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A Phosphate-Binding Pocket within the Platform-PAZ-Connector Helix Cassette of Human Dicer

DC Field Value Language
dc.contributor.authorTian, Yuan-
dc.contributor.authorSimanshu, Dhirendra K.-
dc.contributor.authorMa, Jin-Biao-
dc.contributor.authorPark, Jong-Eun-
dc.contributor.authorHeo, Inha-
dc.contributor.authorKim, V. Narry-
dc.contributor.authorPatel, Dinshaw J.-
dc.date.accessioned2021-01-31T08:10:34Z-
dc.date.available2021-01-31T08:10:34Z-
dc.date.created2020-07-16-
dc.date.created2020-07-16-
dc.date.created2020-07-16-
dc.date.issued2014-02-
dc.identifier.citationMolecular Cell, Vol.53 No.4, pp.606-616-
dc.identifier.issn1097-2765-
dc.identifier.other107073-
dc.identifier.urihttps://hdl.handle.net/10371/171866-
dc.description.abstractWe have solved two families of crystal structures of the human Dicer "platform-PAZ-connector helix'' cassette in complex with small interfering RNAs (siRNAs). The structures possess two adjacently positioned pockets: a 2 nt 3'-overhang-binding pocket within the PAZ domain (3' pocket) and a phosphate-binding pocket within the platform domain (phosphate pocket). One family of complexes contains a knob-like alpha-helical protrusion, designated "hDicer-specific helix,'' that separates the two pockets and orients the bound siRNA away from the surface of Dicer, which could be indicative of a product release/transfer state. In the second complex, the helical protrusion is melted/disordered and the bound siRNA is aligned toward the surface of Dicer, suggestive of a cleavage-competent state. These structures allow us to propose that the transition from the cleavage-competent to the postulated product release/transfer state may involve release of the 5'-phosphate from the phosphate pocket while retaining the 3' overhang in the 3' pocket.-
dc.language영어-
dc.publisherCell Press-
dc.titleA Phosphate-Binding Pocket within the Platform-PAZ-Connector Helix Cassette of Human Dicer-
dc.typeArticle-
dc.contributor.AlternativeAuthor김빛내리-
dc.identifier.doi10.1016/j.molcel.2014.01.003-
dc.citation.journaltitleMolecular Cell-
dc.identifier.wosid000331660200009-
dc.identifier.scopusid2-s2.0-84894274509-
dc.citation.endpage616-
dc.citation.number4-
dc.citation.startpage606-
dc.citation.volume53-
dc.identifier.sci000331660200009-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, V. Narry-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusDOUBLE-STRANDED-RNA-
dc.subject.keywordPlusCAENORHABDITIS-ELEGANS-
dc.subject.keywordPlusMICROPROCESSOR COMPLEX-
dc.subject.keywordPlusDROSHA-DGCR8 COMPLEX-
dc.subject.keywordPlusPRIMARY MICRORNAS-
dc.subject.keywordPlusSTRUCTURAL BASIS-
dc.subject.keywordPlusC-ELEGANS-
dc.subject.keywordPlusINTERFERENCE-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusRIBONUCLEASE-
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  • College of Natural Sciences
  • School of Biological Sciences
Research Area Molecular Biology & Genetics

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