| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 10870867 | FEBS Letters | 2013 | 12 Pages | 
Abstract
												This study demonstrates that both types of enzyme targets, one acting via flux reduction and the other by metabolite accumulation, exist in P. falciparum MEP pathway. These groups of targets can be exploited for independent anti-malarial drugs.
											Keywords
												SBMLPYRIPPDXRDXSMEP1-deoxy-D-xylulose 5-phosphate synthase1-deoxy-D-xylulose 5-phosphateDXPDMAPPPDB1-deoxy-d-xylulose 5-phosphate reductoisomeraseMECPPCCCFCC2-C-methyl-d-erythritol 2,4-cyclodiphosphateHMBPPMethylerythritol phosphatePSI-BLASTBasic Local Alignment Search ToolPosition-Specific Iterated BLASTBlastisopentenyl pyrophosphateMetabolic control analysisdimethylallyl diphosphateGAPflux control coefficientMalariaKinetic modelDrug targetProtein Data BankPyruvateglyceraldehyde 3-phosphate
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											Authors
												Vivek Kumar Singh, Indira Ghosh, 
											