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PRKDC and MRE11
Number of citations of the paper that reports this interaction (PubMedID
10608806
)
247
Data Source:
BioGRID
(unspecified method)
PRKDC
MRE11
Description
protein kinase, DNA-activated, catalytic subunit
MRE11 homolog, double strand break repair nuclease
Image
GO Annotations
Cellular Component
Nuclear Chromosome, Telomeric Region
Nucleus
Nucleoplasm
Transcription Factor Complex
Nucleolus
Cytosol
DNA-dependent Protein Kinase-DNA Ligase 4 Complex
Membrane
Protein-containing Complex
Protein-DNA Complex
Nonhomologous End Joining Complex
Chromosome, Telomeric Region
Nuclear Chromosome, Telomeric Region
Nucleus
Nucleoplasm
Replication Fork
Cytoplasm
Cytosol
PML Body
Mre11 Complex
Site Of Double-strand Break
Molecular Function
Double-stranded DNA Binding
RNA Binding
Protein Kinase Activity
Protein Serine/threonine Kinase Activity
DNA-dependent Protein Kinase Activity
Protein Binding
ATP Binding
Transcription Factor Binding
Enzyme Binding
Protein Domain Specific Binding
Single-stranded DNA Endodeoxyribonuclease Activity
DNA Binding
DNA Helicase Activity
Double-stranded DNA Binding
Nuclease Activity
Endodeoxyribonuclease Activity
Protein Binding
Protein C-terminus Binding
3'-5'-exodeoxyribonuclease Activity
3'-5' Exonuclease Activity
5'-3' Exonuclease Activity
Manganese Ion Binding
Identical Protein Binding
Cadherin Binding
Biological Process
Telomere Maintenance
Somitogenesis
Negative Regulation Of Protein Phosphorylation
Activation Of Innate Immune Response
B Cell Lineage Commitment
Pro-B Cell Differentiation
T Cell Lineage Commitment
Negative Regulation Of Immunoglobulin Production
Double-strand Break Repair
Double-strand Break Repair Via Nonhomologous End Joining
Cellular Protein Modification Process
Protein Phosphorylation
Cellular Response To DNA Damage Stimulus
Brain Development
Heart Development
Intrinsic Apoptotic Signaling Pathway In Response To DNA Damage
Response To Gamma Radiation
Response To Activity
Telomere Capping
Protein Ubiquitination
Peptidyl-serine Phosphorylation
Protein Destabilization
Positive Regulation Of Type I Interferon Production
Cellular Response To Insulin Stimulus
T Cell Differentiation In Thymus
Immunoglobulin V(D)J Recombination
T Cell Receptor V(D)J Recombination
Ectopic Germ Cell Programmed Cell Death
Regulation Of Circadian Rhythm
Positive Regulation Of Apoptotic Process
Negative Regulation Of Apoptotic Process
Innate Immune Response
Positive Regulation Of Transcription By RNA Polymerase II
Positive Regulation Of Fibroblast Proliferation
Rhythmic Process
Spleen Development
Thymus Development
Positive Regulation Of Developmental Growth
Regulation Of Smooth Muscle Cell Proliferation
Regulation Of Epithelial Cell Proliferation
Signal Transduction Involved In Mitotic G1 DNA Damage Checkpoint
Double-strand Break Repair Via Alternative Nonhomologous End Joining
Negative Regulation Of Cellular Senescence
Positive Regulation Of Double-strand Break Repair Via Nonhomologous End Joining
Negative Regulation Of Response To Gamma Radiation
Regulation Of Mitotic Recombination
Telomere Maintenance
Double-strand Break Repair Via Homologous Recombination
DNA Double-strand Break Processing
