MolNFT v1 · #154763 · protein
F-actin of cardiac thin filament in high-calcium state
6KLN · Actin, alpha skeletal muscle: “F-actin of cardiac thin filament in high-calcium state”. Electron microscopy, 2 ligands (ADP, MG), 11 pockets (best druggability 0.79). MolNFT v1 #154763 on GenesisL1: 3D structure, binding sites and…
- PDB
- 6KLN
- Type
- protein
- Length
- 1,488 residues
- Chains
- 4
- Method
- electron microscopy
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Actin, alpha skeletal muscle
- UniProt
- P68134
- Ligands
- ADP, MG
- Pockets
- 11 · best druggability 0.79
Structure
electron microscopy · 1 distinct chain · 35% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Actin, alpha skeletal muscle | protein | 372 | 35% helix, 19% strand | P68134 |
Ligands and binding sites
- ADP · Adenosine-5'-diphosphate · ligand · 4 copies · chains A, B, C, D
- MG · Magnesium ion · metal · 4 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
11 pockets found on a 1 Å grid, 10 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 689 | 0.79 | 0.83 | 79 | empty |
| 2 | 261 | 0.76 | 0.89 | 47 | MG, ADP |
| 3 | 278 | 0.76 | 0.89 | 48 | MG, ADP |
| 4 | 290 | 0.75 | 0.88 | 50 | MG, ADP |
| 5 | 264 | 0.75 | 0.89 | 45 | MG, ADP |
Interfaces
5 interfaces between chains.
- B–D · 1269 Ų buried · 10 hydrogen bonds · protein-protein
- A–C · 1259 Ų buried · 8 hydrogen bonds · protein-protein
- A–B · 445 Ų buried · 4 hydrogen bonds · protein-protein
- C–D · 421 Ų buried · 5 hydrogen bonds · protein-protein
- B–C · 407 Ų buried · 4 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 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 P68134
- Elsewhere: RCSB PDB 6KLN · PDBe 6KLN · UniProt P68134
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