Research workbench
Endogenous retrovirus HML2 capsid ntd
Analyse Endogenous retrovirus HML2 capsid ntd in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 6SA9
- Type
- protein
- Length
- 269 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Endogenous retrovirus group K member 9 pol protein
- EC
- 3.4.23.50, 2.7.7.49, 2.7.7.7, 3.1.26.4
- UniProt
- P63128
- Pockets
- 2 · best druggability 0.61
Structure
x-ray diffraction · 2 distinct chains · 68% helix, 3% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Endogenous retrovirus group K member 9 pol protein (EC 3.4.23.50, 2.7.7.49, 2.7.7.7, 3.1.26.4) | protein | 135 | 67% helix, 1% strand | P63128 |
| B | Endogenous retrovirus group K member 9 pol protein (EC 3.4.23.50, 2.7.7.49, 2.7.7.7, 3.1.26.4) | protein | 134 | 68% helix, 5% strand | P63128 |
Ligands and binding sites
- GOL · Glycerol · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
2 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 281 | 0.61 | 0.80 | 35 | empty |
| 2 | 53 | 0.39 | 0.81 | 16 | empty |
Interfaces
1 interface between chains.
- A–B · 816 Ų buried · 13 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 8 modified (engineered).
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 P63128
- Elsewhere: RCSB PDB 6SA9 · PDBe 6SA9 · UniProt P63128
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