Research workbench
Crystal structure of human KDM4A in complex with compound 15
Analyse Crystal structure of human KDM4A in complex with compound 15 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 5F2S
- Type
- protein
- Length
- 1,390 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Lysine-specific demethylase 4A
- EC
- 1.14.11.-
- UniProt
- O75164
- Ligands
- 5TZ, ZN, CL
- Pockets
- 20 · best druggability 0.73
Structure
x-ray diffraction · 4 distinct chains · 30% helix, 24% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Lysine-specific demethylase 4A (EC 1.14.11.-) | protein | 342 | 31% helix, 25% strand | O75164 |
| B | Lysine-specific demethylase 4A (EC 1.14.11.-) | protein | 352 | 31% helix, 24% strand | O75164 |
| C | Lysine-specific demethylase 4A (EC 1.14.11.-) | protein | 347 | 30% helix, 24% strand | O75164 |
| D | Lysine-specific demethylase 4A (EC 1.14.11.-) | protein | 349 | 30% helix, 24% strand | O75164 |
Ligands and binding sites
- 5TZ · 2-(2-azanyl-1,3-thiazol-4-yl)pyridine-4-carboxylic acid · ligand · 4 copies · chains A, B, C, D
- ZN · Zinc ion · metal · 8 copies · chains A, B, C, D
- CL · Chloride ion · ion · chains D
- EDO · 1,2-ethanediol · additive · 37 copies · chains A, B, C, D
- DMS · Dimethyl sulfoxide · additive · 4 copies · chains A, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 497 | 0.73 | 0.82 | 44 | ZN, 5TZ, EDO |
| 2 | 405 | 0.72 | 0.83 | 42 | ZN, 5TZ, EDO |
| 3 | 437 | 0.72 | 0.82 | 39 | ZN, 5TZ, EDO |
| 4 | 313 | 0.69 | 0.83 | 39 | ZN, 5TZ, EDO |
| 5 | 226 | 0.59 | 0.80 | 30 | EDO |
Interfaces
4 interfaces between chains.
- B–D · 558 Ų buried · 2 hydrogen bonds · protein-protein
- B–C · 422 Ų buried · 8 hydrogen bonds · protein-protein
- A–D · 125 Ų buried · 1 hydrogen bond · protein-protein
- A–B · 34 Ų buried · 0 hydrogen bonds · protein-protein
Compared structures
- 5F2S · Crystal structure of human KDM4A in complex with compound 15 · the same entry in another collection · chain A against A, TM-score 1.00
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt O75164
- Elsewhere: RCSB PDB 5F2S · PDBe 5F2S · UniProt O75164
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