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Literature summary for 4.1.2.47 extracted from

  • Hanefeld, U.; Stranzl, G.; Straathof, A.J.; Heijnen, J.J.; Bergmann, A.; Mittelbach, R.; Glatter, O.; Kratky, C.
    Electrospray ionization mass spectrometry, circular dichroism and SAXS studies of the (S)-hydroxynitrile lyase from Hevea brasiliensis (2001), Biochim. Biophys. Acta, 1544, 133-142.
    View publication on PubMed
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Crystallization (Commentary)

Crystallization (Comment) Organism
-
 Hevea brasiliensis

Molecular Weight [Da]

Molecular Weight [Da] Molecular Weight Maximum [Da] Comment Organism
29210
-
 electrospray mass spectrometry Hevea brasiliensis

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
2-hydroxy-2-methylpropanenitrile Hevea brasiliensis
-
 HCN + acetone
-
 ?

Organism

Organism UniProt Comment Textmining
Hevea brasiliensis
-
 rubber tree
-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
(S)-mandelonitrile highly (S)-selective Hevea brasiliensis HCN + benzaldehyde
-
 ?
2-hydroxy-2-methylpropanenitrile
-
 Hevea brasiliensis HCN + acetone
-
 ?
2-hydroxy-2-methylpropanenitrile liberation of HCN by degradation of acetone cyanohydrin is considerably faster than the consumption of HCN by the formation of (S)-mandelonitrile Hevea brasiliensis HCN + acetone
-
 ?

Synonyms

Synonyms Comment Organism
(S)-Hydroxynitrile lyase
-
 Hevea brasiliensis
(S)-selective hydroxynitrile lyase
-
 Hevea brasiliensis

pH Stability

pH Stability pH Stability Maximum Comment Organism
6
-
 very stable above pH 6.0 Hevea brasiliensis