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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P08397: Variant p.Thr35Met

Porphobilinogen deaminase
Gene: HMBS
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Variant information Variant position: help 35 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 Threonine (T) to Methionine (M) at position 35 (T35M, p.Thr35Met). 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 polar (T) to medium size and hydrophobic (M) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -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
Variant description: help In AIP; severely decreased hydroxymethylbilane synthase activity. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 35 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 361 The length of the canonical sequence.
Location on the sequence: help SPKMRVIRVGTRKSQLARIQ T DSVVATLKASYPGLQFEIIA 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                         SPKMRVIRVGTRKSQLARIQTDSVVATLKASYPGLQFEIIA

Mouse                         GSKMRVIRVGTRKSQLARIQTDTVVAMLKALYPGIQFEIIA

Rat                           GSMMRVIRVGTRKSQLARIQTDTVVAMLKTLYPGIQFEIIA

Bovine                        TPKMRVIRVGTRKSQLARIQTDSVVATLKALYPGLQFEIIA

Slime mold                    ITKRDKVIIGSRKSQLAMLQTEWVRDRIQELNPGIIVEIKT

Baker's yeast                 GPE--TLHIGGRKSKLAVIQSNHVLKLIEEKYPDYDCKVFT

Fission yeast                 MPSCTSFPIGTRKSKLAVIQSEIIREELEKHYPHLEFPIIS
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 2 – 361 Porphobilinogen deaminase
Modified residue 15 – 15 Phosphoserine
Mutagenesis 26 – 26 R -> A. Loss of hydroxymethylbilane synthase activity.
Mutagenesis 34 – 34 Q -> A. Loss of hydroxymethylbilane synthase activity.
Helix 29 – 45



Literature citations
Identification and characterization of two novel mutations that produce acute intermittent porphyria: a 3-base deletion (841-843delGGA) and a missense mutation (T35M).
De Siervi A.; Weiss Cadiz D.E.; Parera V.E.; Batlle A.M.C.; Rossetti M.V.;
Hum. Mutat. 16:373-373(2000)
Cited for: VARIANTS AIP MET-35; ARG-111 AND GLY-281 DEL; From a dominant to an oligogenic model of inheritance with environmental modifiers in acute intermittent porphyria.
Lenglet H.; Schmitt C.; Grange T.; Manceau H.; Karboul N.; Bouchet-Crivat F.; Robreau A.M.; Nicolas G.; Lamoril J.; Simonin S.; Mirmiran A.; Karim Z.; Casalino E.; Deybach J.C.; Puy H.; Peoc'h K.; Gouya L.;
Hum. Mol. Genet. 27:1164-1173(2018)
Cited for: VARIANTS AIP PHE-30 AND GLU-235; CHARACTERIZATION OF VARIANTS AIP SER-24; CYS-26; HIS-26; ASN-28; PHE-30; MET-35; PHE-96; ARG-111; TRP-116; ASP-124; GLN-149; LEU-149; HIS-217; GLU-235; ARG-247; ALA-250; GLN-250; VAL-250; TYR-256 AND MET-267;
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.