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9DP (3s)-6-(3-tert-butyl-5-{[(2,3-dichlorophenyl)carbamoyl]amino}-1h-pyrazol-1-yl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
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Code : 3QRK   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/TRANSFERASE INHIBITOR
Title : The crystal structure of human abl1 kinase domain in complex with DP-987
Release Data : 2011-06-01
Compound :
mol_id molecule chains synonym
1 Tyrosine-protein kinase ABL1 A Abelson murine leukemia viral oncogene homolog 1, Proto-oncogene c-Abl, p150
ec: 2.7.10.2
fragment: Kinase domain, UNP residues 229-499
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human SPODOPTERA FRUGIPERDA  (taxid:7108)
gene: ABL1, ABL, JTK7
expression_system_common: FALL ARMYWORM
expression_system_strain: SF9
expression_system_cell_line: SF9
expression_system_vector_type: BACULOVIRUS
Authors : Chan, W.W., Wise, S.C., Kaufman, M.D., Ahn, Y.M., Ensinger, C.L., Haack, T., Hood, M.M., Jones, J., Lord, J.W., Lu, W.P., Miller, D., Patt, W.C., Smith, B.D., Petillo, P.A., Rutkoski, T.J., Telikepalli, H., Vogeti, L., Yao, T., Chun, L., Clark, R., Evangelista, P., Gavrilescu, L.C., Lazarides, K., Zaleskas, V.M., Stewart, L.J., Van Etten, R.A., Flynn, D.L.
Keywords : ABL1, KINASE, KINASE DOMAIN, TRANSFERASE-TRANSFERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 2.30 Å )
Citation :

Conformational Control Inhibition of the BCR-ABL1 Tyrosine Kinase, Including the Gatekeeper T315I Mutant, by the Switch-Control Inhibitor DCC-2036.

Chan, W.W.,Wise, S.C.,Kaufman, M.D.  et al.
(2011)  Cancer Cell  19 : 556 - 568

PubMed: 21481795
DOI: 10.1016/j.ccr.2011.03.003

Chain : A
UniProt : P00519 (ABL1_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
ATP + L-tyrosyl-[protein] = ADP + H(+) + O-phospho-L-tyrosyl- [protein] 2.7.10.2 PROSITE-ProRule:PRU10028, PubMed:20357770, PubMed:28428613
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