scholarly article | Q13442814 |
P6179 | Dimensions Publication ID | 1049512311 |
P356 | DOI | 10.1186/1471-2180-9-56 |
P932 | PMC publication ID | 2666748 |
P698 | PubMed publication ID | 19291314 |
P5875 | ResearchGate publication ID | 24205611 |
P50 | author | Dieter Oesterhelt | Q1222570 |
Stefan Streif | Q63244739 | ||
P2093 | author name string | Matthias Schlesner | |
Judith Müller | |||
Arthur Miller | |||
Frank Siedler | |||
Beatrix Scheffer | |||
Wilfried F Staudinger | |||
P2860 | cites work | The Methanosarcina barkeri Genome: Comparative Analysis with Methanosarcina acetivorans and Methanosarcina mazei Reveals Extensive Rearrangement within Methanosarcinal Genomes | Q22065484 |
The genome of M. acetivorans reveals extensive metabolic and physiological diversity | Q22065756 | ||
Genome sequence of Halobacterium species NRC-1 | Q22066243 | ||
Evolution in the laboratory: The genome of Halobacterium salinarum strain R1 compared to that of strain NRC-1 | Q22162489 | ||
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools | Q24248165 | ||
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 | ||
Identification of a protein methyltransferase as the cheR gene product in the bacterial sensing system | Q24605658 | ||
The Pfam protein families database | Q24650035 | ||
A genomic perspective on protein families | Q27860913 | ||
Prokaryotic motility structures | Q28181584 | ||
The genome of Methanosarcina mazei: evidence for lateral gene transfer between bacteria and archaea | Q28215173 | ||
Communication modules in bacterial signaling proteins | Q28243451 | ||
Archaeal flagella, bacterial flagella and type IV pili: a comparison of genes and posttranslational modifications | Q28264353 | ||
Purification and characterization of the S-adenosylmethionine:glutamyl methyltransferase that modifies membrane chemoreceptor proteins in bacteria | Q28295318 | ||
Bacillus subtilis CheC and FliY are members of a novel class of CheY-P-hydrolyzing proteins in the chemotactic signal transduction cascade | Q28488846 | ||
Conservation of gene order: a fingerprint of proteins that physically interact | Q29616049 | ||
Temperature-sensitive motility of Sulfolobus acidocaldarius influences population distribution in extreme environments | Q30304099 | ||
The structure of an archaeal pilus | Q30438864 | ||
The bacterial flagellar switch complex is getting more complex | Q30481718 | ||
Phylogenomics of the archaeal flagellum: rare horizontal gene transfer in a unique motility structure | Q33289666 | ||
Microarray analysis in the archaeon Halobacterium salinarum strain R1 | Q33303672 | ||
Physiological sites of deamidation and methyl esterification in sensory transducers of Halobacterium salinarum | Q33339126 | ||
Bacterial tactic responses | Q33740396 | ||
The archaeal flagellum: a different kind of prokaryotic motility structure | Q33938114 | ||
Characterization of flagellum gene families of methanogenic archaea and localization of novel flagellum accessory proteins | Q33997223 | ||
Diversity in chemotaxis mechanisms among the bacteria and archaea. | Q34349346 | ||
The rotary motor of bacterial flagella | Q35034069 | ||
Recent advances in the structure and assembly of the archaeal flagellum | Q35788087 | ||
Fumarate or a fumarate metabolite restores switching ability to rotating flagella of bacterial envelopes | Q36109971 | ||
Cloning and sequencing of a multigene family encoding the flagellins of Methanococcus voltae | Q36165865 | ||
Phenotypic characterization of the archaebacterial genus Sulfolobus: comparison of five wild-type strains | Q36184598 | ||
Phosphorylation-dependent binding of a signal molecule to the flagellar switch of bacteria | Q36553581 | ||
Bacillus subtilis chemotaxis: a deviation from the Escherichia coli paradigm | Q36769193 | ||
The surprisingly diverse ways that prokaryotes move | Q37156434 | ||
A protein methylesterase involved in bacterial sensing | Q37591895 | ||
Bacteriorhodopsin and the purple membrane of halobacteria | Q39246778 | ||
