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4WXB

Crystal Structure of Serine Hydroxymethyltransferase from Streptococcus thermophilus

Summary for 4WXB
Entry DOI10.2210/pdb4wxb/pdb
DescriptorSerine hydroxymethyltransferase, CITRIC ACID, CACODYLATE ION, ... (6 entities in total)
Functional Keywordsaldolase, serine hydrodymethyltransferase, transferase, aldehydes, catalysis, catalytic domain, escherichia coli, chemical, protein binding, protein conformation, protein structure
Biological sourceStreptococcus thermophilus
Total number of polymer chains4
Total formula weight187927.97
Authors
Hernandez, K.,Zelen, I.,Petrillo, G.,Uson, I.,Wandtke, C.,Bujons, J.,Joglar, J.,Parella, T.,Clapes, P. (deposition date: 2014-11-13, release date: 2015-02-04, Last modification date: 2024-01-10)
Primary citationHernandez, K.,Zelen, I.,Petrillo, G.,Uson, I.,Wandtke, C.M.,Bujons, J.,Joglar, J.,Parella, T.,Clapes, P.
Engineered L-Serine Hydroxymethyltransferase from Streptococcus thermophilus for the Synthesis of alpha , alpha-Dialkyl-alpha-Amino Acids.
Angew.Chem.Int.Ed.Engl., 54:3013-3017, 2015
Cited by
PubMed Abstract: α,α-Disubstituted α-amino acids are central to biotechnological and biomedical chemical processes for their own sake and as substructures of biologically active molecules for diverse biomedical applications. Structurally, these compounds contain a quaternary stereocenter, which is particularly challenging for stereoselective synthesis. The pyridoxal-5'-phosphate (PLP)-dependent L-serine hydroxymethyltransferase from Streptococcus thermophilus (SHMT(Sth); EC 2.1.2.1) was engineered to achieve the stereoselective synthesis of a broad structural variety of α,α-dialkyl-α-amino acids. This was accomplished by the formation of quaternary stereocenters through aldol addition of the amino acids D-Ala and D-Ser to a wide acceptor scope catalyzed by the minimalist SHMT(Sth) Y55T variant overcoming the limitation of the native enzyme for Gly. The SHMT(Sth) Y55T variant tolerates aromatic and aliphatic aldehydes as well as hydroxy- and nitrogen-containing aldehydes as acceptors.
PubMed: 25611820
DOI: 10.1002/anie.201411484
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

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