Sequence information
Variant position: 411 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 752 The length of the canonical sequence.
Location on the sequence:
AIMVLASQGIVAGTLTVGDL
V MVNGLLFQLSLPLNFLGTVY
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 AIMVLASQ----GIVAGTLTVGDLV MVNGLLFQLSLPLNFLGTV--Y
Mouse AIMVLASQ----GIVAGALTVGDLV MVNGLLFQLSLPLNFL
Rat AIMVLASQ----GIVAGALTVGDLV MVNGLLFQLSLPLNFL
Slime mold SLLVMGTIIGIYGFAMSQTLSNSIL LLQFILYSLMITASMN
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
Chain
23 – 752
ATP-binding cassette sub-family B member 7, mitochondrial
Transmembrane
410 – 430
Helical
Domain
140 – 436
ABC transmembrane type-1
Literature citations
X-linked cerebellar ataxia and sideroblastic anaemia associated with a missense mutation in the ABC7 gene predicting V411L.
Maguire A.; Hellier K.; Hammans S.; May A.;
Br. J. Haematol. 115:910-917(2001)
Cited for: VARIANT ASAT LEU-411; VARIANTS GLY-315 AND ILE-346;
Disclaimer:
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.