DXP reductoisomerase

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Line 25: Line 25:
**[[2jcy]] – MtDXR (mutant) <br />
**[[2jcy]] – MtDXR (mutant) <br />
**[[4zn6]] – DXR – ''Acinetobacter baumannii'' <br />
**[[4zn6]] – DXR – ''Acinetobacter baumannii'' <br />
 +
**[[4zqe]] – McDXR – ''Moraxella catarrhalis''<br />
*DXP reductoisomerase binary complex
*DXP reductoisomerase binary complex
Line 36: Line 37:
**[[3zhz]] – MtDXR + anti-malaria drug<br />
**[[3zhz]] – MtDXR + anti-malaria drug<br />
**[[1ono]] – EcDXR + Mn<br />
**[[1ono]] – EcDXR + Mn<br />
-
**[[3iie]] – DXR + Mg – ''Yersinia pestis''<br />
+
**[[3iie]] – YpDXR + Mg – ''Yersinia pestis''<br />
 +
**[[5dul]] – YpDXR + NADPH<br />
*DXP reductoisomerase ternary complex
*DXP reductoisomerase ternary complex
Line 49: Line 51:
**[[3a14]] – TmDXR + NADPH + Mg – ''Thermotoga maritima''<br />
**[[3a14]] – TmDXR + NADPH + Mg – ''Thermotoga maritima''<br />
**[[3au8]] – PfDXR + NADPH + Mn – ''Plasmodium falciparum''<br />
**[[3au8]] – PfDXR + NADPH + Mn – ''Plasmodium falciparum''<br />
-
**[[4y67]], [[4y6p]], [[4y6r]], [[4y6s]] – PfDXR + Mn + anti-malaria drug<br />
+
**[[4y67]], [[4y6p]], [[4y6r]], [[4y6s]], [[5jaz]], [[5jbi]], [[5jc1]], [[5jmp]], [[5jmw]], [[5jnl]], [[5jo0]] – PfDXR + Mn + anti-malaria drug<br />
 +
**[[4zqf]] – McDXR + Mg + anti-malaria drug<br />
*DXP reductoisomerase quaternary complex
*DXP reductoisomerase quaternary complex
Line 63: Line 66:
**[[4gae]] – PfDXR (mutant) + NADPH + Mn + pyridine inhibitor <br />
**[[4gae]] – PfDXR (mutant) + NADPH + Mn + pyridine inhibitor <br />
**[[3wqq]], [[3wqr]], [[3wqs]] – PfDXR + NADPH + Mg + inhibitor <br />
**[[3wqq]], [[3wqr]], [[3wqs]] – PfDXR + NADPH + Mg + inhibitor <br />
-
 
+
**[[4zqg]] – McDXR + NAD + Mg + anti-malaria drug<br />
 +
**[[4zqh]] – McDXR + NADPH + Mg + anti-malaria drug<br />
}}
}}
== References ==
== References ==
<references/>
<references/>

Revision as of 06:41, 27 April 2017

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

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3D Structures of DXP reductoisomerase

Updated on 27-April-2017

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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