Detailed Information on Publication Record
2017
Computational characterization of hybrid proteins containing ordered and intrinsically disordered regions
ZAPLETAL, Vojtěch, Arnošt MLÁDEK, Jozef HRITZ and Lukáš ŽÍDEKBasic information
Original name
Computational characterization of hybrid proteins containing ordered and intrinsically disordered regions
Authors
ZAPLETAL, Vojtěch (203 Czech Republic, belonging to the institution), Arnošt MLÁDEK (203 Czech Republic, belonging to the institution), Jozef HRITZ (703 Slovakia, belonging to the institution) and Lukáš ŽÍDEK (203 Czech Republic, guarantor, belonging to the institution)
Edition
42nd Congress of the Federation-of-European-Biochemical-Societies (FEBS) on From Molecules to Cells and Back, 2017
Other information
Language
English
Type of outcome
Konferenční abstrakt
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
United States of America
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 4.530
RIV identification code
RIV/00216224:14740/17:00095560
Organization unit
Central European Institute of Technology
ISSN
UT WoS
000409918904041
Keywords in English
NMR; hybrid proteins
Tags
Změněno: 9/3/2018 15:10, Mgr. Pavla Foltynová, Ph.D.
Abstract
V originále
Intrinsically disordered proteins (IDPs) characterized by polypeptide chains that fail to fold into stable and well defined tertiary structure in an isolated state have been under our interest. IDPs play key roles in processes such as molecular recognition, regulation of transcription and they are related to neurodegenerative diseases. Most of IDPs are in fact intrinsically disordered regions (IDRs) that are tethered to ordered domains (ODs). It is imperative that the biophysical properties of these regions be studied in their naturally occurring contexts, which is tethered to ODs. It is difficult to cope with such systems for the experimental techniques and for computational methods. Typical experimental methods for study of IDPs are nuclear magnetic resonance (NMR) and small angle X-ray scattering (SAXS). The obtained data were used for verification of predicted values from the computational simulations. In our study, we generated structural ensembles of the -subunit of RNA polymerase and regulatory domain of human tyrosine hydroxylase using molecular dynamics simulations. The reliability of the obtained ensembles generated under different force field parameters (AMBER99SB-ILDN/CHARMM22 + TIP3P/TIP4P-D) was checked by the comparison of the corresponding calculated properties with their experimental values. Namely we monitored: NMR chemical shifts, residual dipolar couplings, paramagnetic relaxation enhancement, relaxation rates, and SAXS data. The best agreement was obtained for the AMBER99SB-ILDN/TIP4P-D force field parameters.
Links
EF16_013/0001776, research and development project |
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GA13-16842S, research and development project |
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