MolNFT v1 · #109304 · protein
Crystal structure of human-yeast chimera acetyl CoA carboxylase ct domain bound to compound 1
4WYO · Acetyl-CoA carboxylase: “Crystal structure of human-yeast chimera acetyl CoA carboxylase ct domain bound to compound 1”. X-ray diffraction, 1 ligand (3W2), 15 pockets (best druggability 0.84). MolNFT v1 #109304 on GenesisL1: 3D…
- PDB
- 4WYO
- Type
- protein
- Length
- 1,456 residues
- Chains
- 2
- Method
- x-ray diffraction
- Collection
- MolNFT v1 / PDB
- Contract
- 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
- Owner
- 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
- Molecule
- Acetyl-CoA carboxylase
- EC
- 6.4.1.2, 6.3.4.14
- UniProt
- Q00955
- Ligands
- 3W2
- Pockets
- 15 · best druggability 0.84
Structure
x-ray diffraction · 2 distinct chains · 44% helix, 19% strand (DSSP).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| B | Acetyl-CoA carboxylase (EC 6.4.1.2, 6.3.4.14) | protein | 733 | 44% helix, 19% strand | Q00955 |
| C | Acetyl-CoA carboxylase (EC 6.4.1.2, 6.3.4.14) | protein | 723 | 43% helix, 19% strand | Q00955 |
Ligands and binding sites
- 3W2 · 2'-tert-butyl-1-(2H-indazol-5-ylcarbonyl)-2'H-spiro[piperidine-4,5'-pyrano[3,2-c]pyrazol]-7'(6'H)-one · ligand · 2 copies · chains B, C
Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.
Pockets
15 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 1113 | 0.84 | 0.85 | 110 | 3W2 |
| 2 | 478 | 0.77 | 0.85 | 35 | empty |
| 3 | 587 | 0.75 | 0.82 | 64 | 3W2 |
| 4 | 267 | 0.60 | 0.79 | 37 | empty |
| 5 | 218 | 0.58 | 0.79 | 28 | empty |
Interfaces
1 interface between chains.
- B–C · 6878 Ų buried · 54 hydrogen bonds · protein-protein
Compared structures
- Q00955 · AlphaFold monomer V2.0 prediction for acetyl-CoA carboxylase (Q00955) · a predicted model of the same protein · chain B against A, TM-score 0.98
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 Q00955
- Elsewhere: RCSB PDB 4WYO · PDBe 4WYO · UniProt Q00955
GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.