Blat et al., 1996 - Google Patents
Conserved C-terminus of the phosphatase CheZ is a binding domain for the chemotactic response regulator CheYBlat et al., 1996
- Document ID
- 1877533486314173977
- Author
- Blat Y
- Eisenbach M
- Publication year
- Publication venue
- Biochemistry
External Links
Snippet
CheZ is the phosphatase of the chemotactic response regulator, CheY. There are three conserved domains on CheZ. Here we determined the function of the C-terminal domain (residues 202− 214). A truncated form of CheZ, missing residues 202− 214, hardly bound to …
- 230000003399 chemotactic 0 title abstract description 5
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by the preceding groups
- G01N33/48—Investigating or analysing materials by specific methods not covered by the preceding groups biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2333/00—Assays involving biological materials from specific organisms or of a specific nature
- G01N2333/90—Enzymes; Proenzymes
- G01N2333/914—Hydrolases (3)
- G01N2333/978—Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICRO-ORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING OR MAINTAINING MICRO-ORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES OR MICRO-ORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or micro-organisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2500/00—Screening for compounds of potential therapeutic value
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electro-chemical, or magnetic means
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Sun et al. | Repair of oxidized calmodulin by methionine sulfoxide reductase restores ability to activate the plasma membrane Ca-ATPase | |
Brune et al. | Mechanism of inorganic phosphate interaction with phosphate binding protein from Escherichia coli | |
Kaihara et al. | Locating a protein− protein interaction in living cells via split Renilla luciferase complementation | |
Brown et al. | Inhibition of TEM-2 β-lactamase from Escherichia coli by clavulanic acid: observation of intermediates by electrospray ionization mass spectrometry | |
Tell et al. | Redox potential controls the structure and DNA binding activity of the paired domain | |
Wang et al. | D1 ring is stable and nucleotide-independent, whereas D2 ring undergoes major conformational changes during the ATPase cycle of p97-VCP | |
Fisher et al. | Kinetic comparison of the specificity of the vancomycin resistance kinase VanS for two response regulators, VanR and PhoB | |
Wyka et al. | Replication protein A interactions with DNA: differential binding of the core domains and analysis of the DNA interaction surface | |
Blat et al. | Conserved C-terminus of the phosphatase CheZ is a binding domain for the chemotactic response regulator CheY | |
Levay et al. | Localization of the sites for Ca2+-binding proteins on G protein-coupled receptor kinases | |
Baud et al. | Allosteric communication between signal peptides and the SecA protein DEAD motor ATPase domain | |
Park et al. | Chromophore− apoprotein interactions in Synechocystis sp. PCC6803 phytochrome Cph1 | |
Weber et al. | A linear diubiquitin-based probe for efficient and selective detection of the deubiquitinating enzyme OTULIN | |
Rich et al. | Domain structure of the Staphylococcus aureus collagen adhesin | |
Huse et al. | Semisynthesis of hyperphosphorylated type I TGFβ receptor: addressing the mechanism of kinase activation | |
Quadroni et al. | Phosphorylation of calmodulin alters its potency as an activator of target enzymes | |
Cass et al. | The SF3b155 N-terminal domain is a scaffold important for splicing | |
Bartee et al. | The loop connecting metal-binding domains 3 and 4 of ATP7B is a target of a kinase-mediated phosphorylation | |
Behlke et al. | Hexokinase 2 from Saccharomyces cerevisiae: regulation of oligomeric structure by in vivo phosphorylation at serine-14 | |
Li et al. | An NF-κB-specific inhibitor, IκBα, binds to and inhibits cyclin-dependent kinase 4 | |
Schmitz et al. | Role of the C-terminal Gly-Gly motif of Escherichia coli MoaD, a molybdenum cofactor biosynthesis protein with a ubiquitin fold | |
Storf et al. | Proteomic analysis of the photosystem I light-harvesting antenna in tomato (Lycopersicon esculentum) | |
Wu et al. | Protein phosphatase type-1 and glycogen bind to a domain in the skeletal muscle regulatory subunit containing conserved hydrophobic sequence motifs | |
Féthière et al. | Peripheral stator of the yeast V-ATPase: stoichiometry and specificity of interaction between the EG complex and subunits C and H | |
Safferling et al. | TetL tetracycline efflux protein from Bacillus subtilis is a dimer in the membrane and in detergent solution |