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The human genome codes for 95 non-redundant helicases: 64 RNA helicases and 31 DNA helicases. [2] Many cellular processes, such as DNA replication , transcription , translation , recombination , DNA repair , and ribosome biogenesis involve the separation of nucleic acid strands that necessitates the use of helicases.
Werner syndrome ATP-dependent helicase, also known as DNA helicase, RecQ-like type 3, is an enzyme that in humans is encoded by the WRN gene. WRN is a member of the RecQ Helicase family. [ 5 ] Helicase enzymes generally unwind and separate double-stranded DNA .
DnaC helps the helicase to bind to and to properly accommodate the ssDNA at the 13 bp region; this is accomplished by ATP hydrolysis, after which DnaC is released. Single-strand binding proteins (SSBs) stabilize the single DNA strands in order to maintain the replication bubble. DnaB is a 5'→3' helicase, so it travels on the lagging strand.
The polymerase chain reaction is the most widely used method for in vitro DNA amplification for purposes of molecular biology and biomedical research. [1] This process involves the separation of the double-stranded DNA in high heat into single strands (the denaturation step, typically achieved at 95–97 °C), annealing of the primers to the single stranded DNA (the annealing step) and copying ...
DNA-dependent ATPase, abbreviated Dda and also known as Dda helicase and Dda DNA helicase, is the 439-amino acid 49,897-atomic mass unit protein coded by the Dda gene of the bacteriophage T4 phage, a virus that infects enterobacteria.
The steric model hypothesizes that the helicase encircles dsDNA and, after local melting of the duplex DNA at the origin, translocates away from the origin, dragging a rigid proteinaceous "wedge" (either part of the helicase itself or another associated protein) that separates the DNA strands. [32]
Genetic and biochemical studies have shown that the helicase is essential for plasmid rolling-circle replication and repair of DNA damage caused by exposure to ultraviolet radiation. It catalyzes the unwinding of double-stranded plasmid DNA that has been nicked at the replication origin by the replication initiation protein.
The gene CHD8 encodes the protein chromodomain helicase DNA binding protein 8, [7] which is a chromatin regulator enzyme that is essential during fetal development. [8] CHD8 is an ATP dependent enzyme. [9] The protein contains an Snf2 helicase domain that is responsible for the hydrolysis of ATP to ADP. [9]