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MIRAGE
Extracellular serine/threonine protein kinase FAM20C
Summary
- UniProt ID
- Q8IXL6
- Gene Symbol
-
- DMP4
- FAM20C
- Gene ID
- 56975
- Organism
- Homo sapiens (human)
External Links
- GlyConnect
- GlyGen
- Q8IXL6
- PubChem
- Q8IXL6
- The Human Metabolome Database
- HMDBP07650
- Re-Glyco
- Q8IXL6
Annotation
- Keyword
-
- 3D-structure
- ATP-binding
- Alternative splicing
- Biomineralization
- Calcium
- Direct protein sequencing
- Disease variant
- Disulfide bond
- Endoplasmic reticulum
- Glycoprotein
- Golgi apparatus
- Manganese
- Metal-binding
- Phosphoprotein
- Reference proteome
- Secreted
- Serine/threonine-protein kinase
- Signal-anchor
- Transmembrane helix
- Gene Ontology (GO)
| GO Term |
|---|
| extracellular space |
| Golgi membrane |
| nucleoplasm |
| endoplasmic reticulum lumen |
| Golgi apparatus |
| extracellular exosome |
Sequence
MKMMLVRRFRVLILMVFLVACALHIALDLLPRLERRGARPSGEPGCSCAQPAAEVAAPGWAQVRGRPGEPPAASSAAGDAGWPNKHTLRILQDFSSDPSSNLSSHSLEKLPPAAEPAERALRGRDPGALRPHDPAHRPLLRDPGPRRSESPPGPGGDASLLARLFEHPLYRVAVPPLTEEDVLFNVNSDTRLSPKAAENPDWPHAGAEGAEFLSPGEAAVDSYPNWLKFHIGINRYELYSRHNPAIEALLHDLSSQRITSVAMKSGGTQLKLIMTFQNYGQALFKPMKQTREQETPPDFFYFSDYERHNAEIAAFHLDRILDFRRVPPVAGRMVNMTKEIRDVTRDKKLWRTFFISPANNICFYGECSYYCSTEHALCGKPDQIEGSLAAFLPDLSLAKRKTWRNPWRRSYHKRKKAEWEVDPDYCEEVKQTPPYDSSHRILDVMDMTIFDFLMGNMDRHHYETFEKFGNETFIIHLDNGRGFGKYSHDELSILVPLQQCCRIRKSTYLRLQLLAKEEYKLSLLMAESLRGDQVAPVLYQPHLEALDRRLRVVLKAVRDCVERNGLHSVVDDDLDTEHRAASAR
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 37 |
|
|||
| 41 |
|
|||
| 47 |
|
|||
| 65 |
|
|||
| 74 |
|
|||
| 75 |
|
|||
| 87 |
|
|||
| 101 | N-linked (GlcNAc...) asparagine | |||
| 147 |
|
|||
| 148 |
|
G57321FI
G43417UB
G83460ZZ
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Post-translational protein phosphorylation | Homo sapiens |
| Regulation of IGF Activity by IGFBP | Homo sapiens |
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:2187 | amelogenesis imperfecta |
