Research workbench
Ribonuclease inhibitor complexed with ribonuclease a
Analyse Ribonuclease inhibitor complexed with ribonuclease a in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1DFJ
- Type
- protein
- Length
- 580 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Ribonuclease a; Ribonuclease inhibitor
- EC
- 3.1.27.5
- UniProt
- P61823, P10775
- Ligands
- ACE, SO4
- Pockets
- 3 · best druggability 0.76
Structure
x-ray diffraction · 2 distinct chains · 38% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| E | Ribonuclease a (EC 3.1.27.5) | protein | 124 | 18% helix, 34% strand | P61823 |
| I | Ribonuclease inhibitor | protein | 456 | 44% helix, 12% strand | P10775 |
Ligands and binding sites
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1023 | 0.76 | 0.79 | 99 | empty |
| 2 | 55 | 0.73 | 0.98 | 16 | empty |
| 3 | 231 | 0.67 | 0.84 | 34 | SO4 |
Interfaces
1 interface between chains.
- E–I · 1441 Ų buried · 17 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 disulfide, 1 covalent (disulfide, covalent ligand).
Compared structures
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 P61823
- Every structure of UniProt P10775
- Elsewhere: RCSB PDB 1DFJ · PDBe 1DFJ · UniProt P61823 · UniProt P10775
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