MolNFT v1 · #60522 · protein
Human complement component 5
3CU7 · Complement C5: “Human complement component 5”. X-ray diffraction, 2 ligands (NAG, CD), 20 pockets (best druggability 0.84). MolNFT v1 #60522 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 3CU7
- Type
- protein
- Length
- 3,106 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Complement C5
- UniProt
- P01031
- Ligands
- NAG, CD
- Pockets
- 20 · best druggability 0.84
Structure
x-ray diffraction · 2 distinct chains · 17% helix, 32% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Complement C5 | protein | 1625 | 17% helix, 31% strand | P01031 |
| B | Complement C5 | protein | 1481 | 17% helix, 32% strand | P01031 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 6 copies · chains A, B
- CD · Cadmium ion · metal · 9 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 886 | 0.84 | 0.86 | 77 | CD |
| 2 | 829 | 0.84 | 0.86 | 94 | CD |
| 3 | 840 | 0.83 | 0.86 | 95 | CD |
| 4 | 977 | 0.81 | 0.83 | 99 | empty |
| 5 | 967 | 0.81 | 0.82 | 99 | empty |
Interfaces
1 interface between chains.
- A–B · 1289 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 25 disulfide, 4 glycan (disulfide, N-glycosylation).
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 P01031
- Elsewhere: RCSB PDB 3CU7 · PDBe 3CU7 · UniProt P01031
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