메뉴 건너뛰기




Volumn 6, Issue 1, 2011, Pages

Allosteric interactions between the myristate- and ATP-site of the Abl kinase

Author keywords

[No Author keywords available]

Indexed keywords

ABELSON KINASE; ADENOSINE TRIPHOSPHATE; DASATINIB; GNF 5; MYRISTIC ACID; PHOSPHOTRANSFERASE INHIBITOR; UNCLASSIFIED DRUG; 4 METHYL N (3 (4 METHYLIMIDAZOL 1 YL) 5 (TRIFLUOROMETHYL)PHENYL) 3 ((4 PYRIDIN 3 YLPYRIMIDIN 2 YL)AMINO)BENZAMIDE; 4-METHYL-N-(3-(4-METHYLIMIDAZOL-1-YL)-5-(TRIFLUOROMETHYL)PHENYL)-3-((4-PYRIDIN-3-YLPYRIMIDIN-2-YL)AMINO)BENZAMIDE; ANTINEOPLASTIC AGENT; PROTEIN KINASE INHIBITOR; PYRIMIDINE DERIVATIVE; THIAZOLE DERIVATIVE;

EID: 79251582163     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0015929     Document Type: Article
Times cited : (63)

References (46)
  • 1
    • 69949151386 scopus 로고    scopus 로고
    • Factors underlying sensitivity of cancers to small-molecule kinase inhibitors
    • Janne PA, Gray N, Settleman J (2009) Factors underlying sensitivity of cancers to small-molecule kinase inhibitors. Nat Rev Drug Discov 8: 709-723.
    • (2009) Nat Rev Drug Discov , vol.8 , pp. 709-723
    • Janne, P.A.1    Gray, N.2    Settleman, J.3
  • 2
    • 57749188299 scopus 로고    scopus 로고
    • Targeting cancer with small molecule kinase inhibitors
    • Zhang J, Yang PL, Gray NS (2009) Targeting cancer with small molecule kinase inhibitors. Nat Rev Cancer 9: 28-39.
    • (2009) Nat Rev Cancer , vol.9 , pp. 28-39
    • Zhang, J.1    Yang, P.L.2    Gray, N.S.3
  • 3
    • 0029947186 scopus 로고    scopus 로고
    • Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells
    • Druker BJ, Tamura S, Buchdunger E, Ohno S, Segal GM, et al. (1996) Effects of a selective inhibitor of the Abl tyrosine kinase on the growth of Bcr-Abl positive cells. Nat Med 2: 561-566.
    • (1996) Nat Med , vol.2 , pp. 561-566
    • Druker, B.J.1    Tamura, S.2    Buchdunger, E.3    Ohno, S.4    Segal, G.M.5
  • 5
    • 3142676436 scopus 로고    scopus 로고
    • Overriding imatinib resistance with a novel ABL kinase inhibitor
    • Shah NP, Tran C, Lee FY, Chen P, Norris D, et al. (2004) Overriding imatinib resistance with a novel ABL kinase inhibitor. Science 305: 399-401.
    • (2004) Science , vol.305 , pp. 399-401
    • Shah, N.P.1    Tran, C.2    Lee, F.Y.3    Chen, P.4    Norris, D.5
  • 6
    • 29244482571 scopus 로고    scopus 로고
    • Targeting the kinase activity of the BCR-ABL fusion protein in patients with chronic myeloid leukemia
    • Giles FJ, Cortes JE, Kantarjian HM (2005) Targeting the kinase activity of the BCR-ABL fusion protein in patients with chronic myeloid leukemia. Curr Mol Med 5: 615-623.
    • (2005) Curr Mol Med , vol.5 , pp. 615-623
    • Giles, F.J.1    Cortes, J.E.2    Kantarjian, H.M.3
  • 7
    • 33748885930 scopus 로고    scopus 로고
    • Novel tyrosine kinase inhibitors in chronic myelogenous leukemia
    • Jabbour E, Cortes J, Kantarjian H (2006) Novel tyrosine kinase inhibitors in chronic myelogenous leukemia. Curr Opin Oncol 18: 578-583.
