review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1016/S1369-5266(03)00064-5 |
P698 | PubMed publication ID | 12873524 |
P50 | author | Ulla Bonas | Q1612297 |
P2093 | author name string | Daniela Büttner | |
P2860 | cites work | Cytoskeletal control of plant cell shape: getting the fine points | Q35032029 |
Identifying type III effectors of plant pathogens and analyzing their interaction with plant cells. | Q35077176 | ||
A distinctive role for the Yersinia protein kinase: actin binding, kinase activation, and cytoskeleton disruption. | Q35206375 | ||
The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death | Q35630003 | ||
ExoY, an adenylate cyclase secreted by the Pseudomonas aeruginosa type III system | Q36809802 | ||
Molecular signals required for type III secretion and translocation of the Xanthomonas campestris AvrBs2 protein to pepper plants | Q37293186 | ||
The Hrp pilus of Pseudomonas syringae elongates from its tip and acts as a conduit for translocation of the effector protein HrpZ. | Q39644861 | ||
Supramolecular structure of the Shigella type III secretion machinery: the needle part is changeable in length and essential for delivery of effectors | Q40392389 | ||
Cutting edge: Salmonella AvrA effector inhibits the key proinflammatory, anti-apoptotic NF-kappa B pathway. | Q40705607 | ||
Disruption of signaling by Yersinia effector YopJ, a ubiquitin-like protein protease. | Q40840610 | ||
The Salmonella YopJ-homologue AvrA does not possess YopJ-like activity | Q40904595 | ||
PopP1, a new member of the YopJ/AvrRxv family of type III effector proteins, acts as a host-specificity factor and modulates aggressiveness of Ralstonia solanacearum | Q41469976 | ||
A high-molecular-weight outer membrane protein of Xanthomonas oryzae pv. oryzae exhibits similarity to non-fimbrial adhesins of animal pathogenic bacteria and is required for optimum virulence | Q41470112 | ||
A Yersinia effector and a Pseudomonas avirulence protein define a family of cysteine proteases functioning in bacterial pathogenesis. | Q41471661 | ||
Regulation of mRNA expression in macrophages after Yersinia enterocolitica infection. Role of different Yop effectors. | Q41471973 | ||
Exoenzyme T of Pseudomonas aeruginosa elicits cytotoxicity without interfering with Ras signal transduction | Q41476159 | ||
Recognition of bacterial avirulence proteins occurs inside the plant cell: a general phenomenon in resistance to bacterial diseases? | Q41570707 | ||
RIN4 interacts with Pseudomonas syringae type III effector molecules and is required for RPM1-mediated resistance in Arabidopsis | Q42520168 | ||
A functional screen for the type III (Hrp) secretome of the plant pathogen Pseudomonas syringae. | Q42671228 | ||
Two distinct Pseudomonas effector proteins interact with the Pto kinase and activate plant immunity | Q44025701 | ||
Functional analysis of the type III effectors AvrRpt2 and AvrRpm1 of Pseudomonas syringae with the use of a single-copy genomic integration system | Q44135247 | ||
Direct delivery of bacterial avirulence proteins into resistant Arabidopsis protoplasts leads to hypersensitive cell death | Q44565198 | ||
Targeting the targets of Type III effector proteins secreted by phytopathogenic bacteria. | Q47793680 | ||
The xanthomonas type III effector protein AvrBs3 modulates plant gene expression and induces cell hypertrophy in the susceptible host. | Q48293430 | ||
A salmonella protein antagonizes Rac-1 and Cdc42 to mediate host-cell recovery after bacterial invasion. | Q50124353 | ||
Arabidopsis RIN4 is a target of the type III virulence effector AvrRpt2 and modulates RPS2-mediated resistance. | Q52549320 | ||
Type III-dependent translocation of the Xanthomonas AvrBs3 protein into the plant cell. | Q53956677 | ||
Eukaryotic features of the Xanthomonas type III effector AvrBs3: protein domains involved in transcriptional activation and the interaction with nuclear import receptors from pepper. | Q54002933 | ||
Role of the Hrp pilus in type III protein secretion in Pseudomonas syringae | Q64449530 | ||
Comparison of the genomes of two Xanthomonas pathogens with differing host specificities | Q22122346 | ||
Genome sequence of the plant pathogen Ralstonia solanacearum | Q22122347 | ||
The genome sequence of the plant pathogen Xylella fastidiosa. The Xylella fastidiosa Consortium of the Organization for Nucleotide Sequencing and Analysis | Q22122395 | ||
Plants and animals share functionally common bacterial virulence factors | Q24630477 | ||
