MolNFT v1 · #109373 · protein
The crystal structure of mupain-1-17 in complex with murinised human upa
4X0W: “The crystal structure of mupain-1-17 in complex with murinised human upa”. X-ray diffraction, 2 ligands (MRZ, SO4), 1 pocket (best druggability 0.43). MolNFT v1 #109373 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 4X0W
- Type
- protein
- Length
- 257 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Mupain-1-17; Urokinase-type plasminogen activator
- EC
- 3.4.21.73
- UniProt
- P00749
- Ligands
- MRZ, SO4
- Pockets
- 1 · best druggability 0.43
Structure
x-ray diffraction · 2 distinct chains · 10% helix, 39% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| P | Mupain-1-17 | protein | 10 | 0% helix, 10% strand | — |
| U | Urokinase-type plasminogen activator (EC 3.4.21.73) | protein | 247 | 10% helix, 40% strand | P00749 |
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 | 148 | 0.43 | 0.75 | 21 | SO4 |
Interfaces
1 interface between chains.
- P–U · 417 Ų buried · 5 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 6 disulfide, 1 covalent, 1 d-amino (disulfide, covalent ligand, D-amino acid).
Compared structures
- 4X0W · The crystal structure of mupain-1-17 in complex with murinised human uPA · the same entry in another collection · chain P against P, 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 P00749
- Elsewhere: RCSB PDB 4X0W · PDBe 4X0W · UniProt P00749
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