(Q27702270)

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Three-dimensional structure of CheY, the response regulator of bacterial chemotaxis

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Three-dimensional structure of CheY, the response regulator of bacterial chemotaxis (English)

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author name string

A M Stock

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J M Mottonen

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J B Stock

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C E Schutt

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publication date

23 February 1989

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337

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745-9

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6209

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Homologies between the Salmonella typhimurium CheY protein and proteins involved in the regulation of chemotaxis, membrane protein synthesis, and sporulation

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Two-component regulatory systems responsive to environmental stimuli share strongly conserved domains with the nitrogen assimilation regulatory genes ntrB and ntrC.

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Transmitter and receiver modules in bacterial signaling proteins

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Sensory transduction in bacterial chemotaxis involves phosphotransfer between Che proteins.

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Phosphorylation of three proteins in the signaling pathway of bacterial chemotaxis

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Histidine phosphorylation and phosphoryl group transfer in bacterial chemotaxis.

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Covalent modification of the glnG product, NRI, by the glnL product, NRII, regulates the transcription of the glnALG operon in Escherichia coli

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Phosphorylation of nitrogen regulator I (NRI) of Escherichia coli

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Overexpression and sequence of the Escherichia coli cheY gene and biochemical activities of the CheY protein

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Use of site-directed mutagenesis to obtain isomorphous heavy-atom derivatives for protein crystallography: cysteine-containing mutants of phage T4 lysozyme

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Describing patterns of protein tertiary structure.

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Crosstalk between bacterial chemotaxis signal transduction proteins and regulators of transcription of the Ntr regulon: evidence that nitrogen assimilation and chemotaxis are controlled by a common phosphotransfer mechanism

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Relation between structure and function of alpha/beta-proteins

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Two Ca2+ ATPase genes: homologies and mechanistic implications of deduced amino acid sequences

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Yeast plasma membrane ATPase is essential for growth and has homology with (Na+ + K+), K+- and Ca2+-ATPases

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Sequence homology between two membrane transport ATPases, the Kdp-ATPase of Escherichia coli and the Ca2+-ATPase of sarcoplasmic reticulum

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Twenty Questions Concerning The Reaction Cycle Of The Sarcoplasmic Reticulum Calcium Pum

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2 New M13 vectors for cloning

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32 Oligonucleotide-directed mutagenesis of DNA fragments cloned into M13 vectors

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Rapid and efficient site-specific mutagenesis without phenotypic selection

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DNA sequencing with chain-terminating inhibitors

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16 Plasmids of Escherichia coli as cloning vectors

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