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Literature summary extracted from

  • Chronopoulou, E.; Madesis, P.; Asimakopoulou, B.; Platis, D.; Tsaftaris, A.; Labrou, N.E.
    Catalytic and structural diversity of the fluazifop-inducible glutathione transferases from Phaseolus vulgaris (2012), Planta, 235, 1253-1269.
    View publication on PubMed

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
2.5.1.18 additional information
-
additional information Michaelis-Menten steady-state kinetics Phaseolus vulgaris

Organism

EC Number Organism UniProt Comment Textmining
2.5.1.18 Phaseolus vulgaris
-
isozymes PvGSTF1-1, PvGSTU2-2 and PvGSTU3-3
-

Purification (Commentary)

EC Number Purification (Comment) Organism
2.5.1.18 native fluazifop-p-butyl-inducible GSTs PvGSTF1-1, PvGSTU2-2 and PvGSTU3-3 from leaves by glutathione affinity chromatography and dialysis Phaseolus vulgaris

Reaction

EC Number Reaction Comment Organism Reaction ID
2.5.1.18 RX + glutathione = HX + R-S-glutathione substrate specificity and catalytic mechanism, overview Phaseolus vulgaris

Source Tissue

EC Number Source Tissue Comment Organism Textmining
2.5.1.18 leaf
-
Phaseolus vulgaris
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2.5.1.18 (2,3-dichloro-4-[2-methylenebutyryl]phenoxy)acetic acid + glutathione i.e. ethacrynic acid Phaseolus vulgaris ?
-
?
2.5.1.18 1-bromo-2,4-dinitrobenzene + glutathione
-
Phaseolus vulgaris S-(2,4-dinitrophenyl)glutathione + HBr
-
?
2.5.1.18 1-chloro-2,4-dinitrobenzene + glutathione
-
Phaseolus vulgaris S-(2,4-dinitrophenyl)glutathione + HCl
-
?
2.5.1.18 1-fluoro-2,4-dinitrobenzene + glutathione
-
Phaseolus vulgaris S-(2,4-dinitrophenyl)glutathione + HF
-
?
2.5.1.18 1-iodo-2,4-dinitrobenzene + glutathione
-
Phaseolus vulgaris S-(2,4-dinitrophenyl)glutathione + HI
-
?
2.5.1.18 2-hydroxyethyl disulfide + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 4-chloro-7-nitrobenzofurazan + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 4-nitrobenzyl chloride + glutathione
-
Phaseolus vulgaris S-(4-nitrobenzyl)glutathione + HCl
-
?
2.5.1.18 alachlor + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 allyl isothiocyanate + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 atrazine + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 bromosulfophthalein + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 dehydroascorbate + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 fluazifop-p-butyl + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 fluorodifen + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 metolachlor + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 additional information fluazifop-inducible glutathione transferase isozymes catalyze a broad range of reactions and exhibit quite varied substrate specificity, molecular modeling and structural analysis reveal key structural characteristics, isozynme substrate specificities and catalytic mechanism, overview. Only PvGSTU2-2 shows appreciable activity towards trans-2-nonenal, but the isozymes are also active with cumene hydroperoxide, tert-butyl hydroperoxide, and lauroyl peroxide, no activity of all isozymes with benzoyl peroxide Phaseolus vulgaris ?
-
?
2.5.1.18 phenethyl isothiocyanate + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 trans-2-nonenal + glutathione
-
Phaseolus vulgaris ?
-
?
2.5.1.18 trans-4-phenyl-3-buten-2-one + glutathione
-
Phaseolus vulgaris ?
-
?

Synonyms

EC Number Synonyms Comment Organism
2.5.1.18 GST
-
Phaseolus vulgaris
2.5.1.18 PvGSTF1-1
-
Phaseolus vulgaris
2.5.1.18 PvGSTU2-2
-
Phaseolus vulgaris
2.5.1.18 PvGSTU3-3
-
Phaseolus vulgaris

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
2.5.1.18 37
-
assay at Phaseolus vulgaris

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
2.5.1.18 7
-
assay at Phaseolus vulgaris

Expression

EC Number Organism Comment Expression
2.5.1.18 Phaseolus vulgaris treatment of Phaseolus vulgaris leaves with the aryloxyphenoxypropionic herbicide fluazifop-p-butyl, i.e. butyl 2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoate, results in induction of three GST isozyme activities, i.e. PvGSTF1-1, PvGSTU2-2 and PvGSTU3-3 up