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Results 1 - 6 of 6
EC Number Application Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 3.6.5.5agriculture the edr3 mutant displays enhanced disease resistance to Erysiphe cichoracearum and enhanced susceptibility to Botrytis cinerea 689529
Display the word mapDisplay the reaction diagram Show all sequences 3.6.5.5medicine dynamin-1 interacts with TULP1, TULP1 is a photoreceptor-specific protein that is mutated in retinitis pigmentosa 687201
Display the word mapDisplay the reaction diagram Show all sequences 3.6.5.5medicine it is shown that mitochondrial fission plays a causal role in neuronal demise, blocking fission by dominant-negative mutant Drp1K38A prevents mitochondrial fragmentation and rescues neurons from degeneration and cell death evoked by NO or rotenone 686382
Display the word mapDisplay the reaction diagram Show all sequences 3.6.5.5medicine mitochondrial fission plays a causal role in neuronal demise, blocking fission by wild-type Mfn1 prevents mitochondrial fragmentation and rescues neurons from degeneration and cell death evoked by NO or rotenone 686382
Display the word mapDisplay the reaction diagram Show all sequences 3.6.5.5medicine mutations in the dynamin family GTPase OPA1 are reportedly the cause of autosomal dominant optic atrophy 689227
Display the word mapDisplay the reaction diagram Show all sequences 3.6.5.5medicine three autosomal dominant neuropathies in humans are caused by defects in mitochondrial fusion, and a defect in mitochondrial fission is reported as being lethal, mitochondrial morphology is proposed to be maintained by a balance of mitochondrial fusion and fission involving at least four dynamin-like GTPases 687638
Results 1 - 6 of 6