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UniProtKB/Swiss-Prot P00747: Variant p.His133Gln

Plasminogen
Gene: PLG
Chromosomal location: 6q26
Variant information

Variant position:  133
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Type of variant:  Polymorphism
The variants are classified into three categories: Disease, Polymorphism and Unclassified.
  • Disease: Variants implicated in disease according to literature reports.
  • Polymorphism: Variants not reported to be implicated in disease.
  • Unclassified: Variants with uncertain implication in disease according to literature reports. Evidence against or in favor of a pathogenic role is limited and/or conflicting.

Residue change:  From Histidine (H) to Glutamine (Q) at position 133 (H133Q, p.His133Gln).
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 polar.
The physico-chemical property of the reference and variant residues and the change implicated.

BLOSUM score:  0
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:  133
The position of the amino-acid change on the UniProtKB canonical protein sequence.

Protein sequence length:  810
The length of the canonical sequence.

Location on the sequence:   GTMSKTKNGITCQKWSSTSP  H RPRFSPATHPSEGLEENYCR
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                         GTMSKTKNGITCQKWSSTSPHRPRFSPATHPSEGLEENYCR

Rhesus macaque                GTMSKTRTGITCQKWSSTSPHRPTFSPATHPSEGLEENYCR

Mouse                         GTMSRTKSGVACQKWGATFPHVPNYSPSTHPNEGLEENYCR

Rat                           GTMSKTKTGVTCQKWSDTSPHVPKYSPSTHPSEGLEENYCR

Pig                           GTTSKTKSGVICQKWSVSSPHIPKYSPEKFPLAGLEENYCR

Bovine                        GTTAETKSGVTCQKWSATSPHVPKFSPEKFPLAGLEENYCR

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.

TypePositionsDescription
Chain 20 – 810 Plasminogen
Chain 20 – 580 Plasmin heavy chain A
Chain 79 – 466 Angiostatin
Chain 98 – 580 Plasmin heavy chain A, short form
Domain 103 – 181 Kringle 1
Binding site 134 – 134 Fibrin
Binding site 136 – 136 Fibrin
Binding site 136 – 136 Omega-aminocarboxylic acids
Disulfide bond 103 – 181
Disulfide bond 124 – 164
Beta strand 131 – 133


Literature citations

Submission
SeattleSNPs variation discovery resource;
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA]; VARIANTS LYS-57; GLN-133; HIS-261; TRP-408; ASN-472; VAL-494 AND TRP-523;

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.