protein S

Summary
Gene Symbol
  • PROS1
Organism
Homo sapiens (human)
NCBI Gene
5627
PubChem
5627
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Calcium
  • Cleavage on pair of basic residues
  • Disease variant
  • Disulfide bond
  • EGF-like domain
  • Fibrinolysis
  • Gamma-carboxyglutamic acid
  • Glycoprotein
  • Hydroxylation
  • Proteomics identification
  • Reference proteome
  • Repeat
  • Secreted
  • Signal
  • Thrombophilia
  • Zymogen
Proteins
Displaying all 3 entries
UniProt Protein Name
A0A0S2Z4K3
P07225
A0A0S2Z4L3
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Kinase
Functional Category
  • J: Translation, ribosomal structure and biogenesis
  • K: Transcription
  • T: Signal transduction mechanisms
Displaying all 4 entries
Gene Ontology
ATP binding
kinase activity
nucleotide binding
phosphorylation
Disease
Disease Ontology
Displaying all 4 entries
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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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 7, 2025