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CatecholsManganeseCatechol 2,3-DioxygenaseDioxygenasesCatechol 1,2-DioxygenaseOxygenasesEstrogens, CatecholManganese PoisoningManganese Compounds4-Hydroxyphenylpyruvate DioxygenaseProtocatechuate-3,4-DioxygenaseCysteine DioxygenaseTryptophan OxygenaseCatechol O-MethyltransferaseHomogentisate 1,2-Dioxygenase3-Hydroxyanthranilate 3,4-DioxygenasePseudomonasBiodegradation, EnvironmentalKynureninePseudomonas putidaHydroxybenzoatesRhodococcusPhenolChlorobenzenesTryptophanMolecular Sequence DataSorbic AcidCatechol OxidaseTolueneChlorobenzoatesSuperoxide DismutaseIronSubstrate SpecificityBenzoatesOxidation-ReductionMixed Function OxygenasesSphingomonasBurkholderiaAmino Acid SequenceKineticsBenzoic AcidGentisatesGenes, BacterialAlcaligenesBenzeneAdipatesEquileninComamonasBrevibacteriumHomogentisic AcidEscherichia coliAcinetobacterCloning, MolecularPhenolsPyrogallolBacterial ProteinsHydrocarbons, AromaticElectron Spin Resonance SpectroscopyHydroquinonesHydroxylationFerrous CompoundsRalstoniaBase SequencePlanococcus BacteriaOxygenParabensArthrobacterCatalysisModels, MolecularEnzyme InductionChromatography, High Pressure LiquidSequence Homology, Amino AcidPolychlorinated BiphenylsCresolsGram-Negative Aerobic Rods and CocciSpectrophotometryFerredoxinsMetalsBurkholderiaceae3-Hydroxyanthranilic Acidgamma-Butyrobetaine DioxygenaseBinding SitesAlkaptonuriaKetoglutaric AcidsBiphenyl CompoundsSalicylatesXylenesCrystallography, X-RayHydrogen-Ion ConcentrationRecombinant ProteinsPeroxidasesOxidoreductasesCopperMolecular StructureBiotransformationStereoisomerismIntramolecular Lyasesortho-AminobenzoatesToluidinesStructure-Activity Relationship

EnzymesStructural

Enzymes1

• Likewise, the unrelated enzymes methylmalonyl-CoA epimerase, 3-demethylubiquinone-9 3-O-methyltransferase and numerous dioxygenases such as biphenyl-2,3-diol 1,2-dioxygenase, catechol 2,3-dioxygenase, 3,4-dihydroxyphenylacetate 2,3-dioxygenase and 4-hydroxyphenylpyruvate dioxygenase all resemble glyoxalase I in structure. (wikipedia.org)

Structural3

• 3. Structural motifs and biological studies of new antimony(III) iodide complexes with thiones. (nih.gov)
• 5. Structural diversity in supramolecular complexes of MCl(3) (M = As, Sb, Bi) with constrained thio- and seleno-ether ligands. (nih.gov)
• 7. Synthesis, structural characterization, and computational studies of novel diiodine adducts with the heterocyclic thioamides N-methylbenzothiazole-2-thione and benzimidazole-2-thione: implications with the mechanism of action of antithyroid drugs. (nih.gov)