Annotation inferences using phylogenetic trees

Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara

Combined Automated Annotation using Multiple IEA Methods

UniProtKB entry P49247 (RPIA_HUMAN)

Ribose-5-phosphate isomerase deficiency: new inborn error in the pentose phosphate pathway associated with a slowly progressive leukoencephalopathy.

Towards a proteome-scale map of the human protein-protein interaction network.

Next-generation sequencing to generate interactome datasets.

Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.

A proteome-scale map of the human interactome network.

Widespread macromolecular interaction perturbations in human genetic disorders.

Architecture of the human interactome defines protein communities and disease networks.

An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders.

Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.

A reference map of the human binary protein interactome.

Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.

Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.

The ribose 5-phosphate isomerase-encoding gene is located immediately downstream from that encoding murine immunoglobulin kappa.

RPIA isomerizes ribose 5-phosphate to D-ribulose 5-phosphate

Defective RPIA does not isomerize RU5P to R5P

Defective RPIA does not isomerize R5P to RU5P

RPIA isomerizes D-ribulose 5-phosphate to ribose 5-phosphate

Pentose phosphate pathway