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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot Q2TAA5: Variant p.Leu86Ser

GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
Gene: ALG11
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Variant information Variant position: help 86 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] 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: help From Leucine (L) to Serine (S) at position 86 (L86S, p.Leu86Ser). 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: help Change from medium size and hydrophobic (L) to small size and polar (S) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -2 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: help In CDG1P; no effect on protein expression; no effect on localization to endoplasmic reticulum membrane; decreased GDP-Man:Man3GlcNAc2-PP-Dol alpha-1,2-mannosyltransferase activity. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 86 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 492 The length of the canonical sequence.
Location on the sequence: help AFFHPYCNAGGGGERVLWCA L RALQKKYPEAVYVVYTGDVN 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences. 
Human                         AFFHPYCNAGGGGERVLWCALRALQKKYPEAVYVVYTGD----VN

Mouse                         AFFHPYCNAGGGGERVLWCALRALQKKYPEAVYVVYTGD--

Xenopus laevis                AFFHPYCNAGGGGERVLWCALRSLQKRYKDAIYVIYTGD--

Xenopus tropicalis            AFFHPYCNAGGGGERVLWCALRSLQKRYKDAIYVIYTGD--

Zebrafish                     AFFHPYCNAGGGGERVLWCALRALQNRYQDVSFVVYTGD--

Caenorhabditis elegans        AFFHPYCNAGGGGERVLWAAIRTMQKKFPDHKYFVYSGD--

Slime mold                    GFFHPYCTAGGGGERVLWCAIKSIQEEYPYVRCVVYTGD--

Baker's yeast                 GFFHPYCNAGGGGEKVLWKAVDITLRKDAKNVIVIYSGDFV

Fission yeast                 GFFHPYCNAGGGGERVLWTAVKSVQTEFPNVISVVYTGD--
Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 1 – 492 GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
Topological domain 41 – 233 Cytoplasmic
Mutagenesis 86 – 86 L -> A. No effect on GDP-Man:Man3GlcNAc2-PP-Dol alpha-1,2-mannosyltransferase activity.
Mutagenesis 86 – 86 L -> P. Decreased GDP-Man:Man3GlcNAc2-PP-Dol alpha-1,2-mannosyltransferase activity.



Literature citations
A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip.
Rind N.; Schmeiser V.; Thiel C.; Absmanner B.; Lubbehusen J.; Hocks J.; Apeshiotis N.; Wilichowski E.; Lehle L.; Korner C.;
Hum. Mol. Genet. 19:1413-1424(2010)
Cited for: FUNCTION; CATALYTIC ACTIVITY; PATHWAY; SUBCELLULAR LOCATION; VARIANT CDG1P SER-86; CHARACTERIZATION OF VARIANT CDG1P SER-86; MUTAGENESIS OF LEU-86;
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.