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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q96RP9: Variant p.Asn174Ser

Elongation factor G, mitochondrial
Gene: GFM1
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Variant information Variant position: help 174 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 Asparagine (N) to Serine (S) at position 174 (N174S, p.Asn174Ser). 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 polar (N) to small size and polar (S) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 1 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 COXPD1. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 174 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 751 The length of the canonical sequence.
Location on the sequence: help QTMTVNRQMKRYNVPFLTFI N KLDRMGSNPARALQQMRSKL 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                         QTMTVNRQMKRYNVPFLTFINKLDRMGSNPARALQQMRSKL

Mouse                         QTMTVSRQMKRYNVPFLTFINKLDRMGSNPSRALQQMRSKL

Rat                           QTMTVSRQMKRYNVPFLTFINKLDRMGSNPARALQQMRSKL

Xenopus laevis                QTMTVNRQMKRYNVPFLTFINKLDRMGSNPSRAVLQLRSKL

Zebrafish                     QTVTVNRQMKRYSVPFLTFINKLDRLGANPNRALQQLRTKL

Caenorhabditis elegans        QTFTVNRQLARYNVPFICFVNKMDRNGATPLKALDGLRNKL

Drosophila                    QTLTVNRQMKRYNVPCLAFINKLDRLGSNPYRVLSQMRSKM

Slime mold                    QTITVDRQMRRYNVPRVVFINKLDRTGANPWNVIEQLRKKL

Baker's yeast                 QTVTVDRQMRRYNVPRVTFINKMDRMGSDPFRAIEQLNSKL

Fission yeast                 QTITVDRQMRRYNVPRISFVNKMDRMGADPWKVIQQINTKL

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 37 – 751 Elongation factor G, mitochondrial
Domain 44 – 321 tr-type G
Binding site 174 – 177
Modified residue 175 – 175 N6-acetyllysine



Literature citations
Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency.
Coenen M.J.H.; Antonicka H.; Ugalde C.; Sasarman F.; Rossi R.; Angelien Heister J.G.A.M.; Newbold R.F.; Trijbels F.J.M.F.; van den Heuvel L.P.; Shoubridge E.A.; Smeitink J.A.M.;
N. Engl. J. Med. 351:2080-2086(2004)
Cited for: VARIANT COXPD1 SER-174;
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.