Variant position: 378 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 522 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 VCRDLFTASNDPLLWRFLYL RDFRDNTVRVQDTDWKELYRK
Mouse VCHDLLIASNDPLLWRCLYL RDFRDGTVRGPDTDWKELYRK
Rat VCHDLLIASNDPLLWRCLYL RDFRDSTIRGPDTDWKELYRK
Bovine VCRDLCITSNDQLLWRCLYL RDFRDGSIRGRDTDWKELYKK
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 – 522 F-box only protein 7
The Parkinson's disease-linked proteins Fbxo7 and Parkin interact to mediate mitophagy.
Burchell V.S.; Nelson D.E.; Sanchez-Martinez A.; Delgado-Camprubi M.; Ivatt R.M.; Pogson J.H.; Randle S.J.; Wray S.; Lewis P.A.; Houlden H.; Abramov A.Y.; Hardy J.; Wood N.W.; Whitworth A.J.; Laman H.; Plun-Favreau H.;
Nat. Neurosci. 16:1257-1265(2013)
Cited for: FUNCTION; INTERACTION WITH PRKN AND PINK1; SUBCELLULAR LOCATION; MUTAGENESIS OF THR-22; CHARACTERIZATION OF VARIANT PARK15 GLY-378;
Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays.
Shojaee S.; Sina F.; Banihosseini S.S.; Kazemi M.H.; Kalhor R.; Shahidi G.-A.; Fakhrai-Rad H.; Ronaghi M.; Elahi E.;
Am. J. Hum. Genet. 82:1375-1384(2008)
Cited for: VARIANT PARK15 GLY-378; VARIANT ILE-115;
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.