| scholarly article | Q13442814 |
| P2093 | author name string | Collmer A | |
| Delaney TP | |||
| Alfano JR | |||
| Klm HS | |||
| P433 | issue | 5 | |
| P921 | main subject | Pseudomonas syringae | Q311202 |
| P304 | page(s) | 580-588 | |
| P577 | publication date | 1997-07-01 | |
| P1433 | published in | Molecular Plant-Microbe Interactions | Q15750768 |
| P1476 | title | Evidence that the Pseudomonas syringae pv. syringae hrp-linked hrmA gene encodes an Avr-like protein that acts in an hrp-dependent manner within tobacco cells | |
| P478 | volume | 10 |
| Q50089577 | A chaperone-like HrpG protein acts as a suppressor of HrpV in regulation of the Pseudomonas syringae pv. syringae type III secretion system |
| Q36289429 | A cloned Erwinia chrysanthemi Hrp (type III protein secretion) system functions in Escherichia coli to deliver Pseudomonas syringae Avr signals to plant cells and to secrete Avr proteins in culture |
| Q47793926 | A dsbA mutant of Pseudomonas syringae exhibits reduced virulence and partial impairment of type III secretion |
| Q42555068 | Apoplastic peroxidases are required for salicylic acid-mediated defense against Pseudomonas syringae |
| Q33736489 | Characterization of the hrpC and hrpRS operons of Pseudomonas syringae pathovars syringae, tomato, and glycinea and analysis of the ability of hrpF, hrpG, hrcC, hrpT, and hrpV mutants to elicit the hypersensitive response and disease in plants |
| Q47898214 | Conversion of compatible plant-pathogen interactions into incompatible interactions by expression of the Pseudomonas syringae pv. syringae 61 hrmA gene in transgenic tobacco plants |
| Q30475802 | Crystal structure of the flagellar rotor protein FliN from Thermotoga maritima |
| Q39573090 | DNA sequencing and analysis of the low-Ca2+-response plasmid pCD1 of Yersinia pestis KIM5. |
| Q52613293 | Degeneration of hrpZ gene in Pseudomonas syringae pv. tabaci to evade tobacco defence: an arms race between tobacco and its bacterial pathogen. |
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| Q33536582 | Gene-for-gene interactions: bacterial avirulence proteins specify plant disease resistance. |
| Q41692279 | Hrp-controlled interkingdom protein transport: learning from flagellar assembly? |
| Q35949246 | Identification of Pseudomonas syringae pv. syringae 61 type III secretion system Hrp proteins that can travel the type III pathway and contribute to the translocation of effector proteins into plant cells |
| Q48207372 | Identification of Pseudomonas syringae type III effectors that can suppress programmed cell death in plants and yeast |
| Q37293186 | Molecular signals required for type III secretion and translocation of the Xanthomonas campestris AvrBs2 protein to pepper plants |
| Q33736495 | Negative regulation of hrp genes in Pseudomonas syringae by HrpV. |
| Q48026545 | PIOX, a new pathogen-induced oxygenase with homology to animal cyclooxygenase |
| Q42972443 | Plant immunity directly or indirectly restricts the injection of type III effectors by the Pseudomonas syringae type III secretion system. |
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| Q39743757 | Pseudomonas syringae exchangeable effector loci: sequence diversity in representative pathovars and virulence function in P. syringae pv. syringae B728a |
| Q41873246 | Pseudomonas syringae lytic transglycosylases coregulated with the type III secretion system contribute to the translocation of effector proteins into plant cells |
| Q34087701 | Pseudomonas syringae pv. actinidiae draft genomes comparison reveal strain-specific features involved in adaptation and virulence to Actinidia species |
| Q43318227 | Pseudomonas syringae pv. tomato: the right pathogen, of the right plant, at the right time |
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| Q33992662 | 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. |
| Q35699642 | 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 |
| Q39568015 | 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. |
| Q53871902 | The ShcA protein is a molecular chaperone that assists in the secretion of the HopPsyA effector from the type III (Hrp) protein secretion system of Pseudomonas syringae. |
| Q33699873 | 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 |
| Q42045885 | The insecticidal toxin makes caterpillars floppy 2 (Mcf2) shows similarity to HrmA, an avirulence protein from a plant pathogen |
| Q37423242 | The majority of the type III effector inventory of Pseudomonas syringae pv. tomato DC3000 can suppress plant immunity |
| Q35630003 | The type III (Hrp) secretion pathway of plant pathogenic bacteria: trafficking harpins, Avr proteins, and death |
| Q28290675 | The virulence plasmid of Yersinia, an antihost genome |
| Q48343337 | Type III secretion in plant growth-promoting Pseudomonas fluorescens SBW25. |
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