Molecular secrets of bacterial type III effector proteins | Q28190618 | ||
Structure and composition of the Shigella flexneri "needle complex", a part of its type III secreton | Q28199735 | ||
The leucine-rich repeat as a protein recognition motif | Q28212461 | ||
Structural mimicry in bacterial virulence | Q28212980 | ||
Getting across--bacterial type III effector proteins on their way to the plant cell | Q30320765 | ||
Port of entry--the type III secretion translocon | Q30320840 | ||
Plant disease resistance triggered by pathogen-derived molecules: refined models of specific recognition | Q30320862 | ||
cDNA-AFLP analysis unravels a genome-wide hrpG-regulon in the plant pathogen Xanthomonas campestris pv. vesicatoria | Q30320916 | ||
HecA, a member of a class of adhesins produced by diverse pathogenic bacteria, contributes to the attachment, aggregation, epidermal cell killing, and virulence phenotypes of Erwinia chrysanthemi EC16 on Nicotiana clevelandii seedlings | Q30852463 | ||
Phosphatases and kinases delivered to the host cell by bacterial pathogens | Q33818897 | ||
Pathogenicity islands and the evolution of microbes | Q33920183 | ||
Bacterial adhesins: common themes and variations in architecture and assembly. | Q33991218 | ||
Pathogenic strategies of enteric bacteria. | Q34017362 | ||
Direct biochemical evidence for type III secretion-dependent translocation of the AvrBs2 effector protein into plant cells | Q34032589 | ||
Assembly and function of type III secretory systems | Q34052773 | ||
Pseudomonas aeruginosa exoenzyme S, a bifunctional type-III secreted cytotoxin | Q34101987 | ||
Initiation of RPS2-specified disease resistance in Arabidopsis is coupled to the AvrRpt2-directed elimination of RIN4. | Q34176705 | ||
Common and contrasting themes of plant and animal diseases | Q34292177 | ||
Modulation of Rho GTPases and the actin cytoskeleton by Yersinia outer proteins (Yops). | Q34419980 | ||
Salmonella interactions with host cells: type III secretion at work | Q34425135 | ||
Pseudomonas type III effector AvrPtoB induces plant disease susceptibility by inhibition of host programmed cell death | Q34446089 | ||
Rho family proteins: coordinating cell responses | Q34446303 | ||
Function of the Yersinia effector YopJ. | Q34521795 | ||
Yersinia effectors target mammalian signalling pathways | Q34600556 | ||
Supramolecular structure of the Salmonella typhimurium type III protein secretion system | Q34746894 | ||
Cross-species infections and their analysis | Q34762804 | ||
Genomic mining type III secretion system effectors in Pseudomonas syringae yields new picks for all TTSS prospectors | Q34960211 | ||
P433 | issue | 4 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 312-319 | |
P577 | publication date | 2003-08-01 | |
P1433 | published in | Current Opinion in Plant Biology | Q15756095 |
P1476 | title | Common infection strategies of plant and animal pathogenic bacteria | |
P478 | volume | 6 |
Q28492431 | A J domain virulence effector of Pseudomonas syringae remodels host chloroplasts and suppresses defenses |
Q34154462 | A bacterial acetyltransferase destroys plant microtubule networks and blocks secretion |
Q37692988 | A genetic screen to isolate type III effectors translocated into pepper cells during Xanthomonas infection |
Q45942973 | A novel gene, phcA from Pseudomonas syringae induces programmed cell death in the filamentous fungus Neurospora crassa. |
Q24678382 | An extensive repertoire of type III secretion effectors in Escherichia coli O157 and the role of lambdoid phages in their dissemination |
Q34005300 | Anti-apoptotic machinery protects the necrotrophic fungus Botrytis cinerea from host-induced apoptotic-like cell death during plant infection |
Q35093393 | Breaking dogmas: the plant vascular pathogen Xanthomonas albilineans is able to invade non-vascular tissues despite its reduced genome |
Q33884633 | Changes in race-specific virulence in Pseudomonas syringae pv. phaseolicola are associated with a chimeric transposable element and rare deletion events in a plasmid-borne pathogenicity island |
Q22065748 | Comparative and functional genomic analyses of the pathogenicity of phytopathogen Xanthomonas campestris pv. campestris |
Q38958195 | Comparative genomic analysis of Xanthomonas axonopodis pv. citrumelo F1, which causes citrus bacterial spot disease, and related strains provides insights into virulence and host specificity |
Q33503402 | Comparative in vivo gene expression of the closely related bacteria Photorhabdus temperata and Xenorhabdus koppenhoeferi upon infection of the same insect host, Rhizotrogus majalis |
