MolNFT v1 · #4758 · protein
Inhibition of the hepatitis C virus NS3/4A protease. the crystal structures of two protease-inhibitor complexes (apo structure)
1DXP · PROTEASE/HELICASE NS3 (P70): “Inhibition of the hepatitis C virus NS3/4A protease. the crystal structures of two protease-inhibitor…”. X-ray diffraction, 1 ligand (ZN), 1 pocket (best druggability 0.29). MolNFT v1 #4758 on…
- PDB
- 1DXP
- Type
- protein
- Length
- 374 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- PROTEASE/HELICASE NS3 (P70); Nonstructural protein NS4A (P4)
- EC
- 3.4.22.-
- UniProt
- Q81755
- Ligands
- ZN
- Pockets
- 1 · best druggability 0.29
Structure
x-ray diffraction · 2 distinct chains · 11% helix, 49% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | PROTEASE/HELICASE NS3 (P70) (EC 3.4.22.-) | protein | 175 | 11% helix, 47% strand | Q81755 |
| C, D | Nonstructural protein NS4A (P4) | protein | 12 | 0% helix, 75% strand | Q81755 |
Ligands and binding sites
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 | 55 | 0.29 | 0.75 | 15 | empty |
Interfaces
3 interfaces between chains.
- A–C · 1211 Ų buried · 33 hydrogen bonds · protein-protein
- B–D · 1207 Ų buried · 29 hydrogen bonds · protein-protein
- A–B · 463 Ų buried · 9 hydrogen bonds · protein-protein
Compared structures
- 1DXP · Inhibition of the Hepatitis C Virus NS3/4A Protease. The Crystal Structures of Two… · the same entry in another collection · chain B against B, 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 Q81755
- Elsewhere: RCSB PDB 1DXP · PDBe 1DXP · UniProt Q81755
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