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 |
---|---|---|---|
1feb | FAD | Trypanothione reductase | 1.8.1.12 |
PDB ID | HET | Uniprot Name | EC Number | Cavity Similarity |
Align |
---|---|---|---|---|---|
1feb | FAD | Trypanothione reductase | 1.8.1.12 | 1.000 | |
1bzl | FAD | Trypanothione reductase | 1.8.1.12 | 0.546 | |
3sqp | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.527 | |
1ger | FAD | Glutathione reductase | 1.8.1.7 | 0.526 | |
4kpr | FAD | Thioredoxin reductase 1, cytoplasmic | 1.8.1.9 | 0.524 | |
3qfb | FAD | Thioredoxin reductase 1, cytoplasmic | 1.8.1.9 | 0.521 | |
4gr1 | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.518 | |
1k4q | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.512 | |
1grh | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.510 | |
3grs | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.510 | |
4nev | FAD | Trypanothione reductase | / | 0.507 | |
3dgz | FAD | Thioredoxin reductase 2, mitochondrial | 1.8.1.9 | 0.487 | |
4j56 | FAD | Thioredoxin reductase 2 | 1.8.1.9 | 0.484 | |
2j3n | FAD | Thioredoxin reductase 1, cytoplasmic | 1.8.1.9 | 0.465 | |
1bwc | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.463 | |
1grg | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.463 | |
1fea | FAD | Trypanothione reductase | 1.8.1.12 | 0.462 | |
1gre | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.462 | |
4jq9 | FAD | Dihydrolipoyl dehydrogenase | / | 0.460 | |
2hqm | FAD | Glutathione reductase | 1.8.1.7 | 0.458 | |
1gsn | FAD | Glutathione reductase, mitochondrial | 1.8.1.7 | 0.451 | |
1zk7 | FAD | Mercuric reductase | 1.16.1.1 | 0.447 | |
2jk6 | FAD | Trypanothione reductase | / | 0.445 | |
1fec | FAD | Trypanothione reductase | 1.8.1.12 | 0.443 |