메뉴 건너뛰기




Volumn 417, Issue 3, 2012, Pages 240-252

A novel Pim-1 kinase inhibitor targeting residues that bind the substrate peptide

Author keywords

fluorescent correlation spectroscopy; inhibitor; leukemia cell lethality; Pim 1; substrate peptide binding residue

Indexed keywords

PROTEIN KINASE; PROTEIN KINASE INHIBITOR; PROTEIN KINASE PIM 1; PROTEIN KINASE PIM 1 INHIBITOR; PROTEIN P21; PROTEIN P27; QUERCETIN; UNCLASSIFIED DRUG;

EID: 84857654419     PISSN: 00222836     EISSN: 10898638     Source Type: Journal    
DOI: 10.1016/j.jmb.2012.01.036     Document Type: Article
Times cited : (27)

References (31)
  • 1
    • 77953180976 scopus 로고    scopus 로고
    • PIM serine/threonine kinases in the pathogenesis and therapy of hematologic malignancies and solid cancers
    • Brault L., Gasser C., Bracher F., Huber K., Knapp S., and Schwaller J. PIM serine/threonine kinases in the pathogenesis and therapy of hematologic malignancies and solid cancers Haematologica 95 2010 1004 1015
    • (2010) Haematologica , vol.95 , pp. 1004-1015
    • Brault, L.1    Gasser, C.2    Bracher, F.3    Huber, K.4    Knapp, S.5    Schwaller, J.6
  • 5
    • 34548670994 scopus 로고    scopus 로고
    • Cip1/WAF1 regulates its stability and cellular localization in H1299 cells
    • DOI 10.1158/1541-7786.MCR-06-0388
    • Zhang Y., Wang Z., and Magnuson N.S. Pim-1 kinase-dependent phosphorylation of p21Cip1/WAF1 regulates its stability and cellular localization in H1299 cells Mol. Cancer Res. 5 2007 909 922 (Pubitemid 47416668)
    • (2007) Molecular Cancer Research , vol.5 , Issue.9 , pp. 909-922
    • Zhang, Y.1    Wang, Z.2    Magnuson, N.S.3
  • 6
    • 48549096958 scopus 로고    scopus 로고
    • Pim kinases promote cell cycle progression by phosphorylating and down-regulating p27Kip1 at the transcriptional and posttranscriptional levels
    • Morishita D., Katayama R., Sekimizu K., Tsuruo T., and Fujita N. Pim kinases promote cell cycle progression by phosphorylating and down-regulating p27Kip1 at the transcriptional and posttranscriptional levels Cancer Res. 68 2008 5076 5085
    • (2008) Cancer Res. , vol.68 , pp. 5076-5085
    • Morishita, D.1    Katayama, R.2    Sekimizu, K.3    Tsuruo, T.4    Fujita, N.5
  • 7
    • 3343007095 scopus 로고    scopus 로고
    • 112 gatekeeper site
    • DOI 10.1016/j.febslet.2004.06.050, PII S0014579304008026
    • Aho T.L., Sandholm J., Peltola K.J., Mankonen H.P., Lilly M., and Koskinen P.J. Pim-1 kinase promotes inactivation of the pro-apoptotic Bad protein by phosphorylating it on the Ser112 gatekeeper site FEBS Lett. 571 2004 43 49 (Pubitemid 38992921)
    • (2004) FEBS Letters , vol.571 , Issue.1-3 , pp. 43-49
    • Aho, T.L.T.1    Sandholm, J.2    Peltola, K.J.3    Mankonen, H.P.4    Lilly, M.5    Koskinen, P.J.6
  • 8
    • 67649307131 scopus 로고    scopus 로고
    • Novel benzylidene-thiazolidine-2,4-diones inhibit Pim protein kinase activity and induce cell cycle arrest in leukemia and prostate cancer cells
    • Beharry Z., Zemskova M., Mahajan S., Zhang F., Ma J., and Xia Z. Novel benzylidene-thiazolidine-2,4-diones inhibit Pim protein kinase activity and induce cell cycle arrest in leukemia and prostate cancer cells Mol. Cancer Ther. 8 2009 1473 1483
    • (2009) Mol. Cancer Ther. , vol.8 , pp. 1473-1483
    • Beharry, Z.1    Zemskova, M.2    Mahajan, S.3    Zhang, F.4    Ma, J.5    Xia, Z.6
  • 10
  • 14
    • 34347237194 scopus 로고    scopus 로고
    • Fluorescence correlation spectroscopy: Novel variations of an established technique
    • DOI 10.1146/annurev.biophys.36.040306.132612
    • Haustein E., and Schwille P. Fluorescence correlation spectroscopy: novel variations of an established technique Annu. Rev. Biophys. Biomol. Struct. 36 2007 151 169 (Pubitemid 46998114)
    • (2007) Annual Review of Biophysics and Biomolecular Structure , vol.36 , pp. 151-169
    • Haustein, E.1    Schwille, P.2
  • 15
    • 2442457423 scopus 로고    scopus 로고
