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PMID: 1649998 Published · ppublish English Comparative Study Journal Article Research Support, U.S. Gov't, P.H.S.

Sequence and structure determinants of the nonenzymatic deamidation of asparagine and glutamine residues in proteins.

Protein engineering ·Vol. 4 ·No. 3 ·1991-02-00 ·Pages 283-94

Wright HT

Abstract

The rates of deamidation of Asn and Gln residues in peptides and proteins depend upon both the identity of other nearby amino acid residues, some of which can catalyze the deamidation reaction of the Asn and Gln side chains, and upon polypeptide conformation. Proximal amino acids can be contiguous in sequence or brought close to Asn or Gln side chains by higher order structure of the protein. Local polypeptide conformation can stabilize the oxyanion transition state of the deamidation reaction and also enable deamidation through the beta-aspartyl shift mechanism. In this paper, the environments of Asn and Gln residues in known protein structures are examined to determine the configuration and identity of groups which participate in deamidation reactions. Sequence information is also analyzed and shown to support evolutionary selection against the occurrence of certain potentially catalytic amino acids adjacent to Asn and Gln in proteins. This negative selection supports a functional role for deamidation in those non-mutant proteins in which it occurs.

MeSH Terms
Amino Acid Sequence Asparagine/chemistry,physiology Computer Simulation Cytochrome c Group/chemistry Glutamine/chemistry,physiology Hemoglobin J/chemistry Hemoglobins, Abnormal/chemistry Humans Insulin/chemistry Models, Molecular Molecular Sequence Data Protein Conformation Ribonuclease, Pancreatic/chemistry Triose-Phosphate Isomerase/chemistry
Chemicals
Cytochrome c Group Hemoglobins, Abnormal Insulin hemoglobin Singapore Glutamine Hemoglobin J hemoglobin J Providence Asparagine Ribonuclease, Pancreatic Triose-Phosphate Isomerase
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Wright H T
Department of Biochemistry and Molecular Biophysics, Virginia Commonwealth University, Richmond 23298-0614.
Article Info
Journal
Protein engineering
Abbr.
Protein Eng
ISSN
0269-2139
Published
1991-02-00
Pages
283-94
Language
English
Region
England
NLM ID
8801484
Subset
IM
Grants
NIA NIH HHS · AG07369 · United States
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