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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Choline/ethanolamine kinase
Summary
- UniProt ID
- Q9Y259
- Gene Symbol
-
- CHKB
- CHETK
- CHKL
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q9Y259
- PubChem
- Q9Y259
- SwissLipids
- The Human Metabolome Database
- HMDBP00777
- The O-GlcNAc Database
- Q9Y259
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Acetylation
- Alternative splicing
- Congenital muscular dystrophy
- Direct protein sequencing
- Disease variant
- Kinase
- Phospholipid biosynthesis
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| muscle organ development |
| phosphorylation |
| CDP-choline pathway |
| phosphatidylethanolamine biosynthetic process |
| GO Term |
|---|
| choline kinase activity |
| ethanolamine kinase activity |
| ATP binding |
Sequence
MAAEATAVAGSGAVGGCLAKDGLQQSKCPDTTPKRRRASSLSRDAERRAYQWCREYLGGAWRRVQPEELRVYPVSGGLSNLLFRCSLPDHLPSVGEEPREVLLRLYGAILQGVDSLVLESVMFAILAERSLGPQLYGVFPEGRLEQYIPSRPLKTQELREPVLSAAIATKMAQFHGMEMPFTKEPHWLFGTMERYLKQIQDLPPTGLPEMNLLEMYSLKDEMGNLRKLLESTPSPVVFCHNDIQEGNILLLSEPENADSLMLVDFEYSSYNYRGFDIGNHFCEWVYDYTHEEWPFYKARPTDYPTQEQQLHFIRHYLAEAKKGETLSQEEQRKLEEDLLVEVSRYALASHFFWGLWSILQASMSTIEFGYLDYAQSRFQFYFQQKGQLTSVHSSS
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 130 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Synthesis of PC | Homo sapiens |
| Synthesis of PE | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110461 | X-linked dilated cardiomyopathy | |
| DOID:0050425 | restless legs syndrome | |
| DOID:0050463 | campomelic dysplasia | |
| DOID:0050557 | congenital muscular dystrophy | |
| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | |
| DOID:0060215 | Balo concentric sclerosis | |
| DOID:0060255 | rippling muscle disease 2 | |
| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | |
| DOID:0080033 | craniometaphyseal dysplasia | |
| DOID:0080092 | myofibrillar myopathy 1 |
