5IWG: HDAC2 with ligand BRD4884

HDAC2 with ligand BRD4884. Determined by X-ray diffraction at 1.66 Å resolution. Released 31 Aug 2016.

Method: X-ray diffraction
Resolution: 1.66 Å
Organism: Homo sapiens
Chains: 3
Atoms: 9,747
Mol. weight: 129.27 kDa
Ligands: ZN, CA, IWX, PG5
Released: 31 Aug 2016

Explore 5IWG in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5IWG contains 58 α-helices and 50 β-strands across 3 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 20 helices, 16 β-strands

Element	Residues	Length	Sheet
β-strand	16-19	4	1
α-helix	24-26	3
α-helix	38-49	12
α-helix	52-55	4
β-strand	57-59	3	1
α-helix	60-62	3
α-helix	66-69	4
α-helix	75-83	9
α-helix	86-92	7
α-helix	93-98	6
α-helix	111-130	20
β-strand	136-139	4	1
β-strand	148	1	2
β-strand	151	1	2
β-strand	153	1	3
β-strand	156	1	3
α-helix	160-168	9
β-strand	175-179	5	1
α-helix	186-191	6
β-strand	198-205	8	1
α-helix	222-224	3
β-strand	228-233	6	1
α-helix	239-257	19
β-strand	261-265	5	1
α-helix	268-270	3
β-strand	271	1	4
β-strand	281	1	4
α-helix	283-295	13
β-strand	300-303	4	1
α-helix	310-324	15
β-strand	332	1	5
α-helix	333-335	3
α-helix	339-342	4
β-strand	347	1	5
α-helix	351-353	3
α-helix	361-375	15

Chain B: 19 helices, 16 β-strands

Element	Residues	Length	Sheet
β-strand	16-19	4	6
α-helix	24-26	3
α-helix	38-49	12
α-helix	52-55	4
β-strand	57-59	3	6
α-helix	60-62	3
α-helix	66-69	4
α-helix	75-83	9
α-helix	86-92	7
α-helix	93-99	7
α-helix	111-130	20
β-strand	136-139	4	6
β-strand	148	1	7
β-strand	151	1	7
β-strand	153	1	8
β-strand	156	1	8
α-helix	160-168	9
β-strand	175-179	5	6
α-helix	186-191	6
β-strand	198-205	8	6
α-helix	222-224	3
β-strand	228-233	6	6
α-helix	239-257	19
β-strand	261-265	5	6
α-helix	268-270	3
β-strand	271	1	9
β-strand	281	1	9
α-helix	283-294	12
β-strand	300-303	4	6
α-helix	310-324	15
β-strand	332	1	10
α-helix	333-335	3
α-helix	339-342	4
β-strand	347	1	10
α-helix	361-375	15

Chain C: 19 helices, 18 β-strands

Element	Residues	Length	Sheet
β-strand	16-19	4	11
α-helix	24-26	3
α-helix	38-49	12
α-helix	52-55	4
β-strand	57-59	3	11
α-helix	61-65	5
α-helix	66-69	4
α-helix	75-83	9
α-helix	86-88	3
α-helix	93-99	7
α-helix	111-130	20
β-strand	136-139	4	11
β-strand	148	1	12
β-strand	151	1	12
β-strand	153	1	13
β-strand	156	1	13
α-helix	160-168	9
β-strand	175-179	5	11
α-helix	186-191	6
β-strand	198-205	8	11
α-helix	222-224	3
β-strand	228-233	6	11
β-strand	238	1	14
α-helix	239-257	19
β-strand	261-265	5	11
α-helix	268-270	3
β-strand	271	1	15
β-strand	280	1	14
β-strand	281	1	15
α-helix	283-294	12
β-strand	300-303	4	11
α-helix	310-324	15
β-strand	332	1	16
α-helix	333-335	3
α-helix	339-342	4
β-strand	347	1	16
α-helix	361-375	15

Molecules and chains

Molecule	Chains	Type	Length	Organism	UniProt
Histone deacetylase 2	A, B, C	protein	368	Homo sapiens	Q92769 (AlphaFold model)

Sequence of entity 1 (A, B, C), FASTA

>5IWG_1 Histone deacetylase 2 (chains A, B, C)
GKKKVCYYYDGDIGNYYYGQGHPMKPHRIRMTHNLLLNYGLYRKMEIYRPHKATAEEMTK
YHSDEYIKFLRSIRPDNMSEYSKQMQRFNVGEDCPVFDGLFEFCQLSTGGSVAGAVKLNR
QQTDMAVNWAGGLHHAKKSEASGFCYVNDIVLAILELLKYHQRVLYIDIDIHHGDGVEEA
FYTTDRVMTVSFHKYGEYFPGTGDLRDIGAGKGKYYAVNFPMRDGIDDESYGQIFKPIIS
KVMEMYQPSAVVLQCGADSLSGDRLGCFNLTVKGHAKCVEVVKTFNLPLLMLGGGGYTIR
NVARCWTYETAVALDCEIPNELPYNDYFEYFGPDFKLHISPSNMTNQNTPEYMEKIKQRL
FENLRMLP

Ligands and cofactors

ID	Name	Formula	Copies
ZN	Zinc ion	Zn	3
CA	Calcium ion	Ca	6
IWX	N-(4-amino-4'-fluoro[1,1'-biphenyl]-3-yl)oxane-4-carboxamide	C18 H19 F N2 O2	3
PG5	1-methoxy-2-[2-(2-methoxy-ethoxy]-ethane	C8 H18 O4	1

Water and common crystallization additives (PGE, PEG, PG4) are not listed.

Primary citation

Kinetic and structural insights into the binding of histone deacetylase 1 and 2 (HDAC1, 2) inhibitors. Wagner, F.F., Weiwer, M., Steinbacher, S. et al. Bioorg Med Chem (2016) 24:4008-4015. DOI 10.1016/j.bmc.2016.06.040 · PubMed

Other PDB entries of the same protein (UniProt Q92769 (AlphaFold model), which also has an AlphaFold model), best resolution first:

7KBG 1.26 Å, Structure of Human HDAC2 in complex with a 2-substituted benzamide inhibitor (compound 20)
6WBZ 1.32 Å, Structure of Human HDAC2 in complex with an ethyl ketone inhibitor containing a…
6WBW 1.46 Å, Structure of Human HDAC2 in complex with an ethyl ketone inhibitor
7LTL 1.49 Å, Structure of human HDAC2 in complex with an inhibitor lacking a zinc binding group…
6XEB 1.5 Å, Structure of human HDAC2 in complex with ketone inhibitor (compound E)
7ZZP 1.52 Å, Structure of HDAC2 complexed with an inhibitory ligand
6WHN 1.54 Å, Histone deacetylases complex with peptide macrocycles
7MOT 1.54 Å, Structure of HDAC2 in complex with an inhibitor (compound 9)
7MOZ 1.54 Å, Structure of HDAC2 in complex with a macrocyclic inhibitor (compound 25)
6XDM 1.56 Å, Structure of human HDAC2 in complex with an aryl ketone inhibitor
7ZZT 1.56 Å, Ligand binding to HDAC2
4LY1 1.57 Å, Structure of Human HDAC2 in complex with inhibitor 4-(acetylamino)-N-[2-amino-5-(thiophen…

Browse structure collections

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