1mq0
From Proteopedia
| |||||||
, resolution 2.40Å | |||||||
---|---|---|---|---|---|---|---|
Ligands: | and | ||||||
Activity: | Cytidine deaminase, with EC number 3.5.4.5 | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Crystal Structure of Human Cytidine Deaminase
Contents |
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.
Disease
Known disease associated with this structure: Anemia, congenital dyserythropoietic, type I OMIM:[607465]
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 Thu Mar 20 12:46:46 2008
Categories: Cytidine deaminase | Homo sapiens | Single protein | Chung, S J. | Fromme, J C. | Verdine, G L. | BRD | ZN | Amine hydrolase | Anticancer | Chemotherapy | Diazepinone | Drug | Edge-to-face interaction | Enzyme | Human | Inhibitor | Leukemia | Phi-phi interaction | Protein | Zinc