4e4e

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Crystal Structure of the Y34F mutant of Saccharomyces cerevisiae Manganese Superoxide DismutaseCrystal Structure of the Y34F mutant of Saccharomyces cerevisiae Manganese Superoxide Dismutase

Structural highlights

4e4e is a 4 chain structure with sequence from Atcc 18824. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Ligands:
NonStd Res:
Gene:SOD2, YHR008C (ATCC 18824)
Activity:Superoxide dismutase, with EC number 1.15.1.1
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

[SODM_YEAST] Destroys superoxide anion radicals which are normally produced within the cells and which are toxic to biological systems.

Publication Abstract from PubMed

Reduction of superoxide ( ) by manganese-containing superoxide dismutase occurs through either a "prompt protonation" pathway, or an "inner-sphere" pathway, with the latter leading to formation of an observable Mn-peroxo complex. We recently reported that wild-type (WT) manganese superoxide dismutases (MnSODs) from Saccharomyces cerevisiae and Candida albicans are more gated toward the "prompt protonation" pathway than human and bacterial MnSODs and suggested that this could result from small structural changes in the second coordination sphere of manganese. We report here that substitution of a second-sphere residue, Tyr34, by phenylalanine (Y34F) causes the MnSOD from S. cerevisiae to react exclusively through the "inner-sphere" pathway. At neutral pH, we have a surprising observation that protonation of the Mn-peroxo complex in the mutant yeast enzyme occurs through a fast pathway, leading to a putative six-coordinate Mn(3+) species, which actively oxidizes in the catalytic cycle. Upon increasing pH, the fast pathway is gradually replaced by a slow proton-transfer pathway, leading to the well-characterized five-coordinate Mn(3+). We here propose and compare two hypothetical mechanisms for the mutant yeast enzyme, differing in the structure of the Mn-peroxo complex yet both involving formation of the active six-coordinate Mn(3+) and proton transfer from a second-sphere water molecule, which has substituted for the horizontal line OH of Tyr34, to the Mn-peroxo complex. Because WT and the mutant yeast MnSOD both rest in the 2+ state and become six-coordinate when oxidized up from Mn(2+), six-coordinate Mn(3+) species could also actively function in the mechanism of WT yeast MnSODs.

Six-coordinate manganese(3+) in catalysis by yeast manganese superoxide dismutase.,Sheng Y, Butler Gralla E, Schumacher M, Cascio D, Cabelli DE, Selverstone Valentine J Proc Natl Acad Sci U S A. 2012 Sep 4;109(36):14314-9. Epub 2012 Aug 20. PMID:22908245[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

See Also

References

  1. Sheng Y, Butler Gralla E, Schumacher M, Cascio D, Cabelli DE, Selverstone Valentine J. Six-coordinate manganese(3+) in catalysis by yeast manganese superoxide dismutase. Proc Natl Acad Sci U S A. 2012 Sep 4;109(36):14314-9. Epub 2012 Aug 20. PMID:22908245 doi:http://dx.doi.org/10.1073/pnas.1212367109

4e4e, resolution 1.88Å

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