| human | Q5 |
| P496 | ORCID iD | 0000-0002-4863-0330 |
| P108 | employer | University of Cambridge | Q35794 |
| P734 | family name | Deane | Q26779034 |
| Deane | Q26779034 | ||
| Deane | Q26779034 | ||
| P735 | given name | ??? | Q13553631 |
| ??? | Q13553631 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q28216647 | 1H, 15N and 13C assignments of FLIN4, an intramolecular LMO4:ldb1 complex |
| Q91940625 | Antagonism of PP2A is an independent and conserved function of HIV-1 Vif and causes cell cycle arrest |
| Q27675415 | Architecture of the major component of the type III secretion system export apparatus |
| Q35652295 | Azasugar inhibitors as pharmacological chaperones for Krabbe disease |
| Q40194202 | Characterisation of Shigella Spa33 and Thermotoga FliM/N reveals a new model for C-ring assembly in T3SS. |
| Q37330460 | Competition between LIM-binding domains |
| Q27650631 | Crystal structure of Spa40, the specificity switch for theShigella flexneritype III secretion system |
| Q47742274 | Crystallization of FLINC4, an intramolecular LMO4-ldb1 complex |
| Q74425233 | Design, production and characterization of FLIN2 and FLIN4: the engineering of intramolecular ldb1:LMO complexes |
| Q35846730 | Expression, limited proteolysis and preliminary crystallographic analysis of IpaD, a component of the Shigella flexneri type III secretion system |
| 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 |
| Q27672430 | Insights into Krabbe disease from structures of galactocerebrosidase |
| Q38874171 | Molecular Mechanisms of Disease Pathogenesis Differ in Krabbe Disease Variants |
| Q24670035 | Molecular model of a type III secretion system needle: Implications for host-cell sensing |
| Q92524443 | Molecular models should not be published without the corresponding atomic coordinates |
| Q27653843 | Neisseria meningitidis recruits factor H using protein mimicry of host carbohydrates |
| Q28068142 | New therapeutic approaches for Krabbe disease: The potential of pharmacological chaperones |
| Q35846739 | Self-chaperoning of the type III secretion system needle tip proteins IpaD and BipD. |
| Q42375349 | SepL resembles an aberrant effector in binding to a class 1 type III secretion chaperone and carrying an N-terminal secretion signal |
| Q27670706 | Structural and Functional Studies on the N-terminal Domain of the Shigella Type III Secretion Protein MxiG |
| Q24676096 | Structural basis for the recognition of ldb1 by the N-terminal LIM domains of LMO2 and LMO4 |
| Q24313126 | Structural basis of Vps33A recruitment to the human HOPS complex by Vps16 |
| Q27680741 | Structural snapshots illustrate the catalytic cycle of β-galactocerebrosidase, the defective enzyme in Krabbe disease |
| Q40767844 | Structure of human saposin A at lysosomal pH. |
| Q27649946 | Structures of the Shigella flexneri Type 3 Secretion System Protein MxiC Reveal Conformational Variability Amongst Homologues |
| Q30668579 | TAPBPR alters MHC class I peptide presentation by functioning as a peptide exchange catalyst |
| Q33719590 | TAPBPR bridges UDP-glucose:glycoprotein glucosyltransferase 1 onto MHC class I to provide quality control in the antigen presentation pathway |
| Q60931379 | TAPBPR mediates peptide dissociation from MHC class I using a leucine lever |
| Q40018790 | Tandem LIM domains provide synergistic binding in the LMO4:Ldb1 complex |
| Q39157867 | The Shigella Virulence Factor IcsA Relieves N-WASP Autoinhibition by Displacing the Verprolin Homology/Cofilin/Acidic (VCA) Domain |
| Q30668568 | The binding of TAPBPR and Tapasin to MHC class I is mutually exclusive |
| Q64101666 | The homophilic receptor PTPRK selectively dephosphorylates multiple junctional regulators to promote cell-cell adhesion |
| Q91017318 | The lipid transfer protein Saposin B does not directly bind CD1d for lipid antigen loading |
| Q48263330 | The mechanism of glycosphingolipid degradation revealed by a GALC-SapA complex structure |
| Q96765569 | The receptor PTPRU is a redox sensitive pseudophosphatase |
| Q36303183 | The type III needle and the damage done |
| Q37665331 | Timing is everything: the regulation of type III secretion |
| Q36638746 | What's the point of the type III secretion system needle? |
| Q112305084 | pUL21 is a viral phosphatase adaptor that promotes herpes simplex virus replication and spread |
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