Expasy logo

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q70HW3: Variant p.Val148Gly

Mitochondrial S-adenosylmethionine carrier protein
Gene: SLC25A26
Feedback?
Variant information Variant position: help 148 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance
Residue change: help From Valine (V) to Glycine (G) at position 148 (V148G, p.Val148Gly). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from medium size and hydrophobic (V) to glycine (G) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -3 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page
Variant description: help In COXPD28; decreased S-adenosyl-L-methionine/S-adenosyl-L-homocysteine antiporter activity. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 148 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 274 The length of the canonical sequence.
Location on the sequence: help FSNILYEEGIQGLYRGYKST V LREIPFSLVQFPLWESLKAL 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         FSNILYEEGI-QGLYRGYKSTVLREIPFSLVQFPLWESLKAL

Mouse                         FLTILSEEGI-QGLYRGYKSTVLREIPFSLVQFPLWESLKA

Bovine                        FSNILCQEGI-QGLYRGYKSTVLREIPFSLVQFPLWESLKA

Xenopus laevis                LSVTLREEGI-KGLYRGYKSTVLREIPFSLVQFPLWEFLKN

Xenopus tropicalis            LSATLRQEGI-KGLYRGYKSTVLREIPFSLVQFPLWESLKD

Zebrafish                     LLNSLQEEGF-RGLYRGYGSTVLREIPFSLVQFPLWEYLKA

Drosophila                    LLRAYRTEGLKRGLYRGFGSTIMREIPFSLIQFPLWEYFKL
Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 1 – 274 Mitochondrial S-adenosylmethionine carrier protein
Transmembrane 142 – 162 Helical; Name=4
Repeat 86 – 168 Solcar 2



Literature citations
Intra-mitochondrial methylation deficiency due to mutations in SLC25A26.
Kishita Y.; Pajak A.; Bolar N.A.; Marobbio C.M.; Maffezzini C.; Miniero D.V.; Monne M.; Kohda M.; Stranneheim H.; Murayama K.; Naess K.; Lesko N.; Bruhn H.; Mourier A.; Wibom R.; Nennesmo I.; Jespers A.; Govaert P.; Ohtake A.; Van Laer L.; Loeys B.L.; Freyer C.; Palmieri F.; Wredenberg A.; Okazaki Y.; Wedell A.;
Am. J. Hum. Genet. 97:761-768(2015)
Cited for: INVOLVEMENT IN COXPD28; VARIANTS COXPD28 VAL-102; GLY-148 AND LEU-199; CHARACTERIZATION OF VARIANTS COXPD28 VAL-102; GLY-148 AND LEU-199; FUNCTION; TRANSPORTER ACTIVITY; SUBCELLULAR LOCATION;
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.