Vitamin K-dependent protein S
| GO Term |
|---|
| blood coagulation |
| fibrinolysis |
| positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction |
| GO Term |
|---|
| endopeptidase inhibitor activity |
| calcium ion binding |
| Position | Description |
|---|---|
| 499 | Not glycosylated; in variant Heerlen |
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 91 |
|
|||
| 102 |
|
|||
| 104 |
|
|||
| 122 |
|
|||
| 499 |
|
|
||
| 509 | N-linked (GlcNAc...) asparagine |
|
||
| 530 | N-linked (GlcNAc...) asparagine |
| Pathway Name | Organism |
|---|---|
| Cell surface interactions at the vascular wall | Homo sapiens |
| Common Pathway of Fibrin Clot Formation | Homo sapiens |
| Gamma-carboxylation of protein precursors | Homo sapiens |
| Intrinsic Pathway of Fibrin Clot Formation | Homo sapiens |
| Platelet degranulation | Homo sapiens |
| Regulation of Complement cascade | Homo sapiens |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | Homo sapiens |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | Homo sapiens |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0111900 | autosomal dominant thrombophilia due to protein S deficiency | |
| DOID:0111905 | autosomal recessive thrombophilia due to protein S deficiency | |
| DOID:2451 | protein S deficiency | |
| DOID:3526 | cerebral infarction |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: August 4, 2025