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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Acetylcholinesterase
Summary
- UniProt ID
- P22303
- Gene Symbol
-
- ACHE
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P22303
- PubChem
- P22303
- The Human Metabolome Database
- HMDBP00524
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Blood group antigen
- Cell membrane
- Direct protein sequencing
- Disulfide bond
- GPI-anchor
- Neurotransmitter degradation
- Nucleus
- Reference proteome
- Secreted
- Serine esterase
- Signal
- Synapse
- Gene Ontology (GO)
| GO Term |
|---|
| osteoblast development |
| acetylcholine catabolic process |
| cell adhesion |
| nervous system development |
| synapse assembly |
| GO Term |
|---|
| plasma membrane |
| membrane |
| neuromuscular junction |
Sequence
MRPPQCLLHTPSLASPLLLLLLWLLGGGVGAEGREDAELLVTVRGGRLRGIRLKTPGGPVSAFLGIPFAEPPMGPRRFLPPEPKQPWSGVVDATTFQSVCYQYVDTLYPGFEGTEMWNPNRELSEDCLYLNVWTPYPRPTSPTPVLVWIYGGGFYSGASSLDVYDGRFLVQAERTVLVSMNYRVGAFGFLALPGSREAPGNVGLLDQRLALQWVQENVAAFGGDPTSVTLFGESAGAASVGMHLLSPPSRGLFHRAVLQSGAPNGPWATVGMGEARRRATQLAHLVGCPPGGTGGNDTELVACLRTRPAQVLVNHEWHVLPQESVFRFSFVPVVDGDFLSDTPEALINAGDFHGLQVLVGVVKDEGSYFLVYGAPGFSKDNESLISRAEFLAGVRVGVPQVSDLAAEAVVLHYTDWLHPEDPARLREALSDVVGDHNVVCPVAQLAGRLAAQGARVYAYVFEHRASTLSWPLWMGVPHGYEIEFIFGIPLDPSRNYTAEEKIFAQRLMRYWANFARTGDPNEPRDPKAPQWPPYTAGAQQYVSLDLRPLEVRRGLRAQACAFWNRFLPKLLSATDTLDEAERQWKAEFHRWSSYMVHWKNQFDHYSKQDRCSDL
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 296 | N-linked (GlcNAc...) asparagine | |||
| 381 | N-linked (GlcNAc...) asparagine | |||
| 495 | N-linked (GlcNAc...) asparagine |
|
G83460ZZ
G41247ZX
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Neurotransmitter clearance | Homo sapiens |
| Synthesis of PC | Homo sapiens |
| Synthesis, secretion, and deacylation of Ghrelin | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110639 | congenital muscular dystrophy due to integrin alpha-7 deficiency | |
| DOID:0110640 | congenital muscular dystrophy due to LMNA mutation | |
| DOID:0110667 | congenital myasthenic syndrome 5 | |
| DOID:0110892 | inflammatory bowel disease 1 | |
| DOID:0111064 | autosomal recessive distal hereditary motor neuronopathy 1 | |
| DOID:0111140 | IGSF1 deficiency syndrome | |
| DOID:0111225 | centronuclear myopathy X-linked | |
| DOID:1002 | endometritis | |
| DOID:10112 | sleeping sickness | |
| DOID:10113 | trypanosomiasis |
