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3AUA

Crystal structure of the quaternary complex-2 of an isomerase

Summary for 3AUA
Entry DOI10.2210/pdb3aua/pdb
Related3AU8 3AU9
Descriptor1-deoxy-D-xylulose 5-phosphate reductoisomerase, NADPH DIHYDRO-NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE, MAGNESIUM ION, ... (6 entities in total)
Functional Keywordsnadph binding, isomerase-isomerase inhibitor complex, isomerase/isomerase inhibitor
Biological sourcePlasmodium falciparum
Cellular locationPlastid, apicoplast: O96693
Total number of polymer chains2
Total formula weight113673.08
Authors
Umeda, T.,Tanaka, N.,Kusakabe, Y.,Nakanishi, M.,Kitade, Y.,Nakamura, K.T. (deposition date: 2011-02-01, release date: 2011-08-10, Last modification date: 2024-03-13)
Primary citationUmeda, T.,Tanaka, N.,Kusakabe, Y.,Nakanishi, M.,Kitade, Y.,Nakamura, K.T.
Molecular basis of fosmidomycin's action on the human malaria parasite Plasmodium falciparum
Sci Rep, 1:9-9, 2011
Cited by
PubMed Abstract: The human malaria parasite Plasmodium falciparum is responsible for the deaths of more than a million people each year. Fosmidomycin has been proven to be efficient in the treatment of P. falciparum malaria by inhibiting 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR), an enzyme of the non-mevalonate pathway, which is absent in humans. However, the structural details of DXR inhibition by fosmidomycin in P. falciparum are unknown. Here, we report the crystal structures of fosmidomycin-bound complete quaternary complexes of PfDXR. Our study revealed that (i) an intrinsic flexibility of the PfDXR molecule accounts for an induced-fit movement to accommodate the bound inhibitor in the active site and (ii) a cis arrangement of the oxygen atoms of the hydroxamate group of the bound inhibitor is essential for tight binding of the inhibitor to the active site metal. We expect the present structures to be useful guides for the design of more effective antimalarial compounds.
PubMed: 22355528
DOI: 10.1038/srep00009
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.15 Å)
Structure validation

227111

數據於2024-11-06公開中

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