scholarly article | Q13442814 |
review article | Q7318358 |
P50 | author | Sonja-Verena Albers | Q21264709 |
Behnam Zolghadr | Q114449125 | ||
P2093 | author name string | Ken F Jarrell | |
Sandy Y M Ng | |||
Arnold J M Driessen | |||
P2860 | cites work | Sensing wetness: a new role for the bacterial flagellum | Q24529135 |
In vivo observation of cell division of anaerobic hyperthermophiles by using a high-intensity dark-field microscope | Q24549248 | ||
Natural communities of novel archaea and bacteria growing in cold sulfurous springs with a string-of-pearls-like morphology | Q24550104 | ||
Methane- and sulfur-metabolizing microbial communities dominate the Lost City hydrothermal field ecosystem | Q24674422 | ||
Pyrobaculum aerophilum sp. nov., a novel nitrate-reducing hyperthermophilic archaeum | Q24679510 | ||
Cleavage of preflagellins by an aspartic acid signal peptidase is essential for flagellation in the archaeon Methanococcus voltae | Q28184916 | ||
Pili in gram-positive pathogens | Q28246526 | ||
Archaeal flagella, bacterial flagella and type IV pili: a comparison of genes and posttranslational modifications | Q28264353 | ||
The type III secretion injectisome | Q29617944 | ||
Signal transduction in bacterial chemotaxis | Q30159999 | ||
The structure of an archaeal pilus | Q30438864 | ||
Pyrodictium gen. nov., a New Genus of Submarine Disc-Shaped Sulphur Reducing Archaebacteria Growing Optimally at 105°C. | Q30579063 | ||
Metagenomics: genomic analysis of microbial communities | Q31132850 | ||
Thermococcus gorgonarius sp. nov. and Thermococcus pacificus sp. nov.: heterotrophic extremely thermophilic archaea from New Zealand submarine hot vents | Q32068133 | ||
Cold-adapted archaea | Q33244208 | ||
The archaeal flagellum: a different kind of prokaryotic motility structure | Q33938114 | ||
Posttranslational protein modification in Archaea | Q33940312 | ||
FlaK of the archaeon Methanococcus maripaludis possesses preflagellin peptidase activity | Q33958390 | ||
Glucose transport in the extremely thermoacidophilic Sulfolobus solfataricus involves a high-affinity membrane-integrated binding protein | Q33992567 | ||
Nonspecific adherence by Actinobacillus actinomycetemcomitans requires genes widespread in bacteria and archaea | Q33994822 | ||
Chaperone-assisted pilus assembly and bacterial attachment. | Q34066527 | ||
Pyrodictium cannulae enter the periplasmic space but do not enter the cytoplasm, as revealed by cryo-electron tomography | Q34176085 | ||
The flagellar bundle of Halobacterium salinarium is inserted into a distinct polar cap structure | Q39896564 | ||
Ultrastructure and biochemistry of the cell wall of Methanococcus voltae | Q39956142 | ||
Signal Processing and Flagellar Motor Switching During Phototaxis of Halobacterium salinarum | Q40830292 | ||
Identification of a putative acetyltransferase gene, MMP0350, which affects proper assembly of both flagella and pili in the archaeon Methanococcus maripaludis | Q41341604 | ||
The flagellar filament structure of the extreme acidothermophile Sulfolobus shibatae B12 suggests that archaeabacterial flagella have a unique and common symmetry and design | Q41623624 | ||
The unique structure of archaeal 'hami', highly complex cell appendages with nano-grappling hooks | Q41627393 | ||
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 | ||
Response of the hyperthermophilic archaeon Sulfolobus solfataricus to UV damage | Q41816055 | ||
Flagellar motility and structure in the hyperthermoacidophilic archaeon Sulfolobus solfataricus | Q42619847 | ||
The fla gene cluster is involved in the biogenesis of flagella in Halobacterium salinarum | Q42658358 | ||
Possible nonconductive role of Geobacter sulfurreducens pilus nanowires in biofilm formation | Q42845485 | ||
A quantitative model of the switch cycle of an archaeal flagellar motor and its sensory control | Q42931907 | ||
Multicomponent nature of Halobacterium salinarum flagella | Q43023538 | ||
