Variant position: 575 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 652 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human VIQTMGKDLTPITPSSGFTI ELASAFTVVIASNIGLPVSTT
Mouse VIQTMGKDLTPITPSSGFTI ELASAFTVVIASNIGLPVSTT
Rat VIQTMGKDLTPITPSSGFTI ELASAFTVVIASNIGLPVSTT
Bovine VIQTMGKDLTPITPSSGFTI ELASAFTVVIASNIGLPVSTT
Cat VIQTMGKDLTPITPSSGFTI ELASAFTVVIASNVGLPVSTT
Xenopus laevis VIQTMGKDLTPITPSSGFTI ELASAFTVVVASNIGLPISTT
Xenopus tropicalis VIQTMGKDLTPITPSSGFTI ELASAFTVVVASNIGLPISTT
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 652 Sodium-dependent phosphate transporter 2
572 – 586 Helical
575 – 575 E -> DK. Abolishes sodium-dependent phosphate transport; no effect on retroviral receptor function.
575 – 575 E -> Q. Abolishes phosphate but not sodium uptake; when associated with Q-55 and Q-91.
No reference for the current variant in UniProtKB/Swiss-Prot.
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.