About: Finian J. Leeper

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) researcher (en) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) эрдэмтэн (mn) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy)
rdfs:label	Finian J. Leeper (en) Finian J. Leeper (es) Finian J. Leeper (nl) Finian J. Leeper (tr) Finian J. Leeper (ast)
skos:prefLabel	Finian J. Leeper (en) Finian J. Leeper (es) Finian J. Leeper (nl) Finian J. Leeper (tr) Finian J. Leeper (ast)
name	Finian J. Leeper (en) Finian J. Leeper (es) Finian J. Leeper (nl) Finian J. Leeper (tr) Finian J. Leeper (ast)
instance of	wds:Q56526538-63C50E48-388A-49F2-8723-3C1355EDBBF1
instance of	Homo sapiens
skos:altLabel	Finian Leeper (en)
occupation	wds:Q56526538-37CEB90C-68F7-421D-B31F-C627A25DC027
employer	wds:Q56526538-0AB161D5-DC08-43D3-93F0-C9758043236A
NUKAT ID	wds:Q56526538-9FE381CC-3679-417E-90B0-02611388877E
ISNI	wds:Q56526538-B68049F2-4859-49EB-B84C-799A8D3403D9
VIAF ID	wds:Q56526538-95D88B86-C9B5-47BB-97A3-BB3990A174B2
GND ID	wds:Q56526538-843ffd5e-30a5-4852-bf2b-fdb66962f13f
Bibliothèque nationale de France ID	wds:Q56526538-A76FF8AE-EE01-4F0D-A345-0D751B214B74
IdRef ID	wds:Q56526538-E6DAF41B-56AB-4B0E-963E-780211C0648B
educated at	wds:Q56526538-79B34544-1BEC-4046-BD24-EAB94811C81C
family name	wds:Q56526538-D50AACBE-969A-43E4-90C3-37ADE0B2F594
National Library of Israel J9U ID	wds:Q56526538-845EC989-4E29-42DE-BB75-1E8F3D88F581
VIAF ID	http://viaf.org/viaf/29687979
GND ID	https://d-nb.info/gnd/1158407548
Bibliothèque nationale de France ID	http://data.bnf.fr/ark:/12148/cb13498733z#about
IdRef ID	http://www.idref.fr/05049919X/id
occupation	researcher
employer	John Ffowcs Williams
NUKAT ID	n98010198
ISNI	0000000117545275
VIAF ID	29687979
GND ID	1158407548
Bibliothèque nationale de France ID	13498733z
IdRef ID	05049919X
educated at	John Ffowcs Williams
family name	Leeper
National Library of Israel J9U ID	987007433689205171
ORCID iD	wds:Q56526538-63A48379-1C9A-4BFF-9BD7-BA489153AE93
ORCID iD	https://orcid.org/0000-0003-3408-5199
ORCID iD	0000-0003-3408-5199
Gateway to Research person ID	wds:Q56526538-22C5FCDA-738F-43B0-8502-C93CF9C067FA
Gateway to Research person ID	E8243343-A854-436F-AEFB-4C7D9D57A278
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56526538
is author of	Editorial: Vitamins and cofactors—chemistry, biochemistry and biology Crystallographic snapshots of oxalyl-CoA decarboxylase give insights into catalysis by nonoxidative ThDP-dependent decarboxylases The Serratia gene cluster encoding biosynthesis of the red antibiotic, prodigiosin, shows species- and strain-dependent genome context variation Disruption of the copper efflux pump (CopA) of Serratia marcescens ATCC 274 pleiotropically affects copper sensitivity and production of the tripyrrole secondary metabolite, prodigiosin. Imaging sialylated tumor cell glycans in vivo. Biosynthesis of the red antibiotic, prodigiosin, in Serratia: identification of a novel 2-methyl-3-n-amyl-pyrrole (MAP) assembly pathway, definition of the terminal condensing enzyme, and implications for undecylprodigiosin biosynthesis in Streptomy In vivo trapping of polyketide intermediates from an assembly line synthase using malonyl carba(dethia)-N-acetyl cysteamines. The biosynthesis of porphyrins, chlorophylls, and vitamin B12 Modification of hydroxymethylbilane synthase (porphobilinogen deaminase) by pyridoxal 5'-phosphate. Demonstration of an essential lysine residue The role of His113 and His114 in pyruvate decarboxylase from Zymomonas mobilis. Bacterial biosynthetic gene clusters encoding the anti-cancer haterumalide class of molecules: biogenesis of the broad spectrum antifungal and anti-oomycete compound, oocydin A. Biosynthesis of the antifungal haterumalide, oocydin A, in Serratia, and its regulation by quorum sensing, RpoS and Hfq. (E,E)-1,5-Cyclooctadiene: a small and fast click-chemistry multitalent Anticancer and immunosuppressive properties of bacterial prodiginines The evidence for a spirocyclic intermediate in the formation of uroporphyrinogen III by cosynthase Dual-sugar imaging using isonitrile and azido-based click chemistries Development and evaluation of new cyclooctynes for cell surface glycan imaging in cancer cells. Synthesis and biological evaluation of pyrophosphate mimics of thiamine pyrophosphate based on a triazole scaffold. Imaging Glycosylation In Vivo by Metabolic Labeling and Magnetic Resonance Imaging α-Hydroxy-β-keto acid rearrangement-decarboxylation: impact on thiamine diphosphate-dependent enzymatic transformations. Asymmetric Stetter reactions catalyzed by thiamine diphosphate-dependent enzymes Thiamin diphosphate in biological chemistry: analogues of thiamin diphosphate in studies of enzymes and riboswitches. Validation of a homology model of Mycobacterium tuberculosis DXS: rationalization of observed activities of thiamine derivatives as potent inhibitors of two orthologues of DXS. Biosynthesis of porphyrins and related macrocycles. Part 40. Synthesis of a spiro-lactam related to the proposed spiro-intermediate for porphyrin biosynthesis: inhibition of cosynthetase A fragment-based approach to identifying ligands for riboswitches Fragment screening against the thiamine pyrophosphate riboswitchthiM Dissecting Bottromycin Biosynthesis Using Comparative Untargeted Metabolomics Structure of the Fundamental Lipopeptide Surfactin at the Air/Water Interface Investigated by Sum Frequency Generation Spectroscopy. Snapshots of Catalysis in the E1 Subunit of the Pyruvate Dehydrogenase Multienzyme Complex Molecular mechanism of allosteric substrate activation in a thiamine diphosphate-dependent decarboxylase Structure of the branched-chain keto acid decarboxylase (KdcA) from Lactococcus lactis provides insights into the structural basis for the chemoselective and enantioselective carboligation reaction Identification of novel ligands for thiamine pyrophosphate (TPP) riboswitches Biosynthesis of the polyketide antibiotic ICI139603 in Streptomyces longisporoflavus: assignment of the 13C n.m.r. spectrum by two-dimensional methods, and determination of the origin of the carbon atoms Exploring isonitrile-based click chemistry for ligation with biomolecules. Imaging Glycosylation In Vivo by Metabolic Labeling and Magnetic Resonance Imaging. Gold(I)-catalysed synthesis of a furan analogue of thiamine pyrophosphate.

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