Research workbench
Arginase-descarboxy-nor-noha complex
Analyse Arginase-descarboxy-nor-noha complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 1T4R
- Type
- protein
- Length
- 942 residues
- Chains
- 3
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Arginase 1
- EC
- 3.5.3.1
- UniProt
- P07824
- Ligands
- AHI, MN
- Pockets
- 9 · best druggability 0.80
Structure
x-ray diffraction · 1 distinct chain · 40% helix, 17% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B, C | Arginase 1 (EC 3.5.3.1) | protein | 314 | 40% helix, 17% strand | P07824 |
Ligands and binding sites
- AHI · 3-{[(E)-amino(hydroxyimino)methyl]amino}propan-1-aminium · ligand · 3 copies · chains A, B, C
- MN · Manganese (II) ion · metal · 6 copies · chains A, B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
9 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1197 | 0.80 | 0.81 | 104 | empty |
| 2 | 256 | 0.57 | 0.78 | 30 | empty |
| 3 | 122 | 0.47 | 0.78 | 22 | empty |
| 4 | 84 | 0.45 | 0.81 | 19 | AHI |
| 5 | 97 | 0.45 | 0.80 | 18 | AHI |
Interfaces
3 interfaces between chains.
- B–C · 977 Ų buried · 13 hydrogen bonds · protein-protein
- A–B · 949 Ų buried · 12 hydrogen bonds · protein-protein
- A–C · 945 Ų buried · 14 hydrogen bonds · protein-protein
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 P07824
- Elsewhere: RCSB PDB 1T4R · PDBe 1T4R · UniProt P07824
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