Name: Data for 'Light-Driven, Posttranslation Installation of Reactive Protein Side Chains' Date: 2020-09-23 00:00:00 UTC
Description: C–C side chain alteration within intact proteins has the potential to allow native, chemical, po...
DOI: 10.5287/bodleian:9ewjq268q
Location: https://ora.ox.ac.uk/objects/uuid:2a618e7e-551b-4360-a2de-237453d49a31
Article: Light-driven post-translational installation of reactive protein side chains
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Name: GT-Predict Date: 2018-11-12 00:00:00 UTC
Description: We utilized informatics and machine learning to build predictive software for enzyme functional ...
DOI: 10.5287/bodleian:zg5195kae
Location: https://ora.ox.ac.uk/objects/uuid:1b174bc0-4058-4057-8db4-59872c2b6d99
Article: Functional and informatics analysis enables glycosyltransferase activity prediction
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Name: LanCLs have C-glutathionylation activity with potential to trap the eliminylome Date: 2020-01-01 00:00:00 UTC
Description: Enzyme-mediated damage repair or containment, whilst common for nucleic acids, is rare for prote...
DOI: 10.5287/bodleian:qrn18xodg
Location: https://ora.ox.ac.uk/objects/uuid:d8729aad-ca98-4f06-b14a-0a75ea306584
Article: LanCLs add glutathione to dehydroamino acids generated at phosphorylated sites in the proteome
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Name: Structure of MbQ NMH Date: 2018-01-30 00:00:00 UTC
Description: Structure of MbQ NMH
DOI: 10.2210/pdb5ojb/pdb
Location: http://www.ebi.ac.uk/pdbe-srv/view/entry/5ojb/summary
Article: A Noncanonical Proximal Heme Ligand Affords an Efficient Peroxidase in a Globin Fold
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Name: 1OAF Date: 2020-12-24 00:00:00 UTC
Description: Related Article: Rewiring the “Push-Pull” Catalytic Machinery of a Heme Enzyme Using an Expanded...
DOI:
Location: http://identifiers.org/pdbe/pdb:1OAF
Article: Rewiring the “Push-Pull” Catalytic Machinery of a Heme Enzyme Using an Expanded Genetic Code
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Name: 1ZBY Date: 2020-12-24 00:00:00 UTC
Description: Related Article: Rewiring the “Push-Pull” Catalytic Machinery of a Heme Enzyme Using an Expanded...
DOI:
Location: http://identifiers.org/pdbe/pdb:1ZBY
Article: Rewiring the “Push-Pull” Catalytic Machinery of a Heme Enzyme Using an Expanded Genetic Code
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Name: structure of reductive aminase from neosartorya fumigata in complex with nadp+ Date: 2021-07-13 00:00:00 UTC
Description: Related Article: Asymmetric synthesis of primary amines catalyzed by thermotolerant fungal reduc...
DOI:
Location: http://www.ebi.ac.uk/pdbe-srv/view/entry/6sle/summary
Article: Asymmetric synthesis of primary amines catalyzed by thermotolerant fungal reductive aminases
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Name: structure of reductive aminase from neosartorya fumigata Date: 2021-07-13 00:00:00 UTC
Description: Related Article: Asymmetric synthesis of primary amines catalyzed by thermotolerant fungal reduc...
DOI:
Location: http://www.ebi.ac.uk/pdbe-srv/view/entry/6skx/summary
Article: Asymmetric synthesis of primary amines catalyzed by thermotolerant fungal reductive aminases
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Name: Dataset Underpinning the Southampton Doctoral Thesis "Investigating Nanoscale Catalysts from Primary Growth to Catalytic Activity" Date: 2022-01-01 00:00:00 UTC
Description: Dataset Underpinning the Southampton Doctoral Thesis "Investigating Nanoscale Catalysts from Pri...
DOI: 10.5258/soton/d2092
Location: https://eprints.soton.ac.uk/467645/
Article: Extracting structural information of Au colloids at ultra-dilute concentrations: identification of growth during nanoparticle immobilization
Article: Controlling the Production of Acid Catalyzed Products of Furfural Hydrogenation by Pd/TiO 2
Article: Investigating nanoscale catalysts from primary growth to catalytic activity
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Name: Isolated PdO sites on SiO2-supported NiO nanoparticles as active sites for allylic alcohol selective oxidation Date: 2023-06-07 00:00:00 UTC
Description: Raw data sets that under pin the publication Isolated PdO sites on SiO2-supported NiO nanoparti...
DOI: 10.48420/c.6647102.v1
Location: https://figshare.manchester.ac.uk/collections/Isolated_PdO_sites_on_SiO2-supported_NiO_nanoparticles_as_active_sites_for_allylic_alcohol_selective_oxidation/6647102
Article: Isolated PdO sites on SiO<sub>2</sub>-supported NiO nanoparticles as active sites for allylic alcohol selective oxidation
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