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6D0Z

Polymerase Eta cytarabine (AraC) extension ternary complex

Summary for 6D0Z
Entry DOI10.2210/pdb6d0z/pdb
Related6D0M
DescriptorDNA polymerase eta, DNA (5'-D(*CP*AP*TP*TP*GP*CP*AP*GP*TP*GP*CP*T)-3'), DNA/RNA (5'-D(*AP*GP*CP*AP*CP*TP*G)-R(P*(CAR))-3'), ... (7 entities in total)
Functional Keywordscytarabine, arac, dna damage, translesion, dna synthesis, dna replication, transferase
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains3
Total formula weight55449.75
Authors
Rechkoblit, O.,Aggarwal, A.K. (deposition date: 2018-04-11, release date: 2018-09-05, Last modification date: 2023-10-04)
Primary citationRechkoblit, O.,Choudhury, J.R.,Buku, A.,Prakash, L.,Prakash, S.,Aggarwal, A.K.
Structural basis for polymerase eta-promoted resistance to the anticancer nucleoside analog cytarabine.
Sci Rep, 8:12702-12702, 2018
Cited by
PubMed Abstract: Cytarabine (AraC) is an essential chemotherapeutic for acute myeloid leukemia (AML) and resistance to this drug is a major cause of treatment failure. AraC is a nucleoside analog that differs from 2'-deoxycytidine only by the presence of an additional hydroxyl group at the C2' position of the 2'-deoxyribose. The active form of the drug AraC 5'-triphosphate (AraCTP) is utilized by human replicative DNA polymerases to insert AraC at the 3' terminus of a growing DNA chain. This impedes further primer extension and is a primary basis for the drug action. The Y-family translesion synthesis (TLS) DNA polymerase η (Polη) counteracts this barrier to DNA replication by efficient extension from AraC-terminated primers. Here, we provide high-resolution structures of human Polη with AraC incorporated at the 3'-primer terminus. We show that Polη can accommodate AraC at different stages of the catalytic cycle, and that it can manipulate the conformation of the AraC sugar via specific hydrogen bonding and stacking interactions. Taken together, the structures provide a basis for the ability of Polη to extend DNA synthesis from AraC terminated primers.
PubMed: 30140014
DOI: 10.1038/s41598-018-30796-w
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.75 Å)
Structure validation

237735

数据于2025-06-18公开中

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