| human | Q5 |
| P856 | official website | https://www.imperial.ac.uk/people/d.mavridou |
| P496 | ORCID iD | 0000-0002-7449-1151 |
| P108 | employer | University of Texas at Austin | Q49213 |
| Imperial College London | Q189022 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q93539199 | -Type cytochrome biogenesis can occur via a natural Ccm system lacking CcmH, CcmG, and the heme-binding histidine of CcmE |
| Q42027426 | 1H, 13C and 15N resonance assignments for the oxidized and reduced states of the N-terminal domain of DsbD from Escherichia coli |
| Q40732482 | A pivotal heme-transfer reaction intermediate in cytochrome c biogenesis |
| Q54440365 | Active-site properties of the oxidized and reduced C-terminal domain of DsbD obtained by NMR spectroscopy. |
| Q27681479 | An Extended Active-site Motif Controls the Reactivity of the Thioredoxin Fold |
| Q44401102 | Avoidance of the cytochrome c biogenesis system by periplasmic CXXCH motifs. |
| Q50207579 | Bacteria Use Collective Behavior to Generate Diverse Combat Strategies |
| Q115702735 | Colistin resistance in Escherichia coli confers protection of the cytoplasmic but not outer membrane from the polymyxin antibiotic |
| Q42757366 | Control of periplasmic interdomain thiol:disulfide exchange in the transmembrane oxidoreductase DsbD. |
| Q64990140 | Costs and benefits of provocation in bacterial warfare. |
| Q34323819 | Cytochrome c assembly. |
| Q37940545 | Cytochrome c biogenesis System I. |
| Q90616530 | Detection of Colistin Resistance in Escherichia coli by Use of the MALDI Biotyper Sirius Mass Spectrometry System |
| Q36606851 | Divergence of Erv1-associated mitochondrial import and export pathways in trypanosomes and anaerobic protists |
| Q112730162 | Identification of Tse8 as a Type VI secretion system toxin from Pseudomonas aeruginosa that targets the bacterial transamidosome to inhibit protein synthesis in prey cells |
| Q48592773 | Lifestyle transitions and adaptive pathogenesis of Pseudomonas aeruginosa. |
| Q92969222 | Making the Best of Aggression: The Many Dimensions of Bacterial Toxin Regulation |
| Q33571987 | Novel polycarboxylated EDTA-type cyclodextrins as ligands for lanthanide binding: study of their luminescence, relaxivity properties of Gd(iii) complexes, and PM3 theoretical calculations |
| Q27667688 | Oxidation State-dependent Protein-Protein Interactions in Disulfide Cascades |
| Q57972024 | Plasma membrane profiling during enterohemorrhagic E. coli infection reveals that the metalloprotease StcE cleaves CD55 from host epithelial surfaces |
| Q33356546 | Probing heme delivery processes in cytochrome c biogenesis System I. |
| Q59275382 | Rapid detection and discrimination of chromosome- and MCR-plasmid-mediated resistance to polymyxins by MALDI-TOF MS in Escherichia coli: the MALDIxin test |
| Q112597236 | Staphylococcal DNA Repair Is Required for Infection |
| Q112305667 | The Breadth and Molecular Basis of Hcp-Driven Type VI Secretion System Effector Delivery |
| Q57889649 | The CcmC–CcmE interaction during cytochrome c maturation by System I is driven by protein–protein and not protein–heme contacts |
| Q37565590 | The Paracoccus denitrificans NarK-like nitrate and nitrite transporters-probing nitrate uptake and nitrate/nitrite exchange mechanisms |
| Q64996315 | The Pseudomonas aeruginosa T6SS-VgrG1b spike is topped by a PAAR protein eliciting DNA damage to bacterial competitors. |
| Q91763039 | The clue is in the lipid A: Rapid detection of colistin resistance |
| Q50071867 | The heme auxotroph Caenorhabditis elegans can cleave the thioether bonds of c-type cytochromes. |
| Q41767891 | The interplay between the disulfide bond formation pathway and cytochrome c maturation in Escherichia coli |
| Q40520160 | The pUltra plasmid series: A robust and flexible tool for fluorescent labeling of Enterobacteria. |
| Q28596486 | The uronic acid content of coccolith-associated polysaccharides provides insight into coccolithogenesis and past climate |
| Q34295902 | Vital dye reaction and granule localization in periplasm of Escherichia coli |
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