Sequence information
Variant position: 44 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 557 The length of the canonical sequence.
Location on the sequence:
AEEEEDEDDDEPDDDTLDLG
E VELVEPGLGVGGERDGLLCG
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 AEEEEDEDDDEPDDDTLDLGE VELVEPGLGVGGERDGLLCG
Mouse AEEEEDDDEDEPDDDNLDLGE VELVEPGLGVGGERDGLLCG
Bovine AEEEEDEDDDEPDDDNLDLGE VELVEPGLGVGGERDGLLCG
Xenopus laevis ADEHEDE---------LELGE VELVEAGLS-GSERAG-LCG
Xenopus tropicalis ADEHEDD---------LELGE VELVEAGLS-GSERAG-ICG
Zebrafish EEETADD--------TLELGE VELVDPVVA-GGERDD--CG
Drosophila NVSSGDDGDD-------DFG- ---MEVDLPSSADRQM----
Baker's yeast AT---------------GFIA LHIMNDLLKAG---------
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
1 – 557
E3 ubiquitin-protein ligase ARIH1
Literature citations
Ari-1 Regulates Myonuclear Organization Together with Parkin and Is Associated with Aortic Aneurysms.
Tan K.L.; Haelterman N.A.; Kwartler C.S.; Regalado E.S.; Lee P.T.; Nagarkar-Jaiswal S.; Guo D.C.; Duraine L.; Wangler M.F.; Bamshad M.J.; Nickerson D.A.; Lin G.; Milewicz D.M.; Bellen H.J.;
Dev. Cell 45:226-244(2018)
Cited for: FUNCTION; POSSIBLE INVOLVEMENT IN AORTIC ANEURYSM; VARIANTS GLN-15; GLY-44 AND 171-ARG--ASP-557;
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.