2goz

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(New page: 200px<br /><applet load="2goz" size="350" color="white" frame="true" align="right" spinBox="true" caption="2goz, resolution 2.20&Aring;" /> '''The 2.2 A structure ...)
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==Overview==
==Overview==
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Minimal hammerhead ribozymes have been characterized extensively by static, and time-resolved crystallography as well as numerous biochemical, analyses, leading to mutually contradictory mechanistic explanations for, catalysis. We present the 2.2 A resolution crystal structure of a, full-length Schistosoma mansoni hammerhead ribozyme that permits us to, explain the structural basis for its 1000-fold catalytic enhancement. The, full-length hammerhead structure reveals how tertiary interactions, occurring remotely from the active site prime this ribozyme for catalysis., G-12 and G-8 are positioned consistent with their previously suggested, roles in acid-base catalysis, the nucleophile is aligned with a scissile, phosphate positioned proximal to the A-9 phosphate, and previously, unexplained roles of other conserved nucleotides become apparent within, the context of a distinctly new fold that nonetheless accommodates the, previous structural studies. These interactions permit us to explain the, previously irreconcilable sets of experimental results in a unified, consistent, and unambiguous manner.
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Minimal hammerhead ribozymes have been characterized extensively by static and time-resolved crystallography as well as numerous biochemical analyses, leading to mutually contradictory mechanistic explanations for catalysis. We present the 2.2 A resolution crystal structure of a full-length Schistosoma mansoni hammerhead ribozyme that permits us to explain the structural basis for its 1000-fold catalytic enhancement. The full-length hammerhead structure reveals how tertiary interactions occurring remotely from the active site prime this ribozyme for catalysis. G-12 and G-8 are positioned consistent with their previously suggested roles in acid-base catalysis, the nucleophile is aligned with a scissile phosphate positioned proximal to the A-9 phosphate, and previously unexplained roles of other conserved nucleotides become apparent within the context of a distinctly new fold that nonetheless accommodates the previous structural studies. These interactions permit us to explain the previously irreconcilable sets of experimental results in a unified, consistent, and unambiguous manner.
==About this Structure==
==About this Structure==
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[[Category: Protein complex]]
[[Category: Protein complex]]
[[Category: Martick, M.]]
[[Category: Martick, M.]]
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[[Category: Scott, W.G.]]
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[[Category: Scott, W G.]]
[[Category: a-form helix]]
[[Category: a-form helix]]
[[Category: catalytic rna]]
[[Category: catalytic rna]]
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[[Category: uridine turn]]
[[Category: uridine turn]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Jan 29 20:04:51 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:33:50 2008''

Revision as of 15:33, 21 February 2008


2goz, resolution 2.20Å

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The 2.2 A structure of a full-length catalytically active hammerhead ribozyme

Overview

Minimal hammerhead ribozymes have been characterized extensively by static and time-resolved crystallography as well as numerous biochemical analyses, leading to mutually contradictory mechanistic explanations for catalysis. We present the 2.2 A resolution crystal structure of a full-length Schistosoma mansoni hammerhead ribozyme that permits us to explain the structural basis for its 1000-fold catalytic enhancement. The full-length hammerhead structure reveals how tertiary interactions occurring remotely from the active site prime this ribozyme for catalysis. G-12 and G-8 are positioned consistent with their previously suggested roles in acid-base catalysis, the nucleophile is aligned with a scissile phosphate positioned proximal to the A-9 phosphate, and previously unexplained roles of other conserved nucleotides become apparent within the context of a distinctly new fold that nonetheless accommodates the previous structural studies. These interactions permit us to explain the previously irreconcilable sets of experimental results in a unified, consistent, and unambiguous manner.

About this Structure

2GOZ is a Protein complex structure of sequences from [1]. Full crystallographic information is available from OCA.

Reference

Tertiary contacts distant from the active site prime a ribozyme for catalysis., Martick M, Scott WG, Cell. 2006 Jul 28;126(2):309-20. Epub 2006 Jul 20. PMID:16859740

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