Q35911179 | Disabling surveillance: bacterial type III secretion system effectors that suppress innate immunity |
Q36301108 | Discovery of Novel Plant Interaction Determinants from the Genomes of 163 Root Nodule Bacteria |
Q37191152 | Effect of iron concentration on the growth rate of Pseudomonas syringae and the expression of virulence factors in hrp-inducing minimal medium |
Q36798626 | Elicitation and suppression of microbe-associated molecular pattern-triggered immunity in plant-microbe interactions |
Q35023527 | Elucidation of the hrp clusters of Xanthomonas oryzae pv. oryzicola that control the hypersensitive response in nonhost tobacco and pathogenicity in susceptible host rice |
Q82507286 | EseD, a putative T3SS translocon component of Edwardsiella tarda, contributes to virulence in fish and is a candidate for vaccine development |
Q44245943 | Fungal-specific transcription factor AbPf2 activates pathogenicity in Alternaria brassicicola |
Q34374477 | Hijacking of leguminous nodulation signaling by the rhizobial type III secretion system |
Q28540112 | HopW1 from Pseudomonas syringae disrupts the actin cytoskeleton to promote virulence in Arabidopsis |
Q46884639 | Host-mediated phosphorylation of type III effector AvrPto promotes Pseudomonas virulence and avirulence in tomato. |
Q35991629 | Identification of phenolic compounds that suppress the virulence of Xanthomonas oryzae on rice via the type III secretion system |
Q90679893 | Identifying Pseudomonas syringae Type III Secreted Effector Function via a Yeast Genomic Screen |
Q33664494 | Invertebrate immune systems--not homogeneous, not simple, not well understood |
Q34452499 | Involvement of bacterial TonB-dependent signaling in the generation of an oligogalacturonide damage-associated molecular pattern from plant cell walls exposed to Xanthomonas campestris pv. campestris pectate lyases |
Q50752333 | Localization of Ptr ToxA Produced by Pyrenophora tritici-repentis Reveals Protein Import into Wheat Mesophyll Cells. |
Q35841646 | NopC Is a Rhizobium-Specific Type 3 Secretion System Effector Secreted by Sinorhizobium (Ensifer) fredii HH103. |
Q39469913 | NopP, a phosphorylated effector of Rhizobium sp. strain NGR234, is a major determinant of nodulation of the tropical legumes Flemingia congesta and Tephrosia vogelii. |
Q38083866 | Phytopathogen type III effectors as probes of biological systems |
Q33928688 | Powerful screens for bacterial virulence proteins |
Q51538264 | RIN13 is a positive regulator of the plant disease resistance protein RPM1. |
Q37901375 | Recognition events and host-pathogen co-evolution in gene-for-gene resistance to flax rust. |
Q41336612 | RpoN2- and FliA-regulated fliTX is indispensible for flagellar motility and virulence in Xanthomonas oryzae pv. oryzae |
Q44759878 | SecretP: Identifying bacterial secreted proteins by fusing new features into Chou’s pseudo-amino acid composition |
Q46113948 | Subcellular localization and functional analysis of the Arabidopsis GTPase RabE. |
Q30320104 | Targeting of two effector protein classes to the type III secretion system by a HpaC- and HpaB-dependent protein complex from Xanthomonas campestris pv. vesicatoria |
Q40875002 | The Erwinia chrysanthemi type III secretion system is required for multicellular behavior. |
Q40406118 | The Sinorhizobium (Ensifer) fredii HH103 Nodulation Outer Protein NopI Is a Determinant for Efficient Nodulation of Soybean and Cowpea Plants |
Q27650415 | The crystal structure of pectate lyase peli from soft rot pathogen Erwinia chrysanthemi in complex with its substrate |
Q35980437 | The cytoskeleton as a regulator and target of biotic interactions in plants |
Q91894438 | Transcriptional responses of Xanthomonas oryzae pv. oryzae to type III secretion system inhibitor ortho-coumaric acid |
Q34479457 | Type III effector AvrPtoB requires intrinsic E3 ubiquitin ligase activity to suppress plant cell death and immunity. |
Q41504137 | Type III secretion system and virulence markers highlight similarities and differences between human- and plant-associated pseudomonads related to Pseudomonas fluorescens and P. putida. |
Q36156270 | Unraveling the secret lives of bacteria: use of in vivo expression technology and differential fluorescence induction promoter traps as tools for exploring niche-specific gene expression |
Q30320542 | XopC and XopJ, two novel type III effector proteins from Xanthomonas campestris pv. vesicatoria |
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