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Literature summary for 3.2.1.52 extracted from

  • Slamova, K.; Gazak, R.; Bojarova, P.; Kulik, N.; Ettrich, R.; Pelantova, H.; Sedmera, P.; Kren, V.
    4-Deoxy-substrates for beta-N-acetylhexosaminidases: how to make use of their loose specificity (2010), Glycobiology, 20, 1002-1009.
    View publication on PubMed
Search for more literature for 3.2.1.52

Organism

Organism UniProt Comment Textmining
Penicillium oxalicum
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Penicillium oxalicum CCF 1959
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Talaromyces flavus
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Talaromyces flavus CCF 2573
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information the 4-hydroxy moiety at the substrate pyranose ring is not essential for substrate binding to the enzyme active site. No substrate: 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enodialdo-1,5-pyranoside, 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enopyranoside Penicillium oxalicum ?
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 ?
additional information the 4-hydroxy moiety at the substrate pyranose ring is not essential for substrate binding to the enzyme active site. No substrate: 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enodialdo-1,5-pyranoside, 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enopyranoside Talaromyces flavus ?
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 ?
additional information the 4-hydroxy moiety at the substrate pyranose ring is not essential for substrate binding to the enzyme active site. No substrate: 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enodialdo-1,5-pyranoside, 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enopyranoside Penicillium oxalicum CCF 1959 ?
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 ?
additional information the 4-hydroxy moiety at the substrate pyranose ring is not essential for substrate binding to the enzyme active site. No substrate: 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enodialdo-1,5-pyranoside, 4-nitrophenyl 2-acetamido-2,4-dideoxy-alpha-L-threo-hex-4-enopyranoside Talaromyces flavus CCF 2573 ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-1,5-dialdo-hexopyranoside + H2O poor substrate Penicillium oxalicum ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-1,5-dialdo-hexopyranoside + H2O poor substrate Talaromyces flavus ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-1,5-dialdo-hexopyranoside + H2O poor substrate Penicillium oxalicum CCF 1959 ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-1,5-dialdo-hexopyranoside + H2O poor substrate Talaromyces flavus CCF 2573 ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-hexopyranoside + H2O good substrate, highest binding energy of all 4-deoxy compounds tested, its value lying between that of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-galactopyranoside and 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-glucopyranoside Penicillium oxalicum ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-hexopyranoside + H2O good substrate, highest binding energy of all 4-deoxy compounds tested, its value lying between that of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-galactopyranoside and 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-glucopyranoside Talaromyces flavus ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-hexopyranoside + H2O good substrate, highest binding energy of all 4-deoxy compounds tested, its value lying between that of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-galactopyranoside and 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-glucopyranoside Penicillium oxalicum CCF 1959 ?
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 ?
phenyl 2-acetamido-2,4-dideoxy-beta-D-xylo-hexopyranoside + H2O good substrate, highest binding energy of all 4-deoxy compounds tested, its value lying between that of 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-galactopyranoside and 4-nitrophenyl 2-acetamido-2-deoxy-beta-D-glucopyranoside Talaromyces flavus CCF 2573 ?
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 ?