Cavities are compared using Shaper.
For more information, please see the following publication:
Desaphy J. et al. Comparison and Druggability Prediction of protein-Ligand Binding sites from pharmacophore-annotated cavity shapes J. Chem. Inf. Model., 2012, 52(8), pp2287-2299
| PDB ID | HET | Uniprot Name | EC Number |
|---|---|---|---|
| 4dna | FAD | Probable glutathione reductase |
| PDB ID | HET | Uniprot Name | EC Number | Cavity Similarity |
Align |
|---|---|---|---|---|---|
| 4dna | FAD | Probable glutathione reductase | / | 1.000 | |
| 2jk6 | FAD | Trypanothione reductase | / | 0.581 | |
| 2hqm | FAD | Glutathione reductase | 1.8.1.7 | 0.537 | |
| 1fec | FAD | Trypanothione reductase | 1.8.1.12 | 0.527 | |
| 1tyt | FAD | Trypanothione reductase | 1.8.1.12 | 0.525 | |
| 3sqp | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.517 | |
| 4la1 | FAD | Thioredoxin glutathione reductase | / | 0.516 | |
| 1k4q | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.510 | |
| 1gxf | FAD | Trypanothione reductase | 1.8.1.12 | 0.509 | |
| 1grh | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.505 | |
| 3dgz | FAD | Thioredoxin reductase 2, mitochondrial | 1.8.1.9 | 0.505 | |
| 1feb | FAD | Trypanothione reductase | 1.8.1.12 | 0.502 | |
| 1bzl | FAD | Trypanothione reductase | 1.8.1.12 | 0.487 | |
| 4nev | FAD | Trypanothione reductase | / | 0.486 | |
| 4j56 | FAD | Thioredoxin reductase 2 | 1.8.1.9 | 0.474 | |
| 4kpr | FAD | Thioredoxin reductase 1, cytoplasmic | 1.8.1.9 | 0.473 | |
| 4gr1 | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.471 | |
| 3grs | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.467 | |
| 2wba | FAD | Trypanothione reductase | 1.8.1.12 | 0.462 | |
| 4fx9 | FAD | Coenzyme A disulfide reductase | 1.8.1.14 | 0.456 | |
| 1ger | FAD | Glutathione reductase | 1.8.1.7 | 0.451 | |
| 2f5z | FAD | Dihydrolipoyl dehydrogenase, mitochondrial | 1.8.1.4 | 0.440 | |
| 2x8g | FAD | Thioredoxin glutathione reductase | / | 0.440 |