Tag | Content |
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CPLM ID | CPLM-023117 |
UniProt Accession | |
Genbank Protein ID | |
Genbank Nucleotide ID | |
Protein Name | Isobutyryl-CoA dehydrogenase, mitochondrial |
Protein Synonyms/Alias | Activator-recruited cofactor 42 kDa component; ARC42; Acyl-CoA dehydrogenase family member 8; ACAD-8 |
Gene Name | ACAD8 |
Gene Synonyms/Alias | ARC42; IBD |
Created Date | July 27, 2013 |
Organism | Homo sapiens (Human) |
NCBI Taxa ID | 9606 |
Lysine Modification | Position | Peptide | Type | References |
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144 | GNEEQRHKFCPPLCT | ubiquitination | [1] | 177 | ASLLTSAKKQGDHYI | ubiquitination | [1] | 178 | SLLTSAKKQGDHYIL | ubiquitination | [1] | 213 | RTGGPGPKGISCIVV | ubiquitination | [1] | 232 | PGLSFGKKEKKVGWN | ubiquitination | [1] | 235 | SFGKKEKKVGWNSQP | ubiquitination | [1] | 303 | RDHLNVRKQFGEPLA | ubiquitination | [1] | 345 | VALQEERKDAVALCS | ubiquitination | [1] |
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Reference | [1] Refined preparation and use of anti-diglycine remnant (K-ε-GG) antibody enables routine quantification of 10,000s of ubiquitination sites in single proteomics experiments. Udeshi ND, Svinkina T, Mertins P, Kuhn E, Mani DR, Qiao JW, Carr SA. Mol Cell Proteomics. 2013 Mar;12(3):825-31. [ PMID: 23266961] |
Functional Description | Has very high activity toward isobutyryl-CoA. Is an isobutyryl-CoA dehydrogenase that functions in valine catabolism. Plays a role in transcriptional coactivation within the ARC complex. |
Sequence Annotation | NP_BIND 158 167 FAD. NP_BIND 191 193 FAD. NP_BIND 312 313 FAD; shared with dimeric partner. NP_BIND 371 375 FAD; shared with dimeric partner. NP_BIND 400 402 FAD. REGION 274 277 Substrate binding. ACT_SITE 398 398 Proton acceptor. BINDING 167 167 Substrate; via carbonyl oxygen. BINDING 302 302 FAD; shared with dimeric partner. BINDING 399 399 Substrate; via amide nitrogen. BINDING 410 410 Substrate. |
Keyword | 3D-structure; Activator; Branched-chain amino acid catabolism; Complete proteome; Direct protein sequencing; Disease mutation; FAD; Flavoprotein; Mitochondrion; Oxidoreductase; Reference proteome; Transcription; Transcription regulation; Transit peptide. |
Sequence Source | UniProt (SWISSPROT/TrEMBL); GenBank; EMBL |
Protein Length | 415 AA |
Protein Sequence | MLWSGCRRFG ARLGCLPGGL RVLVQTGHRS LTSCIDPSMG LNEEQKEFQK VAFDFAAREM 60 APNMAEWDQK ELFPVDVMRK AAQLGFGGVY IQTDVGGSGL SRLDTSVIFE ALATGCTSTT 120 AYISIHNMCA WMIDSFGNEE QRHKFCPPLC TMEKFASYCL TEPGSGSDAA SLLTSAKKQG 180 DHYILNGSKA FISGAGESDI YVVMCRTGGP GPKGISCIVV EKGTPGLSFG KKEKKVGWNS 240 QPTRAVIFED CAVPVANRIG SEGQGFLIAV RGLNGGRINI ASCSLGAAHA SVILTRDHLN 300 VRKQFGEPLA SNQYLQFTLA DMATRLVAAR LMVRNAAVAL QEERKDAVAL CSMAKLFATD 360 ECFAICNQAL QMHGGYGYLK DYAVQQYVRD SRVHQILEGS NEVMRILISR SLLQE 415 |
Gene Ontology | GO:0005759; C:mitochondrial matrix; TAS:Reactome. GO:0003995; F:acyl-CoA dehydrogenase activity; EXP:Reactome. GO:0050660; F:flavin adenine dinucleotide binding; IEA:InterPro. GO:0009083; P:branched-chain amino acid catabolic process; TAS:Reactome. GO:0034641; P:cellular nitrogen compound metabolic process; TAS:Reactome. GO:0006629; P:lipid metabolic process; TAS:ProtInc. GO:0006355; P:regulation of transcription, DNA-dependent; IEA:UniProtKB-KW. GO:0006351; P:transcription, DNA-dependent; IEA:UniProtKB-KW. GO:0006574; P:valine catabolic process; IEA:UniProtKB-UniPathway. |
Interpro | |
Pfam | |
SMART | |
PROSITE | |
PRINTS | |