8ca2: Difference between revisions

Revision as of 12:54, 11 July 2008

This article has been automatically seeded. Changes to this page should pertain to the PDB entry only and not to the protein or biomolecule in general.

File:8ca2.png

Template:STRUCTURE 8ca2

ENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE IIENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE II

Template:ABSTRACT PUBMED 1932029

About this StructureAbout this Structure

8CA2 is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

ReferenceReference

Engineering the hydrophobic pocket of carbonic anhydrase II., Alexander RS, Nair SK, Christianson DW, Biochemistry. 1991 Nov 19;30(46):11064-72. PMID:1932029

Page seeded by OCA on Fri Jul 11 12:54:43 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA

@@ Line 1: / Line 1: @@
-[[Image:8ca2.gif|left|200px]]
+{{Seed}}
+[[Image:8ca2.png|left|200px]]
 <!--
@@ Line 9: / Line 10: @@
 {{STRUCTURE_8ca2|  PDB=8ca2  |  SCENE=  }}
-'''ENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE II'''
+===ENGINEERING THE HYDROPHOBIC POCKET OF CARBONIC ANHYDRASE II===
-==Overview==
+<!--
-Wild-type and mutant human carbonic anhydrases II, where mutations have been made in the hydrophobic pocket of the active site, have been studied by X-ray crystallographic methods. Specifically, mutations at Val-143 (the base of the pocket) lead to significant changes in catalytic activity and protein structure. The obliteration of a well-defined pocket in the Val-143----Phe and Val-143----Tyr mutants results in significantly diminished enzyme activity [(5 x 10(4))-fold and (3 x 10(5))-fold, respectively]; however, the activity of the Val-143----His mutant is diminished less (10(2)-fold), and deepening the pocket in the Val-143----Gly mutant results in only a 2-fold decrease in activity [Fierke et al., 1991 (preceding paper in this issue)]. These results indicate that the hydrophobic pocket is important for substrate association with the enzyme, but there are probably several catalytically acceptable substrate trajectories through this region of the enzyme structure. Additionally, each mutant protein exhibits long-range (ca. 10-15 A) compensatory structural changes which accommodate the Val-143 substitution. As such, the genetic-structural approach represented in this work serves as a three-dimensional paradigm for the redesign of specificity pockets in other protein catalysts.
+The line below this paragraph, {{ABSTRACT_PUBMED_1932029}}, adds the Publication Abstract to the page
+(as it appears on PubMed at http://www.pubmed.gov), where 1932029 is the PubMed ID number.
+-->
+{{ABSTRACT_PUBMED_1932029}}
 ==About this Structure==
@@ Line 25: / Line 29: @@
 [[Category: Alexander, R S.]]
 [[Category: Christianson, D W.]]
-''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May  4 22:48:51 2008''
+''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Jul 11 12:54:43 2008''