1mq0
From Proteopedia
Line 1: | Line 1: | ||
- | [[Image:1mq0.gif|left|200px]] | + | [[Image:1mq0.gif|left|200px]] |
- | + | ||
- | '''Crystal Structure of Human Cytidine Deaminase''' | + | {{Structure |
+ | |PDB= 1mq0 |SIZE=350|CAPTION= <scene name='initialview01'>1mq0</scene>, resolution 2.40Å | ||
+ | |SITE= | ||
+ | |LIGAND= <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene> and <scene name='pdbligand=BRD:1-BETA-RIBOFURANOSYL-1,3-DIAZEPINONE'>BRD</scene> | ||
+ | |ACTIVITY= [http://en.wikipedia.org/wiki/Cytidine_deaminase Cytidine deaminase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.4.5 3.5.4.5] | ||
+ | |GENE= | ||
+ | }} | ||
+ | |||
+ | '''Crystal Structure of Human Cytidine Deaminase''' | ||
+ | |||
==Overview== | ==Overview== | ||
Line 10: | Line 19: | ||
==About this Structure== | ==About this Structure== | ||
- | 1MQ0 is a [ | + | 1MQ0 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1MQ0 OCA]. |
==Reference== | ==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:[http:// | + | 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:[http://www.ncbi.nlm.nih.gov/pubmed/15689149 15689149] |
[[Category: Cytidine deaminase]] | [[Category: Cytidine deaminase]] | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
Line 37: | Line 46: | ||
[[Category: zinc]] | [[Category: zinc]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 12:46:46 2008'' |
Revision as of 10:46, 20 March 2008
| |||||||
, 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