILNLYERGEKTLEVSFTLSNVNKIKMDDSPAVFKGKAPIDPLVFGAIPQTKAGLKLTRKVEFRKKVVVKGDEWLFFYDDEMLFKLRILKISRSSR	Probably involved in the biogenesis of the ribosome. {ECO:0000255\|HAMAP-Rule:MF_00699}.
O29170	Y1095_ARCFU	Putative antitoxin AF_1095	MPKIIEAIYENGVFKPLQKVDLKEGERIKLRIEEGILDVIKKYQGKFKLTEKDIEKFLEERR	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
O29173	VPB13_ARCFU	Putative antitoxin VapB13	MPKIIEAIYENGVFKPLQKVDLKEGERVRVVVSEVVAKTRGLLKGCEMEEIIEEIESEGFL	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC13 (Potential).
O29175	Y1090_ARCFU	Putative antitoxin AF_1090	MPKIIEAVYENGVFKPLQKVDLREGEKVKIIAGNLVERLRKYRVKVDSDIVAEFISERR	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
O29178	Y1087_ARCFU	Putative antitoxin AF_1087	MPKIIEAVYENGVFKPLQKVDLKEGEKIRLRIEEGIADVIKEFSRKVDQDVLEEFLRERR	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
O29181	Y1084_ARCFU	Putative antitoxin AF_1084	MPKIIEAIYENGVFKPLQKVDLKEGEKIRILLKKIDVEKFIMAKLPEEKIRELERRFEDENLY	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
O29184	Y1079_ARCFU	Putative antitoxin AF_1079	MPKIIEAVYENGVFKPLQKVDLREGERE	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
O29189	Y1074_ARCFU	Putative antitoxin AF_1074	MPKIIEAIYENGVFKPLQKVDLKEGERVRIKLEKVEEVVDEVFGILKGKDTLKALRELEEWGFC	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.
O29926	VAPB7_ARCFU	Putative antitoxin VapB7	MPKVIEAVYENGVFKPLQKVDLKEGEKVKVELKESVVESVAGILKVSDEKVKKALEMIEYGEDIY	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC7 (Potential).
O29929	VAPB5_ARCFU	Putative antitoxin VapB5	MPKIIEAIYENGVFKPLQKVNFRPGSKVRIVIQEDKKEILRKYKGVFGKAEVEELREYEGEVML	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC5 (Potential).
O29931	VAPB4_ARCFU	Putative antitoxin VapB4	MPKIIEAIYENGVFKPLQKVDLKEGEKAKIVLESISDKTFGILKASETEIKKVLEEIDDFWGVC	Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC4 (Potential).

C6DAH5

SYDP_PECCP

Protein Syd

MEHEVVSALAAFTQRYVDCWQQEKGHLPASEALYGIPSPCIVENHEDTVYWSPQPFAPAAALDGVERALEISLHPDVHAFYTAQYAGDMAAQFDSLSCQLLQVWSEDDFTRMQENLIGHLLTQKRLKLTPTLFLATTDSEMTMVSLCNISGEIILEEFGTKKRQILAPTLAAFLFGLNPLAV

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}.

C6DYS2

YIDD_GEOSM

Putative membrane protein insertion efficiency factor

MLKQIFIGLVVFYQRFISPLKAPSCRFYPTCSHYSLQALEKYGPVKGLWLTAARVLKCHPFHPGGYDPVK

Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.

C6HEL8

LCL2_AJECH

Long chronological lifespan protein 2

MVHIFTGILLGLLLLATGTQAQFQFFEQMFGGGQQQQHDSREQNVPSDSDWYQRTYDNARCSNYLCPGTLACVAVPHHCPCQHPAVEDKFELGDGSAICVSKGGFKFGEAARKVELARKGLL

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

C6UP45

LPMG_ECO5T

mgtA leader peptide (Regulatory leader peptide for mgtA)

MEPDPTPLPRRRLKLFR

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).

C7GLG0

CRS5_YEAS2

Metallothionein-like protein CRS5

MTVKICDCEGECCKDSCHCGSTCLPSCSGGEKCKCDHSTGSPQCKSCGEKCKCETTCTCEKSKCNCEKC

Critical role in copper (specific) homeostasis and detoxification. May protect by directly chelating and sequestering copper ions (By similarity).

C7GQE4

IRC19_YEAS2

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).

C7GQS7

LCL2_YEAS2

Long chronological lifespan protein 2

MSQSRWSIVLIFALFIFGSTGVNAFFNFGHHQQQQQQQQQSYEDQVLNNPCDGYLCPDTLTCVAQQKDCPCPFPKSQLKCVLPDNKFVCISKPATHNEKFRAIYDDPVKGPKAKNKGFRDCGWVSDAYKNH

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

C7GVL2

MTC2_YEAS2

Maintenance of telomere capping protein 2

MGDHNLPDFQTCLKFSVTAKKSFLCMYRDSVSKEKLASSMPSTCDIQLKRAINDAYPGGGIKVTVLNSTTASLDSLATTHVKEFEIVIIPDINSLLQPDQAKLVKIMRDCTVAIEKAQSTRIFIGVVHWNNPVQPSGAAKDGDEAGKPAPKTRIFLPTSLRMGAWLKHKFWFACAPPYLDFESSTESSINTRANNSIGMAEEEKQEPESKRSIILNEEANLNDVFVGSTVRRYILDIMVHLRTHRLTYNAKAGGVYTNSLDDVVLLSRLIGLHSGKMFVSPSHVKEASRWYFPMHLELVQRSSMDSSLLYGSDPNLVDEMLEKLAKIKCEEVNEFENPLFLESLVVKNVLSKVVPPV

May be involved in telomere capping.

C7GVS1

RRG1_YEAS2

Required for respiratory growth protein 1, mitochondrial

MAQNFGKIPSHKSYVLSLYRTVLRNIPKCCHSYAFQYEIKKTLSKQLFKHKHDKSSWSVYTLLNEFSLLNNCLLEGKLQEIKNLMKPLKKMKKQLETTKILNSLTSLGDVKTNDPEEVRRFHVLSAYIKRKQDLGLLPAYIPKTYQHKLLLPLALNEHACLKLFHIQQKLKNGPPSAGLSYTKEGRNQIWFVRSPINKGRQQSKKLGILIRKERKDSQKNIDNLNFCEINAAWALHEAIWEEYLESKKIIKVNLPKYLEYAANIPKSTKCNPSSQYQKIKEWVDPVREIMFELHSKSFQRVEYFNKYKEKLLKNGGQLAYFDKKSKEMYAKRLTLFRKMSKETLPYVTLFIEGRDLPSVLAKYGF

Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).

C7GVY4

RGI2_YEAS2

Respiratory growth induced protein 2

MTKKDKKAKGPKMSTITTKSGESLKVFEDLHDFETYLKGETEDQEFDHVHCQLKYYPPFVLHDAHDDPEKIKETANSHSKKFVRHLHQHVEKHLLKDIKTAINKPELKFHDKKKQESFDRIVWNYGEETELNAKKFKVSVEVVCKHDGAMVDVDYKTEPLQPLI

Involved in the control of energetic metabolism and significantly contribute to cell fitness, especially under respiratory growth conditions.

C7GWA2

SPG4_YEAS2

Stationary phase protein 4

MGSFWDAFAVYDKKKHADPSVYGGNHNNTGDSKTQVMFSKEYRQPRTHQQENLQSMRRSSIGSQDSSDVEDVKEGRLPAEVEIPKNVDISNMSQGEFLRLYESLRRGEPDNKVNR

Stationary phase-essential protein not required for growth on nonfermentable carbon sources.

