1mq0
From Proteopedia
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'''Crystal Structure of Human Cytidine Deaminase''' | '''Crystal Structure of Human Cytidine Deaminase''' | ||
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[[Category: Fromme, J C.]] | [[Category: Fromme, J C.]] | ||
[[Category: Verdine, G L.]] | [[Category: Verdine, G L.]] | ||
- | [[Category: | + | [[Category: Amine hydrolase]] |
- | [[Category: | + | [[Category: Anticancer]] |
- | [[Category: | + | [[Category: Chemotherapy]] |
- | [[Category: | + | [[Category: Cytidine deaminase]] |
- | [[Category: | + | [[Category: Diazepinone]] |
- | [[Category: | + | [[Category: Drug]] |
- | [[Category: | + | [[Category: Edge-to-face interaction]] |
- | [[Category: | + | [[Category: Enzyme]] |
- | [[Category: | + | [[Category: Human]] |
- | [[Category: | + | [[Category: Inhibitor]] |
- | [[Category: | + | [[Category: Leukemia]] |
- | [[Category: | + | [[Category: Phi-phi interaction]] |
- | [[Category: | + | [[Category: Protein]] |
- | [[Category: | + | [[Category: Zinc]] |
- | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 01:34:40 2008'' | |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + |
Revision as of 22:34, 2 May 2008
Crystal Structure of Human Cytidine Deaminase
Overview
Human cytidine deaminase (CDA) is an enzyme prominent for its role in catalyzing metabolic processing of nucleoside-type anticancer and antiviral agents. It is thus a promising target for the development of small molecule therapeutic adjuvants. We report the first crystal structure of human CDA as a complex with a tight-binding inhibitor, diazepinone riboside 1. The structure reveals that inhibitor 1 is able to establish a canonical pi/pi-interaction with a key active site residue, Phe 137.
About this Structure
1MQ0 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Structure of human cytidine deaminase bound to a potent inhibitor., Chung SJ, Fromme JC, Verdine GL, J Med Chem. 2005 Feb 10;48(3):658-60. PMID:15689149 Page seeded by OCA on Sat May 3 01:34:40 2008
Categories: Cytidine deaminase | Homo sapiens | Single protein | Chung, S J. | Fromme, J C. | Verdine, G L. | Amine hydrolase | Anticancer | Chemotherapy | Diazepinone | Drug | Edge-to-face interaction | Enzyme | Human | Inhibitor | Leukemia | Phi-phi interaction | Protein | Zinc