| scholarly article | Q13442814 |
| P2093 | author name string | Wenbo Ma | |
| David S Guttman | |||
| John Stavrinides | |||
| P2860 | cites work | Insights into Genome Plasticity and Pathogenicity of the Plant Pathogenic Bacterium Xanthomonas campestris pv. vesicatoria Revealed by the Complete Genome Sequence | Q22065447 |
| The complete genome sequence of the Arabidopsis and tomato pathogen Pseudomonas syringae pv. tomato DC3000 | Q22066254 | ||
| Comparison of the genomes of two Xanthomonas pathogens with differing host specificities | Q22122346 | ||
| Complete genome sequence of a multiple drug resistant Salmonella enterica serovar Typhi CT18 | Q22122370 | ||
| The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools | Q24248165 | ||
| Type III protein secretion systems in bacterial pathogens of animals and plants | Q24548602 | ||
| MEGA3: Integrated software for Molecular Evolutionary Genetics Analysis and sequence alignment | Q27860726 | ||
| Diversifying selection drives the evolution of the type III secretion system pilus of Pseudomonas syringae. | Q54456461 | ||
| Identification of breakpoints in intergenotypic recombinants of HIV type 1 by bootscanning | Q70929876 | ||
| Analysis of promoters recognized by HrpL, an alternative sigma-factor protein from Pantoea agglomerans pv. gypsophilae | Q80928787 | ||
| A secreted anti-activator, OspD1, and its chaperone, Spa15, are involved in the control of transcription by the type III secretion apparatus activity in Shigella flexneri | Q81785474 | ||
| XopC and XopJ, two novel type III effector proteins from Xanthomonas campestris pv. vesicatoria | Q30320542 | ||
| cDNA-AFLP analysis unravels a genome-wide hrpG-regulon in the plant pathogen Xanthomonas campestris pv. vesicatoria | Q30320916 | ||
| Identification of the YopE and YopH domains required for secretion and internalization into the cytosol of macrophages, using the cyaA gene fusion approach | Q33638561 | ||
| A high-throughput, near-saturating screen for type III effector genes from Pseudomonas syringae | Q33850561 | ||
| Pseudomonas syringae type III chaperones ShcO1, ShcS1, and ShcS2 facilitate translocation of their cognate effectors and can substitute for each other in the secretion of HopO1-1. | Q33855521 | ||
| Mosaic nature of the wolbachia surface protein. | Q33937281 | ||
| Identification of a putative Salmonella enterica serotype typhimurium host range factor with homology to IpaH and YopM by signature-tagged mutagenesis | Q34002724 | ||
| Assembly and function of type III secretory systems | Q34052773 | ||
| Mosaic structure and molecular evolution of the leukotoxin operon (lktCABD) in Mannheimia (Pasteurella) haemolytica, Mannheimia glucosida, and Pasteurella trehalosi | Q34304108 | ||
| Diverse evolutionary mechanisms shape the type III effector virulence factor repertoire in the plant pathogen Pseudomonas syringae | Q34645388 | ||
| Identifying type III effectors of plant pathogens and analyzing their interaction with plant cells. | Q35077176 | ||
| A conserved amino acid sequence directing intracellular type III secretion by Salmonella typhimurium | Q35162771 | ||
| Functions and effectors of the Salmonella pathogenicity island 2 type III secretion system | Q35178637 | ||
| Cysteine proteases in phytopathogenic bacteria: identification of plant targets and activation of innate immunity | Q35825006 | ||
| Nucleotide sequence and evolution of the five-plasmid complement of the phytopathogen Pseudomonas syringae pv. maculicola ES4326. | Q35892099 | ||
| Proposed guidelines for a unified nomenclature and phylogenetic analysis of type III Hop effector proteins in the plant pathogen Pseudomonas syringae | Q36097161 | ||
| Molecular analysis of avirulence gene avrRpt2 and identification of a putative regulatory sequence common to all known Pseudomonas syringae avirulence genes | Q36103789 | ||
| New insights to the function of phytopathogenic bacterial type III effectors in plants | Q36111001 | ||
| Type-III effectors: sophisticated bacterial virulence factors | Q36158672 | ||
| The bacterial injection kit: type III secretion systems | Q36194906 | ||
| Molecular evolution of the dotA gene in Legionella pneumophila | Q36371076 | ||
| Molecular evolution and mosaicism of leptospiral outer membrane proteins involves horizontal DNA transfer | Q37425517 | ||
| A genetic screen to isolate type III effectors translocated into pepper cells during Xanthomonas infection | Q37692988 | ||
| Naturally occurring horizontal gene transfer and homologous recombination in Mycobacterium | Q39149413 | ||
