MolNFT v1 · #124655 · protein
Crystal structure of trypanosoma brucei procyclic specific surface antigen-2
5KLH · Surface glycoprotein: “Crystal structure of trypanosoma brucei procyclic specific surface antigen-2”. X-ray diffraction, 1 ligand (SO4), 3 pockets (best druggability 0.63). MolNFT v1 #124655 on GenesisL1: 3D structure, binding sites…
- PDB
- 5KLH
- Type
- protein
- Length
- 436 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Surface glycoprotein
- UniProt
- Q26806
- Ligands
- SO4
- Pockets
- 3 · best druggability 0.63
Structure
x-ray diffraction · 2 distinct chains · 19% helix, 41% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Surface glycoprotein | protein | 221 | 19% helix, 43% strand | Q26806 |
| B | Surface glycoprotein | protein | 215 | 19% helix, 40% strand | Q26806 |
Ligands and binding sites
- SO4 · Sulfate ion · ion · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 179 | 0.63 | 0.84 | 33 | empty |
| 2 | 142 | 0.49 | 0.78 | 33 | empty |
| 3 | 62 | 0.24 | 0.71 | 15 | empty |
Interfaces
1 interface between chains.
- A–B · 744 Ų buried · 3 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 disulfide (disulfide).
Compared structures
- 5KLH · Crystal Structure of Trypanosoma brucei Procyclic Specific Surface Antigen-2 · 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 Q26806
- Elsewhere: RCSB PDB 5KLH · PDBe 5KLH · UniProt Q26806
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