Variant position: 430 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 721 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 QSLLCDNAEVKERVTLKPRS VLTSQVVVGPNITLPEGSVIS
Mouse QSLLCDRAEVKERVKLKPYC VLTSQVVVGPDITLPEGSVIS
Rat QSLLCDRAEVKERVILKPHC VLTSQVVVGPDIILPEGSVIS
Rabbit QSLLCDHAEVKEQVTLKPHC VLTSQVVVGPNITLPEGSVIS
Slime mold HSIICNGSIIKSSSIIGRGS IIGFNVYIGQSKTLEPFSKIT
Baker's yeast HSLIASNATLGSNVRLNDGC IIGFNVKIDDNMDLDRNTKIS
Fission yeast KAILANSVKIGNNCSIEDGA IVAAGVVIGDNTIIEKNKRLT
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
2 – 721 Translation initiation factor eIF-2B subunit epsilon
450 – 450 Phosphoserine
429 – 431
Subunits of the translation initiation factor eIF2B are mutant in leukoencephalopathy with vanishing white matter.
Leegwater P.A.J.; Vermeulen G.; Koenst A.A.M.; Naidu S.; Mulders J.; Visser A.; Kersbergen P.; Mobach D.; Fonds D.; van Berkel C.G.M.; Lemmers R.J.L.F.; Frants R.R.; Oudejans C.B.M.; Schutgens R.B.H.; Pronk J.C.; van der Knaap M.S.;
Nat. Genet. 29:383-388(2001)
Cited for: VARIANTS VWM GLY-73; ALA-91; PHE-106; HIS-113; HIS-299; GLY-315; HIS-315; PRO-339; GLN-339; TRP-339; VAL-386; ALA-430; ARG-628 AND LYS-650; VARIANT VAL-587;
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.