UniProtKB/Swiss-Prot P35613: Variant p.Lys152Asn

Basigin
Gene: BSG
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Variant information Variant position:

152 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 152 (K152N, p.Lys152Asn). 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
Variant description:

No effect on the interaction with P.falciparum RH5. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs14704 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

AVVLVLEPGTVFTTVEDLGS K ILLTCSLNDSATEVTGHRWL 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                         AVVLVLEPGTVFTTVEDLGSKILLTCSLNDSATEVTGHRWL

Mouse                         ASVVVLEPGTIQTSVQEVNSKTQLTCSLNSSGVDIVGHRWM

Rat                           ASVVVLEPGTIVTSVQEVDSKTQLTCFLNSSGIDIVGHRWM

Rabbit                        ---------TVTTSVQSGDSWVQLTCTLNTSAAGVTGHRWL

Chicken                       ANVLVIERPVITGQYSSSADKVVLSCNISAPPTLIKGHKWM

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	22 – 385	Basigin
Topological domain	138 – 323	Extracellular
Domain	138 – 219	Ig-like C2-type
Glycosylation	160 – 160	N-linked (GlcNAc...) asparagine
Alternative sequence	1 – 209	Missing. In isoform 3.
Alternative sequence	12 – 191	Missing. In isoform 4.
Mutagenesis	160 – 160	N -> D. No effect on the interaction with P.falciparum RH5; when associated with D-268 and D-302.
Beta strand	152 – 159

Literature citations
Basigin is a receptor essential for erythrocyte invasion by Plasmodium falciparum.
Crosnier C.; Bustamante L.Y.; Bartholdson S.J.; Bei A.K.; Theron M.; Uchikawa M.; Mboup S.; Ndir O.; Kwiatkowski D.P.; Duraisingh M.T.; Rayner J.C.; Wright G.J.;
Nature 480:534-537(2011)
Cited for: FUNCTION (ISOFORMS 1 AND 2) (MICROBIAL INFECTION); INTERACTION WITH P.FALCIPARUM RH5 (ISOFORMS 1 AND 2) (MICROBIAL INFECTION); GLYCOSYLATION; VARIANTS ASN-152; LEU-176; PRO-206; LYS-208 AND VAL-269; MUTAGENESIS OF ASN-160; ASN-268 AND ASN-302;

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.