MolNFT v1 · #30328 · protein
Mutant human lysozyme C77A
207L: “Mutant human lysozyme C77A”. X-ray diffraction, 1 ligand (SC2), 1 pocket (best druggability 0.35). MolNFT v1 #30328 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 207L
- Type
- protein
- Length
- 130 residues
- Chains
- 1
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Lysozyme
- EC
- 3.2.1.17
- UniProt
- P00695
- Ligands
- SC2
- Pockets
- 1 · best druggability 0.35
Structure
x-ray diffraction · 1 distinct chain · 38% helix, 12% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Lysozyme (EC 3.2.1.17) | protein | 130 | 38% helix, 12% strand | P00695 |
Ligands and binding sites
- SC2 · N-acetyl-L-cysteine · ligand · chains A
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 | 81 | 0.35 | 0.75 | 14 | empty |
Modifications
Observed in the structure: 3 disulfide, 1 covalent (disulfide, covalent ligand).
Compared structures
- 207L · Mutant human lysozyme C77A · the same entry in another collection · chain A against A, 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 P00695
- Elsewhere: RCSB PDB 207L · PDBe 207L · UniProt P00695
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