C7GXS8

RRG8_YEAS2

Required for respiratory growth protein 8, mitochondrial

MGLPKSAYKKLLIDCPTRVINKNCAQRVKDVSPLITNFEKWSDKRKKLYFKDEEEMVGHFHLENFNLKNNLYGRLLASPMRAEKISKLKSCRELLIPLKVVPSTGKDQHADKDKLKLVPTLDYSKSYKSSYVLNSASIVQDNLAAATSWFPISVLQTSTPKSLEVDSSTFITEYNANLHAFIKARLSVIPNVGPSSINRVLLICDKRKTPPIEIQVVSHGKGLPITQSVFNLGYLHEPTLEAIVSKDAVTKGIYLDADNDKDLIKHLYSTLLFQSVN

Required for respiratory activity and maintenance and expression of the mitochondrial genome.

C7GYE7

IRC6_YEAS2

Increased recombination centers protein 6

MVLQYPQNKILVLSDHPHNFSKTQFLQDLFHCSSTGISIVKDQTWENRYYKVHFDLYIDSCKDIPVWVEEFITPECEPLRNVMAGIILITDIRQTKPQELLHQFMIAAHRNTFVVLVNVNEEVEQDEIDELNEIWSNAFTNVIEFVNWKRSKPTVNHNDYGEKLGLDRIQEIIDTHDWLNCEVLPATKIREEIPNEMPLEQIIRNLQSARLKYKSIENSSEADAFANEMADELSRYL

Involved in gross chromosomal rearrangements (GCRs) and telomere healing.

C7ZKL5

PEP2L_FUSV7

PEP2-like protein NECHADRAFT_97050

MVDLHSLPIGSRPSAAIRNNGPDRLVLERLKLRELAEGWPSYRDSCEWENFESIFHPGAHVYTTWSGRVPYQDFITASKAGMDKGAFIMHRCHGTSTDINAEGTRAVTKLKAIITQRFEVDGAEFDVEADCRFCFFFEKVGSRWGAQLVRHWYEKDKMIPANPARFPAVDEERLKGYPPGYRYLAYWQEATMGVKVLLDMPGHRRHVGTPNLEKHDLLYRQAKQWLEGEQIEI

May contribute to the ability of the fungus to cause disease on pea plants.

C8Z4Y4

RRG1_YEAS8

Required for respiratory growth protein 1, mitochondrial

MAQNFGKIPSHKSYVLSLYRTVLRNIPKCCHSYAFQYEIKKTLSKQLFKHKHDKSSWSVYTLLNEFSLLNNCLLEGKLQEIKNLMKPLKKMKKQLETTKILNSLTSLGDVKTNDPEEVRRFHVLSAYIKRKQDLGLLPAYIPKTYQHKLLLPLALNEHACLKLFHIQQKLKNGPPSAGLSYTKEGRNQIWFVRSPINKGRQQSKKLGILIRKERKDSQKNIDNLNFCEINAAWALHEAIWEEYLESKKIIKVNLPKYLEYAANIPKSTKCNPSSQYQKVKEWVDPVREIMFELHSKSFQRVEYFNKYKEKLLKNGGQLAYFDKKSKEMYAKRLTLFRKMSKETLPYVTLFIEGRDLPSVLAKYGF

Essential for respiratory growth and required for mitochondrial protein synthesis. Required for vacuolar acidification (By similarity).

C8Z7X8

IRC6_YEAS8

Increased recombination centers protein 6

MVLQYPQNKILVLSDHPHNFSKTQFLQDLFHCSSTGISIVKDQTWENRYYKVHFDLYIDSCKDIPVWVEEFITPECEPLRNVMAGIILITDIRQTKPQELLHQFMIAAHRNTFVVLVNVNEEVEQDEIDELNEIWSNAFTNVIEFVNWKRSKPTVNHNDYGEKLGLDRIQEIIDTHDWLNCEVLPATKIREEIPNEMPLEQIIRNLQSARLKYKSIENSSEADAFANEMADELSRYL

Involved in gross chromosomal rearrangements (GCRs) and telomere healing.

C8ZAJ0

RGI2_YEAS8

Respiratory growth induced protein 2

MTKKDKKAKGPKMSTITTKSGESLKVFEDLHDFETYLKGETEDQEFDHVHCQLKYYPPFVLHDAHDDPEKIKETANSHSKKFVRHLHQHVEKHLLKDIKTAINKPELKFHDKKKQESFDRIVWNYGEETELNAKKFKVSVEVVCKHDGAMVDVDYRTEPLQPLI

Involved in the control of energetic metabolism and significantly contribute to cell fitness, especially under respiratory growth conditions.

C8ZC77

MTC2_YEAS8

Maintenance of telomere capping protein 2

MGDHNLPDFQTCLKFSVTAKKSFLCMYRDSVSKEKLASSMPSTCDIQLKRAINDAYPGGGIKVTVLNSTTASLDSLATTHVKEFEIVIIPDINSLLQPDQAKLVKIMRDCTVAIEKAQSTRIFIGVVHWNNPVQPSGAAKDGDEAGKPAPKTRIFLPTSLRMGAWLKHKFWFACAPPYLDFESSTESSINTRANNSIGMAEEEKQEPESKRSIILNEEANLNDVFVGSTVRRYILDIMVHLRTHRLTYNAKAGGVYTNSLDDVVLLSRLIGLHSGKMFVSPSHVKEASRWYFPMHLELVQRSSMDSSLLYGSDPNLVDEMLEKLAKIKCEEVNEFENPLFLESLVVKNVLSKVVPPV

May be involved in telomere capping.

C8ZCU0

IRC19_YEAS8

Increased recombination centers protein 19

MRKPSITITTAKAIITPDYTLIKSHSKYQLPSRFQKLDADSPERSTVVKLFYRRFMRLKPFISNVKMVKDTYRDYVRYKFMKENYELKRYLVFNPDGLRSKIKLELLSNTKCCERIVPVTEMQRTLEFVLKSCSYLPETKVQKWDIARDNTYCRQILKNLLTMQYEKYRSILHRGIGHDELDVKFSHLKTTSSPLTKLNKTEKKKIPLFKVFSDFDTTLIYLNETLGTRL

Involved in sporulation and maintenance of the mitochondrial DNA. Is probably involved in a pathway contributing to genomic integrity (By similarity).

C8ZD75

LCL2_YEAS8

Long chronological lifespan protein 2

MSQSRWSIVLIFALFIFGSTGVNAFFNFGHHQQQQQQQQQSYEDQVLNNPCDGYLCPDTLTCVAQQKDCPCPFPKSQLKCVLPDNKFVCISKPATHNEKFRAIYDDPVKGPKAKNKGFRDCGWVSDAYKNH

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

C8ZEW0

SPG4_YEAS8

Stationary phase protein 4

MGSFWDAFAVYDKKKHADPSVYGGNHNNTGDSKTQVMFSKEYRQPRTHQQENLQSMRRSSIGSQDSSDVEDVKEGRLPAEVEIPKNVDISNMSQGEFLRLYESLRRGEPDNKVNR

Stationary phase-essential protein not required for growth on nonfermentable carbon sources.

C8ZHZ1

CRS5_YEAS8

Metallothionein-like protein CRS5

MTVKICDCEGECCKDSCHCGSTCLPSCSGGEKCKCDHSTGSPQCKSCGEKCKCETTCTCEKSKCNCEKC

Critical role in copper (specific) homeostasis and detoxification. May protect by directly chelating and sequestering copper ions (By similarity).

