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A systematic method for analysing the protein hydration structure of T4 lysozyme

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    0396329 - ÚOCHB 2014 RIV GB eng J - Journal Article
    Kysilka, Jiří - Vondrášek, Jiří
    A systematic method for analysing the protein hydration structure of T4 lysozyme.
    Journal of Molecular Recognition. Roč. 26, č. 10 (2013), s. 479-487. ISSN 0952-3499. E-ISSN 1099-1352
    R&D Projects: GA ČR GAP208/10/0725; GA MŠMT(CZ) LH11020
    Grant - others:GA ČR(CZ) GAP302/10/0427
    Institutional support: RVO:61388963
    Keywords : protein hydration structure * water * X-ray crystallography * cluster algorithm * interaction enthalpy
    Subject RIV: CE - Biochemistry
    Impact factor: 2.337, year: 2013

    A systematic method for the analysis of the hydration structure of proteins is demonstrated on the case study of lysozyme. The method utilises multiple structural data of the same protein deposited in the protein data bank. Clusters of high water occupancy are localised and characterised in terms of their interaction with protein. It is shown that they constitute a network of interconnected hydrogen bonds anchored to the protein molecule. The high occupancy of the clusters does not directly correlate with water-protein interaction energy as was originally hypothesised. The highly occupied clusters rather correspond to the nodes of the hydration network that have the maximum number of hydrogen bonds including both the protein atoms and the surrounding water clusters.
    Permanent Link: http://hdl.handle.net/11104/0224147

     
     
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