The trypanosomiases

MP Barrett, RJS Burchmore, A Stich, JO Lazzari… - The Lancet, 2003 - thelancet.com
The trypanosomiases consist of a group of important animal and human diseases caused by
parasitic protozoa of the genus Trypanosoma. In sub-Saharan Africa, the final decade of the …

Drug targets in Leishmania

B Chawla, R Madhubala - Journal of Parasitic Diseases, 2010 - Springer
Leishmaniasis is a major public health problem and till date there are no effective vaccines
available. The control strategy relies solely on chemotherapy of the infected people …

Antileishmanial drug discovery: Comprehensive review of the last 10 years

JN Sangshetti, FAK Khan, AA Kulkarni, R Arote… - Rsc Advances, 2015 - pubs.rsc.org
Leishmaniasis, a group of diseases caused by hemoflagellate obligate intracellular protozoa
(trypanosomatids) from the genus Leishmania, has not received the attention it deserves …

Glycolysis as a target for the design of new anti-trypanosome drugs

CLMJ Verlinde, V Hannaert, C Blonski, M Willson… - Drug Resistance …, 2001 - Elsevier
Glycolysis is perceived as a promising target for new drugs against parasitic trypanosomatid
protozoa because this pathway plays an essential role in their ATP supply. Trypanosomatid …

Anticancer agents that counteract tumor glycolysis

C Granchi, F Minutolo - ChemMedChem, 2012 - Wiley Online Library
Can we consider cancer to be a “metabolic disease”? Tumors are the result of a metabolic
selection, forming tissues composed of heterogeneous cells that generally express an …

Recent advances in structure-based rational drug design

PJ Gane, PM Dean - Current opinion in structural biology, 2000 - Elsevier
Two approaches to structure-based drug design, that is, the docking of known compounds
into a target protein and molecular assembly in situ, are seen to be merging technologies …

Hierarchical docking of databases of multiple ligand conformations

DM Lorber, BK Shoichet - Current topics in medicinal chemistry, 2005 - ingentaconnect.com
Ligand flexibility is an important problem in molecular docking and virtual screening. To
address this challenge, we investigate a hierarchical pre-organization of multiple …

High-resolution structure of human D-glyceraldehyde-3-phosphate dehydrogenase

JL Jenkins, JJ Tanner - Acta Crystallographica Section D …, 2006 - journals.iucr.org
GAPDH (d-glyceraldehyde-3-phosphate dehydrogenase) is a multifunctional protein that is
a target for the design of antitrypanosomatid and anti-apoptosis drugs. Here, the first high …

Inhibitors of PEX14 disrupt protein import into glycosomes and kill Trypanosoma parasites

M Dawidowski, L Emmanouilidis, VC Kalel… - Science, 2017 - science.org
The parasitic protists of the Trypanosoma genus infect humans and domestic mammals,
causing severe mortality and huge economic losses. The most threatening trypanosomiasis …

Progresses in the field of drug design to combat tropical protozoan parasitic diseases

GEG Linares, EL Ravaschino… - Current Medicinal …, 2006 - ingentaconnect.com
The progresses made in the field of drug design to combat tropical protozoan parasitic
diseases, such as Chagas' disease, leishmaniasis, and sleeping sickness are discussed …