C8ZJD8

RRG8_YEAS8

Required for respiratory growth protein 8, mitochondrial

MGLPKSAYKKLLIDCPTRVINKNCAQRVKDVSPLITNFEKWSDKRKKLYFKDEEEMVGHFHLENFNLKNNLYGRLLASPMRAEKISKLKSCRELLIPLKVVPSTGKDQHADKDKLKLVPTLDYSKSYKSSYVLNSASIVQDNLAAATSWFPISVLQTSTPKSLEVDSSTFITEYNANLHAFIKARLSVIPNVGPSSINRVLLICDKRKTPPIEIQVVSHGKGLPITQSVFNLGYLHEPTLEAIVSKDAVTKGIYLDADNDKDLIKHLYSTLLFQSVN

Required for respiratory activity and maintenance and expression of the mitochondrial genome.

C9SNH6

LCL2_VERA1

Long chronological lifespan protein 2

MRALTSLSVVLLALISTVSAQFGFFEQMFGGQQQGQQQRPQNVPSDSAAYRQQYDRSYCEHYLCPDTLACVHYPHHCPCPWPMNEDKFELSEGQRICVSKGGFAANEAARKVELARKGLL

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

D0UFC9

M1_QRFVE

Probable matrix protein

MACHTGNRRFPSVEELSLGMAQMTLLGTPVSSGTFDSVETLADRMGELKINDKSKVAGLTSVWVASRYNPFQGGALFKSHLRCNSLKKIIYRTDRNKCVKTAKVYLDRGGPPQAEDWEKLFECAIGLLAKQDWGDSQFREETALRLVVAAGGGVKRDACSAGTGGTEEGDSDTEEEPLEKVMERATKRIIEETARLSKRRRPEALEAALELRDSFKILSAQGGPFSKLSKDEKTRWVTAFSKCLQPILDLNEGRLLYDYVKQVGSK

May play a role in virion budding and release by binding the ribonucleocapsid and the host membrane.

D0ZV07

ORGA_SALT1

Oxygen-regulated invasion protein OrgA

MIRRNRQMNRQPLPIIWQRIIFDPLSYIHPQRLQIAPEMIVRPAARAAANELILAAWRLKNGEKECIQNSLTQLWLRQWRRLPQVAYLLGCHKLRADLARQGALLGLPDWAQAFLAMHQGTSLSVCNKAPNHRFLLSVGYAQLNALNEFLPESLAQRFPLLFPPFIEEALKQDAVEMSILLLALQYAQKYPNTVPAFAC

Oxygen-regulated protein required for bacterial internalization.

D3NXD9

COWN_AZOS1

N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)

MDSFDAPDRYVSFKGIDCEGNSRRIIDRLHMHIDDPAKTNAFWERFRAKLAIAEDPLKRQADGLCLLCANIYYIADLFEEHDDEDGLAMLRQLEDECC

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}.

D3QLG0

LPMG_ECOCB

mgtA leader peptide (Regulatory leader peptide for mgtA)

MEPDPTPLPRRRLKLFR

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).

D3RQU0

COWN_ALLVD

N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)

MSQAAVKIDRYITFEGIECDEQARRVLDCIRDCIEAPEASSWSAYFERKLDEITRMGQDELFVVGSQVNYIRALFEHHGHREGLDLLDRIEDECC

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}.

D3WAC0

TERS_BPLP2

Terminase small subunit (Gene product 1) (gp1)

MQTQKGGRPTILPKMYEEPLFSQIIDKIESGCNDREIYTSLHCSAKTFRKWRDDNIKAYDEAKSIARGNLLELAESALASKLTVRTLKETETIYDADGNVEKVKVKEKELDKDSLVAMMVAKAGNPELYNPTEWRRLQQEESSAHDLKAKIEELDDYKLSKYKTPEIEVPEGFE

Probable terminase small subunit. The terminase lies at a unique vertex of the procapsid and is composed of two subunits, a small terminase subunit and a large terminase subunit. Both terminase subunits heterooligomerize and are docked on the portal protein to form the packaging machine. Once the capsid is packaged with the DNA, the terminase complex is substituted by the connector proteins gp15.

D4G3R3

WAPI_BACNB

Immunity protein WapI

MKFFKRYNIDQKTLDEFKKYYVLLHGPFPNDMYDFEEETNTSLDEFYEFFALITGSLNYIIEDKKIPRYQREMLKKTFYEHYPHFRNYKSDILKYQELSECLEFHEKIRILINKLITGG

Immunity protein component of a toxin-immunity protein module, which functions as a cellular contact-dependent growth inhibition (CDI) system. Neutralizes the tRNase activity of cognate toxin WapA upon expression in E.coli. Does not inhibit WapA from other strains of B.subtilis. The WapA C-terminus cannot be expressed on its own in E.coli, however it can be cloned in the presence of its cognate immunity protein gene. Cell contact is probably necessary for growth inhibition.

D4H539

COWN_DENA2

N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)

MCNCKKNIKVDESYVSFKDIDCFENACLVIDNLLRILKEPKNTNAYWEKFIEKIPEAYYTRDSKKDPSEALLYLVCSCTSNIMELFEEIDDEEAIDAMSKCEQECC

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}.

D5ANI6

COWN_RHOCB

N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)

MNDQTPDRYVTFMGIACDTNADRLCEMLAARMAGNDSRWVAYFEKKLAENAQMGHDRLRFIGAQVNALMSFFEEEDDEAALALLWHIEHHCL

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}.

D5V2I8

COWN_ARCNC

N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)

MSNFEIRVNESYESFKNIDCFENACVVIDNMLRVLENPKNMNIYWKKIVPMIPKAYYDRDPKSDTKEELLYLVCSNSFYLDELFEKAEDEQAINALSKCEQECC

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}.

D6RMH5

LCL2_COPC7

Long chronological lifespan protein 2

MSRSSLLLVFFTLFGLAAAQFQFFNDFFGGQQHHQQQQRTGASQYAAFSENVPCSHYLCPGTMDCVERPRDCPCPDVQDVKCLIPDMDSDDDEATVVCVRGGTDCSTVEKLMKRGS

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

E1B9R1

SMIP4_BOVIN

Sperm-associated microtubule inner protein 4

MIPISLPEEHRPKCEPPRVMGKGHQHYGFGGEIWPRLPKPPNSTVGEICSPYPIEHPYHTHISRGAMFPTFTSPKDLYTGIKARTQQPFPPTVPTKPYDTTVLKTRGNPYRYELLDFPMDSKKKALVWPGQRVYFDLPKCVEKNKPVFYPKPPKTFAPNTSLNSWDPITSLKEVNIQRNLEKSHWITSYNHDFTGLGPMNPLELDDYHEKEVAELTGQIGFDPEPQEKVHPALKPTRPLEGRIARLIQNQRPLEAILEQRPSSCPDCTPRVLCTFHTFVPSSTEMMALSDNIPADVTHKNQEIEEKIKEEQSLLSTYALPSCYPTKDLANTYDIKPFPKITDTKKTEDLYWRQLSLKPQLIPYCNPDHYIPYEHLNQYNVYQNPVSLSKPGILQSKPDLKTFDFEHFLSKPEQLTLNMEDDEETKPILGWIPRAGVAKPQTDLLELKNAFSKTGAQKRFHKSVLEDYKDLRDKEHLGKKHQFYGHNSYYFYN

Microtubule inner protein (MIP) part of the dynein-decorated doublet microtubules (DMTs) in flagellum axoneme. May serve to reinforce and thus stabilize the microtubule structure in the sperm flagella.

