2fl3

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(New page: 200px<br /><applet load="2fl3" size="350" color="white" frame="true" align="right" spinBox="true" caption="2fl3, resolution 2.39&Aring;" /> '''Binary Complex of Re...)
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==Overview==
==Overview==
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HinP1I recognizes and cleaves the palindromic tetranucleotide sequence G, downward arrowCGC in DNA. We report three structures of HinP1I-DNA, complexes: in the presence of Ca(2+) (pre-reactive complex), in the, absence of metal ion (binary complex) and in the presence of Mg(2+), (post-reactive complex). HinP1I forms a back-to-back dimer with two active, sites and two DNA duplexes bound on the outer surfaces of the dimer facing, away from each other. The 10 bp DNA duplexes undergo protein-induced, distortions exhibiting features of A-, B- and Z-conformations: bending on, one side (by intercalation of a phenylalanine side chain into the major, groove), base flipping on the other side of the recognition site (by, expanding the step rise distance of the local base pair to Z-form) and a, local A-form conformation between the two central C:G base pairs of the, recognition site (by binding of the N-terminal helix in the minor groove)., In the pre- and post-reactive complexes, two metals (Ca(2+) or Mg(2+)) are, found in the active site. The enzyme appears to cleave DNA sequentially, hydrolyzing first one DNA strand, as seen in the post-reactive complex in, the crystalline state, and then the other, as supported by the observation, that, in solution, a nicked DNA intermediate accumulates before, linearization.
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HinP1I recognizes and cleaves the palindromic tetranucleotide sequence G downward arrowCGC in DNA. We report three structures of HinP1I-DNA complexes: in the presence of Ca(2+) (pre-reactive complex), in the absence of metal ion (binary complex) and in the presence of Mg(2+) (post-reactive complex). HinP1I forms a back-to-back dimer with two active sites and two DNA duplexes bound on the outer surfaces of the dimer facing away from each other. The 10 bp DNA duplexes undergo protein-induced distortions exhibiting features of A-, B- and Z-conformations: bending on one side (by intercalation of a phenylalanine side chain into the major groove), base flipping on the other side of the recognition site (by expanding the step rise distance of the local base pair to Z-form) and a local A-form conformation between the two central C:G base pairs of the recognition site (by binding of the N-terminal helix in the minor groove). In the pre- and post-reactive complexes, two metals (Ca(2+) or Mg(2+)) are found in the active site. The enzyme appears to cleave DNA sequentially, hydrolyzing first one DNA strand, as seen in the post-reactive complex in the crystalline state, and then the other, as supported by the observation that, in solution, a nicked DNA intermediate accumulates before linearization.
==About this Structure==
==About this Structure==
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[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Type II site-specific deoxyribonuclease]]
[[Category: Type II site-specific deoxyribonuclease]]
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[[Category: Horton, J.R.]]
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[[Category: Horton, J R.]]
[[Category: dna superhelix]]
[[Category: dna superhelix]]
[[Category: protein dimerizaton]]
[[Category: protein dimerizaton]]
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[[Category: restriction endonuclease]]
[[Category: restriction endonuclease]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jan 29 19:39:03 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:22:27 2008''

Revision as of 15:22, 21 February 2008


2fl3, resolution 2.39Å

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Binary Complex of Restriction Endonuclease HinP1I with Cognate DNA

Overview

HinP1I recognizes and cleaves the palindromic tetranucleotide sequence G downward arrowCGC in DNA. We report three structures of HinP1I-DNA complexes: in the presence of Ca(2+) (pre-reactive complex), in the absence of metal ion (binary complex) and in the presence of Mg(2+) (post-reactive complex). HinP1I forms a back-to-back dimer with two active sites and two DNA duplexes bound on the outer surfaces of the dimer facing away from each other. The 10 bp DNA duplexes undergo protein-induced distortions exhibiting features of A-, B- and Z-conformations: bending on one side (by intercalation of a phenylalanine side chain into the major groove), base flipping on the other side of the recognition site (by expanding the step rise distance of the local base pair to Z-form) and a local A-form conformation between the two central C:G base pairs of the recognition site (by binding of the N-terminal helix in the minor groove). In the pre- and post-reactive complexes, two metals (Ca(2+) or Mg(2+)) are found in the active site. The enzyme appears to cleave DNA sequentially, hydrolyzing first one DNA strand, as seen in the post-reactive complex in the crystalline state, and then the other, as supported by the observation that, in solution, a nicked DNA intermediate accumulates before linearization.

About this Structure

2FL3 is a Single protein structure of sequence from Haemophilus influenzae. Active as Type II site-specific deoxyribonuclease, with EC number 3.1.21.4 Full crystallographic information is available from OCA.

Reference

DNA nicking by HinP1I endonuclease: bending, base flipping and minor groove expansion., Horton JR, Zhang X, Maunus R, Yang Z, Wilson GG, Roberts RJ, Cheng X, Nucleic Acids Res. 2006 Feb 9;34(3):939-48. Print 2006. PMID:16473850

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