| Sequence diversity and molecular evolution of the heat-modifiable outer membrane protein gene (ompA) of Mannheimia(Pasteurella) haemolytica, Mannheimia glucosida, and Pasteurella trehalosi | Q40000677 | ||
| Pseudomonas syringae type III secretion system targeting signals and novel effectors studied with a Cya translocation reporter | Q40387827 | ||
| Salmonella typhimurium leucine-rich repeat proteins are targeted to the SPI1 and SPI2 type III secretion systems | Q41481295 | ||
| Sequence and expression analysis of the hrpB pathogenicity operon of Xanthomonas campestris pv. vesicatoria which encodes eight proteins with similarity to components of the Hrp, Ysc, Spa, and Fli secretion systems | Q41493133 | ||
| Reduced genetic variation occurs among genes of the highly clonal plant pathogen Xanthomonas axonopodis pv. vesicatoria, including the effector gene avrBs2 | Q42186152 | ||
| The virulence plasmid pWR100 and the repertoire of proteins secreted by the type III secretion apparatus of Shigella flexneri | Q42638971 | ||
| Highly conserved sequences flank avirulence genes: isolation of novel avirulence genes from Pseudomonas syringae pv. pisi | Q42648178 | ||
| A functional screen for the type III (Hrp) secretome of the plant pathogen Pseudomonas syringae. | Q42671228 | ||
| Functional analysis of the type III effectors AvrRpt2 and AvrRpm1 of Pseudomonas syringae with the use of a single-copy genomic integration system | Q44135247 | ||
| The Pseudomonas syringae type III-secreted protein HopPtoD2 possesses protein tyrosine phosphatase activity and suppresses programmed cell death in plants | Q44492738 | ||
| A translocated protein tyrosine phosphatase of Pseudomonas syringae pv. tomato DC3000 modulates plant defence response to infection | Q44492741 | ||
| EspFU is a translocated EHEC effector that interacts with Tir and N-WASP and promotes Nck-independent actin assembly | Q45008620 | ||
| Exposure to host resistance mechanisms drives evolution of bacterial virulence in plants | Q48108253 | ||
| The response regulator SsrB activates transcription and binds to a region overlapping OmpR binding sites at Salmonella pathogenicity island 2. | Q50095966 | ||
| N-terminal conservation of putative type III secreted effectors of Salmonella typhimurium. | Q50120787 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 10 | |
| P921 | main subject | bacterial evolution | Q115395667 |
| P304 | page(s) | e104 | |
| P577 | publication date | 2006-10-01 | |
| P1433 | published in | PLOS Pathogens | Q283209 |
| P1476 | title | Terminal reassortment drives the quantum evolution of type III effectors in bacterial pathogens | |
| P478 | volume | 2 |
| Q28822572 | 3'-NADP and 3'-NAADP - Two Metabolites Formed by the Bacterial Type III Effector AvrRxo1 |
| Q33493436 | A "repertoire for repertoire" hypothesis: repertoires of type three effectors are candidate determinants of host specificity in Xanthomonas |
| Q36065227 | A De-Novo Genome Analysis Pipeline (DeNoGAP) for large-scale comparative prokaryotic genomics studies. |
| Q34782161 | A Ralstonia solanacearum type III effector directs the production of the plant signal metabolite trehalose-6-phosphate |
| Q45346078 | A bacterial toxin-antitoxin module is the origin of inter-bacterial and inter-kingdom effectors of Bartonella. |
| Q51909008 | Adaptive evolution has targeted the C-terminal domain of the RXLR effectors of plant pathogenic oomycetes. |
| Q30315566 | AnnoTALE: bioinformatics tools for identification, annotation, and nomenclature of TALEs from Xanthomonas genomic sequences |
| Q35789603 | BEAN 2.0: an integrated web resource for the identification and functional analysis of type III secreted effectors |
| Q34639643 | Bacterial secreted effectors and caspase-3 interactions |
| Q64902058 | Caspase-3 cleavage of Salmonella type III secreted effector protein SifA is required for localization of functional domains and bacterial dissemination. |
| Q56838695 | Comparative Genomics and Evolution of Bacterial Type III Effectors |
| Q35082974 | Comparative genomics of host-specific virulence in Pseudomonas syringae |
| Q33843911 | Comparative genomics reveals diversity among xanthomonads infecting tomato and pepper. |
| Q46882359 | Comparative large-scale analysis of interactions between several crop species and the effector repertoires from multiple pathovars of Pseudomonas and Ralstonia |
| Q38023077 | Computational analysis of interactomes: current and future perspectives for bioinformatics approaches to model the host-pathogen interaction space. |
| Q24644295 | De novo assembly using low-coverage short read sequence data from the rice pathogen Pseudomonas syringae pv. oryzae |
