DXP reductoisomerase

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Line 27: Line 27:
**[[4zqe]] – McDXR – ''Moraxella catarrhalis''<br />
**[[4zqe]] – McDXR – ''Moraxella catarrhalis''<br />
**[[5kqo]], [[5kry]], [[5ks1]] – VvDXR – ''Vibrio vulnificus''<br />
**[[5kqo]], [[5kry]], [[5ks1]] – VvDXR – ''Vibrio vulnificus''<br />
 +
**[[6mh4]] – SsDXR – ''Staphylococcus schleiferi''<br />
*DXP reductoisomerase binary complex
*DXP reductoisomerase binary complex
Line 42: Line 43:
**[[5krr]] – VvDXR + Mn<br />
**[[5krr]] – VvDXR + Mn<br />
**[[5krv]] – VvDXR + Arg<br />
**[[5krv]] – VvDXR + Arg<br />
 +
**[[6mh5]] – SsDXR + antibiotic<br />
*DXP reductoisomerase ternary complex
*DXP reductoisomerase ternary complex

Revision as of 07:35, 20 July 2020

DXP reductoisomerase complex with NADPH, Mn+2 ion (green) and anti-malaria drug fosmidomycin (PDB code 3zhy)

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3D Structures of DXP reductoisomerase

Updated on 20-July-2020

References

  1. Takahashi S, Kuzuyama T, Watanabe H, Seto H. A 1-deoxy-D-xylulose 5-phosphate reductoisomerase catalyzing the formation of 2-C-methyl-D-erythritol 4-phosphate in an alternative nonmevalonate pathway for terpenoid biosynthesis. Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9879-84. PMID:9707569
  2. Jansson AM, Wieckowska A, Bjorkelid C, Yahiaoui S, Sooriyaarachchi S, Lindh M, Bergfors T, Dharavath S, Desroses M, Suresh S, Andaloussi M, Nikhil R, Sreevalli S, Srinivasa BR, Larhed M, Jones TA, Karlen A, Mowbray SL. DXR inhibition by potent mono- and disubstituted fosmidomycin analogues. J Med Chem. 2013 Aug 8;56(15):6190-9. doi: 10.1021/jm4006498. Epub 2013 Jul 17. PMID:23819803 doi:http://dx.doi.org/10.1021/jm4006498

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