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300D

CAPTURING THE STRUCTURE OF A CATALYTIC RNA INTERMEDIATE: RNA HAMMERHEAD RIBOZYME, MN(II)-SOAKED

Summary for 300D
Entry DOI10.2210/pdb300d/pdb
DescriptorRNA HAMMERHEAD RIBOZYME, MANGANESE (II) ION (3 entities in total)
Functional Keywordsrna hammerhead ribozyme, catalytic rna, loop, ribozyme
Total number of polymer chains2
Total formula weight13519.61
Authors
Scott, W.G.,Murray, J.B.,Arnold, J.R.P.,Stoddard, B.L.,Klug, A. (deposition date: 1996-12-14, release date: 1997-01-24, Last modification date: 2024-02-21)
Primary citationScott, W.G.,Murray, J.B.,Arnold, J.R.,Stoddard, B.L.,Klug, A.
Capturing the structure of a catalytic RNA intermediate: the hammerhead ribozyme.
Science, 274:2065-2069, 1996
Cited by
PubMed Abstract: The crystal structure of an unmodified hammerhead RNA in the absence of divalent metal ions has been solved, and it was shown that this ribozyme can cleave itself in the crystal when divalent metal ions are added. This biologically active RNA fold is the same as that found previously for two modified hammerhead ribozymes. Addition of divalent cations at low pH makes it possible to capture the uncleaved RNA in metal-bound form. A conformational intermediate, having an additional Mg(II) bound to the cleavage-site phosphate, was captured by freeze-trapping the RNA at an active pH prior to cleavage. The most significant conformational changes were limited to the active site of the ribozyme, and the changed conformation requires only small additional movements to reach a proposed transition-state.
PubMed: 8953035
DOI: 10.1126/science.274.5295.2065
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3 Å)
Structure validation

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数据于2024-11-06公开中

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