human | Q5 |
P2798 | Loop ID | 560776 |
P496 | ORCID iD | 0000-0002-7877-3543 |
P3829 | Publons author ID | 2276717 |
P1053 | ResearcherID | F-9182-2016 |
P1153 | Scopus author ID | 56457061400 |
P108 | employer | University of Oxford | Q34433 |
National Cancer Institute | Q664846 | ||
P734 | family name | Johnson | Q1158485 |
Johnson | Q1158485 | ||
Johnson | Q1158485 | ||
P735 | given name | ??? | Q17501985 |
??? | Q17501985 | ||
P106 | occupation | researcher | Q1650915 |
biochemist | Q2919046 | ||
P21 | sex or gender | male | Q6581097 |
Q27651367 | A conserved face of the Jagged/Serrate DSL domain is involved in Notch trans-activation and cis-inhibition |
Q42043588 | A key centriole assembly interaction interface between human PLK4 and STIL appears to not be conserved in flies |
Q34125630 | A mechanism of release of calreticulin from cells during apoptosis |
Q92217539 | An inhibitor of complement C5 provides structural insights into activation |
Q27675415 | Architecture of the major component of the type III secretion system export apparatus |
Q57843582 | Author Correction: Structure of the core of the type III secretion system export apparatus |
Q101476516 | Author Correction: Structures of the stator complex that drives rotation of the bacterial flagellum |
Q27973510 | Biochemical analysis of the Plasmodium falciparum erythrocyte-binding antigen-175 (EBA175)-glycophorin-A interaction: implications for vaccine design |
Q38202459 | Building a secreting nanomachine: a structural overview of the T3SS. |
Q57843658 | Calreticulin comes of age |
Q40194202 | Characterisation of Shigella Spa33 and Thermotoga FliM/N reveals a new model for C-ring assembly in T3SS. |
Q57843640 | Characterization of soluble complexes of theShigella flexneritype III secretion system ATPase |
Q27671051 | Crystal Structure and Functional Characterization of the Complement Regulator Mannose-binding Lectin (MBL)/Ficolin-associated Protein-1 (MAP-1) |
Q27650631 | Crystal structure of Spa40, the specificity switch for theShigella flexneritype III secretion system |
Q41898025 | Crystal structure of the Bacillus subtilis phosphodiesterase PhoD reveals an iron and calcium-containing active site |
Q27679997 | Crystal structures of the CPAP/STIL complex reveal its role in centriole assembly and human microcephaly |
Q27676318 | Defining a protective epitope on factor H binding protein, a key meningococcal virulence factor and vaccine antigen |
Q27675010 | Design and Evaluation of Meningococcal Vaccines through Structure-Based Modification of Host and Pathogen Molecules |
Q27676814 | Dimerization of complement factor H-related proteins modulates complement activation in vivo |
Q34916886 | Distinct binding and immunogenic properties of the gonococcal homologue of meningococcal factor h binding protein |
Q29302052 | Dry roasting enhances peanut-induced allergic sensitization across mucosal and cutaneous routes in mice |
Q27678414 | ErpC, a member of the complement regulator-acquiring family of surface proteins fromBorrelia burgdorferi, possesses an architecture previously unseen in this protein family |
Q57836585 | Erratum: Corrigendum: Three-dimensional reconstruction of the Shigella T3SS transmembrane regions reveals 12-fold symmetry and novel features throughout |
Q57843665 | Evidence That C1q Binds Specifically to CH2-like Immunoglobulin γ Motifs Present in the Autoantigen Calreticulin and Interferes with Complement Activation† |
Q57843649 | Expression and Purification of Mammalian Calreticulin in Pichia pastoris |
Q35846730 | Expression, limited proteolysis and preliminary crystallographic analysis of IpaD, a component of the Shigella flexneri type III secretion system |
Q43167342 | Expression, purification, cocrystallization and preliminary crystallographic analysis of sucrose octasulfate/human complement regulator factor H SCRs 6-8. |
Q35846733 | Expression, purification, crystallization and preliminary crystallographic analysis of BipD, a component of the Burkholderia pseudomallei type III secretion system |
Q35846725 | Expression, purification, crystallization and preliminary crystallographic analysis of MxiH, a subunit of the Shigella flexneri type III secretion system needle |
Q57843653 | Fine specificity of autoantibodies to calreticulin: epitope mapping and characterization |
Q24657819 | High-resolution structures of bacterially expressed soluble human CD59 |
Q53566059 | Identification of minor inner-membrane components of the Shigella type III secretion system 'needle complex'. |
Q40682669 | Investigating the structure of the factor B vWF-A domain/CD55 protein-protein complex using DEER spectroscopy: successes and pitfalls |
Q38301097 | Mechanism of thiosulfate oxidation in the SoxA family of cysteine-ligated cytochromes |
