Detailed Information on Publication Record
2012
BH3-ONLY PROTEINS - FROM STRUCTURE TO FUNCTION
IONESCU, Crina-Maria, Zuzana KLÍMOVÁ, David SEHNAL, Radka SVOBODOVÁ VAŘEKOVÁ, Jaroslav KOČA et. al.Basic information
Original name
BH3-ONLY PROTEINS - FROM STRUCTURE TO FUNCTION
Authors
IONESCU, Crina-Maria, Zuzana KLÍMOVÁ, David SEHNAL, Radka SVOBODOVÁ VAŘEKOVÁ and Jaroslav KOČA
Edition
XXIII. biochemický sjezd České společnosti pro biochemii a molekulární biologii a Slovenské spoločnosti pre biochémiu a molekulárnu biológiu, 2012
Other information
Type of outcome
Prezentace na konferencích
Confidentiality degree
není předmětem státního či obchodního tajemství
Organization unit
Faculty of Science
Keywords in English
apoptosis, BH3 domain
Změněno: 12/4/2024 14:18, Mgr. Marie Šípková, DiS.
Abstract
V originále
Disfunctions in the mechanism of programmed cell death (apoptosis) are directly related to cancer, neurodegenerative and auto-immune diseases. Apoptosis is highly regulated by the interplay of BH3-only proteins [1,2]. How these proteins perform their function at the molecular level is not yet understood, which makes it very hard to develop medical treatment. We recently developed SiteBinder, an effective tool for comparing the 3D structure of multiple protein motifs [3]. Using this tool, we performed a brief structural comparison of the BH3 domain of several BH3-only proteins known to promote cell death. The preliminary results showed that there is a detectable structural trend which correlates with the type of mechanism of action (direct versus indirect) of these proteins. We present here our results of an extensive structural comparison analysis comprising all BH3-only proteins whose structure is known. Our investigations were ultimately meant to determine whether the measures of 3D structural similarity correlate with specificity of binding. The results of our analysis can be useful in studies focused on modulating apoptosis and related diseases.
Links
GD301/09/H004, research and development project |
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MUNI/A/0914/2009, interní kód MU |
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