Hasslacher_1997_Proteins_27_438

Reference

Title : Hydroxynitrile lyase from Hevea brasiliensis: molecular characterization and mechanism of enzyme catalysis - Hasslacher_1997_Proteins_27_438
Author(s) : Hasslacher M , Kratky C , Griengl H , Schwab H , Kohlwein SD
Ref : Proteins , 27 :438 , 1997
Abstract :

(S)-Hydroxynitrile lyase (Hnl) from the tropical rubber tree Hevea brasiliensis is a 29 kDa single chain protein that catalyses the breakdown or formation of a C--C bond by reversible addition of hydrocyanic acid to aldehydes or ketones. The primary sequence of Hnl has no significant homology to known proteins. Detailed homology investigations employing PROFILESEARCH and secondary structure prediction algorithms suggest that Hnl is a member of the alpha/beta hydrolase fold protein family and contains a catalytic triad as functional residues for catalysis. The significance of predicted catalytic residues was tested and confirmed by site-directed mutagenesis and expression of mutant and wild-type proteins in the yeast, Saccharomyces cerevisiae. Based on these data we suggest a mechanistic model for the (S)-cyanohydrin synthesis catalyzed by hydroxynitrile lyase from Hevea brasiliensis.

PubMedSearch : Hasslacher_1997_Proteins_27_438
PubMedID: 9094745
Gene_locus related to this paper: hevbr-hnl

Related information

Inhibitor Histidine
Gene_locus hevbr-hnl
Structure 1YAS

Citations formats

Hasslacher M, Kratky C, Griengl H, Schwab H, Kohlwein SD (1997)
Hydroxynitrile lyase from Hevea brasiliensis: molecular characterization and mechanism of enzyme catalysis
Proteins 27 :438

Hasslacher M, Kratky C, Griengl H, Schwab H, Kohlwein SD (1997)
Proteins 27 :438