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Literature summary extracted from

  • Horibe, T.; Kikuchi, M.; Kawakami, K.
    Interaction of human protein disulfide isomerase and human P5 with drug compounds: Analysis using biosensor technology (2008), Process Biochem., 43, 1330-1337.
No PubMed abstract available

Cloned(Commentary)

EC Number Cloned (Comment) Organism
5.3.4.1 expression in Escherichia coli Homo sapiens

Protein Variants

EC Number Protein Variants Comment Organism
5.3.4.1 additional information analysis of binding and dissociation constants of various antibiotics with PDI and PDI domain deletion mutants lacking domains abb', domains b'a'c, domains aba'c Homo sapiens

Inhibitors

EC Number Inhibitors Comment Organism Structure
5.3.4.1 gentamycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 kanamycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 neomycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 paromomycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 ribostamycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 sisomycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 streptomycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 Vancomycin analysis of binding and dissociation constants with PDI and PDI domain deletion mutants Homo sapiens
5.3.4.1 vincristine inhibits chaperone activity but not isomerase activity of both isoforms PDI and P5 in vitro. A 100:1 molar ratio of vincristine to enzyme is sufficient to almost completely inhibit chaperone activity Homo sapiens

Organism

EC Number Organism UniProt Comment Textmining
5.3.4.1 Homo sapiens
-
isoform PDI
-