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Literature summary extracted from

  • Ralat, L.A.; Ren, M.; Schilling, A.B.; Tang, W.J.
    Protective role of Cys-178 against the inactivation and oligomerization of human insulin-degrading enzyme by oxidation and nitrosylation (2009), J. Biol. Chem., 284, 34005-34018.
    View publication on PubMedView publication on EuropePMC

Cloned(Commentary)

EC Number Cloned (Comment) Organism
3.4.24.56 expressed in BV-2 cells Homo sapiens
3.4.24.56 expression of His-tagged wild-type and mutant IDEs in Escherichia coli strain Rosetta (DE3) Homo sapiens

Protein Variants

EC Number Protein Variants Comment Organism
3.4.24.56 additional information construction of Cys residue mutants of IDE, properties of oxidized and/or nitrosylated mutant enzymes compared to wild-type enzyme, overview Homo sapiens

Inhibitors

EC Number Inhibitors Comment Organism Structure
3.4.24.56 hydrogen peroxide the oxidative burst of BV-2 microglial cells leads to oxidation of secreted IDE at Cys residues, e.g. Cys819, Cys110, Cys257, and Cys178, leading to the reduced activity after 4 h versus amyloid beta degradation, increases IDE oligomerization, and decreases IDE thermostability. Within the first 4 h of incubation at 37°C, the control and H2O2-treated enzyme does not lose any relative activity. The inhibitory response of IDE is substrate-dependent, biphasic for amyloid beta degradation but monophasic for a shorter bradykinin-mimetic substrate, mutational analysis, overview. Only Cys819 modification plays a prominent role in the change of enzyme properties Homo sapiens
3.4.24.56 NEM modifies Cys819 and inhibits IDE Homo sapiens
3.4.24.56 S-nitrosoglutathione the oxidative burst of BV-2 microglial cells leads nitrosylation of secreted IDE at Cys residues, e.g. Cys819, Cys110, Cys257, and Cys178, leading to the reduced activity versus amyloid beta degradation, increases IDE oligomerization, and decreases IDE thermostability. This inhibitory response of IDE is substrate-dependent, biphasic for amyloid beta degradation but monophasic for a shorter bradykinin-mimetic substrate, mutational analysis, overview. Only Cys819 modification plays a prominant role in the change of enzyme properties Homo sapiens

KM Value [mM]

EC Number KM Value [mM] KM Value Maximum [mM] Substrate Comment Organism Structure
3.4.24.56 additional information
-
additional information kinetics of wild-type IDE, IDE mutants, and IDE modified at Cys residues by H2O2 or S-nitrosoglutathione, with substrate amyloidbeta, overview. IDE exhibits substantially different enzyme kinetic parameters with the longer peptide amyloidbeta as compared with a shorter peptide substrate, the bradykinin-mimetic substrate V Homo sapiens
3.4.24.56 0.08
-
amyloid beta pH 8.0, 37°C, wild-type enzyme Homo sapiens

Localization

EC Number Localization Comment Organism GeneOntology No. Textmining
3.4.24.56 extracellular IDE is secreted by BV-2 microglial cells Homo sapiens
-
-

Metals/Ions

EC Number Metals/Ions Comment Organism Structure
3.4.24.56 Zn2+ dependent on, metallopeptidase Homo sapiens

Molecular Weight [Da]

EC Number Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
3.4.24.56 110000
-
monomeric enzyme Homo sapiens
3.4.24.56 150000
-
monomer/dimer mixture of solubilized enzyme, gel filtration Homo sapiens

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.4.24.56 amyloid beta + H2O Homo sapiens
-
amyloid beta peptide fragments
-
?
3.4.24.56 insulin + H2O Homo sapiens
-
insulin peptide fragments
-
?

Organism

EC Number Organism UniProt Comment Textmining
3.4.24.56 Homo sapiens
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
3.4.24.56 recombinant His-tagged wild-type and mutant IDEs from Escherichia coli strain Rosetta (DE3) by nickel affinity chromatography Homo sapiens

Source Tissue

EC Number Source Tissue Comment Organism Textmining
3.4.24.56 microglia
-
Homo sapiens
-

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.4.24.56 amyloid beta + H2O
-
Homo sapiens amyloid beta peptide fragments
-
?
3.4.24.56 insulin + H2O
-
Homo sapiens insulin peptide fragments
-
?
3.4.24.56 peptide V + H2O a bradykinin-mimetic fluorogenic peptide substrate V Homo sapiens ?
-
?

Subunits

EC Number Subunits Comment Organism
3.4.24.56 monomer or dimer in solution the enzyme exists as a monomer/dimer mixture Homo sapiens
3.4.24.56 More oligomeric forms of IDE treated with H2O2 and GSN, 280-290 kDa, overview Homo sapiens

Synonyms

EC Number Synonyms Comment Organism
3.4.24.56 IDE
-
Homo sapiens
3.4.24.56 Insulin-degrading enzyme
-
Homo sapiens

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
3.4.24.56 37
-
assay at Homo sapiens

Temperature Stability [°C]

EC Number Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
3.4.24.56 additional information
-
the oxidative burst of BV-2 microglial cells leads to oxidation or nitrosylation of secreted IDE, leading to decreased IDE thermostability Homo sapiens

Turnover Number [1/s]

EC Number Turnover Number Minimum [1/s] Turnover Number Maximum [1/s] Substrate Comment Organism Structure
3.4.24.56 70
-
amyloid beta pH 8.0, 37°C, wild-type enzyme Homo sapiens

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
3.4.24.56 8
-
assay at Homo sapiens

Ki Value [mM]

EC Number Ki Value [mM] Ki Value maximum [mM] Inhibitor Comment Organism Structure
3.4.24.56 additional information
-
additional information inhibition kinetics, overview Homo sapiens

IC50 Value

EC Number IC50 Value IC50 Value Maximum Comment Organism Inhibitor Structure
3.4.24.56 0.9
-
pH 8.0, 37°C Homo sapiens hydrogen peroxide
3.4.24.56 1.2
-
pH 8.0, 37°C Homo sapiens S-nitrosoglutathione

General Information

EC Number General Information Comment Organism
3.4.24.56 additional information IDE can be intricately regulated by reactive oxygen or nitrogen species, identification of oxidation and nitrosylation sites, structure of IDE, and molecular basis for the long distance interactions, and mechanism of oxidative and nitrosylative modification of IDE, overview Homo sapiens