Novel Binding Mode of Hydroxamate Inhibitors to Human Carbonic Anhydrase II-Reference-Cited by-同舟云学术

Novel Binding Mode of Hydroxamate Inhibitors to Human Carbonic Anhydrase II

Published:1997-01-01 Issue:4 Volume:119 Page:850-851
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Scolnick Laura R.¹,Clements Adrienne M.¹,Liao John¹,Crenshaw Lori¹,Hellberg Mark¹,May Jesse¹,Dean Tom R.¹,Christianson David W.¹

Affiliation:

1. Department of Chemistry, University of Pennsylvania, 231 South 34th Street, Philadelphia, Pennsylvania 19104-6323 Department of Biochemistry and Biophysics University of Pennsylvania, 36th and Hamilton Walk Philadelphia, Pennsylvania 19104-6059 Alcon Laboratories, Inc. 6201 South Freeway, Fort Worth, Texas 76134-2099

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja963832z

Reference34 articles.

1. Peptide hydroxamic acids as inhibitors of thermolysin

2. (b) Powers, J. C.; Harper, J. W. InProteinase Inhibitors; Barrett, A. J. S., Salvensen, G., Eds.; Elsevier: Amsterdam, New York, Oxford, 1986; pp 219−298.

3. Crystal structures of matrilysin-inhibitor complexes

4. X-ray Structures of Human Neutrophil Collagenase Complexed with Peptide Hydroxamate and Peptide Thiol Inhibitors. Implications for Substrate Binding and Rational Drug Design

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