Bos taurus Gene: PYGL
Summary
InnateDB Gene IDBG-646461.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PYGL
Gene Name Glycogen phosphorylase, liver form
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000011494
Encoded Proteins
Glycogen phosphorylase, liver form
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000100504:
This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Feb 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:43800152-43840994
Strand Reverse strand
Band
Transcripts
ENSBTAT00000015277 ENSBTAP00000015277
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 10 interaction(s) predicted by orthology.
Predicted by orthology
Total 10 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0002060 purine nucleobase binding
GO:0003824 catalytic activity
GO:0004645 phosphorylase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0008144 drug binding
GO:0008184 glycogen phosphorylase activity
GO:0016208 AMP binding
GO:0016740 transferase activity
GO:0016757 transferase activity, transferring glycosyl groups
GO:0019842 vitamin binding
GO:0030170 pyridoxal phosphate binding
GO:0032052 bile acid binding
Biological Process
GO:0005975 carbohydrate metabolic process
GO:0005977 glycogen metabolic process
GO:0008152 metabolic process
GO:0042593 glucose homeostasis
GO:0070266 necroptotic process
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
Metabolism of carbohydrates pathway
Myoclonic epilepsy of Lafora pathway
Glycogen storage diseases pathway
Glycogen breakdown (glycogenolysis) pathway
Glucose metabolism pathway
Metabolism pathway
Disease pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
TNFalpha pathway
REACTOME
Glycogen breakdown (glycogenolysis) pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
Metabolism pathway
Disease pathway
Glucose metabolism pathway
Glycogen storage diseases pathway
Disease pathway
Glucose metabolism pathway
Metabolism pathway
Glycogen breakdown (glycogenolysis) pathway
Glycogen storage diseases pathway
Myoclonic epilepsy of Lafora pathway
Metabolism of carbohydrates pathway
KEGG
Insulin signaling pathway pathway
Starch and sucrose metabolism pathway
Insulin signaling pathway pathway
Starch and sucrose metabolism pathway
INOH
PID NCI
Cross-References
SwissProt Q0VCM4
TrEMBL
UniProt Splice Variant
Entrez Gene 505472
UniGene Bt.39311
RefSeq NM_001075203 XM_005211657 XM_005211658
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL BC120097
GenPept AAI20098
RNA Seq Atlas 505472