3.4.13.20: beta-Ala-His dipeptidase
This is an abbreviated version!
For detailed information about beta-Ala-His dipeptidase, go to the full flat file.
Word Map on EC 3.4.13.20
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3.4.13.20
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carnosine
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dipeptide
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nephropathy
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anserine
-
homocarnosine
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beta-alanyl-l-histidine
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l-histidine
-
bestatin
-
n-acetylcarnosine
-
histidine-containing
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carcinine
-
medicine
-
analysis
-
synthesis
- 3.4.13.20
- carnosine
- dipeptide
- nephropathy
- anserine
- homocarnosine
- beta-alanyl-l-histidine
- l-histidine
- bestatin
-
n-acetylcarnosine
-
histidine-containing
-
carcinine
- medicine
- analysis
- synthesis
Reaction
preferential hydrolysis of the beta-Ala-/-His dipeptide (carnosine), and also anserine, Xaa-/-His dipeptides and other dipeptides including homocarnosine =
Synonyms
carnosinase, carnosinase-1, CN1, CN2, CNDP dipeptidase 2, CNDP1, CNDP2, cytosolic non-specific dipeptidase 2, DmpA, EC 3.4.13.13, EC 3.4.13.3, EC 3.4.3.3, serum carnosinase, tissue carnosinase
ECTree
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Substrates Products
Substrates Products on EC 3.4.13.20 - beta-Ala-His dipeptidase
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REACTION DIAGRAM
(beta-homoAla-beta-homoLys-beta-homoPhe)2 + H2O
beta-homoAla + beta-homoLys-beta-homoPhe-beta-homoAla-beta-homoLys-beta-homoPhe
3-(acetylamino)-L-alanyl-L-histidine + H2O
3-(acetylamino)-L-alanine + L-histidine
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3% of the activity with carnosine
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-
?
3-amino-L-alanyl-L-histidine + H2O
3-amino-L-alanine + L-histidine
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30% of the activity with carnosine
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-
?
beta-Ala-Gly + H2O
beta-Ala + Gly
76% of the activity compared to beta-Ala-L-Ala
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-
?
beta-Ala-L-Leu + H2O
beta-Ala + L-Leu
49% of the activity compared to beta-Ala-L-Ala
-
-
?
beta-Ala-NH2 + H2O
beta-Ala + NH3
58% of the activity compared to beta-Ala-L-Ala
-
-
?
beta-homoAla-4-nitroanilide + H2O
beta-homoAla + 4-nitroaniline
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-
-
?
beta-homoAla-beta-homoLeu + H2O
beta-homoAla + beta-homoLeu
hydrolysis at 55% compared to hydrolysis of carnosine
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-
?
beta-homoLeu-Ile-beta-homoTyr + H2O
beta-homoLeu + Ile-beta-homoTyr
hydrolysis at 0.01% compared to hydrolysis of carnosine
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-
?
beta-homoPhe-4-nitroanilide + H2O
beta-homoPhe + 4-nitroaniline
-
-
-
?
beta-homoSer-Ile-beta-homoTyr + H2O
beta-homoSer + Ile-beta-homoTyr
hydrolysis at 0.06% compared to hydrolysis of carnosine
-
-
?
beta-homoVal-beta-homoAla-beta-homoLeu + H2O
beta-homoVal + beta-homoAla-beta-homoLeu
hydrolysis at 0.19% compared to hydrolysis of carnosine
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-
?
beta-homoVal-Ile-beta-homoTyr + H2O
beta-homoVal + Ile-beta-homoTyr
hydrolysis at 0.01% compared to hydrolysis of carnosine
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-
?
beta-homoVal-Ile-Tyr + H2O
beta-homoVal + Ile-Tyr
hydrolysis at 0.09% compared to hydrolysis of carnosine
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-
?
D-Ala-NH2 + H2O
D-Ala + NH3
0.6% of the activity compared to beta-Ala-L-Ala
-
-
?
N-acetyl-3-(acetylamino)-L-alanyl-L-histidine + H2O
N-acetyl-3-(acetylamino)-L-alanine + L-histidine
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63% of the activity with carnosine
-
-
?
beta-homoAla + beta-homoLys-beta-homoPhe-beta-homoAla-beta-homoLys-beta-homoPhe
DmpA cleaves the N-terminal beta-homoAla, no further hydrolysis is observed within 13 days
-
-
?
