HUS1 and NEIL1

Number of citations of the paper that reports this interaction (PubMedID 17395641)
65

Data Source:
BioGRID (far western blotting)

		HUS1	NEIL1
Description		HUS1 checkpoint clamp component	nei like DNA glycosylase 1
Image
GO Annotations	Cellular Component	Nucleus Nucleoplasm Nucleolus Cytoplasm Cytosol Checkpoint Clamp Complex Site Of Double-strand Break	Nucleus Nucleoplasm Chromosome Cytoplasm Centrosome Cytosol Cytoskeleton
	Molecular Function	Protein Binding	Nucleic Acid Binding DNA Binding Damaged DNA Binding Catalytic Activity DNA-(apurinic Or Apyrimidinic Site) Endonuclease Activity Protein Binding Zinc Ion Binding Hydrolase Activity Hydrolase Activity, Acting On Glycosyl Bonds Hydrolase Activity, Hydrolyzing N-glycosyl Compounds Lyase Activity DNA N-glycosylase Activity Class I DNA-(apurinic Or Apyrimidinic Site) Endonuclease Activity
	Biological Process	DNA Damage Checkpoint Signaling Telomere Maintenance Double-strand Break Repair Via Homologous Recombination DNA Repair Nucleotide-excision Repair DNA Damage Response Response To Radiation Response To UV Embryo Development Ending In Birth Or Egg Hatching Mitotic Intra-S DNA Damage Checkpoint Signaling Mitotic DNA Replication Checkpoint Signaling Meiotic DNA Integrity Checkpoint Signaling Cellular Response To Ionizing Radiation	DNA Repair Base-excision Repair Base-excision Repair, Gap-filling DNA Damage Response Response To Oxidative Stress Negative Regulation Of Nuclease Activity Depyrimidination
Pathways		Activation of ATR in response to replication stress HDR through Single Strand Annealing (SSA) 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 Impaired BRCA2 binding to RAD51	Recognition and association of DNA glycosylase with site containing an affected pyrimidine Cleavage of the damaged pyrimidine APEX1-Independent Resolution of AP Sites via the Single Nucleotide Replacement Pathway Defective Base Excision Repair Associated with NEIL1
Drugs			Iron Copper Ferrous gluconate Ferrous succinate Ferrous ascorbate Ferrous fumarate Ferrous glycine sulfate
Diseases
GWAS		Gut microbiota alpha diversity (Shannon index) ( 33208821) Obstructive sleep apnea during REM sleep (apnea hypopnea index) ( 29077507)
Interacting Genes		28 interacting genes: C4orf46 CD200 DCUN1D5 DNAJC7 FEN1 GRIP1 HDAC1 HUS1B MSH2 MSH3 MSH6 NEIL1 NTAQ1 OGG1 PCNA POLB RAD1 RAD17 RAD9A RAD9B RHNO1 RPA1 RPA2 SDCBP SIRT6 TDG TOPBP1 YWHAQ	5 interacting genes: APP HUS1 POLB RAD1 XRCC1
Entrez ID		3364	79661
HPRD ID		04787	12314
Ensembl ID		ENSG00000136273	ENSG00000140398
Uniprot IDs		A4D2F2 O60921	Q96FI4
PDB IDs		3A1J 3G65 3GGR 6J8Y 7Z6H 8GNN 8WU8	1TDH 4NRV 5ITQ 5ITR 5ITT 5ITU 5ITX 5ITY 6LWA 6LWB 6LWC 6LWD 6LWF 6LWG 6LWH 6LWI 6LWJ 6LWK 6LWL 6LWM 6LWN 6LWO 6LWP 6LWQ 6LWR 7TMX 8FTJ
Enriched GO Terms of Interacting Partners?		DNA Repair Damaged DNA Binding DNA Damage Response DNA Metabolic Process Base-excision Repair Cellular Response To Stress DNA Damage Checkpoint Signaling Response To Radiation Signal Transduction In Response To DNA Damage DNA Recombination Nucleic Acid Metabolic Process Mismatch Repair Mitotic DNA Damage Checkpoint Signaling Mitotic DNA Integrity Checkpoint Signaling Checkpoint Clamp Complex Mitotic Intra-S DNA Damage Checkpoint Signaling Double-strand Break Repair Negative Regulation Of Cell Cycle Phase Transition DNA Replication Checkpoint Signaling Site Of Double-strand Break Oxidized Purine DNA Binding Nucleobase-containing Compound Metabolic Process Negative Regulation Of Cell Cycle Process Protein Localization To Site Of Double-strand Break Response To Stress Mismatched DNA Binding Chromosome Organization Response To Ionizing Radiation Negative Regulation Of Cell Cycle Single Guanine Insertion Binding Dinucleotide Insertion Or Deletion Binding Base-excision Repair, Gap-filling Nucleoplasm Chromosome, Telomeric Region Guanine/thymine Mispair Binding Intracellular Signal Transduction Chromatin-protein Adaptor Activity Protein Localization To Chromosome Regulation Of Cell Cycle Phase Transition Negative Regulation Of Mitotic Cell Cycle Macromolecule Metabolic Process Recombinational Repair Regulation Of Cell Cycle Process Maintenance Of DNA Repeat Elements MutLalpha Complex Binding Class I DNA-(apurinic Or Apyrimidinic Site) Endonuclease Activity Response To UV Nucleus Enzyme Binding Depyrimidination	Checkpoint Clamp Complex Damaged DNA Binding Meiotic Cell Cycle Checkpoint Signaling Response To Radiation DNA Repair Response To Ionizing Radiation Intracellular Signal Transduction DNA Metabolic Process Double-strand Break Repair DNA Damage Response DNA Recombination Base-excision Repair Double-strand Break Repair Via Nonhomologous End Joining Enzyme Binding Positive Regulation Of Neuron Apoptotic Process Amyloid-beta Complex Growth Cone Lamellipodium Regulation Of Response To Calcium Ion Amylin Binding Positive Regulation Of Toll Signaling Pathway Cellular Response To Ionizing Radiation Oxidized DNA Binding Positive Regulation Of JNK Cascade Macromolecule Metabolic Process Telomere Maintenance DNA Damage Checkpoint Signaling Acetylcholine Receptor Activator Activity PTB Domain Binding Collateral Sprouting In Absence Of Injury Regulation Of Protein Import Response To Stress Endosome To Plasma Membrane Transport Vesicle Positive Regulation Of Endothelin Production Growth Cone Filopodium Lipoprotein Particle Phospholipase D-activating G Protein-coupled Receptor Signaling Pathway Positive Regulation Of Protein Import Microglia Development Positive Regulation Of G Protein-coupled Receptor Internalization Cellular Response To Stress Telomere Organization Meiotic DNA Integrity Checkpoint Signaling Immunoglobulin Heavy Chain V-D-J Recombination Meiotic Recombination Checkpoint Signaling ADP-D-ribose Modification-dependent Protein Binding Telomeric DNA-containing Double Minutes Formation Negative Regulation Of Protein ADP-ribosylation Negative Regulation Of Protection From Non-homologous End Joining At Telomere Regulation Of JNK Cascade Signal Transduction In Response To DNA Damage
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