About: Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation

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About: Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation Goto Sponge Distinct Permalink

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scientific article published on 01 April 1998

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована у квітні 1998 (uk) article scientifique publié en 1998 (fr) im April 1998 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'abril de 1998 (ast) scientific article published on 01 April 1998 (en)
publication date	wds:Q74457479-C75B85DA-E3F3-4FAB-B9EC-75ACCD4BE0D1
publication date	1998-04-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q74457479-21AA296F-4F2A-457A-A7ED-D32C6B774752
language of work or name	English
author name string	wds:Q74457479-0D031673-7026-4E14-A316-A29E945FD5CF wds:Q74457479-46C54FAD-614A-49D9-980F-91525CD0BF1A wds:Q74457479-E724AF50-5FFD-4CAA-9782-AE61AA54A353
author name string	M J Robins D J Silva V Samano
rdfs:label	Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation (en) Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation (nl)
skos:prefLabel	Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation (en) Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation (nl)
name	Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation (en) Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation (nl)
author	wds:Q74457479-6376138E-424C-46D2-8C6E-0447F604FC74
author	JoAnne Stubbe
title	wds:Q74457479-F7883E3F-1E32-4E84-ADE7-8476501C5853
title	Gemcitabine 5'-triphosphate is a stoichiometric mechanism-based inhibitor of Lactobacillus leichmannii ribonucleoside triphosphate reductase: evidence for thiyl radical-mediated nucleotide radical formation (en)
page(s)	wds:Q74457479-80736390-7CEE-493D-8BF0-392F0F7833FC
page(s)	5528-5535
instance of	wds:Q74457479-36DCB64E-8F0D-4D97-AF0E-049966E810A9
instance of	scholarly article
main subject	wds:Q74457479-9BB494E4-1957-4426-889B-24DF0E3DADAA
main subject	Lactobacillus leichmannii
PubMed ID	wds:Q74457479-677EF730-C865-4824-BE47-AF63453AFC5C
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9548936
PubMed ID	9548936
published in	wds:Q74457479-DA6189B0-D627-41EF-B23F-82A7AF8E7498
published in	Biochemistry
issue	wds:Q74457479-365BD735-5A47-48F2-B957-F06C3F9CB07C
volume	wds:Q74457479-6E5BAF66-71B8-4DE3-A74A-31AB3EA2C5AD
issue	16
volume	37
DOI	wds:Q74457479-7E556EB6-81C6-44C8-A478-2FD506906848
DOI	http://dx.doi.org/10.1021/BI972934E
DOI	10.1021/BI972934E
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74457479
is cites work of	High-field EPR detection of a disulfide radical anion in the reduction of cytidine 5'-diphosphate by the E441Q R1 mutant of Escherichia coli ribonucleotide reductase Insight into the mechanism of inactivation of ribonucleotide reductase by gemcitabine 5'-diphosphate in the presence or absence of reductant Harnessing free radicals: formation and function of the tyrosyl radical in ribonucleotide reductase Enhanced subunit interactions with gemcitabine-5'-diphosphate inhibit ribonucleotide reductases. Inactivation of Lactobacillus leichmannii ribonucleotide reductase by 2',2'-difluoro-2'-deoxycytidine 5'-triphosphate: covalent modification Mechanism of inactivation of human ribonucleotide reductase with p53R2 by gemcitabine 5'-diphosphate Inactivation of Lactobacillus leichmannii ribonucleotide reductase by 2',2'-difluoro-2'-deoxycytidine 5'-triphosphate: adenosylcobalamin destruction and formation of a nucleotide-based radical. Synthesis and characterization of isolable thiolatocobalamin complexes relevant to coenzyme B12-dependent ribonucleoside triphosphate reductase Synthesis and cytostatic evaluation of 4-N-alkanoyl and 4-N-alkyl gemcitabine analogues Inhibition of CHK1 sensitizes Ewing sarcoma cells to the ribonucleotide reductase inhibitor gemcitabine. Ribonucleotide reductase from Pyrococcus furiosus
is cites work of	wds:Q30585705-4BE29922-201D-45FC-AD86-E5333319E354 wds:Q33791851-F4A5D6F7-9F8F-4E43-BAC8-036D8B956008 wds:Q40465500-E20CA56A-7517-4D3B-8034-B16502398681 wds:Q34048376-35136A3B-25BC-4C70-BF01-082593485B37 wds:Q35971682-8EB69143-A114-4254-96CC-A7E1ECD10E34 wds:Q73995678-F3BE0035-900F-49D7-B0F1-ABD6159E1B29 wds:Q34068104-1E4054FC-887D-472C-9269-A0E20806E9E9 wds:Q35591295-23CDFA2A-4007-4997-A057-5E30EDD9EA01 wds:Q42568349-319082D4-2EEA-4934-9261-10A0292D8271 wds:Q47130816-B7F352B0-BACE-43FA-B9BB-BEA5D7325289 wds:Q39042999-63A20136-B729-4369-A281-44821BC06738

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