MolNFT v1 · #72815 · protein
Q118A mutant of SO1698 protein, an aspartic peptidase from shewanella oneidensis
3NJN: “Q118A mutant of SO1698 protein, an aspartic peptidase from shewanella oneidensis”. X-ray diffraction, 1 ligand (CA). MolNFT v1 #72815 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 3NJN
- Type
- protein
- Length
- 243 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Peptidase
- UniProt
- Q8EGA7
- Ligands
- CA
Structure
x-ray diffraction · 3 distinct chains · 0% helix, 55% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, C | Peptidase | protein | 114 | 0% helix, 55% strand | Q8EGA7 |
| B | Peptidase | protein | 8 | 0% helix, 50% strand | Q8EGA7 |
| D | Peptidase | protein | 7 | 0% helix, 57% strand | Q8EGA7 |
Ligands and binding sites
- CA · Calcium ion · metal · 2 copies · chains A, C
- MPD · (4S)-2-methyl-2,4-pentanediol · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Interfaces
3 interfaces between chains.
- A–C · 1255 Ų buried · 26 hydrogen bonds · protein-protein
- A–B · 672 Ų buried · 24 hydrogen bonds · protein-protein
- C–D · 627 Ų buried · 20 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 2 isopeptide (isopeptide).
Compared structures
- 3NJN · Q118A mutant of SO1698 protein, an aspartic peptidase from Shewanella oneidensis · 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 Q8EGA7
- Elsewhere: RCSB PDB 3NJN · PDBe 3NJN · UniProt Q8EGA7
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