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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P55160: Variant p.Pro359Leu

Nck-associated protein 1-like
Gene: NCKAP1L
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Variant information Variant position: help 359 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 Leucine (L) at position 359 (P359L, p.Pro359Leu). 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 Similar physico-chemical property. Both residues are medium size and hydrophobic. 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 IMD72; loss of function; decreased protein levels in T-cells; decreased interaction with WASF2 and poor formation of WAVE2 complex; T-cells display excessive degranulation and granule release; cells exhibit reduced cortical F-actin and aberrant membrane spikes and WAS-mediated puncta, defective cell spreading and lamellipodia and reduced migratory velocity, as well as abnormal activation, blunted proliferation, decreased IL2 and TNF production and defective TCR-induced phosphorylation of mTORC2 complex substrate AKT; homozygous patient neutrophils migrating in chemokine gradients exhibit reduced velocity and directional persistence, unusual elongation and misdirected competing leading edges; no effect on interaction with RICTOR. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 359 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1127 The length of the canonical sequence.
Location on the sequence: help QRRQFLRMAVKELETVLADE P GLLGPKALFAFMALSFIRDE 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                         QRRQFLRMAVKELETVLADEPGLLGPKALFAFMALSFIRDE

Mouse                         QRRQFLRTAVKELETVLNDEPGLLGPKALFAFMALSFIRDE
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 – 1127 Nck-associated protein 1-like



Literature citations
HEM1 deficiency disrupts mTORC2 and F-actin control in inherited immunodysregulatory disease.
Cook S.A.; Comrie W.A.; Poli M.C.; Similuk M.; Oler A.J.; Faruqi A.J.; Kuhns D.B.; Yang S.; Vargas-Hernandez A.; Carisey A.F.; Fournier B.; Anderson D.E.; Price S.; Smelkinson M.; Abou Chahla W.; Forbes L.R.; Mace E.M.; Cao T.N.; Coban-Akdemir Z.H.; Jhangiani S.N.; Muzny D.M.; Gibbs R.A.; Lupski J.R.; Orange J.S.; Cuvelier G.D.E.; Al Hassani M.; Al Kaabi N.; Al Yafei Z.; Jyonouchi S.; Raje N.; Caldwell J.W.; Huang Y.; Burkhardt J.K.; Latour S.; Chen B.; ElGhazali G.; Rao V.K.; Chinn I.K.; Lenardo M.J.;
Science 369:202-207(2020)
Cited for: INVOLVEMENT IN IMD72; VARIANTS IMD72 LEU-258; LEU-359; VAL-371 AND LEU-519; CHARACTERIZATION OF VARIANTS IMD72 LEU-258; LEU-359; VAL-371 AND LEU-519; FUNCTION; INTERACTION WITH MTOR; RICTOR AND WASF2; TISSUE SPECIFICITY;
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.