scholarly article | Q13442814 |
P50 | author | Saheed Imam | Q59179038 |
P2093 | author name string | Mechthild Pohlschröder | |
Manuela Tripepi | |||
P2860 | cites work | The complete genome sequence of Haloferax volcanii DS2, a model archaeon | Q21562676 |
UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation | Q22065690 | ||
Genetic transfer in Halobacterium volcanii. | Q39980511 | ||
Mating variation by DNA inversions of shufflon in plasmid R64. | Q40454039 | ||
Development of additional selectable markers for the halophilic archaeon Haloferax volcanii based on the leuB and trpA genes | Q40604361 | ||
Identification of a putative acetyltransferase gene, MMP0350, which affects proper assembly of both flagella and pili in the archaeon Methanococcus maripaludis | Q41341604 | ||
Response of the hyperthermophilic archaeon Sulfolobus solfataricus to UV damage | Q41816055 | ||
Archaeal signal peptides--a comparative survey at the genome level. | Q41841032 | ||
Appendage-mediated surface adherence of Sulfolobus solfataricus. | Q41920403 | ||
The fla gene cluster is involved in the biogenesis of flagella in Halobacterium salinarum | Q42658358 | ||
Export of the pseudopilin XcpT of the Pseudomonas aeruginosa type II secretion system via the signal recognition particle-Sec pathway | Q42845566 | ||
Signal recognition particle-dependent inner membrane targeting of the PulG Pseudopilin component of a type II secretion system | Q42845651 | ||
Halobacterium volcanii spec. nov., a Dead Sea halobacterium with a moderate salt requirement | Q43016121 | ||
Ca(2+)-dependent cell aggregation of halophilic archaeon, Halobacterium salinarum | Q43019566 | ||
Effects of divalent cations on Halobacterium salinarum cell aggregation | Q43023103 | ||
Characterization of a tightly controlled promoter of the halophilic archaeon Haloferax volcanii and its use in the analysis of the essential cct1 gene | Q43023536 | ||
Genetic analysis of homologous recombination in Archaea: Haloferax volcanii as a model organism. | Q54524431 | ||
Protein N-glycosylation in Archaea: defining Haloferax volcanii genes involved in S-layer glycoprotein glycosylation. | Q54597832 | ||
Mutants in flaI and flaJ of the archaeon Methanococcus voltae are deficient in flagellum assembly | Q64449468 | ||
Charon phages: safer derivatives of bacteriophage lambda for DNA cloning | Q67558978 | ||
Identification of genes involved in the biosynthesis and attachment of Methanococcus voltae N-linked glycans: insight into N-linked glycosylation pathways in Archaea | Q79847600 | ||
The UCSC Archaeal Genome Browser | Q25256865 | ||
Clustal W and Clustal X version 2.0 | Q27860517 | ||
Signal peptidases | Q28217085 | ||
Archaeal flagella, bacterial flagella and type IV pili: a comparison of genes and posttranslational modifications | Q28264353 | ||
A hidden Markov model for predicting transmembrane helices in protein sequences | Q29547468 | ||
Biofilm formation as microbial development | Q29619202 | ||
The structure of an archaeal pilus | Q30438864 | ||
Haloferax volcanii AglB and AglD are involved in N-glycosylation of the S-layer glycoprotein and proper assembly of the surface layer. | Q30837729 | ||
Genome information management and integrated data analysis with HaloLex. | Q31161033 | ||
Purification and characterization of thin pili of IncI1 plasmids ColIb-P9 and R64: formation of PilV-specific cell aggregates by type IV pili. | Q32062583 | ||
Identification of Archaea-specific chemotaxis proteins which interact with the flagellar apparatus | Q33418776 | ||
Genetic approaches to study of biofilms | Q33766182 | ||
Regulation of pap pilin phase variation by a mechanism involving differential dam methylation states | Q33923349 | ||
FlaK of the archaeon Methanococcus maripaludis possesses preflagellin peptidase activity | Q33958390 | ||
Bacterial Motility on a Surface: Many Ways to a Common Goal | Q34267501 | ||
Identification and localization of flagellins FlaA and FlaB3 within flagella of Methanococcus voltae | Q34319213 | ||
Archaeal and bacterial SecD and SecF homologs exhibit striking structural and functional conservation. | Q34354021 | ||
Type III flagellar protein export and flagellar assembly | Q34368259 | ||
Type II protein secretion and its relationship to bacterial type IV pili and archaeal flagella | Q35576644 | ||
Identification of diverse archaeal proteins with class III signal peptides cleaved by distinct archaeal prepilin peptidases. | Q35634559 | ||
Recent advances in the structure and assembly of the archaeal flagellum | Q35788087 | ||
Weapons of mass retraction | Q36223539 | ||
Flagellar glycosylation - a new component of the motility repertoire? | Q36452420 | ||
The archaeabacterial flagellar filament: a bacterial propeller with a pilus-like structure | Q36597264 | ||
Type IV pili: paradoxes in form and function | Q36742465 | ||
Protein translocation across the bacterial cytoplasmic membrane. | Q37031528 | ||
Type IV pili: e pluribus unum? | Q37133352 | ||
The surprisingly diverse ways that prokaryotes move | Q37156434 | ||
Cell surface structures of archaea | Q37214242 | ||
Diversity of archaeal type IV pilin-like structures | Q37434036 | ||
Flagella of Pyrococcus furiosus: multifunctional organelles, made for swimming, adhesion to various surfaces, and cell-cell contacts | Q38503993 | ||
Archaeal homolog of bacterial type IV prepilin signal peptidases with broad substrate specificity. | Q39775185 | ||
The plasmid R64 thin pilus identified as a type IV pilus | Q39845928 | ||
An expression vector for the archaebacterium Haloferax volcanii | Q39952118 | ||
