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 |
|---|---|---|---|
| 4j56 | FAD | Thioredoxin reductase 2 | 1.8.1.9 |
| PDB ID | HET | Uniprot Name | EC Number | Cavity Similarity |
Align |
|---|---|---|---|---|---|
| 4j56 | FAD | Thioredoxin reductase 2 | 1.8.1.9 | 1.000 | |
| 3dgz | FAD | Thioredoxin reductase 2, mitochondrial | 1.8.1.9 | 0.521 | |
| 4kpr | FAD | Thioredoxin reductase 1, cytoplasmic | 1.8.1.9 | 0.518 | |
| 3qfb | FAD | Thioredoxin reductase 1, cytoplasmic | 1.8.1.9 | 0.506 | |
| 3sqp | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.503 | |
| 1bzl | FAD | Trypanothione reductase | 1.8.1.12 | 0.491 | |
| 1grh | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.490 | |
| 1feb | FAD | Trypanothione reductase | 1.8.1.12 | 0.481 | |
| 1k4q | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.479 | |
| 2hqm | FAD | Glutathione reductase | 1.8.1.7 | 0.475 | |
| 1ger | FAD | Glutathione reductase | 1.8.1.7 | 0.473 | |
| 2nvk | FAD | Thioredoxin reductase 1, mitochondrial | 1.8.1.9 | 0.467 | |
| 3grs | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.464 | |
| 4nev | FAD | Trypanothione reductase | / | 0.464 | |
| 4la1 | FAD | Thioredoxin glutathione reductase | / | 0.457 | |
| 4gr1 | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.450 | |
| 1fec | FAD | Trypanothione reductase | 1.8.1.12 | 0.448 | |
| 4dna | FAD | Probable glutathione reductase | / | 0.442 | |
| 2v6o | FAD | Thioredoxin glutathione reductase | / | 0.440 | |
| 4jq9 | FAD | Dihydrolipoyl dehydrogenase | / | 0.440 |