Reaction Details |
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Target | 1-deoxy-D-xylulose 5-phosphate reductoisomerase |
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Ligand | BDBM50181150 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_345851 (CHEMBL860877) |
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IC50 | 156±n/a nM |
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Citation | Haemers, T; Wiesner, J; Van Poecke, S; Goeman, J; Henschker, D; Beck, E; Jomaa, H; Van Calenbergh, S Synthesis of alpha-substituted fosmidomycin analogues as highly potent Plasmodium falciparum growth inhibitors. Bioorg Med Chem Lett16:1888-91 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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1-deoxy-D-xylulose 5-phosphate reductoisomerase |
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Name: | 1-deoxy-D-xylulose 5-phosphate reductoisomerase |
Synonyms: | 1-Deoxy-D-xylulose 5-phosphate reductoisomerase (DXP) | 1-Deoxyxylulose 5-phosphate reductoisomerase (DXR) | 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR) | 2-C-methyl-D-erythritol 4-phosphate synthase | DXP reductoisomerase | DXR_ECOLI | dxr | ispC | yaeM |
Type: | Protein |
Mol. Mass.: | 43384.52 |
Organism: | Escherichia coli |
Description: | P45568 |
Residue: | 398 |
Sequence: | MKQLTILGSTGSIGCSTLDVVRHNPEHFRVVALVAGKNVTRMVEQCLEFSPRYAVMDDEA
SAKLLKTMLQQQGSRTEVLSGQQAACDMAALEDVDQVMAAIVGAAGLLPTLAAIRAGKTI
LLANKESLVTCGRLFMDAVKQSKAQLLPVDSEHNAIFQSLPQPIQHNLGYADLEQNGVVS
ILLTGSGGPFRETPLRDLATMTPDQACRHPNWSMGRKISVDSATMMNKGLEYIEARWLFN
ASASQMEVLIHPQSVIHSMVRYQDGSVLAQLGEPDMRTPIAHTMAWPNRVNSGVKPLDFC
KLSALTFAAPDYDRYPCLKLAMEAFEQGQAATTALNAANEITVAAFLAQQIRFTDIAALN
LSVLEKMDMREPQCVDDVLSVDANAREVARKEVMRLAS
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BDBM50181150 |
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n/a |
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Name | BDBM50181150 |
Synonyms: | 3-(N-hydroxyformamido)-1-(4-methoxyphenyl)propylphosphonic acid | CHEMBL205339 |
Type | Small organic molecule |
Emp. Form. | C11H16NO6P |
Mol. Mass. | 289.2216 |
SMILES | COc1ccc(cc1)C(CCN(O)C=O)P(O)(O)=O |
Structure |
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