2a30: Difference between revisions

From Proteopedia
Jump to navigationJump to search
← Older editNewer edit →
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,328,572 edits
No edit summary
OCA (talk | contribs)
Bots, Bureaucrats, journal, Administrators
3,328,572 edits
No edit summary
Line 1: Line 1:
[[Image:2a30.gif|left|200px]]
{{Seed}}
[[Image:2a30.png|left|200px]]


<!--
<!--
Line 9: Line 10:
{{STRUCTURE_2a30|  PDB=2a30  |  SCENE=  }}  
{{STRUCTURE_2a30|  PDB=2a30  |  SCENE=  }}  


'''Crystal structure of human deoxycytidine kinase in complex with deoxycytidine'''
===Crystal structure of human deoxycytidine kinase in complex with deoxycytidine===




==Overview==
<!--
Human deoxycytidine kinase (dCK) uses nucleoside triphosphates to phosphorylate several clinically important prodrugs in addition to its natural substrates. Although UTP is the preferred phosphoryl donor for this reaction, our previous studies reported dCK structures solely containing ADP in the phosphoryl donor binding site. To determine the molecular basis of the kinetically observed phosphoryl donor preference, we solved crystal structures of a dCK variant lacking a flexible insert (residues 65-79) but having similar catalytic properties as wild type, in complex with deoxycytidine (dC) and UDP, and in the presence of dC but the absence of UDP or ADP. These structures reveal major changes in the donor base binding loop (residues 240-247) between the UDP-bound and ADP-bound forms, involving significant main-chain rearrangement. This loop is disordered in the dCK-dC structure, which lacks a ligand at the phosphoryl donor site. In comparison with the ADP-bound form, in the presence of UDP this loop is shifted inward to make closer contact to the smaller uracil base. These structures illuminate the phosphoryl donor binding and preference mechanisms of dCK.
The line below this paragraph, {{ABSTRACT_PUBMED_16401075}}, adds the Publication Abstract to the page
(as it appears on PubMed at http://www.pubmed.gov), where 16401075 is the PubMed ID number.
-->
{{ABSTRACT_PUBMED_16401075}}


==About this Structure==
==About this Structure==
Line 29: Line 33:
[[Category: Sabini, E.]]
[[Category: Sabini, E.]]
[[Category: Nucleoside kinase]]
[[Category: Nucleoside kinase]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 18:32:14 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat Jul 5 16:22:25 2008''

Revision as of 13:22, 5 July 2008

File:2a30.png

Template:STRUCTURE 2a30

Crystal structure of human deoxycytidine kinase in complex with deoxycytidine

Template:ABSTRACT PUBMED 16401075

About this Structure

2A30 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Structural basis for the preference of UTP over ATP in human deoxycytidine kinase: illuminating the role of main-chain reorganization., Godsey MH, Ort S, Sabini E, Konrad M, Lavie A, Biochemistry. 2006 Jan 17;45(2):452-61. PMID:16401075

Page seeded by OCA on Sat Jul 5 16:22:25 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "https://proteopedia.org/index.php?title=2a30&oldid=636653"