PREDICTED: Niemann-Pick C1-like protein 1, partial [Pseudopodoces humilis]
List of domain hits
Name | Accession | Description | Interval | E-value | |||
2A060601 super family | cl36767 | Niemann-Pick C type protein family; The model describes Niemann-Pick C type protein in ... |
1-103 | 7.68e-23 | |||
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. [Transport and binding proteins, Other] The actual alignment was detected with superfamily member TIGR00917: Pssm-ID: 273337 [Multi-domain] Cd Length: 1205 Bit Score: 91.51 E-value: 7.68e-23
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Name | Accession | Description | Interval | E-value | |||
2A060601 | TIGR00917 | Niemann-Pick C type protein family; The model describes Niemann-Pick C type protein in ... |
1-103 | 7.68e-23 | |||
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. [Transport and binding proteins, Other] Pssm-ID: 273337 [Multi-domain] Cd Length: 1205 Bit Score: 91.51 E-value: 7.68e-23
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Name | Accession | Description | Interval | E-value | |||
2A060601 | TIGR00917 | Niemann-Pick C type protein family; The model describes Niemann-Pick C type protein in ... |
1-103 | 7.68e-23 | |||
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. [Transport and binding proteins, Other] Pssm-ID: 273337 [Multi-domain] Cd Length: 1205 Bit Score: 91.51 E-value: 7.68e-23
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Blast search parameters | ||||
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