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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P00734: Variant p.Arg431His

Prothrombin
Gene: F2
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Variant information Variant position: help 431 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 Arginine (R) to Histidine (H) at position 431 (R431H, p.Arg431His). 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 large size and basic (R) to medium size and polar (H) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 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

Variant description: help In FA2D; Himi-2. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 431 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 622 The length of the canonical sequence.
Location on the sequence: help PPWDKNFTENDLLVRIGKHS R TRYERNIEKISMLEKIYIHP 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                         PPWDKNFTENDLLVRIGKHSRTRYERNIEKISMLEKIYIHP

Mouse                         PPWDKNFTENDLLVRIGKHSRTRYERNVEKISMLEKIYVHP

Rat                           PPWDKNFTENDLLVRIGKHSRTRYERNVEKISMLEKIYIHP

Pig                           PPWDKNFTENDLLVRIGKHSRTRYERNIEKISMLEKIYIHP

Bovine                        PPWDKNFTVDDLLVRIGKHSRTRYERKVEKISMLDKIYIHP

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 44 – 622 Prothrombin
Chain 364 – 622 Thrombin heavy chain
Domain 364 – 618 Peptidase S1
Glycosylation 416 – 416 N-linked (GlcNAc...) (complex) asparagine
Disulfide bond 336 – 482 Interchain (between light and heavy chains)
Beta strand 430 – 433



Literature citations
Prothrombin Himi: a compound heterozygote for two dysfunctional prothrombin molecules (Met-337-->Thr and Arg-388-->His).
Morishita E.; Saito M.; Kumabashiri I.; Asakura H.; Matsuda T.; Yamaguchi K.;
Blood 80:2275-2280(1992)
Cited for: VARIANTS FA2D THR-380 AND HIS-431;
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.