UniProtKB/Swiss-Prot Q9UIQ6: Variant p.Asn594Ile

Leucyl-cystinyl aminopeptidase
Gene: LNPEP
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Variant information Variant position:

594 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 Asparagine (N) to Isoleucine (I) at position 594 (N594I, p.Asn594Ile). 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 polar (N) to medium size and hydrophobic (I) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-3 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:

Haplotypes at the ERAP1-ERAP2-LNPEP locus, which encodes the ERAP1, ERAP2 and LNPEP peptidases that process peptides for MHC display, are strongly associated with DNA load of EBV and HHV-7 viruses. Additional information on the polymorphism described.
Other resources:

Links to websites of interest for the variant.

Variant rs12520455 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

1025 The length of the canonical sequence.
Location on the sequence:

LYLHNHSYASIQSDDLWDSF N EVTNQTLDVKRMMKTWTLQK 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                         LYLHNHSYASIQSDDLWDSFNEVTNQTLDVKRMMKTWTLQK

Mouse                         LYLHNHSYAAIQSDDLWDSFNEVTDKTLDVKKMMKTWTLQK

Rat                           LYLHNHSYAAIQSDDLWDSFNEVTGKTLDVKKMMKTWTLQK

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	1 – 1025	Leucyl-cystinyl aminopeptidase
Chain	155 – 1025	Leucyl-cystinyl aminopeptidase, pregnancy serum form
Topological domain	132 – 1025	Extracellular
Glycosylation	578 – 578	N-linked (GlcNAc...) asparagine
Glycosylation	598 – 598	N-linked (GlcNAc...) asparagine
Helix	586 – 597

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.