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PPT1 and RLF
Data Source:
BioGRID
(affinity chromatography technology, affinity chromatography technology)
PPT1
RLF
Description
palmitoyl-protein thioesterase 1
RLF zinc finger
Image
No pdb structure
GO Annotations
Cellular Component
Extracellular Region
Nucleus
Lysosome
Golgi Apparatus
Cytosol
Synaptic Vesicle
Membrane
Axon
Lysosomal Lumen
Intracellular Membrane-bounded Organelle
Membrane Raft
Extracellular Exosome
Nucleus
Molecular Function
Protein Binding
Palmitoyl-(protein) Hydrolase Activity
Palmitoyl-CoA Hydrolase Activity
Thiolester Hydrolase Activity
Lysophosphatidic Acid Binding
Sulfatide Binding
DNA-binding Transcription Factor Activity, RNA Polymerase II-specific
DNA-binding Transcription Activator Activity, RNA Polymerase II-specific
DNA Binding
Protein Binding
Metal Ion Binding
Biological Process
Protein Depalmitoylation
Receptor-mediated Endocytosis
Pinocytosis
Lysosomal Lumen Acidification
Nervous System Development
Brain Development
Visual Perception
Protein Transport
Lipid Catabolic Process
Protein Phosphopantetheinylation
Sphingolipid Catabolic Process
Protein Catabolic Process
Negative Regulation Of Cell Growth
Membrane Raft Organization
Negative Regulation Of Apoptotic Process
Negative Regulation Of Neuron Apoptotic Process
Fatty-acyl-CoA Biosynthetic Process
Positive Regulation Of Receptor-mediated Endocytosis
Positive Regulation Of Pinocytosis
Neuron Development
Regulation Of Synapse Structure Or Activity
Response To Stimulus
Regulation Of Transcription By RNA Polymerase II
Regulation Of DNA Methylation
Positive Regulation Of Transcription, DNA-templated
Positive Regulation Of Transcription By RNA Polymerase II
Histone H3-K4 Monomethylation
Pathways
Fatty acyl-CoA biosynthesis
Drugs
Hexadecanesulfonyl fluoride
Palmitic Acid
Diseases
Neuronal ceroid lipofuscinosis, including: Infantile Neuronal Ceroid Lipofuscinosis (INCL)/ Santavuori-Haltia Disease (CLN1); Late-Infantile Neuronal Ceroid Lipofuscinosis (LINCL)/ Jansky-Bielschowsky Disease (CLN2); Juvenile Neuronal Ceroid Lipofuscinosis (JNCL)/Batten Disease/ Spielmeyer-Vogt Disease (CLN3); Adult Neuronal Ceroid Lipofuscinosis (ANCL)/ Kufs Disease (CLN4); LINCL variant (CLN5, CLN6, CLN7, CLN8); Batten Disease variant (CLN9); Congenital NCL (CLN10)
Progressive myoclonic epilepsy (PME), including: Lafora disease (LBD); Unverricht-Lundborg disease (ULD); Neuronal ceroid lipofuscinoses (NCL); Type I sialidosis; Action myoclonus-renal failure syndrome (AMRF); Type III Gaucher disease (GD)
GWAS
Blood protein levels (
30072576
29875488
)
Platelet count (
32888494
)
High density lipoprotein cholesterol levels (
30498476
)
Post bronchodilator FEV1 (
26634245
)
Post bronchodilator FEV1/FVC ratio (
26634245
)
Interacting Genes
1 interacting genes:
GNAQ
7 interacting genes:
CLK1
FBXL17
GCH1
PRPF40A
RIT1
RIT2
TRIM14
Entrez ID
5538
6018
HPRD ID
07203
01614
Ensembl ID
ENSG00000131238
ENSG00000117000
Uniprot IDs
P50897
Q13129
PDB IDs
3GRO
Enriched GO Terms of Interacting Partners
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Tagcloud
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Tagcloud (Intersection)
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