UniProtKB/Swiss-Prot P12821: Variant p.Gln1296Pro

Angiotensin-converting enzyme
Gene: ACE
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Variant information Variant position:

1296 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 Glutamine (Q) to Proline (P) at position 1296 (Q1296P, p.Gln1296Pro). 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 (Q) to medium size and hydrophobic (P) 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 rs4981 [ dbSNP | Ensembl ]

Sequence information Variant position:

1296 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length:

1306 The length of the canonical sequence.
Location on the sequence:

LSQRLFSIRHRSLHRHSHGP Q FGSEVELRHS 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                         LSQRLFSIR-HRSLHRHSHGPQFGSEVELRHS

Chimpanzee                    LSQRLFSIR-HRSLHRHSHGPQFDSEVELRH

Mouse                         LAHRLYNIRNHHSLRRPHRGPQFGSEVELRH

Rat                           LAHRLYNIHNHHSLRRPHRGPQFGSEVELRH

Pig                           LTQRLFSIR-HQILRRTHRGPQFGSEVELRH

Bovine                        LTQRLFSIR-HHSLRRPHRGPQFGSEVELRH

Rabbit                        LTQRLFSIR-YQSLRQPHHGPQFGSEVELRH

Chicken                       LGVKLFSSR-RKAFKSS-------SEMELK-

Drosophila                    -------------------------------

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	30 – 1306	Angiotensin-converting enzyme
Topological domain	1278 – 1306	Cytoplasmic
Modified residue	1299 – 1299	Phosphoserine
Alternative sequence	1146 – 1306	Missing. In isoform Somatic-2.
Mutagenesis	1299 – 1299	S -> A. Abolishes phosphorylation and decreases membrane retention.

Literature citations
Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis.
Halushka M.K.; Fan J.-B.; Bentley K.; Hsie L.; Shen N.; Weder A.; Cooper R.; Lipshutz R.; Chakravarti A.;
Nat. Genet. 22:239-247(1999)
Cited for: VARIANTS THR-1018; VAL-1051; GLN-1279; SER-1286 AND PRO-1296;

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.