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Article

Structure-function study of the glucose-6-phosphate transporter, an eukaryotic antiporter deficient in glycogen storage disease type Ib.

Molecular genetics and metabolism - 1 Jan 2009

Pan Chi-Jiunn, Chen Shih-Yin, Lee Soojung, Chou Janice Y

Abstract excerpt

Glycogen storage disease type Ib is caused by deficiencies in the glucose-6-phosphate transporter (G6PT), a phosphate (P(i))-linked antiporter capable of homologous (P(i):P(i)) and heterologous (G6P:P(i)) exchanges similar to the bacterial hexose-6-phosphate transporter, UhpT. Protease protection and glycosylation scanning assays have suggested that G6PT is anchored to the endoplasmic reticulum by 10...

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Identifiers

PMID: 19008136
DOI: 10.1016/j.ymgme.2008.10.005
PMCID: PMC3099254

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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