Title : Structural modeling and molecular dynamics studies on the human LMTK3 domain and the mechanism of ATP binding.

Pub. Date : 2014 May

PMID : 24619340






6 Functional Relationships(s)
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1 Structural modeling and molecular dynamics studies on the human LMTK3 domain and the mechanism of ATP binding. Adenosine Triphosphate lemur tyrosine kinase 3 Homo sapiens
2 In this computational study, we performed structural studies on LMTK3 by structural modeling and molecular dynamics (MD) simulations of the apo state and the ATP bound state. Adenosine Triphosphate lemur tyrosine kinase 3 Homo sapiens
3 Furthermore, MD simulation of the LMTK3-ATP complex was performed and the trajectory analyses confirmed the stability and effective binding of ATP in the dynamic system. Adenosine Triphosphate lemur tyrosine kinase 3 Homo sapiens
4 Furthermore, MD simulation of the LMTK3-ATP complex was performed and the trajectory analyses confirmed the stability and effective binding of ATP in the dynamic system. Adenosine Triphosphate lemur tyrosine kinase 3 Homo sapiens
5 Overall, our computational reports provide more information on the structure-function relationship of LMTK3 with ATP. Adenosine Triphosphate lemur tyrosine kinase 3 Homo sapiens
6 The critical residues Tyr185 and Asp284 found in the ATP binding cavity may be useful in designing potential inhibitors on human LMTK3. Adenosine Triphosphate lemur tyrosine kinase 3 Homo sapiens