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2bf2

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{{STRUCTURE_2bf2| PDB=2bf2 | SCENE= }}
{{STRUCTURE_2bf2| PDB=2bf2 | SCENE= }}
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'''CRYSTAL STRUCTURE OF NATIVE TOLUENE-4-MONOOXYGENASE CATALYTIC EFFECTOR PROTEIN, T4MOD'''
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===CRYSTAL STRUCTURE OF NATIVE TOLUENE-4-MONOOXYGENASE CATALYTIC EFFECTOR PROTEIN, T4MOD===
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==Overview==
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Toluene 4-monooxygenase (T4MO) is a four-component complex that catalyzes the regiospecific, NADH-dependent hydroxylation of toluene to yield p-cresol. The catalytic effector (T4moD) of this complex is a 102-residue protein devoid of metals or organic cofactors. It forms a complex with the diiron hydroxylase component (T4moH) that influences both the kinetics and regiospecificity of catalysis. Here, we report crystal structures for native T4moD and two engineered variants with either four (DeltaN4-) or 10 (DeltaN10-) residues removed from the N-terminal at 2.1-, 1.7-, and 1.9-A resolution, respectively. The crystal structures have C-alpha root-mean-squared differences of less than 0.8 A for the central core consisting of residues 11-98, showing that alterations of the N-terminal have little influence on the folded core of the protein. The central core has the same fold topology as observed in the NMR structures of T4moD, the methane monooxygenase effector protein (MmoB) from two methanotrophs, and the phenol hydroxylase effector protein (DmpM). However, the root-mean-squared differences between comparable C-alpha positions in the X-ray structures and the NMR structures vary from approximately 1.8 A to greater than 6 A. The X-ray structures exhibit an estimated overall coordinate error from 0.095 (0.094) A based on the R-value (R free) for the highest resolution DeltaN4-T4moD structure to 0.211 (0.196) A for the native T4moD structure. Catalytic studies of the DeltaN4-, DeltaN7-, and DeltaN10- variants of T4moD show statistically insignificant changes in k(cat), K(M), k(cat)/K(M), and K(I) relative to the native protein. Moreover, there was no significant change in the regiospecificity of toluene oxidation with any of the T4moD variants. The relative insensitivity to changes in the N-terminal region distinguishes T4moD from the MmoB homologues, which each require the approximately 33 residue N-terminal region for catalytic activity.
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{{ABSTRACT_PUBMED_15882052}}
==About this Structure==
==About this Structure==
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[[Category: Oxidoreductase]]
[[Category: Oxidoreductase]]
[[Category: Toluene oxidation]]
[[Category: Toluene oxidation]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 20:12:21 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 16:59:46 2008''

Revision as of 13:59, 27 July 2008

Image:2bf2.png

Template:STRUCTURE 2bf2

CRYSTAL STRUCTURE OF NATIVE TOLUENE-4-MONOOXYGENASE CATALYTIC EFFECTOR PROTEIN, T4MOD

Template:ABSTRACT PUBMED 15882052

About this Structure

2BF2 is a Single protein structure of sequence from Pseudomonas mendocina. Full crystallographic information is available from OCA.

Reference

Crystal structures and functional studies of T4moD, the toluene 4-monooxygenase catalytic effector protein., Lountos GT, Mitchell KH, Studts JM, Fox BG, Orville AM, Biochemistry. 2005 May 17;44(19):7131-42. PMID:15882052

Page seeded by OCA on Sun Jul 27 16:59:46 2008

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