UniProtKB/Swiss-Prot P04637: Variant p.Pro89Leu

Cellular tumor antigen p53
Gene: TP53
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Variant information Variant position:

89 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

US 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:

From Proline (P) to Leucine (L) at position 89 (P89L, p.Pro89Leu). 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 hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-3 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:

In sporadic cancers; somatic mutation. Any additional useful information about the variant.
Other resources:

Links to websites of interest for the variant.

Variant rs730881994 [ dbSNP | Ensembl ]

Sequence information Variant position:

89 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

393 The length of the canonical sequence.
Location on the sequence:

AAPPVAPAPAAPTPAAPAPA P SWPLSSSVPSQKTYQGSYGF 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                         AAPPVAPAPAAPTPAAPAPAPSWPLSSSVPSQKTYQGSYGF

                              T----------SAPTAPGPAPSWPLSSSVPSPKTYPGTYGF

Rhesus macaque                AAPPMAPTPAAPTPAAPAPAPSWPLSSSVPSQKTYHGSYGF

Mouse                         APAAQDPVTETPGPVAPAPATPWPLSSFVPSQKTYQGNYGF

Rat                           PAAQ-EPGTEAPAPVAPASATPWPLSSSVPSQKTYQGNYGF

Pig                           P-----PAATAPAPAAPAPATSWPLSSFVPSQKTYPGSYDF

Bovine                        P-----SAPAAPPPATPAPATSWPLSSFVPSQKTYPGNYGF

Rabbit                        APAPEAPAPAAPALAAPAPATSWPLSSSVPSQKTYHGNYGF

Sheep                         P----------PAQAALAPATSWPLSSFVPSQKTYPGNYGF

Cat                           V-----PAPAAPAPATPAPAISWPLSSFVPSQKTYPGAYGF

Chicken                       PPPPLPLAAAAPPPLNPPTPPRAAPSPVVPSTEDYGGDFDF

Xenopus laevis                AADMTVLQEGLMGNAVPTVT-----SCAVPSTDDYAGKYGL

Zebrafish                     PNFFENVLEEQPQPSTLPP------TSTVPETSDYPGDHGF

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.

Type	Positions	Description
Chain	1 – 393	Cellular tumor antigen p53
Region	1 – 320	Interaction with CCAR2
Region	50 – 96	Disordered
Region	66 – 110	Interaction with WWOX
Compositional bias	64 – 92	Pro residues
Alternative sequence	1 – 132	Missing. In isoform 7, isoform 8 and isoform 9.

Literature citations
No reference for the current variant in UniProtKB/Swiss-Prot.

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.