MolNFT v1 · #36542 · protein
Structure of full length telethonin in complex with the N-terminus of titin
2F8V · N2B-titin isoform: “Structure of full length telethonin in complex with the N-terminus of titin”. X-ray diffraction, 1 ligand (SO4), 8 pockets (best druggability 0.79). MolNFT v1 #36542 on GenesisL1: 3D structure, binding sites and…
- PDB
- 2F8V
- Type
- protein
- Length
- 951 residues
- Chains
- 6
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- N2B-titin isoform; Telethonin
- UniProt
- Q8WZ42, O15273
- Ligands
- SO4
- Pockets
- 8 · best druggability 0.79
Structure
x-ray diffraction · 5 distinct chains · 3% helix, 63% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | N2B-titin isoform | protein | 194 | 3% helix, 63% strand | Q8WZ42 |
| B | N2B-titin isoform | protein | 197 | 3% helix, 63% strand | Q8WZ42 |
| T, Y | Telethonin | protein | 88 | 0% helix, 69% strand | O15273 |
| C | N2B-titin isoform | protein | 191 | 3% helix, 61% strand | Q8WZ42 |
| D | N2B-titin isoform | protein | 193 | 3% helix, 61% strand | Q8WZ42 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · 5 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
8 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1112 | 0.79 | 0.80 | 89 | empty |
| 2 | 410 | 0.68 | 0.80 | 38 | empty |
| 3 | 513 | 0.63 | 0.76 | 54 | SO4 |
| 4 | 186 | 0.57 | 0.80 | 28 | empty |
| 5 | 149 | 0.51 | 0.79 | 26 | empty |
Interfaces
8 interfaces between chains.
- D–Y · 1932 Ų buried · 46 hydrogen bonds · protein-protein
- B–T · 1921 Ų buried · 43 hydrogen bonds · protein-protein
- A–T · 1626 Ų buried · 37 hydrogen bonds · protein-protein
- C–Y · 1618 Ų buried · 32 hydrogen bonds · protein-protein
- A–D · 458 Ų buried · 7 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 Q8WZ42
- Every structure of UniProt O15273
- Elsewhere: RCSB PDB 2F8V · PDBe 2F8V · UniProt Q8WZ42 · UniProt O15273
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