We apologize for Proteopedia being slow to respond. For the past two years, a new implementation of Proteopedia has been being built. Soon, it will replace this 18-year old system. All existing content will be moved to the new system at a date that will be announced here.

2pnu

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:2pnu.jpg|left|200px]]
+
{{Seed}}
 +
[[Image:2pnu.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_2pnu| PDB=2pnu | SCENE= }}
{{STRUCTURE_2pnu| PDB=2pnu | SCENE= }}
-
'''Crystal structure of human androgen receptor ligand-binding domain in complex with EM-5744'''
+
===Crystal structure of human androgen receptor ligand-binding domain in complex with EM-5744===
-
==Overview==
+
<!--
-
Antiandrogens are commonly used to treat androgen-dependent disorders. The currently used drugs unfortunately possess very weak affinity for the human AR (hAR), thus indicating the need to develop new high-affinity steroidal antiandrogens. Our compounds are specially designed to impede repositioning of the mobile carboxyl-terminal helix 12, which blocks the ligand-dependent transactivation function (AF-2) located in the AR ligand-binding domain (ARLBD). Using crystal structures of the hARLBD, we first found that H12 could be directly reached from the ligand-binding pocket (LBP) by a chain positioned on the C18 atom of an androgen steroid nucleus. A set of 5alpha-dihydrotestosterone-derived molecules bearing various C18 chains were thus synthesized and tested for their capacity to bind hAR and act as antagonists. Although most of those having very high affinity for hAR were agonists, several very potent antagonists were obtained, confirming the structural importance of the C18 chain. To understand the role of the C18 chain in their agonistic/antagonistic properties, the structure of the hARLBD complexed with one of these agonists, EM5744, was determined at a 1.65-A resolution. We have identified new interactions involving Gln(738), Met(742), and His(874) that explain both the high affinity of this compound and the inability of its bulky chain to prevent the repositioning of H12. This structural information will be helpful to refine the structure of the chains placed on the C18 atom to obtain efficient H12-directed steroidal antiandrogens.
+
The line below this paragraph, {{ABSTRACT_PUBMED_17711855}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 17711855 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_17711855}}
==About this Structure==
==About this Structure==
Line 38: Line 42:
[[Category: Lbd]]
[[Category: Lbd]]
[[Category: Ligand binding domain]]
[[Category: Ligand binding domain]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 13:30:23 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 18:39:45 2008''

Revision as of 15:39, 27 July 2008

Image:2pnu.png

Template:STRUCTURE 2pnu

Crystal structure of human androgen receptor ligand-binding domain in complex with EM-5744

Template:ABSTRACT PUBMED 17711855

About this Structure

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

Reference

Structural characterization of the human androgen receptor ligand-binding domain complexed with EM5744, a rationally designed steroidal ligand bearing a bulky chain directed toward helix 12., Cantin L, Faucher F, Couture JF, de Jesus-Tran KP, Legrand P, Ciobanu LC, Frechette Y, Labrecque R, Singh SM, Labrie F, Breton R, J Biol Chem. 2007 Oct 19;282(42):30910-9. Epub 2007 Aug 21. PMID:17711855

Page seeded by OCA on Sun Jul 27 18:39:45 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/2pnu"
Personal tools