thrombomodulin; TM; fetomodulin; CD141 (THBD, THRM)
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Function
- specific endothelial cell receptor
- forms a 1:1 stoichiometric complex with thrombin
- thrombin-thrombomodulin complex activates protein C
- activated protein C scissions the activated cofactors of the coagulation mechanism, factor Va & factor VIIIa, thus diminishes the amount of thrombin generated
- iron & 2-oxoglutarate dependent 3-hydroxylation of Asp & Asn is (R) stereospecific within EGF domains
Thrombomodulin stimulates:
- thrombin-mediated activatation of protein C
- antithrombin III inactivation of thrombin
Thrombomodulin inhibits:
- thrombin-mediated proteolysis of fibrinogen
- thrombin-mediated proteolysis of factor V
- thrombin activation of platelets
Structure
- N-glycosylated
- contains 1 C-type lectin domain
- contains 6 EGF-like domains
Compartment
membrane
Expression
- uniquely expressed by endothelial cells
Pathology
- defects in THBD are the cause of thrombophilia due to thrombomodulin defect
More general terms
More specific terms
References
- ↑ Textbook of Biochemistry with Clinical Correlations, 3rd ed., TM Devlin (ed), Wiley-Liss, NY 1992 pg 973
- ↑ Walker FJ, Fay PJ. Regulation of blood coagulation by the protein C system. FASEB J. 1992 May;6(8):2561-7. Review. PMID: https://www.ncbi.nlm.nih.gov/pubmed/1317308