E1XTG1

CAPSD_BPSAV

Major capsid protein (Major head protein)

MTKKLVTEEMRKQWLPVLQKESEAIQPLSAENVTIRLMQNQAEWNAKNLGESDAPGSVNSTVGKWQPVLIDMAKRLAPINIAMDFFGVQPLSGPDGQIFALRARQGVGDGSTTAQARKELFMNEADSGYSGDGTVQAGDPSGFSQAEIEGSGSVVTTIGKGMPSTDAELLGTTTNPWARVGITVQKATVTAKSRGLYADYSHELRQDMMAIHGEDVDNILSDVMVTEIQAEMNREFIRTMNFSAVRFKKFGTNGVVDIAQDISGRWALEKWKFLTFMLEVEANGIGVDTRRGKGNRVLCSPNVASALAMSGMLDYAPVLQENTKLAVDPTGQTFAGVLSNGMRVYVDPYAVAEYITLAYKGATALDAGIFFAPYVPLEMYRTQGETTFSPRMAFKTRYGICANPFVQIPANQDPQVYVTADGIAQDSNPYFRKGLIKSLF

Major capsid protein that self-associates to form the icosahedral capsid.

E3I7Z1

COWN_RHOVT

N(2)-fixation sustaining protein CowN (CO weal-nitrogenase)

MSEQIDRYVSFKNIDCNARAGQMMDALQPYIQAAENPFWAYFQQKRAEFNAKGYDDLRVLHNYLPTLKELIEDDELLAQLEDLEYTCM

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}.

E3QVL2

LCL2_COLGM

Long chronological lifespan protein 2

MRFFASLPLVILALISSAQAQFGFFDQMFGGQQQQQQQPQNVPSDPSQYQQRYDGSYCENYLCPDTLACVHFPHHCPCPWPANQDKFELTEGSSRICVSKGGFAAGEAARKVELARKGLL

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

E4UUB3

LCL2_ARTGP

Long chronological lifespan protein 2

MASILRTALLGLLLFTTAQAQFQFFEQMFGGGQQHQESSGQGGNVPSDSAWYQNTYNGAQCSNYLCPGTLACVAVPHHCPCAHPKVEEKFELGEGSAICASKGGFKAGETARKIELARKGLL

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

E5A960

LCL2_LEPMJ

Long chronological lifespan protein 2

MARPYMIFAVLTAWFFGCNAQFGFFDQMFGGGGGGGQQQQQPQNVRSDSVWYQQQYEAAQCSHYLCPGTLSCVHFPHHCPCAWEGVEEKIELGEGIAICASKGGWAEGEFAKKVELARKGML

Probable component of the endoplasmic reticulum-associated degradation (ERAD) pathway.

F5HC16

UL34_HCMVM

Transcriptional regulator UL34

MNFIITTRDFSNDDSVLRAAEMRDNVAGSISKAYKGTVRAEGKKKLLLKHLPVPPGGCSRRNSNLFVFCTERDYRKFHQGIAQLKRAPAELDPHEIQQVTASIRCRLQPSLREPPTPADELQTAVSRVCALFNQLVFTAQLRHYCEHQDKVVSYARDELTKRCGEKSALGVEVHQLVALLPHERHRELCHVLIGLLHQTPHMWARSIRLIGHLRHYLQNSFLHLLMNSGLDIAQVFDGCYHSEAYRMLFQIGHTDSVSAALELSHSAAAGPPEADENNDEGEEDDDELRHSDPAPLHDSKKPRNARRPRTRVPPHEQKPEENEEEEEELFPSCKATAAFLRAEPSVSNDDGNGGERCDTLATALRHRADEEDGPLASQTSVRVAATPSPSVTSALTPVTSPITPLCI

Acts as a transcriptional repressor of the US3 gene expression through a specific DNA sequence named the transcriptional repressive element (tre).

F5HH39

UL21A_HCMVM

Uncharacterized protein UL21A

MGGSPVPQLTTVTQGLMPSVRMDFRARRPLRRLAFYAPRARRRLFQNHIHPEQRRVLVGEGDEEMLPDLPMEIDIVIDRPPQQPLPNPLVLLLDDVPPHVPGFAPYRVPRPHPMIPEEHWDQF

Required for efficient viral DNA synthesis and the late accumulation of viral IE transcripts.

G0KYB0

TRI10_TRIAR

Trichothecene biosynthesis transcription regulator TRI10 (Trichothecene biosynthesis protein 10)

MILPKRTQEKEISLLMHYLDEVFPLQFPFHERRYVGKREWLLTILASTRPVYYATLSLSLLHKEACLHEFEAELAEIWQKEKMRYYILALQESQQQLDALDTAYGIAKMKGNIHALASTLQLISFESSSLSKGDWQLHLRAGTSLIPVLIDGWAVALKSDKVASSSSLWTELDASDFNATHDEDSLSYEYVGALKFFANVLAMFGIFSCISIGPSSPFMEYRFLMDQAGLIQMDQIMGCRNWAMLAILEIGTLDKWKREEQENRRLSLKALTSRAMAIEGVLESGLREASGSALVDLITSIYATSALTYLHTVVSGLNPNLSEVQESVAATIVLLKRLPDLRAAKSLVWPLGVTGCMASRSQEDFFRGLIISAGATPRALRNCWGLMKVWEDTWKMREYMSKQPPERWEEVVSGQGPPMLLM

Transcriptional activator of all of the trichothecene biosynthesis genes. Acts upstream of the cluster-encoded transcription factor TRI6 and is necessary for full expression of both the other trichothecene genes and the genes for the primary metabolic pathway that precedes the trichothecene biosynthetic pathway.

G2K048

HRCA_LISM4

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}.

G2TRS2

STEEP_SCHPO

ER exit protein

MSNQGKDSFKAYSYFCPCGQLFLTIHVSLTRLPQRQLDKRHVVDEKLNHIAHFSTGNKYYITRSDGGYEQRIQLLCRRCTLECAYALEAAPGYIYVDPTLVNEKPVTVSVSNLKE

May stimulate membrane curvature formation and subsequent endoplasmic reticulum exit site (ERES) establishment.

G4NYJ5

WAPI_BACS4

Immunity protein WapI

MILSSFLKIERMSSMHELKFRDLNVEVNEEDTVLLSMTESEIIVLTKKEIDYGAKYINHIVLYCNTDGRFLNSFSIQTNEQVINVQKVDDSFLFLIDKEYEDSVRDVEPNIYLWNPIEGFHQSFYAGRYINSMIIDQNKNLWVGYDETGIFSCVDQEISTRGINKFVLKNGKYELYFHGVSSYVIDQYFSTFVSEDAIYLYYRSMGEDYLQKLNLLGETLERVEVGIECSSCIKNGSSIYLFSRDDDSYNIEKVFKTNDMQNYVEQKISNENNGESLCFTQVASYKDKVAGIDHNNKLFLLNNQSL

Immunity protein component of a toxin-immunity protein module, which functions as a cellular contact-dependent growth inhibition (CDI) system. Neutralizes the tRNase activity of cognate toxin WapA upon expression in E.coli. Does not inhibit WapA from other strains of B.subtilis. The WapA C-terminus cannot be expressed on its own in E.coli, however it can be cloned in the presence of its cognate immunity protein gene. Cell contact is probably necessary for growth inhibition.

