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PDBsum entry 1sb3
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Oxidoreductase
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PDB id
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1sb3
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Contents |
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761 a.a.
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323 a.a.
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161 a.a.
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References listed in PDB file
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Key reference
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Title
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Structure of a xanthine oxidase-Related 4-Hydroxybenzoyl-Coa reductase with an additional [4fe-4s] cluster and an inverted electron flow.
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Authors
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M.Unciuleac,
E.Warkentin,
C.C.Page,
M.Boll,
U.Ermler.
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Ref.
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Structure, 2004,
12,
2249-2256.
[DOI no: ]
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PubMed id
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Abstract
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The Mo-flavo-Fe/S-dependent heterohexameric protein complex 4-hydroxybenzoyl-CoA
reductase (4-HBCR, dehydroxylating) is a central enzyme of the anaerobic
degradation of phenolic compounds and belongs to the xanthine oxidase (XO)
family of molybdenum enzymes. Its X-ray structure was established at 1.6 A
resolution. The most pronounced difference between 4-HBCR and other structurally
characterized members of the XO family is the insertion of 40 amino acids within
cluster at a distance of
16.5 A to the isoalloxazine ring of FAD. The architecture of 4-HBCR and
concomitantly performed electron transfer rate calculations suggest an inverted
cluster to
the Mo over a distance of 55 A. The binding site of 4-hydroxybenzoyl-CoA is
located in an 18 A long channel lined up by several aromatic side chains around
the aromatic moiety, which are proposed to shield and stabilize the postulated
radical intermediates during catalysis.
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Figure 1.
Figure 1. Reaction Catalyzed by 4-Hydroxybenzoyl-CoA
Reductase 
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The above figure is
reprinted
by permission from Cell Press:
Structure
(2004,
12,
2249-2256)
copyright 2004.
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Secondary reference #1
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Title
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Crystallization of 4-Hydroxybenzoyl-Coa reductase and the structure of its electron donor ferredoxin.
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Authors
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M.Unciuleac,
M.Boll,
E.Warkentin,
U.Ermler.
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Ref.
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Acta Crystallogr D Biol Crystallogr, 2004,
60,
388-391.
[DOI no: ]
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PubMed id
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Figure 1.
Figure 1 Reactions catalyzed by benzoyl-CoA reductase (1) and
4-hydroxybenzoyl-CoA reductase (2). In T. aromatica, reduced
ferredoxin serves as in vivo electron donor for both reactions;
it is regenerated by 2-oxoglutarate:ferredoxin oxidoreductase.
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The above figure is
reproduced from the cited reference
with permission from the IUCr
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