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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial
Summary
- UniProt ID
- Q16836
- Gene Symbol
-
- HADH
- HAD
- HAD1
- HADHSC
- SCHAD
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q16836
- PubChem
- Q16836
- SwissLipids
- The Human Metabolome Database
- HMDBP00381
- The O-GlcNAc Database
- Q16836
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Disease variant
- Fatty acid metabolism
- Hydroxylation
- Mitochondrion
- NAD
- Oxidoreductase
- Reference proteome
- Transferase
- Transit peptide
- Gene Ontology (GO)
| GO Term |
|---|
| mitochondrion |
| mitochondrial matrix |
| nucleoplasm |
| cytoplasm |
| GO Term |
|---|
| identical protein binding |
| 3-hydroxyacyl-CoA dehydrogenase activity |
| NAD+ binding |
| transferase activity |
Sequence
MAFVTRQFMRSVSSSSTASASAKKIIVKHVTVIGGGLMGAGIAQVAAATGHTVVLVDQTEDILAKSKKGIEESLRKVAKKKFAENLKAGDEFVEKTLSTIATSTDAASVVHSTDLVVEAIVENLKVKNELFKRLDKFAAEHTIFASNTSSLQITSIANATTRQDRFAGLHFFNPVPVMKLVEVIKTPMTSQKTFESLVDFSKALGKHPVSCKDTPGFIVNRLLVPYLMEAIRLYERGDASKEDIDTAMKLGAGYPMGPFELLDYVGLDTTKFIVDGWHEMDAENPLHQPSPSLNKLVAENKFGKKTGEGFYKYK
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Beta oxidation of butanoyl-CoA to acetyl-CoA | Homo sapiens |
| Beta oxidation of decanoyl-CoA to octanoyl-CoA-CoA | Homo sapiens |
| Beta oxidation of hexanoyl-CoA to butanoyl-CoA | Homo sapiens |
| Beta oxidation of lauroyl-CoA to decanoyl-CoA-CoA | Homo sapiens |
| Beta oxidation of octanoyl-CoA to hexanoyl-CoA | Homo sapiens |
| Mitochondrial protein degradation | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0014667 | disease of metabolism | |
| DOID:0050572 | cone-rod dystrophy | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0050782 | Zollinger-Ellison syndrome | |
| DOID:0060262 | gallbladder disease | |
| DOID:0070215 | familial hyperinsulinemic hypoglycemia 4 | |
| DOID:0070218 | familial hyperinsulinemic hypoglycemia 2 | |
| DOID:0070219 | familial hyperinsulinemic hypoglycemia 1 | |
| DOID:0080108 | myoglobinuria | |
| DOID:0080326 | familial hypertrophic cardiomyopathy |
