1epp: Difference between revisions

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New page: left|200px<br /><applet load="1epp" size="450" color="white" frame="true" align="right" spinBox="true" caption="1epp, resolution 1.9Å" /> '''ANALYSES OF LIGAND BI...
 
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[[Image:1epp.gif|left|200px]]<br /><applet load="1epp" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1epp.gif|left|200px]]<br /><applet load="1epp" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1epp, resolution 1.9&Aring;" />
caption="1epp, resolution 1.9&Aring;" />
'''ANALYSES OF LIGAND BINDING IN FIVE ENDOTHIAPEPSIN CRYSTAL COMPLEXES AND THEIR USE IN THE DESIGN AND EVALUATION OF NOVEL RENIN INHIBITORS'''<br />
'''ANALYSES OF LIGAND BINDING IN FIVE ENDOTHIAPEPSIN CRYSTAL COMPLEXES AND THEIR USE IN THE DESIGN AND EVALUATION OF NOVEL RENIN INHIBITORS'''<br />


==Overview==
==Overview==
Five renin inhibitors were cocrystallized with endothiapepsin, a fungal, enzyme homologous to renin. Crystal structures of inhibitor-bound, complexes have provided invaluable insight regarding the three-dimensional, structure of the aspartic proteinase family of enzymes, as well as the, steric and polar interactions that occur between the proteins and the, bound ligands. Beyond this, subtleties of binding have been revealed, including multiple subsite binding modes and subsite interdependencies., This information has been applied in the design of novel potent renin, inhibitors and in the understanding of structure-activity relationships, and enzyme selectivities.
Five renin inhibitors were cocrystallized with endothiapepsin, a fungal enzyme homologous to renin. Crystal structures of inhibitor-bound complexes have provided invaluable insight regarding the three-dimensional structure of the aspartic proteinase family of enzymes, as well as the steric and polar interactions that occur between the proteins and the bound ligands. Beyond this, subtleties of binding have been revealed, including multiple subsite binding modes and subsite interdependencies. This information has been applied in the design of novel potent renin inhibitors and in the understanding of structure-activity relationships and enzyme selectivities.


==About this Structure==
==About this Structure==
1EPP is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ] with SO4, MAS and MTF as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Endothiapepsin Endothiapepsin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.22 3.4.23.22] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1EPP OCA].  
1EPP is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ] with <scene name='pdbligand=SO4:'>SO4</scene>, <scene name='pdbligand=MAS:'>MAS</scene> and <scene name='pdbligand=MTF:'>MTF</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Endothiapepsin Endothiapepsin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.22 3.4.23.22] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EPP OCA].  


==Reference==
==Reference==
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[[Category: Endothiapepsin]]
[[Category: Endothiapepsin]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Blundell, T.L.]]
[[Category: Blundell, T L.]]
[[Category: Cooper, J.B.]]
[[Category: Cooper, J B.]]
[[Category: Wallace, B.A.]]
[[Category: Wallace, B A.]]
[[Category: MAS]]
[[Category: MAS]]
[[Category: MTF]]
[[Category: MTF]]
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[[Category: hydrolase(acid proteinase)]]
[[Category: hydrolase(acid proteinase)]]


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Revision as of 13:30, 21 February 2008

File:1epp.gif


1epp, resolution 1.9Å

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ANALYSES OF LIGAND BINDING IN FIVE ENDOTHIAPEPSIN CRYSTAL COMPLEXES AND THEIR USE IN THE DESIGN AND EVALUATION OF NOVEL RENIN INHIBITORS

OverviewOverview

Five renin inhibitors were cocrystallized with endothiapepsin, a fungal enzyme homologous to renin. Crystal structures of inhibitor-bound complexes have provided invaluable insight regarding the three-dimensional structure of the aspartic proteinase family of enzymes, as well as the steric and polar interactions that occur between the proteins and the bound ligands. Beyond this, subtleties of binding have been revealed, including multiple subsite binding modes and subsite interdependencies. This information has been applied in the design of novel potent renin inhibitors and in the understanding of structure-activity relationships and enzyme selectivities.

About this StructureAbout this Structure

1EPP is a Single protein structure of sequence from [1] with , and as ligands. Active as Endothiapepsin, with EC number 3.4.23.22 Full crystallographic information is available from OCA.

ReferenceReference

Analyses of ligand binding in five endothiapepsin crystal complexes and their use in the design and evaluation of novel renin inhibitors., Lunney EA, Hamilton HW, Hodges JC, Kaltenbronn JS, Repine JT, Badasso M, Cooper JB, Dealwis C, Wallace BA, Lowther WT, et al., J Med Chem. 1993 Nov 26;36(24):3809-20. PMID:8254610

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