Promiscuous scaffolds in proteins - non-native, non-additive and non-trivial

dc.contributorHáskóli Íslandsen_US
dc.contributorUniversity of Icelanden_US
dc.contributor.authorChakraborty, Sandeep
dc.contributor.authorÁsgeirsson, Bjarni
dc.contributor.authorDutta, Mouparna
dc.contributor.authorGhosh, Anindya S.
dc.contributor.authorOda, Masataka
dc.contributor.authorRendón, Adela
dc.contributor.authorGoñi, Felix
dc.contributor.authorFrere, Jean-Marie
dc.contributor.authorVenkatramani, Ravindra
dc.contributor.authorDandekar, Abhaya M.
dc.contributor.authorRao, Basuthkar J.
dc.contributor.departmentRaunvísindadeild (HÍ)en_US
dc.contributor.departmentFaculty of Physical Sciences (UI)en_US
dc.contributor.departmentRaunvísindastofnun (HÍ)en_US
dc.contributor.departmentScience Institute (UI)en_US
dc.contributor.schoolVerkfræði- og náttúruvísindasvið (HÍ)en_US
dc.contributor.schoolSchool of Engineering and Natural Sciences (UI)en_US
dc.date.accessioned2020-08-25T10:39:38Z
dc.date.available2020-08-25T10:39:38Z
dc.date.issued2014-01-20
dc.descriptionPublisher's version (útgefin grein)en_US
dc.description.abstractPromiscuity, the ability of an enzyme to catalyze diverse activities using the same active site, sets up the stage for the evolution of complex organisms through gene duplication and specialization. The detection of promiscuous motifs is crucial to understand the physiological relevance of a protein, or for any endeavor that intends to rationally modify these latent capabilities to design new proteins under laboratory conditions. We have established a methodology for identifying catalytic residues based on spatial and electrostatic congruence with known active site configurations. Here, we discuss insights gained in several initiatives using our method on different enzymes.en_US
dc.description.sponsorshipIcelandic reasearch fund (RANNÍS) No. 141619en_US
dc.description.versionPeer revieweden_US
dc.identifier.citationChakraborty S, Asgeirsson B, Dutta M et al. Promiscuous scaffolds in proteins - non-native, non-additive and non-trivial [version 2; peer review: 1 approved with reservations, 2 not approved]. F1000Research 2014, 2:260 (https://doi.org/10.12688/f1000research.2-260.v2)en_US
dc.identifier.doi10.12688/f1000research.2-260.v2
dc.identifier.issn2046-1402
dc.identifier.journalF1000Researchen_US
dc.identifier.urihttps://hdl.handle.net/20.500.11815/2016
dc.language.isoenen_US
dc.publisherF1000Researchen_US
dc.relation.ispartofseriesF1000Research;2(260)
dc.relation.urlhttps://f1000research.com/articles/2-260en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titlePromiscuous scaffolds in proteins - non-native, non-additive and non-trivialen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dcterms.license© 2014 Chakraborty S et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US

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