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Inhibition of recombinant human SRR expressed in Escherichia coli assessed as reduction in conversion of L-serine to D-serine at 0.3 mM incubated for => 8 hrs in presence of PLP and recombinant D-serine dehydratase 1 by spectrophotometry relative to control
Assay data:5 Tested
SummaryRelated BioAssays by Target
Inhibition of recombinant human SRR expressed in Escherichia coli assessed as reduction in conversion of L-serine to D-serine at 0.1 mM incubated for => 8 hrs in presence of PLP and recombinant D-serine dehydratase 1 by spectrophotometry relative to control
Assay data:39 Tested
Inhibition of recombinant human SRR expressed in Escherichia coli assessed as reduction in conversion of L-serine to D-serine at 1 mM incubated for => 8 hrs in presence of PLP and recombinant D-serine dehydratase 1 by spectrophotometry relative to control
Assay data:62 Tested
Inhibition of mouse serine racemase assessed as remaining enzyme activity by measuring D-serine production using L-serine as substrate at 1 mM incubated for > 8 hrs
Assay data:4 Tested
SummaryPubMed CitationRelated BioAssays by Target
Inhibition of serine racemase mutant (unknown origin)
Assay data:1 Tested
Inhibition of wild-type serine racemase (unknown origin) assessed as residual activity by measuring D-serine level using Dsd1 as substrate and PLP as co-factor pretreated for 30 mins followed by substrate and co-factor addition measured after 30 mins
Assay data:2 Tested
Inhibition of wild-type serine racemase (unknown origin) assessed as residual activity by measuring D-serine level at 1 mM using Dsd1 as substrate and PLP as co-factor pretreated for 30 mins followed by substrate and co-factor addition measured after 30 mins relative to control
Assay data:18 Tested
Inhibition of human recombinant serine racemase expressed in Escherichia coli Rosetta 2 (DE3) cells using L-serine as substrate by horseradish peroxidase based couple assay
Inhibition of hexa-His-tagged purified human recombinant serine racemase expressed in Escherichia coli BL21 Codonplus (DE3)-RIL cells assessed as reduction in beta-elimination of L-serine at by spectrophotomtery
Assay data:7 Tested
Inhibition of hexa-His-tagged purified human recombinant serine racemase expressed in Escherichia coli BL21 Codonplus (DE3)-RIL cells assessed as reduction in beta-elimination of L-serine at 330 uM by spectrophotomtery
Inhibition of hexa-His-tagged purified human recombinant serine racemase expressed in Escherichia coli BL21 Codonplus (DE3)-RIL cells assessed as reduction in beta-elimination of L-serine at 1.2 mM by spectrophotomtery
Inhibition of hexa-His-tagged purified human recombinant serine racemase expressed in Escherichia coli BL21 Codonplus (DE3)-RIL cells assessed as reduction in beta-elimination of L-serine at 2.8 mM by spectrophotomtery
Assay data:3 Tested
Inhibition of hexa-His-tagged purified human recombinant serine racemase expressed in Escherichia coli BL21 Codonplus (DE3)-RIL cells assessed as reduction in beta-elimination of L-serine at 5 mM by spectrophotomtery
Binding affinity to serine recemase (unknown origin)
Inhibition of full length human recombinant serine recemase C2DC6D mutant expressed in Escherichia coli BL21 (DE3) assessed as D-serine production at 1 mM after 10 mins by Saccharomyces cerevisiae Dsd1SC based D-serine detection assay
Assay data:38 Tested
Inhibition of full length human recombinant serine recemase C2DC6D mutant expressed in Escherichia coli BL21 (DE3) assessed as D-serine production after 10 mins by Saccharomyces cerevisiae Dsd1SC based D-serine detection assay
Assay data:6 Tested
Inhibition of mouse serine racemase by Lineweaver-Burk plot
Inhibition of mouse serine racemase using L-serine substrate by reversed-phase HPLC analysis
Assay data:10 Tested
Inhibition of human recombinant N-terminal His-tagged serine racemase expressed in Escherichia coli BL21(DE3) using L-serine as substrate after 10 mins by fluorescence assay
Assay data:26 Tested
Inhibition of human recombinant serine racemase assessed as formation of D-serine at 5 mM treated for 15 to 20 mins before addition of substrate by HPLC analysis in presence of increasing concentration of PLP
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