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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Choline O-acetyltransferase
Summary
- UniProt ID
- P28329
- Gene Symbol
-
- CHAT
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P28329
- PubChem
- P28329
- The Human Metabolome Database
- HMDBP00025
- The O-GlcNAc Database
- P28329
Annotation
- Keyword
-
- 3D-structure
- Acyltransferase
- Alternative splicing
- Congenital myasthenic syndrome
- Direct protein sequencing
- Disease variant
- Neurotransmitter biosynthesis
- Phosphoprotein
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| phosphatidylcholine biosynthetic process |
| neurotransmitter transport |
| neuromuscular synaptic transmission |
| acetylcholine biosynthetic process |
| GO Term |
|---|
| cytosol |
| nucleus |
| cytoplasm |
| neuron projection |
| synapse |
| GO Term |
|---|
| choline O-acetyltransferase activity |
Sequence
MGLRTAKKRGLGGGGKWKREEGGGTRGRREVRPACFLQSGGRGDPGDVGGPAGNPGCSPHPRAATRPPPLPAHTPAHTPEWCGAASAEAAEPRRAGPHLCIPAPGLTKTPILEKVPRKMAAKTPSSEESGLPKLPVPPLQQTLATYLQCMRHLVSEEQFRKSQAIVQQFGAPGGLGETLQQKLLERQEKTANWVSEYWLNDMYLNNRLALPVNSSPAVIFARQHFPGTDDQLRFAASLISGVLSYKALLDSHSIPTDCAKGQLSGQPLCMKQYYGLFSSYRLPGHTQDTLVAQNSSIMPEPEHVIVACCNQFFVLDVVINFRRLSEGDLFTQLRKIVKMASNEDERLPPIGLLTSDGRSEWAEARTVLVKDSTNRDSLDMIERCICLVCLDAPGGVELSDTHRALQLLHGGGYSKNGANRWYDKSLQFVVGRDGTCGVVCEHSPFDGIVLVQCTEHLLKHVTQSSRKLIRADSVSELPAPRRLRWKCSPEIQGHLASSAEKLQRIVKNLDFIVYKFDNYGKTFIKKQKCSPDAFIQVALQLAFYRLHRRLVPTYESASIRRFQEGRVDNIRSATPEALAFVRAVTDHKAAVPASEKLLLLKDAIRAQTAYTVMAITGMAIDNHLLALRELARAMCKELPEMFMDETYLMSNRFVLSTSQVPTTTEMFCCYGPVVPNGYGACYNPQPETILFCISSFHSCKETSSSKFAKAVEESLIDMRDLCSLLPPTESKPLATKEKATRPSQGHQP
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 366 |
|
|||
| 372 |
|
|||
| 373 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Acetylcholine Neurotransmitter Release Cycle | Homo sapiens |
| Synthesis of PC | 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:10652 | Alzheimer's disease | |
| DOID:10914 | amnestic disorder | |
| DOID:11119 | Gilles de la Tourette syndrome | |
| DOID:11771 | spontaneous ocular nystagmus | |
| DOID:14445 | chronic closed-angle glaucoma | |
| DOID:14525 | Reye syndrome | |
| DOID:3683 | lung benign neoplasm | |
| DOID:11832 | visual epilepsy | |
| DOID:11836 | clubfoot | |
| DOID:11847 | coronary thrombosis |
