1get

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1get.gif|left|200px]]
+
{{Seed}}
 +
[[Image:1get.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1get| PDB=1get | SCENE= }}
{{STRUCTURE_1get| PDB=1get | SCENE= }}
-
'''ANATOMY OF AN ENGINEERED NAD-BINDING SITE'''
+
===ANATOMY OF AN ENGINEERED NAD-BINDING SITE===
-
==Overview==
+
<!--
-
The coenzyme specificity of Escherichia coli glutathione reductase was switched from NADP to NAD by modifying the environment of the 2'-phosphate binding site through a set of point mutations: A179G, A183G, V197E, R198M, K199F, H200D, and R204P (Scrutton NS, Berry A, Perham RN, 1990, Nature 343:38-43). In order to analyze the structural changes involved, we have determined 4 high-resolution crystal structures, i.e., the structures of the wild-type enzyme (1.86 A resolution, R-factor of 16.8%), of the wild-type enzyme ligated with NADP (2.0 A, 20.8%), of the NAD-dependent mutant (1.74 A, 16.8%), and of the NAD-dependent mutant ligated with NAD (2.2 A, 16.9%). A comparison of these structures reveals subtle differences that explain details of the specificity change. In particular, a peptide rotation occurs close to the adenosine ribose, with a concomitant change of the ribose pucker. The mutations cause a contraction of the local chain fold. Furthermore, the engineered NAD-binding site assumes a less rigid structure than the NADP site of the wild-type enzyme. A superposition of the ligated structures shows a displacement of NAD versus NADP such that the electron pathway from the nicotinamide ring to FAD is elongated, which may explain the lower catalytic efficiency of the mutant. Because the nicotinamide is as much as 15 A from the sites of the mutations, this observation reminds us that mutations may have important long-range consequences that are difficult to anticipate.
+
The line below this paragraph, {{ABSTRACT_PUBMED_7833810}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 7833810 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_7833810}}
==About this Structure==
==About this Structure==
Line 25: Line 29:
[[Category: Mittl, P R.E.]]
[[Category: Mittl, P R.E.]]
[[Category: Schulz, G E.]]
[[Category: Schulz, G E.]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 17:28:57 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 1 05:10:54 2008''

Revision as of 02:10, 1 July 2008

Image:1get.png

Template:STRUCTURE 1get

ANATOMY OF AN ENGINEERED NAD-BINDING SITE

Template:ABSTRACT PUBMED 7833810

About this Structure

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

Reference

Anatomy of an engineered NAD-binding site., Mittl PR, Berry A, Scrutton NS, Perham RN, Schulz GE, Protein Sci. 1994 Sep;3(9):1504-14. PMID:7833810

Page seeded by OCA on Tue Jul 1 05:10:54 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/1get"
Personal tools