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KRT31 and PSMA1
Number of citations of the paper that reports this interaction (PubMedID
25416956
)
381
Data Source:
BioGRID
(two hybrid)
KRT31
PSMA1
Description
keratin 31
proteasome 20S subunit alpha 1
Image
No pdb structure
GO Annotations
Cellular Component
Extracellular Space
Cytosol
Intermediate Filament
Extracellular Exosome
Proteasome Complex
Nucleus
Nucleoplasm
Cytoplasm
Centrosome
Cytosol
Proteasome Core Complex
Polysome
Proteasome Core Complex, Alpha-subunit Complex
Extracellular Exosome
Molecular Function
Structural Constituent Of Cytoskeleton
Protein Binding
Lipopolysaccharide Binding
RNA Binding
Endopeptidase Activity
Threonine-type Endopeptidase Activity
Protein Binding
Biological Process
Cytoskeleton Organization
Epidermis Development
Keratinization
Cornification
MAPK Cascade
Protein Polyubiquitination
Stimulatory C-type Lectin Receptor Signaling Pathway
Antigen Processing And Presentation Of Exogenous Peptide Antigen Via MHC Class I, TAP-dependent
Negative Regulation Of Inflammatory Response To Antigenic Stimulus
Regulation Of Cellular Amino Acid Metabolic Process
Proteasomal Protein Catabolic Process
Proteasomal Ubiquitin-independent Protein Catabolic Process
Negative Regulation Of G2/M Transition Of Mitotic Cell Cycle
Protein Deubiquitination
Anaphase-promoting Complex-dependent Catabolic Process
SCF-dependent Proteasomal Ubiquitin-dependent Protein Catabolic Process
Tumor Necrosis Factor-mediated Signaling Pathway
NIK/NF-kappaB Signaling
Fc-epsilon Receptor Signaling Pathway
Proteasome-mediated Ubiquitin-dependent Protein Catabolic Process
Regulation Of MRNA Stability
Post-translational Protein Modification
T Cell Receptor Signaling Pathway
Transmembrane Transport
Wnt Signaling Pathway, Planar Cell Polarity Pathway
Regulation Of Transcription From RNA Polymerase II Promoter In Response To Hypoxia
Interleukin-1-mediated Signaling Pathway
Negative Regulation Of Canonical Wnt Signaling Pathway
Positive Regulation Of Canonical Wnt Signaling Pathway
Regulation Of Mitotic Cell Cycle Phase Transition
Regulation Of Hematopoietic Stem Cell Differentiation
Pathways
Keratinization
Formation of the cornified envelope
Activation of NF-kappaB in B cells
Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha
ER-Phagosome pathway
Cross-presentation of soluble exogenous antigens (endosomes)
Autodegradation of Cdh1 by Cdh1:APC/C
SCF-beta-TrCP mediated degradation of Emi1
APC/C:Cdc20 mediated degradation of Securin
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1
Cdc20:Phospho-APC/C mediated degradation of Cyclin A
Vpu mediated degradation of CD4
Vif-mediated degradation of APOBEC3G
SCF(Skp2)-mediated degradation of p27/p21
Degradation of beta-catenin by the destruction complex
Downstream TCR signaling
Regulation of activated PAK-2p34 by proteasome mediated degradation
Separation of Sister Chromatids
FCERI mediated NF-kB activation
Autodegradation of the E3 ubiquitin ligase COP1
Regulation of ornithine decarboxylase (ODC)
ABC-family proteins mediated transport
AUF1 (hnRNP D0) binds and destabilizes mRNA
Asymmetric localization of PCP proteins
Degradation of AXIN
Degradation of DVL
Hedgehog ligand biogenesis
Hh mutants that don't undergo autocatalytic processing are degraded by ERAD
Dectin-1 mediated noncanonical NF-kB signaling
CLEC7A (Dectin-1) signaling
Degradation of GLI1 by the proteasome
Degradation of GLI2 by the proteasome
GLI3 is processed to GLI3R by the proteasome
Hedgehog 'on' state
Regulation of RAS by GAPs
TNFR2 non-canonical NF-kB pathway
