Research workbench
Cryo-EM structure of unmodified nucleosome
Analyse Cryo-EM structure of unmodified nucleosome in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7XD1
- Type
- protein + DNA
- Length
- 1,054 residues
- Chains
- 10
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Histone H3; Histone H4; Histone H2A type 1-B/E; DNA (147-mer); Histone H2B type 1-K
- UniProt
- A0A6I9KHI6, A0A0P9AXL3, P04908, O60814
- Pockets
- 20 · best druggability 0.79
Structure
electron microscopy · 8 distinct chains · 60% helix, 6% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Histone H3 | protein | 98 | 61% helix, 4% strand | A0A6I9KHI6 |
| B | Histone H4 | protein | 80 | 61% helix, 9% strand | A0A0P9AXL3 |
| C, G | Histone H2A type 1-B/E | protein | 109 | 50% helix, 6% strand | P04908 |
| E | Histone H3 | protein | 97 | 63% helix, 4% strand | A0A6I9KHI6 |
| F | Histone H4 | protein | 79 | 59% helix, 9% strand | A0A0P9AXL3 |
| I | DNA (147-mer) | dna | 147 | — | — |
| J | DNA (147-mer) | dna | 147 | — | — |
| D, H | Histone H2B type 1-K | protein | 94 | 69% helix, 4% strand | O60814 |
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1143 | 0.79 | 0.81 | 86 | empty |
| 2 | 395 | 0.74 | 0.85 | 49 | empty |
| 3 | 241 | 0.73 | 0.88 | 33 | empty |
| 4 | 234 | 0.72 | 0.88 | 33 | empty |
| 5 | 357 | 0.72 | 0.85 | 36 | empty |
Interfaces
33 interfaces between chains.
- I–J · 6769 Ų buried · 733 hydrogen bonds · nucleic-nucleic
- A–B · 2582 Ų buried · 18 hydrogen bonds · protein-protein
- G–H · 2568 Ų buried · 18 hydrogen bonds · protein-protein
- C–D · 2566 Ų buried · 18 hydrogen bonds · protein-protein
- E–F · 2443 Ų buried · 20 hydrogen bonds · protein-protein
Compared structures
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 A0A6I9KHI6
- Every structure of UniProt A0A0P9AXL3
- Every structure of UniProt P04908
- Every structure of UniProt O60814
- Elsewhere: RCSB PDB 7XD1 · PDBe 7XD1 · UniProt A0A6I9KHI6 · UniProt A0A0P9AXL3 · UniProt P04908 · UniProt O60814
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