Difference between revisions of "YOL090W"

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'''Description of YOL090W:''' Protein that forms heterodimers with Msh3p and Msh6p that bind to DNA mismatches to initiate the mismatch repair process; contains a Walker ATP-binding motif required for repair activity; Msh2p-Msh6p binds to and hydrolyzes ATP<ref name='S000073894'>Kijas AW, et al. (2003) Msh2 separation of function mutations confer defects in the initiation steps of mismatch repair. J Mol Biol 331(1):123-38 {{SGDpaper|S000073894}} PMID 12875840</ref><ref name='S000073568'>Antony E and Hingorani MM (2003) Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair. Biochemistry 42(25):7682-93
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'''Description of YOL090W:''' Protein that forms heterodimers with Msh3p and Msh6p that bind to DNA mismatches to initiate the mismatch repair process; contains a Walker ATP-binding motif required for repair activity; Msh2p-Msh6p binds to and hydrolyzes ATP<ref name='S000073568'>Antony E and Hingorani MM (2003) Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair. Biochemistry 42(25):7682-93 {{SGDpaper|S000073568}} PMID 12820877</ref><ref name='S000073894'>Kijas AW, et al. (2003) Msh2 separation of function mutations confer defects in the initiation steps of mismatch repair. J Mol Biol 331(1):123-38
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  {{SGDpaper|S000073894}} PMID 12875840</ref>
 
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Revision as of 13:05, 31 March 2009

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Systematic name YOL090W
Gene name MSH2
Aliases PMS5
Feature type ORF, Verified
Coordinates Chr XV:147382..150276
Primary SGDID S000005450


Description of YOL090W: Protein that forms heterodimers with Msh3p and Msh6p that bind to DNA mismatches to initiate the mismatch repair process; contains a Walker ATP-binding motif required for repair activity; Msh2p-Msh6p binds to and hydrolyzes ATP[1][2]




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References

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  1. Antony E and Hingorani MM (2003) Mismatch recognition-coupled stabilization of Msh2-Msh6 in an ATP-bound state at the initiation of DNA repair. Biochemistry 42(25):7682-93 SGD PMID 12820877
  2. Kijas AW, et al. (2003) Msh2 separation of function mutations confer defects in the initiation steps of mismatch repair. J Mol Biol 331(1):123-38 SGD PMID 12875840

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