序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
1 Crystal structures of bacterial guanylate kinases US11122793 2005-05-05 US20060073581A1 2006-04-06 Aled Edwards; Akil Dharamsi; Masoud Vedadi; Nicole Brufatto; Teresa Clarke
The present invention relates to novel drug targets for pathogenic bacteria. Accordingly, the invention provides purified protein comprising the amino acid sequence set forth in SEQ ID NO: 4. The invention also provides biochemical and biophysical characteristics of the polypeptides of the invention.
2 Method of killing cancer cells US10385163 2003-03-10 US20040180844A1 2004-09-16 Stephen W. Fesik; Donald N. Halbert; Randy E. Metzger; Jeffrey A. McDowell; Mark E. Schurdak; Susan E. Morgan-Lappe; Aparna V. Sarthy
A method of killing cancer cells comprising inhibiting the function of a gene selected from the group consisting of CDK8, STK33, PRKCM, PRKACA, ACVR1B, CDK5R1, CDC42BPB, MPP6, and CDC42BPA; pharmaceutical compositions comprising an inhibitor of the same, and a method of detecting cellular hyperplasia.
3 Modulating the interaction between ZO-2/TJP2 and a Snail zinc finger transcription factor family member US14380583 2013-02-28 US09963704B2 2018-05-08 Walter Hunziker; Choon Peng Goh
There is provided a method of identifying candidate agents capable of modulating interaction between a first polypeptide and a second polypeptide, wherein the first polypeptide is ZO-2/TJP2 or a functional variant thereof and the second polypeptide is a Snail zinc finger transcription factor family member or a functional variant thereof.
4 MODULATING THE INTERACTION BETWEEN ZO-2/TJP2 AND A SNAIL ZINC FINGER TRANSCRIPTION FACTOR FAMILY MEMBER US14380583 2013-02-28 US20150031748A1 2015-01-29 Walter Hunziker; Choon Peng Goh
There is provided a method of identifying candidate agents capable of modulating interaction between a first polypeptide and a second polypeptide, wherein the first polypeptide is ZO-2/TJP2 or a functional variant thereof and the second polypeptide is a Snail zinc finger transcription factor family member or a functional variant thereof.
5 Novel purified polypeptides from bacteria US10958216 2004-10-04 US20050181388A1 2005-08-18 Aled Edwards; Akil Dharamsi; Masoud Vedadi; Muhammad Alam; Cheryl Arrowsmith; Donald Awrey; Bryan Beattie; Kristina Buzadzija; Veronica Canadien; Megan Domagala; Simon Houston; Dhushy Kanagarajah; Qin Li; Kamran Mansoury; Merry-Lynn McDonald; Kathleen Nethery-Brokx; Ivy Ng; Hui Ouyang; Benjamin Pinder; Dawn Richards; Matthew Tai; Rosanne Thalakada; Francois Vallee; Cristina Virag
The present invention relates to polypeptide targets for pathogenic bacteria. The invention also provides biochemical and biophysical characteristics of those polypeptides.
6 Method of killing cancer cells US10796177 2004-03-09 US20040180848A1 2004-09-16 Stephen W. Fesik; Donald N. Halbert; Randy E. Metzger; Jeffrey A. McDowell; Mark E. Schurdak; Susan E. Morgan-Lappe; Aparna V. Sarthy
A method of killing cancer cells comprising inhibiting the function of a gene selected from the group consisting of CDK8, STK33, PRKCM, PRKACA, ACVR1B, CDK5R1, CDC42BPB, MPP6, and CDC42BPA; pharmaceutical compositions comprising an inhibitor of the same, and a method of detecting cellular hyperplasia.
7 METHOD OF KILLING CANCER CELLS PCT/US2004007177 2004-03-10 WO2004080287A3 2005-03-17 FESIK STEPHEN W; HALBERT DONALD N; METZGER RANDY E; MCDOWELL JEFFREY A; SCHURDAK MARK E; MORGAN-LAPPE SUSAN E; SARTHY APARNA V
A method of killing cancer cells comprising inhibiting the function of a gene selected from the group consisting of CDK8, STK33, PRKCM, PRKACA, ACVR1B, CDK5R1, CDC42BPB, MPP6, and CDC42BPA; pharmaceutical compositions comprising an inhibitor of the same, and a method of detecting cellular hyperplasia. More specifically, the inhibitors are oligonucleotides and siRNA.
8 CRYSTAL STRUCTURES OF BACTERIAL GUANYLATE KINASES PCT/CA0301673 2003-11-05 WO2004042044A3 2005-02-24 EDWARDS ALED; DHARAMSI AKIL; VEDADI MASOUD; DOMAGALA MEGAN; PINDER BENJAMIN; ALAM MUHAMMAD ZAHOOR; KIMBER MATTHEW; CLARKE TERESA; LAM ROBERT
The present invention relates to novel drug targets for pathogenic bacteria. Accordingly, the invention provides purified protein comprising the amino acid sequence set forth in SEQ ID NO: 4. The invention also provides biochemical and biophysical characteristics of the polypeptides of the invention.
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