UniProtKB/Swiss-Prot Q92878: Variant p.Lys616Glu

DNA repair protein RAD50
Gene: RAD50
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Variant information Variant position:

616 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 Lysine (K) to Glutamate (E) at position 616 (K616E, p.Lys616Glu). 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 basic (K) to medium size and acidic (E) 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
Other resources:

Links to websites of interest for the variant.

Variant rs1047380 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

1312 The length of the canonical sequence.
Location on the sequence:

KLNKELASSEQNKNHINNEL K RKEEQLSSYEDKLFDVCGSQ 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                         KLNKELASSEQNKNHINN--------ELKRKEEQLSSYE----D----------KLFDVCGSQ

Mouse                         KLNKELASAEQNKNHINN--------ELKKKEEQLSSYE--

Rat                           KLNKELASAEQNKNHINN--------ELKKKEEQLSSYE--

Caenorhabditis elegans        IMEEDLRDVQLNVQKLET-----MQHQYRKQEESLTAQELK

Drosophila                    TQKLKEQSYEIKRKNLIS--------DISRMEKELKDSE--

Slime mold                    ELKQQFQILQNKKNQIDAQLTSSIEPQLKKKQIELESYE--

Baker's yeast                 ELDRRYTNALYNLNTIEK----DLQDNQKSKEKVIQLLS--

Fission yeast                 RLEIRISLSVQSINDLTE--------NKKIKTKTLKSYS--

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 – 1312	DNA repair protein RAD50
Modified residue	635 – 635	Phosphoserine; by ATM
Mutagenesis	635 – 635	S -> G. Abolished phosphorylation by ATM, leading to impaired ability to mediate DNA repair.
Helix	586 – 632

Literature citations
Submission
Offenberg H.H.;
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2); VARIANTS GLU-616; ALA-697; HIS-964 AND MET-973;

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.