DNA recognition by beta-sheets in the Arc repressor-operator crystal structure.
By B. Raumann, M. A. Rould, C. Pabo, R. Sauer. 1994
How researchers see this paper
The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.
- M. V. van Dijk
- Alexandre M. J. J. Bonvin
- A. V. van Dijk
- V. Hsu
- R. Monnat
- Eric A. Galburt
- Rolf Boelens
- Meggen S. Chadsey
Citations in the corpus
- Pushing the limits of what is achievable in protein–DNA docking: benchmarking HADDOCK’s performance (2010, methodology): “The protocol was initially tested by docking the unbound structures of three monomeric transcription factors to their respective operator half-sites [phage 434 Cro (21), phage (cid:2) Arc (22) and Escherichia coli Lac (23)].”
- Conformational changes and cleavage by the homing endonuclease I-PpoI: a critical role for a leucine residue in the active site. (2000, background): “, 1993, 1994), arc repressor (Bowie & Sauer, 1989; Raumann et al., 1994), and l”
- Information-driven protein–DNA docking using HADDOCK: it is a matter of flexibility (2006, background): “We evaluated our approach on the monomeric repressor DNA complexes formed by bacteriophage 434 Cro, the Escherichia coli Lac headpiece and bacteriophage P22 Arc.”