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Literature summary extracted from

  • Kanzaki, H.; Kobayashi, M.; Nagasawa, T.; Yamada, H.
    Purification and characterization of cystathionine gamma-synthase type II from Bacillus sphaericus (1987), Eur. J. Biochem., 163, 105-112.
    View publication on PubMed

Inhibitors

EC Number Inhibitors Comment Organism Structure
2.5.1.48 3-Methyl-2-benzothiazolinone hydrazone
-
Lysinibacillus sphaericus
2.5.1.48 D-cycloserine
-
Lysinibacillus sphaericus
2.5.1.48 hydroxylamine
-
Lysinibacillus sphaericus
2.5.1.48 additional information not inhibited by p-chloromercuribenzoate, iodoacetate, N-ethylmaleimide, 5,5'-dithiobis(2-nitrobenzoate), NaCN Lysinibacillus sphaericus
2.5.1.48 phenylhydrazine
-
Lysinibacillus sphaericus
2.5.1.48 Semicarbazide
-
Lysinibacillus sphaericus

Molecular Weight [Da]

EC Number Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
2.5.1.48 43000
-
4 * 43000, SDS-PAGE Lysinibacillus sphaericus
2.5.1.48 165000
-
gel filtration Lysinibacillus sphaericus

Organism

EC Number Organism UniProt Comment Textmining
2.5.1.48 Lysinibacillus sphaericus
-
-
-

Purification (Commentary)

EC Number Purification (Comment) Organism
2.5.1.48
-
Lysinibacillus sphaericus

Specific Activity [micromol/min/mg]

EC Number Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
2.5.1.48 118
-
-
Lysinibacillus sphaericus

Storage Stability

EC Number Storage Stability Organism
2.5.1.48 -20°C, 10 mM potassium phosphate buffer, pH 7.5, 50% glycerol Lysinibacillus sphaericus

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
2.5.1.48 additional information beta-elimination and gamma-elimination barely catalyzed Lysinibacillus sphaericus ?
-
?
2.5.1.48 O-acetyl-L-homoserine + 2-mercaptoethanol 150% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-hydroxyethyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + 2-mercaptopropionate 50% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-methylcarboxymethyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + 3-mercaptopropionate 65% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-carboxyethyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + allyl mercaptan 4% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-allyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + benzyl mercaptan 41% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-benzyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + CH3SH 11% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus L-methionine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + D-Cys 101% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus D-allocystathionine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + D-homocysteine 125% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus meso-homolanthionine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + ethyl mercaptan 24% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus L-thionine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + isobutyl mercaptan 13% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-isobutyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + isopropyl mercaptan 1% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-isopropyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + L-Cys ethyl ester 15% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-[(2R)-2-amino-3-ethoxy-3-oxopropyl]-L-homocysteine + acetate i.e. L-cystathionine monoethyl ester + acetate ?
2.5.1.48 O-acetyl-L-homoserine + L-Cys methyl ester 20% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-(L-2-amino-2-methoxycarbonyl)-L-homocysteine + acetate i.e. L-cystathionine monomethyl ester + acetate ?
2.5.1.48 O-acetyl-L-homoserine + L-cysteine
-
Lysinibacillus sphaericus L-cystathionine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + L-homocysteine 92% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus L-homolanthionine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + m-thiocresol 150% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-m-tolyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + N-acetyl-L-Cys 12% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-(L-acetylamino-2-carboxyethyl)-L-homocysteine + acetate i.e. mono-N-acetyl-L-cystathionine + acetate ?
2.5.1.48 O-acetyl-L-homoserine + n-butyl mercaptan 5% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-n-butyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + n-propyl mercaptan 13% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-n-propyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + o-thiocresol 3% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-o-tolyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + p-nitrothiophenol 41% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-p-nitrophenyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + p-thiocresol 25% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-p-tolyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + phenyl mercaptan 98% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-phenyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + S2- 163% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + sec-butyl mercaptan 5% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-sec-butyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + tert-butyl mercaptan 2% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-tert-butyl-L-homosysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + thioacetic acid 3% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-acetyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + thioglycolate ethyl ester 348% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-ethoxycarbonyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + thioglycolate n-butyl ester 274% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-n-butoxycarbonyl-L-homocysteine + acetate
-
?
2.5.1.48 O-acetyl-L-homoserine + thiosalicylic acid 63% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus S-o-carboxyphenyl-L-homocysteine + acetate
-
?
2.5.1.48 O-malonyl-L-homoserine + L-cysteine 14% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus L-cystathionine + malonate
-
?
2.5.1.48 O-phenyl-L-homoserine + L-cysteine 1% relative activity to O-acetyl-L-homoserine + L-cysteine Lysinibacillus sphaericus L-cystathionine + phenol
-
?
2.5.1.48 O-succinyl-L-homoserine + L-cysteine
-
Lysinibacillus sphaericus L-cystathionine + succinate
-
?

Subunits

EC Number Subunits Comment Organism
2.5.1.48 tetramer 4 * 43000, SDS-PAGE Lysinibacillus sphaericus

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
2.5.1.48 40
-
-
Lysinibacillus sphaericus

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
2.5.1.48 7.5
-
-
Lysinibacillus sphaericus

Cofactor

EC Number Cofactor Comment Organism Structure
2.5.1.48 pyridoxal 5'-phosphate 4 mol per mol of enzyme, Km: 0.021 mM Lysinibacillus sphaericus