2p94: Difference between revisions

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New page: left|200px<br /> <applet load="2p94" size="450" color="white" frame="true" align="right" spinBox="true" caption="2p94, resolution 1.80Å" /> '''Factor xa in comple...
 
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[[Image:2p94.gif|left|200px]]<br />
[[Image:2p94.jpg|left|200px]]<br /><applet load="2p94" size="350" color="white" frame="true" align="right" spinBox="true"  
<applet load="2p94" size="450" color="white" frame="true" align="right" spinBox="true"  
caption="2p94, resolution 1.80&Aring;" />
caption="2p94, resolution 1.80&Aring;" />
'''Factor xa in complex with the inhibitor 3-chloro-N-((1R,2S)-2-(4-(2-oxopyridin-1(2H)-yl)benzamido)cyclohexyl)-1H-indole-6-carboxamide'''<br />
'''Factor xa in complex with the inhibitor 3-chloro-N-((1R,2S)-2-(4-(2-oxopyridin-1(2H)-yl)benzamido)cyclohexyl)-1H-indole-6-carboxamide'''<br />
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==Overview==
==Overview==
In the search of Factor Xa (FXa) inhibitors structurally different from, the pyrazole-based series, we identified a viable series of enantiopure, cis-(1R,2S)-cycloalkyldiamine derivatives as potent and selective, inhibitors of FXa. Among them, cyclohexyldiamide 7 and cyclopentyldiamide, 9 were the most potent neutral compounds, and had good anticoagulant, activity comparable to the pyrazole-based analogs. Crystal structures of, 7-FXa and 9-FXa illustrate binding similarities and differences between, the five- and the six-membered core systems, and provide rationales for, the observed SAR of P1 and linker moieties.
In the search of Factor Xa (FXa) inhibitors structurally different from, the pyrazole-based series, we identified a viable series of enantiopure, cis-(1R,2S)-cycloalkyldiamine derivatives as potent and selective, inhibitors of FXa. Among them, cyclohexyldiamide 7 and cyclopentyldiamide, 9 were the most potent neutral compounds, and had good anticoagulant, activity comparable to the pyrazole-based analogs. Crystal structures of, 7-FXa and 9-FXa illustrate binding similarities and differences between, the five- and the six-membered core systems, and provide rationales for, the observed SAR of P1 and linker moieties.
==Disease==
Known disease associated with this structure: Factor X deficiency OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=227600 227600]]


==About this Structure==
==About this Structure==
2P94 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with ME4 as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Coagulation_factor_Xa Coagulation factor Xa], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.6 3.4.21.6] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2P94 OCA].  
2P94 is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] with <scene name='pdbligand=ME4:'>ME4</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Coagulation_factor_Xa Coagulation factor Xa], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.6 3.4.21.6] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2P94 OCA].  


==Reference==
==Reference==
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[[Category: serine protease]]
[[Category: serine protease]]


''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 23:21:45 2007''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jan 23 14:26:13 2008''