Literature DB >> 2381905

Comparative modeling methods: application to the family of the mammalian serine proteases.

J Greer1.   

Abstract

Comparative modeling methods are described that can be used to construct a three-dimensional model structure of a new protein from knowledge of its sequence and of the experimental structures and sequences of other members of its homology family. The methods are illustrated with the mammalian serine protease family, for which seven experimental structures have been reported in the literature, and the sequences for over 35 different protein members of the family are available. The strategy for modeling these proteins is presented, and criteria are developed for determining and assigning the reliability of the modeled structure. Criteria are described that are specially designed to help detect cases in which it is likely that the local structure diverges significantly from the usual conformation of the family.

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Year:  1990        PMID: 2381905     DOI: 10.1002/prot.340070404

Source DB:  PubMed          Journal:  Proteins        ISSN: 0887-3585


  70 in total

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8.  Simultaneous modeling of multiple loops in proteins.

Authors:  D Rosenbach; R Rosenfeld
Journal:  Protein Sci       Date:  1995-03       Impact factor: 6.725

9.  Three-dimensional structure of human basic fibroblast growth factor, a structural homolog of interleukin 1 beta.

Authors:  J D Zhang; L S Cousens; P J Barr; S R Sprang
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10.  Prediction of the three-dimensional structures of the nerve growth factor and epidermal growth factor binding proteins (kallikreins) and an hypothetical structure of the high molecular weight complex of epidermal growth factor with its binding protein.

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Journal:  Protein Sci       Date:  1993-08       Impact factor: 6.725

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