1xs7

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
(New page: 200px<br /> <applet load="1xs7" size="450" color="white" frame="true" align="right" spinBox="true" caption="1xs7, resolution 2.8&Aring;" /> '''Crystal Structure of...)
Line 1: Line 1:
-
[[Image:1xs7.gif|left|200px]]<br />
+
[[Image:1xs7.gif|left|200px]]<br /><applet load="1xs7" size="350" color="white" frame="true" align="right" spinBox="true"
-
<applet load="1xs7" size="450" color="white" frame="true" align="right" spinBox="true"
+
caption="1xs7, resolution 2.8&Aring;" />
caption="1xs7, resolution 2.8&Aring;" />
'''Crystal Structure of a cycloamide-urethane-derived novel inhibitor bound to human brain memapsin 2 (beta-secretase).'''<br />
'''Crystal Structure of a cycloamide-urethane-derived novel inhibitor bound to human brain memapsin 2 (beta-secretase).'''<br />
==Overview==
==Overview==
-
A series of novel macrocyclic amide-urethanes was designed and synthesized, based upon the X-ray crystal structure of our lead inhibitor (1, OM99-2, with eight residues) bound to memapsin 2. Ring size and substituent, effects have been investigated. Cycloamide-urethanes containing 14- to, 16-membered rings exhibited low nanomolar inhibitory potencies against, human brain memapsin 2 (beta-secretase).
+
A series of novel macrocyclic amide-urethanes was designed and synthesized based upon the X-ray crystal structure of our lead inhibitor (1, OM99-2 with eight residues) bound to memapsin 2. Ring size and substituent effects have been investigated. Cycloamide-urethanes containing 14- to 16-membered rings exhibited low nanomolar inhibitory potencies against human brain memapsin 2 (beta-secretase).
==About this Structure==
==About this Structure==
-
1XS7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with MMI as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Memapsin_2 Memapsin 2], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.46 3.4.23.46] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1XS7 OCA].
+
1XS7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=MMI:'>MMI</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Memapsin_2 Memapsin 2], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.46 3.4.23.46] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1XS7 OCA].
==Reference==
==Reference==
Line 35: Line 34:
[[Category: memapsin2]]
[[Category: memapsin2]]
-
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:10:12 2007''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:58:07 2008''

Revision as of 13:58, 21 February 2008


1xs7, resolution 2.8Å

Drag the structure with the mouse to rotate

Crystal Structure of a cycloamide-urethane-derived novel inhibitor bound to human brain memapsin 2 (beta-secretase).

Overview

A series of novel macrocyclic amide-urethanes was designed and synthesized based upon the X-ray crystal structure of our lead inhibitor (1, OM99-2 with eight residues) bound to memapsin 2. Ring size and substituent effects have been investigated. Cycloamide-urethanes containing 14- to 16-membered rings exhibited low nanomolar inhibitory potencies against human brain memapsin 2 (beta-secretase).

About this Structure

1XS7 is a Single protein structure of sequence from Homo sapiens with as ligand. Active as Memapsin 2, with EC number 3.4.23.46 Full crystallographic information is available from OCA.

Reference

Structure-based design of cycloamide-urethane-derived novel inhibitors of human brain memapsin 2 (beta-secretase)., Ghosh AK, Devasamudram T, Hong L, DeZutter C, Xu X, Weerasena V, Koelsch G, Bilcer G, Tang J, Bioorg Med Chem Lett. 2005 Jan 3;15(1):15-20. PMID:15582402

Page seeded by OCA on Thu Feb 21 15:58:07 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools