1mq0: Difference between revisions
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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'' | |||
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Revision as of 01:34, 3 May 2008
Crystal Structure of Human Cytidine Deaminase
OverviewOverview
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 StructureAbout this Structure
1MQ0 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
ReferenceReference
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