<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Silva MC</submitter><funding>Conselho Nacional de Desenvolvimento Científico e Tecnológico - CNPq</funding><funding>Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPES</funding><funding>Fundação de Amparo à Pesquisa do Estado de Minas Gerais - FAPEMIG</funding><pagination>E223</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4963855</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>8(7)</volume><pubmed_abstract>Tumor necrosis factor (TNF) is a major cytokine in inflammatory processes and its deregulation plays a pivotal role in several diseases. Here, we report that a zinc metalloprotease extracted from Bothrops moojeni venom (BmooMP-alpha-I) inhibits TNF directly by promoting its degradation. This inhibition was demonstrated by both in vitro and in vivo assays, using known TLR ligands. These findings are supported by molecular docking results, which reveal interaction between BmooMP-alpha-I and TNF. The major cluster of interaction between BmooMP-alpha-I and TNF was confirmed by the structural alignment presenting Ligand Root Mean Square Deviation LRMS = 1.05 Å and Interactive Root Mean Square Deviation IRMS = 1.01 Å, this result being compatible with an accurate complex. Additionally, we demons</pubmed_abstract><journal>Toxins</journal><pubmed_title>Interaction between TNF and BmooMP-Alpha-I, a Zinc Metalloprotease Derived from Bothrops moojeni Snake Venom, Promotes Direct Proteolysis of This Cytokine: Molecular Modeling and Docking at a Glance.</pubmed_title><pmcid>PMC4963855</pmcid><funding_grant_id>308183/2009-6</funding_grant_id><funding_grant_id>APQ-00412-09</funding_grant_id><funding_grant_id>AUXPE-PNPD-2314.2009</funding_grant_id><pubmed_authors>Lopes Silva T</pubmed_authors><pubmed_authors>Silva MC</pubmed_authors><pubmed_authors>Mota CM</pubmed_authors><pubmed_authors>Mineo TW</pubmed_authors><pubmed_authors>Oliveira F</pubmed_authors><pubmed_authors>Fonseca KC</pubmed_authors><pubmed_authors>Mineo JR</pubmed_authors><pubmed_authors>Silva MV</pubmed_authors><pubmed_authors>Santiago FM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Interaction between TNF and BmooMP-Alpha-I, a Zinc Metalloprotease Derived from Bothrops moojeni Snake Venom, Promotes Direct Proteolysis of This Cytokine: Molecular Modeling and Docking at a Glance.</name><description>Tumor necrosis factor (TNF) is a major cytokine in inflammatory processes and its deregulation plays a pivotal role in several diseases. Here, we report that a zinc metalloprotease extracted from Bothrops moojeni venom (BmooMP-alpha-I) inhibits TNF directly by promoting its degradation. This inhibition was demonstrated by both in vitro and in vivo assays, using known TLR ligands. These findings are supported by molecular docking results, which reveal interaction between BmooMP-alpha-I and TNF. The major cluster of interaction between BmooMP-alpha-I and TNF was confirmed by the structural alignment presenting Ligand Root Mean Square Deviation LRMS = 1.05 Å and Interactive Root Mean Square Deviation IRMS = 1.01 Å, this result being compatible with an accurate complex. Additionally, we demons</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Jul</publication><modification>2025-04-19T21:51:05.262Z</modification><creation>2019-03-27T02:19:22Z</creation></dates><accession>S-EPMC4963855</accession><cross_references><pubmed>27447669</pubmed><doi>10.3390/toxins8070223</doi></cross_references></HashMap>