MolNFT v1 · #161819 · protein
The room temperature structure of lysozyme via the acoustic levitation of a droplet
6QQ3 · Lysozyme C: “The room temperature structure of lysozyme via the acoustic levitation of a droplet”. X-ray diffraction, 2 ligands (NA, CL), 1 pocket (best druggability 0.34). MolNFT v1 #161819 on GenesisL1: 3D structure, binding sites…
- PDB
- 6QQ3
- Type
- protein
- Length
- 129 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Lysozyme C
- EC
- 3.2.1.17
- UniProt
- P00698
- Ligands
- NA, CL
- Pockets
- 1 · best druggability 0.34
Structure
x-ray diffraction · 1 distinct chain · 40% helix, 11% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | Lysozyme C (EC 3.2.1.17) | protein | 129 | 40% helix, 11% strand | P00698 |
Ligands and binding sites
- NA · Sodium ion · metal · 5 copies · chains B
- CL · Chloride ion · ion · chains B
- ACT · Acetate ion · additive · chains B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
1 pocket found on a 1 Å grid, 0 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 56 | 0.34 | 0.77 | 14 | ACT |
Modifications
Observed in the structure: 4 disulfide (disulfide).
Compared structures
- 6QQ3 · The room temperature structure of lysozyme via the acoustic levitation of a droplet · the same entry in another collection · chain B against B, TM-score 1.00
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 P00698
- Elsewhere: RCSB PDB 6QQ3 · PDBe 6QQ3 · UniProt P00698
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