1joa

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1joa.jpg|left|200px]]<br /><applet load="1joa" size="350" color="white" frame="true" align="right" spinBox="true"
+
[[Image:1joa.jpg|left|200px]]
-
caption="1joa, resolution 2.8&Aring;" />
+
 
-
'''NADH PEROXIDASE WITH CYSTEINE-SULFENIC ACID'''<br />
+
{{Structure
 +
|PDB= 1joa |SIZE=350|CAPTION= <scene name='initialview01'>1joa</scene>, resolution 2.8&Aring;
 +
|SITE= <scene name='pdbsite=ACT:Cso+42+Is+The+Native,+Active+CYS-Sulfenic+Acid+(Soh)'>ACT</scene>
 +
|LIGAND= <scene name='pdbligand=FAD:FLAVIN-ADENINE DINUCLEOTIDE'>FAD</scene>
 +
|ACTIVITY= [http://en.wikipedia.org/wiki/NADH_peroxidase NADH peroxidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.11.1.1 1.11.1.1]
 +
|GENE=
 +
}}
 +
 
 +
'''NADH PEROXIDASE WITH CYSTEINE-SULFENIC ACID'''
 +
 
==Overview==
==Overview==
Line 7: Line 16:
==About this Structure==
==About this Structure==
-
1JOA is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Enterococcus_faecalis Enterococcus faecalis] with <scene name='pdbligand=FAD:'>FAD</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/NADH_peroxidase NADH peroxidase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.11.1.1 1.11.1.1] Known structural/functional Site: <scene name='pdbsite=ACT:Cso+42+Is+The+Native,+Active+CYS-Sulfenic+Acid+(Soh)'>ACT</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JOA OCA].
+
1JOA is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Enterococcus_faecalis Enterococcus faecalis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1JOA OCA].
==Reference==
==Reference==
-
Structure of the native cysteine-sulfenic acid redox center of enterococcal NADH peroxidase refined at 2.8 A resolution., Yeh JI, Claiborne A, Hol WG, Biochemistry. 1996 Aug 6;35(31):9951-7. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=8756456 8756456]
+
Structure of the native cysteine-sulfenic acid redox center of enterococcal NADH peroxidase refined at 2.8 A resolution., Yeh JI, Claiborne A, Hol WG, Biochemistry. 1996 Aug 6;35(31):9951-7. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/8756456 8756456]
[[Category: Enterococcus faecalis]]
[[Category: Enterococcus faecalis]]
[[Category: NADH peroxidase]]
[[Category: NADH peroxidase]]
Line 21: Line 30:
[[Category: oxidoreductase]]
[[Category: oxidoreductase]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 13:24:49 2008''
+
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 12:06:07 2008''

Revision as of 10:06, 20 March 2008


PDB ID 1joa

Drag the structure with the mouse to rotate
, resolution 2.8Å
Sites:
Ligands:
Activity: NADH peroxidase, with EC number 1.11.1.1
Coordinates: save as pdb, mmCIF, xml



NADH PEROXIDASE WITH CYSTEINE-SULFENIC ACID


Overview

In order to obtain the crystal structure of the flavoprotein NADH peroxidase with its native Cys42-sulfenic acid redox center, a strategy combining reduced exposure of crystals to ambient oxygen and data collection at -160 degrees C was applied. The structure of the native enzyme to 2.8 A resolution is described; these results conclusively establish the existence of the Cys42-sulfenic acid as the functional non-flavin redox center of the peroxidase and provide the first structure for any naturally occurring protein-sulfenic acid. The Cys42-sulfenic acid atoms C alpha-C beta-S gamma-O roughly define a planar arrangement which is stacked parallel to the si face of the FAD isoalloxazine and positions the sulfenyl oxygen atom only 3.3 A from FAD-C4A. His10-N epsilon 2 contributes a hydrogen bond to the sulfenic acid oxygen, at a distance of 3.2 A. Although one oxygen atom (OX1) of the non-native Cys42-sulfonic acid derivative identified in the earlier wild-type peroxidase structure was taken to represent the native Cys42-sulfenic acid oxygen [Stehle, T., Ahmed, S. A., Claiborne, A., & Schulz, G. E. (1991) J. Mol. Biol. 221, 1325-1344], this structure shows that the sulfenic acid oxygen does not occupy this position, nor is it hydrogen-bonded to Cys42-N as was OX1. Comparison of the native Cys42-sulfenic acid structure with that of two-electron reduced glutathione reductase provides an insight into the sulfenic acid FAD charge-transfer interaction observed with both wild-type and His10 mutant peroxidases. A model of the E.NADH intermediate recently observed in stopped-flow analyses of the enzyme [Crane, E. J., III, Parsonage, D., Poole, L. B., & Claiborne, A. (1995) Biochemistry 34, 14114-14124] has also been generated to assist in analyzing the chemical mechanism of sulfenic acid reduction.

About this Structure

1JOA is a Single protein structure of sequence from Enterococcus faecalis. Full crystallographic information is available from OCA.

Reference

Structure of the native cysteine-sulfenic acid redox center of enterococcal NADH peroxidase refined at 2.8 A resolution., Yeh JI, Claiborne A, Hol WG, Biochemistry. 1996 Aug 6;35(31):9951-7. PMID:8756456

Page seeded by OCA on Thu Mar 20 12:06:07 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools