MolNFT v1 · #9773 · protein
Structure of a star mutant crp-camp at 2.2 a
1I6X · Catabolite gene activator protein: “Structure of a star mutant crp-camp at 2.2 a”. X-ray diffraction, 1 ligand (CMP), 5 pockets (best druggability 0.76). MolNFT v1 #9773 on GenesisL1: 3D structure, binding sites and pockets in GL1X.
- PDB
- 1I6X
- Type
- protein
- Length
- 401 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Catabolite gene activator protein
- UniProt
- P0ACJ8
- Ligands
- CMP
- Pockets
- 5 · best druggability 0.76
Structure
x-ray diffraction · 2 distinct chains · 39% helix, 30% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Catabolite gene activator protein | protein | 201 | 39% helix, 29% strand | P0ACJ8 |
| B | Catabolite gene activator protein | protein | 200 | 39% helix, 31% strand | P0ACJ8 |
Ligands and binding sites
- CMP · Adenosine-3',5'-cyclic-monophosphate · ligand · 3 copies · chains A, B
- TRS · 2-amino-2-hydroxymethyl-propane-1,3-diol · additive · chains A
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
5 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 435 | 0.76 | 0.85 | 49 | TRS, CMP |
| 2 | 127 | 0.71 | 0.92 | 27 | CMP |
| 3 | 246 | 0.58 | 0.79 | 22 | empty |
| 4 | 106 | 0.35 | 0.73 | 18 | empty |
| 5 | 75 | 0.30 | 0.74 | 18 | empty |
Interfaces
1 interface between chains.
- A–B · 1678 Ų buried · 5 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 P0ACJ8
- Elsewhere: RCSB PDB 1I6X · PDBe 1I6X · UniProt P0ACJ8
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