Reactome: A Curated Pathway Database
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Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

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Details on Person Before rejoining of the broken DNA ends can occur, endonucle...

Class:IdSummation:353291
_displayNameBefore rejoining of the broken DNA ends can occur, endonucle...
_timestamp2009-02-23 15:56:29
created[InstanceEdit:353491] Saxena, A, 2008-06-12 16:39:18
modified[InstanceEdit:391641] Saxena, A, 2009-02-23 15:55:32
textBefore rejoining of the broken DNA ends can occur, endonucleases removes possible 3' phospho-glycolate residues so that a DNA-PK synaptic complex with ligatable DNA is formed at the DSB. Rejoining of ionizing radiation (IR)-induced DNA DSBs usually follows biphasic kinetics with a fast (t(1/2): 5-30 min) component attributed to DNA PK dependent non homologous end joining (NHEJ) and a slow (t(1/2): 1-20 h) component of as yet uncharacterized reaction. In a systematic genetic study using the chicken DT40 cell line and employing a series of mutants defective in homologous recombination (HR), it was suggested that NHEJ is the main pathway for rejoining of IR-induced DNA DSBs in vertebrates. It is speculated that the contribution of homologous recombination repair (HRR) occurs at a stage after the initial rejoining.
(summation)[Reaction:353313] Removal of 3'-phosphoglycolate (PG) moiety from DSB ends [Gallus gallus]
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