1tmg

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{{STRUCTURE_1tmg| PDB=1tmg | SCENE= }}
{{STRUCTURE_1tmg| PDB=1tmg | SCENE= }}
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'''crystal structure of the complex of subtilisin BPN' with chymotrypsin inhibitor 2 M59F mutant'''
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===crystal structure of the complex of subtilisin BPN' with chymotrypsin inhibitor 2 M59F mutant===
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==Overview==
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A series of mutants of chymotrypsin inhibitor 2 (CI2), at residues that interact with the inhibited enzyme subtilisin BPN', were studied to determine the relative importance of intermolecular contacts on either side of the scissile bond. Mutants were tested for inhibition of subtilisin, rates of hydrolysis by subtilisin, and ability to acylate subtilisin. Additionally, crystal structures of the mutant CI2 complexes with subtilisin were obtained. Ordered water molecules were found to play an important role in inhibitor recognition, and features of the crystal structures, in combination with biochemical data, support a transition-state stabilization role for the P(1) residue in subtilisin catalysis. Consistent with the proposed mechanism of inhibition, in which rapid acylation is followed by religation, leaving-group contacts with the enzyme were found to be more critical determinants of inhibition than acylating-group contacts in the mutants studied here.
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(as it appears on PubMed at http://www.pubmed.gov), where 15504027 is the PubMed ID number.
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{{ABSTRACT_PUBMED_15504027}}
==About this Structure==
==About this Structure==
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[[Category: Inhibitor]]
[[Category: Inhibitor]]
[[Category: Serine protease]]
[[Category: Serine protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 10:07:44 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 15:26:22 2008''

Revision as of 12:26, 28 July 2008

Image:1tmg.png

Template:STRUCTURE 1tmg

crystal structure of the complex of subtilisin BPN' with chymotrypsin inhibitor 2 M59F mutant

Template:ABSTRACT PUBMED 15504027

About this Structure

1TMG is a Protein complex structure of sequences from Bacillus amyloliquefaciens and Hordeum vulgare subsp. vulgare. Full crystallographic information is available from OCA.

Reference

Binding, proteolytic, and crystallographic analyses of mutations at the protease-inhibitor interface of the subtilisin BPN'/chymotrypsin inhibitor 2 complex., Radisky ES, Kwan G, Karen Lu CJ, Koshland DE Jr, Biochemistry. 2004 Nov 2;43(43):13648-56. PMID:15504027

Page seeded by OCA on Mon Jul 28 15:26:22 2008

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