Structure of protein kinase C theta

A method of identifying a candidate agent capable of altering a catalytic activity of PKCθ comprising:

• (a) generating a three-dimensional model of the catalytic domain of PKCθ defined by the three-dimensional structural coordinates of the complex of the catalytic domain of PKCθ and staurosporine according to Table 2, ± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å, wherein the catalytic domain of PKCθ in the complex according to Table 2 consists of amino acids Ile377 to Pro649 and Gln688 to Phe696 of SEQ ID NO:
• 1;
• (b) identifying the amino acid residues forming the ATP-binding pocket of the catalytic domain of PKCθ from the three-dimensional model in step (a) in order to generate a three-dimensional representation of the ATP-binding pocket which comprises the structural coordinates of residues Leu386, Gly387, Gly389, Val394, Ala407, Lys409, Val422, Met458, Glu459, Tyr460, Leu461, Gly464, Leu466, Arg503, Asp504, Asp508, Asn509, Leu511, Ala521, Asp522, Lys527, Thr536, and Thr538 according to Table 2± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å;
• (c) studying the interaction of a plurality of candidate agents with the three-dimensional representation of the ATP-binding pocket from step (b);
• (d) selecting from the plurality of candidate agents an agent which is predicted to alter a catalytic activity of the catalytic domain of PKCθ;
• and
• (e) determining a catalytic activity of the catalytic domain of a PKCθ polypeptide in the presence or the absence of the candidate agent.

A method of designing an agent that binds to a PKCθ polypeptide, comprising:

• (a) generating a three-dimensional model of the catalytic domain of PKCθ defined by the three-dimensional structural coordinates of the crystalline complex of the catalytic domain of PKCθ and staurosporine according to Table 2, ± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å, wherein the catalytic domain of PKCθ in the complex according to Table 2 consists of amino acids Ile377 to Pro649 and Gln688 to Phe696 of SEQ ID NO:
• 1;
• (b) identifying the amino acid residues forming the ATP-binding pocket of the catalytic domain of PKCθ from the three-dimensional model in step (a) in order to generate a three-dimensional representation of the ATP-binding pocket which comprises the structural coordinates of residues Leu386, Gly387, Gly389, Val394, Ala407, Lys409, Lys413, Val416, Leu417, Val422, Met426, Glu428, Lys429, Thr447, Gln449, Leu454, Phe456, Met458, Glu459, Tyr460, Leu461, Gly464, Leu466, Arg503, Asp504, Asp508, Asn509, Leu511, Ala521, Asp522, Lys527, Thr536, Thr538, Phe691, Arg692, Asn693, Phe694, and Ser695 according to Table 2± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å;
• (c) selecting a candidate agent by performing rational drug design with the three-dimensional representation of the ATP-binding pocket from step (b);
• (d) altering the structure of the candidate agent in the three-dimensional representation from step (b);
• (e) contacting the candidate agent with the catalytic domain of a PKCθ polypeptide;
• and
• (f) detecting the ability of the candidate agent to bind to the catalytic domain of the PKCθ polypeptide.

A method of designing a candidate agent that interacts with protein kinase C theta (PKCθ), comprising:

• generating a three-dimensional model of a crystalline complex comprising the structural coordinates of a crystalline complex of a catalytic domain of a PKCθ and staurosporine defined by Table 2, ± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å, wherein the PKCθ in the complex according to Table 2 consists of the amino acid sequence of SEQ ID NO:
• 2, said structural coordinates of the crystalline complex being obtained by subjecting a co-crystal comprising the catalytic domain of PKCθ and staurosporine to X-ray diffraction and collecting data sufficient to determine the three-dimensional structure of said crystalline complex, wherein the crystalline complex has a space group symmetry C2, with dimensions a=139.6 Å, b=42.4 Å, c=67.7 Å and β=116.2°;
• determining a fit between the structural coordinates of atoms of the three-dimensional model of the catalytic domain of PKCθ and a candidate;
• altering the structure of the candidate agent in the three-dimensional model,
• obtaining the candidate agent;
• and
• detecting the ability of the candidate agent to bind to the catalytic domain of a PKCθ polypeptide.

A method of designing a candidate agent that interacts with protein kinase C theta (PKCθ), comprising:

• (a) generating a three-dimensional model of the catalytic domain of PKCθ defined by the three-dimensional structural coordinates of the crystalline complex of the catalytic domain of PKCθ and staurosporine according to Table 2± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å, wherein the catalytic domain of PKCθ in the complex according to Table 2 consists of amino acids lle377 to Pro649 and Gln688 to Phe696 of SEQ ID NO:
• 1;
• (b) identifying the amino acid residues forming the ATP-binding pocket of the catalytic domain of PKCθ from the three-dimensional model in step (a) in order to generate a three-dimensional representation of the ATP-binding pocket which comprises the structural coordinates of residues Leu386, Gly387, Gly389, Val394, Ala407, Lys409, Lys413, Val416, Leu417, Va1422, Met426, Glu428, Lys429, Thr447, Gln449, Leu454, Phe456, Met458, Glu459, Tyr460, Leu461, Gly464, Leu466, Arg503, Asp504, Asp508, Asn509, Leu511, Ala521, Asp522, Lys527, Thr536, Thr538, Phe691, Arg692, Asn693, Phe694, and Ser695 according to Table 2± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å, wherein the ATP-binding pocket of the catalytic domain of PKCθ has a closed conformation;
• (c) determining a fit between said three-dimensional model and a candidate agent;
• (d) altering the structure of the candidate agent in the three-dimensional model,
• (e) synthesizing the candidate agent;
• and
• (f) detecting the ability of the candidate agent to bind to the catalytic domain of a PKCθ polypeptide.

A method of designing a candidate agent that interacts with protein kinase C theta (PKCθ), comprising:

• (a) generating a three-dimensional model of the catalytic domain of PKCθ defined by the three-dimensional structural coordinates of the complex of the catalytic domain of PKCθ and staurosporine according to Table 2, ± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å, wherein the catalytic domain of PKCθ of the complex according to Table 2 consists of amino acids Ile377 to Pro649 and Gln688 to Phe696 of SEQ ID NO:
• 1;
• (b) identifying the amino acid residues forming the ATP-binding pocket of the catalytic domain of PKCθ from the three-dimensional model in step (a) in order to generate a three-dimensional representation of the ATP-binding pocket which comprises the structural coordinates of residues Leu386, Gly387, Gly389, Val394, Ala407, Lys409, Val422, Glu428, Met458, Glu459, Tyr460, Leu461, Gly464, Leu466, Arg503, Asp504, Asp508, Asn509, Leu511, Ala521, Asp522, Lys527, Thr536, and Thr538 according to Table 2± a root mean square deviation for alpha carbon atoms of not more than 0.5 Å;
• (c) employing said three-dimensional representation from step (b) to design said candidate agent;
• (d) obtaining said candidate agent;
• and
• (e) contacting said candidate agent with said catalytic domain of PKCθ to determine the ability of said candidate agent to interact or bind with said three-dimensional model of the catalytic domain of PKCθ,
• whereby the detection of the ability of said candidate agent to interact or bind said catalytic domain of PKCθ thereby identifies said candidate agent as an agent that interacts with PKCθ.