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PDBsum entry 1sxt

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Superantigen PDB id
1sxt
Contents
Protein chains
224 a.a. *
Metals
_ZN ×2
* Residue conservation analysis

References listed in PDB file
Key reference
Title The co-Crystal structure of staphylococcal enterotoxin type a with zn2+ at 2.7 a resolution. Implications for major histocompatibility complex class ii binding.
Authors M.Sundström, D.Hallén, A.Svensson, E.Schad, M.Dohlsten, L.Abrahmsén.
Ref. J Biol Chem, 1996, 271, 32212-32216. [DOI no: 10.1074/jbc.271.50.32212]
PubMed id 8943278
Abstract
Superantigens form complexes with major histocompatibility complex (MHC) class II molecules and T-cell receptors resulting in extremely strong immunostimulatory properties. Staphylococcus aureus enterotoxin A (SEA) belongs to a subgroup of the staphylococcal superantigens that utilizes Zn2+ in the high affinity interaction with MHC class II molecules. A high affinity metal binding site was described previously in SEA co-crystallized with Cd2+ in which the metal ion was octahedrally co-ordinated, involving the N-terminal serine. We have now co-crystallized SEA with its native co-factor Zn2+ and determined its crystal structure at 2.7 A resolution. As expected for a Zn2+ ion, the co-ordination was found to be tetrahedral. Three of the ligands are located on the SEA surface on a C-terminal domain beta-sheet, while the fourth varies with the conditions. Further analysis of the zinc binding event was performed using titration microcalorimetry, which showed that SEA binds Zn2+ with an affinity of KD = 0.3 microM in an entropy driven process. The differential Zn2+ co-ordination observed here has implications for the mechanism of the SEA-MHC class II interaction.
Figure 1.
Fig. 1. A representative part of the 2F[o]F[c] electron density map of SEA-Zn2+ in the core of the superantigen molecule. Observe the interactions between tyrosine residues that possibly contribute to the resistance^ of SEA to environmental factors such as high temperature or protease^ degradation. The 2F[o]F[c] electron density map is contoured at 1.2^ above the mean.
Figure 3.
Fig. 3. The zinc binding site of SEA co-crystallized with Zn2+. A, tetrahedral zinc co-ordination in molecule one (yellow) in the asymmetric unit. Note that the use of His61 from the neighboring molecule (cyan) as zinc ligand leads to the loop 59-63, absent in the SEA-Cd^2+ structure, here becoming ordered. B, tetrahedral zinc co-ordination in the second molecule of the asymmetric unit. The three high affinity SEA ligands are used and in addition a water molecule^ (H[2]O) is used as the fourth Zn2+ ligand. The figures were drawn using Molscript (30) and Raster3D^ (31).
The above figures are reprinted by permission from the ASBMB: J Biol Chem (1996, 271, 32212-32216) copyright 1996.
PROCHECK
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