Research workbench
Crystal structure of nitrophorin 1 from rhodnius prolixus
Analyse Crystal structure of nitrophorin 1 from rhodnius prolixus in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.
- PDB
- 2NP1
- Type
- protein
- Length
- 368 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Nitrophorin 1
- UniProt
- Q26239
- Ligands
- HEM, NH4, 2HP
- Pockets
- 3 · best druggability 0.75
Structure
x-ray diffraction · 1 distinct chain · 13% helix, 45% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A, B | Nitrophorin 1 | protein | 184 | 13% helix, 45% strand | Q26239 |
Ligands and binding sites
- HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains A, B
- NH4 · Ammonium ion · ion · 2 copies · chains A, B
- 2HP · Dihydrogenphosphate ion · ion · 2 copies · chains A, B
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
3 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 428 | 0.75 | 0.84 | 43 | NH4, HEM |
| 2 | 456 | 0.73 | 0.82 | 43 | NH4, HEM |
| 3 | 78 | 0.39 | 0.78 | 20 | empty |
Interfaces
1 interface between chains.
- A–B · 48 Ų buried · 0 hydrogen bonds · protein-protein
Modifications
Observed in the structure: 4 disulfide (disulfide).
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 Q26239
- Elsewhere: RCSB PDB 2NP1 · PDBe 2NP1 · UniProt Q26239
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