UniProtKB/Swiss-Prot P17947: Variant p.Val241Gly

• Variant information
• Sequence information
• Literature citations
• All

Variant information

Variant position: 241 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: LP/P [Disclaimer: Variants classification is intended for research purposes only, not for clinical and diagnostic use. The label disease variant is assigned according to literature reports on probable disease-association that can be based on theoretical reasons. This label must not be considered as a definitive proof for the pathogenic role of a variant.] 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 Valine (V) to Glycine (G) at position 241 (V241G, p.Val241Gly). 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 hydrophobic (V) to glycine (G) 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 AGM10; very low protein expression, if any, in peripheral blood mononuclear cells; when tested in transfected cells, decreased transcription activation; in vitro, fails to bind PU motif-containing DNA probes; does not affect interaction with IRF4 and IRF8, nor nuclear localization. Any additional useful information about the variant.
Other resources: Links to websites of interest for the variant.

• Variant rs2095906404 [ dbSNP | Ensembl ]

Sequence information

Variant position: 241 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 270 The length of the canonical sequence.
Location on the sequence: KKMTYQKMARALRNYGKTGE V KKVKKKLTYQFSGEVLGRGG 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.
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 – 270	Transcription factor PU.1
DNA binding	170 – 253	ETS
Binding site	230 – 230	contacts bases in the GGAA sequence in the major groove
Binding site	233 – 233	contacts bases in the GGAA sequence in the major groove
Binding site	243 – 243	contacts the phosphate backbone of the GGAA sequence in the minor groove upstream
Beta strand	239 – 243

Literature citations

Constrained chromatin accessibility in PU.1-mutated agammaglobulinemia patients.
Le Coz C.; Nguyen D.N.; Su C.; Nolan B.E.; Albrecht A.V.; Xhani S.; Sun D.; Demaree B.; Pillarisetti P.; Khanna C.; Wright F.; Chen P.A.; Yoon S.; Stiegler A.L.; Maurer K.; Garifallou J.P.; Rymaszewski A.; Kroft S.H.; Olson T.S.; Seif A.E.; Wertheim G.; Grant S.F.A.; Vo L.T.; Puck J.M.; Sullivan K.E.; Routes J.M.; Zakharova V.; Shcherbina A.; Mukhina A.; Rudy N.L.; Hurst A.C.E.; Atkinson T.P.; Boggon T.J.; Hakonarson H.; Abate A.R.; Hajjar J.; Nicholas S.K.; Lupski J.R.; Verbsky J.; Chinn I.K.; Gonzalez M.V.; Wells A.D.; Marson A.; Poon G.M.K.; Romberg N.;
J. Exp. Med. 218:0-0(2021)
Cited for: INVOLVEMENT IN AGM10; VARIANTS AGM10 110-GLN--HIS-270 DEL; 121-TYR--HIS-270 DEL; PRO-211 AND GLY-241; CHARACTERIZATION OF VARIANTS AGM10 110-GLN--HIS-270 DEL; 121-TYR--HIS-270 DEL; PRO-211 AND GLY-241; SUBCELLULAR LOCATION; TISSUE SPECIFICITY; INTERACTION WITH IRF4 AND IRF8;