MolNFT v1 · #74881 · protein
Structure of I274C variant of E. COLI kate
3P9Q · Catalase hpii: “Structure of I274C variant of E. COLI kate”. X-ray diffraction, 3 ligands (HDD, HDE, H2S), 20 pockets (best druggability 0.89). MolNFT v1 #74881 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 3P9Q
- Type
- protein
- Length
- 2,904 residues
- Chains
- 4
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Catalase hpii
- EC
- 1.11.1.6
- UniProt
- P21179
- Ligands
- HDD, HDE, H2S
- Pockets
- 20 · best druggability 0.89
Structure
x-ray diffraction · 1 distinct chain · 32% helix, 18% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C, D | Catalase hpii (EC 1.11.1.6) | protein | 726 | 32% helix, 18% strand | P21179 |
Ligands and binding sites
- HDD · Cis-heme D hydroxychlorin gamma-spirolactone · ligand · 4 copies · chains A, D, B, C
- HDE · Cis-heme D hydroxychlorin gamma-spirolactone 17R, 18S · ligand · 4 copies · chains A, D, B, C
- H2S · Hydrosulfuric acid · ion · 4 copies · chains A, B, C, D
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
20 pockets found on a 1 Å grid, 18 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 488 | 0.89 | 0.96 | 58 | empty |
| 2 | 500 | 0.88 | 0.96 | 57 | empty |
| 3 | 376 | 0.86 | 0.95 | 45 | empty |
| 4 | 294 | 0.86 | 0.96 | 50 | HDD, HDE |
| 5 | 293 | 0.85 | 0.96 | 47 | HDD, HDE, H2S |
Interfaces
6 interfaces between chains.
- A–D · 6223 Ų buried · 118 hydrogen bonds · protein-protein
- B–C · 6208 Ų buried · 118 hydrogen bonds · protein-protein
- B–D · 5898 Ų buried · 85 hydrogen bonds · protein-protein
- A–C · 5868 Ų buried · 82 hydrogen bonds · protein-protein
- C–D · 2281 Ų buried · 40 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 covalent (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 P21179
- Elsewhere: RCSB PDB 3P9Q · PDBe 3P9Q · UniProt P21179
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.