1ctt

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[[Image:1ctt.gif|left|200px]]
[[Image:1ctt.gif|left|200px]]
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{{Structure
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<!--
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|PDB= 1ctt |SIZE=350|CAPTION= <scene name='initialview01'>1ctt</scene>, resolution 2.2&Aring;
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The line below this paragraph, containing "STRUCTURE_1ctt", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=DHZ:3,4-DIHYDRO-1H-PYRIMIDIN-2-ONE+NUCLEOSIDE'>DHZ</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Cytidine_deaminase Cytidine deaminase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.5.4.5 3.5.4.5] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1ctt| PDB=1ctt | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1ctt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ctt OCA], [http://www.ebi.ac.uk/pdbsum/1ctt PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1ctt RCSB]</span>
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}}
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'''TRANSITION-STATE SELECTIVITY FOR A SINGLE OH GROUP DURING CATALYSIS BY CYTIDINE DEAMINASE'''
'''TRANSITION-STATE SELECTIVITY FOR A SINGLE OH GROUP DURING CATALYSIS BY CYTIDINE DEAMINASE'''
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[[Category: Wolfenden, R.]]
[[Category: Wolfenden, R.]]
[[Category: Xiang, S.]]
[[Category: Xiang, S.]]
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[[Category: hydrolase]]
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[[Category: Hydrolase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 13:06:18 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 19:28:20 2008''
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Revision as of 10:06, 2 May 2008

Template:STRUCTURE 1ctt

TRANSITION-STATE SELECTIVITY FOR A SINGLE OH GROUP DURING CATALYSIS BY CYTIDINE DEAMINASE


Overview

Cytidine deaminase binds transition-state analog inhibitors approximately 10(7) times more tightly than corresponding 3,4-dihydro analogs containing a proton in place of the 4-hydroxyl group. X-ray crystal structures of complexes with the two matched inhibitors differ only near a "trapped" water molecule in the complex with the 3,4-dihydro analog, where contacts are substantially less favorable than those with the hydroxyl group of the transition-state analog. The hydrogen bond between the hydroxyl group and the Glu 104 carboxylate shortens in that complex, and may become a "low-barrier" hydrogen bond, since at the same time the bond between zinc and the Cys 132 thiolate ligand lengthens. These differences must therefore account for most of the differential binding affinity related to catalysis. Moreover, the trapped water molecule retains some of the binding energy stabilizing the hydroxyl group in the transition-state analog complex. To this extent, the ratio of binding affinities for the two compounds is smaller than the true contribution of the hydroxyl group, a conclusion with significant bearing on interpreting difference free energies derived from substituent effects arising from chemical modification and/or mutagenesis.

About this Structure

1CTT is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.

Reference

Transition-state selectivity for a single hydroxyl group during catalysis by cytidine deaminase., Xiang S, Short SA, Wolfenden R, Carter CW Jr, Biochemistry. 1995 Apr 11;34(14):4516-23. PMID:7718553 Page seeded by OCA on Fri May 2 13:06:18 2008

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