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New page: left|200px<br /><applet load="1tx3" size="450" color="white" frame="true" align="right" spinBox="true" caption="1tx3, resolution 2.50Å" /> '''HINCII BOUND TO COGN...
 
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[[Image:1tx3.gif|left|200px]]<br /><applet load="1tx3" size="450" color="white" frame="true" align="right" spinBox="true"  
[[Image:1tx3.gif|left|200px]]<br /><applet load="1tx3" size="350" color="white" frame="true" align="right" spinBox="true"  
caption="1tx3, resolution 2.50&Aring;" />
caption="1tx3, resolution 2.50&Aring;" />
'''HINCII BOUND TO COGNATE DNA'''<br />
'''HINCII BOUND TO COGNATE DNA'''<br />


==Overview==
==Overview==
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.
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.


==About this Structure==
==About this Structure==
1TX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Haemophilus_influenzae Haemophilus influenzae] with NA as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Type_II_site-specific_deoxyribonuclease Type II site-specific deoxyribonuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.21.4 3.1.21.4] Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1TX3 OCA].  
1TX3 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Haemophilus_influenzae Haemophilus influenzae] with <scene name='pdbligand=NA:'>NA</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/Type_II_site-specific_deoxyribonuclease Type II site-specific deoxyribonuclease], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.21.4 3.1.21.4] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1TX3 OCA].  


==Reference==
==Reference==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Type II site-specific deoxyribonuclease]]
[[Category: Type II site-specific deoxyribonuclease]]
[[Category: Dorner, L.F.]]
[[Category: Dorner, L F.]]
[[Category: Horton, N.C.]]
[[Category: Horton, N C.]]
[[Category: Perona, J.J.]]
[[Category: Perona, J J.]]
[[Category: NA]]
[[Category: NA]]
[[Category: blunt cutting]]
[[Category: blunt cutting]]
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[[Category: restriction endonuclease]]
[[Category: restriction endonuclease]]


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