UniProtKB/Swiss-Prot P53597: Variant p.Gly37Ala

Succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial
Gene: SUCLG1
Feedback?

Variant information Variant position:

37 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 Glycine (G) to Alanine (A) at position 37 (G37A, p.Gly37Ala). 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 glycine (G) 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 rs369610897 [ dbSNP | Ensembl ]

Sequence information Variant position:

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

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

GSSGLAAARLLSRSFLLPQN G IRHCSYTASRQHLYVDKNTK 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                         GSSGLAAARLLSRSFLLPQNGIR-HCSYTASRQHLYVDKNTK

Mouse                         SSSGLAAARLLSRTFLLQQNGIR-HGSYTASRKHIYIDKNT

Rat                           GSSGLAAARLLSRTFLLQQNGIR-HGSYTASRKNIYIDKNT

Pig                           GSSGLAAARLLSRSFLLQQNGIR-HCSYTASRKHLYVDKNT

Bovine                        GSSGLAAARLLSRAFLLQQNGIR-HCSYTTSRKHLYVDRNT

Caenorhabditis elegans        SQQIANNARTLQKGA---------ARFYNSTYNNLKINKDT

Drosophila                    MAASMRALLKVRDGFVA---GVRCNSQYNKTRGNLKLNGDS

Slime mold                    ----MISAGMIARNF-----GKR----FFSTKPSVLINKHT

Baker's yeast                 RSTVSKASLKICRHF------HRESIPYDKTIKNLLLPKDT

Fission yeast                 QTTLLTSLRRFSSSSQLKNS----KSLYEQTIPNLMINSDT

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
Transit peptide	1 – 40	Mitochondrion
Modified residue	54 – 54	N6-acetyllysine
Modified residue	57 – 57	N6-acetyllysine; alternate
Modified residue	57 – 57	N6-succinyllysine; alternate

Literature citations
Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.
Rafiullah R.; Aslamkhan M.; Paramasivam N.; Thiel C.; Mustafa G.; Wiemann S.; Schlesner M.; Wade R.C.; Rappold G.A.; Berkel S.;
J. Med. Genet. 53:138-144(2016)
Cited for: VARIANT ALA-37;

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.