G9M952

CAPSD_BPPS4

Major capsid protein (Major head protein)

MAEKSTKNETALLVAQSAKSALQDFNHTYSKSWTFGDKWDNSNTMFETFVNKFLFPKINETLLIDIALGNRFNWLAKEQDFIGQYSEEYVIMDTVPINMDLSKNEELMLKRNYPRMATKLYGSGIVKKQKFTLNNNDTRFNFQTLADATNYALGVYKKKISDINVLEEKEMRAMLVDYSLNQLSESNVRKATSKEDLASKVFEAILNLQNNSAKYNEVHRASGGAIGQYTTVSKLKDIVILTTDSLKSYLLDTKIANTFQVAGIDFTDHVISFDDLGGVFKVTKDIVVSSDESVNFLRAYGDYQTHKGDTIPVGSVFTYDVSKLSEFKDSVEEIKPKSDLYAFILDINSIKYKRYTKGMLKQPFYNGEFDEVTHWIHYYSFKAISPFFNKILITDQDVTPRTE

Assembles to form an icosahedral capsid. {ECO:0000305|Ref.2}.

G9M973

CAPSD_BPPSP

Major capsid protein (Major head protein)

MAEKSTKNETALLVAQSAKSALQDFNHTYSKSWTFGDKWDNSNTMFETFVNKFLFPKINETLLIDIALGNRFNWLAKEQDFIGQYSEEYVIMDTVPINMDLSKNEELMLKRNYPRMATKLYGSGIVKKQKFTLNNNDTRFNFQTLADATNYALGVYKKKISDINVLEEKEMRAMLVDYSLNQLSESNVRKATSKQDLASKVFEAILNLQNNSAKYNEVHRASGGAIGQYTTVSKLKDIVILTTDSLKSYLLDTKIANTFQVAGIDFTDHVISFDDLGGVFKVTKDIVVSSDESVAFLRAYGDYQTHKGDTIPVGSVFTYDVSNLSEFKSNVEEIKPKSDLYAFILDINSIKYKRYTKGMLKQPFYNGEFDEVTHWIHYYSFKAISPFFNKILITDQDVTPRTE

Assembles to form an icosahedral capsid.

I1R9A8

GRA5_GIBZE

Gramillins biosynthetic cluster protein FGSG_00039

MHLDHKLPWKTIASHFTLARDGSSPNYNLIALGLSTQDAALGHFSRIFIATIEEFSNTETSKINLNQVDGKLFSDDVLNFPEHHFGLGPHDTNSALNNPLDAKHQELKYWKGRASTASEYGTSPEYSASYSTADGDLADAAKMLVITAAVSDNQAIRREALSALCQLSAHVPMSDLRGLSWGHGFGLSLVASEALKLYMLLNLIEAVQSRGAQQVSLLRVKILLCALGNYSLQNYDFPAQNIPHRAFWHSLGITESWADRQADGVRESDEPVVDPLGLGDDEIHQEARINLKKYLKDCFAILYVYDVFLKQIASEEERKEFWSYEINRVILYL

Part of the gene cluster that mediates the biosynthesis of gramillins A and B, bicyclic lipopeptides that induce cell death in maize leaves but not in wheat leaves. The nonribosomal peptide synthetase GRA1 incorporates respectively a glutamic adic (Glu), a leucine (Leu), a serine (Ser), a hydroxyglutamine (HOGln), a 2-amino decanoic acid, and 2 cysteins (CysB and CysA) (Probable). The biosynthesis of 2-amino decanoic acid incorporated in gramillins could be initiated by a fatty acid synthase composed of the alpha and beta subunits FGSG_00036 and FGSG_11656 (Probable). The cytochrome P450 monooxygenase FGSG_15680 could hydroxylate the fatty acid chain (Probable). Subsequent oxidation to the ketone by the oxidoreductase FGSG_00048 and transamination by aminotransferase FGSG_00049 could form 2-amino-decanoic acid (Probable). On the other hand, FGSG_15680 could also be responsible for the HO-modified glutamine at the gamma-position (Probable). Whether hydroxylation occurs on the fully assembled product or on the Gln residue prior to assembly into the gramillins requires further proof (Probable). The thioredoxin FGSG_00043 could also be required for the disulfide-bond formation between CysA and CysB (Probable). The specific involvement of the remaining proteins from the cluster is more difficult to discern, but could have broader regulatory (FGSG_00040 and FGSG_11657) or enzymatic functions (FGSG_00044 and FGSG_00045) (Probable). The final C-domain of GRA1 does not possess the expected sequence of a termination CT domain, often implicated in macrocyclization and release of a cyclopeptidein fungal NRPs and the thioesterase FGSG_00047 may act in concert with the terminal C-domain of GRA1 to catalyze the formation of the macrocyclic anhydride and release of the products (Probable).

I6WXS6

VPB51_MYCTU

Putative antitoxin VapB51

MAKHLVDIDEQALNMARTELGTTTIKDTVNAALRQATSQRVQRVAAALDTLAAAPPEDRAEAWR

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC51.

L0TGF0

VPC50_MYCTU

Putative ribonuclease VapC50 (RNase VapC50) (EC 3.1.-.-) (Toxin VapC50)

MPCCGSLTRAPIGLCGRRTSWPRLGEPWSTASTSAPNGLTTAFAFGYNDLIAAMNNHYKDRHVLAAAVRERAEVIVTTNLKHFPDDALKPYQIKALHPDDFLLDQLDLYEEATKAVILGMVDAYIDPPFTPHSLLDALGEQVPQFAAKARRLFPSGSPFGLGVLLPFDQ

Toxic component of a type II toxin-antitoxin (TA) system. An RNase. The cognate antitoxin is VapB50.

M1L9M3

PG087_MONPV

Late transcription elongation factor OPG087

MPFRDLILFNLSKFLLTEDEESLEIVSSLCRGFEISYDDLISYFPDRKYHKYISKVFEHVDLSEELSMEFHDTTLRDLVYLRLYKYSKYIRPCYKLGDNLKGIVVIKDRNIYIREANDDLIEYLLKEYTPQIYTYSNERVPIAGSKLILCGFSQVTFMAYTTSHITTNKKVDVLVSKKCIDELVDPINYQILQNLFDKGSGTINKILRKIFYSVTGGQTP

Involved in postreplicative transcription elongation on intermediate and late genes.

O05070

VGAM_HAEIN

Mu-like prophage FluMu host-nuclease inhibitor protein gam

MATKVKSQAKLRFVSVEQVQSAIKEIGDLSREHTRLATEMNDKIGATSEHYAPKLKALKEEIEPLQKAVQEYCEANRDELTEFGKTKTANFVTGEVQWRQRPPSVAIRGAEAVMEFLQRMGFDRFIRTRQEINKEALLNEPEVAKGIAGVTIKQGLEDFVIKPFEQDAR

Protects linear double-stranded DNA of Mu genome from exonuclease degradation.

O05073

VPI_HAEIN

Mu-like prophage FluMu I protein

MKAEKTSLAVLTAQLTSPDGWQQLLPKGEFRSRDGSPTDVAHWFIDGTIAQNLIHKARQLNQDLLVDYDHETILKAKKGIDAGNVVAAGWFNADEIQWFDDETRQGLYIKPRWTPKAYQQIKDGEFAFLSAVFPYDENGTPLELRMAALTNDPGITGMQRLAVLSATLNPQENVKMPESLRKLLAKLGVEIAEGVELTEEQANTALNALETLQTDKTKADEQVATLSAKNTEVDLSQYVPKATYDAVMSQVAVLSAKTDDVEIDNHISKARNEGRAVEAEVEYLKQFGKQQGVAALSAMLEKRPQIAVLSAQQTQTTKVEKPVEKGTAVLSAADKEAAKLLGISEQDYAKELEAK

Potential protease involved in virion morphogenesis.

