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PDBsum entry 1sb3

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Oxidoreductase PDB id
1sb3
Contents
Protein chains
761 a.a.
323 a.a.
161 a.a.
Ligands
PCD ×2
EPE
FAD ×2
SF4 ×2
FES ×4
SO4 ×2
Waters ×1042

References listed in PDB file
Key reference
Title Structure of a xanthine oxidase-Related 4-Hydroxybenzoyl-Coa reductase with an additional [4fe-4s] cluster and an inverted electron flow.
Authors M.Unciuleac, E.Warkentin, C.C.Page, M.Boll, U.Ermler.
Ref. Structure, 2004, 12, 2249-2256. [DOI no: 10.1016/j.str.2004.10.008]
PubMed id 15576037
Abstract
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.
Figure 1.
Figure 1. Reaction Catalyzed by 4-Hydroxybenzoyl-CoA Reductase

The above figure is reprinted by permission from Cell Press: Structure (2004, 12, 2249-2256) copyright 2004.
Secondary reference #1
Title Crystallization of 4-Hydroxybenzoyl-Coa reductase and the structure of its electron donor ferredoxin.
Authors M.Unciuleac, M.Boll, E.Warkentin, U.Ermler.
Ref. Acta Crystallogr D Biol Crystallogr, 2004, 60, 388-391. [DOI no: 10.1107/S0907444903028506]
PubMed id 14747735
Full text Abstract
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.
The above figure is reproduced from the cited reference with permission from the IUCr
PROCHECK
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 Headers

 

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