| Analysis | rpsblast_cdd | Start | 122 |
| End | 1275 | Strand | + |
| Length | 1154 | Note | Gaps:146 |
| Hit Coverage | 100.00 | Hit Length | 1204 |
| Hit Pident | 53.49 | E Val | 0.0 |
| Hit Description | TIGR00917 2A060601 Niemann-Pick C type protein family. The model describes Niemann-Pick C type protein in eukaryotes. The defective protein has been associated with Niemann-Pick disease which is described in humans as autosomal recessive lipidosis. It is characterized by the lysosomal accumulation of unestrified cholesterol. It is an integral membrane protein which indicates that this protein is most likely involved in cholesterol transport or acts as some component of cholesterol homeostasis. | Hit Pcons | 14.12 |
| Name | Qrob_P0251840.2 |
| Protein Identifier |
Organism . Name |
Score | Score Type | Protein Description | Alias (in v1) | Code Enzyme | Gene Prediction Quality |
|---|---|---|---|---|---|---|---|
| Qrob_P0251840.2 | Quercus robur | 93.0 | egn | (M=2) K12385 - Niemann-Pick C1 protein | validated |
Powered by
