4ZW1

Crystal structure of hBRD4 in complex with BL-BI06 reveals a novel synthesized inhibitor that induces Beclin1-independent/ATG5-dependent autophagic cell death in breast cancer

Functional Information from PDB Data

site_id	AC1
Number of Residues	10
Details	binding site for residue 4V1 A 201

Chain	Residue
A	TRP81
A	HOH361
A	PRO82
A	PHE83
A	GLN85
A	LEU92
A	LEU94
A	ASN140
A	HOH303
A	HOH304

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site_id	AC2
Number of Residues	4
Details	binding site for residue EDO A 202

Chain	Residue
A	THR109
A	LYS112
A	HOH314
A	HOH365

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site_id	AC3
Number of Residues	4
Details	binding site for residue EDO A 203

Chain	Residue
A	PRO53
A	PRO56
A	GLN84
A	LYS99

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Functional Information from PROSITE/UniProt

site_id	PS00633
Number of Residues	60
Details	BROMODOMAIN_1 Bromodomain signature. AwpFqqpvDavklnlpDYYkiIktpMdmgtIkkrlenny..Ywnaqeciqdfnt.MftNCyiY

Chain	Residue	Details
A	ALA80-TYR139

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Functional Information from SwissProt/UniProt

site_id	SWS_FT_FI1
Number of Residues	1
Details	SITE: Acetylated histone binding => ECO:0000269|PubMed:22464331

Chain	Residue	Details
A	ASN140

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site_id	SWS_FT_FI2
Number of Residues	2
Details	CROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2) => ECO:0007744|PubMed:28112733

Chain	Residue	Details
A	LYS99

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