about
Isolation of an Escherichia coli K-12 mutant strain able to form biofilms on inert surfaces: involvement of a new ompR allele that increases curli expressionA small diffusible signal molecule is responsible for the global control of virulence and exoenzyme production in the plant pathogen Erwinia carotovoraThe Rhizobium meliloti rhizopine mos locus is a mosaic structure facilitating its symbiotic regulationIsolation and characterization of a regulatory gene affecting rhamnolipid biosurfactant synthesis in Pseudomonas aeruginosaRewiring cell signalling through chimaeric regulatory protein engineeringBiologically inspired strategies for combating bacterial biofilmsCooperative Formation of Chiral Patterns during Growth of Bacterial ColoniesCrystal structure of activated CheY. Comparison with other activated receiver domainsCrystal structure of the CheA histidine phosphotransfer domain that mediates response regulator phosphorylation in bacterial chemotaxisCrystallographic structure reveals phosphorylated pilin from Neisseria: phosphoserine sites modify type IV pilus surface chemistry and fibre morphologyStructural Investigation of a Phosphorylation-Catalyzed, Isoaspartate-Free, Protein Succinimide: Crystallographic Structure of Post-Succinimide His15Asp Histidine-Containing Protein † ‡Crystal Structure of the -Kinase Domain of Dictyostelium Myosin Heavy Chain Kinase AX-ray crystallographic snapshots of reaction intermediates in the G117H mutant of human butyrylcholinesterase, a nerve agent target engineered into a catalytic bioscavengerPhosphotyrosine-independent binding of SHC to the NPLH sequence of murine protein-tyrosine phosphatase-PEST. Evidence for extended phosphotyrosine binding/phosphotyrosine interaction domain recognition specificityBacterial signalling involving eukaryotic-type protein kinasesCloning and identification of a two-component signal-transducing regulatory system from Bacteroides fragilisCloning and phenotypic characterization of fleS and fleR, new response regulators of Pseudomonas aeruginosa which regulate motility and adhesion to mucinA transcriptional activator, FleQ, regulates mucin adhesion and flagellar gene expression in Pseudomonas aeruginosa in a cascade mannerOuter membrane protein genes and their small non-coding RNA regulator genes in Photorhabdus luminescensTransduction of the light signal during complementary chromatic adaptation in the cyanobacterium Calothrix sp. PCC 7601: DNA-binding proteins and modulation by phosphorylationPhosphoproteomics--more than meets the eye.Expression cloning of different bacterial phosphatase-encoding genes by histochemical screening of genomic libraries onto an indicator medium containing phenolphthalein diphosphate and methyl green.Arabidopsis ARR1 and ARR2 response regulators operate as transcriptional activators.Use of a transposon with luciferase as a reporter to identify environmentally responsive genes in a cyanobacterium.Chemotaxis of bacteria in glass capillary arrays. Escherichia coli, motility, microchannel plate, and light scatteringCloning of the complete biosynthetic gene cluster for an aminonucleoside antibiotic, puromycin, and its regulated expression in heterologous hosts.Genome-wide survey of putative serine/threonine protein kinases in cyanobacteria.A response regulator of cyanobacteria integrates diverse environmental signals and is critical for survival under extreme conditions.A Campylobacter jejuni homolog of the LcrD/FlbF family of proteins is necessary for flagellar biogenesis.Microbial biofilms: their development and significance for medical device-related infections.Aberrant cell division and random FtsZ ring positioning in Escherichia coli cpxA* mutants.A high-throughput TNP-ATP displacement assay for screening inhibitors of ATP-binding in bacterial histidine kinasesRegulation of virulence by a two-component system in group B streptococcus.Receptor-mediated protein kinase activation and the mechanism of transmembrane signaling in bacterial chemotaxis.Serine/threonine protein kinase SpkG is a candidate for high salt resistance in the unicellular cyanobacterium Synechocystis sp. PCC 6803.The bacterial enhancer-dependent sigma(54) (sigma(N)) transcription factorActivation of the phosphosignaling protein CheY. I. Analysis of the phosphorylated conformation by 19F NMR and protein engineeringMutational analysis of the phoD promoter in Bacillus subtilis: implications for PhoP binding and promoter activation of Pho regulon promotersThe periplasmic murein peptide-binding protein MppA is a negative regulator of multiple antibiotic resistance in Escherichia coliFunctionality of purified sigma(N) (sigma(54)) and a NifA-like protein from the hyperthermophile Aquifex aeolicus.
