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The toeprinting assay has been utilized to examine the formation of the translation initiation complex.
These general factors include components of the initiation complex that assemble on promoters or involved in transcription elongation.
Once the initiation complex is formed and the cells pass into the S phase, the complex then becomes a replisome.
Extension inhibition analysis of translation initiation complexes.
Formation of initiation complex.
During this transformation, the pre-RC is disassembled with the loss of Cdc6, creating the initiation complex.
Cell division cycle 45 (Cdc45) protein is a critical component for the conversion of the pre-replicative complex to the initiation complex.
IF3 is required by the small subunit to form initiation complexes, but has to be released to allow the 50S subunit to bind.
Cdc45 binding is also required for chromatin association of DNA polymerase α to the initiation complex.
The protein RLI is known to have an essential, probably catalytic role in the formation of initiation complexes as well.
The polymerase catalyses the formation of the initiation complex between the terminal protein and the chromosome ends at an adenine residue.
Their signaling will converge at the translation initiation complex on the 5' end of mRNA, and thus activate translation.
PDCD4 is a tumor suppressor that binds to eIF4A and prevents it from being incorporated into the initiation complex.
The completed assembly of transcription factors and RNA polymerase bind to the promoter, forming a transcription initiation complex.
In addition to microtubules, Dr. Nogales explores the structural and functional aspects of large macromolecular assemblies such as eukaryotic transcription and translation initiation complexes.
It has also been demonstrated that the Mediator complex is involved in activator-independent transcription, implying that it may provide a fundamental control of the formation of the initiation complex.
Usually, in eukaryotes, translation can be initiated only at the 5' end of the mRNA molecule, since 5' cap recognition is required for the assembly of the initiation complex.
Enhancers are sites on the DNA helix that are bound to by activators in order to loop the DNA bringing a specific promoter to the initiation complex.
It does this by binding DNA at the transcription initiation complex and preventing elongation of RNA chain by RNA polymerase.
It does so by preventing the formation of the initiation complex, composed of the 30S and 50S subunits of the ribosome, tRNA, and mRNA.
The nonphosphorylated form, RNAPIIA, is recruited to the initiation complex, whereas the elongating polymerase is found with RNAPII0.
The ORC, a component of the initiation complex, binds the ACS in vivo throughout the cell cycle, and in vitro in an ATP dependent manner.
The small subunit of the ribosome usually starts by binding to one end of the mRNA and is joined there by various other eukaryotic initiation factors, forming the initiation complex.
In contrast, the DRE motif that is part of the recognition site for an alternative transcription initiation complex that utilizes TRF2 [ 26] is more frequent than previously thought.
At the onset of the S phase, the pre-replicative complex must be activated by two S phase specific kinases in order to form an initiation complex at an origin of replication.