scholarly article | Q13442814 |
P50 | author | Christoph Dehio | Q18599888 |
Alexander Harms | Q56252263 | ||
Maxime Québatte | Q64667707 | ||
Jonas Körner | Q89740882 | ||
Philipp Engel | Q48076385 | ||
P2093 | author name string | Marius Liesch | |
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Within-host competition selects for plasmid-encoded toxin-antitoxin systems. | Q53068164 | ||
A plant phosphoswitch platform repeatedly targeted by type III effector proteins regulates the output of both tiers of plant immune receptors. | Q54316623 | ||
Molecular recognition determinants for type IV secretion of diverse families of conjugative relaxases. | Q54374307 | ||
DNA-independent transport of plasmid primase protein between bacteria by the I1 conjugation system | Q64449645 | ||
VirB/D4-dependent protein translocation from Agrobacterium into plant cells | Q73149678 | ||
Selection for plasmid post-segregational killing depends on multiple infection: evidence for the selection of more virulent parasites through parasite-level competition | Q81447949 | ||
Cre Reporter Assay for Translocation (CRAfT): a tool for the study of protein translocation into host cells | Q85216862 | ||
Social behavior and decision making in bacterial conjugation | Q38210215 | ||
VgrG, Tae, Tle, and beyond: the versatile arsenal of Type VI secretion effectors | Q38231827 | ||
Towards an integrated model of bacterial conjugation | Q38242996 | ||
New insights into the role of Bartonella effector proteins in pathogenesis | Q38280761 | ||
The relaxase of the Rhizobium etli symbiotic plasmid shows nic site cis-acting preference. | Q38310561 | ||
Secretion systems in Gram-negative bacteria: structural and mechanistic insights. | Q38482854 | ||
Toxin-antitoxin systems in bacterial growth arrest and persistence | Q38779945 | ||
Biological Diversity and Molecular Plasticity of FIC Domain Proteins. | Q38915969 | ||
A new type IV secretion system promotes conjugal transfer in Agrobacterium tumefaciens | Q39680036 | ||
The primase of broad-host-range plasmid R1162 is active in conjugal transfer | Q39843640 | ||
Helicobacter exploits integrin for type IV secretion and kinase activation | Q40066287 | ||
Specification of surface mating systems among conjugative drug resistance plasmids in Escherichia coli K-12. | Q40337368 | ||
The BID Domain of Type IV Secretion Substrates Forms a Conserved Four-Helix Bundle Topped with a Hook | Q40435058 | ||
The VirB type IV secretion system of Bartonella henselae mediates invasion, proinflammatory activation and antiapoptotic protection of endothelial cells | Q40572442 | ||
Adenylylation of Gyrase and Topo IV by FicT Toxins Disrupts Bacterial DNA Topology | Q41037330 | ||
Silent mischief: bacteriophage Mu insertions contaminate products of Escherichia coli random mutagenesis performed using suicidal transposon delivery plasmids mobilized by broad-host-range RP4 conjugative machinery. | Q41430239 | ||
The Fic protein Doc uses an inverted substrate to phosphorylate and inactivate EF-Tu | Q42050878 | ||
Interbacterial macromolecular transfer by the Campylobacter fetus subsp. venerealis type IV secretion system | Q42156667 | ||
Diversity of bacterial type II toxin-antitoxin systems: a comprehensive search and functional analysis of novel families | Q42836520 | ||
Dual input control: activation of the Bartonella henselae VirB/D4 type IV secretion system by the stringent sigma factor RpoH1 and the BatR/BatS two-component system | Q43836715 | ||
Functional divergence and horizontal transfer of type IV secretion systems | Q43872014 | ||
Genomic analysis of Bartonella identifies type IV secretion systems as host adaptability factors | Q48076322 | ||
The VirB/VirD4 type IV secretion system of Bartonella is essential for establishing intraerythrocytic infection | Q48274738 | ||
Postsegregational killing does not increase plasmid stability but acts to mediate the exclusion of competing plasmids | Q24679732 | ||
Parallel evolution of a type IV secretion system in radiating lineages of the host-restricted bacterial pathogen Bartonella | Q27342991 | ||
Type VI secretion apparatus and phage tail-associated protein complexes share a common evolutionary origin | Q27653977 | ||
The Legionella effector protein DrrA AMPylates the membrane traffic regulator Rab1b | Q27663583 | ||