Primary structure and glycosylation of the S-layer protein of Haloferax volcanii | Q39952123 | ||
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Haloferax volcanii | Q16982678 |
P304 | page(s) | 3093-3102 | |
P577 | publication date | 2010-04-02 | |
P1433 | published in | Journal of Bacteriology | Q478419 |
P1476 | title | Haloferax volcanii flagella are required for motility but are not involved in PibD-dependent surface adhesion | |
P478 | volume | 192 |
Q33786757 | An Acidic Exopolysaccharide from Haloarcula hispanica ATCC33960 and Two Genes Responsible for Its Synthesis |
Q27001111 | Archaea in symbioses |
Q90879981 | Archaeal biofilm formation |
Q38077258 | Archaeal biofilms: widespread and complex |
Q64448582 | Archaeal cell surface biogenesis |
Q35129642 | Archaeal membrane-associated proteases: insights on Haloferax volcanii and other haloarchaea |
Q35212015 | Archaeal type IV pili and their involvement in biofilm formation |
Q34160723 | Assembly and function of the archaeal flagellum. |
Q21146693 | Biofilms formed by the archaeon Haloferax volcanii exhibit cellular differentiation and social motility, and facilitate horizontal gene transfer |
Q49444291 | Candidatus Nitrosocaldus cavascurensis, an Ammonia Oxidizing, Extremely Thermophilic Archaeon with a Highly Mobile Genome. |
Q30630847 | CetZ tubulin-like proteins control archaeal cell shape |
Q39450584 | Direct observation of rotation and steps of the archaellum in the swimming halophilic archaeon Halobacterium salinarum |
Q43022438 | Dissection of key determinants of cleavage activity in signal peptidase III (SPaseIII) PibD. |
Q36023357 | Diversity and Evolution of Type IV pili Systems in Archaea |
Q36070868 | Diversity and subcellular distribution of archaeal secreted proteins |
Q35564578 | Effects of N-glycosylation site removal in archaellins on the assembly and function of archaella in Methanococcus maripaludis |
Q34108405 | Functional genomic and advanced genetic studies reveal novel insights into the metabolism, regulation, and biology of Haloferax volcanii. |
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. |
Q35569977 | Getting a hold on archaeal type IV pili: an expanding repertoire of cellular appendages implicates complex regulation and diverse functions |
Q34343383 | Haloferax volcanii archaeosortase is required for motility, mating, and C-terminal processing of the S-layer glycoprotein. |
Q37332257 | Haloferax volcanii cells lacking the flagellin FlgA2 are hypermotile |
Q34290402 | Halophiles 2010: Life in Saline Environments |
Q36898217 | Identification of Haloferax volcanii Pilin N-Glycans with Diverse Roles in Pilus Biosynthesis, Adhesion, and Microcolony Formation. |
Q35080773 | Identification of an additional minor pilin essential for piliation in the archaeon Methanococcus maripaludis |
Q50508304 | Influence of cell surface structures on crenarchaeal biofilm formation using a thermostable green fluorescent protein. |
Q64093463 | Limited Cross-Complementation Between PilB1-C1 and PilB3-C3 Paralogs |
Q90629791 | Lipid Anchoring of Archaeosortase Substrates and Midcell Growth in Haloarchaea |
Q42582867 | Mass spectrometry unmasks mystery Methanococcus pilin |
Q38093569 | Mechanisms of metal resistance and homeostasis in haloarchaea |
Q64283764 | Motor torque measurement of Halobacterium salinarum archaellar suggests a general model for ATP-driven rotary motors |
Q36197559 | N-glycosylation of Haloferax volcanii flagellins requires known Agl proteins and is essential for biosynthesis of stable flagella |
Q33743511 | N-linked glycosylation in Archaea: a structural, functional, and genetic analysis |
Q37124947 | Novel archaeal adhesion pilins with a conserved N terminus |
Q34936965 | Novel pili-like surface structures of Halobacterium salinarum strain R1 are crucial for surface adhesion |
Q27321892 | Permuting the PGF Signature Motif Blocks both Archaeosortase-Dependent C-Terminal Cleavage and Prenyl Lipid Attachment for the Haloferax volcanii S-Layer Glycoprotein |
Q39427949 | Pilin Processing Follows a Different Temporal Route than That of Archaellins in Methanococcus maripaludis |
Q38061206 | Post-translation modification in Archaea: lessons from Haloferax volcanii and other haloarchaea |
Q99584387 | Proteolytic systems of archaea: slicing, dicing, and mincing in the extreme |
Q37780957 | S-layer glycoproteins and flagellins: reporters of archaeal posttranslational modifications |
Q57059590 | Salt-dependent regulation of archaellins in Haloarcula marismortui |
Q36206586 | Screening of a Haloferax volcanii Transposon Library Reveals Novel Motility and Adhesion Mutants |
Q64899897 | Several One-Domain Zinc Finger µ-Proteins of Haloferax Volcanii Are Important for Stress Adaptation, Biofilm Formation, and Swarming. |
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 |
Q48191378 | Structure and function of the archaeal response regulator CheY. |
Q38265133 | Surface appendages of archaea: structure, function, genetics and assembly |
Q34185088 | The archaeal cell envelope |
Q38362614 | The archaellum: how Archaea swim |
Q37248438 | The nucleotide-dependent interaction of FlaH and FlaI is essential for assembly and function of the archaellum motor. |
Q92025952 | The structure of the periplasmic FlaG-FlaF complex and its essential role for archaellar swimming motility |
Q49791507 | Transcriptional landscape and regulatory roles of small non-coding RNAs in the oxidative stress response of the haloarchaeon Haloferax volcanii |
Q46250170 | Versatile cell surface structures of archaea. |