2a5m
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(New page: 200px<br /><applet load="2a5m" size="450" color="white" frame="true" align="right" spinBox="true" caption="2a5m" /> '''NMR structure of murine gamma-S crystallin f...)
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Revision as of 05:48, 21 November 2007
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NMR structure of murine gamma-S crystallin from joint refinement with SAXS data
Overview
Determination of the 3D structures of multidomain proteins by solution NMR, methods presents a number of unique challenges related to their larger, molecular size and the usual scarcity of constraints at the interdomain, interface, often resulting in a decrease in structural accuracy. In this, respect, experimental information from small-angle scattering of X-ray, radiation in solution (SAXS) presents a suitable complement to the NMR, data, as it provides an independent constraint on the overall molecular, shape. A computational procedure is described that allows incorporation of, such SAXS data into the mainstream high-resolution macromolecular, structure refinement. The method is illustrated for a two-domain, 177-amino-acid protein, gammaS crystallin, using an experimental SAXS data, set fitted at resolutions from approximately 200 A to approximately 30 A., Inclusion of these data during structure refinement decreases the backbone, coordinate root-mean-square difference between the derived model and the, high-resolution crystal structure of a 54% homologous gammaB crystallin, from 1.96 +/- 0.07 A to 1.31 +/- 0.04 A. Combining SAXS data with NMR, restraints can be accomplished at a moderate computational expense and is, expected to become useful for multidomain proteins, multimeric assemblies, and tight macromolecular complexes.
About this Structure
2A5M is a Single protein structure of sequence from Mus musculus. Full crystallographic information is available from OCA.
Reference
Refinement of multidomain protein structures by combination of solution small-angle X-ray scattering and NMR data., Grishaev A, Wu J, Trewhella J, Bax A, J Am Chem Soc. 2005 Nov 30;127(47):16621-8. PMID:16305251
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