| Q41911735 | Distribution, functional expression, and genetic organization of Cif, a phage-encoded type III-secreted effector from enteropathogenic and enterohemorrhagic Escherichia coli. |
| Q31025558 | Dynamic evolution of pathogenicity revealed by sequencing and comparative genomics of 19 Pseudomonas syringae isolates |
| Q40347879 | E622, a miniature, virulence-associated mobile element |
| Q34672479 | Effective identification of bacterial type III secretion signals using joint element features. |
| Q39313194 | Evolution of RXLR-class effectors in the oomycete plant pathogen Phytophthora ramorum |
| Q30962327 | Evolutionary diversification of an ancient gene family (rhs) through C-terminal displacement |
| Q33592109 | Evolutionary microbial genomics: insights into bacterial host adaptation |
| Q28262210 | From bacterial avirulence genes to effector functions via the hrp delivery system: an overview of 25 years of progress in our understanding of plant innate immunity |
| Q37850977 | Functional domains and motifs of bacterial type III effector proteins and their roles in infection |
| Q33417110 | Gene Ontology annotation highlights shared and divergent pathogenic strategies of type III effector proteins deployed by the plant pathogen Pseudomonas syringae pv tomato DC3000 and animal pathogenic Escherichia coli strains |
| Q34905508 | Gene duplication and fragment recombination drive functional diversification of a superfamily of cytoplasmic effectors in Phytophthora sojae. |
| Q35032941 | Genome sequence of Xanthomonas fuscans subsp. fuscans strain 4834-R reveals that flagellar motility is not a general feature of xanthomonads |
| Q35091377 | Genomic plasticity enables phenotypic variation of Pseudomonas syringae pv. tomato DC3000 |
| Q41968421 | Host immune responses accelerate pathogen evolution |
| Q35549489 | Host-microbe and microbe-microbe interactions in the evolution of obligate plant parasitism |
| Q37012231 | Host-pathogen interplay and the evolution of bacterial effectors |
| Q63976022 | In planta conditions induce genomic changes in Pseudomonas syringae pv. phaseolicola |
| Q37830741 | Insects as alternative hosts for phytopathogenic bacteria |
| Q30572104 | Involvement of Type IV Pili in Pathogenicity of Plant Pathogenic Bacteria |
| Q99604969 | Keeping in Touch with Type-III Secretion System Effectors: Mass Spectrometry-Based Proteomics to Study Effector-Host Protein-Protein Interactions |
| Q36974212 | Manipulation of host-cell pathways by bacterial pathogens |
| Q34053316 | Miniature transposable sequences are frequently mobilized in the bacterial plant pathogen Pseudomonas syringae pv. phaseolicola. |
| Q36489643 | Mobile effector proteins on phage genomes |
| Q64072106 | Molecular Evolution of Type III Secreted Effector Proteins |
| Q43112689 | Naturally occurring nonpathogenic isolates of the plant pathogen Pseudomonas syringae lack a type III secretion system and effector gene orthologues. |
| Q33553931 | Novel insights into the genomic basis of citrus canker based on the genome sequences of two strains of Xanthomonas fuscans subsp. aurantifolii |
| Q35305175 | Potential origins and horizontal transfer of type III secretion systems and effectors |
| Q41517374 | Promoter propagation in prokaryotes |
| Q60921530 | Recombination of ecologically and evolutionarily significant loci maintains genetic cohesion in the Pseudomonas syringae species complex |
| Q36054725 | Salmonella effectors: important players modulating host cell function during infection |
| Q34055715 | Sequence and role in virulence of the three plasmid complement of the model tumor-inducing bacterium Pseudomonas savastanoi pv. savastanoi NCPPB 3335. |
| Q27317165 | Sequence-based prediction of type III secreted proteins |
| Q37619690 | Ten things to know about oomycete effectors. |
| Q38803183 | The HopF family of Pseudomonas syringae type III secreted effectors |
| Q34611109 | The apoptogenic toxin AIP56 is a metalloprotease A-B toxin that cleaves NF-κb P65 |
| Q52722868 | The bacterial type III-secreted protein AvrRps4 is a bipartite effector. |
| Q37619687 | The evolution of Pseudomonas syringae host specificity and type III effector repertoires |
| Q36598993 | The mangotoxin biosynthetic operon (mbo) is specifically distributed within Pseudomonas syringae genomospecies 1 and was acquired only once during evolution |
| Q37148107 | The multilevel and dynamic interplay between plant and pathogen |
| Q21559423 | The signal for signaling, found |
| Q37619685 | The type III effectors of Xanthomonas |
| Q35082188 | Variable suites of non-effector genes are co-regulated in the type III secretion virulence regulon across the Pseudomonas syringae phylogeny |
Search more.