O05290

P13_MYCMY

Probable UPF0122 protein (p13)

MKLKNNLLEKTLELSELFKIYKELLTDKQKQYFELYIDEDLSLSEIADEFNISKTAVYDSISKTSKLLFSLETKLHLKQKQDLLISLINKIETNQIDEKQFIKSLKEVIWWKY

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 (By similarity).

O06723

YISJ_BACSU

Inner spore coat protein H-like protein

MERVHLFFHREQLKRKGTAKGLFVTDRSVSPILLTQRDRAEKASYEISWEKSLLGERTLFLNAEQDDPSLMRRRLAYCFFDQIGVPAPVASYSFLTINGQPEGIYLNIKNHQPAGKRSYGVKTADPRVPLSLFNNDSSAFLHEFFILIRTAGDDELAERIKLYLDVKLFFLWLIGNTCTNQGFYYTFCLNESGRLYVSPMETRSLAVQEWYEEDPLLTKGKTLSSRLLSIPAFRSQYHTLMKNVLKRSFTIERLSPLINEWHLDICQSAADDPFIKKSPFQIEKEQTNILREIEERQDFLQAHLARL

Involved in the assembly of several proteins in the inner and outer layer of the spore coat.

O06775

VAPB8_MYCTU

Putative antitoxin VapB8

MEKSRCHAVAHGGGCAGSAKSHKSGGRCGQGRGAGDSHGTRGAGRRYRAASAPHPLAVGAHLRDELAKRSADPRLTDELNDLAGHTLDDL

Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC8.

O06777

VAPB7_MYCTU

Putative antitoxin VapB7

MSMRLAHRLQILLDDECHRRITAVARERGVPVATVVREAIDRGLVSPAGRRKSAGRRLLDAADMSVPEPRELKQELEALRARRG

Antitoxin component of a possible type II toxin-antitoxin (TA) system. The cognate toxin is VapC7.

O06779

MAZE2_MYCTU

Probable antitoxin MazE2

MLSFRADDHDVDLADAWARRLHIGRSELLRDALRRHLAALAADQDVQAYTERPLTDDENALAEIADWGPAEDWADWADAAR

Antitoxin component of a type II toxin-antitoxin (TA) system.

O10276

VE26_NPVOP

Putative early 21.8 kDa protein

METAQPPISYAPPKRGAVCAYVRTVVTTTTVSDSGGNNEDRLTQIVAQLQRTRLNFSKLSQLQRRRVRNMQKLIRKKNSVIANLAARLTTQKKTKHFAVTIRKNVIHTTSGSEQFVRQRVLELCANGGEQVFCARRADCARDRRRVAEALATALGAGVVASAANKRFEIEDEEKLVSAKLIVQQVLHDGDHSDTCAD

This protein is required for viral late gene expression.

O10277

VE18_NPVOP

Putative early 22.7 kDa protein

MEITVTLVPINLRGAEEPERNQRFRLKPLCAAAEVCLAVKCRSPFAKFKVLISVTNFDNKHLQATVCSRHAAVCVVNAPGQREVVFDGFAKPDDEGATVPLVVGPLFAARQAGRCVRAAVDAIQRQQTVLKVFINEAYLQSAWGAVRGLFFSDNNHESDLTSNVGKFISVDPTDVGARGANSSKWVPAINYVTGRQLLTILFIFKFI

This protein is required for viral late gene expression.

O10278

VE41_NPVOP

Putative early 40.3 kDa protein

MDRVASQIYSGALPYITTMDMEDRLRNRIAAKAGAKFFKACFEAVVADKSGLFVLSGGAATACHIGDDRNVLKCLDFDYYNATQEWLQLARLQQRLQACVQDNLEILSRLAQSVRMQDDLFVVKCFQNGAFCFNGPVQARLVPCVETVRTSFNGEFDLLRFALQVELKALNGVDEYVDQKVIVDRGAAVFNVFFVNIRAMKGPLTMERCVRTLAVFGDAYRVVVSPLQSVINDQIMCLLKDIFTDKPEFRVARPKALICALFAKLPREAYDECINSHHGAEPTRRRDETVTSFCRRTLHIHGPALGCRKLVYAYFKTDSFARQMPDYVANRAIYPHTDCEMKWKEFIHFFVVAKV

This protein is required for viral late gene expression.

O10300

VP47_NPVOP

Viral transcription regulator p47

MANVSMFAQSLHYTTQFLPAVCRAHDDVLLRYNLYISGAGAQLPRRVTRTVQIDADGFVRFVFDVKVFHLERLTVVERATAGDLDDYVEVTRPELSAHDAAIFKLVCRDRWCKGDAQRLRRILQQPRVDNLIKFACNVIWERGYEDHYTIGQQLSILITTKLIQSGLDFKHQPDTAAPASVRGWQDETFEKYLLSLSSVNEIIKRHVFSKKYICLEVAAAHWRSVVQALQDEGFKLAFNAHTPHVLLICVDDDKNSMVYMLKLAHLLQTRVVNLLFATDVEFYMRANHFTFYVYNSLKFYYYCLKNKFAFESNDKMLMFLLYTIVSLEWFNKGHLNSFTLEKSELYNPLELATRRLNSIKRAAQQNRVVECDSEIGVDYVRGKRVRTGTHYGQRAVQFE

It is involved in regulating viral transcription at late times postinfection.

O10311

LEF10_NPVOP

Late expression factor 10

MTHVLSAAANDLIACVLRDNLFSADGECLRYVVCKEAGHVESVYIGEIGAAQAHSGDQNAVLDASSASDVSSSASSRRVS

Involved in late/very late gene activation.

O10319

LEF9_NPVOP

Late expression factor 9

MVSFLDRPPTEFDLILDPAKLNSAAFFSNDEFRAVLKSLIGDLKKNQRPNYFNSLVDQMINVYAHISAGEHADALVRIIDATCVVVTNLPSNVFLKKLKTNKFTDSIDYLILPHFILWDYNFVVFLNNTFNSKHENSLVDISGALQKIKLTHGVIKDQLQSKNGYAVQYSYSTFLNTASFYANVQCLNGVNEVMPPLHSVRRYFGRDVPHARAWTTRHPNISQLSTQVSDVRVNDRDTDWNVKVGLGIFPGANTDCDGDKKIITYLPRPNSLIDLECLLYGDPRYSFICFDKNRLTFVSQQIFYLHKNVEAVERLLKTMPLAFALWRIHANVKFSARLELLLRDFCLVASSNASYLLFKQLTELIKDEEMVCADEELFGLSGQFTDMVNSGAKGSAALIESTRQYARTRATDIDIVSTRATTSLNSYISSHNKVQVCGADIYHNTAVLQNLYIKNNYICYKNDDRRIASICALPSEYLFPEHLLDLFIE

Involved in late/very late gene activation.

