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4X4N

Crystal structure of the A.fulgidus CCA-adding enzyme in complex with a G70A arginyl-tRNA minihelix

Summary for 4X4N
Entry DOI10.2210/pdb4x4n/pdb
Related4X4O 4X4P 4X4Q 4X4R 4X4S 4X4U 4X4V 4X4W
DescriptorCCA-adding enzyme, G70A tRNA minihelix, RNA (5'-D(P*CP*G)-3'), ... (7 entities in total)
Functional Keywordsprotein-rna complex, trna, non-coding rna, cca-adding enzyme, nucleotidyltransferase, ncrna, transferase-rna complex, transferase/rna
Biological sourceArchaeoglobus fulgidus (strain ATCC 49558 / VC-16 / DSM 4304 / JCM 9628 / NBRC 100126)
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Total number of polymer chains8
Total formula weight247324.67
Authors
Kuhn, C.-D.,Joshua-Tor, L. (deposition date: 2014-12-03, release date: 2015-02-11, Last modification date: 2023-12-27)
Primary citationKuhn, C.D.,Wilusz, J.E.,Zheng, Y.,Beal, P.A.,Joshua-Tor, L.
On-Enzyme Refolding Permits Small RNA and tRNA Surveillance by the CCA-Adding Enzyme.
Cell, 160:644-658, 2015
Cited by
PubMed Abstract: Transcription in eukaryotes produces a number of long noncoding RNAs (lncRNAs). Two of these, MALAT1 and Menβ, generate a tRNA-like small RNA in addition to the mature lncRNA. The stability of these tRNA-like small RNAs and bona fide tRNAs is monitored by the CCA-adding enzyme. Whereas CCA is added to stable tRNAs and tRNA-like transcripts, a second CCA repeat is added to certain unstable transcripts to initiate their degradation. Here, we characterize how these two scenarios are distinguished. Following the first CCA addition cycle, nucleotide binding to the active site triggers a clockwise screw motion, producing torque on the RNA. This ejects stable RNAs, whereas unstable RNAs are refolded while bound to the enzyme and subjected to a second CCA catalytic cycle. Intriguingly, with the CCA-adding enzyme acting as a molecular vise, the RNAs proofread themselves through differential responses to its interrogation between stable and unstable substrates.
PubMed: 25640237
DOI: 10.1016/j.cell.2015.01.005
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.953 Å)
Structure validation

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数据于2024-11-06公开中

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