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ABHD17C and VCP
Number of citations of the paper that reports this interaction (PubMedID
27762274
)
3
Data Source:
BioGRID
(two hybrid, affinity chromatography technology)
ABHD17C
VCP
Description
abhydrolase domain containing 17C, depalmitoylase
valosin containing protein
Image
No pdb structure
GO Annotations
Cellular Component
Cell Junction
Dendritic Spine
Recycling Endosome Membrane
Postsynaptic Density Membrane
Glutamatergic Synapse
Proteasome Complex
Extracellular Region
Nucleus
Nucleoplasm
Cytoplasm
Endoplasmic Reticulum
Endoplasmic Reticulum Membrane
Lipid Droplet
Cytosol
Cytoplasmic Stress Granule
Protein-containing Complex
VCP-NPL4-UFD1 AAA ATPase Complex
Secretory Granule Lumen
Azurophil Granule Lumen
Site Of Double-strand Break
Derlin-1 Retrotranslocation Complex
Intracellular Membrane-bounded Organelle
Perinuclear Region Of Cytoplasm
Extracellular Exosome
Glutamatergic Synapse
Ficolin-1-rich Granule Lumen
ATPase Complex
VCP-NSFL1C Complex
Molecular Function
Palmitoyl-(protein) Hydrolase Activity
RNA Binding
Protein Binding
ATP Binding
Lipid Binding
ATPase Activity
Protein Phosphatase Binding
Protein Domain Specific Binding
Polyubiquitin Modification-dependent Protein Binding
Ubiquitin Protein Ligase Binding
Deubiquitinase Activator Activity
K48-linked Polyubiquitin Modification-dependent Protein Binding
MHC Class I Protein Binding
Identical Protein Binding
ADP Binding
Ubiquitin-like Protein Ligase Binding
BAT3 Complex Binding
Ubiquitin-specific Protease Binding
Biological Process
Protein Depalmitoylation
Protein Palmitoylation
Regulation Of Postsynapse Organization
Negative Regulation Of Protein Localization To Microtubule
Positive Regulation Of Protein Localization To Endosome
DNA Repair
Double-strand Break Repair
Protein Folding
NADH Metabolic Process
ER To Golgi Vesicle-mediated Transport
Autophagy
Activation Of Cysteine-type Endopeptidase Activity Involved In Apoptotic Process
Cellular Response To DNA Damage Stimulus
Proteasomal Protein Catabolic Process
Positive Regulation Of Mitochondrial Membrane Potential
Macroautophagy
Protein Ubiquitination
Protein Deubiquitination
Viral Genome Replication
Translesion Synthesis
Ubiquitin-dependent ERAD Pathway
Endoplasmic Reticulum Unfolded Protein Response
Retrograde Protein Transport, ER To Cytosol
Positive Regulation Of Protein Complex Assembly
Positive Regulation Of Proteasomal Ubiquitin-dependent Protein Catabolic Process
Endosome To Lysosome Transport Via Multivesicular Body Sorting Pathway
Cellular Response To Heat
Stress Granule Disassembly
ERAD Pathway
Regulation Of Apoptotic Process
Proteasome-mediated Ubiquitin-dependent Protein Catabolic Process
Neutrophil Degranulation
Establishment Of Protein Localization
Positive Regulation Of Protein Catabolic Process
ATP Metabolic Process
Regulation Of Synapse Organization
Mitotic Spindle Disassembly
Transmembrane Transport
Endoplasmic Reticulum Stress-induced Pre-emptive Quality Control
Aggresome Assembly
Error-free Translesion Synthesis
ER-associated Misfolded Protein Catabolic Process
Flavin Adenine Dinucleotide Catabolic Process
Positive Regulation Of Canonical Wnt Signaling Pathway
Autophagosome Maturation
Positive Regulation Of Protein K63-linked Deubiquitination
Positive Regulation Of Lys63-specific Deubiquitinase Activity
Regulation Of Aerobic Respiration
Cellular Response To Arsenite Ion
Positive Regulation Of Oxidative Phosphorylation
Positive Regulation Of Ubiquitin-specific Protease Activity
Positive Regulation Of ATP Biosynthetic Process
Pathways
Translesion Synthesis by POLH
HSF1 activation
ABC-family proteins mediated transport
N-glycan trimming in the ER and Calnexin/Calreticulin cycle
Hedgehog ligand biogenesis
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD
Defective CFTR causes cystic fibrosis
Josephin domain DUBs
Ovarian tumor domain proteases
Neutrophil degranulation
E3 ubiquitin ligases ubiquitinate target proteins
Protein methylation
Aggrephagy
Drugs
Phosphoaminophosphonic Acid-Adenylate Ester
Phenethyl Isothiocyanate
Diseases
Frontotemporal lobar degeneration (FTLD), including: Pick disease of brain; Frontotemporal dementia (FTD); Ubiquitin-positive frontotemporal dementia (UP-FTD); Progressive supranuclear palsy type 1 (PSNP1); Inclusion body myopathy with early-onset paget disease and frontotemporal dementia (IBMPFD); Frontotemporal dementia, chromosome 3-linked (FTD3)
GWAS
Hand grip strength (
29691431
)
Systolic blood pressure (
28135244
)
Response to quetiapine in schizophrenia (
29503163
)
Interacting Genes
1 interacting genes:
VCP
84 interacting genes:
ABHD17C
AMFR
ANKRD13A
AR
ATG5
ATXN1
ATXN3
ATXN7
BRCA1
BRSK2
BUD23
CEP19
CLUAP1
CRMP1
CSTF1
DERL1
DGCR6
DTNB
ELAVL1
EPSTI1
ESR1
FAF2
FAM104A
GZMK
HDAC6
HERPUD1
HTT
INSIG1
INSIG2
JAK2
LNX1
LZIC
MAPK8IP2
MFN2
NDRG1
NF1
NFKBIA
NGLY1
NOD2
NSFL1C
NTAQ1
NUB1
OTULIN
PIK3R3
PLAA
PPP1R11
PRKCD
PSMA1
PSMA7
PSMC1
PTPN3
RNF115
RNF19A
RNF8
RPL9
RPS6KA1
SELENOS
SH2D2A
SIGMAR1
SLC43A3
STUB1
STX5
SUMO4
SVIP
TOM1L1
TOMM34
UBC
UBE4A
UBE4B
UBOX5
UBXN10
UBXN11
UBXN2A
UBXN2B
UBXN4
UBXN6
UBXN7
UFD1
VAMP2
VCPIP1
VCPKMT
WAC
WRN
YWHAZ
Entrez ID
58489
7415
HPRD ID
19350
03013
Ensembl ID
ENSG00000136379
ENSG00000165280
Uniprot IDs
Q6PCB6
P55072
V9HW80
PDB IDs
3EBB
3HU1
3HU2
3HU3
3QC8
3QQ7
3QQ8
3QWZ
3TIW
4KDI
4KDL
4KLN
4KO8
4KOD
4P0A
5B6C
5C18
5C19
5C1A
5C1B
5DYG
5DYI
5EPP
5FTJ
5FTK
5FTL
5FTM
5FTN
5GLF
5IFS
5IFW
5KIW
5KIY
5X4L
6G2V
6G2W
6G2X
6G2Y
6G2Z
6G30
6HD0
6MCK
Enriched GO Terms of Interacting Partners
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