Equilibrium studies of the cyclic AMP receptor protein-DNA interaction (Q70186335)

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9 October 2019

title

Equilibrium studies of the cyclic AMP receptor protein-DNA interaction (English)

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9 October 2019

2

D M Crothers

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9 October 2019

author name string

M G Fried

series ordinal

1

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9 October 2019

publication date

1 January 1984

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Journal of Molecular Biology

9 October 2019

published in

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9 October 2019

volume

172

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9 October 2019

issue

3

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9 October 2019

page(s)

241-262

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Diffusion-driven mechanisms of protein translocation on nucleic acids. 1. Models and theory

9 October 2019

cites work

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lac Repressor-operator interaction. IX. The binding of lac repressor to operators containing Oc mutations

7 January 2021

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7 January 2021

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A new method for sequencing DNA

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Structure of catabolite gene activator protein at 2.9 A resolution suggests binding to left-handed B-DNA.

7 January 2021

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The Location of the Repressor Binding Sites in the lac Operon

7 January 2021

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Diffusion controlled reaction rates in spheroidal geometry. Application to repressor--operator association and membrane bound enzymes

7 January 2021

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The lac repressor-operator interaction. 3. Kinetic studies

7 January 2021

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Cyclic AMP receptor protein interacts with lactose operator DNA

7 January 2021

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Rate enhancement by guided diffusion. Chain length dependence of repressor-operator association rates

7 January 2021

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DNA flexibility studied by covalent closure of short fragments into circles

7 January 2021

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Diffusion-driven mechanisms of protein translocation on nucleic acids. 3. The Escherichia coli lac repressor--operator interaction: kinetic measurements and conclusions

7 January 2021

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Effect of cyclic guanosine 3,5-monophosphate on the synthesis of enzymes sensitive to caatabolite repression in intact cells of Escherichia coli

7 January 2021

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7 January 2021

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Nature of Col E 1 plasmid replication in Escherichia coli in the presence of the chloramphenicol

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inferred from DOI database lookup

7 January 2021

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Identifiers

DOI

10.1016/S0022-2836(84)80025-X

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9 October 2019

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