| scholarly article | Q13442814 |
| P50 | author | Damien Meyer | Q55590619 |
| Sebastien Cunnac | Q56859921 | ||
| P2093 | author name string | Frédérique Van Gijsegem | |
| Matthieu Arlat | |||
| Emmanuelle Lauber | |||
| Christian Boucher | |||
| Céline Declercq | |||
| Mareva Guéneron | |||
| P2860 | cites work | Characterization of Nops, nodulation outer proteins, secreted via the type III secretion system of NGR234 | Q73936219 |
| Biology and epidemiology of bacterial wilt caused by pseudomonas solanacearum | Q81274475 | ||
| The genome sequence of Xanthomonas oryzae pathovar oryzae KACC10331, the bacterial blight pathogen of rice | Q22065983 | ||
| Complete Genome Structure of the Nitrogen-fixing Symbiotic Bacterium Mesorhizobium loti | Q22066064 | ||
| 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 | ||
| Genome sequence of the plant pathogen Ralstonia solanacearum | Q22122347 | ||
| The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools | Q24248165 | ||
| CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice | Q24286950 | ||
| The Yersinia Yop virulon: LcrV is required for extrusion of the translocators YopB and YopD. | Q24520677 | ||
| Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 | Q25938983 | ||
| Bacterial type III secretion systems are ancient and evolved by multiple horizontal-transfer events | Q28156326 | ||
| The virulence plasmid of Yersinia, an antihost genome | Q28290675 | ||
| Molecular basis of symbiosis between Rhizobium and legumes | Q29393489 | ||
| The type III-dependent Hrp pilus is required for productive interaction of Xanthomonas campestris pv. vesicatoria with pepper host plants | Q30320262 | ||
| Functional analysis of HrpF, a putative type III translocon protein from Xanthomonas campestris pv. vesicatoria | Q30320829 | ||
| Port of entry--the type III secretion translocon | Q30320840 | ||
| Two novel type III-secreted proteins of Xanthomonas campestris pv. vesicatoria are encoded within the hrp pathogenicity island | Q30320855 | ||
| Extracellular proteins involved in soybean cultivar-specific nodulation are associated with pilus-like surface appendages and exported by a type III protein secretion system in Sinorhizobium fredii USDA257. | Q30959859 | ||
| NopB, a type III secreted protein of Rhizobium sp. strain NGR234, is associated with pilus-like surface appendages. | Q31142460 | ||
| Xanthomonas campestrisContains a Cluster ofhrpGenes Related to the LargerhrpCluster ofPseudomonas solanacearum | Q33241847 | ||
| Identification of two novel hrp-associated genes in the hrp gene cluster of Xanthomonas oryzae pv. oryzae | Q33601534 | ||
| The hrpK operon of Pseudomonas syringae pv. tomato DC3000 encodes two proteins secreted by the type III (Hrp) protein secretion system: HopB1 and HrpK, a putative type III translocator | Q33699873 | ||
| Role of predicted transmembrane domains for type III translocation, pore formation, and signaling by the Yersinia pseudotuberculosis YopB protein | Q33769194 | ||
| A high-throughput, near-saturating screen for type III effector genes from Pseudomonas syringae | Q33850561 | ||
| HrpZPsph from the plant pathogen Pseudomonas syringae pv. phaseolicola binds to lipid bilayers and forms an ion-conducting pore in vitro | Q33929605 | ||
| 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 | ||
| Type III secretion system effector proteins: double agents in bacterial disease and plant defense | Q34337243 | ||
| Quorum sensing regulates type III secretion in Vibrio harveyi and Vibrio parahaemolyticus | Q34351491 | ||
| NolX of Sinorhizobium fredii USDA257, a type III-secreted protein involved in host range determination, Iis localized in the infection threads of cowpea (Vigna unguiculata [L.] Walp) and soybean (Glycine max [L.] Merr.) nodules | Q34434362 | ||
| Bacterial blight of soybean: regulation of a pathogen gene determining host cultivar specificity | Q34544077 | ||
| Yersinia type III secretion: send in the effectors | Q34774578 | ||
| Characterization of the Xanthomonas axonopodis pv. glycines Hrp Pathogenicity Island | Q34977390 | ||
| Recognition and Response in the Plant Immune System | Q35583005 | ||
| The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death | Q35630003 | ||
