1g37

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(New page: 200px<br /> <applet load="1g37" size="450" color="white" frame="true" align="right" spinBox="true" caption="1g37, resolution 2.0&Aring;" /> '''CRYSTAL STRUCTURE OF...)
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[[Image:1g37.gif|left|200px]]<br />
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[[Image:1g37.gif|left|200px]]<br /><applet load="1g37" size="350" color="white" frame="true" align="right" spinBox="true"
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<applet load="1g37" size="450" color="white" frame="true" align="right" spinBox="true"
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caption="1g37, resolution 2.0&Aring;" />
caption="1g37, resolution 2.0&Aring;" />
'''CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE'''<br />
'''CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE'''<br />
==Overview==
==Overview==
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Bicyclic piperazinone based thrombin inhibitors of general structure 2, were prepared and evaluated in vitro and in vivo. These inhibitors, having, in common an electrophilic basic trans-cyclohexylamine P1 residue, displayed high thrombin affinity, high selectivity against trypsin and, good in vivo efficacy in the rat arterial thrombosis model.
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Bicyclic piperazinone based thrombin inhibitors of general structure 2 were prepared and evaluated in vitro and in vivo. These inhibitors, having in common an electrophilic basic trans-cyclohexylamine P1 residue, displayed high thrombin affinity, high selectivity against trypsin and good in vivo efficacy in the rat arterial thrombosis model.
==Disease==
==Disease==
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==About this Structure==
==About this Structure==
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1G37 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 110 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=1G37 OCA].
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1G37 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=110:'>110</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=1G37 OCA].
==Reference==
==Reference==
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[[Category: Thrombin]]
[[Category: Thrombin]]
[[Category: Bachand, B.]]
[[Category: Bachand, B.]]
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[[Category: Edmunds, J.J.]]
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[[Category: Edmunds, J J.]]
[[Category: Leblond, L.]]
[[Category: Leblond, L.]]
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[[Category: Siddiqui, M.A.]]
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[[Category: Siddiqui, M A.]]
[[Category: St-Denis, Y.]]
[[Category: St-Denis, Y.]]
[[Category: Tarazi, M.]]
[[Category: Tarazi, M.]]
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[[Category: Winocour, P.D.]]
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[[Category: Winocour, P D.]]
[[Category: 110]]
[[Category: 110]]
[[Category: inhibitor]]
[[Category: inhibitor]]
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[[Category: thrombin]]
[[Category: thrombin]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 17:00:05 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:45:32 2008''

Revision as of 10:45, 21 February 2008


1g37, resolution 2.0Å

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CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN COMPLEXED WITH BCH-10556 AND EXOSITE-DIRECTED PEPTIDE

Contents

Overview

Bicyclic piperazinone based thrombin inhibitors of general structure 2 were prepared and evaluated in vitro and in vivo. These inhibitors, having in common an electrophilic basic trans-cyclohexylamine P1 residue, displayed high thrombin affinity, high selectivity against trypsin and good in vivo efficacy in the rat arterial thrombosis model.

Disease

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

About this Structure

1G37 is a Single protein structure of sequence from Homo sapiens with as ligand. Active as Thrombin, with EC number 3.4.21.5 Full crystallographic information is available from OCA.

Reference

Potent and selective bicyclic lactam inhibitors of thrombin. Part 4: transition state inhibitors., Bachand B, Tarazi M, St-Denis Y, Edmunds JJ, Winocour PD, Leblond L, Siddiqui MA, Bioorg Med Chem Lett. 2001 Feb 12;11(3):287-90. PMID:11212093

Page seeded by OCA on Thu Feb 21 12:45:32 2008

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