Variant position: 466 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 542 The length of the canonical sequence.
Location on the sequence:
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 DLPNRQLKVQVADRRVISTT DAERQAVTPPGLQEAINDLVK
Mouse DLPNRQLKVKVADRRVISTT DAERQAVTPPGLQEAINDLVK
Pig DLPNRQLKVKVADRQVISTT DAERQVVKPPGLQEAINDLVK
Baker's yeast DLPNKLVKCIVPDRSIFQTT DQERKLLNPVGLQDKIDLVVA
Fission yeast DLPNKLAKVKVSDRTIYKST DAERRLVSPDGLQEKIDALVA
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
1 – 542 Phosphoacetylglucosamine mutase
Functional cloning and mutational analysis of the human cDNA for phosphoacetylglucosamine mutase: identification of the amino acid residues essential for the catalysis.
Mio T.; Yamada-Okabe T.; Arisawa M.; Yamada-Okabe H.;
Biochim. Biophys. Acta 1492:369-376(2000)
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1); MUTAGENESIS; ACTIVE SITE; VARIANT ASN-466;
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
The MGC Project Team;
Genome Res. 14:2121-2127(2004)
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1); VARIANT ASN-466;
Identification of human phosphoglucomutase 3 (PGM3) as N-acetylglucosamine-phosphate mutase (AGM1).
Pang H.; Koda Y.; Soejima M.; Kimura H.;
Ann. Hum. Genet. 66:139-144(2002)
Cited for: VARIANT ASN-466;
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