UniProtKB/Swiss-Prot P06213: Variant p.Lys1095Glu

Insulin receptor
Gene: INSR
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Variant information Variant position:

1095 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

LB/B 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 Lysine (K) to Glutamate (E) at position 1095 (K1095E, p.Lys1095Glu). 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 basic (K) to medium size and acidic (E) 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 a subject with non-insulin dependent diabetes mellitus. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs909008899 [ dbSNP | Ensembl ]

Sequence information Variant position:

1095 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

1382 The length of the canonical sequence.
Location on the sequence:

ASVMKGFTCHHVVRLLGVVS K GQPTLVVMELMAHGDLKSYL 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                         ASVMKGFTCHHVVRLLGVVSKGQPTLVVMELMAHGDLKSYL

Mouse                         ASVMKGFTCHHVVRLLGVVSKGQPTLVVMELMAHGDLKSHL

Rat                           ASVMKGFTCHHVVRLLGVVSKGQPTLVVMELMAHGDLKSHL

Xenopus laevis                ASVMKAFNCHHVVRLLGVVSKGQPTLVIMELMAHGDLKSYL

Caenorhabditis elegans        ANIMKNFKTNFIVKLYGVISTVQPAMVVMEMMDLGNLRDYL

Drosophila                    ASVMKEFDTYHVVRLLGVCSRGQPALVVMELMKKGDLKSYL

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.

Type	Positions	Description
Chain	763 – 1382	Insulin receptor subunit beta
Topological domain	980 – 1382	Cytoplasmic
Domain	1023 – 1298	Protein kinase
Modified residue	1083 – 1083	S-nitrosocysteine
Mutagenesis	1083 – 1083	C -> A. Reduced S-nitrosylation by BLVRB, leading to increased receptor tyrosine kinase activity.
Beta strand	1095 – 1098

Literature citations
Detection of mutations in insulin-receptor gene in NIDDM patients by analysis of single-stranded conformation polymorphisms.
O'Rahilly S.; Choi W.H.; Patel P.; Turner R.C.; Flier J.S.; Moller D.E.;
Diabetes 40:777-782(1991)
Cited for: VARIANT GLU-1095;

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.