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Journal of Infectious Diseases

Volumn 192, Issue 4, 2005, Pages 705-706

Antimalarial effects of HIV proteinase inhibitors: Common compounds but structurally distinct enzymes [2]

(2) Wyatt, David M a Berry, Colin a

a CARDIFF UNIVERSITY (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ANTIMALARIAL AGENT; CATHEPSIN D; CATHEPSIN E; PLASMEPSIN II; PROTEINASE; PROTEINASE INHIBITOR; RITONAVIR; SAQUINAVIR;

DIMERIZATION; ENZYME ACTIVE SITE; ENZYME STRUCTURE; HUMAN; HUMAN IMMUNODEFICIENCY VIRUS; LETTER; MALARIA; NONHUMAN; PLASMODIUM FALCIPARUM; PRIORITY JOURNAL; PROTEINASE INHIBITION;

ANIMALS; ANTIMALARIALS; ASPARTIC ENDOPEPTIDASES; HIV PROTEASE; HIV PROTEASE INHIBITORS; HIV-1; HUMANS; PLASMODIUM FALCIPARUM;

EID: 23244467899 PISSN: 00221899 EISSN: None Source Type: Journal
DOI: 10.1086/432079 Document Type: Letter

Times cited : (6)

References (8)

1
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2
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- Aspartic proteases of Plasmodium falciparum as the target of HIV-1 protease inhibitors
- Savarino A, Cauda R, Cassone A. Aspartic proteases of Plasmodium falciparum as the target of HIV-1 protease inhibitors [letter]. J Infect Dis 2005; 191:1381-2.
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3
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- Barrett AJ, Rawlings ND, Woessner JF Handbook of proteolytic enzymes. London: Elsevier Academic Press, 2004.
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4
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- Aspartic proteases of Plasmodium falciparum and other parasitic protozoa as drug targets
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- (2001) Trends Parasitol , vol.17 , pp. 532-537
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5
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- Activity and inhibition of plasmepsin IV, a new aspartic proteinase from the malaria parasite Plasmodium falciparum
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6
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7
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