The protease inhibitor chagasin of Trypanosoma cruzi adopts an immunoglobulin-type fold and may have arisen by horizontal gene transfer

• Autor(a) principal: Rigden, Daniel John
• Data de Publicação: 2001
• Outros Autores: Monteiro, Ana Carolina dos Santos, Sá, Maria Fatima Grossi de
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UCB
• Texto Completo: http://twingo.ucb.br:8080/jspui/handle/10869/593; https://repositorio.ucb.br:9443/jspui/handle/123456789/7770
• topic: Chagasin; Protease inhibitor; Immunoglobulin-like domain; Threading; Horizontal gene transfer; Trypanosoma cruzi

Abstract Chagasin, a protein from Trypanosoma cruzi, is the first member of a new family of cysteine protease inhibitors. Despite its lack of significant sequence identity with known proteins, convincing structural models, using variable light chain templates, could be constructed on the basis of threading results. Experimental support for the final structure came from inhibition data for overlapping oligopeptides spanning the chagasin sequence. Chagasin therefore exemplifies a new protease inhibitor structural class and a new natural use for an immunoglobulin-like domain. Limited sequence resemblance suggests that chagasin may represent the result of a rare horizontal gene transfer from host to parasite. ß 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.