Homo sapiens Protein: BCKDK | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-27752.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | BCKDK | ||||||||||||||||||
Protein Name | branched chain ketoacid dehydrogenase kinase | ||||||||||||||||||
Synonyms | BCKDKD; BDK; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000219794 | ||||||||||||||||||
InnateDB Gene | IDBG-27748 (BCKDK) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Catalyzes the phosphorylation and inactivation of the branched-chain alpha-ketoacid dehydrogenase complex, the key regulatory enzyme of the valine, leucine and isoleucine catabolic pathways. Key enzyme that regulate the activity state of the BCKD complex (By similarity). {ECO:0000250}. | ||||||||||||||||||
Subcellular Localization | Mitochondrion matrix. | ||||||||||||||||||
Disease Associations | Branched-chain ketoacid dehydrogenase kinase deficiency (BCKDKD) [MIM:614923]: A metabolic disorder characterized by autism, epilepsy, intellectual disability, and reduced branched- chain amino acids. {ECO:0000269PubMed:22956686}. Note=The disease is caused by mutations affecting the gene represented in this entry. A diet enriched in branched amino acids (BCAAs) allows to normalize plasma BCAA levels. This suggests that it may be possible to treat patients with mutations in BCKDK with BCAA supplementation. | ||||||||||||||||||
Tissue Specificity | Ubiquitous. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 20 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR003594
Histidine kinase-like ATPase, C-terminal domain IPR004358 Signal transduction histidine kinase-related protein, C-terminal IPR005467 Signal transduction histidine kinase, core IPR018955 Branched-chain alpha-ketoacid dehydrogenase kinase/Pyruvate dehydrogenase kinase, N-terminal |
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PFAM |
PF02518
PF13581 PF10436 |
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PRINTS |
PR00344
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PIRSF | |||||||||||||||||||
SMART |
SM00387
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | O14874 | ||||||||||||||||||
PhosphoSite | PhosphoSite-O14874 | ||||||||||||||||||
TrEMBL | H3BQP2 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 10295 | ||||||||||||||||||
UniGene | Hs.513520 | ||||||||||||||||||
RefSeq | NP_005872 | ||||||||||||||||||
HUGO | HGNC:16902 | ||||||||||||||||||
OMIM | 614901 | ||||||||||||||||||
CCDS | CCDS10705 | ||||||||||||||||||
HPRD | 12523 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AC135050 AF026548 AK130145 BC007363 BC009872 CH471192 CR542093 | ||||||||||||||||||
GenPept | AAB82714 AAH07363 AAH09872 CAG46890 EAW52160 EAW52161 EAW52162 EAW52163 | ||||||||||||||||||