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3.4.21.72: IgA-specific serine endopeptidase

This is an abbreviated version!
For detailed information about IgA-specific serine endopeptidase, go to the full flat file.

Word Map on EC 3.4.21.72

Reaction

Cleavage of immunoglobulin A molecules at certain Pro-/- bonds in the hinge region. No small molecule substrates are known =

Synonyms

Iga, IgA protease, IgA protease A1, IgA protease B2, IgA proteinase, IgA-specific proteinase, IgA1 protease, IgA1-protease, IgA1-specific protease, IgA1?P, IgA1P, IgA1pr, IgaA1, IgaA2, IgaB2, IgAP, Immunoglobulin A protease, Immunoglobulin A proteinase, immunoglobulin A1 protease, NMB IgA1 protease, Proteinase, immunoglobulin A, serine-type IgA1 protease, serine-type immunoglobulin A1 protease, ST-11 IgA protease, type 2 IgA1 protease

ECTree

     3 Hydrolases
         3.4 Acting on peptide bonds (peptidases)
             3.4.21 Serine endopeptidases
                3.4.21.72 IgA-specific serine endopeptidase

Purification

Purification on EC 3.4.21.72 - IgA-specific serine endopeptidase

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PURIFICATION (Commentary)
ORGANISM
UNIPROT
LITERATURE
development and evaluation of a method for isolation and purification of IgA1 protease from a culture of Neisseria meningitidis serogroup A, purification involves absorption, hydrophobic interaction, anion exchange, and jacalin affinity chromatography steps, to homogeneity, overview
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native enzyme by hydrophobic interaction chromatography, ultrafiltration, anion exchange chromatography, dialysis, gel filtration, and again ultrafiltration
native enzyme from three inactivated intermediates of meningococcal vaccine production
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Ni-NTA agarose column chromatography
recombinant extracellular His6-tagged IgA protease from Escherichia coli culture medium by nickel affinity chromatography, dialysis, and ultrafiltration, to over 95% purity
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recombinant His-tagged enzyme variants solubilized from Escherichia coli inclusion bodies by nickel affinity chromatography, dialysis, and anion exchange chromatography
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recombinant His-tagged IgA1 protease by nickel affinity chromatography, anion exchange chromatography, and gel filtration
recombinant isolated surface-exposed SD domain from Escherichia coli to homogeneity
recombinant refolded enzyme solubilized from Escherichia coli inclusion bodies by ion exchange and hydrophobic interaction chromatography, followed by ultrafiltration and diafiltration
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