UniProtKB/Swiss-Prot P05362: Variant p.Lys155Asn

Intercellular adhesion molecule 1
Gene: ICAM1
Feedback?

Variant information Variant position:

155 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 Asparagine (N) at position 155 (K155N, p.Lys155Asn). 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 polar (N) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

0 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
Polymorphism:

Variant p.Lys56Met, known as ICAM1-Kilifi, may influence susceptibility to cerebral malaria [MIM:611162]. Additional information on the polymorphism described.
Other resources:

Links to websites of interest for the variant.

Variant rs5492 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

CQVEGGAPRANLTVVLLRGE K ELKREPAVGEPAEVTTTVLV 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                         CQVEGGAPRANLTVVLLRGEKELKREPAV-G---EPAEVTTTVLV

Gorilla                       CQVEGGAPRANLIVVLLRGEEELKREPAV-G---EPAEVTT

Rhesus macaque                CQVEGGAPRANLTVMLLRGEKELSRQSAV-G---EPAEVTT

Chimpanzee                    CQVEGGAPRANLTVVLLRGEKELKREPAV-G---EPAEVTT

Mouse                         CHVDGGAPRTQLSAVLLRGEEILSRQPVG-GHPKDPKEITF

Rat                           CLVEGGAPRTQLSVVLLRGNETLSRQAVD-G---DPKEITF

Bovine                        CLVSGGAPRAHLSVVLLRGEEELGRQPVGKG---EPAKVMF

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	28 – 532	Intercellular adhesion molecule 1
Topological domain	28 – 480	Extracellular
Domain	128 – 193	Ig-like C2-type 2
Glycosylation	145 – 145	N-linked (GlcNAc...) (complex) asparagine
Disulfide bond	135 – 186
Beta strand	155 – 161

Literature citations
No reference for the current variant in UniProtKB/Swiss-Prot.

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.