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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial
Summary
- UniProt ID
- P08559
- Gene Symbol
-
- PDHA1
- PHE1A
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P08559
- PubChem
- P08559
- The Human Metabolome Database
- HMDBP00046
- The O-GlcNAc Database
- P08559
- O-GlcNAcAtlas
- P08559
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Glucose metabolism
- Leigh syndrome
- Mitochondrion
- Oxidoreductase
- Phosphoprotein
- Pyruvate
- Reference proteome
- Thiamine pyrophosphate
- Transit peptide
- Tricarboxylic acid cycle
- Gene Ontology (GO)
| GO Term |
|---|
| glucose metabolic process |
| tricarboxylic acid cycle |
| acetyl-CoA biosynthetic process from pyruvate |
| GO Term |
|---|
| nucleus |
| nucleolus |
| mitochondrion |
| mitochondrial matrix |
| mitochondrial pyruvate dehydrogenase complex |
| pyruvate dehydrogenase complex |
| GO Term |
|---|
| pyruvate dehydrogenase (acetyl-transferring) activity |
| pyruvate dehydrogenase (NAD+) activity |
Sequence
MRKMLAAVSRVLSGASQKPASRVLVASRNFANDATFEIKKCDLHRLEEGPPVTTVLTREDGLKYYRMMQTVRRMELKADQLYKQKIIRGFCHLCDGQEACCVGLEAGINPTDHLITAYRAHGFTFTRGLSVREILAELTGRKGGCAKGKGGSMHMYAKNFYGGNGIVGAQVPLGAGIALACKYNGKDEVCLTLYGDGAANQGQIFEAYNMAALWKLPCIFICENNRYGMGTSVERAAASTDYYKRGDFIPGLRVDGMDILCVREATRFAAAYCRSGKGPILMELQTYRYHGHSMSDPGVSYRTREEIQEVRSKSDPIMLLKDRMVNSNLASVEELKEIDVEVRKEIEDAAQFATADPEPPLEELGYHIYSSDPPFEVRGANQWIKFKSVS
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 13 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Mitochondrial protein degradation | Homo sapiens |
| PDH complex synthesizes acetyl-CoA from PYR | Homo sapiens |
| Regulation of pyruvate dehydrogenase (PDH) complex | Homo sapiens |
| Signaling by Retinoic Acid | 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:10584 | retinitis pigmentosa | |
| DOID:1059 | intellectual disability | |
| DOID:10907 | microcephaly | |
| DOID:10908 | hydrocephalus | |
| DOID:10965 | spastic diplegia | |
| DOID:10968 | spastic monoplegia | |
| DOID:10969 | hemiplegia | |
| DOID:10970 | spastic quadriplegic cerebral palsy | |
| DOID:1107 | esophageal carcinoma | |
| DOID:11105 | fundus albipunctatus |
