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A Look Inside HIV Resistance through Retroviral Protease Interaction Maps
Author(s) -
Aleksejs Kontijevskis,
Peteris Prūsis,
Ramona Petrovska,
Sviatlana Yahorava,
Felikss Mutulis,
Ilze Mutule,
Jan Komorowski,
Jarl E. S. Wikberg
Publication year - 2007
Publication title -
plos computational biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.628
H-Index - 182
eISSN - 1553-7358
pISSN - 1553-734X
DOI - 10.1371/journal.pcbi.0030048
Subject(s) - proteases , protease , cleave , biology , computational biology , cleavage (geology) , genetics , peptide sequence , biochemistry , gene , enzyme , paleontology , fracture (geology)
Retroviruses affect a large number of species, from fish and birds to mammals and humans, with global socioeconomic negative impacts. Here the authors report and experimentally validate a novel approach for the analysis of the molecular networks that are involved in the recognition of substrates by retroviral proteases. Using multivariate analysis of the sequence-based physiochemical descriptions of 61 retroviral proteases comprising wild-type proteases, natural mutants, and drug-resistant forms of proteases from nine different viral species in relation to their ability to cleave 299 substrates, the authors mapped the physicochemical properties and cross-dependencies of the amino acids of the proteases and their substrates, which revealed a complex molecular interaction network of substrate recognition and cleavage. The approach allowed a detailed analysis of the molecular–chemical mechanisms involved in substrate cleavage by retroviral proteases.

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