dc.contributor.author | Moore, B. | |
dc.contributor.author | Miles, A.J. | |
dc.contributor.author | Guerra-Giraldez, C. | |
dc.contributor.author | Simpson, P. | |
dc.contributor.author | Iwata, M. | |
dc.contributor.author | Wallace, B.A. | |
dc.contributor.author | Matthews, S.J. | |
dc.contributor.author | Smith, D.F. | |
dc.contributor.author | Brown, K.A. | |
dc.date.accessioned | 2022-01-18T19:26:50Z | |
dc.date.available | 2022-01-18T19:26:50Z | |
dc.date.issued | 2011 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12866/10927 | |
dc.description.abstract | The 57-residue small hydrophilic endoplasmic reticulum-associated protein (SHERP) shows highly specific, stageregulated expression in the non-replicative vector-transmitted stages of the kinetoplastid parasite, Leishmania major, the causative agent of human cutaneous leishmaniasis. Previous studies have demonstrated that SHERP localizes as a peripheral membrane protein on the cytosolic face of the endoplasmic reticulum and on outer mitochondrial membranes, whereas its high copy number suggests a critical function in vivo. However, the absence of defined domains or identifiable orthologues, together with lack of a clear phenotype in transgenic parasites lacking SHERP, has limited functional understanding of this protein. Here, we use a combination of biophysical and biochemical methods to demonstrate that SHERP can be induced to adopt a globular fold in the presence of anionic lipids or SDS. Cross-linking and binding studies suggest that SHERP has the potential to form a complex with the vacuolar type H+-ATPase. Taken together, these results suggest that SHERP may function in modulating cellular processes related to membrane organization and/or acidification during vector transmission of infective Leishmania. | en_US |
dc.language.iso | eng | |
dc.publisher | Elsevier | |
dc.relation.ispartofseries | Journal of Biological Chemistry | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es | |
dc.subject | Controlled Study | en_US |
dc.subject | Unclassified Drug | en_US |
dc.subject | Protein Binding | en_US |
dc.subject | Protozoan Proteins | en_US |
dc.subject | Leishmania | en_US |
dc.subject | Bacterial Strain | en_US |
dc.subject | In-Vivo | en_US |
dc.subject | Protein Analysis | en_US |
dc.subject | Plants (Botany) | en_US |
dc.subject | Protein Function | en_US |
dc.subject | Protein Localization | en_US |
dc.subject | Protein Structure | en_US |
dc.subject | Biochemistry | en_US |
dc.subject | Biological Membranes | en_US |
dc.subject | Causative Agents | en_US |
dc.subject | Cell Membranes | en_US |
dc.subject | Cellular Process | en_US |
dc.subject | Complex Formation | en_US |
dc.subject | Copy Number | en_US |
dc.subject | Critical Functions | en_US |
dc.subject | Cytosolic | en_US |
dc.subject | Endoplasmic Reticulum | en_US |
dc.subject | Kinetoplastida | en_US |
dc.subject | Leishmania Major | en_US |
dc.subject | Membrane Protein | en_US |
dc.subject | Membrane Surface | en_US |
dc.subject | Mitochondrial Membrane | en_US |
dc.subject | Molecular Biology | en_US |
dc.subject | Molecular Recognition | en_US |
dc.subject | Orthologues | en_US |
dc.subject | Outer Mitochondrial Membranes | en_US |
dc.subject | Peripheral Membranes | en_US |
dc.subject | Protein Cross Linking | en_US |
dc.subject | Protein Folding | en_US |
dc.subject | Protein Structure Tertiary | en_US |
dc.subject | Small Hydrophilic Endoplasmic Reticulum Associated Protein | en_US |
dc.subject | Structural Basis | en_US |
dc.subject | Transgenics | en_US |
dc.subject | Vacuolar Proton-Translocating Atpases | en_US |
dc.subject | Vector Transmission | en_US |
dc.title | Structural basis of molecular recognition of the Leishmania Small Hydrophilic Endoplasmic Reticulum-associated Protein (SHERP) at membrane surfaces | en_US |
dc.type | info:eu-repo/semantics/article | |
dc.identifier.doi | https://doi.org/10.1074/jbc.M110.130427 | |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.01.00 | |
dc.relation.issn | 1083-351X |
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