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PMID: 10074945 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Crystal structure of a lead-dependent ribozyme revealing metal binding sites relevant to catalysis.

Nature structural biology ·Vol. 6 ·No. 3 ·1999-03-00 ·Pages 261-8

Wedekind JE, McKay DB

Abstract

The leadzyme is a small RNA motif that catalyzes a site-specific, Pb2+-dependent cleavage reaction. As such, it is an example of a metal-dependent RNA enzyme. Here we describe the X-ray crystallographic structure of the leadzyme, which reveals two independent molecules per asymmetric unit. Both molecules feature an internal loop in which a bulged purine base stack twists away from the helical stem. This kinks the backbone, rendering the phosphodiester bond susceptible to cleavage. The independent molecules have different conformations: one leadzyme copy coordinates Mg2+, whereas the other binds only Ba2+ or Pb2+. In the active site of the latter molecule, a single Ba2+ ion coordinates the 2'-OH nucleophile, and appears to mimic the binding of catalytic lead. These observations allow a bond cleavage reaction to be modeled, which reveals the minimal structural features necessary for catalysis by this small ribozyme.

MeSH Terms
Base Sequence Binding Sites Catalytic Domain Crystallography, X-Ray Lead/metabolism Nucleic Acid Conformation RNA, Catalytic/chemistry,metabolism
Chemicals
RNA, Catalytic leadzyme Lead
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Wedekind J E
Department of Structural Biology, Stanford University School of Medicine, California 94305-5126, USA. Wedekind@ribose.stanford.edu
McKay D B
Article Info
Journal
Nature structural biology
Abbr.
Nat Struct Biol
ISSN
1072-8368
Published
1999-03-00
Pages
261-8
Language
English
Region
United States
NLM ID
9421566
Subset
IM
Databases
PDB
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