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2HO7

Pre-cleavage state of the Thermoanaerobacter tengcongensis glmS ribozyme bound to glucose-6-phosphate

Summary for 2HO7
Entry DOI10.2210/pdb2ho7/pdb
Related2HO6
DescriptorglmS ribozyme substrate RNA, glmS ribozyme RNA, 6-O-phosphono-alpha-D-glucopyranose, ... (5 entities in total)
Functional Keywordsrna; ribozyme; pseudoknot; helix, rna
Total number of polymer chains2
Total formula weight49564.59
Authors
Klein, D.J.,Ferre-D'Amare, A.R. (deposition date: 2006-07-13, release date: 2006-09-26, Last modification date: 2024-02-14)
Primary citationKlein, D.J.,Ferre-D'Amare, A.R.
Structural basis of glmS ribozyme activation by glucosamine-6-phosphate
Science, 313:1752-1756, 2006
Cited by
PubMed Abstract: The glmS ribozyme is the only natural catalytic RNA known to require a small-molecule activator for catalysis. This catalytic RNA functions as a riboswitch, with activator-dependent RNA cleavage regulating glmS messenger RNA expression. We report crystal structures of the glmS ribozyme in precleavage states that are unliganded or bound to the competitive inhibitor glucose-6-phosphate and in the postcleavage state. All structures superimpose closely, revealing a remarkably rigid RNA that contains a preformed active and coenzyme-binding site. Unlike other riboswitches, the glmS ribozyme binds its activator in an open, solvent-accessible pocket. Our structures suggest that the amine group of the glmS ribozyme-bound coenzyme performs general acid-base and electrostatic catalysis.
PubMed: 16990543
DOI: 10.1126/science.1129666
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.9 Å)
Structure validation

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