CD59 and C9

Number of citations of the paper that reports this interaction (PubMedID 1377690)
22

Data Source:
BioGRID (pull down, pull down)
HPRD (in vitro)

		CD59	C9
Description		CD59 molecule (CD59 blood group)	complement C9
Image
GO Annotations	Cellular Component	Golgi Membrane Extracellular Space Endoplasmic Reticulum Membrane Plasma Membrane Focal Adhesion Cell Surface ER To Golgi Transport Vesicle Membrane Membrane Transport Vesicle Anchored Component Of External Side Of Plasma Membrane Vesicle Endoplasmic Reticulum-Golgi Intermediate Compartment Membrane Specific Granule Membrane Extracellular Exosome Tertiary Granule Membrane	Extracellular Region Membrane Attack Complex Extracellular Space Plasma Membrane Other Organism Cell Membrane Extracellular Exosome Blood Microparticle
	Molecular Function	Complement Binding Protein Binding
	Biological Process	Negative Regulation Of Activation Of Membrane Attack Complex ER To Golgi Vesicle-mediated Transport Cell Surface Receptor Signaling Pathway Blood Coagulation Regulation Of Complement Activation Neutrophil Degranulation COPII Vesicle Coating Regulation Of Complement-dependent Cytotoxicity	Cell Killing Complement Activation, Alternative Pathway Complement Activation, Classical Pathway Cytolysis Regulation Of Complement Activation Protein Homooligomerization
Pathways		COPII-mediated vesicle transport Cargo concentration in the ER Neutrophil degranulation COPI-mediated anterograde transport Regulation of Complement cascade	Terminal pathway of complement Regulation of Complement cascade
Drugs			Copper
Diseases		Complement regulatory protein defects, including the following six diseases: C1 inhibitor deficiency (hereditary angioedema); C4 binding protein alpha deficiency; C4 binding protein beta deficiency; Factor I deficiency; Decay-accelerating factor (CD55) deficiency; CD59 deficiency	Late complement pathway defects, including the following seven diseases: C5 deficiency; C6 deficiency; C7 deficiency; C8 alpha-chain deficiency; C8 beta-chain deficiency; C8 gamma-chain deficiency; C9 deficiency
GWAS		Blood protein levels ( 30072576 29875488) Chronotype ( 30696823) Morning person ( 30696823)	Advanced age-related macular degeneration ( 26691988) Blood protein levels ( 30072576 29875488) Chronic kidney disease ( 20383146) Health literacy ( 31250787) Systemic lupus erythematosus ( 19838195)
Interacting Genes		13 interacting genes: C8A C9 CD2 CD8A CD9 EGFR GNAI3 NCR1 NCR3 SLC6A8 SMAD4 SRC WFS1	4 interacting genes: C8A CD59 CLU LAMTOR5
Entrez ID		966	735
HPRD ID		00117	00408
Ensembl ID		ENSG00000085063	ENSG00000113600
Uniprot IDs		P13987 Q6FHM9	P02748
PDB IDs		1CDQ 1CDR 1CDS 1ERG 1ERH 2J8B 2OFS 2UWR 2UX2 4BIK 5IMT 5IMY	5FMW 6DLW 6H03 6H04
Enriched GO Terms of Interacting Partners?
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