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Structure of ribonuclease A: results of joint neutron and x-ray refinement at 2.0-.ANG. resolution

Wlodawer, Alexander, Sjoelin, Lennart·1983·Biochemistry

Abstract

The structure of ribonuclease A has been refined jointly with the neutron and X-ray data extending to 2.0 A. The results of an earlier X-ray refinement provided the starting model [Wlodawer, A., Bott, R., & Sjölin, L. (1982) J. Biol. Chem. 257, 1325-1332]. The final R factors were 0.159 (X-ray) and 0.183 (neutron) for a model containing all of the atoms expected in the protein, 128 waters, and a phosphate molecule in the active site. The joint refinement necessitated modifications in the orientation of a number of side chains, including the catalytically active lysine-41, which is now thought to form a salt link to the phosphate. Major modifications of the previous model of the bound solvent were necessary. The refinement of all atom occupancies with the neutron data only provided the information about the amide hydrogen exchange. A fourth of all amide hydrogens were found to be at least partially protected from exchange after a year of exchange with D2O.

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Authors
Wlodawer, A., & Sjoelin, L.
Venue
Biochemistry
Published
1983-05-01
Volume
22
Issue
11
Pages
2720-2728
ISSN
  • 0006-2960 (ISSN-L)
  • 1520-4995
OpenAlex
W2085260075
Cited by
171
References
0
FWCI
14.20
Type
journal article
Language
en
Open access
closed

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