Identification of the archaeal alg7 gene homolog (encoding N-acetylglucosamine-1-phosphate transferase) of the N-linked glycosylation system by cross-domain complementation in Saccharomyces cerevisiae | Q43064367 | ||
Halobacterial flagellins are encoded by a multigene family. Characterization of five flagellin genes | Q44033712 | ||
Identification and characterization of the unique N-linked glycan common to the flagellins and S-layer glycoprotein of Methanococcus voltae. | Q45277086 | ||
Growth-saturation in vitro of Salmonella flagella | Q50230859 | ||
Analysis of ATPases of putative secretion operons in the thermoacidophilic archaeon Sulfolobus solfataricus. | Q51531093 | ||
Deletion analysis of the che operon in the archaeon Halobacterium salinarium. | Q52887608 | ||
The Mth60 fimbriae of Methanothermobacter thermoautotrophicus are functional adhesins. | Q54419304 | ||
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 | ||
Tubular spinae are long-distance connectors between bacteria | Q67932701 | ||
Further evidence to suggest that archaeal flagella are related to bacterial type IV pili | Q74285563 | ||
Two immunologically distinct types of protofilaments can be identified in Natrialba magadii flagella | Q74333437 | ||
A twisted tale: the origin and evolution of motility and chemotaxis in prokaryotes | Q74602001 | ||
Identification of genes involved in the biosynthesis and attachment of Methanococcus voltae N-linked glycans: insight into N-linked glycosylation pathways in Archaea | Q79847600 | ||
An archaeal bi-species biofilm formed by Pyrococcus furiosus and Methanopyrus kandleri | Q81157750 | ||
How Bacteria Assemble Flagella | Q34194719 | ||
New insights into the lifestyle of the cold-loving SM1 euryarchaeon: natural growth as a monospecies biofilm in the subsurface | Q34316005 | ||
Identification and localization of flagellins FlaA and FlaB3 within flagella of Methanococcus voltae | Q34319213 | ||
Molecular analysis of archael flagellins: similarity to the type IV pilin-transport superfamily widespread in bacteria | Q34322226 | ||
Dual flagellar systems enable motility under different circumstances | Q34323741 | ||
Bees aren't the only ones: swarming in gram-negative bacteria | Q34328004 | ||
Diversity in chemotaxis mechanisms among the bacteria and archaea. | Q34349346 | ||
Active-site residues in the type IV prepilin peptidase homologue PibD from the archaeon Sulfolobus solfataricus. | Q34354030 | ||
Type III flagellar protein export and flagellar assembly | Q34368259 | ||
Archaeal habitats--from the extreme to the ordinary | Q34502659 | ||
Bacterial lateral flagella: an inducible flagella system. | Q34566431 | ||
Nitrogen fixation at 92 degrees C by a hydrothermal vent archaeon | Q34591247 | ||
Type II protein secretion and its relationship to bacterial type IV pili and archaeal flagella | Q35576644 | ||
Isolation and characterization of flagella and flagellin proteins from the Thermoacidophilic archaea Thermoplasma volcanium and Sulfolobus shibatae | Q35602117 | ||
Identification of diverse archaeal proteins with class III signal peptides cleaved by distinct archaeal prepilin peptidases. | Q35634559 | ||
Pulling together with type IV pili | Q35788091 | ||
Physical characterization of the flagella and flagellins from Methanospirillum hungatei | Q35983647 | ||
Isolation and Ultrastructure of the Flagella of Methanococcus thermolithotrophicus and Methanospirillum hungatei | Q36071805 | ||
Microbial community genomics in the ocean | Q36123645 | ||
Cloning and sequencing of a multigene family encoding the flagellins of Methanococcus voltae | Q36165865 | ||
Weapons of mass retraction | Q36223539 | ||
Rice Cluster I methanogens, an important group of Archaea producing greenhouse gas in soil | Q36452223 | ||
Flagellar glycosylation - a new component of the motility repertoire? | Q36452420 | ||
Protein secretion in the Archaea: multiple paths towards a unique cell surface | Q36498040 | ||
