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1okx

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{{STRUCTURE_1okx| PDB=1okx | SCENE= }}
{{STRUCTURE_1okx| PDB=1okx | SCENE= }}
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'''BINDING STRUCTURE OF ELASTASE INHIBITOR SCYPTOLIN A'''
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===BINDING STRUCTURE OF ELASTASE INHIBITOR SCYPTOLIN A===
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==Overview==
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Natural bioactive compounds are of general interest to pharmaceutical research because they may be used as leads in drug development campaigns. Among them, scyptolin A and B from Scytonema hofmanni PCC 7110 are known to inhibit porcine pancreatic elastase, which in turn resembles the attractive drug target neutrophil elastase. The crystal structure of scyptolin A as bound to pancreatic elastase was solved at 2.8 A resolution. The inhibitor occupies the most prominent subsites S1 through S4 of the elastase and prevents a hydrolytic attack by covering the active center with its rigid ring structure. The observed binding structure may help to design potent elastase inhibitors.
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(as it appears on PubMed at http://www.pubmed.gov), where 14583266 is the PubMed ID number.
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{{ABSTRACT_PUBMED_14583266}}
==About this Structure==
==About this Structure==
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[[Category: Inhibitor]]
[[Category: Inhibitor]]
[[Category: Protease]]
[[Category: Protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 10:25:14 2008''

Revision as of 07:25, 28 July 2008

Image:1okx.png

Template:STRUCTURE 1okx

BINDING STRUCTURE OF ELASTASE INHIBITOR SCYPTOLIN A

Template:ABSTRACT PUBMED 14583266

About this Structure

1OKX is a Protein complex structure of sequences from Scytonema hofmanni and Sus scrofa. Full crystallographic information is available from OCA.

Reference

Binding structure of elastase inhibitor scyptolin A., Matern U, Schleberger C, Jelakovic S, Weckesser J, Schulz GE, Chem Biol. 2003 Oct;10(10):997-1001. PMID:14583266

Page seeded by OCA on Mon Jul 28 10:25:14 2008

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