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Protein Ontology report - methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant MCCB E99Q (human) PR:000026119 - http://purl.obolibrary.org/obo/PR_000026119        Annotations       Ontology Information Show OBO stanza / PAF / GPI   PRO ID PR:000026119      PRO name methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant MCCB E99Q (human)    Synonyms PRO-Short-label: EXACT: hMCCC2/var:MCCB E99Q PRO-proteoform-std: EXACT: UniProtKB:Q9HCC0, Glu-99, CHEBI:30011 NARROW: UniProtKB:Q9HCC0-1, Glu-99, CHEBI:30011   Definition "A methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant (human) that has a Gln residue at the position equivalent to Glu-99 of the amino acid sequence represented by UniProtKB:Q9HCC0-1. Example: UniProtKB:Q9HCC0-1, Glu-99, CHEBI:30011." [PMID:11181649, PRO:CNA]    PRO Category organism-sequence    Parent PR:000026117 methylcrotonoyl-CoA carboxylase beta chain, mitochondrial sequence variant (human)   Taxon NCBITaxon:9606 Homo sapiens   Term Hierarchy   Visualization DAG: OLS: Back to top Related Cross References   Db identifiers UniProtKB_VAR:VAR_012792 Back to top Functional Annotation (GO-centric view) Switch to PRO Centric View       Disease Associated GO Term Protein Forms & Complexes Evidence DO:0050710 3-methylcrotonyl-CoA carboxylase deficiency PR:000026119 hMCCC2/var:MCCB E99Q PMID:11181649