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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Structural studies of BmooMP alpha-I, a non-hemorrhagic metalloproteinase from Bothrops moojeni venom

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Author(s):
Akao, P. K. [1, 2] ; Tonoli, C. C. C. [2] ; Navarro, M. S. [2] ; Cintra, A. C. O. [3] ; Neto, J. R. [1] ; Arni, R. K. [1, 4] ; Murakami, M. T. [2]
Total Authors: 7
Affiliation:
[1] UNESP, IBILCE, Dept Phys, Sao Jose Do Rio Preto, SP - Brazil
[2] Brazilian Synchrotron Light Lab, Ctr Struct Mol Biol, BR-13083970 Campinas, SP - Brazil
[3] USP, FCFRP, Dept Clin Toxicol & Bromatol Anal, Ribeirao Preto - Brazil
[4] Butantan Inst, CAT CEPID, Ctr Appl Toxicol, Sao Paulo - Brazil
Total Affiliations: 4
Document type: Journal article
Source: Toxicon; v. 55, n. 2-3, p. 361-368, FEB-MAR 2010.
Web of Science Citations: 24
Abstract

Hemostatically active snake venom metalloproteinases (SVMPs) perturb the blood coagulation cascade at specific points and due to their potential application as thrombolytic agents, the fibrin(ogen)olytic non-hemorrhagic SVMPs have been employed as biochemical tools in coagulation research and diagnosis. Structural studies complemented by the design of metalloproteinase inhibitors have been instrumental in understanding their stereo specificity and action mechanism. We present here, details of the crystal structure of BmooMP alpha-I, a 22.6 kDa non-hemorrhagic P-I class SVMP isolated from Bothrops moojeni venom, determined at 1.76 angstrom resolution. In this structure, the catalytic zinc ion displays an unusual octahedral coordination formed by the three canonical histiclines (His(142), HiS(146) and His(152)) and additionally, by three solvent molecules. Comparative sequence and structural studies indicate that the motif comprising amino acid segments 153-164 and 167-176 adjacent to the methionine-turn is a salient feature that differentiates both non and hemorrhagic P-I class SVMPs and could directly be involved in the development of the hemorrhagic activity. (C) 2009 Elsevier Ltd. All rights reserved. (AU)

FAPESP's process: 98/14138-2 - Center for Structural Molecular Biotechnology
Grantee:Glaucius Oliva
Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC