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1.
J Comput Chem ; 31(16): 2967-70, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20928852

ABSTRACT

We herein present the graphical user interface (GUI) TmoleX for the quantum chemical program package TURBOMOLE. TmoleX allows users to execute the complete workflow of a quantum chemical investigation from the initial building of a structure to the visualization of the results in a user friendly graphical front end. The purpose of TmoleX is to make TURBOMOLE easy to use and to provide a high degree of flexibility. Hence, it should be a valuable tool for most users from beginners to experts. The program is developed in Java and runs on Linux, Windows, and Mac platforms. It can be used to run calculations on local desktops as well as on remote computers.


Subject(s)
Quantum Theory , User-Computer Interface , Molecular Dynamics Simulation
2.
J Biol Chem ; 277(23): 20541-8, 2002 Jun 07.
Article in English | MEDLINE | ID: mdl-11927598

ABSTRACT

Human cell extracts support the replication of SV40 DNA, whereas mouse cell extracts do not. Species specificity is determined at the level of initiation of DNA replication, and it was previously found that this requires the large subunit, p180, of DNA polymerase alpha-primase to be of human origin. Furthermore, a functional interaction between SV40 large T antigen (TAg) and p180 is essential for viral DNA replication. In this study we determined that the N-terminal regions of human p180, which contain the TAg-binding sites, can be replaced with those of murine origin without losing the ability to support SV40 DNA replication in vitro. The same substitutions do not prevent SV40 TAg from stimulating the activity of DNA polymerase alpha-primase on single-stranded DNA in the presence of replication protein A. Furthermore, biophysical studies show that the interactions of human and murine DNA polymerase alpha-primase with SV40 TAg are of a similar magnitude. These studies strongly suggest that requirement of SV40 DNA replication for human DNA polymerase alpha depends neither on the TAg-binding site being of human origin nor on the strength of the binary interaction between SV40 TAg and DNA polymerase alpha-primase but rather on sequences in the C-terminal region of human p180.


Subject(s)
DNA Polymerase I/physiology , DNA Replication/physiology , DNA, Viral/biosynthesis , Simian virus 40/genetics , Animals , DNA Polymerase I/genetics , DNA Polymerase I/metabolism , DNA, Single-Stranded/metabolism , Humans , Mice , Mutagenesis, Site-Directed , Species Specificity
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