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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P08397: Variant p.Gln34Lys

Porphobilinogen deaminase
Gene: HMBS
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Variant information Variant position: help 34 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 Glutamine (Q) to Lysine (K) at position 34 (Q34K, p.Gln34Lys). 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 (Q) to large size and basic (K) 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. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 34 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 NSPKMRVIRVGTRKSQLARI Q TDSVVATLKASYPGLQFEII 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                         NSPKMRVIRVGTRKSQLARIQTDSVVATLKASYPGLQFEII

Mouse                         NGSKMRVIRVGTRKSQLARIQTDTVVAMLKALYPGIQFEII

Rat                           NGSMMRVIRVGTRKSQLARIQTDTVVAMLKTLYPGIQFEII

Bovine                        DTPKMRVIRVGTRKSQLARIQTDSVVATLKALYPGLQFEII

Slime mold                    SITKRDKVIIGSRKSQLAMLQTEWVRDRIQELNPGIIVEIK

Baker's yeast                 MGPE--TLHIGGRKSKLAVIQSNHVLKLIEEKYPDYDCKVF

Fission yeast                 -MPSCTSFPIGTRKSKLAVIQSEIIREELEKHYPHLEFPII
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
Detection of seven point mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria, by direct sequencing of in vitro amplified cDNA.
Mgone C.S.; Lanyon W.G.; Moore M.R.; Connor J.M.;
Hum. Genet. 90:12-16(1992)
Cited for: VARIANTS AIP LYS-34; GLN-167; ARG-177 AND ASN-256;
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.