2uwp
From Proteopedia
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FACTOR XA INHIBITOR COMPLEX
Disease
Known disease associated with this structure: Factor X deficiency OMIM:[227600]
About this Structure
2UWP is a Single protein structure of sequence from Homo sapiens with , and as ligands. Active as Coagulation factor Xa, with EC number 3.4.21.6 Known structural/functional Site: . Full crystallographic information is available from OCA.
Page seeded by OCA on Thu Feb 21 18:51:01 2008
Categories: Coagulation factor Xa | Homo sapiens | Single protein | Brown, D. | Burns-Kurtis, C L. | Chan, C. | Convery, M A. | Hubbard, J A. | Kelly, H A. | Pateman, A J. | Patikis, A. | Senger, S. | Shah, G P. | Thorpe, J H. | Toomey, J R. | Watson, N S. | Young, R J. | Zhou, P. | 894 | CA | MG | Blood coagulation | Calcium | Cleavage on pair of basic residues | Complex | Egf-like domain | Gamma-carboxyglutamic acid | Glycoprotein | Hydrolase | Hydroxylation | Polymorphism | Protease | Serine protease | Target hopping | Zymogen
