MolNFT v1 · #180872 · protein
Improved feline drugs as SARS-cov-2 mpro inhibitors: structure- activity studies & micellar solubilization for enhanced bioavailability
7LDL: “Improved feline drugs as SARS-cov-2 mpro inhibitors: structure- activity studies & micellar solubilization…”. X-ray diffraction, 1 ligand (XV4). MolNFT v1 #180872 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 7LDL
- Type
- protein
- Length
- 612 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- UniProt
- P0DTD1
- Ligands
- XV4
Structure
x-ray diffraction · 1 distinct chain.
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | — | protein | 306 | — | P0DTD1 |
Ligands and binding sites
- XV4 · N-[(2S)-1-({(2S)-1-hydroxy-3-[(3S)-2-oxopyrrolidin-3-yl]propan-2-yl}amino)-4-methyl-1-oxopentan-2-yl]-4-methoxy-1H-indole-2-carboxamide · ligand · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Compared structures
- 7LDL · Improved Feline Drugs as SARS-CoV-2 Mpro Inhibitors: Structure-Activity Studies &… · 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 P0DTD1
- Elsewhere: RCSB PDB 7LDL · PDBe 7LDL · UniProt P0DTD1
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