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MIBiG 3.0: a community-driven effort to annotate experimentally validated biosynthetic gene clusters.

Barbara R TerlouwKai BlinJorge C Navarro-MuñozNicole E AvalonMarc G ChevretteSusan EgbertSanghoon LeeDavid MeijerMichael J J RecchiaZachary L ReitzJeffrey A van SantenNelly Selem-MojicaThomas TørringLiana ZaroubiMohammad AlanjaryGajender AletiCésar AguilarSuhad A A Al-SalihiHannah E AugustijnJ Abraham Avelar-RivasLuis A Avitia-DomínguezFrancisco Barona-GómezJordan Bernaldo-AgüeroVincent A BielinskiFriederike BiermannThomas J BoothVíctor J CarriónRaquel Castelo-BrancoFernanda Oliveira ChagasPablo Cruz-MoralesChao DuKatherine R DuncanAthina GavrilidouDamien GayrardFrancisco Barona-GómezKristina HaslingerEric J N HelfrichJustin Johan Jozias van der HooftAfif P JatiEdward KalkreuterNikolaos KalyvasKyo-Bin KangSatria A KautsarWonyong KimAditya M KunjapurYong-Xin LiGeng-Min LinCatarina LoureiroJoris J R LouwenNico L L LouwenGeorge LundJonathan ParraBenjamin PhilmusBita PourmohseninLotte J U PronkAdriana RegoDevasahayam Arokiar Balaya RexSerina L RobinsonL Rodrigo Rosas-BecerraEve T RoxboroughMichelle A SchornDarren J ScobieKumar Saurabh SinghNika SokolovaXiaoyu TangDaniel W UdwaryAruna VigneshwariKristiina VindSophie P J M VromansValentin WaschulinSam E WilliamsJaclyn M WinterThomas E WitteHuali XieDong YangJingwei YuMitja M ZdoucZheng ZhongJérôme CollemareRoger G LiningtonTilmann WeberMarnix H Medema
Published in: Nucleic acids research (2022)
With an ever-increasing amount of (meta)genomic data being deposited in sequence databases, (meta)genome mining for natural product biosynthetic pathways occupies a critical role in the discovery of novel pharmaceutical drugs, crop protection agents and biomaterials. The genes that encode these pathways are often organised into biosynthetic gene clusters (BGCs). In 2015, we defined the Minimum Information about a Biosynthetic Gene cluster (MIBiG): a standardised data format that describes the minimally required information to uniquely characterise a BGC. We simultaneously constructed an accompanying online database of BGCs, which has since been widely used by the community as a reference dataset for BGCs and was expanded to 2021 entries in 2019 (MIBiG 2.0). Here, we describe MIBiG 3.0, a database update comprising large-scale validation and re-annotation of existing entries and 661 new entries. Particular attention was paid to the annotation of compound structures and biological activities, as well as protein domain selectivities. Together, these new features keep the database up-to-date, and will provide new opportunities for the scientific community to use its freely available data, e.g. for the training of new machine learning models to predict sequence-structure-function relationships for diverse natural products. MIBiG 3.0 is accessible online at https://mibig.secondarymetabolites.org/.
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