Rotation and switching of the flagellar motor assembly in Halobacterium halobium | Q39940913 | ||
Signal transduction schemes of bacteria | Q40710183 | ||
Phosphorylation in halobacterial signal transduction | Q40789246 | ||
Chemotaxis and phototaxis require a CheA histidine kinase in the archaeon Halobacterium salinarium | Q40805752 | ||
Signal Processing and Flagellar Motor Switching During Phototaxis of Halobacterium salinarum | Q40830292 | ||
Signal transduction in Halobacterium depends on fumarate | Q41201916 | ||
The structure of the archeabacterial flagellar filament of the extreme halophile Halobacterium salinarum R1M1 and its relation to eubacterial flagellar filaments and type IV pili | Q41629969 | ||
Assembly of an MCP receptor, CheW, and kinase CheA complex in the bacterial chemotaxis signal transduction pathway | Q42016227 | ||
The fla gene cluster is involved in the biogenesis of flagella in Halobacterium salinarum | Q42658358 | ||
A quantitative model of the switch cycle of an archaeal flagellar motor and its sensory control | Q42931907 | ||
Transformation methods for halophilic archaebacteria | Q43018042 | ||
Phosphorylation of the response regulator CheV is required for adaptation to attractants during Bacillus subtilis chemotaxis | Q43735115 | ||
Correlation between phosphorylation of the chemotaxis protein CheY and its activity at the flagellar motor | Q43831042 | ||
Bacillus subtilis CheD is a chemoreceptor modification enzyme required for chemotaxis | Q43993817 | ||
Assembly and function of a quaternary signal transduction complex monitored by surface plasmon resonance | Q45107695 | ||
Structure and function of an unusual family of protein phosphatases: the bacterial chemotaxis proteins CheC and CheX. | Q45152405 | ||
MpcT is the transducer for membrane potential changes in Halobacterium salinarum | Q45307973 | ||
Phosphatase localization in bacterial chemotaxis: divergent mechanisms, convergent principles. | Q46004876 | ||
Quantitation of photochromism of sensory rhodopsin-I by computerized tracking of Halobacterium halobium cells | Q46161620 | ||
Phosphorylation of three proteins in the signaling pathway of bacterial chemotaxis | Q46219823 | ||
Flagellar rotation in the archaeon Halobacterium salinarum depends on ATP. | Q46373303 | ||
Histidine phosphorylation and phosphoryl group transfer in bacterial chemotaxis | Q46988302 | ||
Quantitative analysis of signal transduction in motile and phototactic cells by computerized light stimulation and model based tracking. | Q48858073 | ||
The N terminus of the flagellar switch protein, FliM, is the binding domain for the chemotactic response regulator, CheY. | Q50130656 | ||
Multiple forms of the CheB methylesterase in bacterial chemosensing. | Q50205296 | ||
Sensory rhodopsin-controlled release of the switch factor fumarate in Halobacterium salinarium. | Q50778085 | ||
Deletion analysis of the che operon in the archaeon Halobacterium salinarium. | Q52887608 | ||
Morphology, function and isolation of halobacterial flagella | Q64331245 | ||
Systematic deletion analyses of the fla genes in the flagella operon identify several genes essential for proper assembly and function of flagella in the archaeon, Methanococcus maripaludis | Q64331261 | ||
Mutants in flaI and flaJ of the archaeon Methanococcus voltae are deficient in flagellum assembly | Q64449468 | ||
Insertional inactivation of the flaH gene in the archaeon Methanococcus voltae results in non-flagellated cells | Q64449566 | ||
Phototrophic growth of halobacteria and its use for isolation of photosynthetically-deficient mutants | Q71092583 | ||
Mechanism of photosensory adaptation in Halobacterium salinarium | Q72595045 | ||
Modelling the CheY(D10K,Yl00W) Halobacterium salinarum mutant: sensitivity analysis allows choice of parameter to be modified in the phototaxis model | Q80816893 | ||
The CheC phosphatase regulates chemotactic adaptation through CheD | Q81380787 | ||
P921 | main subject | chemotaxis | Q658145 |
Archaea | Q10872 | ||
