This invention relates to progesterone receptor/ligand complex, and related methods and software systems. Methods for designing and/or selecting ligands of the progesterone receptor using the three-dimensional structural coordinates of the progesterone receptor and/or nonsteroidal ligands are disclo
This invention relates to progesterone receptor/ligand complex, and related methods and software systems. Methods for designing and/or selecting ligands of the progesterone receptor using the three-dimensional structural coordinates of the progesterone receptor and/or nonsteroidal ligands are disclosed.
대표청구항▼
What is claimed is: 1. A method of designing or selecting a non-steroidal candidate agent that interacts with a progesterone receptor, comprising: (a) utilizing the three-dimensional structural coordinates of the progesterone receptor ligand binding domain:non-steroidal ligand complex of Table 2 ��
What is claimed is: 1. A method of designing or selecting a non-steroidal candidate agent that interacts with a progesterone receptor, comprising: (a) utilizing the three-dimensional structural coordinates of the progesterone receptor ligand binding domain:non-steroidal ligand complex of Table 2 �� a root mean square deviation for alpha carbon atoms of not more than 1.5 Å, to generate a three-dimensional model wherein said non-steroidal ligand from Table 2 forms a favorable hydrogen bond, hydrophobic and/or electrostatic interaction between said non-steroid ligand and Asn719 and Gln725, and between one or more of Leu797, Arg766, Thr894 or Cys891; (b) identifying the amino acid residues forming a non-steroidal ligand binding pocket of the progesterone receptor ligand binding domain from the three-dimensional model in step (a) in order to generate a three-dimensional representation of the non-steroidal ligand binding pocket, wherein the non-steroidal ligand binding pocket comprises amino acids Ile699, Ala701, Leu714, Leu715, Leu718, Asn719, Leu721, Gln725, Trp755, Met756, Met759, Val760, Leu763, Arg766, Ser767, Tyr777, Phe778, Ala779, Leu782, Phe794, Leu797, Cys798, Met801, Ile804, Leu887, His888, Tyr890, Cys891, Asn893, Thr894, Phe895, Ser898, Leu901, Val903, Phe905, Met909, Ile913, and Leu917 according to Table 2, �� a root mean square deviation for alpha carbon atoms of not more than 1.5 Å, and wherein said three-dimensional representation of the non-steroidal ligand binding pocket optionally has the non-steroidal ligand from step (a) present or absent; (c) employing said three dimensional representation from step (b) to design or select said candidate agent such that the favorable interactions from step (a) are maintained between the candidate non-steroidal ligand and the progesterone receptor ligand binding pocket; (d) synthesizing said candidate agent; and (e) contacting said candidate agent with said progesterone receptor ligand binding domain to determine the ability of said candidate agent to interact or bind said progesterone receptor ligand binding domain; whereby the detection of the ability of said candidate agent to interact or bind said progesterone receptor ligand binding domain thereby identifies said candidate agent as an agent that interacts with the progesterone receptor. 2. A method of designing or selecting a non-steroidal candidate agent that interacts with a progesterone receptor, comprising: (a) utilizing the three-dimensional structural coordinates of the progesterone receptor ligand binding domain:non-steroidal ligand complex of Table 2�� a root mean square deviation for alpha carbon atoms of not more than 1.5 Å, to generate a three-dimensional model wherein said non-steroidal ligand from Table 2 forms a favorable hydrogen bond, hydrophobic and/or electrostatic interaction between said non-steroid ligand and Asn719 and Gln725, and between one or more of Leu797, Arg766, Thr894 or Cys891; (b) identifying the amino acid residues forming a non-steroidal ligand binding pocket of the progesterone receptor ligand binding domain from the three-dimensional model in step (a) in order to generate a three-dimensional representation of the non-steroidal ligand binding pocket, wherein the non-steroidal ligand binding pocket comprises amino acids Ile699, Ala701, Leu714, Leu715, Leu718, Asn719, Leu721, Gln725, Trp755, Met756, Met759, Val760, Leu763, Arg766, Ser767, Tyr777, Phe778, Ala779, Leu782, Phe794, Leu797, Cys798, Met801, Ile804, Leu887, His888, Tyr890, Cys891, Asn893, Thr894, Phe895, Ser898, Leu901, Val903, Phe905, Met909, Ile913, and Leu917, according to Table 2, �� a root mean square deviation for alpha carbon atoms of not more than 1.5 Å and wherein said three-dimensional representation of the non-steroidal ligand binding pocket optionally has the non-steroidal ligand from step(a) present or absent; (c) employing said three dimensional representation from step (b) to design or select said candidate agent such that the favorable interactions from step (a) are maintained between the candidate non-steroidal ligand and the progesterone receptor ligand binding pocket; (d) obtaining said candidate agent; and (e) contacting in vitro or in vivo said candidate agent with a polypeptide comprising said progesterone receptor ligand binding domain to determine the ability of said candidate agent to interact or bind said progesterone receptor ligand binding domain; whereby the detection of the ability of said candidate agent to interact or bind said progesterone receptor ligand binding domain thereby identifies said candidate agent as an agent that interacts with the progesterone receptor. 3. The method of claim 1 or 2, wherein the progesterone receptor ligand binding domain comprises amino acids Gln682 to Lys932 of SEQ ID NO:4. 