    • (2006) Curr Opin Oncol , vol.18 , pp. 578-583
    • Jabbour, E.1    Cortes, J.2    Kantarjian, H.3
  • 8
    • 14644425319 scopus 로고    scopus 로고
    • Mechanisms of BCR-ABL in the pathogenesis of chronic myelogenous leukaemia
    • Ren R (2005) Mechanisms of BCR-ABL in the pathogenesis of chronic myelogenous leukaemia. Nat Rev Cancer 5: 172-183.
    • (2005) Nat Rev Cancer , vol.5 , pp. 172-183
    • Ren, R.1
  • 10
    • 0035800507 scopus 로고    scopus 로고
    • Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification
    • Gorre ME, Mohammed M, Ellwood K, Hsu N, Paquette R, et al. (2001) Clinical resistance to STI-571 cancer therapy caused by BCR-ABL gene mutation or amplification. Science 293: 876-880.
    • (2001) Science , vol.293 , pp. 876-880
    • Gorre, M.E.1    Mohammed, M.2    Ellwood, K.3    Hsu, N.4    Paquette, R.5
  • 11
    • 0001686739 scopus 로고    scopus 로고
    • Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia
    • Shah NP, Nicoll JM, Nagar B, Gorre ME, Paquette RL, et al. (2002) Multiple BCR-ABL kinase domain mutations confer polyclonal resistance to the tyrosine kinase inhibitor imatinib (STI571) in chronic phase and blast crisis chronic myeloid leukemia. Cancer Cell 2: 117-125.
    • (2002) Cancer Cell , vol.2 , pp. 117-125
    • Shah, N.P.1    Nicoll, J.M.2    Nagar, B.3    Gorre, M.E.4    Paquette, R.L.5
  • 12
    • 33845444046 scopus 로고    scopus 로고
    • Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia
    • Druker BJ, Guilhot F, O'Brien SG, Gathmann I, Kantarjian H, et al. (2006) Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia. N Engl J Med 355: 2408-2417.
    • (2006) N Engl J Med , vol.355 , pp. 2408-2417
    • Druker, B.J.1    Guilhot, F.2    O'Brien, S.G.3    Gathmann, I.4    Kantarjian, H.5
  • 13
    • 0037459344 scopus 로고    scopus 로고
    • Mechanisms of autoinhibition and STI-571/imatinib resistance revealed by mutagenesis of BCR-ABL
    • Azam M, Latek RR, Daley GQ (2003) Mechanisms of autoinhibition and STI-571/imatinib resistance revealed by mutagenesis of BCR-ABL. Cell 112: 831-843.
    • (2003) Cell , vol.112 , pp. 831-843
    • Azam, M.1    Latek, R.R.2    Daley, G.Q.3
  • 14
    • 34548548332 scopus 로고    scopus 로고
    • Crystal structure of the T315I Abl mutant in complex with the aurora kinases inhibitor PHA-739358
    • Modugno M, Casale E, Soncini C, Rosettani P, Colombo R, et al. (2007) Crystal structure of the T315I Abl mutant in complex with the aurora kinases inhibitor PHA-739358. Cancer Res 67: 7987-7990.
    • (2007) Cancer Res , vol.67 , pp. 7987-7990
    • Modugno, M.1    Casale, E.2    Soncini, C.3    Rosettani, P.4    Colombo, R.5
  • 16
    • 33845806858 scopus 로고    scopus 로고
    • In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinibresistant Bcr-Abl+ neoplastic cells
    • Puttini M, Coluccia AM, Boschelli F, Cleris L, Marchesi E, et al. (2006) In vitro and in vivo activity of SKI-606, a novel Src-Abl inhibitor, against imatinibresistant Bcr-Abl+ neoplastic cells. Cancer Res 66: 11314-11322.
