UniProtKB/Swiss-Prot Q96P20: Variant p.Gln705Lys

NACHT, LRR and PYD domains-containing protein 3
Gene: NLRP3
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Variant information Variant position:

705 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 Glutamine (Q) to Lysine (K) at position 705 (Q705K, p.Gln705Lys). 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 (Q) 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 rs35829419 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

1036 The length of the canonical sequence.
Location on the sequence:

HNMPKEEEEEEKEGRHLDMV Q CVLPSSSHAACSHGLVNSHL 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                         HNMPKEEEEEEKEGRHLDMVQCVLPSSSHAACSHGLVNSHL

Rhesus macaque                HNMPKEEEEEEKEGRHLDMVQCVLP-GSHAACSHRLVNSHL

Mouse                         HNSPKEEEEERRGGRPLDQVQCVFP-DTHVACSSRLVNCCL

Rat                           HNSPKEEEEEKRGSQPLDQVQCVFP-DPHVACSSRLVNCCL

Bovine                        HNSPKEEEEEE-EVRHSHMDRSVLS-DFEVAYSQGLVN-YL

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 – 1036	NACHT, LRR and PYD domains-containing protein 3
Cross	689 – 689	Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
Mutagenesis	689 – 689	K -> R. Abolished ubiquitination by the SCF(FBXL2) complex.
Mutagenesis	707 – 707	V -> R. Decreased ability to activate the NLRP3 inflammasome.

Literature citations
Fine structure mapping of CIAS1: identification of an ancestral haplotype and a common FCAS mutation, L353P.
Hoffman H.M.; Gregory S.G.; Mueller J.L.; Tresierras M.; Broide D.H.; Wanderer A.A.; Kolodner R.D.;
Hum. Genet. 112:209-216(2003)
Cited for: VARIANT FCAS1 PRO-355; VARIANT LYS-705;

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.