3.5.1.87: N-carbamoyl-L-amino-acid hydrolase
This is an abbreviated version!
For detailed information about N-carbamoyl-L-amino-acid hydrolase, go to the full flat file.
Word Map on EC 3.5.1.87
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3.5.1.87
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hydantoinase
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arthrobacter
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hydantoin
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biocatalyst
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racemase
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stearothermophilus
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aurescens
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synthesis
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racemic
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l-specific
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l-tryptophan
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geobacillus
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kaustophilus
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brevibacillus
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beta-alanine
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l-homophenylalanine
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amidohydrolases
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l-forms
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biotechnology
- 3.5.1.87
- hydantoinase
- arthrobacter
- hydantoin
-
biocatalyst
- racemase
- stearothermophilus
- aurescens
- synthesis
-
racemic
-
l-specific
- l-tryptophan
-
geobacillus
- kaustophilus
-
brevibacillus
- beta-alanine
- l-homophenylalanine
-
amidohydrolases
-
l-forms
- biotechnology
Reaction
Synonyms
ADS79_04835, AtcC, BsLcar, carbamoylated amino acid carbamoylase, hyuC, immobilized L-N-carbamoylase, L-carbamoylase, L-methionine-N-carbamoylase, L-N-carbamoylamino acid aminohydrolase, L-N-carbamoylase, L-NCC amidohydrolase, Lnc, LNCA, N-carbamoyl-amino-acid amidohydrolase, N-carbamoyl-L-alpha-amino acid amidohydrolase, N-carbamoyl-L-amino acid amidohydrolase, N-carbamoyl-L-amino-acid amidohydrolase, N-carbamoyl-L-amino-acid hydrolase, N-carbamoyl-L-cysteine amidohydrolase, N-carbamoyl-L-cysteine-acid amidohydrolase, N-carbamyl-L-amino acid amidohydrolase, NCC amidohydrolase, SmLcar
ECTree
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Metals Ions
Metals Ions on EC 3.5.1.87 - N-carbamoyl-L-amino-acid hydrolase
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Ca2+
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similar enzyme activity of non 8-hydroxyquinoline-5-sulfonic acid (HQSA) treated enzyme and HQSA pretreated enzyme compared to activity without addition of any effectors
Co2+
Cu2+
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slightly activated activity of non 8-hydroxyquinoline-5-sulfonic acid (HQSA) treated enzyme and HQSA pretreated enzyme compared to activity without addition of any effectors
Mn2+
Ni2+
Zn2+
additional information
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0.5 mM, 195% activation of 8-hydroxyquinoline treated enzyme with 38% of initial
Co2+
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0.5 mM, strong activation, no activity of partially purified enzyme without Co2+, Mn2+ or Ni2+
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0.3 mM, 360% activation of 8-hydroxyquinoline treated enzyme with 38% of initial activity
Mn2+
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0.5 mM, strong activation, no activity of partially purified enzyme without Co2+, Mn2+ or Ni2+
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0.3 mM, 200% activation of 8-hydroxyquinoline treated enzyme with 38% of initial activity
Ni2+
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5.0 mM, strong activation, no activity of partially purified enzyme without Co2+, Mn2+ or Ni2+
Zn2+
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slightly activated activity of non 8-hydroxyquinoline-5-sulfonic acid (HQSA) treated enzyme, similar activity of 8-hydroxyquinoline-5-sulfonic acid pretreated enzyme compared to activity of non 8-hydroxyquinoline-5-sulfonic acid treated enzyme without addition of any effectors
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no significant effect by Fe2+, Ca2+, and Ni2+ at low concentrations, overview
additional information
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the enzymatic function is not affected by the sulfhydryl reagent iodoacetamide and is only slightly affected by 5,5'-dithiobis(2-nitrobenzoic acid)
additional information
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other divalent cations (Ni2+, Cu2+, Fe2+, Hg2+) at the low concentration (0.1 mM) are ineffective, although they cause an inhibitory effect at the high concentration