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OPTN and GABARAPL1
Data Source:
BioGRID
(pull down, proximity labelling technology, affinity chromatography technology)
OPTN
GABARAPL1
Description
optineurin
GABA type A receptor associated protein like 1
Image
GO Annotations
Cellular Component
Golgi Membrane
Nucleus
Nucleoplasm
Cytoplasm
Autophagosome
Golgi Apparatus
Trans-Golgi Network
Cytosol
Perinuclear Region Of Cytoplasm
Recycling Endosome Membrane
Autophagosome Membrane
Mitochondrion
Autophagosome
Endoplasmic Reticulum
Golgi Apparatus
Cytosol
Microtubule
Cytoplasmic Vesicle Membrane
Dendrite Membrane
Dendrite Cytoplasm
Cell Body
Molecular Function
Protein Binding
Protein C-terminus Binding
Protein-macromolecule Adaptor Activity
Small GTPase Binding
Polyubiquitin Modification-dependent Protein Binding
Identical Protein Binding
Metal Ion Binding
K63-linked Polyubiquitin Modification-dependent Protein Binding
Protein Binding
Tat Protein Binding
Ubiquitin Protein Ligase Binding
Beta-tubulin Binding
GABA Receptor Binding
Biological Process
G2/M Transition Of Mitotic Cell Cycle
Negative Regulation Of Receptor Recycling
Autophagy
Golgi Organization
Signal Transduction
Cell Death
Positive Regulation Of Autophagy
Viral Process
Protein Localization To Golgi Apparatus
Cellular Response To Unfolded Protein
Golgi To Plasma Membrane Protein Transport
Regulation Of I-kappaB Kinase/NF-kappaB Signaling
Negative Regulation Of I-kappaB Kinase/NF-kappaB Signaling
Innate Immune Response
Defense Response To Gram-negative Bacterium
Parkin-mediated Stimulation Of Mitophagy In Response To Mitochondrial Depolarization
Golgi Ribbon Formation
Positive Regulation Of Xenophagy
Autophagosome Assembly
Autophagy Of Mitochondrion
Cellular Response To Nitrogen Starvation
Macroautophagy
Autophagosome Maturation
Pathways
Regulation of PLK1 Activity at G2/M Transition
TBC/RABGAPs
Macroautophagy
Drugs
Diseases
Amyotrophic lateral sclerosis (ALS); Lou Gehrig's disease
Primary open angle glaucoma
GWAS
Cerebrospinal fluid p-tau levels (
29274321
)
Cerebrospinal fluid p-tau levels in mild cognitive impairment (
29274321
)
Paget's disease (
21623375
20436471
)
Interacting Genes
69 interacting genes:
AIMP1
ARRDC3
ATG16L1
ATG5
CALM1
CCDC13
CDC23
CLTC
CMYA5
DAZAP2
DYSF
DZIP1
FAM189A2
FLII
FOS
FTH1
GABARAP
GABARAPL1
GABARAPL2
GNAS
GRM1
GTF3A
HACE1
HSF2BP
HSPB1
HTT
IRAK1
KANSL1L
LITAF
LNX2
MAP1LC3A
MAP1LC3C
MPP1
MYH3
MYO6
PIAS4
PICK1
POU6F2
RAB11A
RAB11B
RAB12
RAB14
RAB25
RAB8A
RBM12
RFFL
RNF11
RNF216
SDCBP
SLF2
SNX6
TBC1D15
TBC1D17
TNIP1
UBB
UBC
UQCRQ
USP2
VCP
WASHC3
WIPI2
ZNF17
ZNF181
ZNF302
ZNF329
ZNF398
ZNF426
ZNF670
ZNF711
73 interacting genes:
AHNAK2
AMBRA1
ANK2
ATG13
ATG4A
ATG4B
ATG4D
BNIP3L
BSCL2
BSDC1
CALCOCO1
CALCOCO2
CREB3L2
CUL3
DISC1
DVL2
DYNLL1
ERBB2
ERBB3
FUNDC1
HSP90AA1
HSP90AB1
KBTBD7
KRTAP10-3
KRTAP10-7
KRTAP10-9
KXD1
MAPK15
MEFV
MLX
NEDD4
NFIA
OPRK1
OPTN
OSBPL3
PBXIP1
PSMB4
PTPRR
RABGAP1
RABGAP1L
RB1CC1
RCN2
RETREG3
SCYL3
SNCA
SQSTM1
SRPK1
SRPK2
STRN3
TAX1BP1
TBC1D1
TBC1D10A
TBC1D10B
TBC1D16
TBC1D17
TBC1D2
TBC1D25
TBC1D2B
TBC1D5
TBC1D7
TBC1D9
TBC1D9B
THAP7
TMEM131
TNIP1
TP53INP1
TRIM21
TRIM32
ULK1
UMAD1
VDR
WDFY3
ZBTB22
Entrez ID
10133
23710
HPRD ID
03891
07601
Ensembl ID
ENSG00000123240
ENSG00000139112
Uniprot IDs
Q96CV9
A0A024RAP5
Q9H0R8
PDB IDs
2LO4
2LUE
3VTV
3VTW
5AAZ
5B83
5EOA
5EOF
2L8J
2R2Q
5DPT
5LXH
5LXI
6HOI
6HOL
Enriched GO Terms of Interacting Partners
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