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Results 1 - 10 of 69 > >>
EC Number Protein Variants Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3A178Q mutation in subunit DmsA. About 1200% of wild-type catalytic efficiency 711886
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3A178Q mutation in subunit DmsA. Mutant is functionally impairment, with abnormal anaerobic growth with dimethylsulfoxide as the sole terminal acceptor, in a recombinant strain deleted for chromosomal dmsABC 711886
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3A181T mutation in subunit DmsA. About 300% of wild-type catalytic efficiency 711886
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3C102S mutation in electron transfer subunit DmsB. Iron-sulfur centre FS4 is assembled as a [3Fe-4S] cluster. The midpoint potential of FS4[3Fe-4S] is insensitive to inhibitor 2-n-heptyl-4-hydroxyquinoline N-oxide as well as to changes in pH from 5 to 7 711196
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3C38S the spin-spin interaction between the reduced [4Fe-4S] cluster of subunit DmsB and the Mo(V) of the molybdo bis(molybdopterin guanine dinucleotide) cofactor of subunit DmsA is significantly modified in DmsA-C38S mutant that contains a [3Fe-4S] cluster in DmsA. In ferricyanide-oxidized glycerol-inhibited DmsAC38SBC, there is no detectable interaction between the oxidized [3Fe-4S] cluster and the molybdo bis(molybdopterin guanine dinucleotide) cofactor 712341
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3C59S mutantion renders enzyme maturation sensitive to molybdenum cofactor availability. Residue C59 is a ligand to the FS0 [4Fe-4S] cluster. In the presence of trace amounts of molybdate, the C59S variant assembles normally to the cytoplasmic membrane and supports respiratory growth on DMSO, although the ground state of FS0 as determined by EPR is converted from high-spin, S = 3/2, to low-spin, S = 1/2. In the presence of the molybdenum antagonist tungstate, wild-type enzyme lacks molybdo-bis(pyranopterin guanine dinucleotide), but is translocated via the Tat translocon and assembles on the periplasmic side of the membrane as an apoenzyme. The C59S variant cannot overcome the dual insults of amino acid substitution plus lack of molybdo-bis(pyranopterin guanine dinucleotide) , leading to degradation of the DmsABC subunits 724457
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3D95A mutation in electron transfer subunit DmsB 711196
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3D95A/C102S mutation in electron transfer subunit DmsB. Iron-sulfur centre FS4 is assembled as a [3Fe-4S] cluster 711196
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3D95K/C102S mutation in electron transfer subunit DmsB. Iron-sulfur centre FS4 is assembled as a [3Fe-4S] cluster 711196
Display the word mapDisplay the reaction diagram Show all sequences 1.8.5.3D97A mutation in electron transfer subunit DmsB 711196
Results 1 - 10 of 69 > >>