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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P62805: Variant p.Arg36Trp

Histone H4
Gene: H4C16
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Variant information Variant position: help 36 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 Arginine (R) to Tryptophan (W) at position 36 (R36W, p.Arg36Trp). 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 large size and basic (R) to large size and aromatic (W) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -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: help In TEBIVANED3; results in early developmental defects when expressed in zebrafish embryos. Any additional useful information about the variant.


Sequence information Variant position: help 36 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 103 The length of the canonical sequence.
Location on the sequence: help AKRHRKVLRDNIQGITKPAI R RLARRGGVKRISGLIYEETR 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                         AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Mouse                         AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Rat                           AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Pig                           AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Bovine                        AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Chicken                       AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Xenopus laevis                AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Xenopus tropicalis            AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Caenorhabditis elegans        AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Drosophila                    AKRHRKVLRDNIQGITKPAIRRLARRGGVKRISGLIYEETR

Slime mold                    AKRHKKTQKEHINGITKPAIRRLARRGGVKRISFPIYEETR

Baker's yeast                 AKRHRKILRDNIQGITKPAIRRLARRGGVKRISGLIYEEVR

Fission yeast                 AKRHRKILRDNIQGITKPAIRRLARRGGVKRISALVYEETR
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 2 – 103 Histone H4
Modified residue 17 – 17 N6-(2-hydroxyisobutyryl)lysine; alternate
Modified residue 17 – 17 N6-acetyllysine; alternate
Modified residue 17 – 17 N6-butyryllysine; alternate
Modified residue 17 – 17 N6-crotonyllysine; alternate
Modified residue 17 – 17 N6-lactoyllysine; alternate
Modified residue 17 – 17 N6-propionyllysine; alternate
Modified residue 21 – 21 N6,N6,N6-trimethyllysine; alternate
Modified residue 21 – 21 N6,N6-dimethyllysine; alternate
Modified residue 21 – 21 N6-methyllysine; alternate
Modified residue 32 – 32 N6-(2-hydroxyisobutyryl)lysine; alternate
Modified residue 32 – 32 N6-(beta-hydroxybutyryl)lysine; alternate
Modified residue 32 – 32 N6-acetyllysine; alternate
Modified residue 32 – 32 N6-butyryllysine; alternate
Modified residue 32 – 32 N6-glutaryllysine; alternate
Modified residue 32 – 32 N6-lactoyllysine; alternate
Modified residue 32 – 32 N6-propionyllysine; alternate
Modified residue 32 – 32 N6-succinyllysine; alternate
Modified residue 45 – 45 N6-(2-hydroxyisobutyryl)lysine; alternate
Modified residue 45 – 45 N6-butyryllysine; alternate
Modified residue 45 – 45 N6-propionyllysine; alternate
Modified residue 48 – 48 Phosphoserine; by PAK2
Modified residue 52 – 52 Phosphotyrosine
Cross 21 – 21 Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2); alternate
Cross 32 – 32 Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO2); alternate
Cross 32 – 32 Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in UFM1); alternate
Mutagenesis 32 – 32 K -> R. Abolished ufmylation.
Helix 32 – 41



Literature citations
Recurrent de novo missense variants across multiple histone H4 genes underlie a neurodevelopmental syndrome.
Tessadori F.; Duran K.; Knapp K.; Fellner M.; Smithson S.; Beleza Meireles A.; Elting M.W.; Waisfisz Q.; O'Donnell-Luria A.; Nowak C.; Douglas J.; Ronan A.; Brunet T.; Kotzaeridou U.; Svihovec S.; Saenz M.S.; Thiffault I.; Del Viso F.; Devine P.; Rego S.; Tenney J.; van Haeringen A.; Ruivenkamp C.A.L.; Koene S.; Robertson S.P.; Deshpande C.; Pfundt R.; Verbeek N.; van de Kamp J.M.; Weiss J.M.M.; Ruiz A.; Gabau E.; Banne E.; Pepler A.; Bottani A.; Laurent S.; Guipponi M.; Bijlsma E.; Bruel A.L.; Sorlin A.; Willis M.; Powis Z.; Smol T.; Vincent-Delorme C.; Baralle D.; Colin E.; Revencu N.; Calpena E.; Wilkie A.O.M.; Chopra M.; Cormier-Daire V.; Keren B.; Afenjar A.; Niceta M.; Terracciano A.; Specchio N.; Tartaglia M.; Rio M.; Barcia G.; Rondeau S.; Colson C.; Bakkers J.; Mace P.D.; Bicknell L.S.; van Haaften G.;
Am. J. Hum. Genet. 109:750-758(2022)
Cited for: VARIANTS TEBIVANED1 ALA-33; LEU-33 AND GLN-92; VARIANT TEBIVANED2 CYS-41; VARIANTS TEBIVANED3 THR-32; ARG-33; TRP-36; PRO-38; CYS-41; CYS-46 AND HIS-99; VARIANTS TEBIVANED4 LEU-41 AND ARG-76; CHARACTERIZATION OF VARIANT TEBIVANED1 GLN-92; CHARACTERIZATION OF VARIANT TEBIVANED2 CYS-41; CHARACTERIZATION OF VARIANTS TEBIVANED3 THR-32; ARG-33; TRP-36; PRO-38; CYS-41 AND HIS-99; CHARACTERIZATION OF VARIANTS TEBIVANED4 LEU-41 AND ARG-76; VARIANTS HIS-41 AND ARG-95; CHARACTERIZATION OF VARIANTS HIS-41 AND ARG-95; INVOLVEMENT IN TEBIVANED1; INVOLVEMENT IN TEBIVANED2; INVOLVEMENT IN TEBIVANED3; INVOLVEMENT IN TEBIVANED4;
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.