| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Sonja-Verena Albers | Q21264709 |
| P2093 | author name string | Mecky Pohlschröder | |
| P2860 | cites work | UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation | Q22065690 |
| Methanogenic Archaea and human periodontal disease | Q24568024 | ||
| Hexameric structures of the archaeal secretion ATPase GspE and implications for a universal secretion mechanism | Q27643662 | ||
| Flagellar and twitching motility are necessary for Pseudomonas aeruginosa biofilm development | Q27976516 | ||
| Pilus retraction powers bacterial twitching motility | Q28138923 | ||
| Cleavage of preflagellins by an aspartic acid signal peptidase is essential for flagellation in the archaeon Methanococcus voltae | Q28184916 | ||
| Extracellular electron transfer via microbial nanowires | Q28485746 | ||
| The secretion apparatus of Pseudomonas aeruginosa: identification of a fifth pseudopilin, XcpX (GspK family) | Q28493060 | ||
| Bacterial biofilms: from the natural environment to infectious diseases | Q29547677 | ||
| Type IV pili and twitching motility | Q29615262 | ||
| The structure of an archaeal pilus | Q30438864 | ||
| Phylogenetic diversity and ecology of environmental Archaea | Q33225541 | ||
| Human methanogen diversity and incidence in healthy and diseased colonic groups using mcrA gene analysis. | Q33336207 | ||
| FlaK of the archaeon Methanococcus maripaludis possesses preflagellin peptidase activity | Q33958390 | ||
| Posttranslational processing of Methanococcus voltae preflagellin by preflagellin peptidases of M. voltae and other methanogens | Q33993723 | ||
| The underlying mechanisms of type II protein secretion | Q64449375 | ||
| Mutants in flaI and flaJ of the archaeon Methanococcus voltae are deficient in flagellum assembly | Q64449468 | ||
| A function of Pseudomonas aeruginosa PAO polar pili: twitching motility | Q72430032 | ||
| Cell surface localization and processing of the ComG proteins, required for DNA binding during transformation of Bacillus subtilis | Q77179906 | ||
| 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 | ||
| A mouthful of microbes | Q81575228 | ||
| New processes and players in the nitrogen cycle: the microbial ecology of anaerobic and archaeal ammonia oxidation. | Q34008413 | ||
| Type III flagellar protein export and flagellar assembly | Q34368259 | ||
| Archaeal habitats--from the extreme to the ordinary | Q34502659 | ||
| The role of microorganisms in coral health, disease and evolution | Q34612195 | ||
| The microbial engines that drive Earth's biogeochemical cycles. | Q34780678 | ||
| Pili in Gram-negative and Gram-positive bacteria - structure, assembly and their role in disease. | Q34866500 | ||
| 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 | ||
| Protein transport in Archaea: Sec and twin arginine translocation pathways | Q36300549 | ||
| 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 | ||
| Quantitative analysis of three hydrogenotrophic microbial groups, methanogenic archaea, sulfate-reducing bacteria, and acetogenic bacteria, within plaque biofilms associated with human periodontal disease | Q36672768 | ||
| Archaeal signal peptidases | Q36720738 | ||
| Type IV pili: paradoxes in form and function | Q36742465 | ||
| Type IV pili: e pluribus unum? | Q37133352 | ||
| The surprisingly diverse ways that prokaryotes move | Q37156434 | ||
| Cell surface structures of archaea | Q37214242 | ||
| Methanogenic archaea in health and disease: a novel paradigm of microbial pathogenesis | Q37256022 | ||
| A macromolecular complex formed by a pilin-like protein in competent Bacillus subtilis | Q37310146 | ||
| Identification of a system required for the functional surface localization of sugar binding proteins with class III signal peptides in Sulfolobus solfataricus. | Q38302318 | ||
| Flagella of Pyrococcus furiosus: multifunctional organelles, made for swimming, adhesion to various surfaces, and cell-cell contacts | Q38503993 | ||
| Type IV-Like Pili Formed by the Type II Secreton: Specificity, Composition, Bundling, Polar Localization, and Surface Presentation of Peptides | Q39753852 | ||
| Archaeal homolog of bacterial type IV prepilin signal peptidases with broad substrate specificity. | Q39775185 | ||
| The flagellar bundle of Halobacterium salinarium is inserted into a distinct polar cap structure | Q39896564 | ||
| The flagellar filament structure of the extreme acidothermophile Sulfolobus shibatae B12 suggests that archaeabacterial flagella have a unique and common symmetry and design | Q41623624 | ||
| Type IV pilus structure by cryo-electron microscopy and crystallography: implications for pilus assembly and functions | Q41625721 | ||
| Response of the hyperthermophilic archaeon Sulfolobus solfataricus to UV damage | Q41816055 | ||
| Archaeal signal peptides--a comparative survey at the genome level. | Q41841032 | ||
| 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 | ||
| 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 | ||
