This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.

Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


1y2g

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1y2g.gif|left|200px]]
+
{{Seed}}
 +
[[Image:1y2g.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1y2g| PDB=1y2g | SCENE= }}
{{STRUCTURE_1y2g| PDB=1y2g | SCENE= }}
-
'''Crystal STructure of ZipA in complex with an inhibitor'''
+
===Crystal STructure of ZipA in complex with an inhibitor===
-
==Overview==
+
<!--
-
In this paper, we describe the first prospective application of the shape-comparison program ROCS (Rapid Overlay of Chemical Structures) to find new scaffolds for small molecule inhibitors of the ZipA-FtsZ protein-protein interaction, a proposed antibacterial target. The shape comparisons are made relative to the crystallographically determined, bioactive conformation of a high-throughput screening (HTS) hit. The use of ROCS led to the identification of a set of novel, weakly binding inhibitors with scaffolds presenting synthetic opportunities to further optimize biological affinity and lacking development issues associated with the HTS lead. These ROCS-identified scaffolds would have been missed using other structural similarity approaches such as ISIS 2D fingerprints. X-ray crystallographic analysis of one of the new inhibitors bound to ZipA reveals that the shape comparison approach very accurately predicted the binding mode. These experimental results validate this use of ROCS for chemotype switching or "lead hopping" and suggest that it is of general interest for lead identification in drug discovery endeavors.
+
The line below this paragraph, {{ABSTRACT_PUBMED_15743191}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 15743191 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_15743191}}
==About this Structure==
==About this Structure==
Line 25: Line 29:
[[Category: Rush, T S.]]
[[Category: Rush, T S.]]
[[Category: Cell cycle]]
[[Category: Cell cycle]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 15:48:21 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 21:18:15 2008''

Revision as of 18:18, 27 July 2008

Image:1y2g.png

Template:STRUCTURE 1y2g

Crystal STructure of ZipA in complex with an inhibitor

Template:ABSTRACT PUBMED 15743191

About this Structure

1Y2G is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.

Reference

A shape-based 3-D scaffold hopping method and its application to a bacterial protein-protein interaction., Rush TS 3rd, Grant JA, Mosyak L, Nicholls A, J Med Chem. 2005 Mar 10;48(5):1489-95. PMID:15743191

Page seeded by OCA on Sun Jul 27 21:18:15 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/1y2g"
Personal tools