ILP-2 modeling and virtual screening of an FDA-approved library:a possible anticancer therapy
Author(s) -
Saeed Khalili,
Hemn Mohammadpour,
Mahdieh Shokrollahi Barough,
Parviz Kokhaei
Publication year - 2016
Publication title -
turkish journal of medical sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.277
H-Index - 27
eISSN - 1303-6165
pISSN - 1300-0144
DOI - 10.3906/sag-1503-2
Subject(s) - medicine , virtual screening , pharmacology , medical physics , bioinformatics , drug discovery , biology
The members of the inhibitors of apoptosis protein (IAP) family inhibit diverse components of the caspase signaling pathway, notably caspase 3, 7, and 9. ILP-2 (BIRC-8) is the most recently identified member of the IAPs, mainly interacting with caspase 9. This interaction would eventually lead to death resistance in the case of cancerous cells. Therefore, structural modeling of ILP-2 and finding applicable inhibitors of its interaction with caspase 9 are a compelling challenge.
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