NIK - noncanonical NF-kB signaling
Defective CFTR causes cystic fibrosis
MAPK6/MAPK4 signaling
UCH proteinases
Ub-specific processing proteases
CDT1 association with the CDC6:ORC:origin complex
Orc1 removal from chromatin
CDK-mediated phosphorylation and removal of Cdc6
G2/M Checkpoints
Ubiquitin Mediated Degradation of Phosphorylated Cdc25A
Ubiquitin-dependent degradation of Cyclin D
The role of GTSE1 in G2/M progression after G2 checkpoint
FBXL7 down-regulates AURKA during mitotic entry and in early mitosis
RUNX1 regulates transcription of genes involved in differentiation of HSCs
Regulation of RUNX2 expression and activity
Regulation of RUNX2 expression and activity
Regulation of RUNX3 expression and activity
Regulation of PTEN stability and activity
Neddylation
Regulation of expression of SLITs and ROBOs
Interleukin-1 signaling
Negative regulation of NOTCH4 signaling
Antigen processing: Ubiquitination & Proteasome degradation
Drugs
(3AR,6R,6AS)-6-((S)-((S)-CYCLOHEX-2-ENYL)(HYDROXY)METHYL)-6A-METHYL-4-OXO-HEXAHYDRO-2H-FURO[3,2-C]PYRROLE-6-CARBALDEHYDE
Diseases
GWAS
Brown vs. black hair color (
30531825
)
Alzheimer's disease (cognitive decline) (
23535033
)
Bipolar disorder (
31043756
)
Diastolic blood pressure (
27841878
)
High chromosomal aberration frequency (total) (
31586183
)
Systolic blood pressure (
27841878
)
Vitamin D levels (
25208829
)
Interacting Genes
184 interacting genes:
ABI2
AGR2
ALDH3B1
AMOT
AMOTL2
ANKRD36BP1
AQP1
AQP5
ARHGAP35
ARMC7
ARSJ
ASMTL
ASPSCR1
ATG9A
ATN1
ATXN7L1
BEX2
BTC
BYSL
C12orf49
C19orf73
C1orf109
C1orf216
C2CD6
C5orf60
CA6
CARD9
CATIP
CCDC112
CCDC120
CCDC17
CCDC196
CCDC93
CCER1
CCHCR1
CCNC
CD33
CDC20B
CDK18
CDKN1A
CEP57
CEP57L1
CEP70
CFAP206
CHCHD2
CHRNG
CLDN2
COA5
COMT
COX5A
COX5B
CRH
CTSG
DGCR6L
DHX37
DMRT3
DTNB
EIF4E2
EXOC8
FAM110A
FAM124B
FAM71C
FAM74A4
FAM90A1
FARS2
FBF1
FBXW5
FKBP1B
FOXB1
GAD1
GEM
GFOD1
GLRX3
GNAI2
GNE
GNG10
GNG5
GPS2
GSTP1
HAUS1
HDAC4
HGS
HNRNPLL
HOXA1
HSPA12B
HSPD1
ICAM4
INPP5D
INPP5K
INSR
JOSD1
KIFC3
KLC1
KLC4
KLHL38
KRT2
KRT5
KRT6A
KRT6B
KRT6C
KRT71
KRT77
KRT79
KRT8
KRT81
KRT83
LATS1
LCE4A
LENG1
LIN37
LINC00526
LMF2
LMO4
LONRF1
MAP3K7CL
MAPKBP1
MARK4
MRPL40
NAV1
NAXD
NEK6
NPBWR2
NTAQ1
OTUB2
P2RX7
PDE4DIP
PGLS
PIN1
PKN1
PPP1R18
PRF1
PRKAA2
PRR19
PSMA1
PSMG2
PSPC1
PTGER3
PTPMT1
RADIL
RAMAC
RCOR3
RIBC1
RPUSD3
RSPH14
SCNM1
SEMA4C
SHC3
SIRPA
SLC15A3
SLC23A1
SLC25A6
SMARCE1
SMCP
SMG9
SNAI1
SNRNP25
SPATA24
SPON2
SRSF2
SSX2IP
TAPBPL
THAP7
TLE5
TMEM106C
TMEM231
TMSB4X
TRAF4
TROAP
TSG101
TTC23
TXLNA
USHBP1
UTP23
UXT
WDR25
ZFYVE21
ZNF124
ZNF148
ZNF20
ZNF569
ZNF572
ZNF688
ZNF69
ZNRF2P1
89 interacting genes:
ABCD3
ABI3
ACTN1
APIP
APP
BLZF1
C11orf49
CALCOCO2
CBS
CCDC102B
CCDC85B
CCNH
CDA
CEP70
CEP72
COIL
DLEU1
EHMT2
GNPTAB
GOLGA2
HOMER3
HSD17B14
IFT20
IKZF1
IKZF3
INO80E
KCTD1
KCTD17
KCTD9
KRT15
KRT31
KRT38
KRT40
KRTAP5-9
LDB1
LDOC1
LZTS2
MAD1L1
MAPRE1
MAPRE3
MCM6
MID2
MKRN3
MLH1
MRFAP1L1
MT-CO2
MTUS2
NECAB2
NMI
NOP53
NOTCH2NLA
PLK1
PNMA1
PNMA2
PNMA5
POMP
PPCDC
PRDM14
PRKN
PSMA2
PSMA3
PSMA4
PSMA7
PSMB1
PSMB10
PSMB2
PSMB5
RAD54B
REL
ROPN1
SFMBT1
SH3BP4
SH3GLB1
SSX2IP
TCF12
TCF4
TDO2
TNFAIP1
TNR
TRAF1
TRIM10
TRIM23
TRIM27
TRIM42
TSC22D4
UBXN11
VCP
VIM
ZFAND1
Entrez ID
3881
5682
HPRD ID
03047
04170
Ensembl ID
ENSG00000094796
ENSG00000129084
Uniprot IDs
Q15323
B4E0X6
P25786
PDB IDs
4R3O
4R67
5A0Q
5GJQ
5GJR
5L4G
5LE5
5LEX
5LEY
5LEZ
5LF0
5LF1
5LF3
5LF4
5LF6
5LF7
5LN3
5M32
5T0C
5T0G
5T0H
5T0I
5T0J
5VFO
5VFP
5VFQ
5VFR
5VFS
5VFT
5VFU
6AVO
6E5B
6MSB
6MSD
6MSE
6MSG
6MSH
6MSJ
6MSK
6R70
6REY
6RGQ
Enriched GO Terms of Interacting Partners
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