2any
From Proteopedia
Contents |
Expression, Crystallization and the Three-dimensional Structure of the Catalytic Domain of Human Plasma Kallikrein: Implications for Structure-Based Design of Protease Inhibitors
Template:ABSTRACT PUBMED 16199530
Disease
[KLKB1_HUMAN] Defects in KLKB1 are the cause of prekallikrein deficiency (PKK deficiency) [MIM:612423]; also known as Fletcher factor deficiency. This disorder is a blood coagulation defect.
Function
[KLKB1_HUMAN] The enzyme cleaves Lys-Arg and Arg-Ser bonds. It activates, in a reciprocal reaction, factor XII after its binding to a negatively charged surface. It also releases bradykinin from HMW kininogen and may also play a role in the renin-angiotensin system by converting prorenin into renin.
About this Structure
2any is a 1 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
- Tang J, Yu CL, Williams SR, Springman E, Jeffery D, Sprengeler PA, Estevez A, Sampang J, Shrader W, Spencer J, Young W, McGrath M, Katz BA. Expression, crystallization, and three-dimensional structure of the catalytic domain of human plasma kallikrein. J Biol Chem. 2005 Dec 9;280(49):41077-89. Epub 2005 Sep 30. PMID:16199530 doi:10.1074/jbc.M506766200
Categories: Homo sapiens | Plasma kallikrein | Estevez, A. | Jeffery, D. | Katz, B A. | McGrath, M E. | Sampang, J. | Shrader, W. | Spencer, J R. | Sprengeler, P A. | Springman, E. | Tang, J. | Williams, S R. | Young, W B. | Yu, C L. | Blood clotting | Hydrolase | Mutagenically deglycosyalted human plasma kallikrein protease domain | Trypsin-like serine protease