O10340

LEF4_NPVOP

Late expression factor 4

MGADVLIEQEISYTINFSQDLLYLILDSYIKKRCAAPAERYTDLYDANNVRTRQTADSAVSVHKTNLRDERFVHWLRSSNALVPLVRRENRETAVPHDRVSRHIASLIETTVYKLDGVDVKFEHVYMQSGPADRYESTAAHKIAALKTALLGVDCARPSQNLQLGSDAVLARVRLELEFEGAAPAAASLDAFCELVVQMETLADHHNIAPCLPYTTLLDSATPRRFTREQRIAYGAQAPDSTGVKKWAFKLDGVRGRGAFRRGYCLVQTDDMQLHAACISSPFGLNNVVTFQCEVVADKIFVTDLLQVFRYKYNNRTQYECNLHDAYPINADVAVECLNRLHCAVGSVPWPGLGELRFQQFFDPPLAPTHYTTIPIDGYIVLDEQLQYAKYKWLPTVELEYDAPSGALHSIDGPLLGKTVVADLQLKHGAVYECAITDNAINVLKCRPDRIVPSKVC

Required for late and very late gene expression.

O10344

LEF5_NPVOP

Late expression factor 5

MALVKGVAQSQTRPLAFHGEQWTPRALFTVFGAFRASKDYAKLIEFLTNNFACYVKNKTFNFAGTGHLFHSLYAFVPNVSELVKERKQIRLQIDCVMRLFKNTTNDFKMYVELFAFIDAHGGAECPCLLLQQSKLNAVSFVENLNCKLFDIKPPKFKKEPFDSILSKYSLNYKALCFKKKEKCTVGCVTKRQKKMKRRQLLSDRVIYLHNKNDVLDERTLLHGPSGTSLAPCLHRYATVERQTRAGDEMVSFIRYCELCQMRA

Required for late and very late gene expression.

O10362

LEF7_NPVOP

Late expression factor 7

MEPPLKRCRLCHQALPKLPQLPFEMIDKILSHLPFDLHVDVVGASAATRLRALRRPDRLTRYHEYDLAADELFAAHWNIEAADPARPYVGQLCRSTCASAAQKFFNERVPRAAAMCMLNAPRAESDSVLTRRWNWWGLTRTLLIHEANSGRGRRPARVRVDADEACIGYHAPFCDASVFEFNAQPDHVVFVLLDDDKIELNMYGKRVYRIV

Involved in late/very late gene activation.

O10365

VP74_NPVOP

Protein p74

MAVLTAVDLTNASRYAGHMHRLEFINRWRERLPHILIDYTLRPASSDDDYYVPPNLRNRALAVKLAFSRRGCDSMSCFPFHETGVVSSQTPFAYTQTSETSVAYAQPACYHLDRAAAMREGAENEVQSAEFTYTPNNQCVLVDSTSKMYFNSPYLRTEEHTIMGVDDVPAFNVRPDPDPLFPERFKGEFNEAYCRRFGRDLINGGCSFRWWESLIGFVLGDTIYVTFKMLANNIFSELRDFDYAAPSPLLPPRPAADSNAVLAQWRAVRDRAVDWDFEKQFSEAPTLQQLGMDANGVLMQLSYTAETGFTKTPIAYSARGAVRVARESRAADRAMSDDDLEAIVASFLEEYALVFGIATDIGFDMLLTAFKAMLKKINTALIPALKRMLVGTSQRVTVRLLGETYKAALVHSMNRIAIKTLTTAAKALTRVAIKASSVVGIVLILFTLADLVLALWDPFGYNNMFPREFPDDLSRTFLTAYFETLDSNTSREIIEFLPEFFADIVETDDDATFQSLFHLLDYVAALEVNSDGQMLALDESDEIKDFDEATLVGQALASSSLYTRLEFMQYTYRQNTLLAMNKNNNKLNGVIAGLFLTNTAVALAAFIAHKELTFFVYFAIFLMLAFYYLVKEPYEYFKTVDLLF

Essential for virulence of baculovirus occlusion bodies for insect larvae.

O15602

ACTO_ENTHI

Actobindin homolog

DAKALAGIADAKLKHTETGDKSAPVIENVEIKKGDRNELLSGIKEGKELKKAETNDRSAPVIPADAKVQEDNRGALLADIQATAK

Is able to bind two actin monomers at high concentrations of G-actin.

O15926

CAPSD_CPVKS

Capsid protein (CP) (Coat protein)

MITSFESIEKKNAVYYPVDLKFVTDLSSDLSNTADGLGQAWYKISQVAVEHIILTALKINYVLNHRTLLLIYNKKVPDMDLINIIQSSIMVPRFVRDLIREILRPMHHSGITYIPDLDLSTRPTPHLLDTFYPIAEHLTRWNNVCQKLGFEMVPILPEAVQSVSLTFYSYETDELLSFDNLINLDWRIEAFGWTKHLVHNPTSEVDELGKSQTATSRKRVQEKDYECDDFRKVYERPLQNRRILGMIVYRYTCAPYTMRLGHLSPNCRFPTEKNHSETPPTSNRVLLSEQTMVHSIQKNRSKPKKVKIVTTECSADRSH

The capsid protein self-assembles to form an icosahedral capsid with a T=2 symmetry made of 120 subunits.

O18638

OAF_DROVI

Out at first protein

MAYGAPQCAQHLPPIGTPTLRQRSVSCYHFFRHSRGFLWFVLCNLLLTPNISDAQLLINVQNQGGEVIQESITSNIGEDLITLEFQKTDGTLITQLIDFRNEVQILKALVLGEEERGQSQYQVMCFATKFNKGDFISSDAMAKLRQKNPHTIRTPEEDKGRETYTMSSWVQLNRSLPITRHLQSLCAEATDATYVRDVDLKAWAELPGSSISSLEAATEKFPDALSTRCNEVSSLWAPCLCTLETCIGWYPCGLKYCKGKSVGGDTSGTQQQQQQTNYRCGIKTCRKCTQFTYYVRQKQQCLWDE

Vital for proper neuronal development and hatching.

O21869

TERS_BPLSK

Terminase small subunit (Gene product 1) (gp1)

MQTQKGGRPTILPKMYEEPLFSQIIDKIESGCNDREIYTSLHCSAKTFRKWRDDNIKAYDEAKGIARGNLLELAESALASKLTVRTLKETETIYDADGNVEKVKVKEKELDKDSLVAMMVAKAGNPELYNPTEWRRLQQEESSAHDLKAKIEELDDYKLSKYKTPEIEVPEGFE

Probable terminase small subunit. The terminase lies at a unique vertex of the procapsid and is composed of two subunits, a small terminase subunit and a large terminase subunit. Both terminase subunits heterooligomerize and are docked on the portal protein to form the packaging machine. Once the capsid is packaged with the DNA, the terminase complex is substituted by the connector proteins gp15.

O21894

SAV_BPLSK

SaV protein (Gene product 26) (Gp26)

MNYGTNNHYANEYGMELNEYFKHHFNYEELAGWYTMQVLKYLVRAGKKEGESYDKDRNKALDYAGELANLSNENELTEYTTDDIMGFAQDIADDFKQWKDERNNFKSEFTKEEIKAIDERYLEFIEEV

Involved in the sensitivity of the virus to the host AbiV system.

O22005

TFA_BPSF5

Probable tail fiber assembly protein (P37)

MSRTLDLILLCRLVQDTAHLLMRITLQWDINEMSYFYSASTNGFYSTEFHGTNIPDDAVEISESEWETLINSQGVTKMITCGENGHPVIVDRPSPTPERLALINDEKKSALIAEATNVIAPLQDAVDLGMATDDETKLLLAWEKYRVLLMRVDIKNTEWPKKPEGNK

Chaperone involved in tail fiber assembly.

