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5UEE

RNA primer-template complex with guanosine dinucleotide ligand G(5')ppp(5')G

Summary for 5UEE
Entry DOI10.2210/pdb5uee/pdb
Related5UED 5UEF 5UEG
DescriptorRNA (5'-R(*(LCC)P*(LCC)P*(LCC)P*GP*AP*CP*UP*UP*AP*AP*GP*UP*CP*G)-3'), DIGUANOSINE-5'-TRIPHOSPHATE, MAGNESIUM ION, ... (4 entities in total)
Functional Keywordsrna, dinucleotide
Biological sourcesynthetic construct
Total number of polymer chains2
Total formula weight10724.23
Authors
Zhang, W.,Tam, C.P.,Szostak, J.W. (deposition date: 2017-01-01, release date: 2017-07-05, Last modification date: 2023-10-04)
Primary citationZhang, W.,Tam, C.P.,Walton, T.,Fahrenbach, A.C.,Birrane, G.,Szostak, J.W.
Insight into the mechanism of nonenzymatic RNA primer extension from the structure of an RNA-GpppG complex.
Proc. Natl. Acad. Sci. U.S.A., 114:7659-7664, 2017
Cited by
PubMed Abstract: The nonenzymatic copying of RNA templates with imidazole-activated nucleotides is a well-studied model for the emergence of RNA self-replication during the origin of life. We have recently discovered that this reaction can proceed through the formation of an imidazolium-bridged dinucleotide intermediate that reacts rapidly with the primer. To gain insight into the relationship between the structure of this intermediate and its reactivity, we cocrystallized an RNA primer-template complex with a close analog of the intermediate, the triphosphate-bridged guanosine dinucleotide GpppG, and solved a high-resolution X-ray structure of the complex. The structure shows that GpppG binds the RNA template through two Watson-Crick base pairs, with the primer 3'-hydroxyl oriented to attack the 5'-phosphate of the adjacent G residue. Thus, the GpppG structure suggests that the bound imidazolium-bridged dinucleotide intermediate would be preorganized to react with the primer by in-line S2 substitution. The structures of bound GppG and GppppG suggest that the length and flexibility of the 5'-5' linkage are important for optimal preorganization of the complex, whereas the position of the 5'-phosphate of bound pGpG explains the slow rate of oligonucleotide ligation reactions. Our studies provide a structural interpretation for the observed reactivity of the imidazolium-bridged dinucleotide intermediate in nonenzymatic RNA primer extension.
PubMed: 28673998
DOI: 10.1073/pnas.1704006114
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.9 Å)
Structure validation

226707

건을2024-10-30부터공개중

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