(beta-homoAla-beta-homoLys-beta-homoPhe)2 + H2O
beta-homoAla + beta-homoLys-beta-homoPhe-beta-homoAla-beta-homoLys-beta-homoPhe
Brucella anthropi LMG7991
DmpA cleaves the N-terminal beta-homoAla, no further hydrolysis is observed within 13 days
-
-
?
anserine + H2O
beta-Ala + Ntau-methyl-L-histidine
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88% of the activity with carnosine
-
?
anserine + H2O
beta-Ala + Ntau-methyl-L-histidine
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splitting in the blood stream
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-
?
beta-Ala + beta-Ala
48% of the activity compared to beta-Ala-L-Ala
-
-
?
beta-Ala-beta-Ala + H2O
beta-Ala + beta-Ala
48% of the activity compared to beta-Ala-L-Ala
-
-
?
beta-Ala + Ile-beta-homoTyr
hydrolysis at 1.3% compared to hydrolysis of carnosine
-
-
?
beta-Ala-Ile-beta-homoTyr + H2O
beta-Ala + Ile-beta-homoTyr
Brucella anthropi LMG7991
hydrolysis at 1.3% compared to hydrolysis of carnosine
-
-
?
beta-Ala + L-His
i.e. carnosine, preferred substrate
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-
?
beta-Ala-L-His + H2O
beta-Ala + L-His
Brucella anthropi LMG7991
i.e. carnosine, preferred substrate
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-
?
beta-Ala-L-His + H2O
beta-Ala + L-His
i.e. carnosine, 57% of the activity compared to beta-Ala-L-Ala
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-
?
beta-Ala-L-His + H2O
beta-Ala + L-His
i.e. carnosine, 57% of the activity compared to beta-Ala-L-Ala
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-
?
D-Ala-4-nitroanilide + H2O
D-Ala + 4-nitroaniline
30% of the activity with Gly-p-nitroanilide, partially purified enzyme
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-
?
D-Ala-4-nitroanilide + H2O
D-Ala + 4-nitroaniline
Brucella anthropi LMG7991
30% of the activity with Gly-p-nitroanilide, partially purified enzyme
-
-
?
D-Ala-4-nitroanilide + H2O
D-Ala + 4-nitroaniline
16% of the activity compared to beta-Ala-L-Ala. D-Ala-4-nitroanilide is hydrolyzed with 5.8 times high efficiency than L-Ala-4-nitroanilide
-
-
?
D-Ala-4-nitroanilide + H2O
D-Ala + 4-nitroaniline
16% of the activity compared to beta-Ala-L-Ala. D-Ala-4-nitroanilide is hydrolyzed with 5.8 times high efficiency than L-Ala-4-nitroanilide
-
-
?
L-Ala-4-nitroanilide + H2O
L-Ala + 4-nitroaniline
9% of the activity with Gly-p-nitroanilide, partially purified enzyme
-
-
?
L-Ala-4-nitroanilide + H2O
L-Ala + 4-nitroaniline
Brucella anthropi LMG7991
9% of the activity with Gly-p-nitroanilide, partially purified enzyme
-
-
?
L-Ala-4-nitroanilide + H2O
L-Ala + 4-nitroaniline
3% of the activity compared to beta-Ala-L-Ala. D-Ala-4-nitroanilide is hydrolyzed with 5.8 times high efficiency than L-Ala-4-nitroanilide
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-
?
L-Ala-4-nitroanilide + H2O
L-Ala + 4-nitroaniline
3% of the activity compared to beta-Ala-L-Ala. D-Ala-4-nitroanilide is hydrolyzed with 5.8 times high efficiency than L-Ala-4-nitroanilide
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-
?
?
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cleaves beta- and mixed alpha,beta-peptides and amides, but a short side chain of the N-terminal beta-amino acid residue seems to be a prerequisite, since only peptides carrying N-terminal betahGly and betahAla are hydrolyzed with good efficiencies. Tripeptides carrying two consecutive N-terminal beta-homoamino acids as well as peptides with alpha-amino acids in the N-terminal position do not serve as substrates for DmpA
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-
?
additional information
?
