1sca

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(New page: 200px<br /><applet load="1sca" size="450" color="white" frame="true" align="right" spinBox="true" caption="1sca, resolution 2.0&Aring;" /> '''ENZYME CRYSTAL STRUCT...)
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[[Image:1sca.gif|left|200px]]<br /><applet load="1sca" size="350" color="white" frame="true" align="right" spinBox="true"
caption="1sca, resolution 2.0&Aring;" />
caption="1sca, resolution 2.0&Aring;" />
'''ENZYME CRYSTAL STRUCTURE IN A NEAT ORGANIC SOLVENT'''<br />
'''ENZYME CRYSTAL STRUCTURE IN A NEAT ORGANIC SOLVENT'''<br />
==Overview==
==Overview==
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The crystal structure of the serine protease subtilisin Carlsberg in, anhydrous acetonitrile was determined at 2.3 A resolution. It was found to, be essentially identical to the three-dimensional structure of the enzyme, in water; the differences observed were smaller than those between two, independently determined structures in aqueous solution. The hydrogen bond, system of the catalytic triad is intact in acetonitrile. The majority (99, of 119) of enzyme-bound, structural water molecules have such a great, affinity to subtilisin that they are not displaced even in anhydrous, acetonitrile. Of the 12 enzyme-bound acetonitrile molecules, 4 displace, water molecules and 8 bind where no water had been observed before., One-third of all subtilisin-bound acetonitrile molecules reside in the, active center, occupying the same region (P1, P2, and P3 binding sites) as, the specific protein inhibitor eglin c.
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The crystal structure of the serine protease subtilisin Carlsberg in anhydrous acetonitrile was determined at 2.3 A resolution. It was found to be essentially identical to the three-dimensional structure of the enzyme in water; the differences observed were smaller than those between two independently determined structures in aqueous solution. The hydrogen bond system of the catalytic triad is intact in acetonitrile. The majority (99 of 119) of enzyme-bound, structural water molecules have such a great affinity to subtilisin that they are not displaced even in anhydrous acetonitrile. Of the 12 enzyme-bound acetonitrile molecules, 4 displace water molecules and 8 bind where no water had been observed before. One-third of all subtilisin-bound acetonitrile molecules reside in the active center, occupying the same region (P1, P2, and P3 binding sites) as the specific protein inhibitor eglin c.
==About this Structure==
==About this Structure==
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1SCA is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_licheniformis Bacillus licheniformis] with CA and NA as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1SCA OCA].
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1SCA is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Bacillus_licheniformis Bacillus licheniformis] with <scene name='pdbligand=CA:'>CA</scene> and <scene name='pdbligand=NA:'>NA</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [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] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1SCA OCA].
==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Subtilisin]]
[[Category: Subtilisin]]
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[[Category: Fitzpatrick, P.A.]]
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[[Category: Fitzpatrick, P A.]]
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[[Category: Klibanov, A.M.]]
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[[Category: Klibanov, A M.]]
[[Category: Ringe, D.]]
[[Category: Ringe, D.]]
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[[Category: Steinmetz, A.C.U.]]
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[[Category: Steinmetz, A C.U.]]
[[Category: CA]]
[[Category: CA]]
[[Category: NA]]
[[Category: NA]]
[[Category: serine protease]]
[[Category: serine protease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:00:05 2008''

Revision as of 13:00, 21 February 2008


1sca, resolution 2.0Å

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ENZYME CRYSTAL STRUCTURE IN A NEAT ORGANIC SOLVENT

Overview

The crystal structure of the serine protease subtilisin Carlsberg in anhydrous acetonitrile was determined at 2.3 A resolution. It was found to be essentially identical to the three-dimensional structure of the enzyme in water; the differences observed were smaller than those between two independently determined structures in aqueous solution. The hydrogen bond system of the catalytic triad is intact in acetonitrile. The majority (99 of 119) of enzyme-bound, structural water molecules have such a great affinity to subtilisin that they are not displaced even in anhydrous acetonitrile. Of the 12 enzyme-bound acetonitrile molecules, 4 displace water molecules and 8 bind where no water had been observed before. One-third of all subtilisin-bound acetonitrile molecules reside in the active center, occupying the same region (P1, P2, and P3 binding sites) as the specific protein inhibitor eglin c.

About this Structure

1SCA is a Single protein structure of sequence from Bacillus licheniformis with and as ligands. Active as Subtilisin, with EC number 3.4.21.62 Full crystallographic information is available from OCA.

Reference

Enzyme crystal structure in a neat organic solvent., Fitzpatrick PA, Steinmetz AC, Ringe D, Klibanov AM, Proc Natl Acad Sci U S A. 1993 Sep 15;90(18):8653-7. PMID:8378343

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