UniProtKB/Swiss-Prot Q9GZR1: Variant p.Tyr1106Cys

Sentrin-specific protease 6
Gene: SENP6
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Variant information Variant position:

1106 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant:

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:

From Tyrosine (Y) to Cysteine (C) at position 1106 (Y1106C, p.Tyr1106Cys). 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 large size and aromatic (Y) to medium size and polar (C) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

-2 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.

Variant rs9250 [ dbSNP | Ensembl ]

Sequence information Variant position:

1106 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

1112 The length of the canonical sequence.
Location on the sequence:

KRKHKDTYSTEAPLGEGTEQ Y VNSISD 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                         KRKHKDTYSTEAPLGEGTEQYVNSI--SD

Mouse                         KKLLKDSLA-ETSLGDGAEQYASASGG

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 – 1112	Sentrin-specific protease 6
Region	666 – 1112	Protease
Region	1082 – 1112	Disordered
Compositional bias	1098 – 1112	Polar residues
Modified residue	1111 – 1111	Phosphoserine

Literature citations
A new SUMO-1-specific protease, SUSP1, that is highly expressed in reproductive organs.
Kim K.I.; Baek S.H.; Jeon Y.-J.; Nishimori S.; Suzuki T.; Uchida S.; Shimbara N.; Saitoh H.; Tanaka K.; Chung C.H.;
J. Biol. Chem. 275:14102-14106(2000)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); VARIANTS MET-121 AND CYS-1106; CHARACTERIZATION; Prediction of the coding sequences of unidentified human genes. XI. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.
Nagase T.; Ishikawa K.; Suyama M.; Kikuno R.; Miyajima N.; Tanaka A.; Kotani H.; Nomura N.; Ohara O.;
DNA Res. 5:277-286(1998)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1); VARIANTS MET-121 AND CYS-1106;

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.