UniProtKB/SwissProt variant VAR

Variant information

Variant position:

387

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

Type of variant:

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:

From Cysteine (C) to Arginine (R) at position 387 (C387R, p.Cys387Arg).

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:

Change from medium size and polar (C) to large size and basic (R)

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 IBDIMDE; loss of TGFB1-mediated activation of SMAD signaling; mutant TGFB1 is not secreted.

Any additional useful information about the variant.

Sequence information

Variant position:

387

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

Protein sequence length:

390

The length of the canonical sequence.

Location on the sequence:

VYYVGRKPKVEQLSNMIVRS C KCS

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                         VYYVGRKPKVEQLSNMIVRSCKCS

                              VYYVGRKPKVEQLSNMIVRSCKCS

Mouse                         VYYVGRKPKVEQLSNMIVRSCKCS

Rat                           VYYVGRKPKVEQLSNMIVRSCKCS

Pig                           VYYVGRKPKVEQLSNMIVRSCKCS

Bovine                        VYYVGRKPKVEQLSNMIVRSCKCS

Sheep                         VYYVGRKPKVEQLSNMIVRSCKCS

Horse                         VYYVGRKPKVEQLSNMIVRSCKCS

Chicken                       IYYVGRNVRVEQLSNMVVRACKCS

Xenopus laevis                IYYVGRTAKVEQLSNMVVRSCNCS

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	279 – 390	Transforming growth factor beta-1
Disulfide bond	322 – 387
Disulfide bond	326 – 389
Beta strand	373 – 390

Literature citations

Human TGF-beta1 deficiency causes severe inflammatory bowel disease and encephalopathy.
Kotlarz D.; Marquardt B.; Baroey T.; Lee W.S.; Konnikova L.; Hollizeck S.; Magg T.; Lehle A.S.; Walz C.; Borggraefe I.; Hauck F.; Bufler P.; Conca R.; Wall S.M.; Schumacher E.M.; Misceo D.; Frengen E.; Bentsen B.S.; Uhlig H.H.; Hopfner K.P.; Muise A.M.; Snapper S.B.; Stroemme P.; Klein C.;
Nat. Genet. 50:344-348(2018)
Cited for: FUNCTION; SUBCELLULAR LOCATION; INVOLVEMENT IN IBDIMDE; VARIANTS IBDIMDE CYS-45; CYS-110 AND ARG-387; CHARACTERIZATION OF VARIANTS IBDIMDE CYS-45; CYS-110 AND ARG-387;

UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P01137: Variant p.Cys387Arg