Q24670035 | Molecular model of a type III secretion system needle: Implications for host-cell sensing |
Q112598798 | Molecular structure of the intact bacterial flagellar basal body |
Q27653843 | Neisseria meningitidis recruits factor H using protein mimicry of host carbohydrates |
Q38328071 | Nonfunctional variant 3 factor H binding proteins as meningococcal vaccine candidates |
Q27681812 | Polymorphisms in the Human Inhibitory Signal-regulatory Protein Do Not Affect Binding to Its Ligand CD47 |
Q26828812 | Putting the structure into complement |
Q35846739 | Self-chaperoning of the type III secretion system needle tip proteins IpaD and BipD. |
Q27972850 | Semaphorin-7A is an erythrocyte receptor for P. falciparum merozoite-specific TRAP homolog, MTRAP |
Q42375349 | SepL resembles an aberrant effector in binding to a class 1 type III secretion chaperone and carrying an N-terminal secretion signal |
Q27665874 | Shigella flexneri Spa15 Crystal Structure Verified in Solution by Double Electron Electron Resonance |
Q42224464 | Structural Basis for Mitotic Centrosome Assembly in Flies |
Q27678091 | Structural Basis for Recognition of the Pore-Forming Toxin Intermedilysin by Human Complement Receptor CD59 |
Q27670706 | Structural and Functional Studies on the N-terminal Domain of the Shigella Type III Secretion Protein MxiG |
Q24676448 | Structural basis for complement factor H linked age-related macular degeneration |
Q24622871 | Structural basis for complement factor I control and its disease-associated sequence polymorphisms |
Q36435139 | Structural basis for specificity and promiscuity in a carrier protein/enzyme system from the sulfur cycle |
Q27704314 | Structural basis for therapeutic inhibition of complement C5 |
Q47098372 | Structural basis of cholesterol binding by a novel clade of dendritic cell modulators from ticks. |
Q112608608 | Structure and mechanism of the proton-driven motor that powers type 9 secretion and gliding motility |
Q27675340 | Structure of the TatC core of the twin-arginine protein transport system |
Q57843586 | Structure of the core of the type III secretion system export apparatus |
Q55403226 | Structure-based design of chimeric antigens for multivalent protein vaccines. |
Q27677459 | Structures of CD200/CD200 Receptor Family and Implications for Topology, Regulation, and Evolution |
Q35943010 | Structures of CD6 and Its Ligand CD166 Give Insight into Their Interaction |
Q89881502 | Structures of SALSA/DMBT1 SRCR domains reveal the conserved ligand-binding mechanism of the ancient SRCR fold |
Q27649946 | Structures of the Shigella flexneri Type 3 Secretion System Protein MxiC Reveal Conformational Variability Amongst Homologues |
Q27671061 | Structures of the rat complement regulator CrrY |
Q99418490 | Structures of the stator complex that drives rotation of the bacterial flagellum |
Q91874790 | Symmetry mismatch in the MS-ring of the bacterial flagellar rotor explains the structural coordination of secretion and rotation |
Q38002809 | Tetartohedral twinning could happen to you too |
Q27644514 | The Structure of OMCI, a Novel Lipocalin Inhibitor of the Complement System |
Q93023860 | The Structure of an Injectisome Export Gate Demonstrates Conservation of Architecture in the Core Export Gate between Flagellar and Virulence Type III Secretion Systems |
Q35127642 | The centrosome-specific phosphorylation of Cnn by Polo/Plk1 drives Cnn scaffold assembly and centrosome maturation. |
Q54049232 | The conformation of calreticulin is influenced by the endoplasmic reticulum luminal environment. |
Q39896038 | The extreme C terminus of Shigella flexneri IpaB is required for regulation of type III secretion, needle tip composition, and binding. |
Q42425294 | The homo-oligomerisation of both Sas-6 and Ana2 is required for efficient centriole assembly in flies |
Q34221174 | The ins and outs of calreticulin: from the ER lumen to the extracellular space. |
Q90207511 | The substrate specificity switch FlhB assembles onto the export gate to regulate type three secretion |
Q36303183 | The type III needle and the damage done |
Q24644829 | Three-dimensional reconstruction of the Shigella T3SS transmembrane regions reveals 12-fold symmetry and novel features throughout |
Q37665331 | Timing is everything: the regulation of type III secretion |
Q55286804 | Virulence Associated Gene 8 of Bordetella pertussis Enhances Contact System Activity by Inhibiting the Regulatory Function of Complement Regulator C1 Inhibitor. |
Q36638746 | What's the point of the type III secretion system needle? |
Q39968674 | With phases: how two wrongs can sometimes make a right |
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