Substitutions in the Escherichia coli RNA polymerase inhibitor T7 Gp2 that allow inhibition of transcription when the primary interaction interface between Gp2 and RNA polymerase becomes compromised.
about
Phage T7 Gp2 inhibition of Escherichia coli RNA polymerase involves misappropriation of 70 domain 1.1Full shut-off of Escherichia coli RNA-polymerase by T7 phage requires a small phage-encoded DNA-binding protein.A non-bacterial transcription factor inhibits bacterial transcription by a multipronged mechanism.Transcriptional downregulation of agr expression in Staphylococcus aureus during growth in human serum can be overcome by constitutively active mutant forms of the sensor kinase AgrC.Overexpression of Escherichia coli udk mimics the absence of T7 Gp2 function and thereby abrogates successful infection by T7 phage.Phenotypic consequences of RNA polymerase dysregulation in Escherichia coli.
P2860
Substitutions in the Escherichia coli RNA polymerase inhibitor T7 Gp2 that allow inhibition of transcription when the primary interaction interface between Gp2 and RNA polymerase becomes compromised.
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Substitutions in the Escherich ...... olymerase becomes compromised.
@en
Substitutions in the Escherich ...... olymerase becomes compromised.
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type
label
Substitutions in the Escherich ...... olymerase becomes compromised.
@en
Substitutions in the Escherich ...... olymerase becomes compromised.
@nl
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Substitutions in the Escherich ...... olymerase becomes compromised.
@en
Substitutions in the Escherich ...... olymerase becomes compromised.
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P2093
P2860
P356
P1433
P1476
Substitutions in the Escherich ...... olymerase becomes compromised.
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P2093
Andrey Shadrin
Carol Sheppard
Konstantin Severinov
Sivaramesh Wigneshweraraj
Steve Matthews
P2860
P304
P356
10.1099/MIC.0.062547-0
P577
2012-09-13T00:00:00Z