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1wvv

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(New page: 200px<br /><applet load="1wvv" size="450" color="white" frame="true" align="right" spinBox="true" caption="1wvv, resolution 2.00&Aring;" /> '''Crystal structure of...)
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caption="1wvv, resolution 2.00&Aring;" />
'''Crystal structure of chitinase C mutant E147Q'''<br />
'''Crystal structure of chitinase C mutant E147Q'''<br />
==Overview==
==Overview==
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Chitinase C (ChiC) from Streptomyces griseus HUT6037 was the first, glycoside hydrolase family 19 chitinase that was found in an organism, other than higher plants. An N-terminal chitin-binding domain and a, C-terminal catalytic domain connected by a linker peptide constitute ChiC., We determined the crystal structure of full-length ChiC, which is the only, representative of the two-domain chitinases in the family. The catalytic, domain has an alpha-helix-rich fold with a deep cleft containing a, catalytic site, and lacks three loops on the domain surface compared with, the catalytic domain of plant chitinases. The chitin-binding domain is an, all-beta protein with two tryptophan residues (Trp59 and Trp60) aligned on, the surface. We suggest the binding mechanism of tri-N-acetylchitotriose, onto the chitin-binding domain on the basis of molecular dynamics (MD), simulations. In this mechanism, the ligand molecule binds well on the, surface-exposed binding site through two stacking interactions and two, hydrogen bonds and only Trp59 and Trp60 are involved in the binding., Furthermore, the flexibility of the Trp60 side-chain, which may be, involved in adjusting the binding surface to fit the surface of, crystalline chitin by the rotation of chi2 angle, is shown.
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Chitinase C (ChiC) from Streptomyces griseus HUT6037 was the first glycoside hydrolase family 19 chitinase that was found in an organism other than higher plants. An N-terminal chitin-binding domain and a C-terminal catalytic domain connected by a linker peptide constitute ChiC. We determined the crystal structure of full-length ChiC, which is the only representative of the two-domain chitinases in the family. The catalytic domain has an alpha-helix-rich fold with a deep cleft containing a catalytic site, and lacks three loops on the domain surface compared with the catalytic domain of plant chitinases. The chitin-binding domain is an all-beta protein with two tryptophan residues (Trp59 and Trp60) aligned on the surface. We suggest the binding mechanism of tri-N-acetylchitotriose onto the chitin-binding domain on the basis of molecular dynamics (MD) simulations. In this mechanism, the ligand molecule binds well on the surface-exposed binding site through two stacking interactions and two hydrogen bonds and only Trp59 and Trp60 are involved in the binding. Furthermore, the flexibility of the Trp60 side-chain, which may be involved in adjusting the binding surface to fit the surface of crystalline chitin by the rotation of chi2 angle, is shown.
==About this Structure==
==About this Structure==
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1WVV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptomyces_chryseus Streptomyces chryseus] with CL and GOL as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Chitinase Chitinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.14 3.2.1.14] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1WVV OCA].
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1WVV is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Streptomyces_chryseus Streptomyces chryseus] with <scene name='pdbligand=CL:'>CL</scene> and <scene name='pdbligand=GOL:'>GOL</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Active as [http://en.wikipedia.org/wiki/Chitinase Chitinase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.2.1.14 3.2.1.14] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WVV OCA].
==Reference==
==Reference==
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[[Category: whole structure]]
[[Category: whole structure]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 00:51:57 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:48:39 2008''

Revision as of 13:48, 21 February 2008


1wvv, resolution 2.00Å

Drag the structure with the mouse to rotate

Crystal structure of chitinase C mutant E147Q

Overview

Chitinase C (ChiC) from Streptomyces griseus HUT6037 was the first glycoside hydrolase family 19 chitinase that was found in an organism other than higher plants. An N-terminal chitin-binding domain and a C-terminal catalytic domain connected by a linker peptide constitute ChiC. We determined the crystal structure of full-length ChiC, which is the only representative of the two-domain chitinases in the family. The catalytic domain has an alpha-helix-rich fold with a deep cleft containing a catalytic site, and lacks three loops on the domain surface compared with the catalytic domain of plant chitinases. The chitin-binding domain is an all-beta protein with two tryptophan residues (Trp59 and Trp60) aligned on the surface. We suggest the binding mechanism of tri-N-acetylchitotriose onto the chitin-binding domain on the basis of molecular dynamics (MD) simulations. In this mechanism, the ligand molecule binds well on the surface-exposed binding site through two stacking interactions and two hydrogen bonds and only Trp59 and Trp60 are involved in the binding. Furthermore, the flexibility of the Trp60 side-chain, which may be involved in adjusting the binding surface to fit the surface of crystalline chitin by the rotation of chi2 angle, is shown.

About this Structure

1WVV is a Single protein structure of sequence from Streptomyces chryseus with and as ligands. Active as Chitinase, with EC number 3.2.1.14 Full crystallographic information is available from OCA.

Reference

Structural studies of a two-domain chitinase from Streptomyces griseus HUT6037., Kezuka Y, Ohishi M, Itoh Y, Watanabe J, Mitsutomi M, Watanabe T, Nonaka T, J Mol Biol. 2006 Apr 28;358(2):472-84. Epub 2006 Feb 21. PMID:16516924

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