Homo sapiens Protein: PPM1K
Summary
InnateDB Protein IDBP-29592.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol PPM1K
Protein Name protein phosphatase, Mg2+/Mn2+ dependent, 1K
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000295908
InnateDB Gene IDBG-29590 (PPM1K)
Protein Structure
UniProt Annotation
Function Regulates the mitochondrial permeability transition pore and is essential for cellular survival and development. {ECO:0000269PubMed:17374715}.
Subcellular Localization Mitochondrion matrix {ECO:0000269PubMed:17336929, ECO:0000269PubMed:17374715}.
Disease Associations Maple syrup urine disease, mild variant (MSUDMV) [MIM:615135]: A mild form of maple syrup urine disease, a metabolic disorder due to an enzyme defect in the catabolic pathway of the branched-chain amino acids leucine, isoleucine, and valine. Accumulation of these 3 amino acids and their corresponding keto acids leads to encephalopathy and progressive neurodegeneration. Clinical features include mental and physical retardation, feeding problems, and a maple syrup odor to the urine. The keto acids of the branched-chain amino acids are present in the urine. If untreated, maple syrup urine disease can lead to seizures, coma, and death. The disease is often classified by its pattern of signs and symptoms. The most common and severe form of the disease is the classic type, which becomes apparent soon after birth. Variant forms of the disorder become apparent later in infancy or childhood and are typically milder, but they still involve developmental delay and other medical problems if not treated. MSUDMV is characterized by increased plasma levels of branched-chain amino acids (BCAA) apparent at birth. Treatment with a low-protein diet free of BCAA can result in normal psychomotor development and lack of metabolic episodes. {ECO:0000269PubMed:23086801}. Note=The gene represented in this entry is involved in disease pathogenesis.
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 2 [view]
Protein-Protein 2 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003824 catalytic activity
GO:0004722 protein serine/threonine phosphatase activity
Biological Process
GO:0006470 protein dephosphorylation
GO:0008152 metabolic process
Cellular Component
Protein Structure and Domains
PDB ID
InterPro IPR001932 Protein phosphatase 2C (PP2C)-like domain
PFAM PF00481
PF07228
PRINTS
PIRSF
SMART SM00331
SM00332
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt
PhosphoSite PhosphoSite-Q8N3J5
TrEMBL V9GYS8
UniProt Splice Variant
Entrez Gene 152926
UniGene Hs.43744
RefSeq XP_005262832
HUGO HGNC:25415
OMIM 611065
CCDS
HPRD 15167
IMGT
EMBL AC097484 AC107067 AC108213
GenPept