6USP
Telomerase Reverse Transcriptase product complex, TERT:DNA
Summary for 6USP
Entry DOI | 10.2210/pdb6usp/pdb |
Descriptor | Telomerase reverse transcriptase, DNA (5'-D(P*GP*GP*TP*CP*AP*GP*GP*TP*CP*AP*GP*GP*TP*CP*AP*G)-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'), ... (4 entities in total) |
Functional Keywords | telomerase, reverse transcriptase, polymerase, nuclear protein, transferase-rna-dna complex, transferase/rna/dna |
Biological source | Tribolium castaneum (Red flour beetle) More |
Total number of polymer chains | 3 |
Total formula weight | 80648.38 |
Authors | Schaich, M.A.,Freudenthal, B.D. (deposition date: 2019-10-28, release date: 2020-06-17, Last modification date: 2023-10-11) |
Primary citation | Schaich, 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: 32501800DOI: 10.7554/eLife.55438 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3.56 Å) |
Structure validation
Download full validation report