Literature DB >> 11580238

Crystallographic analysis of Lac repressor bound to natural operator O1.

C E Bell1, M Lewis.   

Abstract

Previous structures of Lac repressor bound to DNA used a fully symmetric "ideal" operator sequence that is missing the central G-C base-pair present in the three natural operator sequences. Here we have determined the X-ray crystal structure of a dimeric Lac repressor bound to a 22 base-pair DNA with the natural operator O1 sequence and the anti-inducer ONPF, at 4.0 A resolution. The natural operator is bent in the same way as the symmetric sequence, due to the binding of the hinge helices of the repressor to the minor groove at the central GCGG sequence of O1. Comparison of the structures of the repressor bound to the natural and symmetric operators shows very similar overall structures, with only slight rearrangements of the headpiece domains of the repressor. Analysis of crystals with iodinated DNA shows that the operator is uniquely positioned and allows for the sequence registration of the DNA relative to the repressor to be determined. The kink in the operator is centered between the left half-site and the central G-C base-pair of O1. Our results are most consistent with a previously proposed model in which, relative to the complex with the symmetric operator, the repressor accommodates binding to the natural operator sequence by shifting the position of the right headpiece by one base-pair step towards the center of O1. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11580238     DOI: 10.1006/jmbi.2001.5024

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  26 in total

1.  Plasticity in protein-DNA recognition: lac repressor interacts with its natural operator 01 through alternative conformations of its DNA-binding domain.

Authors:  Charalampos G Kalodimos; Alexandre M J J Bonvin; Roberto K Salinas; Rainer Wechselberger; Rolf Boelens; Robert Kaptein
Journal:  EMBO J       Date:  2002-06-17       Impact factor: 11.598

2.  Looping charged elastic rods: applications to protein-induced DNA loop formation.

Authors:  A G Cherstvy
Journal:  Eur Biophys J       Date:  2010-10-21       Impact factor: 1.733

3.  Influence of chemical shift tolerances on NMR structure calculations using ARIA protocols for assigning NOE data.

Authors:  Michele Fossi; Jens Linge; Dirk Labudde; Dietmar Leitner; Michael Nilges; Hartmut Oschkinat
Journal:  J Biomol NMR       Date:  2005-01       Impact factor: 2.835

4.  Modeling the Lac repressor-operator assembly: the influence of DNA looping on Lac repressor conformation.

Authors:  David Swigon; Bernard D Coleman; Wilma K Olson
Journal:  Proc Natl Acad Sci U S A       Date:  2006-06-19       Impact factor: 11.205

5.  Extrinsic interactions dominate helical propensity in coupled binding and folding of the lactose repressor protein hinge helix.

Authors:  Hongli Zhan; Liskin Swint-Kruse; Kathleen Shive Matthews
Journal:  Biochemistry       Date:  2006-05-09       Impact factor: 3.162

6.  Structure of the apo form of the catabolite control protein A (CcpA) from Bacillus megaterium with a DNA-binding domain.

Authors:  Rajesh Kumar Singh; Gottfried J Palm; Santosh Panjikar; Winfried Hinrichs
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2007-03-12

7.  Functional consequences of exchanging domains between LacI and PurR are mediated by the intervening linker sequence.

Authors:  Sudheer Tungtur; Susan M Egan; Liskin Swint-Kruse
Journal:  Proteins       Date:  2007-07-01

8.  Switching control of expression of ptsG from the Mlc regulon to the NagC regulon.

Authors:  Samir El Qaidi; Jacqueline Plumbridge
Journal:  J Bacteriol       Date:  2008-05-09       Impact factor: 3.490

9.  High-resolution specificity from DNA sequencing highlights alternative modes of Lac repressor binding.

Authors:  Zheng Zuo; Gary D Stormo
Journal:  Genetics       Date:  2014-09-09       Impact factor: 4.562

10.  Ligand-induced conformational changes and conformational dynamics in the solution structure of the lactose repressor protein.

Authors:  Marc Taraban; Hongli Zhan; Andrew E Whitten; David B Langley; Kathleen S Matthews; Liskin Swint-Kruse; Jill Trewhella
Journal:  J Mol Biol       Date:  2007-11-28       Impact factor: 5.469

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