| What can bacterial genome research teach us about bacteria-plant interactions? | Q35683383 | ||
| Lessons learned from the genome analysis of ralstonia solanacearum. | Q35850397 | ||
| Type III protein secretion mechanism in mammalian and plant pathogens | Q35951971 | ||
| Hrp pilus: an hrp-dependent bacterial surface appendage produced by Pseudomonas syringae pv. tomato DC3000 | Q36086934 | ||
| A type III secretion system is required for Aeromonas hydrophila AH-1 pathogenesis | Q36576242 | ||
| Mutational analysis of Xanthomonas harpin HpaG identifies a key functional region that elicits the hypersensitive response in nonhost plants | Q37494542 | ||
| Gene-for-gene complementarity in plant-pathogen interactions | Q37794706 | ||
| Genome-wide analysis of gene expression in Ralstonia solanacearum reveals that the hrpB gene acts as a regulatory switch controlling multiple virulence pathways. | Q38320943 | ||
| Identification of open reading frames unique to a select agent: Ralstonia solanacearum race 3 biovar 2. | Q39014880 | ||
| The Hrp pilus of Pseudomonas syringae elongates from its tip and acts as a conduit for translocation of the effector protein HrpZ. | Q39644861 | ||
| A cloned avirulence gene from Pseudomonas solanacearum determines incompatibility on Nicotiana tabacum at the host species level | Q39960103 | ||
| Pseudomonas syringae type III secretion system targeting signals and novel effectors studied with a Cya translocation reporter | Q40387827 | ||
| PopA1, a protein which induces a hypersensitivity-like response on specific Petunia genotypes, is secreted via the Hrp pathway of Pseudomonas solanacearum. | Q40790729 | ||
| Characterization of the cis-acting regulatory element controlling HrpB-mediated activation of the type III secretion system and effector genes in Ralstonia solanacearum. | Q40867634 | ||
| The YopB protein of Yersinia pseudotuberculosis is essential for the translocation of Yop effector proteins across the target cell plasma membrane and displays a contact-dependent membrane disrupting activity | Q41077827 | ||
| 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 | ||
| LcrV is a channel size-determining component of the Yop effector translocon of Yersinia | Q41477086 | ||
| HrpB2 and HrpF from Xanthomonas are type III-secreted proteins and essential for pathogenicity and recognition by the host plant | Q41477472 | ||
| Yersinia enterocolitica type III secretion-translocation system: channel formation by secreted Yops | Q41481194 | ||
| Insertion of a Yop translocation pore into the macrophage plasma membrane by Yersinia enterocolitica: requirement for translocators YopB and YopD, but not LcrG. | Q41481875 | ||
| Functional conservation of the effector protein translocators PopB/YopB and PopD/YopD of Pseudomonas aeruginosa and Yersinia pseudotuberculosis | Q41484833 | ||
| Translocation of a hybrid YopE-adenylate cyclase from Yersinia enterocolitica into HeLa cells | Q41497627 | ||
| hrpf of Xanthomonas campestris pv. vesicatoria encodes an 87-kDa protein with homology to NoIX of Rhizobium fredii | Q42656003 | ||
| Inventory and functional analysis of the large Hrp regulon in Ralstonia solanacearum: identification of novel effector proteins translocated to plant host cells through the type III secretion system | Q47269339 | ||
| Two novel proteins, PopB, which has functional nuclear localization signals, and PopC, which has a large leucine-rich repeat domain, are secreted through the hrp-secretion apparatus of Ralstonia solanacearum | Q47863693 | ||
| PrhA controls a novel regulatory pathway required for the specific induction of Ralstonia solanacearum hrp genes in the presence of plant cells | Q48040015 | ||
| In vitro insertional mutagenesis with a selectable DNA fragment | Q48387759 | ||
| Genes for gentamicin-(3)-N-acetyltransferases III and IV: I. Nucleotide sequence of the AAC(3)-IV gene and possible involvement of an IS140 element in its expression. | Q48393805 | ||
| Unified nomenclature for broadly conserved hrp genes of phytopathogenic bacteria. | Q48786134 | ||
| Genetic dissection of Ralstonia solanacearum hrp gene cluster reveals that the HrpV and HrpX proteins are required for Hrp pilus assembly. | Q49167670 | ||
