glycosylphosphatidylinositol anchor attachment 1 [Homo sapiens]

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Structural modelling of the lumenal domain of human GPAA1, the metallo-peptide synthetase subunit of the transamidase complex, reveals zinc-binding mode and two flaps surrounding the active site. [Biol Direct. 2020]
Structural modelling of the lumenal domain of human GPAA1, the metallo-peptide synthetase subunit of the transamidase complex, reveals zinc-binding mode and two flaps surrounding the active site.
Su CT, Sinha S, Eisenhaber B, Eisenhaber F. Version 2. Biol Direct. 2020 Sep 29; 15(1):14. Epub 2020 Sep 29.
A novel variant in GPAA1, encoding a GPI transamidase complex protein, causes inherited vascular anomalies with various phenotypes. [Hum Genet. 2020]
A novel variant in GPAA1, encoding a GPI transamidase complex protein, causes inherited vascular anomalies with various phenotypes.
Li Y, Yang L, Yang J, Shi J, Chai P, Ge S, Wang Y, Fan X, Jia R. Hum Genet. 2020 Dec; 139(12):1499-1511. Epub 2020 Jun 12.
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia. [Am J Hum Genet. 2017]
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.
Nguyen TTM, Murakami Y, Sheridan E, Ehresmann S, Rousseau J, St-Denis A, Chai G, Ajeawung NF, Fairbrother L, Reimschisel T, et al. Am J Hum Genet. 2017 Nov 2; 101(5):856-865.

RefSeq protein
See the reference protein sequence for glycosylphosphatidylinositol anchor attachment 1 protein (NP_003792.1).

Nucleotide
Nucleotide sequence from coding region
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Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
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ExactAntigen/Labome

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Protein