    • High-throughput screening with quantitation of ATP consumption: A universal non-radioisotope homogeneous assay for protein kinase
    • Koresawa M., and Okabe T. High-throughput screening with quantitation of ATP consumption: a universal non-radioisotope, homogeneous assay for protein kinase Assay Drug Dev. Technol. 2 2004 153 160 (Pubitemid 38647425)
    • (2004) Assay and Drug Development Technologies , vol.2 , Issue.2 , pp. 153-160
    • Koresawa, M.1    Okabe, T.2
  • 16
    • 77952744088 scopus 로고    scopus 로고
    • A fluorescence correlation spectroscopy-based assay for fragment screening of slowly inhibiting protein-peptide interaction inhibitors
    • Mikuni J., Kato M., Taruya S., Tsuganezawa K., Mori M., and Ogawa N. A fluorescence correlation spectroscopy-based assay for fragment screening of slowly inhibiting protein-peptide interaction inhibitors Anal. Biochem. 402 2010 26 31
    • (2010) Anal. Biochem. , vol.402 , pp. 26-31
    • Mikuni, J.1    Kato, M.2    Taruya, S.3    Tsuganezawa, K.4    Mori, M.5    Ogawa, N.6
  • 18
    • 28144464847 scopus 로고    scopus 로고
    • Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase
    • DOI 10.1021/jm0504858
    • Bullock A.N., Debreczeni J.E., Fedorov O.Y., Nelson A., Marsden B.D., and Knapp S. Structural basis of inhibitor specificity of the human protooncogene proviral insertion site in moloney murine leukemia virus (PIM-1) kinase J. Med. Chem. 48 2005 7604 7614 (Pubitemid 41698801)
    • (2005) Journal of Medicinal Chemistry , vol.48 , Issue.24 , pp. 7604-7614
    • Bullock, A.N.1    Debreczeni, J.E.2    Fedorov, O.Y.3    Nelson, A.4    Marsden, B.D.5    Knapp, S.6
  • 21
    • 64549120239 scopus 로고    scopus 로고
    • Hit to lead account of the discovery of a new class of inhibitors of Pim kinases and crystallographic studies revealing an unusual kinase binding mode
    • Qian K., Wang L., Cywin C.L., Farmer B.T. II, Hickey E., and Homon C. Hit to lead account of the discovery of a new class of inhibitors of Pim kinases and crystallographic studies revealing an unusual kinase binding mode J. Med. Chem. 52 2009 1814 1827
    • (2009) J. Med. Chem. , vol.52 , pp. 1814-1827
    • Qian, K.1    Wang, L.2    Cywin, C.L.3    Farmer, I.I.B.T.4    Hickey, E.5    Homon, C.6
  • 24
    • 0032923295 scopus 로고    scopus 로고
    • Cell-free production and stable-isotope labeling of milligram quantities of proteins
    • DOI 10.1016/S0014-5793(98)01620-2, PII S0014579398016202
    • Kigawa T., Yabuki T., Yoshida Y., Tsutsui M., Ito Y., Shibata T., and Yokoyama S. Cell-free production and stable-isotope labeling of milligram quantities of proteins FEBS Lett. 442 1999 15 19 (Pubitemid 29065369)
    • (1999) FEBS Letters , vol.442 , Issue.1 , pp. 15-19
    • Kigawa, T.1    Yabuki, T.2    Yoshida, Y.3    Tsutsui, M.4    Ito, Y.5    Shibata, T.6    Yokoyama, S.7
  • 27
    • 17144422830 scopus 로고    scopus 로고
    • Pim-1 ligand-bound structures reveal the mechanism of serine/threonine kinase inhibition by LY294002
    • DOI 10.1074/jbc.M413155200
    • Jacobs M.D., Black J., Futer O., Swenson L., Hare B., Fleming M., and Saxena K. Pim-1 ligand-bound structures reveal the mechanism of serine/threonine kinase inhibition by LY294002 J. Biol. Chem. 280 2005 13728 13734 (Pubitemid 40517268)
    • (2005) Journal of Biological Chemistry , vol.280 , Issue.14 , pp. 13728-13734
    • Jacobs, M.D.1    Black, J.2    Futer, O.3    Swenson, L.4    Hare, B.5    Fleming, M.6    Saxena, K.7
  • 29
    • 0028103275 scopus 로고
    • The CCP4 suite: Programs for protein crystallography
    • Collaborative Computational Project, No. 4
    • Collaborative Computational Project, No. 4 The CCP4 suite: programs for protein crystallography Acta Crystallogr., Sect. D: Biol. Crystallogr. 50 1994 760 763
    • (1994) Acta Crystallogr., Sect. D: Biol. Crystallogr. , vol.50 , pp. 760-763


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.