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Results 1 - 5 of 5
EC Number Reaction Commentary Reference
Show all pathways known for 5.4.99.2Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.2(R)-methylmalonyl-CoA = succinyl-CoA evidence for radical intermediates 3517
Show all pathways known for 5.4.99.2Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.2(R)-methylmalonyl-CoA = succinyl-CoA intrinsic hydrogen isotope effect is 51 due to multidimensional tunneling. Corner-cutting tunneling decreases the distance over which the system tunnels without a comparable increase in either the effective potential barrier or the effective mass for tunneling 682544
Show all pathways known for 5.4.99.2Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.2(R)-methylmalonyl-CoA = succinyl-CoA mechanism 3502, 3516, 3519
Show all pathways known for 5.4.99.2Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.2(R)-methylmalonyl-CoA = succinyl-CoA mechanism, overview, a gradual weakening of the electrostatic energy between the protein and the ribose leads to a progressive increase in the activation energy barrier for Co-C bond homolysis, key role for the conserved polar glutamate residue in controlling the initial generation of radical species 727036
Show all pathways known for 5.4.99.2Display the word mapDisplay the reaction diagram Show all sequences 5.4.99.2(R)-methylmalonyl-CoA = succinyl-CoA ONIOM calculations based on protein structure. Homolytic Co-C5’ bond cleavage in the 5’-deoxyadenosylcobalamin cofactor is a stepwise process in which conformational changens in the 5’-deoxyadenosine moiety proceed the actual homolysis step. The movement of the deoxyadenosine moity during homolysis positions the resulting 5’-deoxyadenosyl radical for the subsequent hydrogen atom transfer from the substrate 680348
Results 1 - 5 of 5