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PCNA and MSH2
Data Source:
HPRD
(in vitro)
PCNA
MSH2
Description
proliferating cell nuclear antigen
mutS homolog 2
Image
GO Annotations
Cellular Component
Cyclin-dependent Protein Kinase Holoenzyme Complex
Chromosome, Telomeric Region
Chromatin
Nucleus
Nuclear Lamina
Nucleoplasm
Replication Fork
Centrosome
Nuclear Body
Replisome
Nuclear Replication Fork
PCNA Complex
Extracellular Exosome
PCNA-p21 Complex
Chromosome, Telomeric Region
Nucleus
Nucleoplasm
Membrane
Mismatch Repair Complex
MutSalpha Complex
MutSbeta Complex
Molecular Function
Purine-specific Mismatch Base Pair DNA N-glycosylase Activity
Chromatin Binding
Damaged DNA Binding
Protein Binding
Protein C-terminus Binding
Enzyme Binding
Estrogen Receptor Binding
DNA Polymerase Processivity Factor Activity
Receptor Tyrosine Kinase Binding
Dinucleotide Insertion Or Deletion Binding
MutLalpha Complex Binding
Histone Acetyltransferase Binding
Identical Protein Binding
Protein-containing Complex Binding
DNA Polymerase Binding
Magnesium Ion Binding
Four-way Junction DNA Binding
Double-strand/single-strand DNA Junction Binding
DNA Binding
Chromatin Binding
Double-stranded DNA Binding
Single-stranded DNA Binding
Protein Binding
ATP Binding
Protein C-terminus Binding
DNA-dependent ATPase Activity
ATPase Activity
Centromeric DNA Binding
Enzyme Binding
Protein Kinase Binding
Mismatched DNA Binding
Guanine/thymine Mispair Binding
Dinucleotide Insertion Or Deletion Binding
Single Guanine Insertion Binding
Single Thymine Insertion Binding
Dinucleotide Repeat Insertion Binding
Oxidized Purine DNA Binding
MutLalpha Complex Binding
Protein Homodimerization Activity
ADP Binding
Biological Process
Regulation Of Transcription Involved In G1/S Transition Of Mitotic Cell Cycle
Negative Regulation Of Transcription By RNA Polymerase II
Telomere Maintenance
Leading Strand Elongation
Transcription-coupled Nucleotide-excision Repair
Base-excision Repair, Gap-filling
Nucleotide-excision Repair, DNA Incision, 5'-to Lesion
Nucleotide-excision Repair, DNA Gap Filling
Mismatch Repair
DNA Damage Response, Signal Transduction By P53 Class Mediator Resulting In Cell Cycle Arrest
Heart Development
Viral Process
Protein Ubiquitination
Translesion Synthesis
Epithelial Cell Differentiation
Replication Fork Processing
Positive Regulation Of Deoxyribonuclease Activity
Telomere Maintenance Via Semi-conservative Replication
Response To Estradiol
Nucleotide-excision Repair, DNA Incision
Cellular Response To UV
Error-prone Translesion Synthesis
DNA Damage Response, Detection Of DNA Damage
Estrous Cycle
Positive Regulation Of DNA Repair
Positive Regulation Of DNA Replication
Response To Cadmium Ion
Cellular Response To Hydrogen Peroxide
Error-free Translesion Synthesis
Cellular Response To Xenobiotic Stimulus
Response To Dexamethasone
Liver Regeneration
Positive Regulation Of DNA-directed DNA Polymerase Activity
Response To L-glutamate
Mitotic Telomere Maintenance Via Semi-conservative Replication
In Utero Embryonic Development
Somatic Recombination Of Immunoglobulin Genes Involved In Immune Response
Oxidative Phosphorylation
DNA Repair
Mismatch Repair
Postreplication Repair
Double-strand Break Repair
DNA Recombination
Cell Cycle Arrest
Germ Cell Development
Determination Of Adult Lifespan
Male Gonad Development
Response To X-ray
Response To UV-B
Somatic Hypermutation Of Immunoglobulin Genes
Somatic Recombination Of Immunoglobulin Gene Segments
B Cell Mediated Immunity
B Cell Differentiation
Intra-S DNA Damage Checkpoint
Intrinsic Apoptotic Signaling Pathway In Response To DNA Damage By P53 Class Mediator
Negative Regulation Of Neuron Apoptotic Process
Maintenance Of DNA Repeat Elements
