Values CatLog read from this paper

Characterization of disease-related 5beta-reductase (AKR1D1) mutations reveals their potential to cause bile acid deficiency

PMID 20522910doi:10.1074/jbc.m110.127779Open in Browse

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CatLog read 6 records (14 values) from this paper: AKR1D1 from Homo sapiens.

Read from the paper by an AI model and checked against the paper by a second, separate AI run; code converted the units. Values are in CatLog's units; each record opens in Browse with the line the paper prints and the checks.

EC 1.3.1.3

Records read from this paper
EnzymeOrganismSubstratekcat (s⁻¹)Km (mM)kcat/Km (mM⁻¹ s⁻¹)ConditionsOpen record
AKR1D1Homo sapiens17alpha,21-dihydroxypregn-4-ene-3,11,20-trione0.1650.015111Open record: AKR1D1, 17alpha,21-dihydroxypregn-4-ene-3,11,20-trione
AKR1D1Homo sapiens17beta-hydroxyandrost-4-en-3-onefluorimetric assay; saturating NADPH; steroid 0.60-40 µM0.1180.002743.8Open record: AKR1D1, 17beta-hydroxyandrost-4-en-3-one
AKR1D1Homo sapiens17beta-hydroxyandrost-4-en-3-oneintact transfected HEK 293 cells in DMEM; untagged—0.004—Open record: AKR1D1, 17beta-hydroxyandrost-4-en-3-one
AKR1D1Homo sapiens7alpha-hydroxycholest-4-en-3-one—8 × 10⁻⁴—Open record: AKR1D1, 7alpha-hydroxycholest-4-en-3-one
AKR1D1variant P133RHomo sapiens17alpha,21-dihydroxypregn-4-ene-3,11,20-trione0.010.00137.7Open record: AKR1D1 variant P133R, 17alpha,21-dihydroxypregn-4-ene-3,11,20-trione
AKR1D1variant P133RHomo sapiens17beta-hydroxyandrost-4-en-3-one0.0450.01273.5Open record: AKR1D1 variant P133R, 17beta-hydroxyandrost-4-en-3-one