DNA Replication
DNA Repair
Double-strand Break Repair
Double-strand Break Repair Via Nonhomologous End Joining
DNA Recombination
Cellular Response To DNA Damage Stimulus
Telomere Maintenance Via Telomerase
Sister Chromatid Cohesion
Mitotic G2 DNA Damage Checkpoint
Synapsis
Reciprocal Meiotic Recombination
Cell Proliferation
Viral Process
Intra-S DNA Damage Checkpoint
Telomeric 3' Overhang Formation
Positive Regulation Of Protein Autophosphorylation
Positive Regulation Of Telomere Maintenance
Positive Regulation Of Type I Interferon Production
DNA Duplex Unwinding
Positive Regulation Of Kinase Activity
Meiotic DNA Double-strand Break Formation
Negative Regulation Of Apoptotic Process
Mitochondrial Double-strand Break Repair Via Homologous Recombination
DNA Strand Resection Involved In Replication Fork Processing
Regulation Of Signal Transduction By P53 Class Mediator
Pathways
Cytosolic sensors of pathogen-associated DNA
IRF3-mediated induction of type I IFN
Nonhomologous End-Joining (NHEJ)
E3 ubiquitin ligases ubiquitinate target proteins
Cytosolic sensors of pathogen-associated DNA
DNA Damage/Telomere Stress Induced Senescence
IRF3-mediated induction of type I IFN
HDR through Single Strand Annealing (SSA)
HDR through MMEJ (alt-NHEJ)
HDR through Homologous Recombination (HRR)
Sensing of DNA Double Strand Breaks
Resolution of D-loop Structures through Synthesis-Dependent Strand Annealing (SDSA)
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
Resolution of D-loop Structures through Holliday Junction Intermediates
Nonhomologous End-Joining (NHEJ)
Homologous DNA Pairing and Strand Exchange
Processing of DNA double-strand break ends
Presynaptic phase of homologous DNA pairing and strand exchange
Regulation of TP53 Activity through Phosphorylation
G2/M DNA damage checkpoint
Meiotic recombination
Drugs
Caffeine
SF1126
Diseases
DNA repair defects, including the following six diseases: Ataxia telangiectasia (AT); Ataxia-talangiectasia-like syndrome; Nijmegen syndrome; DNA ligase I deficiency; DNA ligase IV deficiency; Bloom's syndrome
Ataxia with ocular apraxia (AOA), including: Ataxia telangiectasia (AT); Ataxia telangiectasia like disorder (ATLD); Ataxia oculomotor apraxia type 1 (AOA1); Ataxia oculomotor apraxia type 2 (AOA2)
GWAS
Interacting Genes
89 interacting genes:
ABL1
AICDA
AKT1
AKT2
AP1B1
ATM
ATRIP
BRCA1
C1D
CASP3
CCNB1
CHEK1
CHEK2
CHUK
CIB1
CLK1
CTDP1
DCAF1
DCLRE1C
E4F1
EIF2S2
EIF4EBP1
EP300
ERG
FH
GSK3A
GSK3B
GZMB
H1-1
H1-2
H2AX
HDAC3
HMGB1
HMGB2
HNRNPA1
HNRNPC
HOXC4
HSF1
HSP90AA1
IKBKB
ILF2
JUN
KAT2A
LIG4
LYN
MAPK8
MBP
MKNK1
MRE11
MTNR1B
NBN
NCF1
NCF2
NCF4
NCOA6
NR3C1
PARP1
PCNA
PDX1
PGR
POU2F1
PPP6C
PPP6R1
PPP6R3
PRKCD
RAD17
RASSF1
RBBP8
RPA1
RPA2
SGO1
SP1
SRF
SUMO2
THRA
THRB
TOP1
TP53
TREX1
UBE2I
USF1
WRN
XPA
XRCC4
XRCC5
XRCC6
YWHAG
YWHAQ
ZBTB7A
19 interacting genes:
ATM
ATR
CCNE1
CDK2
DCLRE1C
DYNLL1
EP300
FANCD2
H2AX
LIG1
MAPK8IP2
NBN
NEK1
PRKDC
RAD50
RECQL5
SPOP
SUMO2
XRCC6
Entrez ID
5591
4361
HPRD ID
02941
02889
Ensembl ID
ENSG00000253729
ENSG00000020922
Uniprot IDs
P78527
A0A024R395
F8W7U8
P49959
Q05D78
PDB IDs
5LUQ
5W1R
5Y3R
3T1I
Enriched GO Terms of Interacting Partners
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