PDB ID: 6O0O
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F3Q | ~{N}-(4-hydroxyphenyl)-3-[6-[[(3~{S})-3-(morpholin-4-ylmethyl)-3,4-dihydro-1~{H}-isoquinolin-2-yl]carbonyl]-1,3-benzodioxol-5-yl]-~{N}-phenyl-5,6,7,8-tetrahydroindolizine-1-carboxamide | PoSSuM |
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Download interaction data: 6O0O
Structure summary
Code : | 6O0O PDBj RCSB PDB PDBe | ||||||||||||
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Header : | APOPTOSIS | ||||||||||||
Title : | crystal structure of BCL-2 G101V mutation with S55746 | ||||||||||||
Release Data : | 2019-05-22 | ||||||||||||
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Authors : | Birkinshaw, R.W., Luo, C.S., Colman, P.M., Czabotar, P.E. | ||||||||||||
Keywords : | BCL-2, S55746, complex, Protein-protein interface inhibitor, resistance mutation, APOPTOSIS | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.998 Å ) | ||||||||||||
Citation : |
Structures of BCL-2 in complex with venetoclax reveal the molecular basis of resistance mutations.
Birkinshaw, R.W.,Gong, J.N.,Luo, C.S.
et al.
PubMed: 31160589 |
Reaction
Chain : | A, C |
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UniProt : | P10415 (BCL2_HUMAN) |
Reaction : | - |
Chain : | A, C |
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UniProt : | Q07817 (B2CL1_HUMAN) |
Reaction : | - |