XK, Kell blood group complex subunit-related family, member 8, isoform CRA_a [Homo sapiens]
List of domain hits
Name | Accession | Description | Interval | E-value | |||
XK-related super family | cl20385 | XK-related protein; Members of this family comprise various XK-related proteins, that are ... |
17-162 | 1.85e-24 | |||
XK-related protein; Members of this family comprise various XK-related proteins, that are involved in sodium-dependent transport of neutral amino acids or oligopeptides. These proteins are responsible for the Kx blood group system - defects results in McLeod syndrome [MIM:314850], an X-linked multi-system disorder characterized by late onset abnormalities in the neuromuscular and hematopoietic systems. The actual alignment was detected with superfamily member pfam09815: Pssm-ID: 462912 Cd Length: 332 Bit Score: 96.53 E-value: 1.85e-24
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Name | Accession | Description | Interval | E-value | |||
XK-related | pfam09815 | XK-related protein; Members of this family comprise various XK-related proteins, that are ... |
17-162 | 1.85e-24 | |||
XK-related protein; Members of this family comprise various XK-related proteins, that are involved in sodium-dependent transport of neutral amino acids or oligopeptides. These proteins are responsible for the Kx blood group system - defects results in McLeod syndrome [MIM:314850], an X-linked multi-system disorder characterized by late onset abnormalities in the neuromuscular and hematopoietic systems. Pssm-ID: 462912 Cd Length: 332 Bit Score: 96.53 E-value: 1.85e-24
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Name | Accession | Description | Interval | E-value | |||
XK-related | pfam09815 | XK-related protein; Members of this family comprise various XK-related proteins, that are ... |
17-162 | 1.85e-24 | |||
XK-related protein; Members of this family comprise various XK-related proteins, that are involved in sodium-dependent transport of neutral amino acids or oligopeptides. These proteins are responsible for the Kx blood group system - defects results in McLeod syndrome [MIM:314850], an X-linked multi-system disorder characterized by late onset abnormalities in the neuromuscular and hematopoietic systems. Pssm-ID: 462912 Cd Length: 332 Bit Score: 96.53 E-value: 1.85e-24
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Blast search parameters | ||||
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