Pages that link to "Q39568015"

The following pages link to The Pseudomonas syringae pv. tomato HrpW protein has domains similar to harpins and pectate lyases and can elicit the plant hypersensitive response and bind to pectate. (Q39568015):

Displaying 50 items.

• Commonalities and differences of T3SSs in rhizobia and plant pathogenic bacteria (Q27023604) (← links)
• Identification of harpins in Pseudomonas syringae pv. tomato DC3000, which are functionally similar to HrpK1 in promoting translocation of type III secretion system effectors (Q28492424) (← links)
• Role of type III effector secretion during bacterial pathogenesis in another kingdom (Q28775800) (← links)
• Protein export according to schedule: architecture, assembly, and regulation of type III secretion systems from plant- and animal-pathogenic bacteria (Q30318075) (← links)
• A two-genome microarray for the rice pathogens Xanthomonas oryzae pv. oryzae and X. oryzae pv. oryzicola and its use in the discovery of a difference in their regulation of hrp genes (Q30482750) (← links)
• Transcriptional profile of Pseudomonas syringae pv. phaseolicola NPS3121 in response to tissue extracts from a susceptible Phaseolus vulgaris L. cultivar (Q33517975) (← links)
• Identification of two novel hrp-associated genes in the hrp gene cluster of Xanthomonas oryzae pv. oryzae (Q33601534) (← links)
• 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) (← links)
• The hrpZ Gene of Pseudomonas syringae pv. phaseolicola Enhances Resistance to Rhizomania Disease in Transgenic Nicotiana benthamiana and Sugar Beet (Q33843338) (← links)
• HrpZPsph from the plant pathogen Pseudomonas syringae pv. phaseolicola binds to lipid bilayers and forms an ion-conducting pore in vitro (Q33929605) (← links)
• Pseudomonas syringae Hrp type III secretion system and effector proteins. (Q33988466) (← links)
• The Avr (effector) proteins HrmA (HopPsyA) and AvrPto are secreted in culture from Pseudomonas syringae pathovars via the Hrp (type III) protein secretion system in a temperature- and pH-sensitive manner. (Q33992662) (← links)
• Genomewide identification of Pseudomonas syringae pv. tomato DC3000 promoters controlled by the HrpL alternative sigma factor (Q34013057) (← links)
• Functional mapping of harpin HrpZ of Pseudomonas syringae reveals the sites responsible for protein oligomerization, lipid interactions and plant defence induction (Q34157255) (← links)
• Plant innate immunity induced by flagellin suppresses the hypersensitive response in non-host plants elicited by Pseudomonas syringae pv. averrhoi (Q34387636) (← links)
• Harpin mediates cell aggregation in Erwinia chrysanthemi 3937. (Q34513609) (← links)
• A highly-conserved single-stranded DNA-binding protein in Xanthomonas functions as a harpin-like protein to trigger plant immunity (Q34589927) (← links)
• Diverse evolutionary mechanisms shape the type III effector virulence factor repertoire in the plant pathogen Pseudomonas syringae (Q34645388) (← links)
• Molecular evolution of pathogenicity-island genes in Pseudomonas viridiflava (Q34667554) (← links)
• Characterization of the Xanthomonas axonopodis pv. glycines Hrp Pathogenicity Island (Q34977390) (← links)
• The gene coding for the Hrp pilus structural protein is required for type III secretion of Hrp and Avr proteins in Pseudomonas syringae pv. tomato (Q35052377) (← links)
• Pseudomonas syringae HrpJ is a type III secreted protein that is required for plant pathogenesis, injection of effectors, and secretion of the HrpZ1 Harpin (Q35075234) (← links)
• Comparative genomics of host-specific virulence in Pseudomonas syringae (Q35082974) (← links)
• Eggplant and related species are promising genetic resources to dissect the plant immune response to Pseudomonas syringae and Xanthomonas euvesicatoria and to identify new resistance determinants (Q35135532) (← links)
• The Xanthomonas Hrp type III system secretes proteins from plant and mammalian bacterial pathogens (Q35604617) (← links)
