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@article{571889, author = {Novák, Petr and Macek, Pavel}, article_location = {Praha}, article_number = {1}, keywords = {molecular dynamics; MUP;}, language = {eng}, issn = {1211-5894}, journal = {Materials Structure}, title = {Analysis of Internal Motion from Molecular Dynamics of Major Urinary Protein I}, volume = {11}, year = {2004} }
TY - JOUR ID - 571889 AU - Novák, Petr - Macek, Pavel PY - 2004 TI - Analysis of Internal Motion from Molecular Dynamics of Major Urinary Protein I JF - Materials Structure VL - 11 IS - 1 SP - 51-51 EP - 51-51 PB - The Czech and Slovak Cryst. Assoc. SN - 12115894 KW - molecular dynamics KW - MUP; N2 - Investigation of the protein of mouse urine has shown that it consists predominantly of a group of closely related proteins termed the Major Urinary Proteins (MUPs). These are acidic proteins (pI values from 4.2 to 4.7) with molecular masses of approximately 19 kDa. The MUPs are associated with pheromonally active ligands including relatively tightly bound 2-sec-butyl-4,5-dihydrothiazole. Thus MUPs may serve as a model of proteins binding small, hydrophobic ligands that are known to possess the capability of chemical signaling. Structure of MUP-I was determined crystallographically. The X-ray structures of MUP-I with and without ligand were taken and hydrogens, counter-ions and box of explicit water molecules were added. The system was minimized, heated and equilibrated and then the molecular dynamics was ran. From whole trajectory a 6ns-long part was taken and used for further analysis of internal motions of MUP-I. Correlation functions and frequency dependent order parameters have been calculated.All molecular dynamics was performed with AMBER7 software package. ER -
NOVÁK, Petr a Pavel MACEK. Analysis of Internal Motion from Molecular Dynamics of Major Urinary Protein I. \textit{Materials Structure}. Praha: The Czech and Slovak Cryst. Assoc., 2004, roč.~11, č.~1, s.~51-51. ISSN~1211-5894.
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