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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
propionyl-CoA carboxylase subunit alpha
Summary
- Gene Symbol
-
- PCCA
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Acetylation
- Alternative splicing
- Biotin
- Direct protein sequencing
- Disease variant
- Ligase
- Lipid degradation
- Magnesium
- Manganese
- Metal-binding
- Mitochondrion
- Phosphoprotein
- Reference proteome
- Transit peptide
- Proteins
| UniProt | Protein Name |
|---|---|
| P05165 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid metabolic process |
|
|
| branched-chain amino acid metabolic process |
|
|
| short-chain fatty acid catabolic process |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol |
|
|
| catalytic complex | ||
| mitochondrial matrix | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| propionyl-CoA carboxylase activity | ||
| enzyme binding | ||
| metal ion binding | ||
| ATP binding | ||
| protein binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:1588 | thrombocytopenia | |
| DOID:1826 | epilepsy | |
| DOID:2089 | obsolete constipation | |
| DOID:2355 | anemia | |
| DOID:2361 | macrocytic anemia | |
| DOID:2723 | dermatitis | |
| DOID:2913 | acute pancreatitis | |
| DOID:299 | adenocarcinoma | |
| DOID:3650 | lactic acidosis | |
| DOID:4480 | achondroplasia |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003128 | Lactic acidosis |
| HP:0003353 | Propionyl-CoA carboxylase deficiency |
| HP:0004322 | Short stature |
| HP:0004396 | Poor appetite |
| HP:0006846 | Acute encephalopathy |
| HP:0008872 | Feeding difficulties in infancy |
| HP:0008936 | Axial hypotonia |
| HP:0010978 | Abnormality of immune system physiology |
| HP:0011675 | Arrhythmia |
| HP:0011695 | Cerebellar hemorrhage |
| Disease ID | Disease Name |
|---|---|
| ORPHA:35 |
|
| OMIM:606054 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP000403
- Gene Name
- propionyl CoA carboxylase, alpha polypeptide
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 115597071 | SPAAU10427 | ||
| 734347 | Xenbase:XB-GENE-944990 | ||
| 100493552 | Xenbase:XB-GENE-944987 | ||
| 101939034 | CHRPI13726 | ||
| 109305487 | CROPO03955 | ||
| 103812620 | SERCA01908 | ||
| 100681981 | ORNAN01585 | ||
| 100412765 | CALJA20118 | ||
| 105574441 | CERAT08415 | ||
| 699844 | MACMU17032 |
