<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Baroni, Renata Moro</dc:creator>
  <dc:creator>Luo, Zhipu</dc:creator>
  <dc:creator>Darwiche, Rabih</dc:creator>
  <dc:creator>Hudspeth, Elissa M.</dc:creator>
  <dc:creator>Schneiter, Roger</dc:creator>
  <dc:creator>Pereira, Gonçalo A. G.</dc:creator>
  <dc:creator>Mondego, Jorge M. C.</dc:creator>
  <dc:creator>Asojo, Oluwatoyin A.</dc:creator>
  <dc:date>2017-08-10</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The pathogenic fungi Moniliophthora perniciosa causes Witches’ Broom Disease  (WBD) of cacao. The structure of MpPR-1i, a protein expressed by M. perniciosa  when it infects cacao, are presented. This is the first reported de novo structure  determined by single-wavelength anomalous dispersion phasing upon soaking with  selenourea. Each monomer has flexible loop regions linking the core alpha-beta-alpha  sandwich topology that comprise ~50% of the structure, making it difficult to generate  an accurate homology model of the protein. MpPR-1i is monomeric in solution but is  packed as a high ~70% solvent content, crystallographic heptamer. The greatest  conformational flexibility between monomers is found in loops exposed to the solvent  channel that connect the two longest strands. MpPR-1i lacks the conserved CAP  tetrad and is incapable of binding divalent cations. MpPR-1i has the ability to bind  lipids, which may have roles in its infection of cacao. These lipids likely bind in the  palmitate binding cavity as observed in tablysin-15, since MpPR-1i binds palmitate  with comparable affinity as tablysin-15. Further studies are required to clarify the  possible roles and underlying mechanisms of neutral lipid binding, as well as their  effects on the pathogenesis of M. perniciosa so as to develop new interventions for  WBD.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/306073</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306073/files/sch_csm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/306073/files/sch_cm_sm.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1038/s41598-017-07887-1</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>Scientific Reports. - 2017, vol. 7, no. 1, p. 7818</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Crystal structure of MpPR-1i, a SCP/TAPS protein from Moniliophthora perniciosa , the fungus that causes witches’ broom disease of cacao</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
