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Results 1 - 9 of 9
EC Number Protein Variants Commentary Reference
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36F448V site-directed mutagenesis, the mutant shows activity similar to the wild-type enzyme -, 717290
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36F448Y site-directed mutagenesis, the mutant shows activity similar to the wild-type enzyme -, 717290
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36more construction of several truncation mutants, deletion of about 180-211 amino acids, DELTA420 and DELTA389, from the C-terminal region results in approximately 50% reduction in residual activitycompared to the wild-type enzyme -, 717290
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36more enzyme-deficient transfectants due to expression of enzyme antisense mRNA show increased generation time, altered cell morphology, accumulation of cells in G2/M phase of cell cycle, and increased numbers of binucleate cells with one or two kinetoplasts. Growth of transfectants can be stimulated by addition of a fusion protein containing the fibronectin-like SRYD motif and the zinc-binding domain of enzyme 669539
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36more Leishmaina major gp63ko strain has all seven gp63 genes deleted. In general these ko parasites show a decreased virulence, but are still able to cause significant footpad swelling. Proliferation of interleukin-2-activated purified natural killer cells is suppressed after exposure to the wild-type but not to gp63ko promastigotes. gp63ko Leishmaina major induces no natural killer cell proliferation when natural killer cells are co-cultured with peripheral blood mononuclear cells populations such as CD14+ monocytes or T cells 697408
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36more leishmanolysin-knock out mutants show a substantially higher sensitivity to inhibitors and their antileishmanial activity, such as members of the alpha- and phi-defensins, magainins and cathelicidins, pexiganan-treatment of knock out mutants induces disruption of surface-membrane permeability and expression of features of apoptosis including smaller cell size, loss of mitochondrial membrane potential, exposure of surface phosphatidyl serine as well as induction of caspase 3/7 activity, phenotype and pexiganan cleavage products generated by leishmanolysin degradation, overview 683897
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36more preparation of active enzyme immobilized by glutaraldehyde 683079
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36S446A site-directed mutagenesis, the mutant shows 50% reduced activity and altered kinetics compared to the wild-type enzyme -, 717290
Display the word mapDisplay the reaction diagram Show all sequences 3.4.24.36S446T site-directed mutagenesis, the mutant shows activity similar to the wild-type enzyme -, 717290
Results 1 - 9 of 9