Wiki-MPM
About
Search
Browse
People
Funding
Updates
Search
KARS1 and SPTAN1
Data Source:
BioGRID
(two hybrid)
KARS1
SPTAN1
Description
lysyl-tRNA synthetase 1
spectrin alpha, non-erythrocytic 1
Image
GO Annotations
Cellular Component
Extracellular Space
Nucleus
Mitochondrion
Mitochondrial Matrix
Cytosol
Plasma Membrane
Aminoacyl-tRNA Synthetase Multienzyme Complex
Extracellular Region
Cytosol
Spectrin
Microtubule Cytoskeleton
Membrane
Specific Granule Lumen
Intracellular Membrane-bounded Organelle
Extracellular Exosome
Extracellular Vesicle
Tertiary Granule Lumen
Molecular Function
TRNA Binding
ATP Adenylyltransferase Activity
Lysine-tRNA Ligase Activity
Protein Binding
ATP Binding
Amino Acid Binding
Identical Protein Binding
Protein Homodimerization Activity
Actin Binding
Structural Constituent Of Cytoskeleton
Calcium Ion Binding
Protein Binding
Calmodulin Binding
Cadherin Binding
Biological Process
Basophil Activation Involved In Immune Response
Positive Regulation Of Inflammatory Response To Antigenic Stimulus
TRNA Aminoacylation For Protein Translation
Lysyl-tRNA Aminoacylation
TRNA Processing
Response To X-ray
Diadenosine Tetraphosphate Biosynthetic Process
Viral Process
Positive Regulation Of Macrophage Activation
Positive Regulation Of Transcription, DNA-templated
ERK1 And ERK2 Cascade
MAPK Cascade
Endoplasmic Reticulum To Golgi Vesicle-mediated Transport
Cytoskeleton Organization
Axon Guidance
Neutrophil Degranulation
Actin Filament Capping
Pathways
Selenoamino acid metabolism
Cytosolic tRNA aminoacylation
Mitochondrial tRNA aminoacylation
Caspase-mediated cleavage of cytoskeletal proteins
Nephrin family interactions
NCAM signaling for neurite out-growth
NCAM signaling for neurite out-growth
Interaction between L1 and Ankyrins
Interaction between L1 and Ankyrins
RAF/MAP kinase cascade
Neutrophil degranulation
COPI-mediated anterograde transport
Drugs
L-Lysine
Diseases
Charcot-Marie-Tooth disease (CMT); Hereditary motor and sensory neuropathy; Peroneal muscular atrophy
Early infantile epileptic encephalopathy; Ohtahara syndrome
GWAS
Axial length (
24144296
)
Body mass index (
26426971
)
Interacting Genes
84 interacting genes:
AIMP2
CDC42
DARS2
DYSF
EEF1D
EEF1G
ESR1
FRS3
GAPDH
GEMIN4
LINC01554
MAPK1
MIR1-1
MIR1-2
MIR106A
MIR106B
MIR107
MIR10B
MIR122
MIR128-1
MIR128-2
MIR138-1
MIR138-2
MIR140
MIR141
MIR143
MIR145
MIR155
MIR15A
MIR15B
MIR16-2
MIR18B
MIR199A1
MIR19A
MIR19B1
MIR19B2
MIR200A
MIR200B
MIR200C
MIR205
MIR206
MIR20A
MIR20B
MIR21
MIR214
MIR221
MIR25
MIR29A
MIR29B1
MIR29C
MIR31
MIR34A
MIR34B
MIR34C
MIR363
MIR429
MIR451A
MIR7-1
MIR7-2
MIR7-3
MIR9-1
MIR9-3
MIR92A1
MIR92A2
MIR93
MIRLET7A1
MIRLET7A2
MIRLET7A3
MIRLET7B
MIRLET7C
MIRLET7D
MIRLET7E
MIRLET7F1
MIRLET7F2
MIRLET7G
MIRLET7I
PAFAH1B1
PIK3R3
RPSA
SLC25A6
SOD1
SPTAN1
SUMO2
VIM
56 interacting genes:
ABI1
ABL1
ACP1
ACTA1
ACTB
AKIP1
ANK1
CAPN1
CASP3
CASP7
CEP63
CTNNA1
DDX24
DES
EPB41
EPB41L2
EPB42
ERCC4
EVL
EXOC1
FANCA
FANCC
GAP43
GRIA2
GRIN1
GRIN2A
GRIN2B
GRIN2D
KALRN
KARS1
MAPK6
NEFL
PDE4D
PIN4
PLEC
PLEKHA5
PRKCB
PTEN
PTOV1
SHANK1
SHANK3
SLC9A2
SOS1
SPTB
SPTBN1
SPTBN2
SPTBN4
SRC
STAT1
SUMO2
SYN1
TAF1
TANC1
TES
TSSC4
ZNF333
Entrez ID
3735
6709
HPRD ID
03249
01684
Ensembl ID
ENSG00000065427
ENSG00000197694
Uniprot IDs
Q15046
A0A384P5S9
Q13813
PDB IDs
3BJU
4DPG
4YCU
4YCW
6CHD
6ILD
6ILH
2FOT
3F31
3FB2
5FW9
5FWB
5FWC
6ZEH
Enriched GO Terms of Interacting Partners
?
Tagcloud
?
Tagcloud (Difference)
?
Tagcloud (Intersection)
?