In vertebrate cells, the DNA damage response is controlled by three related kinases: ATM, ATR, and DNA-PK. It has been 20 years since the cloning of ATR, the last of the three to be identified. During this time, our understanding of how these kinases regulate DNA repair and associated events has grown profoundly, although major questions remain unanswered. Here, we provide a historical perspective of their discovery and discuss their established functions in sensing and responding to genotoxic stress. We also highlight what is known regarding their structural similarities and common mechanisms of regulation, as well as emerging non-canonical roles and how our knowledge of ATM, ATR, and DNA-PK is being translated to benefit human health
Deoxycytidine kinase (dCK) (EC 2.7.1.74) is a key enzyme for salvage of deoxynucleosides and activat...
The ATM (Ataxia-telangiectasia mutated) kinase is one of the major players of the DNA damage respon...
SummaryDNA double-strand breaks (DSBs) elicit the so-called DNA damage response (DDR), largely relyi...
In vertebrate cells, the DNA damage response is controlled by three related kinases: ATM, ATR, and D...
In vertebrate cells, the DNA damage response is controlled by three related kinases: ATM, ATR, and D...
In eukaryotic cells, maintenance of genomic stability relies on the coordinated action of a network ...
The maintenance of genomic integrity is crucial for the survival of all organisms. In humans, compro...
ATM is the most significant molecule involved in monitoring the genomic integrity of the cell. Any d...
DNA damage is a key factor both in the evolution and treatment of cancer. Genomic instability is a c...
ATM and ATR signaling pathways are well conserved throughout evolution and are central to the mainte...
A functional DNA damage response is essential for maintaining genome integrity in the presence of DN...
Deoxycytidine kinase (dCK) catalyses the first and rate limiting step of the deoxynucleoside salvage...
AbstractIn order to maintain genomic stability, cells have developed sophisticated signalling pathwa...
Ataxia-telangiectasia mutated kinase (ATM) is a DNA damage-inducible protein kinase, which phosphory...
DNA damage triggers Atm- and/or Atr-dependent signaling pathways to control cell cycle progression, ...
Deoxycytidine kinase (dCK) (EC 2.7.1.74) is a key enzyme for salvage of deoxynucleosides and activat...
The ATM (Ataxia-telangiectasia mutated) kinase is one of the major players of the DNA damage respon...
SummaryDNA double-strand breaks (DSBs) elicit the so-called DNA damage response (DDR), largely relyi...
In vertebrate cells, the DNA damage response is controlled by three related kinases: ATM, ATR, and D...
In vertebrate cells, the DNA damage response is controlled by three related kinases: ATM, ATR, and D...
In eukaryotic cells, maintenance of genomic stability relies on the coordinated action of a network ...
The maintenance of genomic integrity is crucial for the survival of all organisms. In humans, compro...
ATM is the most significant molecule involved in monitoring the genomic integrity of the cell. Any d...
DNA damage is a key factor both in the evolution and treatment of cancer. Genomic instability is a c...
ATM and ATR signaling pathways are well conserved throughout evolution and are central to the mainte...
A functional DNA damage response is essential for maintaining genome integrity in the presence of DN...
Deoxycytidine kinase (dCK) catalyses the first and rate limiting step of the deoxynucleoside salvage...
AbstractIn order to maintain genomic stability, cells have developed sophisticated signalling pathwa...
Ataxia-telangiectasia mutated kinase (ATM) is a DNA damage-inducible protein kinase, which phosphory...
DNA damage triggers Atm- and/or Atr-dependent signaling pathways to control cell cycle progression, ...
Deoxycytidine kinase (dCK) (EC 2.7.1.74) is a key enzyme for salvage of deoxynucleosides and activat...
The ATM (Ataxia-telangiectasia mutated) kinase is one of the major players of the DNA damage respon...
SummaryDNA double-strand breaks (DSBs) elicit the so-called DNA damage response (DDR), largely relyi...