4kbd
From Proteopedia
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[[Image:4kbd.gif|left|200px]] | [[Image:4kbd.gif|left|200px]] | ||
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'''DNA STRUCTURE OF A MUTATED KB SITE''' | '''DNA STRUCTURE OF A MUTATED KB SITE''' | ||
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==About this Structure== | ==About this Structure== | ||
| - | + | Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4KBD OCA]. | |
==Reference== | ==Reference== | ||
NF-kappa B binding mechanism: a nuclear magnetic resonance and modeling study of a GGG --> CTC mutation., Tisne C, Hartmann B, Delepierre M, Biochemistry. 1999 Mar 30;38(13):3883-94. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10194299 10194299] | NF-kappa B binding mechanism: a nuclear magnetic resonance and modeling study of a GGG --> CTC mutation., Tisne C, Hartmann B, Delepierre M, Biochemistry. 1999 Mar 30;38(13):3883-94. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/10194299 10194299] | ||
| - | [[Category: Protein complex]] | ||
[[Category: Delepierre, M.]] | [[Category: Delepierre, M.]] | ||
[[Category: Hartmann, B.]] | [[Category: Hartmann, B.]] | ||
[[Category: Tisne, C.]] | [[Category: Tisne, C.]] | ||
| - | [[Category: | + | [[Category: Deoxyribonucleic acid]] |
| - | [[Category: | + | [[Category: Dna structure]] |
| - | [[Category: | + | [[Category: Modelling]] |
| - | [[Category: | + | [[Category: Nmr]] |
| - | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 22:25:49 2008'' | |
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | |
Revision as of 19:25, 4 May 2008
DNA STRUCTURE OF A MUTATED KB SITE
Overview
We present the solution structure of the nonpalindromic 16 bp DNA 5'd(CTGCTCACTTTCCAGG)3'. 5'd(CCTGGAAAGTGAGCAG)3' containing a mutated kappaB site for which the mutation of a highly conserved GGG tract of the native kappaB HIV-1 site to CTC abolishes NF-kappaB binding. 1H and 31P NMR spectroscopies have been used together with molecular modeling to determine the fine structure of the duplex. NMR data show evidence for a BI-BII equilibrium of the CpA.TpG steps at the 3'-end of the oligomer. Models for the extreme conformations reached by the mutated duplex (denoted 16M) are proposed in agreement with the NMR data. Since the distribution of BII sites is changed in the mutated duplex compared to that of the native duplex (denoted 16N), large differences are induced in the intrinsic structural properties of both duplexes. In particular, in BII structures, 16M shows a kink located at the 3'-end of the duplex, and in contrast, 16N exhibits an intrinsic global curvature toward the major groove. Whereas 16N can reach a conformation very favorable for the interaction with NF-kappaB, 16M cannot mimic such a conformation and, moreover, its deeper and narrower major groove could hinder the DNA-protein interactions.
About this Structure
Full crystallographic information is available from OCA.
Reference
NF-kappa B binding mechanism: a nuclear magnetic resonance and modeling study of a GGG --> CTC mutation., Tisne C, Hartmann B, Delepierre M, Biochemistry. 1999 Mar 30;38(13):3883-94. PMID:10194299 Page seeded by OCA on Sun May 4 22:25:49 2008
