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6USQ

Telomerase Reverse Transcriptase binary complex with Y256A mutation, TERT:DNA

Summary for 6USQ
Entry DOI10.2210/pdb6usq/pdb
DescriptorTelomerase reverse transcriptase, DNA (5'-D(*GP*GP*TP*CP*AP*GP*GP*TP*CP*AP*GP*GP*TP*CP*A)-3'), DNA/RNA (5'-R(*CP*UP*GP*AP*CP*CP*UP*GP*AP*C)-D(P*CP*T)-R(P*GP*AP*C)-D(P*C)-3'), ... (5 entities in total)
Functional Keywordstelomerase, reverse transcriptase, polymerase, nuclear protein, transferase-rna-dna complex, transferase/rna/dna
Biological sourceTribolium castaneum (Red flour beetle)
More
Total number of polymer chains3
Total formula weight80251.38
Authors
Schaich, M.A.,Freudenthal, B.D.,Khoang, T.H. (deposition date: 2019-10-28, release date: 2020-06-17, Last modification date: 2023-10-11)
Primary citationSchaich, M.A.,Sanford, S.L.,Welfer, G.A.,Johnson, S.A.,Khoang, T.H.,Opresko, P.L.,Freudenthal, B.D.
Mechanisms of nucleotide selection by telomerase.
Elife, 9:-, 2020
Cited by
PubMed Abstract: Telomerase extends telomere sequences at chromosomal ends to protect genomic DNA. During this process it must select the correct nucleotide from a pool of nucleotides with various sugars and base pairing properties, which is critically important for the proper capping of telomeric sequences by shelterin. Unfortunately, how telomerase selects correct nucleotides is unknown. Here, we determined structures of telomerase reverse transcriptase (TERT) throughout its catalytic cycle and mapped the active site residues responsible for nucleoside selection, metal coordination, triphosphate binding, and RNA template stabilization. We found that TERT inserts a mismatch or ribonucleotide ~1 in 10,000 and ~1 in 14,000 insertion events, respectively. At biological ribonucleotide concentrations, these rates translate to ~40 ribonucleotides inserted per 10 kilobases. Human telomerase assays determined a conserved tyrosine steric gate regulates ribonucleotide insertion into telomeres. Cumulatively, our work provides insight into how telomerase selects the proper nucleotide to maintain telomere integrity.
PubMed: 32501800
DOI: 10.7554/eLife.55438
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.62 Å)
Structure validation

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