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in the reverse direction the enzyme catalyzes the oligomerization of beta-amino acids and the synthesis of mixed peptides with N-terminal beta-amino acid residues. As substrates the beta-homoamino acid derivatives beta-Ala-p-nitroanilide, beta-homoAla-p-nitroanilide, (R)-beta-homoAla-p-nitroanilide, beta-homoPhe-p-nitroanilide, (R)-beta-homoPhe-p-nitroanilide, and beta-homoLeu-p-nitroanilide are utilized
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-
?
additional information
?
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the enzyme also shows activity with various dipeptides and tripeptides
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?
additional information
?
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Brucella anthropi LMG7991
the enzyme also shows activity with various dipeptides and tripeptides
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-
?
additional information
?
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Brucella anthropi LMG7991
cleaves beta- and mixed alpha,beta-peptides and amides, but a short side chain of the N-terminal beta-amino acid residue seems to be a prerequisite, since only peptides carrying N-terminal betahGly and betahAla are hydrolyzed with good efficiencies. Tripeptides carrying two consecutive N-terminal beta-homoamino acids as well as peptides with alpha-amino acids in the N-terminal position do not serve as substrates for DmpA
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-
?
additional information
?
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Brucella anthropi LMG7991
in the reverse direction the enzyme catalyzes the oligomerization of beta-amino acids and the synthesis of mixed peptides with N-terminal beta-amino acid residues. As substrates the beta-homoamino acid derivatives beta-Ala-p-nitroanilide, beta-homoAla-p-nitroanilide, (R)-beta-homoAla-p-nitroanilide, beta-homoPhe-p-nitroanilide, (R)-beta-homoPhe-p-nitroanilide, and beta-homoLeu-p-nitroanilide are utilized
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?
additional information
?
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no hydrolysis of L-Ala-His, Gly-His or N-acetylhistidine
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?
additional information
?
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dipeptide with histidine in the C-terminal position is preferred
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?
additional information
?
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homocarnosinosis: the lack of serum carnosinase is the defect probably responsible for elevated brain and CSF homocarnosine
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?
additional information
?
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enzyme activities in patients with idiopathic epilepsy and motor neurone disease are similar to the control group. Reduced serum carnosinase activity is observed in patients with multiple sclerosis and patients following a cerebrovascular accident
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?
additional information
?
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non Xaa-His dipeptides like Ala-Ala, or Ala-Pro, as well as tripeptides containing histidine in central or C-terminal position such as Gly-His-Gly or Gly-Gly-His, are not degraded
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?
additional information
?
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non Xaa-His dipeptides like Ala-Ala, or Ala-Pro, as well as tripeptides containing histidine in central or C-terminal position such as Gly-His-Gly or Gly-Gly-His, are not degraded
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?
additional information
?
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does not hydrolyse beta-Ala-D-His, (3S)-3-amino-4-(phenylbutanoyl)-D-histidine, (3S)-3-(aminobutanoyl)-D-histidine, (3S)-3-amino-4-(4-methoxyphenyl)butanoyl-D-histidine, (3S)-3-amino-3-(3,4-methylenedioxyphenyl)propanoyl-D-histidine, 3-amino-2-(S)-(phenylpropanoyl)-D-histidine, (2R,3S)-3-amino-2-hydroxy-4-(phenylbutanoyl)-D-histidine, (3S)-3-amino-3-(phenylpropanoyl)-D-histidine, (3S)-3-amino-4-(4-hydroxyphenyl)butanoyl-D-histidine, and (3S)-3-amino-3-(4-metoxyphenyl)propanoyl-D-histidine
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?
additional information
?
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S-trolox-L-carnosine (STC) and R-trolox-L-carnosine are resistant toward hydrolytic degradation by human carnosinase
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-
?
additional information
?
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no activity on the peptides containing proteinogenic amino acids or their D-counterparts for N-terminal residues. gamma-Aminobutyryl-L-His (L-homocarnosine) is not hydrolyzed
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-
?
additional information
?
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no activity on the peptides containing proteinogenic amino acids or their D-counterparts for N-terminal residues. gamma-Aminobutyryl-L-His (L-homocarnosine) is not hydrolyzed
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-
?