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PMID: 2553124 Published · ppublish English Journal Article

The use of folding patterns in a multisolution approach of the all-beta protein three-dimensional structure. A beta-roll structure is predicted in the retroviral glycoprotein.

Biochimica et biophysica acta ·Vol. 998 ·No. 3 ·1989-10-19 ·Pages 301-9

Busetta B

Abstract

An automatic macromolecular modelling package of unknown protein structures was developed using the intimate correlation which appears between the observed X-ray structures and their associated predicted folding patterns. The method can be considered as a generalization of both the combinatorial [1] and the template identification [2,3] approaches which were proposed some years ago, and provide a fast way of selecting 'structural motifs' to build new proteins. As an illustration, the tertiary fold of the all-beta-domain of the retroviral outermembrane glycoprotein is proposed.

MeSH Terms
Amino Acid Sequence Capsid Disulfides Friend murine leukemia virus Glycoproteins Human T-lymphotropic virus 1 Human T-lymphotropic virus 2 Leukemia Virus, Bovine Membrane Glycoproteins Models, Molecular Molecular Sequence Data Moloney murine leukemia virus Peptide Hydrolases Protein Conformation Retroviridae Proteins Thermodynamics
Chemicals
Disulfides Glycoproteins Membrane Glycoproteins Retroviridae Proteins Peptide Hydrolases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Busetta B
Laboratoire de cristallographie U.A. 144, Université de Bordeaux, Talence, France.
Article Info
Journal
Biochimica et biophysica acta
Abbr.
Biochim Biophys Acta
ISSN
0006-3002
Published
1989-10-19
Pages
301-9
Language
English
Region
Netherlands
NLM ID
0217513
Subset
IM
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