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PDBsum entry 1yat

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Binding protein PDB id
1yat
Jmol
Contents
Protein chain
113 a.a.
Ligands
FK5
Waters ×41

References listed in PDB file
Key reference
Title Improved calcineurin inhibition by yeast fkbp12-Drug complexes. Crystallographic and functional analysis.
Authors J.Rotonda, J.J.Burbaum, H.K.Chan, A.I.Marcy, J.W.Becker.
Ref. J Biol Chem, 1993, 268, 7607-7609.
PubMed id 7681823
Abstract
The protein phosphatase calcineurin is the putative target for the immunosuppressive drug FK-506. The enzyme is inhibited by the complex of the drug with its intracellular receptor, the 12-kDa FK-506-binding protein (FKBP12), and the strength of inhibition usually correlates strongly with immunosuppressive potency. We find, however, that the complex of yeast FKBP12 with L-685,818, a well characterized antagonist of FK-506 immunosuppression, is a potent inhibitor of calcineurin. The corresponding human complex does not inhibit the enzyme, and both human and yeast complexes with FK-506 do inhibit. To understand the structural basis of these findings, we have determined the three-dimensional structure of the complex of yeast FKBP12 with FK-506 by x-ray crystallography, and have found that the structure of the yeast complex is strikingly similar to its human homolog. These observations indicate that specific sequence elements in the yeast protein provide stronger binding interactions with a heterologous calcineurin than do the corresponding elements in the human protein, and suggest structural modifications that may improve the potency of this class of immunosuppressants.
Secondary reference #1
Title Fk-506-Binding protein: three-Dimensional structure of the complex with the antagonist l-685,818.
Authors J.W.Becker, J.Rotonda, B.M.Mckeever, H.K.Chan, A.I.Marcy, G.Wiederrecht, J.D.Hermes, J.P.Springer.
Ref. J Biol Chem, 1993, 268, 11335-11339.
PubMed id 7684380
Abstract
PROCHECK
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