UniProtKB/Swiss-Prot O60462: Variant p.Glu602Lys

Neuropilin-2
Gene: NRP2
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Variant information Variant position:

602 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 Glutamate (E) to Lysine (K) at position 602 (E602K, p.Glu602Lys). 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 medium size and acidic (E) to large size and basic (K) 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
Other resources:

Links to websites of interest for the variant.

Variant rs1128169 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

GIGMRLEVLGCDWTDSKPTV E TLGPTVKSEETTTPYPTEEE 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                         GIGMRLEVLGCDWTDSKPTVETLGPTVKSEETTTPYPTEEE

Mouse                         GIGMRLEVLGCDWTDSKPTVETLGPTVKSEETTTPYPMDED

Rat                           GIGMRLEVLGCDWTDSKPTVETLGPTVKSEETTTPYPMDED

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	21 – 931	Neuropilin-2
Topological domain	21 – 864	Extracellular
Region	601 – 622	Disordered
Compositional bias	601 – 620	Polar residues
Alternative sequence	556 – 931	Missing. In isoform s9.

Literature citations
Neuropilin-2, a novel member of the neuropilin family, is a high affinity receptor for the semaphorins Sema E and Sema IV but not Sema III.
Chen H.; Chedotal A.; He Z.-G.; Goodman C.S.; Tessier-Lavigne M.;
Neuron 19:547-559(1997)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS A0 AND A17); VARIANT LYS-602; Genomic organization of human neuropilin-1 and neuropilin-2 genes: identification and distribution of splice variants and soluble isoforms.
Rossignol M.; Gagnon M.L.; Klagsbrun M.;
Genomics 70:211-222(2000)
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA] (ISOFORMS B0; B5 AND S9); VARIANT LYS-602; ALTERNATIVE SPLICING; SUBCELLULAR LOCATION;

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.