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Mechanism of PARP1 Elongation Reaction Revealed by Molecular Modeling
by
Nilov, Dmitry K
, Pushkarev, Sergey V
, Kirilin, Evgeny M
, Švedas, Vytas K
in
Adenosine diphosphate
/ Biochemistry
/ DNA damage
/ DNA repair
/ Elongated structure
/ Elongation
/ Enzymes
/ Equilibrium
/ Gene regulation
/ Internet resources
/ Modelling
/ Molecular modelling
/ Molecular structure
/ Poly(ADP-ribose)
/ Poly(ADP-ribose) polymerase
/ Proteins
/ Protons
/ Quantum physics
/ Relay systems
/ Ribose
/ Simulation
/ Substrate inhibition
/ Transcription factors
2024
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Mechanism of PARP1 Elongation Reaction Revealed by Molecular Modeling
by
Nilov, Dmitry K
, Pushkarev, Sergey V
, Kirilin, Evgeny M
, Švedas, Vytas K
in
Adenosine diphosphate
/ Biochemistry
/ DNA damage
/ DNA repair
/ Elongated structure
/ Elongation
/ Enzymes
/ Equilibrium
/ Gene regulation
/ Internet resources
/ Modelling
/ Molecular modelling
/ Molecular structure
/ Poly(ADP-ribose)
/ Poly(ADP-ribose) polymerase
/ Proteins
/ Protons
/ Quantum physics
/ Relay systems
/ Ribose
/ Simulation
/ Substrate inhibition
/ Transcription factors
2024
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Do you wish to request the book?
Mechanism of PARP1 Elongation Reaction Revealed by Molecular Modeling
by
Nilov, Dmitry K
, Pushkarev, Sergey V
, Kirilin, Evgeny M
, Švedas, Vytas K
in
Adenosine diphosphate
/ Biochemistry
/ DNA damage
/ DNA repair
/ Elongated structure
/ Elongation
/ Enzymes
/ Equilibrium
/ Gene regulation
/ Internet resources
/ Modelling
/ Molecular modelling
/ Molecular structure
/ Poly(ADP-ribose)
/ Poly(ADP-ribose) polymerase
/ Proteins
/ Protons
/ Quantum physics
/ Relay systems
/ Ribose
/ Simulation
/ Substrate inhibition
/ Transcription factors
2024
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Mechanism of PARP1 Elongation Reaction Revealed by Molecular Modeling
Journal Article
Mechanism of PARP1 Elongation Reaction Revealed by Molecular Modeling
2024
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Overview
Poly(ADP-ribose) polymerase 1 (PARP1) plays a major role in the DNA damage repair and transcriptional regulation, and is targeted by a number of clinical inhibitors. Despite this, catalytic mechanism of PARP1 remains largely underexplored because of the complex substrate/product structure. Using molecular modeling and metadynamics simulations we have described in detail elongation of poly(ADP-ribose) chain in the PARP1 active site. It was shown that elongation reaction proceeds via the SN1-like mechanism involving formation of the intermediate furanosyl oxocarbenium ion. Intriguingly, nucleophilic 2′A-OH group of the acceptor substrate can be activated by the general base Glu988 not directly but through the proton relay system including the adjacent 3′A-OH group.
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