2jbs

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[[Image:2jbs.gif|left|200px]]<br /><applet load="2jbs" size="450" color="white" frame="true" align="right" spinBox="true"
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[[Image:2jbs.gif|left|200px]]<br /><applet load="2jbs" size="350" color="white" frame="true" align="right" spinBox="true"
caption="2jbs, resolution 2.80&Aring;" />
caption="2jbs, resolution 2.80&Aring;" />
'''STRUCTURE OF THE MONOOXYGENASE COMPONENT OF P-HYDROXYPHENYLACETATE HYDROXYLASE FROM ACINETOBACTER BAUMANNII'''<br />
'''STRUCTURE OF THE MONOOXYGENASE COMPONENT OF P-HYDROXYPHENYLACETATE HYDROXYLASE FROM ACINETOBACTER BAUMANNII'''<br />
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==About this Structure==
==About this Structure==
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2JBS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Acinetobacter_baumannii Acinetobacter baumannii] with FMN as [http://en.wikipedia.org/wiki/ligand ligand]. Known structural/functional Site: <scene name='pdbsite=AC1:Fmn Binding Site For Chain D'>AC1</scene>. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=2JBS OCA].
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2JBS is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Acinetobacter_baumannii Acinetobacter baumannii] with <scene name='pdbligand=FMN:'>FMN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Known structural/functional Site: <scene name='pdbsite=AC1:Fmn+Binding+Site+For+Chain+D'>AC1</scene>. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2JBS OCA].
==Reference==
==Reference==
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[[Category: oxidoreductase]]
[[Category: oxidoreductase]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Tue Dec 18 19:59:11 2007''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Feb 3 10:43:49 2008''

Revision as of 08:43, 3 February 2008


2jbs, resolution 2.80Å

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STRUCTURE OF THE MONOOXYGENASE COMPONENT OF P-HYDROXYPHENYLACETATE HYDROXYLASE FROM ACINETOBACTER BAUMANNII

Overview

p-Hydroxyphenylacetate hydroxylase from Acinetobacter baumannii is a, two-component system consisting of a NADH-dependent FMN reductase and a, monooxygenase (C2) that uses reduced FMN as substrate. The crystal, structures of C2 in the ligand-free and substrate-bound forms reveal a, preorganized pocket that binds reduced FMN without large conformational, changes. The Phe-266 side chain swings out to provide the space for, binding p-hydroxyphenylacetate that is oriented orthogonal to the flavin, ring. The geometry of the substrate-binding site of C2 is significantly, different from that of p-hydroxybenzoate hydroxylase, a single-component, flavoenzyme that catalyzes a similar reaction. The C2 overall structure, resembles the folding of medium-chain acyl-CoA dehydrogenase. An, outstanding feature in the C2 structure is a cavity located in front of, reduced FMN; it has a spherical shape with a 1.9-A radius and a 29-A3, volume and is interposed between the flavin C4a atom and the substrate, atom to be hydroxylated. The shape and position of this cavity are, perfectly fit for housing the oxygen atoms of the flavin C4a-hydroperoxide, intermediate that is formed upon reaction of the C2-bound reduced flavin, with molecular oxygen. The side chain of His-396 is predicted to act as a, hydrogen-bond donor to the oxygen atoms of the intermediate. This, architecture promotes the nucleophilic attack of the substrate onto the, terminal oxygen of the hydroperoxyflavin. Comparative analysis with the, structures of other flavoenzymes indicates that a distinctive feature of, monooxygenases is the presence of specific cavities that encapsulate and, stabilize the crucial hydroperoxyflavin intermediate.

About this Structure

2JBS is a Single protein structure of sequence from Acinetobacter baumannii with as ligand. Known structural/functional Site: . Full crystallographic information is available from OCA.

Reference

Structure of the monooxygenase component of a two-component flavoprotein monooxygenase., Alfieri A, Fersini F, Ruangchan N, Prongjit M, Chaiyen P, Mattevi A, Proc Natl Acad Sci U S A. 2007 Jan 23;104(4):1177-82. Epub 2007 Jan 16. PMID:17227849

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