1 Ocak 2020 Dergi makalesi Açık Erişim

Polatoglu, Ilker; Karatas, Deniz

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  <identifier identifierType="URL">https://aperta.ulakbim.gov.tr/record/4015</identifier>
  <creators>
    <creator>
      <creatorName>Polatoglu, Ilker</creatorName>
      <givenName>Ilker</givenName>
      <familyName>Polatoglu</familyName>
      <affiliation>Manisa Celal Bayar Univ, Bioengn Dept, TR-45140 Yunusemre, Manisa, Turkey</affiliation>
    </creator>
    <creator>
      <creatorName>Karatas, Deniz</creatorName>
      <givenName>Deniz</givenName>
      <familyName>Karatas</familyName>
      <affiliation>Istanbul Tech Univ, Mineral Proc Engn Dept, TR-34469 Istanbul, Turkey</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Modeling Of Molecular Interaction Between Catechol And Tyrosinase By Dft</title>
  </titles>
  <publisher>Aperta</publisher>
  <publicationYear>2020</publicationYear>
  <dates>
    <date dateType="Issued">2020-01-01</date>
  </dates>
  <resourceType resourceTypeGeneral="Text">Journal article</resourceType>
  <alternateIdentifiers>
    <alternateIdentifier alternateIdentifierType="url">https://aperta.ulakbim.gov.tr/record/4015</alternateIdentifier>
  </alternateIdentifiers>
  <relatedIdentifiers>
    <relatedIdentifier relatedIdentifierType="DOI" relationType="IsIdenticalTo">10.1016/j.molstruc.2019.127192</relatedIdentifier>
  </relatedIdentifiers>
  <rightsList>
    <rights rightsURI="http://www.opendefinition.org/licenses/cc-by">Creative Commons Attribution</rights>
    <rights rightsURI="info:eu-repo/semantics/openAccess">Open Access</rights>
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  <descriptions>
    <description descriptionType="Abstract">In this study, the synthetic active site model of tyrosinase enzyme's "(His(3))(CuOHCu)-O-center dot center dot-Cu-center dot center dot(His(3)) arrangement" is constituted by applying the density functional theory (DFT) to reveal the enzymatic conversion of catechol in molecular basis. This is the first time the binding mechanisms of catechol in relation to the enzyme active site (met-tyrosinase) in a vacuum environment, explicit water, and solvent (ethanol, acetone)/water mixture have been studied using the DFT. The theoretical results are supported along with the experimental ones to clarify the structure-activity relationship in these models. As understood from the mechanisms, the initial H abstraction from catechol is the most probable rate-limiting step. The parameters that cause the copper region to become congested or comfortable for H abstraction, such as the ordered structure of water molecules, Cu-Cu distance, H-bond distance, orientation and conformation of histidine residues around the copper center, and electrostatic potential of the system, play a significant role in the catechol/met-tyrosinase interaction. (C) 2019 Elsevier B.V. All rights reserved.</description>
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