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PMID: 3470737 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Mechanism of carboxypeptidase A: hydration of a ketonic substrate analogue.

Christianson DW, David PR, Lipscomb WN

Abstract

The structure of the complex between carboxypeptidase A alpha (EC 3.4.17.1) and the ketonic substrate analogue 5-benzamido-2-benzyl-4-oxopentanoic acid (BOP) has been determined by x-ray crystallographic methods to a resolution of 1.7 A (final R = 0.191). Interestingly, BOP was observed to bind to the active site of carboxypeptidase A alpha as the covalent hydrate adduct. Because BOP is probably less than 0.2% hydrated in aqueous solution, this result was unexpected. One possibility is that the zinc-bound water of the native enzyme added to the ketone carbonyl. Alternatively, the enzyme may preferentially scavenge the hydrated ketone as it is continuously maintained at equilibrium in the solution in which the carboxypeptidase A alpha crystals were immersed. In either case, this mode of binding of BOP to carboxypeptidase A alpha provides an example of the preferred binding of a model of a structure along the reaction coordinate of a hydrolytic reaction.

MeSH Terms
Carboxypeptidases/antagonists & inhibitors Carboxypeptidases A Hydrogen Bonding Keto Acids X-Ray Diffraction Zinc
Chemicals
Keto Acids 5-benzamido-2-benzyl-4-oxopentanoic acid Carboxypeptidases Carboxypeptidases A Zinc
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Christianson D W
David P R
Lipscomb W N
References (10)
10 references, click to expand
  1. Antiproteolytic aldehydes and ketones: substituent and secondary deuterium isotope effects on equilibrium addition of water and other nucleophiles.
    Biochemistry. 1977 Nov 1;16(22):4886-90 PMID: 911797
  2. Carbonic anhydrase: structure catalytic versatility, and inhibition.
    Adv Enzymol Relat Areas Mol Biol. 1978;47:149-274 PMID: 31766
  3. Catalytic role of the metal ion of carboxypeptidase A in ester hydrolysis.
    J Biol Chem. 1979 Jan 25;254(2):356-66 PMID: 33168
  4. Hydrolysis of esters by carboxypeptidase A requires a penta-coordinate metal ion.
    J Biol Chem. 1982 Jan 10;257(1):24-7 PMID: 6273427
  5. X-ray crystallographic investigation of substrate binding to carboxypeptidase A at subzero temperature.
    Proc Natl Acad Sci U S A. 1986 Oct;83(20):7568-72 PMID: 3463986
  6. Inhibition of carboxypeptidase A by aldehyde and ketone substrate analogues.
    Biochemistry. 1984 Apr 24;23(9):2083-7 PMID: 6547054
  7. Site-directed mutagenesis shows that tyrosine 248 of carboxypeptidase A does not play a crucial role in catalysis.
    Nature. 1985 Oct 10-16;317(6037):551-5 PMID: 3840231
  8. Binding of a possible transition state analogue to the active site of carboxypeptidase A.
    Proc Natl Acad Sci U S A. 1985 Oct;82(20):6840-4 PMID: 3863130
  9. Inhibition of carboxypeptidase A by ketones and alcohols that are isosteric with peptide substrates.
    Biochemistry. 1985 Dec 17;24(26):7612-7 PMID: 4092029
  10. Refined crystal structure of the potato inhibitor complex of carboxypeptidase A at 2.5 A resolution.
    J Mol Biol. 1982 Sep 25;160(3):475-98 PMID: 7154070
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1987-03-00
Pages
1512-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC304464
Subset
IM
Grants
NIGMS NIH HHS · GM 06920 · United States
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