4. The method of claim 1 or 2, wherein the non-steroidal ligand is tanaproget. 5. The method of claim 1 or 2, wherein the three dimensional model of step (a) comprises structural coordinates of atoms of the candidate agent. 6. The method of claim 1 or 2, wherein the structural coordinates of the progesterone receptor ligand binding domain: non-steroidal ligand complex are according to Table 2, �� a root mean square deviation for alpha carbon atoms of not more than 1.0 Å. 7. The method of claim 1 or 2, wherein the structural coordinates of the progesterone receptor ligand binding domain:non-steroidal ligand complex are according to Table 2, �� a root mean square deviation for alpha carbon atoms of not more than 0.5 Å. 8. The method of claim 1 or 2, further comprising altering a computer-displayed representation of the non-steroidal ligand in the three dimensional model of step (a) or (b). 9. The method of claim 8, wherein altering the computer-displayed representation of the non-steroidal ligand comprises changing the structural coordinates of the non-steroidal ligand. 10. The method of claim 8, wherein altering the computer-displayed representation of the non-steroidal ligand comprises changing the chemical structure of the non-steroidal ligand. 11. The method of claim 8, wherein altering the computer-displayed representation of the non-steroidal ligand comprises superimposing a three dimensional structure of the candidate agent over the computer-displayed representation of the non-steroidal ligand. 12. The method of claim 1 or 2, further comprising determining a fit between the structural coordinates of the amino acids of the non-steroidal ligand binding pocket and a three-dimensional structure of the candidate agent. 13. The method of claim 12, wherein determining the fit comprises calculating a distance between an atom of the non-steroidal binding pocket and an atom of the candidate agent. 14. The method of claim 1, further comprising comparing a predicted interaction between the candidate agent and the non-steroidal ligand binding pocket progesterone receptor with the interaction between the non-steroidal ligand and the non-steroidal ligand binding pocket progesterone receptor. 15. The method of claim 12, wherein determining the fit comprises docking a three-dimensional model of the candidate agent to the three-dimensional model of the ligand binding domain of the progesterone receptor. 16. The method of claim 14, further comprising comparing the interaction of the candidate agent with the progesterone receptor to an interaction of a second agent with the progesterone receptor. 17. The method of claim 2, wherein the step of obtaining the agent comprises synthesizing the agent. 18. A method of designing or selecting an agent that interacts with a progesterone receptor, comprising: (a) providing a three-dimensional structure of a complex comprising a human progesterone receptor ligand binding domain (hPR-LBD) and tanoproget, said three-dimensional structure being obtained by subjecting a co-crystal comprising the hPR-LBD in complex with tanoproget, wherein said hPR-LBD consists of SEQ ID NO:2 and said co-crystal is characterized by space group P21, with dimensions a=57.52 Å, b=64.50 Å, c=70.41 Å and β3=95.76, to X-ray diffraction and collecting data sufficient to determine the three-dimensional structure of said complex; (b) generating a three-dimensional model from the three-dimensional structure of said complex; (c) identifying the amino acid residues forming a non-steroidal ligand binding pocket of the progesterone receptor ligand binding domain from the three-dimensional model in step (b) in order to generate a three-dimensional representation of the non-steroidal ligand binding pocket, wherein the non-steroidal ligand binding pocket comprises amino acids Ile699, Ala701, Leu714, Leu715, Leu718, Asn719, Leu721, Gln725, Trp755, Met756, Met759, Val76O, Leu763, Arg766, Ser767, Tyr777, Phe778, Ala779, Leu782, Phe794, Leu797, Cys798, Met801, Ile804, Leu887, His888, Tyr890, Cys891, Asn893, Thr894, Phe895, Ser898, Leu901, Val903, Phe905, Met909, Ile913, and Leu917 of SEQ ID NO:4, according to Table 2, �� a root mean square deviation for alpha carbon atoms of not more than 1.5 Å and wherein said three-dimensional representation of the non-steroidal ligand binding pocket optionally has the non-steroidal ligand from step(b) present or absent; (d) employing said three dimensional representation from step (c) to design or select said candidate agent; (e) synthesizing said candidate agent; and (f) contacting said candidate agent with said progesterone receptor ligand binding domain to determine the ability of said candidate agent to interact or bind said progesterone receptor ligand binding domain; whereby the detection of the ability of said candidate agent to interact or bind said progesterone receptor ligand binding domain thereby identifies said candidate agent as an agent that interacts with the progesterone receptor.
연구과제 타임라인
LOADING...
LOADING...
LOADING...
LOADING...
LOADING...
이 특허에 인용된 특허 (4)
Wilson Keith P. ; Griffith James P. ; Kim Eunice E. ; Livingston David J., Crystal structure and mutants of interleukin-1 beta converting enzyme.
Becker Joseph W. ; Nicholson Donald W.,CAX ; Rotonda Jennifer ; Thornberry Nancy A. ; Fazil Kimberly M.,CAX ; Gallant Michel,CAX ; Gareau Yves,CAX ; Labelle Marc,CAX ; Peterson Erin P. ; Rasper Dita , Method for identifying inhibitors for apopain based upon the crystal structure of the apopain: Ac-DEVD-CHO complex.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.