Variant position: 873 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 1500 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 GGKFPVDGRVIEGHSMVDES LITGEAMPVAKKPGSTVIAGS
Mouse GGKFPVDGRVIEGHSMVDES LITGEAMPVAKKPGSTVIAGS
Rat GGKFPVDGRVIEGHSMVDES LITGEAMPVAKKPGSTVIAGS
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 – 1500 Copper-transporting ATPase 1
803 – 936 Cytoplasmic
42 – 1038 Missing. In isoform 3.
82 – 1499 Missing. In isoform 6.
872 – 875
The copper-transporting capacity of ATP7A mutants associated with Menkes disease is ameliorated by COMMD1 as a result of improved protein expression.
Vonk W.I.; de Bie P.; Wichers C.G.; van den Berghe P.V.; van der Plaats R.; Berger R.; Wijmenga C.; Klomp L.W.; van de Sluis B.;
Cell. Mol. Life Sci. 69:149-163(2012)
Cited for: INTERACTION WITH ATOX1 AND COMMD1; CHARACTERIZATION OF VARIANT OHS SER-1304; CHARACTERIZATION OF VARIANTS MNK ARG-873; ARG-1000 AND ASP-1362;
Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease.
Ogawa A.; Yamamoto S.; Takayanagi M.; Kogo T.; Kanazawa M.; Kohno Y.;
J. Hum. Genet. 44:206-209(1999)
Cited for: VARIANT MNK ARG-873;
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.