1no9

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[[Image:1no9.png|left|200px]]
[[Image:1no9.png|left|200px]]
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{{STRUCTURE_1no9| PDB=1no9 | SCENE= }}
{{STRUCTURE_1no9| PDB=1no9 | SCENE= }}
===Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies.===
===Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies.===
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{{ABSTRACT_PUBMED_12885234}}
{{ABSTRACT_PUBMED_12885234}}
==About this Structure==
==About this Structure==
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[[1no9]] is a 3 chain structure of [[Hirudin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NO9 OCA].
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[[1no9]] is a 3 chain structure of [[Hirudin]] and [[Thrombin]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1NO9 OCA].
==See Also==
==See Also==
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*[[Hirudin]]
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*[[Hirudin|Hirudin]]
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*[[Thrombin|Thrombin]]
==Reference==
==Reference==
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<ref group="xtra">PMID:12885234</ref><references group="xtra"/>
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<ref group="xtra">PMID:012885234</ref><references group="xtra"/>
[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Thrombin]]
[[Category: Thrombin]]
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[[Category: Blood coagulation]]
[[Category: Blood coagulation]]
[[Category: Hydrolase]]
[[Category: Hydrolase]]
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[[Category: Hydrolase-hydrolase inhibitor complex]]
[[Category: N-diphenylcarbamoyl-aminoguanidine]]
[[Category: N-diphenylcarbamoyl-aminoguanidine]]
[[Category: Serine proteinase inhibition]]
[[Category: Serine proteinase inhibition]]

Revision as of 17:46, 25 July 2012

Template:STRUCTURE 1no9

Contents

Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies.

Template:ABSTRACT PUBMED 12885234

About this Structure

1no9 is a 3 chain structure of Hirudin and Thrombin with sequence from Homo sapiens. Full crystallographic information is available from OCA.

See Also

Reference

  • De Simone G, Menchise V, Omaggio S, Pedone C, Scozzafava A, Supuran CT. Design of weakly basic thrombin inhibitors incorporating novel P1 binding functions: molecular and X-ray crystallographic studies. Biochemistry. 2003 Aug 5;42(30):9013-21. PMID:12885234 doi:10.1021/bi020512l

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