Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Glucose-6-phosphate transporter and receptor functions of the glucose 6-phosphatase system analyzed from a consensus defined by multiple alignments.

Proteins - 1 Nov 2000

Méchin M C, van de Werve G

Abstract excerpt

The cDNA encoding the protein (P46) that is mutated in glycogen storage disease type-1b (GSD-1b) has been previously cloned by homology with bacterial sequences of the uhp (upper hexose phosphate) system. Hydropathic profiles, transmembrane-prediction analysis, and a multiple alignment of 14 sequences related to P46 (with percentage of identity around 30%) allowed to identify two large domains in the proteins...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Amino Acid Motifs
Share to Antiporters
Share to Consensus Sequence

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glucose-6-Phosphatase

Share to Glucose-6-Phosphate

Share to Isoenzymes

Share to Monosaccharide Transport Proteins

Share to Phosphotransferases

Source

Identifiers

PMID: 10966570
DOI: 10.1002/1097-0134(20001101)41:2<164::aid-prot20>3.0.co;2-2

Provenance

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

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Glucose-6-phosphate transporter and receptor functions of the glucose 6-phosphatase system analyzed from a consensus defined by multiple alignments.PMID 10966570Read ↗

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

Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib.Semantic proximity Read ↗

The Biochemistry and Molecular Biology of the Glucose-6-Phosphatase System 1Semantic proximity Read ↗

Glucose-6-phosphatase catalytic subunit gene family.Semantic proximity Read ↗

Homology modeling of the human microsomal glucose 6-phosphate transporter explains the mutations that cause the glycogen storage disease type Ib.Semantic proximity Read ↗

The molecular basis of glycogen storage disease type 1a: structure and function analysis of mutations in glucose-6-phosphatase.Semantic proximity Read ↗

Histidine 167 is the phosphate acceptor in glucose-6-phosphatase-beta forming a phosphohistidine enzyme intermediate during catalysis.Semantic proximity Read ↗

Molecular analysis of human solute carrier SLC26 anion transporter disease-causing mutations using 3-dimensional homology modeling.Semantic proximity Read ↗

Toward a blueprint for UDP-glucose pyrophosphorylase structure/function properties: homology-modeling analyses.Semantic proximity Read ↗

Enzymatic characterization of four new mutations in the glucose-6 phosphatase (G6PC) gene which cause glycogen storage disease type 1a.Semantic proximity Read ↗

Identification of a novel missense mutation (T16A) in the glucose-6-phosphatase gene in a Taiwan Chinese patient with glycogen storage disease Ia (Von Gierke disease).Semantic proximity Read ↗

Proposed carrier lipid-binding site of undecaprenyl pyrophosphate phosphatase from Escherichia coli.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.