1wn7

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{{STRUCTURE_1wn7| PDB=1wn7 | SCENE= }}
{{STRUCTURE_1wn7| PDB=1wn7 | SCENE= }}
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'''Crystal structure of archaeal family B DNA polymerase mutant'''
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===Crystal structure of archaeal family B DNA polymerase mutant===
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==Overview==
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A novel mechanism for controlling the proofreading and polymerase activities of archaeal DNA polymerases was studied. The 3'-5'exonuclease (proofreading) activity and PCR performance of the family B DNA polymerase from Thermococcus kodakaraensis KOD1 (previously Pyrococcus kodakaraensis KOD1) were altered efficiently by mutation of a "unique loop" in the exonuclease domain. Interestingly, eight different H147 mutants showed considerable variations in respect to their 3'-5'exonuclease activity, from 9% to 276%, as against that of the wild-type (WT) enzyme. We determined the 2.75A crystal structure of the H147E mutant of KOD DNA polymerase that shows 30% of the 3'-5'exonuclease activity, excellent PCR performance and WT-like fidelity. The structural data indicate that the properties of the H147E mutant were altered by a conformational change of the Editing-cleft caused by an interaction between the unique loop and the Thumb domain. Our data suggest that electrostatic and hydrophobic interactions between the unique loop of the exonuclease domain and the tip of the Thumb domain are essential for determining the properties of these DNA polymerases.
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{{ABSTRACT_PUBMED_16019029}}
==About this Structure==
==About this Structure==
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==Reference==
==Reference==
Structural mechanism for coordination of proofreading and polymerase activities in archaeal DNA polymerases., Kuroita T, Matsumura H, Yokota N, Kitabayashi M, Hashimoto H, Inoue T, Imanaka T, Kai Y, J Mol Biol. 2005 Aug 12;351(2):291-8. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16019029 16019029]
Structural mechanism for coordination of proofreading and polymerase activities in archaeal DNA polymerases., Kuroita T, Matsumura H, Yokota N, Kitabayashi M, Hashimoto H, Inoue T, Imanaka T, Kai Y, J Mol Biol. 2005 Aug 12;351(2):291-8. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/16019029 16019029]
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Crystal structure of DNA polymerase from hyperthermophilic archaeon Pyrococcus kodakaraensis KOD1., Hashimoto H, Nishioka M, Fujiwara S, Takagi M, Imanaka T, Inoue T, Kai Y, J Mol Biol. 2001 Feb 23;306(3):469-77. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11178906 11178906]
[[Category: DNA-directed DNA polymerase]]
[[Category: DNA-directed DNA polymerase]]
[[Category: Hashimoto, H.]]
[[Category: Hashimoto, H.]]
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[[Category: Yokota, N.]]
[[Category: Yokota, N.]]
[[Category: Transferase]]
[[Category: Transferase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 13:54:15 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 16:22:06 2008''

Revision as of 13:22, 27 July 2008

Image:1wn7.png

Template:STRUCTURE 1wn7

Crystal structure of archaeal family B DNA polymerase mutant

Template:ABSTRACT PUBMED 16019029

About this Structure

Full crystallographic information is available from OCA.

Reference

Structural mechanism for coordination of proofreading and polymerase activities in archaeal DNA polymerases., Kuroita T, Matsumura H, Yokota N, Kitabayashi M, Hashimoto H, Inoue T, Imanaka T, Kai Y, J Mol Biol. 2005 Aug 12;351(2):291-8. PMID:16019029

Crystal structure of DNA polymerase from hyperthermophilic archaeon Pyrococcus kodakaraensis KOD1., Hashimoto H, Nishioka M, Fujiwara S, Takagi M, Imanaka T, Inoue T, Kai Y, J Mol Biol. 2001 Feb 23;306(3):469-77. PMID:11178906

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