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H2AX and RPS6KA3
Data Source:
BioGRID
(enzymatic study)
H2AX
RPS6KA3
Description
H2A.X variant histone
ribosomal protein S6 kinase A3
Image
GO Annotations
Cellular Component
Chromosome, Telomeric Region
Nucleosome
Condensed Nuclear Chromosome
Male Germ Cell Nucleus
XY Body
Nucleus
Nucleoplasm
Replication Fork
Centrosome
Nuclear Speck
Site Of Double-strand Break
Extracellular Exosome
Site Of DNA Damage
Nucleoplasm
Nucleolus
Cytoplasm
Cytosol
Molecular Function
DNA Binding
Damaged DNA Binding
Protein Binding
Enzyme Binding
Histone Binding
Protein Heterodimerization Activity
Magnesium Ion Binding
Protein Kinase Activity
Protein Serine/threonine Kinase Activity
Ribosomal Protein S6 Kinase Activity
Protein Binding
ATP Binding
Protein Kinase Binding
Cysteine-type Endopeptidase Inhibitor Activity Involved In Apoptotic Process
Protein Serine Kinase Activity
Protein Threonine Kinase Activity
Biological Process
DNA Damage Checkpoint
Double-strand Break Repair Via Homologous Recombination
Double-strand Break Repair
Double-strand Break Repair Via Nonhomologous End Joining
Nucleosome Assembly
Chromatin Silencing
Cellular Response To DNA Damage Stimulus
Spermatogenesis
Response To Ionizing Radiation
Viral Process
Cerebral Cortex Development
Positive Regulation Of DNA Repair
Meiotic Cell Cycle
Cellular Response To Gamma Radiation
Cellular Senescence
Skeletal System Development
Toll-like Receptor Signaling Pathway
Apoptotic Process
Cell Cycle
Signal Transduction
Central Nervous System Development
Peptidyl-serine Phosphorylation
Positive Regulation Of Cell Growth
Response To Lipopolysaccharide
Intracellular Signal Transduction
Negative Regulation Of Apoptotic Process
Negative Regulation Of Cysteine-type Endopeptidase Activity Involved In Apoptotic Process
Regulation Of Translation In Response To Stress
Regulation Of DNA-templated Transcription In Response To Stress
Positive Regulation Of Cell Differentiation
Positive Regulation Of Transcription By RNA Polymerase II
Pathways
Recognition and association of DNA glycosylase with site containing an affected pyrimidine
Cleavage of the damaged pyrimidine
Recognition and association of DNA glycosylase with site containing an affected purine
Recognition and association of DNA glycosylase with site containing an affected purine
Cleavage of the damaged purine
Cleavage of the damaged purine
Meiotic synapsis
Packaging Of Telomere Ends
Pre-NOTCH Transcription and Translation
Formation of the beta-catenin:TCF transactivating complex
Formation of the beta-catenin:TCF transactivating complex
PRC2 methylates histones and DNA
Condensation of Prophase Chromosomes
Oxidative Stress Induced Senescence
Senescence-Associated Secretory Phenotype (SASP)
DNA Damage/Telomere Stress Induced Senescence
RMTs methylate histone arginines
SIRT1 negatively regulates rRNA expression
ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression
NoRC negatively regulates rRNA expression
NoRC negatively regulates rRNA expression
B-WICH complex positively regulates rRNA expression
DNA methylation
Transcriptional regulation by small RNAs
Activation of anterior HOX genes in hindbrain development during early embryogenesis
Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3
Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks
Nonhomologous End-Joining (NHEJ)
Processing of DNA double-strand break ends
Deposition of new CENPA-containing nucleosomes at the centromere
G2/M DNA damage checkpoint
RNA Polymerase I Promoter Opening
RNA Polymerase I Promoter Escape
RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function
RUNX1 regulates transcription of genes involved in differentiation of HSCs
Estrogen-dependent gene expression
Meiotic recombination
Transcriptional regulation of granulopoiesis
Inhibition of DNA recombination at telomere
Amyloid fiber formation
ERK/MAPK targets
CREB phosphorylation
Senescence-Associated Secretory Phenotype (SASP)
Senescence-Associated Secretory Phenotype (SASP)
Recycling pathway of L1
CREB1 phosphorylation through NMDA receptor-mediated activation of RAS signaling
RSK activation
RSK activation
Gastrin-CREB signalling pathway via PKC and MAPK
Drugs
Acetylsalicylic acid
Fostamatinib
Diseases
Non-syndromic X-linked mental retardation
Coffin-Lowry syndrome (CLS)
GWAS
Refractive error (
32231278
)
Interacting Genes
46 interacting genes:
A2M
ACTB
ALG9
ATM
ATR
BARD1
BMI1
BRCA1
BRCA2
BRD1
CALM1
COPG1
DDX21
DHX9
EYA1
HUWE1
KAT5
MASP1
MDC1
MRE11
NBN
NCL
NGFR
OTUB1
PAXIP1
PBK
PPP1CA
PRKDC
PTPA
QARS1
RNF168
RNF8
RPS6KA3
SMARCA4
SSRP1
SUPT16H
SUPT5H
TAF1C
TAF5L
TERF2
TIAM2
TOPORS
TP53BP1
TRAF6
TSSK6
WRN
40 interacting genes:
ATP5PF
BAD
BARX1
CREB1
CREBBP
CTNND1
EIF3C
ESR1
FBXO7
FGF2
FGFR1
FGFR3
FYN
GRIN1
GRIN2D
H2AX
H3-4
H3C1
HMGN1
HMGN2
HTR2A
ILKAP
KRT18
MAGI1
MAPK1
MAPK3
MAPT
MASP1
NEDD4
NFKBIA
NR4A1
PDPK1
PEA15
SHANK1
SMS
SRC
STK11
SUMO2
TP53
YBX1
Entrez ID
3014
6197
HPRD ID
03465
02092
Ensembl ID
ENSG00000188486
ENSG00000177189
Uniprot IDs
P16104
A0A384MDW3
B1AXG1
B4DG22
B7ZB17
P51812
PDB IDs
1YDP
2AZM
2D31
2DYP
3SHV
3SQD
3SZM
3U3Z
6K1I
6K1J
6K1K
4D9T
4D9U
4JG6
4JG7
4JG8
4NUS
4NW5
4NW6
5D9K
5D9L
Enriched GO Terms of Interacting Partners
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