Research workbench
Cryo-EM structure of SET8-cenp-a-nucleosome complex
Analyse Cryo-EM structure of SET8-cenp-a-nucleosome complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 7D20
- Type
- protein + DNA
- Length
- 1,186 residues
- Chains
- 11
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Histone H3-like centromeric protein a; Histone H4; Histone H2A type 1-B/E; Histone H2B…
- EC
- 2.1.1.-, 2.1.1.361
- UniProt
- P49450, P62805, P04908, P06899, Q9NQR1
- Pockets
- 20 · best druggability 0.82
Structure
electron microscopy · 11 distinct chains · 54% helix, 9% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Histone H3-like centromeric protein a | protein | 89 | 60% helix, 2% strand | P49450 |
| E | Histone H3-like centromeric protein a | protein | 91 | 60% helix, 4% strand | P49450 |
| B | Histone H4 | protein | 80 | 65% helix, 8% strand | P62805 |
| C | Histone H2A type 1-B/E | protein | 107 | 53% helix, 6% strand | P04908 |
| D | Histone H2B type 1-J | protein | 93 | 75% helix, 4% strand | P06899 |
| F | Histone H4 | protein | 87 | 55% helix, 5% strand | P62805 |
| G | Histone H2A type 1-B/E | protein | 109 | 50% helix, 6% strand | P04908 |
| I | DNA (145-mer) | dna | 136 | — | — |
| J | DNA (145-mer) | dna | 136 | — | — |
| K | Isoform 2 of N-lysine methyltransferase KMT5A (EC 2.1.1.-, 2.1.1.361) | protein | 166 | 20% helix, 30% strand | Q9NQR1 |
| H | Histone H2B type 1-J | protein | 92 | 76% helix, 4% strand | P06899 |
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 | 984 | 0.82 | 0.84 | 96 | empty |
| 2 | 353 | 0.76 | 0.87 | 47 | empty |
| 3 | 322 | 0.75 | 0.87 | 41 | empty |
| 4 | 497 | 0.72 | 0.82 | 51 | empty |
| 5 | 243 | 0.71 | 0.87 | 35 | empty |
Interfaces
44 interfaces between chains.
- I–J · 6036 Ų buried · 502 hydrogen bonds · nucleic-nucleic
- C–D · 2633 Ų buried · 16 hydrogen bonds · protein-protein
- G–H · 2563 Ų buried · 21 hydrogen bonds · protein-protein
- E–B · 2475 Ų buried · 20 hydrogen bonds · protein-protein
- A–F · 2448 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 P49450
- Every structure of UniProt P62805
- Every structure of UniProt P04908
- Every structure of UniProt P06899
- Every structure of UniProt Q9NQR1
- Elsewhere: RCSB PDB 7D20 · PDBe 7D20 · UniProt P49450 · UniProt P62805 · UniProt P04908 · UniProt P06899 · UniProt Q9NQR1
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