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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P00450: Variant p.Ile63Thr

Ceruloplasmin
Gene: CP
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Variant information Variant position: help 63 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LB/B 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 Isoleucine (I) to Threonine (T) at position 63 (I63T, p.Ile63Thr). 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 (I) to medium size and polar (T) 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 Retained in the endoplasmic reticulum. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 63 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 1065 The length of the canonical sequence.
Location on the sequence: help KLISVDTEHSNIYLQNGPDR I GRLYKKALYLQYTDETFRTT 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                         KLISVDTEHSNIYLQNGPDRIGRLYKKALYLQYTDETFRTT

Mouse                         KLISVDTEQSNFYLQNGPDRIGRKYKKALYFEYTDGTFSKT

Rat                           ELISVDTEQSNFYLRNGPDRIGRKYKKALYSEYTDGTFTKT

Sheep                         KLISVDTEHSNIYLQNGPNRIGSVYKKAVYLQYTDENFRTV

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 20 – 1065 Ceruloplasmin
Domain 20 – 357 F5/8 type A 1
Domain 20 – 200 Plastocyanin-like 1
Binding site 55 – 55
Binding site 64 – 64
Binding site 67 – 67



Literature citations
Ceruloplasmin gene variations and substantia nigra hyperechogenicity in Parkinson disease.
Hochstrasser H.; Bauer P.; Walter U.; Behnke S.; Spiegel J.; Csoti I.; Zeiler B.; Bornemann A.; Pahnke J.; Becker G.; Riess O.; Berg D.;
Neurology 63:1912-1917(2004)
Cited for: VARIANTS THR-63; LEU-477; ILE-551; HIS-793 AND ARG-841; Functional relevance of ceruloplasmin mutations in Parkinson's disease.
Hochstrasser H.; Tomiuk J.; Walter U.; Behnke S.; Spiegel J.; Krueger R.; Becker G.; Riess O.; Berg D.;
FASEB J. 19:1851-1853(2005)
Cited for: CHARACTERIZATION OF VARIANTS THR-63 AND HIS-793; FUNCTION; CATALYTIC ACTIVITY; SUBCELLULAR LOCATION;
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.