1zgi

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(New page: 200px<br /> <applet load="1zgi" size="450" color="white" frame="true" align="right" spinBox="true" caption="1zgi, resolution 2.2&Aring;" /> '''thrombin in complex ...)
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'''thrombin in complex with an oxazolopyridine inhibitor 21'''<br />
'''thrombin in complex with an oxazolopyridine inhibitor 21'''<br />
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==About this Structure==
==About this Structure==
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1ZGI 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 382 as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Thrombin Thrombin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.5 3.4.21.5] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1ZGI OCA].
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1ZGI 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=382:'>382</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Thrombin Thrombin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.5 3.4.21.5] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1ZGI OCA].
==Reference==
==Reference==
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[[Category: thrombin inhibitor complex]]
[[Category: thrombin inhibitor complex]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 20:33:57 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:13:15 2008''

Revision as of 15:13, 15 February 2008


1zgi, resolution 2.2Å

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thrombin in complex with an oxazolopyridine inhibitor 21

Contents

Overview

Thrombin-inhibitor X-ray crystal structures, in combination with the, installation of binding elements optimized within the pyrazinone series of, thrombin inhibitors, were utilized to transform a weak triazolopyrimidine, lead into a series of potent oxazolopyridines. A modification intended to, attenuate plasma protein binding (i.e., conversion of the P3 pyridine to a, piperidine) conferred significant factor Xa activity to this series., Ultimately, these dual thrombin/factor Xa inhibitors demonstrated, excellent in vitro and in vivo anticoagulant efficacy.

Disease

Known diseases associated with this structure: Dysprothrombinemia OMIM:[176930], Hyperprothrombinemia OMIM:[176930], Hypoprothrombinemia OMIM:[176930]

About this Structure

1ZGI is a Protein complex structure of sequences from Homo sapiens with as ligand. Active as Thrombin, with EC number 3.4.21.5 Full crystallographic information is available from OCA.

Reference

Development of an oxazolopyridine series of dual thrombin/factor Xa inhibitors via structure-guided lead optimization., Deng JZ, McMasters DR, Rabbat PM, Williams PD, Coburn CA, Yan Y, Kuo LC, Lewis SD, Lucas BJ, Krueger JA, Strulovici B, Vacca JP, Lyle TA, Burgey CS, Bioorg Med Chem Lett. 2005 Oct 15;15(20):4411-6. PMID:16137886

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