MolNFT v1 · #21753 · protein
Structure-based rational drug design: crystal structure of the complex formed between phospholipase A2 and a pentapeptide val-ala-phe-arg- ser
1SKG: “Structure-based rational drug design: crystal structure of the complex formed between phospholipase A2 and a…”. X-ray diffraction, 1 ligand (SO4). MolNFT v1 #21753 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1SKG
- Type
- protein
- Length
- 126 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Phospholipase A2; Vafrs
- EC
- 3.1.1.4
- Ligands
- SO4
Structure
x-ray diffraction · 2 distinct chains · 46% helix, 8% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Phospholipase A2 (EC 3.1.1.4) | protein | 121 | 48% helix, 8% strand | — |
| B | Vafrs | protein | 5 | 0% helix, 0% strand | — |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Interfaces
1 interface between chains.
- A–B · 484 Ų buried · 7 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 7 disulfide (disulfide).
Compared structures
- 1SKG · Structure-based rational drug design: Crystal structure of the complex formed between… · 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
- Elsewhere: RCSB PDB 1SKG · PDBe 1SKG
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