| P50 | author | Eugene Koonin | Q3699974 |
| | Kira Makarova | Q63964276 |
| | Sonja-Verena Albers | Q21264709 |
| P2860 | cites work | Archaeal homolog of bacterial type IV prepilin signal peptidases with broad substrate specificity. | Q39775185 |
| | The bindosome is a structural component of the Sulfolobus solfataricus cell envelope. | Q42091471 |
| | The one-component system ArnR: a membrane-bound activator of the crenarchaeal archaellum | Q44106091 |
| | Mutation analysis of the flp operon in Actinobacillus actinomycetemcomitans | Q46572008 |
| | The archaellum: an old motility structure with a new name | Q48636424 |
| | The Mth60 fimbriae of Methanothermobacter thermoautotrophicus are functional adhesins. | Q54419304 |
| | Regulation of archaella expression by the FHA and von Willebrand domain-containing proteins ArnA and ArnB inSulfolobus acidocaldarius | Q61945037 |
| | 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 |
| | A conserved type IV pilin signal peptide H-domain is critical for the post-translational regulation of flagella-dependent motility | Q64448836 |
| | UV-inducible cellular aggregation of the hyperthermophilic archaeon Sulfolobus solfataricus is mediated by pili formation | Q22065690 |
| | The HHpred interactive server for protein homology detection and structure prediction | Q24530456 |
| | Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 |
| | MUSCLE: multiple sequence alignment with high accuracy and high throughput | Q24613456 |
| | The deep archaeal roots of eukaryotes | Q24642710 |
| | Exceptionally widespread nanomachines composed of type IV pilins: the prokaryotic Swiss Army knives | Q26999020 |
| | The 2.2-Å structure of the HP0958 protein from Helicobacter pylori reveals a kinked anti-parallel coiled-coil hairpin domain and a highly conserved ZN-ribbon domain | Q27664359 |
| | The crystal structure of GXGD membrane protease FlaK | Q27670846 |
| | Predicting transmembrane protein topology with a hidden Markov model: application to complete genomes | Q27860838 |
| | Isolation of an autotrophic ammonia-oxidizing marine archaeon | Q28273549 |
| | fleN, a gene that regulates flagellar number in Pseudomonas aeruginosa | Q28492712 |
| | A single bifunctional enzyme, PilD, catalyzes cleavage and N-methylation of proteins belonging to the type IV pilin family | Q28492973 |
| | FastTree 2--approximately maximum-likelihood trees for large alignments | Q28748616 |
| | SignalP 4.0: discriminating signal peptides from transmembrane regions | Q29547202 |
| | Dark matter in archaeal genomes: a rich source of novel mobile elements, defense systems and secretory complexes. | Q30365589 |
| | A p-loop motif and two basic regions in the regulatory protein GvpD are important for the repression of gas vesicle formation in the archaeon Haloferax mediterranei | Q31843083 |
| | Comparative genomics of the FtsK-HerA superfamily of pumping ATPases: implications for the origins of chromosome segregation, cell division and viral capsid packaging | Q33207648 |
| | Identification of Archaea-specific chemotaxis proteins which interact with the flagellar apparatus | Q33418776 |
| | FlaK of the archaeon Methanococcus maripaludis possesses preflagellin peptidase activity | Q33958390 |
| | Haloferax volcanii flagella are required for motility but are not involved in PibD-dependent surface adhesion. | Q33983376 |
| | The archaeal cell envelope | Q34185088 |
| | Recent advances in the structural and molecular biology of type IV secretion systems | Q34276673 |
| | A circadian clock nanomachine that runs without transcription or translation | Q34338187 |
| | Methanomassiliicoccus luminyensis gen. nov., sp. nov., a methanogenic archaeon isolated from human faeces | Q34364025 |
| | Molecular analysis of the UV-inducible pili operon from Sulfolobus acidocaldarius. | Q34376227 |
| | Phylogeny of genes for secretion NTPases: identification of the widespread tadA subfamily and development of a diagnostic key for gene classification | Q34469628 |
| | Genetic and mass spectrometry analyses of the unusual type IV-like pili of the archaeon Methanococcus maripaludis. | Q34528534 |
| | Signal peptides of secreted proteins of the archaeon Sulfolobus solfataricus: a genomic survey | Q34573139 |
| | Pseudomonas aeruginosa minor pilins prime type IVa pilus assembly and promote surface display of the PilY1 adhesin | Q34801714 |
| | Novel pili-like surface structures of Halobacterium salinarum strain R1 are crucial for surface adhesion | Q34936965 |
| | Identification of an additional minor pilin essential for piliation in the archaeon Methanococcus maripaludis | Q35080773 |
| | MinD-like ATPase FlhG effects location and number of bacterial flagella during C-ring assembly | Q35189933 |
| | Archaeal type IV pili and their involvement in biofilm formation | Q35212015 |
| | Archaeal Clusters of Orthologous Genes (arCOGs): An Update and Application for Analysis of Shared Features between Thermococcales, Methanococcales, and Methanobacteriales | Q35334249 |
| | FlaF Is a β-Sandwich Protein that Anchors the Archaellum in the Archaeal Cell Envelope by Binding the S-Layer Protein. | Q35586999 |
| | Identification of diverse archaeal proteins with class III signal peptides cleaved by distinct archaeal prepilin peptidases. | Q35634559 |
| | S-layers at second glance? Altiarchaeal grappling hooks (hami) resemble archaeal S-layer proteins in structure and sequence | Q35699837 |
| | Type IV pilus structure and bacterial pathogenicity | Q35752406 |
| | Updated clusters of orthologous genes for Archaea: a complex ancestor of the Archaea and the byways of horizontal gene transfer | Q36500812 |
| | The tad locus: postcards from the widespread colonization island | Q36792557 |
| | Novel archaeal adhesion pilins with a conserved N terminus | Q37124947 |
| | Cell surface structures of archaea | Q37214242 |
| | The nucleotide-dependent interaction of FlaH and FlaI is essential for assembly and function of the archaellum motor. | Q37248438 |
| | Structure and function of the phosphothreonine-specific FHA domain. | Q37358429 |
| | Signaling mechanisms of the Mycobacterium tuberculosis receptor Ser/Thr protein kinases | Q37633245 |
| | Lrs14 transcriptional regulators influence biofilm formation and cell motility of Crenarchaea. | Q37662320 |
| | Architecture of the type II secretion and type IV pilus machineries | Q37781062 |
| | Archaeal type IV pilus-like structures--evolutionarily conserved prokaryotic surface organelles | Q37863882 |
| | Pseudomonas aeruginosa twitching motility: type IV pili in action | Q38022664 |
| | Diversity, assembly and regulation of archaeal type IV pili-like and non-type-IV pili-like surface structures | Q38059325 |
| | Diversity of KaiC-based timing systems in marine Cyanobacteria | Q38175653 |
| | Type II secretion system: a magic beanstalk or a protein escalator | Q38175754 |
| | The archaellum: how Archaea swim | Q38362614 |
| | Secretion systems in Gram-negative bacteria: structural and mechanistic insights. | Q38482854 |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Archaea | Q10872 |
| | biodiversity | Q47041 |
| P304 | page(s) | 667 | |
| P577 | publication date | 2016-05-06 | |
| P1433 | published in | Frontiers in Microbiology | Q27723481 |
| P1476 | title | Diversity and Evolution of Type IV pili Systems in Archaea | |
| P478 | volume | 7 | |