UniProtKB/Swiss-Prot P61586: Variant p.Glu47Lys

• Variant information
• Sequence information
• Literature citations
• All

Variant information

Variant position: 47 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 Glutamate (E) to Lysine (K) at position 47 (E47K, p.Glu47Lys). 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 acidic (E) to large size and basic (K) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: 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: In EDFAOB; somatic mosaic variant; decreased Rho protein signal transduction; decreased substrate adhesion-dependent cell spreading; decreased number of stress fibers assembly; decreased cytoplasmic microtubule organization. Any additional useful information about the variant.

Sequence information

Variant position: 47 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 193 The length of the canonical sequence.
Location on the sequence: KDQFPEVYVPTVFENYVADI E VDGKQVELALWDTAGQEDYD 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 – 190	Transforming protein RhoA
Modified residue	34 – 34	(Microbial infection) O-AMP-tyrosine; by Haemophilus IbpA; alternate
Modified residue	37 – 37	(Microbial infection) O-AMP-threonine; by Vibrio VopS
Modified residue	41 – 41	(Microbial infection) ADP-ribosylasparagine; by botulinum toxin
Modified residue	63 – 63	5-glutamyl serotonin
Glycosylation	34 – 34	(Microbial infection) O-linked (GlcNAc) tyrosine; by Photorhabdus PAU_02230; alternate
Glycosylation	37 – 37	(Microbial infection) O-alpha-linked (GlcNAc) threonine; by C.novyi toxin TcdA; alternate
Glycosylation	37 – 37	(Microbial infection) O-linked (Glc) threonine; by C.difficile toxins TcdA and TcdB; alternate
Mutagenesis	34 – 34	Y -> A. Abolishes interaction with DGKQ.
Mutagenesis	34 – 34	Y -> F. Abolishes AMPylation by Haemophilus IbpA.
Mutagenesis	37 – 37	T -> A. Abolished monoglucosylation by C.difficile toxin TcdA. Abolished O-GlcNAcylation by C.novyi toxin TcdA.
Mutagenesis	63 – 63	Q -> L. Causes constitutive activation.
Beta strand	42 – 48

Literature citations

Postzygotic inactivating mutations of RHOA cause a mosaic neuroectodermal syndrome.
Vabres P.; Sorlin A.; Kholmanskikh S.S.; Demeer B.; St-Onge J.; Duffourd Y.; Kuentz P.; Courcet J.B.; Carmignac V.; Garret P.; Bessis D.; Boute O.; Bron A.; Captier G.; Carmi E.; Devauchelle B.; Genevieve D.; Gondry-Jouet C.; Guibaud L.; Lafon A.; Mathieu-Dramard M.; Thevenon J.; Dobyns W.B.; Bernard G.; Polubothu S.; Faravelli F.; Kinsler V.A.; Thauvin C.; Faivre L.; Ross M.E.; Riviere J.B.;
Nat. Genet. 51:1438-1441(2019)
Cited for: INVOLVEMENT IN EDFAOB; VARIANTS EDFAOB LYS-47 AND SER-71; CHARACTERIZATION OF VARIANTS EDFAOB LYS-47 AND SER-71; FUNCTION; MUTAGENESIS OF GLY-14 AND THR-19;