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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot O00255: Variant p.Ala160Pro

Menin
Gene: MEN1
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Variant information Variant position: help 160 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 Alanine (A) to Proline (P) at position 160 (A160P, p.Ala160Pro). 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 small size and hydrophobic (A) to medium size and hydrophobic (P) 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 In MEN1; strong decrease in JUND-binding. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 160 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 610 The length of the canonical sequence.
Location on the sequence: help IQSLFSFITGTKLDSSGVAF A VVGACQALGLRDVHLALSED 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                         IQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED

                              IQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED

Mouse                         IQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED

Rat                           IQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED

Bovine                        IQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED
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 1 – 610 Menin
Alternative sequence 148 – 148 T -> TGWSPV. In isoform 2.
Alternative sequence 148 – 148 Missing. In isoform 3.
Helix 154 – 167



Literature citations
Menin interacts with the AP1 transcription factor JunD and represses JunD-activated transcription.
Agarwal S.K.; Guru S.C.; Heppner C.; Erdos M.R.; Collins R.M.; Park S.Y.; Saggar S.; Chandrasekharappa S.C.; Collins F.S.; Spiegel A.M.; Marx S.J.; Burns A.L.;
Cell 96:143-152(1999)
Cited for: INTERACTION WITH JUND; VARIANTS MEN1 LEU-12; ARG-22; ASP-139; TYR-139; PRO-160; PRO-176; VAL-242; PRO-286; PRO-309; ARG-344 AND ARG-436; Characterization of mutations in patients with multiple endocrine neoplasia type 1.
Bassett J.H.D.; Forbes S.A.; Pannett A.A.J.; Lloyd S.E.; Christie P.T.; Wooding C.; Harding B.; Besser G.M.; Edwards C.R.; Monson J.P.; Sampson J.; Wass J.A.H.; Wheeler M.H.; Thakker R.V.;
Am. J. Hum. Genet. 62:232-244(1998)
Cited for: VARIANTS MEN1 ASP-42; PRO-160; ASP-164; SER-183 AND GLU-284; Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.
Wautot V.; Vercherat C.; Lespinasse J.; Chambe B.; Lenoir G.M.; Zhang C.X.; Porchet N.; Cordier M.; Beroud C.; Calender A.;
Hum. Mutat. 20:35-47(2002)
Cited for: VARIANTS MEN1 TRP-39; ASP-42; LEU-98; PRO-160; THR-160; PHE-162; ASP-164; ARG-165; TYR-172; PRO-223; PHE-240; ARG-281; PRO-311; PRO-314; TYR-317; ARG-317; ASP-337; ARG-341; HIS-357; ASP-368; MET-372; ASN-418; CYS-527; ASN-555 AND ARG-555;
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.