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PMID: 8182748 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Satisfying hydrogen bonding potential in proteins.

Journal of molecular biology ·Vol. 238 ·No. 5 ·1994-05-20 ·Pages 777-93

McDonald IK, Thornton JM

Abstract

We have analysed the frequency with which potential hydrogen bond donors and acceptors are satisfied in protein molecules. There are a small percentage of nitrogen or oxygen atoms that do not form hydrogen bonds with either solvent or protein atoms, when standard criteria are used. For high resolution structures 9.5% and 5.1% of buried main-chain nitrogen and oxygen atoms, respectively, fail to hydrogen bond under our standard criteria, representing 5.8% and 2.1% of all main-chain nitrogen and oxygen atoms. We find that as the resolution of the data improves, the percentages fall. If the hydrogen bond criteria are relaxed many of these unsatisfied atoms form weak hydrogen bonds. However, there remain some buried atoms (1.3% NH and 1.8% CO) that fail to hydrogen bond without any immediately obvious compensating interactions.

MeSH Terms
Algorithms Amino Acids/chemistry Hydrogen/chemistry Hydrogen Bonding Nitrogen/chemistry Oxygen/chemistry Protein Structure, Secondary Proteins/chemistry
Chemicals
Amino Acids Proteins Hydrogen Nitrogen Oxygen
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
McDonald I K
Department of Biochemistry and Molecular Biology, University College London, U.K.
Thornton J M
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
1994-05-20
Pages
777-93
Language
English
Region
England
NLM ID
2985088R
Subset
IM
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