• The Pseudomonas syringae Hrp pathogenicity island has a tripartite mosaic structure composed of a cluster of type III secretion genes bounded by exchangeable effector and conserved effector loci that contribute to parasitic fitness and pathogenicity (Q35699642) (← links)
• Bioinformatics Analysis of the Complete Genome Sequence of the Mango Tree Pathogen Pseudomonas syringae pv. syringae UMAF0158 Reveals Traits Relevant to Virulence and Epiphytic Lifestyle (Q35757616) (← links)
• The signal peptide-like segment of hpaXm is required for its association to the cell wall in transgenic tobacco plants (Q36265087) (← links)
• A family of conserved bacterial effectors inhibits salicylic acid-mediated basal immunity and promotes disease necrosis in plants (Q36449475) (← links)
• A bacterial sensor of plant cell contact controls the transcriptional induction of Ralstonia solanacearum pathogenicity genes. (Q37350400) (← links)
• Type III protein secretion in plant pathogenic bacteria (Q37490586) (← links)
• Mutational analysis of Xanthomonas harpin HpaG identifies a key functional region that elicits the hypersensitive response in nonhost plants (Q37494542) (← links)
• Key steps in type III secretion system (T3SS) towards translocon assembly with potential sensor at plant plasma membrane. (Q38282188) (← links)
• The alternative sigma factor RpoN is required for hrp activity in Pseudomonas syringae pv. maculicola and acts at the level of hrpL transcription (Q39539015) (← links)
• HrpW of Erwinia amylovora, a new harpin that contains a domain homologous to pectate lyases of a distinct class (Q39568007) (← links)
• Productivity and biochemical properties of green tea in response to full-length and functional fragments of HpaG Xooc, a harpin protein from the bacterial rice leaf streak pathogen Xanthomonas oryzae pv. oryzicola (Q39605502) (← links)
• Pseudomonas syringae exchangeable effector loci: sequence diversity in representative pathovars and virulence function in P. syringae pv. syringae B728a (Q39743757) (← links)
• New protein-protein interactions identified for the regulatory and structural components and substrates of the type III Secretion system of the phytopathogen Xanthomonas axonopodis Pathovar citri. (Q39963895) (← links)
• Dickeya dadantii pectic enzymes necessary for virulence are also responsible for activation of the Arabidopsis thaliana innate immune system. (Q40420652) (← links)
• HopX1 in Erwinia amylovora functions as an avirulence protein in apple and is regulated by HrpL. (Q40596580) (← links)
• The Erwinia chrysanthemi type III secretion system is required for multicellular behavior. (Q40875002) (← links)
• Hpa2 Required by HrpF To Translocate Xanthomonas oryzae Transcriptional Activator-Like Effectors into Rice for Pathogenicity (Q42782111) (← links)
• PopW of Ralstonia solanacearum, a new two-domain harpin targeting the plant cell wall (Q43071890) (← links)
• PMR6, a pectate lyase-like gene required for powdery mildew susceptibility in Arabidopsis (Q44128046) (← links)
• Differential volatile emissions and salicylic acid levels from tobacco plants in response to different strains of Pseudomonas syringae (Q44415157) (← links)
• HrpN of Erwinia amylovora functions in the translocation of DspA/E into plant cells. (Q47826079) (← links)
• AtHIPM, an ortholog of the apple HrpN-interacting protein, is a negative regulator of plant growth and mediates the growth-enhancing effect of HrpN in Arabidopsis (Q47838183) (← links)
• Ferredoxin from sweet pepper (Capsicum annuum L.) intensifying harpin(pss)-mediated hypersensitive response shows an enhanced production of active oxygen species (AOS). (Q48244319) (← links)
• Genome-based classification of micromonosporae with a focus on their biotechnological and ecological potential (Q48262869) (← links)
• Degeneration of hrpZ gene in Pseudomonas syringae pv. tabaci to evade tobacco defence: an arms race between tobacco and its bacterial pathogen (Q52613293) (← links)