PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 34052343-2 2021 In the present study, we hypothesized that glutathionylation would fulfill a similar role for the O2 -/H2O2 sources sn-glycerol-3-phosphate dehydrogenase (G3PDH), proline dehydrogenase (PRODH), and branched chain keto acid dehydrogenase (BCKDH). Hydrogen Peroxide 103-107 proline dehydrogenase 1 Homo sapiens 186-191 18430561-3 2008 POX catalyzes the degradation of pyruvate to acetylphosphate, CO(2) and H(2)O(2) in the presence of phosphate and oxygen. Hydrogen Peroxide 72-80 proline dehydrogenase 1 Homo sapiens 0-3 15817612-11 2005 Compared with control cells, MnSOD-expressing DLD-1 POX cells generated a higher concentration of H2O2 owing to dismutation of superoxide radicals, which was elevated by POX. Hydrogen Peroxide 98-102 proline dehydrogenase 1 Homo sapiens 52-55 15817612-11 2005 Compared with control cells, MnSOD-expressing DLD-1 POX cells generated a higher concentration of H2O2 owing to dismutation of superoxide radicals, which was elevated by POX. Hydrogen Peroxide 98-102 proline dehydrogenase 1 Homo sapiens 170-173 33679014-6 2021 H2O2 treatment also protected the sensitive cultivars from drought stress by increasing CAT, POX, APX, MDHAR and GR enzymes. Hydrogen Peroxide 0-4 proline dehydrogenase 1 Homo sapiens 93-96 32200704-8 2020 Our results demonstrate that ABA-induced intracellular H2O2 accumulation triggers NO production leading stomatal closure.Abbreviations: ABA: abscisic acid; CAT: catalase; cGMP: cyclic guanosine monophosphate; DAF-2DA: 4,5-diaminofluorescein-2 diacetate; H2DCF-DA: 2",7"-dichlorodihydrofluorescein diacetate; MeJA: methyljasmonate; NOS: nitric oxide synthetase; NR: nitrate reductase; POX: peroxidase; ROS: reactive oxygen species; SNAP: S-nitroso-N-acetyl-DL-penicillamine; SNP: sodium nitroprusside; NOX: NADP(H) oxidase. Hydrogen Peroxide 55-59 proline dehydrogenase 1 Homo sapiens 385-388 25184115-9 2014 Even with combinations of substrates and respiratory chain inhibitors designed to minimize the contributions of other sites and maximize any superoxide/H2O2 production from proline dehydrogenase itself, there was no significant direct contribution of proline dehydrogenase to the observed H2O2 production. Hydrogen Peroxide 152-156 proline dehydrogenase 1 Homo sapiens 173-194 31821902-2 2020 POx oxidizes several monosaccharides including D-glucose, D-galactose, and D-xylose, while concurrently oxygen is reduced to hydrogen peroxide. Hydrogen Peroxide 125-142 proline dehydrogenase 1 Homo sapiens 0-3 26147088-13 2015 The NFs with POX showed a loss of structural integrity in the presence of hydrogen peroxide as seen using SEM. Hydrogen Peroxide 74-91 proline dehydrogenase 1 Homo sapiens 13-16 26147088-15 2015 We anticipate that nanofibrous PVA/POX can potentially be used to target numerous inflammatory diseases that overproduce hydrogen peroxide and may become a potential candidate for use as a local drug delivery vehicle. Hydrogen Peroxide 121-138 proline dehydrogenase 1 Homo sapiens 35-38 25184115-10 2014 Thus proline oxidation by proline dehydrogenase drives superoxide/H2O2 production, but it does so mainly or exclusively by providing anaplerotic carbon for other mitochondrial dehydrogenases and not by producing superoxide/H2O2 directly. Hydrogen Peroxide 66-70 proline dehydrogenase 1 Homo sapiens 26-47 22796327-0 2012 Proline dehydrogenase is essential for proline protection against hydrogen peroxide-induced cell death. Hydrogen Peroxide 66-83 proline dehydrogenase 1 Homo sapiens 0-21 22796327-12 2012 Knockdown of PRODH in PC3 cells attenuated phosphorylated levels of Akt and FoxO3a and decreased cell survival during hydrogen peroxide stress. Hydrogen Peroxide 118-135 proline dehydrogenase 1 Homo sapiens 13-18 22796327-13 2012 The results provide evidence that PRODH is essential in proline protection against hydrogen peroxide-mediated cell death and that proline/PRODH helps activate Akt in cancer cells. Hydrogen Peroxide 83-100 proline dehydrogenase 1 Homo sapiens 34-39