    • (2006) Cancer Res , vol.66 , pp. 11314-11322
    • Puttini, M.1    Coluccia, A.M.2    Boschelli, F.3    Cleris, L.4    Marchesi, E.5
  • 17
    • 19944428353 scopus 로고    scopus 로고
    • Discovery of N-(2-chloro-6-methyl- phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4- ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays
    • Lombardo LJ, Lee FY, Chen P, Norris D, Barrish JC, et al. (2004) Discovery of N-(2-chloro-6-methyl- phenyl)-2-(6-(4-(2-hydroxyethyl)- piperazin-1-yl)-2-methylpyrimidin-4- ylamino)thiazole-5-carboxamide (BMS-354825), a dual Src/Abl kinase inhibitor with potent antitumor activity in preclinical assays. J Med Chem 47: 6658-6661.
    • (2004) J Med Chem , vol.47 , pp. 6658-6661
    • Lombardo, L.J.1    Lee, F.Y.2    Chen, P.3    Norris, D.4    Barrish, J.C.5
  • 18
    • 43749086323 scopus 로고    scopus 로고
    • SGX393 inhibits the CML mutant Bcr-AblT315I and preempts in vitro resistance when combined with nilotinib or dasatinib
    • O'Hare T, Eide CA, Tyner JW, Corbin AS, Wong MJ, et al. (2008) SGX393 inhibits the CML mutant Bcr-AblT315I and preempts in vitro resistance when combined with nilotinib or dasatinib. Proc Natl Acad Sci U S A 105: 5507-5512.
    • (2008) Proc Natl Acad Sci U S A , vol.105 , pp. 5507-5512
    • O'Hare, T.1    Eide, C.A.2    Tyner, J.W.3    Corbin, A.S.4    Wong, M.J.5
  • 19
    • 68549115413 scopus 로고    scopus 로고
    • 9-(Arenethenyl)purines as dual Src/Abl kinase inhibitors targeting the inactive conformation: Design, synthesis, and biological evaluation
    • Huang WS, Zhu X, Wang Y, Azam M, Wen D, et al. (2009) 9-(Arenethenyl)purines as dual Src/Abl kinase inhibitors targeting the inactive conformation: design, synthesis, and biological evaluation. J Med Chem 52: 4743-4756.
    • (2009) J Med Chem , vol.52 , pp. 4743-4756
    • Huang, W.S.1    Zhu, X.2    Wang, Y.3    Azam, M.4    Wen, D.5
  • 20
    • 65549152514 scopus 로고    scopus 로고
    • Equally potent inhibition of c-Src and Abl by compounds that recognize inactive kinase conformations
    • Seeliger MA, Ranjitkar P, Kasap C, Shan Y, Shaw DE, et al. (2009) Equally potent inhibition of c-Src and Abl by compounds that recognize inactive kinase conformations. Cancer Res 69: 2384-2392.
    • (2009) Cancer Res , vol.69 , pp. 2384-2392
    • Seeliger, M.A.1    Ranjitkar, P.2    Kasap, C.3    Shan, Y.4    Shaw, D.E.5
  • 21
    • 77953636478 scopus 로고    scopus 로고
    • Discovery of a small-molecule type II inhibitor of wild-type and gatekeeper mutants of BCRABL, PDGFRalpha, Kit, and Src kinases: Novel type II inhibitor of gatekeeper mutants
    • Weisberg E, Choi HG, Ray A, Barrett R, Zhang J, et al. (2010) Discovery of a small-molecule type II inhibitor of wild-type and gatekeeper mutants of BCRABL, PDGFRalpha, Kit, and Src kinases: novel type II inhibitor of gatekeeper mutants. Blood 115: 4206-4216.
    • (2010) Blood , vol.115 , pp. 4206-4216
    • Weisberg, E.1    Choi, H.G.2    Ray, A.3    Barrett, R.4    Zhang, J.5
  • 22
    • 70350507997 scopus 로고    scopus 로고
    • AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance
    • O'Hare T, Shakespeare WC, Zhu X, Eide CA, Rivera VM, et al. (2009) AP24534, a pan-BCR-ABL inhibitor for chronic myeloid leukemia, potently inhibits the T315I mutant and overcomes mutation-based resistance. Cancer Cell 16: 401-412.