P2860
Q24520852-0075CCCB-695F-4544-8DDE-A7F73BF1711DQ24564606-E79F8D18-E455-45BB-A36A-B47DE4FA8DD9Q24669866-CC8FC32A-80D3-4C7E-9CFF-A01AF2B98056Q24685284-4C75A459-5669-4BF6-AF06-E6DBC20D0891Q26822574-2DA3F753-43D3-4E30-8DDF-3A394DAA5238Q27006003-A2A63A10-087B-4401-908E-3F8666532218Q27450489-A705E988-E7AC-4206-A7B3-C49295A2539BQ27630942-E5A212A6-3CDA-41D0-971A-04D6C0E55FDCQ27632267-87130C56-8ACB-4FDE-9F0B-6E9B7B786939Q27639839-7404AE74-1923-4046-859C-1AC335A2EE70Q27651575-4B4AAFD2-16A4-4C82-8C20-7A7904052A26Q27660090-BC991E68-8D8B-4A2E-ADDB-724F9976005AQ27665984-226BFD8B-413A-4950-9326-A9F82D96350AQ28278276-DB861F2F-DFBA-499E-B72F-8AEFA577EFD7Q28293209-FF55900E-6587-4B0E-A135-B4A5A1302E96Q28491975-58FE6F52-23A7-4208-8F69-99B060376A51Q28492811-6DE42B1E-73A2-417C-8971-091DB2ADFED1Q28492817-C39558B5-B72A-42AA-97FA-37D82564BB6BQ28768503-D8DD2D19-7143-410C-9D5F-CCC878022081Q28775867-FE3B82C4-3B7C-44AA-89A2-0435AF3B3E90Q30429237-2C0B1BDE-21E2-44DA-BD05-7BA9DED70E4DQ30871091-8724B849-1277-4E90-913E-66C7F7FDCD3CQ30977438-B4C46B0C-8DC3-444E-9921-66413BFF99F1Q31019151-FA8D30C6-A2E1-4DFE-8415-BA751F5B9750Q31054313-3754FC48-B2C7-4AFE-A766-FBA00208D9B1Q31112814-493A50EB-6B83-42F7-A9FF-634C8E95FBB2Q33304398-7857F197-199D-44F3-BC80-12882039CB53Q33568988-548F538F-6E80-45D4-8361-A22E5760A215Q33602825-4EAF3B5D-A2EF-4E53-9C77-B7BAE6FDCA69Q33725393-844C9288-27E5-4165-BD5F-D4C88EE72D1CQ33733032-9052A204-68D2-4E80-9160-0E35A7ADD058Q33738068-1AECFC7A-116D-440D-9983-67C8A0F00C95Q33758224-3D9F9646-22E5-47B5-AA03-5D9FA694AFA2Q33887857-9916E40C-E05F-4C97-8141-D1211A968973Q33920789-04989560-5EF8-4E44-A661-88BB9DC1D0C3Q33968426-AFF77728-6305-4F8F-B6CC-90A0D820462DQ33973483-6C447565-6E46-4937-9E74-486BC55B9C40Q33991585-FAEE117E-C70F-46B2-AE9F-D8C7461AA9FFQ33992682-4D1C2DF4-6894-4DC5-A395-1E969A0F109BQ33994046-E63C3C71-D302-4DF2-A02C-D11A58DD9773
P2860
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on March 1990
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Signal transduction in bacteria.
@en
Signal transduction in bacteria.
@nl
type
label
Signal transduction in bacteria.
@en
Signal transduction in bacteria.
@nl
prefLabel
Signal transduction in bacteria.
@en
Signal transduction in bacteria.
@nl
P2093
P356
P1433
P1476
Signal transduction in bacteria.
@en
P2093
J M Mottonen
P2888
P304
P356
10.1038/344395A0
P407
P577
1990-03-01T00:00:00Z
P6179
1024637414