O22010

VXIS_BPSF5

Excisionase

MHGMGYDSRLDRLAATSWYPFFNNVTARGEIMEPYSLTLDEACDFLKISRPTAINWIRTGRLQATRKDPTKSKSPYLTTRQACIAALQSPLHTVQVSAGDGITEERKCHSSAEVKYGTPVSHCRTVKDLNSLLEQRTKGRRQNSMTS

Excisionase and integrase are necessary for the excision of prophage from the host genome by site-specific recombination.

O22426

NO40_LOTJA

Early nodulin-40

MRFCWQKSIHGS

Modulates the action of auxin, and may function as plant growth regulator that alters phytohormone responses.

O24369

NO40_SESRO

Early nodulin-40

MKLCWQKSIHGS

Modulates the action of auxin, and may function as plant growth regulator that alters phytohormone responses.

O25156

PLPHP_HELPY

Pyridoxal phosphate homeostasis protein (PLP homeostasis protein)

MLDYRQKIDALITKIEKARTAYSRHHIVKIVAVSKNASPEAIQHYYNCSQRAFGENKVQDLKTKMHSLEHLPLEWHMIGSLQENKINALLSLKPALLHSLDSLKLALKIEKRCEILGVNLNALLQVNSAYEESKSGVVPEEALEIYSQISETCKHLKLKGLMCIGAHTDDEKEIEKSFITTKKLFDQIKNASVLSMGMSDDFELAIACGANLLRIGSFLFKE

Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis. {ECO:0000255|HAMAP-Rule:MF_02087}.

O25988

YIDD_HELPY

Putative membrane protein insertion efficiency factor

MRNNKTPFLSAIFTASIRGYQRFFSAFTPSSCRFYPTCSNYALWLLCFESPLSAMGKIAIRILSCNPFCSGGIAYPTTRLKRPSLIQSHKDSNRNFKTITFWLVPTKSHATYYIIKV

Could be involved in insertion of integral membrane proteins into the membrane. {ECO:0000255|HAMAP-Rule:MF_00386}.

O26776

BRIX_METTH

Probable Brix domain-containing ribosomal biogenesis protein

MLLTTSRKPSQRTRSFSQRLSRIMGWRYINRGKMSLRDVLIEARGPVAVVSERHGNPARITFLDERGGERGYILFNPSFEMKKPELADKAVRVSSCPPGSEGLCNLMGLEVDESSSRDAWSIRTDEEYAWVMELMDARGTPAGFKLLIRDFRVGE

Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.

O28071

VPB21_ARCFU

Putative antitoxin VapB21

MPKIIEAVYENGVFKPLQKVDLKEGERVKIKLELKVEPIDLGEPVSVEEIKKIRDGTWMSS

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC21 (Potential).

O28282

VPB18_ARCFU

Putative antitoxin VapB18

MTKTISISDDVYEMLVKIKGKRSFSEVIRELVKKEGNFDLLMVAFGTRSEEEVEKLKREMKEVEEWMQSLCNH

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC18 (Potential). {ECO:0000255|HAMAP-Rule:MF_00794}.

O28301

CUTA_ARCFU

Divalent-cation tolerance protein CutA

MHNFIYITAPSLEEAERIAKRLLEKKLAACVNIFPIKSFFWWEGKIEAATEFAMIVKTRSEKFAEVRDEVKAMHSYTTPCICAIPIERGLKEFLDWIDETVE

Involved in resistance toward heavy metals.

O28561

VPB17_ARCFU

Putative antitoxin VapB13

MGEIIEAVYQKGVLKPLRKVSLREGEIVKVEIRETKKVTGRFYAKLRELEKRIERVEGAHRELEEIRDDRY

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC17 (Potential).

O28584

VPB16_ARCFU

Putative antitoxin VapB16

MKNIMVRDEVYEKLQKMKKGRESFSDVILRLIEGRKKRGIEILERYAGSLSDSELEKIVMEERRKFRVRSFDS

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC16 (Potential). {ECO:0000255|HAMAP-Rule:MF_00794}.

O28791

Y1481_ARCFU

Putative antitoxin AF_1481

MKTISIRDDVYRKLLEMKDEEDSFSDVIEKLLKRKKTDIRRYFGVLKDSEVLDEIEKSLNARKSARFRV

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. {ECO:0000255|HAMAP-Rule:MF_00794}.

O28794

VPB15_ARCFU

Putative antitoxin VapB15

MPTKTITITLEAYERLKREKREGESFSDVIIRLTEKRRDLLEFAGKWKDSGEEIEKIILEGRKEFDKHVLS

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC15 (Potential). {ECO:0000255|HAMAP-Rule:MF_00794}.

O29159

BRIX_ARCFU

Probable Brix domain-containing ribosomal biogenesis protein

MQVLTTSRKPGRKTRRFAKVLARFFNWKYVNRGKLSLEDLAGIAERFWIISEVKGNPAILNLYERGEKTLEVSFTLSNVNKIKMDDSPAVFKGKAPIDPLVFGAIPQTKAGLKLTRKVEFRKKVVVKGDEWLFFYDDEMLFKLRILKISRSSR

Probably involved in the biogenesis of the ribosome. {ECO:0000255|HAMAP-Rule:MF_00699}.

O29170

Y1095_ARCFU

Putative antitoxin AF_1095

MPKIIEAIYENGVFKPLQKVDLKEGERIKLRIEEGILDVIKKYQGKFKLTEKDIEKFLEERR

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.

O29173

VPB13_ARCFU

Putative antitoxin VapB13

MPKIIEAIYENGVFKPLQKVDLKEGERVRVVVSEVVAKTRGLLKGCEMEEIIEEIESEGFL

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC13 (Potential).

O29175

Y1090_ARCFU

Putative antitoxin AF_1090

MPKIIEAVYENGVFKPLQKVDLREGEKVKIIAGNLVERLRKYRVKVDSDIVAEFISERR

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.

O29178

Y1087_ARCFU

Putative antitoxin AF_1087

MPKIIEAVYENGVFKPLQKVDLKEGEKIRLRIEEGIADVIKEFSRKVDQDVLEEFLRERR

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.

O29181

Y1084_ARCFU

Putative antitoxin AF_1084

MPKIIEAIYENGVFKPLQKVDLKEGEKIRILLKKIDVEKFIMAKLPEEKIRELERRFEDENLY

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.

O29184

Y1079_ARCFU

Putative antitoxin AF_1079

MPKIIEAVYENGVFKPLQKVDLREGERE

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.

O29189

Y1074_ARCFU

Putative antitoxin AF_1074

MPKIIEAIYENGVFKPLQKVDLKEGERVRIKLEKVEEVVDEVFGILKGKDTLKALRELEEWGFC

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system.

O29926

VAPB7_ARCFU

Putative antitoxin VapB7

MPKVIEAVYENGVFKPLQKVDLKEGEKVKVELKESVVESVAGILKVSDEKVKKALEMIEYGEDIY

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC7 (Potential).

O29929

VAPB5_ARCFU

Putative antitoxin VapB5

MPKIIEAIYENGVFKPLQKVNFRPGSKVRIVIQEDKKEILRKYKGVFGKAEVEELREYEGEVML

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC5 (Potential).

O29931

VAPB4_ARCFU

Putative antitoxin VapB4

MPKIIEAIYENGVFKPLQKVDLKEGEKAKIVLESISDKTFGILKASETEIKKVLEEIDDFWGVC

Possibly the antitoxin component of a type II toxin-antitoxin (TA) system. Its cognate toxin is VapC4 (Potential).