    • (2009) Cancer Cell , vol.16 , pp. 401-412
    • O'Hare, T.1    Shakespeare, W.C.2    Zhu, X.3    Eide, C.A.4    Rivera, V.M.5
  • 24
    • 33644889108 scopus 로고    scopus 로고
    • Allosteric inhibitors of Bcr-abl-dependent cell proliferation
    • Adrian FJ, Ding Q, Sim T, Velentza A, Sloan C, et al. (2006) Allosteric inhibitors of Bcr-abl-dependent cell proliferation. Nat Chem Biol 2: 95-102.
    • (2006) Nat Chem Biol , vol.2 , pp. 95-102
    • Adrian, F.J.1    Ding, Q.2    Sim, T.3    Velentza, A.4    Sloan, C.5
  • 25
    • 75749146563 scopus 로고    scopus 로고
    • Targeting Bcr-Abl by combining allosteric with ATP-binding-site inhibitors
    • Zhang J, Adrian FJ, Jahnke W, Cowan-Jacob SW, Li AG, et al. (2010) Targeting Bcr-Abl by combining allosteric with ATP-binding-site inhibitors. Nature 463: 501-506.
    • (2010) Nature , vol.463 , pp. 501-506
    • Zhang, J.1    Adrian, F.J.2    Jahnke, W.3    Cowan-Jacob, S.W.4    Li, A.G.5
  • 28
    • 0023571161 scopus 로고
    • Nucleotide sequence of testis-derived c-abl cDNAs: Implications for testis-specific transcription and abl oncogene activation
    • Oppi C, Shore SK, Reddy EP (1987) Nucleotide sequence of testis-derived c-abl cDNAs: implications for testis-specific transcription and abl oncogene activation. Proc Natl Acad Sci U S A 84: 8200-8204.
    • (1987) Proc Natl Acad Sci U S A , vol.84 , pp. 8200-8204
    • Oppi, C.1    Shore, S.K.2    Reddy, E.P.3
  • 29
    • 28844458822 scopus 로고    scopus 로고
    • High yield bacterial expression of active c-Abl and c-Src tyrosine kinases
    • Seeliger MA, Young M, Henderson MN, Pellicena P, King DS, et al. (2005) High yield bacterial expression of active c-Abl and c-Src tyrosine kinases. Protein Sci 14: 3135-3139.
    • (2005) Protein Sci , vol.14 , pp. 3135-3139
    • Seeliger, M.A.1    Young, M.2    Henderson, M.N.3    Pellicena, P.4    King, D.S.5
  • 30
    • 51549121010 scopus 로고    scopus 로고
    • High-speed and highresolution UPLC separation at zero degrees Celsius
    • Wales TE, Fadgen KE, Gerhardt GC, Engen JR (2008) High-speed and highresolution UPLC separation at zero degrees Celsius. Anal Chem 80: 6815-6820.
    • (2008) Anal Chem , vol.80 , pp. 6815-6820
    • Wales, T.E.1    Fadgen, K.E.2    Gerhardt, G.C.3    Engen, J.R.4
  • 31
    • 33644761306 scopus 로고    scopus 로고
    • Hydrogen exchange mass spectrometry for the analysis of protein dynamics
    • Wales TE, Engen JR (2006) Hydrogen exchange mass spectrometry for the analysis of protein dynamics. Mass Spectrom Rev 25: 158-170.
    • (2006) Mass Spectrom Rev , vol.25 , pp. 158-170
    • Wales, T.E.1    Engen, J.R.2
  • 32
    • 0020855355 scopus 로고
    • Hydrogen exchange and structural dynamics of proteins and nucleic acids
    • Englander SW, Kallenbach NR (1983) Hydrogen exchange and structural dynamics of proteins and nucleic acids. Q Rev Biophys 16: 521-655.
    • (1983) Q Rev Biophys , vol.16 , pp. 521-655
    • Englander, S.W.1    Kallenbach, N.R.2
  • 33
    • 33751337111 scopus 로고    scopus 로고
    • Semi-automated data processing of hydrogen exchange mass spectra using HX-Express
    • Weis DD, Engen JR, Kass IJ (2006) Semi-automated data processing of hydrogen exchange mass spectra using HX-Express. J Am Soc Mass Spectrom 17: 1700-1703.
