Literature DB >> 2924921

Mode of binding of E-64-c, a potent thiol protease inhibitor, to papain as determined by X-ray crystal analysis of the complex.

K Matsumoto1, D Yamamoto, H Ohishi, K Tomoo, T Ishida, M Inoue, T Sadatome, K Kitamura, H Mizuno.   

Abstract

The three-dimensional structure of the E-64-c-papain complex has been determined by X-ray crystal analysis at 2.5 A resolution (conventional R = 26.9%). The structure determined indicates that: (i) the C2 atom of the oxirane ring of E-64-c is covalently bound by the S gamma atom of Cys-25 of papain; (ii) this covalent bond formation results in a configurational conversion of the oxirane C2 atom from the S- to the R-form; and (iii) extensive hydrogen bonding and hydrophobic interactions are responsible for the specific interaction of the E-64-c molecule with papain.

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Year:  1989        PMID: 2924921     DOI: 10.1016/0014-5793(89)80216-9

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  2 in total

1.  Crystal structure of papain-E64-c complex. Binding diversity of E64-c to papain S2 and S3 subsites.

Authors:  M J Kim; D Yamamoto; K Matsumoto; M Inoue; T Ishida; H Mizuno; S Sumiya; K Kitamura
Journal:  Biochem J       Date:  1992-11-01       Impact factor: 3.857

2.  Insights into the Interactions of Fasciola hepatica Cathepsin L3 with a Substrate and Potential Novel Inhibitors through In Silico Approaches.

Authors:  Lilian Hernández Alvarez; Dany Naranjo Feliciano; Jorge Enrique Hernández González; R O Soares; Rosemberg de Oliveira Soares; Diego Enry Barreto Gomes; Pedro Geraldo Pascutti
Journal:  PLoS Negl Trop Dis       Date:  2015-05-15
  2 in total

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