KIAA0094 [Homo sapiens]

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METAP1 mutation is a novel candidate for autosomal recessive intellectual disability. [J Hum Genet. 2021]
METAP1 mutation is a novel candidate for autosomal recessive intellectual disability.
Caglayan AO, Aktar F, Bilguvar K, Baranoski JF, Akgumus GT, Harmanci AS, Erson-Omay EZ, Yasuno K, Caksen H, Gunel M. J Hum Genet. 2021 Feb; 66(2):215-218. Epub 2020 Aug 6.
Identification, biochemical and structural evaluation of species-specific inhibitors against type I methionine aminopeptidases. [J Med Chem. 2013]
Identification, biochemical and structural evaluation of species-specific inhibitors against type I methionine aminopeptidases.
Kishor C, Arya T, Reddi R, Chen X, Saddanapu V, Marapaka AK, Gumpena R, Ma D, Liu JO, Addlagatta A. J Med Chem. 2013 Jul 11; 56(13):5295-305. Epub 2013 Jun 27.
Elucidation of the function of type 1 human methionine aminopeptidase during cell cycle progression. [Proc Natl Acad Sci U S A. 2006]
Elucidation of the function of type 1 human methionine aminopeptidase during cell cycle progression.
Hu X, Addlagatta A, Lu J, Matthews BW, Liu JO. Proc Natl Acad Sci U S A. 2006 Nov 28; 103(48):18148-53. Epub 2006 Nov 17.

RefSeq protein isoforms
See 27 reference sequence protein isoforms for the METAP1 gene.

Nucleotide
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Protein