    • (2006) J Am Soc Mass Spectrom , vol.17 , pp. 1700-1703
    • Weis, D.D.1    Engen, J.R.2    Kass, I.J.3
  • 34
    • 33745777632 scopus 로고    scopus 로고
    • UPLC/MS(E); a new approach for generating molecular fragment information for biomarker structure elucidation
    • Plumb RS, Johnson KA, Rainville P, Smith BW, Wilson ID, et al. (2006) UPLC/MS(E); a new approach for generating molecular fragment information for biomarker structure elucidation. Rapid Commun Mass Spectrom 20: 1989-1994.
    • (2006) Rapid Commun Mass Spectrom , vol.20 , pp. 1989-1994
    • Plumb, R.S.1    Johnson, K.A.2    Rainville, P.3    Smith, B.W.4    Wilson, I.D.5
  • 35
    • 15744380263 scopus 로고    scopus 로고
    • Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition
    • Ohren JF, Chen H, Pavlovsky A, Whitehead C, Zhang E, et al. (2004) Structures of human MAP kinase kinase 1 (MEK1) and MEK2 describe novel noncompetitive kinase inhibition. Nat Struct Mol Biol 11: 1192-1197.
    • (2004) Nat Struct Mol Biol , vol.11 , pp. 1192-1197
    • Ohren, J.F.1    Chen, H.2    Pavlovsky, A.3    Whitehead, C.4    Zhang, E.5
  • 36
    • 77954615408 scopus 로고    scopus 로고
    • MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo
    • Hirai H, Sootome H, Nakatsuru Y, Miyama K, Taguchi S, et al. (2010) MK-2206, an allosteric Akt inhibitor, enhances antitumor efficacy by standard chemotherapeutic agents or molecular targeted drugs in vitro and in vivo. Mol Cancer Ther 9: 1956-1967.
    • (2010) Mol Cancer Ther , vol.9 , pp. 1956-1967
    • Hirai, H.1    Sootome, H.2    Nakatsuru, Y.3    Miyama, K.4    Taguchi, S.5
  • 37
    • 0001640528 scopus 로고
    • Di- and triphosphopyridine nucleotide isocitric dehydrogenases in yeast
    • Kornberg A, Pricer WE, Jr. (1951) Di- and triphosphopyridine nucleotide isocitric dehydrogenases in yeast. J Biol Chem 189: 123-136.
    • (1951) J Biol Chem , vol.189 , pp. 123-136
    • Kornberg, A.1    Pricer Jr., W.E.2
  • 38
    • 33745283618 scopus 로고    scopus 로고
    • The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants
    • Tokarski JS, Newitt JA, Chang CY, Cheng JD, Wittekind M, et al. (2006) The structure of Dasatinib (BMS-354825) bound to activated ABL kinase domain elucidates its inhibitory activity against imatinib-resistant ABL mutants. Cancer Res 66: 5790-5797.
    • (2006) Cancer Res , vol.66 , pp. 5790-5797
    • Tokarski, J.S.1    Newitt, J.A.2    Chang, C.Y.3    Cheng, J.D.4    Wittekind, M.5
  • 39
    • 33750989362 scopus 로고    scopus 로고
    • 2-aminothiazole as a novel kinase inhibitor template. Structure-activity relationship studies toward the discovery of N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1- piperazinyl)]-2-methyl-4-pyrimidinyl]amino)]-1,3-thiazole-5-carboxamide (dasatinib, BMS-354825) as a potent pan-Src kinase inhibitor
    • Das J, Chen P, Norris D, Padmanabha R, Lin J, et al. (2006) 2-aminothiazole as a novel kinase inhibitor template. Structure-activity relationship studies toward the discovery of N-(2-chloro-6-methylphenyl)-2-[[6-[4-(2-hydroxyethyl)-1- piperazinyl)]-2-methyl-4-pyrimidinyl]amino)]-1,3-thiazole-5-carboxamide (dasatinib, BMS-354825) as a potent pan-Src kinase inhibitor. J Med Chem 49: 6819-6832.
