Target Binding Site Detail
Target General Information | Top | ||||
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Target ID | T40556 | Target Info | |||
Target Name | Bromodomain-containing protein 4 (BRD4) | ||||
Synonyms | Protein HUNK1; HUNK1 | ||||
Target Type | Clinical trial Target | ||||
Gene Name | BRD4 | ||||
Biochemical Class | Bromodomain | ||||
UniProt ID |
Ligand General Information | Top | ||||
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Ligand Name | N-(1-[1,1-di(pyridin-2-yl)ethyl]-6-{1-methyl-6-oxo-5-[(piperidin-4-yl)amino]-1,6-dihydropyridin-3-yl}-1H-indol-4-yl)ethanesulfonamide | Ligand Info | |||
Canonical SMILES | CCS(=O)(=O)NC1=C2C=CN(C2=CC(=C1)C3=CN(C(=O)C(=C3)NC4CCNCC4)C)C(C)(C5=CC=CC=N5)C6=CC=CC=N6 | ||||
InChI | 1S/C33H37N7O3S/c1-4-44(42,43)38-27-19-23(24-20-28(32(41)39(3)22-24)37-25-11-16-34-17-12-25)21-29-26(27)13-18-40(29)33(2,30-9-5-7-14-35-30)31-10-6-8-15-36-31/h5-10,13-15,18-22,25,34,37-38H,4,11-12,16-17H2,1-3H3 | ||||
InChIKey | RDWRDUFEWMSPGQ-UHFFFAOYSA-N | ||||
PubChem Compound ID | 156583302 |
Drug Binding Sites of Target | Top | |||||
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PDB ID: 7JKZ Bromodomain-containing protein 4 (BRD4) bromodomain 2 (BD2) complexed with YF3-126 | ||||||
Method | X-ray diffraction | Resolution | 2.49 Å | Mutation | No | [1] |
PDB Sequence |
KVSEQLKCCS
358 GILKEMFAKK368 HAAYAWPFYK378 PVDVEALGLH388 DYCDIIKHPM398 DMSTIKSKLE 408 AREYRDAQEF418 GADVRLMFSN428 CYKYNPPDHE438 VVAMARKLQD448 VFEMRFAKMP 458 D
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PDB ID: 7JKY Bromodomain-containing protein 4 (BRD4) bromodomain 1 (BD1) complexed with YF3-126 | ||||||
Method | X-ray diffraction | Resolution | 1.16 Å | Mutation | No | [1] |
PDB Sequence |
LENPPPPETS
51 NPNKPKRQTN61 QLQYLLRVVL71 KTLWKHQFAW81 PFQQPVDAVK91 LNLPDYYKII 101 KTPMDMGTIK111 KRLENNYYWN121 AQECIQDFNT131 MFTNCYIYNK141 PGDDIVLMAE 151 ALEKLFLQKI161 NELPTEE
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References | Top | ||||
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REF 1 | Novel Pyrrolopyridone Bromodomain and Extra-Terminal Motif (BET) Inhibitors Effective in Endocrine-Resistant ER+ Breast Cancer with Acquired Resistance to Fulvestrant and Palbociclib. J Med Chem. 2020 Jul 9;63(13):7186-7210. |
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