Fic domain-catalyzed adenylylation: Insight provided by the structural analysis of the type IV secretion system effector BepA | Q27666512 | ||
Bacterial killing via a type IV secretion system | Q27698110 | ||
Contact-Dependent Growth Inhibition (CDI) and CdiB/CdiA Two-Partner Secretion Proteins | Q28083323 | ||
The non-flagellar type III secretion system evolved from the bacterial flagellum and diversified into host-cell adapted systems | Q28276177 | ||
3'-NADP and 3'-NAADP - Two Metabolites Formed by the Bacterial Type III Effector AvrRxo1 | Q28822572 | ||
ProtTest 3: fast selection of best-fit models of protein evolution | Q29547651 | ||
The Phyre2 web portal for protein modeling, prediction and analysis | Q29616136 | ||
Bartonella schoenbuchii sp. nov., isolated from the blood of wild roe deer | Q30658064 | ||
A gene transfer agent and a dynamic repertoire of secretion systems hold the keys to the explosive radiation of the emerging pathogen Bartonella. | Q31114566 | ||
General mutagenesis of F plasmid TraI reveals its role in conjugative regulation | Q33254725 | ||
Terminal reassortment drives the quantum evolution of type III effectors in bacterial pathogens | Q33260347 | ||
Type III effector diversification via both pathoadaptation and horizontal transfer in response to a coevolutionary arms race | Q33267844 | ||
Fido, a novel AMPylation domain common to fic, doc, and AvrB. | Q33463423 | ||
The Trw type IV secretion system of Bartonella mediates host-specific adhesion to erythrocytes | Q33604841 | ||
A bipartite signal mediates the transfer of type IV secretion substrates of Bartonella henselae into human cells | Q33756268 | ||
Gene Transfer Agent Promotes Evolvability within the Fittest Subpopulation of a Bacterial Pathogen | Q33871108 | ||
Natural conjugative plasmids induce bacterial biofilm development | Q33953756 | ||
Toxin-antitoxin systems: why so many, what for? | Q34147381 | ||
Programmed cell death in bacteria: proteic plasmid stabilization systems | Q34289952 | ||
gyrA mutations in ciprofloxacin-resistant Bartonella bacilliformis strains obtained in vitro | Q34720856 | ||
Potential origins and horizontal transfer of type III secretion systems and effectors | Q35305175 | ||
Transfer of R388 derivatives by a pathogenesis-associated type IV secretion system into both bacteria and human cells | Q35530988 | ||
AvrRxo1 Is a Bifunctional Type III Secreted Effector and Toxin-Antitoxin System Component with Homologs in Diverse Environmental Contexts | Q36070937 | ||
The effector AvrRxo1 phosphorylates NAD in planta. | Q36409276 | ||
The role of bacteriocins as selfish genetic elements. | Q36818453 | ||
Genomic analysis of 38 Legionella species identifies large and diverse effector repertoires. | Q37309818 | ||
Replication and conjugative mobilization of broad host-range IncQ plasmids | Q37493631 | ||
Evolutionary Dynamics of Pathoadaptation Revealed by Three Independent Acquisitions of the VirB/D4 Type IV Secretion System in Bartonella | Q37738564 | ||
The YopJ superfamily in plant-associated bacteria. | Q37897282 | ||
Agrobacterium infection and plant defense-transformation success hangs by a thread | Q38175980 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 10 | |
P304 | page(s) | e1007077 | |
P577 | publication date | 2017-10-26 | |
P1433 | published in | PLOS Genetics | Q1893441 |
P1476 | title | A bacterial toxin-antitoxin module is the origin of inter-bacterial and inter-kingdom effectors of Bartonella | |
P478 | volume | 13 |
Q92526712 | Bacteria-Killing Type IV Secretion Systems |
Q92974374 | Bartonella gene transfer agent: Evolution, function, and proposed role in host adaptation |
Q64082357 | Biological and Structural Diversity of Type IV Secretion Systems |
Q64120325 | Quantitative contribution of efflux to multi-drug resistance of clinical Escherichia coli and Pseudomonas aeruginosa strains |
Q64258770 | Role of distinct type-IV-secretion systems and secreted effector sets in host adaptation by pathogenic Bartonella species |
Q92999216 | Stenotrophomonas maltophilia Encodes a VirB/VirD4 Type IV Secretion System That Modulates Apoptosis in Human Cells and Promotes Competition against Heterologous Bacteria, Including Pseudomonas aeruginosa |
Q64068054 | Versatility of the BID Domain: Conserved Function as Type-IV-Secretion-Signal and Secondarily Evolved Effector Functions Within Bartonella-Infected Host Cells |
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