Isotype Switching
Negative Regulation Of DNA Recombination
Positive Regulation Of Isotype Switching To IgA Isotypes
Positive Regulation Of Isotype Switching To IgG Isotypes
Positive Regulation Of Helicase Activity
Protein Localization To Chromatin
Pathways
Translesion synthesis by REV1
Recognition of DNA damage by PCNA-containing replication complex
Translesion Synthesis by POLH
Transcription of E2F targets under negative control by DREAM complex
Polymerase switching on the C-strand of the telomere
Processive synthesis on the C-strand of the telomere
Telomere C-strand (Lagging Strand) Synthesis
Removal of the Flap Intermediate from the C-strand
SUMOylation of DNA replication proteins
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha)
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta)
PCNA-Dependent Long Patch Base Excision Repair
Translesion synthesis by POLK
Translesion synthesis by POLI
Termination of translesion DNA synthesis
HDR through Homologous Recombination (HRR)
Gap-filling DNA repair synthesis and ligation in GG-NER
Dual Incision in GG-NER
Dual incision in TC-NER
Gap-filling DNA repair synthesis and ligation in TC-NER
TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest
Polymerase switching
Removal of the Flap Intermediate
Processive synthesis on the lagging strand
G1/S-Specific Transcription
E3 ubiquitin ligases ubiquitinate target proteins
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha)
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta)
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta)
Defective Mismatch Repair Associated With MSH3
Defective Mismatch Repair Associated With MSH2
Defective Mismatch Repair Associated With MSH6
TP53 Regulates Transcription of DNA Repair Genes
Drugs
Liothyronine
Acetylsalicylic acid
Diseases
Colorectal cancer
Mismatch repair deficiency, including: Hereditary non-polyposis colorectal cancer (HNPCC); Lynch syndrome; Muir-Torre syndrome; Turcot syndrome
Ovarian cancer
GWAS
Electroencephalogram traits (
25387704
)
Post bronchodilator FEV1/FVC ratio (
26634245
)
Interacting Genes
139 interacting genes:
ALDOA
APEX1
APEX2
ATAD5
BAZ1B
CBX1
CCNB1
CCND1
CCND3
CCNO
CDC25C
CDC6
CDK1
CDK2
CDK5
CDK6
CDKN1A
CDKN1C
CDKN2A
CDT1
CHAF1A
CHTF18
CHTF8
CMTM5
CREBBP
DHX9
DNMT1
DNTT
DNTTIP2
DSCC1
DTL
EGFR
ENO1
EP300
ERCC5
ERCC6
ERRFI1
ESCO2
EXO1
FAN1
FANCD2
FANCL
FEN1
GADD45A
GADD45B
GADD45G
GAPDH
GCK
GPI
HDAC1
HUS1
HUWE1
IGF1R
ING1
KCTD13
KMT5A
LDHA
LIG1
LMNA
MCL1
MGMT
MLH1
MSH2
MSH3
MSH6
MUTYH
MYBBP1A
NMRAL1
NSD2
NTHL1
NUTF2
PARP1
PARP10
PARPBP
PCLAF
PFKM
PGAM1
PGK1
PKLR
PMS2
POLB
POLD1
POLD2
POLD3
POLD4
POLDIP2
POLE
POLH
POLI
POLK
POLL
POLM
PPP1CA
PRKDC
PTEN
PTMA
RAD18
RAD9A
RBBP8
RFC1
RFC2
RFC3
RFC4
RFC5
RFWD3
RNF8
RPA1
SDE2
SEC23IP
SIVA1
SLC30A8
SMARCAD1
SPG21
SUB1
SUMO1
TCOF1
TDG
TIRAP
TMEM218
TPI1
TRIM28
UBB
UBE2A
UBE2B
UBE2D3
UHRF1
UNG
USP1
USP2
USP4
WDR48
WRN
WRNIP1
XPA
XRCC1
XRCC5
XRCC6
YBX1
ZBTB1
48 interacting genes:
AKT1
ANXA7
APPBP2
ATR
BARD1
BRCA1
CCDC180
CDC14B
CDC42
CDKN1A
CHEK2
CREBBP
DVL1
EPHA2
ESR1
ESR2
EXO1
FBP1
FBP2
FGFR4
GALNT12
GRB7
HDAC6
HRAS
HUS1
LEF1
MAX
MSH3
MSH6
MYC
PCNA
PPP3R2
RAD1
RAD9A
RPA4
RPP14
SMAD1
SMC1A
SMN1
STX17
SUMO2
TDRD7
TK1
TREX1
TRIM29
USP10
XPA
ZNF510
Entrez ID
5111
4436
HPRD ID
01456
00389
Ensembl ID
ENSG00000132646
ENSG00000095002
Uniprot IDs
P12004
A0A2R8Y6P0
P43246
PDB IDs
1AXC
1U76
1U7B
1UL1
1VYJ
1VYM
1W60
2ZVK
2ZVL
2ZVM
3JA9
3P87
3TBL
3VKX
3WGW
4D2G
4RJF
4ZTD
5E0T
5E0U
5E0V
5IY4
5MAV
5MLO
5MLW
5MOM
5YCO
5YD8
6CBI
6EHT
6FCM
6FCN
6GIS
6GWS
6HVO
6K3A
6QC0
6QCG
6S1M
6S1N
6S1O
6TNY
6TNZ
6VVO
2O8B
2O8C
2O8D
2O8E
2O8F
3THW
3THX
3THY
3THZ
Enriched GO Terms of Interacting Partners
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