MolNFT v1 · #26680 · protein
Crystal structure of CD14
1WWL · Monocyte differentiation antigen CD14: “Crystal structure of CD14”. X-ray diffraction, 1 ligand (NAG), 7 pockets (best druggability 0.79). MolNFT v1 #26680 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1WWL
- Type
- protein
- Length
- 620 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Monocyte differentiation antigen CD14
- UniProt
- P10810
- Ligands
- NAG
- Pockets
- 7 · best druggability 0.79
Structure
x-ray diffraction · 2 distinct chains · 16% helix, 22% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Monocyte differentiation antigen CD14 | protein | 308 | 18% helix, 22% strand | P10810 |
| B | Monocyte differentiation antigen CD14 | protein | 312 | 14% helix, 22% strand | P10810 |
Ligands and binding sites
- NAG · 2-acetamido-2-deoxy-beta-D-glucopyranose · sugar · 10 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
7 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 742 | 0.79 | 0.83 | 49 | empty |
| 2 | 746 | 0.79 | 0.82 | 43 | empty |
| 3 | 125 | 0.68 | 0.89 | 21 | empty |
| 4 | 86 | 0.38 | 0.77 | 20 | empty |
| 5 | 76 | 0.38 | 0.77 | 19 | empty |
Interfaces
1 interface between chains.
- A–B · 643 Ų buried · 14 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 9 disulfide, 6 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 P10810
- Elsewhere: RCSB PDB 1WWL · PDBe 1WWL · UniProt P10810
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