UniProtKB/Swiss-Prot O14777 : Variant p.Ser66Ala
Kinetochore protein NDC80 homolog
Gene: NDC80
Feedback ?
Variant information
Variant position:
66
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 Serine (S) to Alanine (A) at position 66 (S66A, p.Ser66Ala).
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 small size and polar (S) to small size and hydrophobic (A)
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.
Sequence information
Variant position:
66
The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:
642
The length of the canonical sequence.
Location on the sequence:
NKPTSERKVSLFGKRTSGHG
S RNSQLGIFSSSEKIKDPRPL
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 NKP---TSERKVSLFGKRTSG-H-------GS RNS-------QLGIFSSS-EKIKDPRPL
Mouse HKP---TSERKVSIFGKRTSG-H-------GS RNS------
Chicken SKTTSATSERKVSFFGKRASGAG-------GS RNS------
Xenopus laevis SKPHSGTSEKKTSFFGKRASN-G-------TA RTS------
Xenopus tropicalis SKPHSGTSERKTSFFGKRMSN-G-------TA RTS------
Zebrafish PKPQSTTSERRTSFFGKGIGA-G-------GQ RNS------
Caenorhabditis elegans SQP-------RVSLFNTKNSS-V--------- ---------
Baker's yeast PTGGINKNKRTRSTVAGGTNGTALALNDKSNS RNSVSRLSI
Fission yeast SSRVLTPTMRPSLAPNTRRSS-V-------RV SNA------
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 – 642
Kinetochore protein NDC80 homolog
Region
1 – 445
Interaction with the N-terminus of CDCA1
Region
1 – 250
Nuclear localization
Region
1 – 74
Disordered
Modified residue
53 – 53
N6-acetyllysine
Modified residue
55 – 55
Phosphoserine
Modified residue
59 – 59
N6-acetyllysine
Modified residue
62 – 62
Phosphoserine
Modified residue
69 – 69
Phosphoserine
Mutagenesis
53 – 53
K -> Q. Mimics acetylation, leading to increased kinetochore-microtubule attachment; when associated with Q-59.
Mutagenesis
53 – 53
K -> R. Impaired acetylation, leading to reduced kinetochore-microtubule attachment; when associated with R-59.
Mutagenesis
59 – 59
K -> Q. Mimics acetylation, leading to increased kinetochore-microtubule attachment; when associated with Q-53.
Mutagenesis
59 – 59
K -> R. Impaired acetylation, leading to reduced kinetochore-microtubule attachment; when associated with R-53.
Literature citations
No reference for the current variant in UniProtKB/Swiss-Prot.
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.