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Inhibition of PHGDH D175A mutant (unknown origin) preincubated for 30 mins followed by substrate addition and measured after 5 mins
Assay data:2 Tested
SummaryRelated BioAssays by Target
Inhibition of wild type PHGDH (unknown origin) preincubated for 30 mins followed by substrate addition and measured after 5 mins
Assay data:2 Active, 1 Activity ≤ 1 µM, 2 Tested
Binding affinity to his-tagged PHGDH (127 to 722 residues) (unknown origin) assessed as dissociation constant by SPR analysis
Assay data:1 Active, 1 Tested
Binding affinity to PHGDH (unknown origin) assessed as dissociation constant incubated for 60 mins by microscale thermophoresis analysis
Competitive inhibition of PHGDH (unknown origin) at 100 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Assay data:1 Tested
Non-competitive inhibition of PHGDH (unknown origin) 6.3 uM using 3-PG as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Non-competitive inhibition of PHGDH (unknown origin) 12.5 uM using 3-PG as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Non-competitive inhibition of PHGDH (unknown origin) 25 uM using 3-PG as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Non-competitive inhibition of PHGDH (unknown origin) assessed as Km at 6.3 uM using 3-PG as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Non-competitive inhibition of PHGDH (unknown origin) assessed as Km at 12.5 uM using 3-PG as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Non-competitive inhibition of PHGDH (unknown origin) assessed as Km at 25 uM using 3-PG as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) assessed as Km at 3.1 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) assessed as Km at 6.3 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) assessed as Km at 12.5 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) assessed as Km at 25 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) at 3.1 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) at 6.3 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) at 12.5 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) at 25 uM using NAD+ as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
Competitive inhibition of PHGDH (unknown origin) assessed as inhibition constant using 3-PG as substrate preincubated for 30 mins followed by substrate addition and measured after 5 mins by Lineweaver-Burk plot analysis
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