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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q9UMS0: Variant p.Pro183Arg

NFU1 iron-sulfur cluster scaffold homolog, mitochondrial
Gene: NFU1
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Variant information Variant position: help 183 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 Proline (P) to Arginine (R) at position 183 (P183R, p.Pro183Arg). 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 (P) to large size and basic (R) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 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 SPG93; likely pathogenic. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 183 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 254 The length of the canonical sequence.
Location on the sequence: help SEEDDEVVAMIKELLDTRIR P TVQEDGGDVIYKGFEDGIVQ 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                         SEEDDEVVAMIKELLDTRIRPTVQEDGGDVIYKGFE--DGIVQ

Mouse                         SEEDDEVVAMIKELLDTRIRPTVQEDGGDVIYRGFE--DGI

Drosophila                    LEDDDETVMMIKELLDTRIRPTVQEDGGDIVFMGYE--GGV

Baker's yeast                 TEEDEEVSELIEELIDTRIRPAILEDGGDIDYRGWDPKTGT
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 10 – 254 NFU1 iron-sulfur cluster scaffold homolog, mitochondrial
Region 173 – 241 NifU
Mutagenesis 189 – 189 G -> A. Alters protein structure. Increases likelihood of existing as monomer. Decreases ability to receive a Fe/S clusters from donor proteins. Decreases delivery rates of [2Fe-2S] cluster to target proteins.
Mutagenesis 189 – 189 G -> K. Alters protein structure. Increases likelihood of existing as monomer. Decreases ability to receive a Fe/S clusters from donor proteins. Decreases delivery rates of [2Fe-2S] cluster to target proteins.
Helix 167 – 188



Literature citations
Phenotypic continuum of NFU1-related disorders.
Kaiyrzhanov R.; Zaki M.S.; Lau T.; Sen S.; Azizimalamiri R.; Zamani M.; Sayin G.Y.; Hilander T.; Efthymiou S.; Chelban V.; Brown R.; Thompson K.; Scarano M.I.; Ganesh J.; Koneev K.; Guelacar I.M.; Person R.; Sadykova D.; Maidyrov Y.; Seifi T.; Zadagali A.; Bernard G.; Allis K.; Elloumi H.Z.; Lindy A.; Taghiabadi E.; Verma S.; Logan R.; Kirmse B.; Bai R.; Khalaf S.M.; Abdel-Hamid M.S.; Sedaghat A.; Shariati G.; Issa M.; Zeighami J.; Elbendary H.M.; Brown G.; Taylor R.W.; Galehdari H.; Gleeson J.J.; Carroll C.J.; Cowan J.A.; Moreno-De-Luca A.; Houlden H.; Maroofian R.;
Ann. Clin. Transl. Neurol. 9:2025-2035(2022)
Cited for: VARIANTS SPG93 SER-88; VAL-99; PRO-100; GLY-101; ALA-121; PRO-133; ARG-183; ARG-189; PHE-210 AND LEU-241; INVOLVEMENT IN SPG93;
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.