Specific Inhibition of the Bifunctional Farnesyl/Geranylgeranyl Diphosphate Synthase in Malaria Parasites via a New Small-Molecule Binding Site-Reference-Cited by-同舟云学术

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Specific Inhibition of the Bifunctional Farnesyl/Geranylgeranyl Diphosphate Synthase in Malaria Parasites via a New Small-Molecule Binding Site

Published:2018-02 Issue:2 Volume:25 Page:185-193.e5
ISSN:2451-9456
Container-title:Cell Chemical Biology
language:en
Short-container-title:Cell Chemical Biology

Author:

Gisselberg Jolyn E.,Herrera Zachary,Orchard Lindsey M.,Llinás Manuel,Yeh Ellen

Funder

Stanford Consortium for Innovation, Design, Evaluation and Action

NIH

Burroughs Wellcome Fund

Stanford School of Medicine

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,Biochemistry

Reference72 articles.

1. A method for rapid genetic integration into Plasmodium falciparum utilizing mycobacteriophage Bxb1 integrase;Adjalley;Methods Mol. Biol.,2010

2. Metabolomic profiling of the malaria box reveals antimalarial target pathways;Allman;Antimicrob. Agents Chemother.,2016

3. Small molecule inhibition of apicomplexan FtsH1 disrupts plastid biogenesis in human pathogens;Amberg-Johnson;Elife,2017

4. Molecular characterization of a novel geranylgeranyl pyrophosphate synthase from Plasmodium parasites;Artz;J. Biol. Chem.,2011

5. Galaxy: a web-based genome analysis tool for experimentalists;Blankenberg;Curr. Protoc. Mol. Biol.,2010

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