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Crystallographic analysis of PheLeu substitution in the hydrophobic core of barnase

Chen, Y.-W; Fersht, A.R; Henrick, K
Acta Crystallographica Section D: Biological Crystallography , Volume 51 (2): 220 International Union of CrystallographyMar 1, 1995

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Crystallographic analysis of PheLeu substitution in the hydrophobic core of barnase

Abstract

The crystal structure of a barnase mutant, PheLeu7 has been determined to 2.2 A resolution. No structural rearrangement is observed near the mutated residue. The F7L mutation is highly destabilizing and this is caused by the loss of extensive van der Waals contacts that wild-type Phe7 made with its neighbouring residues, and the exposure of a large hydrophobic pocket on the surface of the protein. The side-chain conformations of the mutated Leu7 residue have torsion angles 1 ranging from -138Degrees to -168Degrees and 2 ranging from +16Degrees to +70Degrees, for the three molecules in the asymmetric unit. These angles do not agree with the most frequently observed conformations in the protein side-chain rotamer library Ponder & Richards (1987). J. Mol. Biol. 193, 775-791 . However, when compared to a more recent `backbone-dependent' rotamer library Dunbrack & Karplus (1993). J. Mol. Biol. 230, 543-574, the side-chain conformation of Leu7 agrees well with that of the most frequently observed rotamers. The side-chain conformation of Leu7 was found to be dictated by two factors: it has the lowest conformational energy and it buries the most hydrophobic surface area.
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Title
Crystallographic analysis of PheLeu substitution in the hydrophobic core of barnase
Author(s)
Chen, Y.-W; Fersht, A.R; Henrick, K
Journal
Acta Crystallographica Section D: Biological Crystallography , Volume 51 (2): 220 International Union of Crystallography – Mar 1, 1995
Publisher
International Union of Crystallography
Copyright
Copyright (c) 1995 International Union of Crystallography
ISSN
0907-4449
eISSN
1399-0047
D.O.I.
10.1107/S0907444994008851
Publisher site
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