MolNFT v1 · #171848 · protein
Bovine ATP synthase rotor domain, state 3
6ZIK · ATP synthase subunit gamma, mitochondrial: “Bovine ATP synthase rotor domain, state 3”. Electron microscopy, 8 pockets (best druggability 0.84). MolNFT v1 #171848 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 6ZIK
- Type
- protein
- Length
- 1,048 residues
- Chains
- 11
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- ATP synthase subunit gamma, mitochondrial; ATP synthase subunit delta, mitochondrial; ATP…
- UniProt
- P05631, P05630, P05632, P07926
- Pockets
- 8 · best druggability 0.84
Structure
electron microscopy · 5 distinct chains · 62% helix, 15% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| G | ATP synthase subunit gamma, mitochondrial | protein | 272 | 64% helix, 14% strand | P05631 |
| H | ATP synthase subunit delta, mitochondrial | protein | 132 | 26% helix, 39% strand | P05630 |
| I | ATP synthase subunit epsilon, mitochondrial | protein | 47 | 55% helix, 9% strand | P05632 |
| K, L, P | ATP synthase F(0) complex subunit C2, mitochondrial | protein | 74 | 91% helix, 0% strand | P07926 |
| M, N, Q, R, O | ATP synthase F(0) complex subunit C2, mitochondrial | protein | 75 | 95% helix, 0% strand | P07926 |
Pockets
8 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 449 | 0.84 | 0.91 | 50 | empty |
| 2 | 324 | 0.81 | 0.91 | 36 | empty |
| 3 | 103 | 0.69 | 0.92 | 26 | empty |
| 4 | 90 | 0.67 | 0.92 | 22 | empty |
| 5 | 208 | 0.57 | 0.80 | 35 | empty |
Interfaces
29 interfaces between chains.
- P–Q · 1648 Ų buried · 9 hydrogen bonds · protein-protein
- Q–R · 1565 Ų buried · 6 hydrogen bonds · protein-protein
- P–O · 1529 Ų buried · 4 hydrogen bonds · protein-protein
- L–M · 1516 Ų buried · 1 hydrogen bond · protein-protein
- N–O · 1499 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 modified (methylation).
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 P05631
- Every structure of UniProt P05630
- Every structure of UniProt P05632
- Every structure of UniProt P07926
- Elsewhere: RCSB PDB 6ZIK · PDBe 6ZIK · UniProt P05631 · UniProt P05630 · UniProt P05632 · UniProt P07926
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