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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Propionyl-CoA carboxylase alpha chain, mitochondrial
Summary
- UniProt ID
- P05165
- Gene Symbol
-
- PCCA
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P05165
- PubChem
- P05165
- The Human Metabolome Database
- HMDBP00259
- The O-GlcNAc Database
- P05165
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
- Gene Ontology (GO)
| GO Term |
|---|
| fatty acid metabolic process |
| short-chain fatty acid catabolic process |
| branched-chain amino acid metabolic process |
| GO Term |
|---|
| catalytic complex |
| mitochondrion |
| mitochondrial matrix |
| cytosol |
| GO Term |
|---|
| propionyl-CoA carboxylase activity |
| urea carboxylase activity |
| ATP binding |
| biotin binding |
| enzyme binding |
| metal ion binding |
| methylcrotonoyl-CoA carboxylase activity |
Sequence
MAGFWVGTAPLVAAGRRGRWPPQQLMLSAALRTLKHVLYYSRQCLMVSRNLGSVGYDPNEKTFDKILVANRGEIACRVIRTCKKMGIKTVAIHSDVDASSVHVKMADEAVCVGPAPTSKSYLNMDAIMEAIKKTRAQAVHPGYGFLSENKEFARCLAAEDVVFIGPDTHAIQAMGDKIESKLLAKKAEVNTIPGFDGVVKDAEEAVRIAREIGYPVMIKASAGGGGKGMRIAWDDEETRDGFRLSSQEAASSFGDDRLLIEKFIDNPRHIEIQVLGDKHGNALWLNERECSIQRRNQKVVEEAPSIFLDAETRRAMGEQAVALARAVKYSSAGTVEFLVDSKKNFYFLEMNTRLQVEHPVTECITGLDLVQEMIRVAKGYPLRHKQADIRINGWAVECRVYAEDPYKSFGLPSIGRLSQYQEPLHLPGVRVDSGIQPGSDISIYYDPMISKLITYGSDRTEALKRMADALDNYVIRGVTHNIALLREVIINSRFVKGDISTKFLSDVYPDGFKGHMLTKSEKNQLLAIASSLFVAFQLRAQHFQENSRMPVIKPDIANWELSVKLHDKVHTVVASNNGSVFSVEVDGSKLNVTSTWNLASPLLSVSVDGTQRTVQCLSREAGGNMSIQFLGTVYKVNILTRLAAELNKFMLEKVTEDTSSVLRSPMPGVVVAVSVKPGDAVAEGQEICVIEAMKMQNSMTAGKTGTVKSVHCQAGDTVGEGDLLVELE
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 655 |
|
|||
| 659 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Biotin transport and metabolism | Homo sapiens |
| Defective HLCS causes multiple carboxylase deficiency | Homo sapiens |
| Propionyl-CoA catabolism | 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:9993 | hypoglycemia | |
| DOID:0014667 | disease of metabolism | |
| DOID:0050590 | severe congenital neutropenia | |
| DOID:0050700 | cardiomyopathy | |
| DOID:0050742 | nicotine dependence | |
| DOID:0060270 | pontocerebellar hypoplasia type 2D | |
| DOID:0080199 | colorectal carcinoma | |
| DOID:0110425 | dilated cardiomyopathy 1A | |
| DOID:10534 | stomach cancer | |
| DOID:1059 | intellectual disability |