| Characterization of the hrpF pathogenicity peninsula of Xanthomonas oryzae pv. oryzae. | Q53853294 | ||
| Type III-dependent translocation of the Xanthomonas AvrBs3 protein into the plant cell. | Q53956677 | ||
| Role of the Hrp pilus in type III protein secretion in Pseudomonas syringae | Q64449530 | ||
| Visualization of secreted Hrp and Avr proteins along the Hrp pilus during type III secretion in Erwinia amylovora and Pseudomonas syringae | Q64449576 | ||
| Ralstonia solanacearum produces hrp-dependent pili that are required for PopA secretion but not for attachment of bacteria to plant cells | Q64449692 | ||
| Transcriptional Organization and Expression of the LargehrpGene Cluster ofPseudomonas solanacearum | Q68181966 | ||
| Flavonoid inducers of nodulation genes stimulate Rhizobium fredii USDA257 to export proteins into the environment | Q72799467 | ||
| P433 | issue | 13 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Ralstonia solanacearum | Q2710840 |
| P304 | page(s) | 4903-4917 | |
| P577 | publication date | 2006-07-01 | |
| P1433 | published in | Journal of Bacteriology | Q478419 |
| P1476 | title | PopF1 and PopF2, two proteins secreted by the type III protein secretion system of Ralstonia solanacearum, are translocators belonging to the HrpF/NopX family | |
| P478 | volume | 188 |
| Q58056337 | A Eucalyptus bacterial wilt isolate from South Africa is pathogenic on Arabidopsis and manipulates host defences |
| Q64945132 | A genome-wide scan for genes under balancing selection in the plant pathogen Ralstonia solanacearum. |
| Q38183945 | Assembly of the bacterial type III secretion machinery. |
| Q36422269 | AvrAC(Xcc8004), a type III effector with a leucine-rich repeat domain from Xanthomonas campestris pathovar campestris confers avirulence in vascular tissues of Arabidopsis thaliana ecotype Col-0. |
| Q27023604 | Commonalities and differences of T3SSs in rhizobia and plant pathogenic bacteria |
| Q41050348 | Comparative Genomics Identifies a Novel Conserved Protein, HpaT, in Proteobacterial Type III Secretion Systems that Do Not Possess the Putative Translocon Protein HrpF. |
| Q36539493 | Comparative Secretome Analysis of Ralstonia solanacearum Type 3 Secretion-Associated Mutants Reveals a Fine Control of Effector Delivery, Essential for Bacterial Pathogenicity |
| Q33525006 | Experimental evolution of a plant pathogen into a legume symbiont |
| Q47826079 | HrpN of Erwinia amylovora functions in the translocation of DspA/E into plant cells. |
| Q28492424 | Identification of harpins in Pseudomonas syringae pv. tomato DC3000, which are functionally similar to HrpK1 in promoting translocation of type III secretion system effectors |
| Q49308826 | Iron Starvation Conditions Upregulate Ehrlichia ruminantium Type IV Secretion System, tr1 Transcription Factor and map1 Genes Family through the Master Regulatory Protein ErxR. |
| Q38282188 | Key steps in type III secretion system (T3SS) towards translocon assembly with potential sensor at plant plasma membrane. |
| Q33274647 | Plant carbohydrate scavenging through tonB-dependent receptors: a feature shared by phytopathogenic and aquatic bacteria |
| Q30318075 | Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria |
| Q28501148 | Protein-protein interactions within type III secretion system-dependent pili of Rhizobium sp. strain NGR234 |
| Q34390259 | Repertoire, unified nomenclature and evolution of the Type III effector gene set in the Ralstonia solanacearum species complex. |
| Q47744378 | The Pseudomonas syringae HrpJ protein controls the secretion of type III translocator proteins and has a virulence role inside plant cells |
| Q27027103 | The SPI-1-like Type III secretion system: more roles than you think |
| Q98465479 | Three Proteins (Hpa2, HrpF and XopN) Are Concomitant Type III Translocators in Bacterial Blight Pathogen of Rice |
| Q37490586 | Type III protein secretion in plant pathogenic bacteria |
| Q34982818 | Xanthomonas oryzae pv. oryzae type III effector XopN targets OsVOZ2 and a putative thiamine synthase as a virulence factor in rice |
| Q34952022 | xopAC-triggered immunity against Xanthomonas depends on Arabidopsis receptor-like cytoplasmic kinase genes PBL2 and RIPK. |
Search more.