1tx3

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{{STRUCTURE_1tx3| PDB=1tx3 | SCENE= }}
{{STRUCTURE_1tx3| PDB=1tx3 | SCENE= }}
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'''HINCII BOUND TO COGNATE DNA'''
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===HINCII BOUND TO COGNATE DNA===
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==Overview==
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The 2.8 A crystal structure of the type II restriction endonuclease HincII bound to Ca(2+) and cognate DNA containing GTCGAC is presented. The DNA is uncleaved, and one calcium ion is bound per active site, in a position previously described as site I in the related blunt cutting type II restriction endonuclease EcoRV [Horton, N. C., Newberry, K. J., and Perona, J. J. (1998) Proc. Natl. Acad. Sci. U.S.A. 95 (23), 13489-13494], as well as that found in other related enzymes. Unlike the site I metal in EcoRV, but similar to that of PvuII, NgoMIV, BamHI, BglII, and BglI, the observed calcium cation is directly ligated to the pro-S(p) oxygen of the scissile phosphate. A calcium ion-ligated water molecule is well positioned to act as the nucleophile in the phosphodiester bond cleavage reaction, and is within hydrogen bonding distance of the conserved active site lysine (Lys 129), as well as the pro-R(p) oxygen of the phosphate group 3' of the scissile phosphate, suggesting possible roles for these groups in the catalytic mechanism. Kinetic data consistent with an important role for the 3'-phosphate group in DNA cleavage by HincII are presented. The previously observed sodium ion [Horton, N. C., Dorner, L. F., and Perona, J. J. (2002) Nat. Struct. Biol. 9, 42-47] persists in the active sites of the Ca(2+)-bound structure; however, kinetic data show little effect on the single-turnover rate of DNA cleavage in the absence of Na(+) ions.
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(as it appears on PubMed at http://www.pubmed.gov), where 15491133 is the PubMed ID number.
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{{ABSTRACT_PUBMED_15491133}}
==About this Structure==
==About this Structure==
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==Reference==
==Reference==
Ca2+ binding in the active site of HincII: implications for the catalytic mechanism., Etzkorn C, Horton NC, Biochemistry. 2004 Oct 26;43(42):13256-70. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15491133 15491133]
Ca2+ binding in the active site of HincII: implications for the catalytic mechanism., Etzkorn C, Horton NC, Biochemistry. 2004 Oct 26;43(42):13256-70. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/15491133 15491133]
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Sequence selectivity and degeneracy of a restriction endonuclease mediated by DNA intercalation., Horton NC, Dorner LF, Perona JJ, Nat Struct Biol. 2002 Jan;9(1):42-7. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11742344 11742344]
[[Category: Haemophilus influenzae]]
[[Category: Haemophilus influenzae]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Protein-dna]]
[[Category: Protein-dna]]
[[Category: Restriction endonuclease]]
[[Category: Restriction endonuclease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 10:28:34 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jul 29 13:22:05 2008''

Revision as of 10:22, 29 July 2008

Image:1tx3.png

Template:STRUCTURE 1tx3

HINCII BOUND TO COGNATE DNA

Template:ABSTRACT PUBMED 15491133

About this Structure

1TX3 is a Single protein structure of sequence from Haemophilus influenzae. Full crystallographic information is available from OCA.

Reference

Ca2+ binding in the active site of HincII: implications for the catalytic mechanism., Etzkorn C, Horton NC, Biochemistry. 2004 Oct 26;43(42):13256-70. PMID:15491133

Sequence selectivity and degeneracy of a restriction endonuclease mediated by DNA intercalation., Horton NC, Dorner LF, Perona JJ, Nat Struct Biol. 2002 Jan;9(1):42-7. PMID:11742344

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