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UniProtKB/Swiss-Prot Q92743: Variant p.Phe286Val

Serine protease HTRA1
Gene: HTRA1
Variant information

Variant position:  286
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  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:  From Phenylalanine (F) to Valine (V) at position 286 (F286V, p.Phe286Val).
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:  Change from large size and aromatic (F) to medium size and hydrophobic (V)
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  -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:  In CADASIL2; loss of proteolytic activity.
Any additional useful information about the variant.



Sequence information

Variant position:  286
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  480
The length of the canonical sequence.

Location on the sequence:   LLGRSSELRPGEFVVAIGSP  F SLQNTVTTGIVSTTQRGGKE
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                         LLGRSSELRPGEFVVAIGSPFSLQNTVTTGIVSTTQRGGKE

Mouse                         LLGRSSELRPGEFVVAIGSPFSLQNTVTTGIVSTTQRGGKE

Rat                           LLGRSSELRPGEFVVAIGSPFSLQNTVTTGIVSTTQRGGKE

Bovine                        LLGRSSELRPGEFVVAIGSPFSLQNTVTTGIVSTTQRGGKE

Xenopus laevis                LLGRSEELRPGEFVVAIGSPFSLQNTVTTGIVSTAQRGGKE

Xenopus tropicalis            LLGRSEDLRPGEFVVAIGSPFSLQNTVTTGIVSTAQRGGKE

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.

TypePositionsDescription
Chain 23 – 480 Serine protease HTRA1
Region 204 – 364 Serine protease
Site 278 – 278 Involved in trimer stabilization
Beta strand 278 – 286


Literature citations

Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel disease.
Verdura E.; Herve D.; Scharrer E.; del Mar Amador M.; Guyant-Marechal L.; Philippi A.; Corlobe A.; Bergametti F.; Gazal S.; Prieto-Morin C.; Beaufort N.; Le Bail B.; Viakhireva I.; Dichgans M.; Chabriat H.; Haffner C.; Tournier-Lasserve E.;
Brain 138:2347-2358(2015)
Cited for: INVOLVEMENT IN CADASIL2; VARIANTS CADASIL2 ARG-121; SER-123; GLY-133; LEU-166; PRO-173; ARG-284; GLY-284; GLN-285; VAL-286 AND HIS-450; VARIANTS VAL-20 AND GLY-51; CHARACTERIZATION OF VARIANTS CADASIL2 ARG-121; LEU-166; PRO-173; ARG-284; GLY-284; GLN-285; VAL-286 AND HIS-450;

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.