Abstract
We provide detailed datasets from our analysis of proteins that are identified in human liver, lung, kidney and intestine microsomes by MS-based proteomics. Also included is a set of CYP450 enzymes and microsomal glutathione-S-transferase (MGSTs) activities in human liver microsomes. The data presented in this paper support the research article “Targeted label-free approach for quantification of epoxide hydrolase and glutathione transferases in microsomes” (Song et al., 2015) [1]. We expect that the data will contribute to the study of metabolism enzymes.
Highlights
We provide detailed datasets from our analysis of proteins that are identified in human liver, lung, kidney and intestine microsomes by MS-based proteomics
Biology Proteomics, biology Text file, Table UPLC was used for enzyme activities assay, Nano-LC-MS/MS identification of proteins
A) The difference of liver enzyme activities related age or gender. b) The different metabolism enzymes identified in human liver, lung, kidney and intestine microsomes
Summary
Dataset from proteomic analysis of human liver, lung, kidney and intestine microsomes. We provide detailed datasets from our analysis of proteins that are identified in human liver, lung, kidney and intestine microsomes by MS-based proteomics. Included is a set of CYP450 enzymes and microsomal glutathione-S-transferase (MGSTs) activities in human liver microsomes. The data presented in this paper support the research article “Targeted label-free approach for quantification of epoxide hydrolase and glutathione transferases in microsomes” (Song et al, 2015) [1]. We expect that the data will contribute to the study of metabolism enzymes.
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