1tmg

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|PDB= 1tmg |SIZE=350|CAPTION= <scene name='initialview01'>1tmg</scene>, resolution 1.67&Aring;
|PDB= 1tmg |SIZE=350|CAPTION= <scene name='initialview01'>1tmg</scene>, resolution 1.67&Aring;
|SITE=
|SITE=
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|LIGAND= <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=CIT:CITRIC+ACID'>CIT</scene>, <scene name='pdbligand=1PE:PENTAETHYLENE+GLYCOL'>1PE</scene> and <scene name='pdbligand=15P:POLYETHYLENE GLYCOL (N=34)'>15P</scene>
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|LIGAND= <scene name='pdbligand=15P:POLYETHYLENE+GLYCOL+(N=34)'>15P</scene>, <scene name='pdbligand=1PE:PENTAETHYLENE+GLYCOL'>1PE</scene>, <scene name='pdbligand=CA:CALCIUM+ION'>CA</scene>, <scene name='pdbligand=CIT:CITRIC+ACID'>CIT</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/Subtilisin Subtilisin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.62 3.4.21.62]
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Subtilisin Subtilisin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.21.62 3.4.21.62] </span>
|GENE= APR ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1390 Bacillus amyloliquefaciens])
|GENE= APR ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1390 Bacillus amyloliquefaciens])
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|DOMAIN=
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|RELATEDENTRY=[[1tm1|1TM1]], [[1tm3|1TM3]], [[1tm4|1TM4]], [[1tm5|1TM5]], [[1tm7|1TM7]]
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1tmg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1tmg OCA], [http://www.ebi.ac.uk/pdbsum/1tmg PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1tmg RCSB]</span>
}}
}}
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[[Category: Lu, C J.Karen.]]
[[Category: Lu, C J.Karen.]]
[[Category: Radisky, E S.]]
[[Category: Radisky, E S.]]
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[[Category: 15P]]
 
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[[Category: 1PE]]
 
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[[Category: CA]]
 
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[[Category: CIT]]
 
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[[Category: NA]]
 
[[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 Thu Mar 20 14:20:24 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:58:09 2008''

Revision as of 20:58, 30 March 2008


PDB ID 1tmg

Drag the structure with the mouse to rotate
, resolution 1.67Å
Ligands: , , , ,
Gene: APR (Bacillus amyloliquefaciens)
Activity: Subtilisin, with EC number 3.4.21.62
Related: 1TM1, 1TM3, 1TM4, 1TM5, 1TM7


Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



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


Overview

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.

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

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