Type IV pilin structures: insights on shared architecture, fiber assembly, receptor binding and type II secretion | Q36597261 | ||
The archaeabacterial flagellar filament: a bacterial propeller with a pilus-like structure | Q36597264 | ||
Archaeal signal peptidases | Q36720738 | ||
The surprisingly diverse ways that prokaryotes move | Q37156434 | ||
Identification of a system required for the functional surface localization of sugar binding proteins with class III signal peptides in Sulfolobus solfataricus. | Q38302318 | ||
Sugar transport in Sulfolobus solfataricus is mediated by two families of binding protein-dependent ABC transporters | Q38303090 | ||
Flagella of Pyrococcus furiosus: multifunctional organelles, made for swimming, adhesion to various surfaces, and cell-cell contacts | Q38503993 | ||
Regulation of switching frequency and bias of the bacterial flagellar motor by CheY and fumarate | Q39566492 | ||
Archaeal homolog of bacterial type IV prepilin signal peptidases with broad substrate specificity. | Q39775185 | ||
The archaeal flagellum: a unique motility structure | Q39842473 | ||
P433 | issue | 18 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Archaea | Q10872 |
P304 | page(s) | 6039-6047 | |
P577 | publication date | 2008-07-11 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Cell surface structures of archaea | |
P478 | volume | 190 |
Q35542657 | Archaeal flagellar ATPase motor shows ATP-dependent hexameric assembly and activity stimulation by specific lipid binding. |
Q42072751 | Biosynthesis and role of N-linked glycosylation in cell surface structures of archaea with a focus on flagella and s layers |
Q46259306 | Community composition and ultrastructure of a nitrate-dependent anaerobic methane-oxidizing enrichment culture |
Q34019155 | Different minimal signal peptide lengths recognized by the archaeal prepilin-like peptidases FlaK and PibD |
Q36023357 | Diversity and Evolution of Type IV pili Systems in Archaea |
Q37434036 | Diversity of archaeal type IV pilin-like structures |
Q50041521 | Electron microscopic observations of prokaryotic surface appendages |
Q54224628 | Genetic analysis of a type IV pili-like locus in the archaeon Methanococcus maripaludis. |
Q34528534 | Genetic and mass spectrometry analyses of the unusual type IV-like pili of the archaeon Methanococcus maripaludis. |
Q37332257 | Haloferax volcanii cells lacking the flagellin FlgA2 are hypermotile |
Q33983376 | Haloferax volcanii flagella are required for motility but are not involved in PibD-dependent surface adhesion. |
Q35080773 | Identification of an additional minor pilin essential for piliation in the archaeon Methanococcus maripaludis |
Q41462874 | Mechanisms involved in Fe(III) respiration by the hyperthermophilic archaeon Ferroglobus placidus. |
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 |
Q35597432 | Salinity regulation of the interaction of halovirus SNJ1 with its host and alteration of the halovirus replication strategy to adapt to the variable ecosystem |
Q37776655 | Shaping the archaeal cell envelope |
Q90204283 | Species-Specific Recognition of Sulfolobales Mediated by UV-Inducible Pili and S-Layer Glycosylation Patterns |
Q30413924 | Structure and function of the adhesive type IV pilus of Sulfolobus acidocaldarius |
Q38265133 | Surface appendages of archaea: structure, function, genetics and assembly |
Q30508514 | Swimming behavior of selected species of Archaea |
Q42569999 | The Iho670 fibers of Ignicoccus hospitalis: a new type of archaeal cell surface appendage |
Q34185088 | The archaeal cell envelope |
Q21562676 | The complete genome sequence of Haloferax volcanii DS2, a model archaeon |
Q44106091 | The one-component system ArnR: a membrane-bound activator of the crenarchaeal archaellum |
Q58835264 | The origin of eukaryotes and their relationship with the Archaea: are we at a phylogenomic impasse? |
Q46250170 | Versatile cell surface structures of archaea. |
Search more.