1bus

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(New page: 200px<br /><applet load="1bus" size="450" color="white" frame="true" align="right" spinBox="true" caption="1bus" /> '''SOLUTION CONFORMATION OF PROTEINASE INHIBITO...)
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Revision as of 09:49, 20 November 2007


1bus

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SOLUTION CONFORMATION OF PROTEINASE INHIBITOR IIA FROM BULL SEMINAL PLASMA BY 1H NUCLEAR MAGNETIC RESONANCE AND DISTANCE GEOMETRY

Overview

A determination of the solution conformation of the proteinase inhibitor, IIA from bull seminal plasma (BUSI IIA) is described. Two-dimensional, nuclear Overhauser enhancement spectroscopy (NOESY) was used to obtain a, list of 202 distance constraints between individually assigned hydrogen, atoms of the polypeptide chain, to identify the positions of the three, disulfide bridges, and to locate the single cis peptide bond., Supplementary geometric constraints were derived from the vicinal, spin-spin couplings and the locations of certain hydrogen bonds, as, determined by nuclear magnetic resonance (n.m.r.). Using a new distance, geometry program (DISGEO) which is capable of computing all-atom, structures for proteins the size of BUSI IIA, five conformers were, computed from the NOE distance constraints alone, and another five were, computed with the supplementary constraints included. Comparison of the, different structures computed from the n.m.r. data among themselves and, with the crystal structures of two homologous proteins shows that the, global features of the conformation of BUSI IIA (i.e. the overall, dimensions of the molecule and the threading of the polypeptide chain), were well-defined by the available n.m.r. data. In the Appendix, we, describe a preliminary energy refinement of the structure, which showed, that the constraints derived from the n.m.r. data are compatible with a, low energy spatial structure.

About this Structure

1BUS is a Single protein structure of sequence from Bos taurus. Full crystallographic information is available from OCA.

Reference

Solution conformation of proteinase inhibitor IIA from bull seminal plasma by 1H nuclear magnetic resonance and distance geometry., Williamson MP, Havel TF, Wuthrich K, J Mol Biol. 1985 Mar 20;182(2):295-315. PMID:3839023

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