| Alternative flagellar filament types in the haloarchaeon Haloarcula marismortui. | Q44559689 | ||
| The pilus-retraction protein PilT: ultrastructure of the biological assembly. | Q44855130 | ||
| The Mth60 fimbriae of Methanothermobacter thermoautotrophicus are functional adhesins. | Q54419304 | ||
| Refining the Structure of the Halobacterium salinarum Flagellar Filament Using the Iterative Helical Real Space Reconstruction Method: Insights into Polymorphism | Q56937818 | ||
| 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 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 403-410 | |
| P577 | publication date | 2009-04-05 | |
| P1433 | published in | Extremophiles | Q15766992 |
| P1476 | title | Diversity of archaeal type IV pilin-like structures | |
| P478 | volume | 13 |
| Q41920403 | Appendage-mediated surface adherence of Sulfolobus solfataricus. |
| Q38077258 | Archaeal biofilms: widespread and complex |
| 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. |
| Q57063387 | Biological role of Actinobacillus pleuropneumoniae type IV pilus proteins encoded by the apf and pil operons |
| Q43023386 | Biology of a widespread uncultivated archaeon that contributes to carbon fixation in the subsurface |
| Q42072751 | Biosynthesis and role of N-linked glycosylation in cell surface structures of archaea with a focus on flagella and s layers |
| Q33760721 | Crenarchaeal biofilm formation under extreme conditions |
| Q38742221 | Cyclic AMP-Independent Control of Twitching Motility in Pseudomonas aeruginosa. |
| Q34019155 | Different minimal signal peptide lengths recognized by the archaeal prepilin-like peptidases FlaK and PibD |
| Q43022438 | Dissection of key determinants of cleavage activity in signal peptidase III (SPaseIII) PibD. |
| Q30405338 | Distinct docking and stabilization steps of the Pseudopilus conformational transition path suggest rotational assembly of type IV pilus-like fibers |
| Q36070868 | Diversity and subcellular distribution of archaeal secreted proteins |
| Q36171501 | Effects of antimicrobial peptides on methanogenic archaea. |
| Q41894122 | First insights into the entry process of hyperthermophilic archaeal viruses. |
| 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. |
| Q34117081 | Identification of surprisingly diverse type IV pili, across a broad range of gram-positive bacteria |
| Q50508304 | Influence of cell surface structures on crenarchaeal biofilm formation using a thermostable green fluorescent protein |
| Q42582867 | Mass spectrometry unmasks mystery Methanococcus pilin |
| Q38093569 | Mechanisms of metal resistance and homeostasis in haloarchaea |
| Q27939366 | Minor pseudopilin self-assembly primes type II secretion pseudopilus elongation. |
| Q30361258 | Mycobacterium tuberculosis pili (MTP), a putative biomarker for a tuberculosis diagnostic test. |
| Q38988491 | Nonconventional cation-coupled flagellar motors derived from the alkaliphilic Bacillus and Paenibacillus species |
| Q37124947 | Novel archaeal adhesion pilins with a conserved N terminus |
| Q39427949 | Pilin Processing Follows a Different Temporal Route than That of Archaellins in Methanococcus maripaludis |
| Q43025780 | Production of halophilic proteins using Haloferax volcanii H1895 in a stirred-tank bioreactor. |
| Q37780957 | S-layer glycoproteins and flagellins: reporters of archaeal posttranslational modifications |
| Q35699837 | S-layers at second glance? Altiarchaeal grappling hooks (hami) resemble archaeal S-layer proteins in structure and sequence |
| Q37776655 | Shaping the archaeal cell envelope |
| Q90204283 | Species-Specific Recognition of Sulfolobales Mediated by UV-Inducible Pili and S-Layer Glycosylation Patterns |
| Q36283781 | Structural and functional studies of the Pseudomonas aeruginosa minor pilin, PilE. |
| Q38265133 | Surface appendages of archaea: structure, function, genetics and assembly |
| Q37138120 | The Conserved Tetratricopeptide Repeat-Containing C-Terminal Domain of Pseudomonas aeruginosa FimV Is Required for Its Cyclic AMP-Dependent and -Independent Functions |
| Q34443421 | The genome of the ammonia-oxidizing Candidatus Nitrososphaera gargensis: insights into metabolic versatility and environmental adaptations. |
| Q44106091 | The one-component system ArnR: a membrane-bound activator of the crenarchaeal archaellum |
| Q39615099 | The platform protein is essential for type IV pilus biogenesis |
| Q97538102 | The structures of two archaeal type IV pili illuminate evolutionary relationships |
| Q64102664 | Two membrane-bound transcription factors regulate expression of various type-IV-pili surface structures in |
| Q27024174 | Type IV pilin proteins: versatile molecular modules |
| Q22065689 | UV-inducible DNA exchange in hyperthermophilic archaea mediated by type IV pili |
| Q55029170 | Validation of a Hypothesis: Colonization of Black Smokers by Hyperthermophilic Microorganisms. |
| Q46250170 | Versatile cell surface structures of archaea. |
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