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1w3p

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[[Image:1w3p.jpg|left|200px]]<br /><applet load="1w3p" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:1w3p.jpg|left|200px]]
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caption="1w3p, resolution 1.80&Aring;" />
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'''NIMA FROM D. RADIODURANS WITH A HIS71-PYRUVATE RESIDUE'''<br />
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{{Structure
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|PDB= 1w3p |SIZE=350|CAPTION= <scene name='initialview01'>1w3p</scene>, resolution 1.80&Aring;
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|SITE= <scene name='pdbsite=AC1:Act+Binding+Site+For+Chain+A'>AC1</scene>
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|LIGAND= <scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene> and <scene name='pdbligand=PYR:PYRUVIC ACID'>PYR</scene>
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|ACTIVITY=
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|GENE=
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}}
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'''NIMA FROM D. RADIODURANS WITH A HIS71-PYRUVATE RESIDUE'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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1W3P is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Deinococcus_radiodurans Deinococcus radiodurans] with <scene name='pdbligand=ACT:'>ACT</scene> and <scene name='pdbligand=PYR:'>PYR</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Known structural/functional Site: <scene name='pdbsite=AC1:Act+Binding+Site+For+Chain+A'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1W3P OCA].
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1W3P is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Deinococcus_radiodurans Deinococcus radiodurans]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1W3P OCA].
==Reference==
==Reference==
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Structural basis of 5-nitroimidazole antibiotic resistance: the crystal structure of NimA from Deinococcus radiodurans., Leiros HK, Kozielski-Stuhrmann S, Kapp U, Terradot L, Leonard GA, McSweeney SM, J Biol Chem. 2004 Dec 31;279(53):55840-9. Epub 2004 Oct 18. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15492014 15492014]
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Structural basis of 5-nitroimidazole antibiotic resistance: the crystal structure of NimA from Deinococcus radiodurans., Leiros HK, Kozielski-Stuhrmann S, Kapp U, Terradot L, Leonard GA, McSweeney SM, J Biol Chem. 2004 Dec 31;279(53):55840-9. Epub 2004 Oct 18. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15492014 15492014]
[[Category: Deinococcus radiodurans]]
[[Category: Deinococcus radiodurans]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: antibiotic resistance]]
[[Category: antibiotic resistance]]
[[Category: catalytic mechanism]]
[[Category: catalytic mechanism]]
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[[Category: deinococcus radiodurans]]
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[[Category: deinococcus radioduran]]
[[Category: nim gene]]
[[Category: nim gene]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 15:40:07 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 14:51:42 2008''

Revision as of 12:51, 20 March 2008


PDB ID 1w3p

Drag the structure with the mouse to rotate
, resolution 1.80Å
Sites:
Ligands: and
Coordinates: save as pdb, mmCIF, xml



NIMA FROM D. RADIODURANS WITH A HIS71-PYRUVATE RESIDUE


Overview

5-Nitroimidazole-based antibiotics are compounds extensively used for treating infections in humans and animals caused by several important pathogens. They are administered as prodrugs, and their activation depends upon an anaerobic 1-electron reduction of the nitro group by a reduction pathway in the cells. Bacterial resistance toward these drugs is thought to be caused by decreased drug uptake and/or an altered reduction efficiency. One class of resistant strains, identified in Bacteroides, has been shown to carry Nim genes (NimA, -B, -C, -D, and -E), which encode for reductases that convert the nitro group on the antibiotic into a non-bactericidal amine. In this paper, we have described the crystal structure of NimA from Deinococcus radiodurans (drNimA) at 1.6 A resolution. We have shown that drNimA is a homodimer in which each monomer adopts a beta-barrel fold. We have identified the catalytically important His-71 along with the cofactor pyruvate and antibiotic binding sites, all of which are found at the monomer-monomer interface. We have reported three additional crystal structures of drNimA, one in which the antibiotic metronidazole is bound to the protein, one with pyruvate covalently bound to His-71, and one with lactate covalently bound to His-71. Based on these structures, a reaction mechanism has been proposed in which the 2-electron reduction of the antibiotic prevents accumulation of the toxic nitro radical. This mechanism suggests that Nim proteins form a new class of reductases, conferring resistance against 5-nitroimidazole-based antibiotics.

About this Structure

1W3P is a Single protein structure of sequence from Deinococcus radiodurans. Full crystallographic information is available from OCA.

Reference

Structural basis of 5-nitroimidazole antibiotic resistance: the crystal structure of NimA from Deinococcus radiodurans., Leiros HK, Kozielski-Stuhrmann S, Kapp U, Terradot L, Leonard GA, McSweeney SM, J Biol Chem. 2004 Dec 31;279(53):55840-9. Epub 2004 Oct 18. PMID:15492014

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