    • (2006) J Med Chem , vol.49 , pp. 6819-6832
    • Das, J.1    Chen, P.2    Norris, D.3    Padmanabha, R.4    Lin, J.5
  • 40
    • 49649108911 scopus 로고    scopus 로고
    • Solution conformations and dynamics of ABL kinase-inhibitor complexes determined by NMR substantiate the different binding modes of imatinib/nilotinib and dasatinib
    • Vajpai N, Strauss A, Fendrich G, Cowan-Jacob SW, Manley PW, et al. (2008) Solution conformations and dynamics of ABL kinase-inhibitor complexes determined by NMR substantiate the different binding modes of imatinib/nilotinib and dasatinib. J Biol Chem 283: 18292-18302.
    • (2008) J Biol Chem , vol.283 , pp. 18292-18302
    • Vajpai, N.1    Strauss, A.2    Fendrich, G.3    Cowan-Jacob, S.W.4    Manley, P.W.5
  • 41
    • 33947384902 scopus 로고    scopus 로고
    • In silico profiling of tyrosine kinases binding specificity and drug resistance using Monte Carlo simulations with the ensembles of protein kinase crystal structures
    • Verkhivker GM (2007) In silico profiling of tyrosine kinases binding specificity and drug resistance using Monte Carlo simulations with the ensembles of protein kinase crystal structures. Biopolymers 85: 333-348.
    • (2007) Biopolymers , vol.85 , pp. 333-348
    • Verkhivker, G.M.1
  • 42
    • 0030199899 scopus 로고    scopus 로고
    • Mass spectrometric determination of isotopic exchange rates of amide hydrogens located on the surfaces of proteins
    • Dharmasiri K, Smith DL (1996) Mass spectrometric determination of isotopic exchange rates of amide hydrogens located on the surfaces of proteins. Anal Chem 68: 2340-2344.
    • (1996) Anal Chem , vol.68 , pp. 2340-2344
    • Dharmasiri, K.1    Smith, D.L.2
  • 43
    • 75749148378 scopus 로고    scopus 로고
    • Investigating solution-phase protein structure and dynamics by hydrogen exchange mass spectrometry
    • Morgan CR, Engen JR (2009) Investigating solution-phase protein structure and dynamics by hydrogen exchange mass spectrometry. Curr Protoc Protein Sci Chapter 17: Unit 17 16: 11-17.
    • (2009) Curr Protoc Protein Sci Chapter 17: Unit , vol.17 , Issue.16 , pp. 11-17
    • Morgan, C.R.1    Engen, J.R.2
  • 44
    • 70350365399 scopus 로고    scopus 로고
    • Nmyristoylated c-Abl tyrosine kinase localizes to the endoplasmic reticulum upon binding to an allosteric inhibitor
    • Choi Y, Seeliger MA, Panjarian SB, Kim H, Deng X, et al. (2009) Nmyristoylated c-Abl tyrosine kinase localizes to the endoplasmic reticulum upon binding to an allosteric inhibitor. J Biol Chem 284: 29005-29014.
    • (2009) J Biol Chem , vol.284 , pp. 29005-29014
    • Choi, Y.1    Seeliger, M.A.2    Panjarian, S.B.3    Kim, H.4    Deng, X.5
  • 45
    • 33644871166 scopus 로고    scopus 로고
    • Organization of the SH3-SH2 unit in active and inactive forms of the c-Abl tyrosine kinase
    • Nagar B, Hantschel O, Seeliger M, Davies JM, Weis WI, et al. (2006) Organization of the SH3-SH2 unit in active and inactive forms of the c-Abl tyrosine kinase. Mol Cell 21: 787-798.
    • (2006) Mol Cell , vol.21 , pp. 787-798
    • Nagar, B.1    Hantschel, O.2    Seeliger, M.3    Davies, J.M.4    Weis, W.I.5
  • 46
    • 31644438945 scopus 로고    scopus 로고
    • Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680
    • Young MA, Shah NP, Chao LH, Seeliger M, Milanov ZV, et al. (2006) Structure of the kinase domain of an imatinib-resistant Abl mutant in complex with the Aurora kinase inhibitor VX-680. Cancer Res 66: 1007-1014.
    • (2006) Cancer Res , vol.66 , pp. 1007-1014
    • Young, M.A.1    Shah, N.P.2    Chao, L.H.3    Seeliger, M.4    Milanov, Z.V.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.