2v23

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:2v23.jpg|left|200px]]
+
{{Seed}}
 +
[[Image:2v23.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_2v23| PDB=2v23 | SCENE= }}
{{STRUCTURE_2v23| PDB=2v23 | SCENE= }}
-
'''STRUCTURE OF CYTOCHROME C PEROXIDASE MUTANT N184R Y36A'''
+
===STRUCTURE OF CYTOCHROME C PEROXIDASE MUTANT N184R Y36A===
-
==Overview==
+
<!--
-
Isoniazid (INH, isonicotinic acid hydrazine) is one of only two therapeutic agents effective in treating tuberculosis. This prodrug is activated by the heme enzyme catalase peroxidase (KatG) endogenous to Mycobacterium tuberculosis but the mechanism of activation is poorly understood, in part because the binding interaction has not been properly established. The class I peroxidases ascorbate peroxidase (APX) and cytochrome c peroxidase (CcP) have active site structures very similar to KatG and are also capable of activating isoniazid. We report here the first crystal structures of complexes of isoniazid bound to APX and CcP. These are the first structures of isoniazid bound to any activating enzymes. The structures show that isoniazid binds close to the delta-heme edge in both APX and CcP, although the precise binding orientation varies slightly in the two cases. A second binding site for INH is found in APX at the gamma-heme edge close to the established ascorbate binding site, indicating that the gamma-heme edge can also support the binding of aromatic substrates. We also show that in an active site mutant of soybean APX (W41A) INH can bind directly to the heme iron to become an inhibitor and in a different mode when the distal histidine is replaced by alanine (H42A). These structures provide the first unambiguous evidence for the location of the isoniazid binding site in the class I peroxidases and provide rationalization of isoniazid resistance in naturally occurring KatG mutant strains of M. tuberculosis.
+
The line below this paragraph, {{ABSTRACT_PUBMED_18056997}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 18056997 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_18056997}}
==About this Structure==
==About this Structure==
Line 41: Line 45:
[[Category: Peroxidase]]
[[Category: Peroxidase]]
[[Category: Transit peptide]]
[[Category: Transit peptide]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 18:04:34 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 19:29:43 2008''

Revision as of 16:29, 27 July 2008

Image:2v23.png

Template:STRUCTURE 2v23

STRUCTURE OF CYTOCHROME C PEROXIDASE MUTANT N184R Y36A

Template:ABSTRACT PUBMED 18056997

About this Structure

2V23 is a Single protein structure of sequence from Saccharomyces cerevisiae. Full crystallographic information is available from OCA.

Reference

The Tuberculosis Prodrug Isoniazid Bound to Activating Peroxidases., Metcalfe C, Macdonald IK, Murphy EJ, Brown KA, Raven EL, Moody PC, J Biol Chem. 2008 Mar 7;283(10):6193-6200. Epub 2007 Dec 5. PMID:18056997

Page seeded by OCA on Sun Jul 27 19:29:43 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/2v23"
Personal tools