UniProtKB/Swiss-Prot Q8NCW5 : Variant p.Val19Leu
NAD(P)H-hydrate epimerase
Gene: NAXE
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Variant information
Variant position:
19
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 Valine (V) to Leucine (L) at position 19 (V19L, p.Val19Leu).
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:
Similar physico-chemical property. Both residues are medium size and hydrophobic.
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.
Sequence information
Variant position:
19
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:
288
The length of the canonical sequence.
Location on the sequence:
MSRLRALLGLGLLVAGSR
V PRIKSQTIACRSGPTWWGPQ
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 MSRLRALLGLGLLVAGSRV ----PRIKSQTIACRSGPTWWGPQ
MSALRALLGLGLLAAGSRL ----RRVPGRAGACPAGSAW
Mouse MSGLRTLLGLGLLVAGSRL ----PRVISQQSVCRARPIW
Rat MSGLRTLLGLGLLVAGSRL ----PRIASRQSVCRAGPIW
Pig MSGLRALLGLGLPVAGSRL ----PRVRVQAGACRARPTW
Bovine MSGLRALLGLGLLVAGSRL ----SRVRVQAGSCRAGATW
Xenopus tropicalis MYGLRTLFSLGLLVGGARL GARVAQVGALGGTCPLGQGL
Zebrafish MLGVRALFGIGLLVTSRG- ----GFVLTHTRACSSAASN
Caenorhabditis elegans ------------------- --------------------
Drosophila ------------------- --------------------
Slime mold ------------------- --------------------
Baker's yeast ------------------- --------------------
Fission yeast ------------------- --------------------
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
Transit peptide
1 – 47
Mitochondrion
Alternative sequence
1 – 103
Missing. In isoform 2.
Literature citations
Cloning and characterization of a novel apolipoprotein A-I-binding protein, AI-BP, secreted by cells of the kidney proximal tubules in response to HDL or ApoA-I.
Ritter M.; Buechler C.; Boettcher A.; Barlage S.; Schmitz-Madry A.; Orso E.; Bared S.M.; Schmiedeknecht G.; Baehr C.H.; Fricker G.; Schmitz G.;
Genomics 79:693-702(2002)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); VARIANT LEU-19; TISSUE SPECIFICITY; INTERACTION WITH APOA1 AND APOA2; SUBCELLULAR LOCATION;
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORMS 1 AND 2); VARIANT LEU-19;
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.