UniProtKB/Swiss-Prot P00846: Variant p.Thr59Ala

ATP synthase subunit a
Gene: MT-ATP6
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Variant information Variant position:

59 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 Threonine (T) to Alanine (A) at position 59 (T59A, p.Thr59Ala). 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 polar (T) to small size and hydrophobic (A) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score:

0 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 rs2000975 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

NNRLITTQQWLIKLTSKQMM T MHNTKGRTWSLMLVSLIIFI 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                         NNRLITTQQ----WLIKLTSKQMMTMHNTKGRTWSL---MLVSLIIFI--

Gorilla                       NNRLIATQQ----WLIQLTSKQMMTMHNAKGRTWSL---ML

                              NNRLISIQQ----WLIQLTSKQMLAIHNQKGRTWAL---ML

Chimpanzee                    NNRLITTQQ----WLIQLTSKQMMTMHSTKGRTWSL---ML

Mouse                         NNRLHSFQH----WLVKLIIKQMMLIHTPKGRTWTL---MI

Rat                           SNRLHSFQH----WLIKLIIKQMMLIHTPKGRTWAL---MI

Pig                           NNRTISIQQ----WLIQLTSKQMMAIHNQKGQTWSL---ML

Bovine                        SNRFVTLQQ----WMLQLVSKQMMSIHNSKGQTWTL---ML

Rabbit                        NNRLVSTQQ----WLAQLILKQMMLMHSPKGRTWSL---ML

Goat                          NNRLVSLQQ----WALQLMSKQMMSIHNTKGQTWTL---ML

Sheep                         NNRLISLQQ----WMLQLVSKQMMSIHNTKGQTWAL---ML

Cat                           NNRLVSLQQ----WLVQLTSKQMLAIHNHKGQTWAL---ML

Horse                         NNRLISIQQ----WLVQLTSKQMMAIHNSKGQTWTL---ML

Chicken                       NNRLSTIQL----WFTHLITKQLMTPLNKAGHKWAL---LL

Xenopus laevis                NNRLITLQS----WFLHNFTTIFYQLTSP-GHKWAL---LL

Zebrafish                     NNRLITVQT----WLTGRFTNQLMTPLNFSGHKWAL---LF

Caenorhabditis elegans        -------------MLNTLVKKFLNSLVGVFSYTNTLPLSSV

Drosophila                    PSRYNIMWN----SILLTLHKEFKTLLGPSGHNGSTF--IF

Slime mold                    GNNWQHIGEMIYEFVVDLIIEQV-------GKPGILFFPFI

Baker's yeast                 GSRWLISQEAIYDTIMNMTKGQI------GGKNWGLYFPMI

Fission yeast                 PQKFGIAMEAIYFTMLNLVENQIHSSKTVSGQSYFP---FI

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 – 226	ATP synthase subunit a

Literature citations
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy.
Wallace D.C.; Singh G.; Lott M.T.; Hodge J.A.; Schurr T.G.; Lezza A.M.; Elsas L.J. II; Nikoskelainen E.K.;
Science 242:1427-1430(1988)
Cited for: VARIANTS ALA-59 AND ILE-213; Normal variants of human mitochondrial DNA and translation products: the building of a reference data base.
Marzuki S.; Noer A.S.; Lertrit P.; Thyagarajan D.; Kapsa R.; Utthanaphol P.; Byrne E.;
Hum. Genet. 88:139-145(1991)
Cited for: VARIANTS SER-33; ALA-59; TYR-61; TYR-90; ALA-112; THR-155; ILE-213 AND GLY-219;

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.