P304 | page(s) | 56 | |
P577 | publication date | 2009-03-16 | |
P1433 | published in | BMC Microbiology | Q15759430 |
P1476 | title | Identification of Archaea-specific chemotaxis proteins which interact with the flagellar apparatus | |
P478 | volume | 9 |
Q31060885 | A comparative genomics perspective on the genetic content of the alkaliphilic haloarchaeon Natrialba magadii ATCC 43099T. |
Q35542657 | Archaeal flagellar ATPase motor shows ATP-dependent hexameric assembly and activity stimulation by specific lipid binding. |
Q34160723 | Assembly and function of the archaeal flagellum. |
Q55233983 | Characterization of the ATPase FlaI of the motor complex of the Pyrococcus furiosus archaellum and its interactions between the ATP-binding protein FlaH. |
Q30209651 | Chemosensory regulation of a HEAT-repeat protein couples aggregation and sporulation in Myxococcus xanthus |
Q22064357 | Complete genome sequence of Archaeoglobus profundus type strain (AV18) |
Q37336843 | Complete genome sequence of Methanoculleus bourgensis strain MAB1, the syntrophic partner of mesophilic acetate-oxidising bacteria (SAOB). |
Q55436577 | Cross-kymography analysis to simultaneously quantify the function and morphology of the archaellum. |
Q36023357 | Diversity and Evolution of Type IV pili Systems in Archaea |
Q37122326 | Ecophysiological Distinctions of Haloarchaea from a Hypersaline Antarctic Lake as Determined by Metaproteomics |
Q35586999 | FlaF Is a β-Sandwich Protein that Anchors the Archaellum in the Archaeal Cell Envelope by Binding the S-Layer Protein. |
Q42424999 | FlaX, a unique component of the crenarchaeal archaellum, forms oligomeric ring-shaped structures and interacts with the motor ATPase FlaI |
Q34039121 | Functional and genomic analyses of alpha-solenoid proteins |
Q92155986 | Genome Analyses and Genome-Centered Metatranscriptomics of Methanothermobacter wolfeii Strain SIV6, Isolated from a Thermophilic Production-Scale Biogas Fermenter |
Q33983376 | Haloferax volcanii flagella are required for motility but are not involved in PibD-dependent surface adhesion. |
Q50097018 | Light-controlled motility in prokaryotes and the problem of directional light perception |
Q30401069 | Methyl-accepting chemotaxis proteins: a core sensing element in prokaryotes and archaea. |
Q37832278 | Model organisms for genetics in the domain Archaea: methanogens, halophiles, Thermococcales and Sulfolobales |
Q42512675 | Morphology of the archaellar motor and associated cytoplasmic cone in Thermococcus kodakaraensis |
Q64064083 | Positioning of the Motility Machinery in Halophilic Archaea |
Q41613456 | Pyrococcus furiosus flagella: biochemical and transcriptional analyses identify the newly detected flaB0 gene to encode the major flagellin |
Q37780957 | S-layer glycoproteins and flagellins: reporters of archaeal posttranslational modifications |
Q36206586 | Screening of a Haloferax volcanii Transposon Library Reveals Novel Motility and Adhesion Mutants |
Q37776655 | Shaping the archaeal cell envelope |
Q38842409 | Structural conservation of chemotaxis machinery across Archaea and Bacteria |
Q48191378 | Structure and function of the archaeal response regulator CheY. |
Q41059794 | Structure and in situ organisation of the Pyrococcus furiosus archaellum machinery |
Q93053911 | Structure of the archaeal chemotaxis protein CheY in a domain-swapped dimeric conformation |
Q38265133 | Surface appendages of archaea: structure, function, genetics and assembly |
Q35007386 | Tandem-repeat protein domains across the tree of life |
Q37279593 | Taxis toward hydrogen gas by Methanococcus maripaludis |
Q34185088 | The archaeal cell envelope |
Q38362614 | The archaellum: how Archaea swim |
Q28589802 | The landscape of microbial phenotypic traits and associated genes |
Q34484501 | The protein interaction network of a taxis signal transduction system in a halophilic archaeon |
Q46250170 | Versatile cell surface structures of archaea. |
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