DPM2 and DPM1

Number of citations of the paper that reports this interaction (PMID 10835346)
25

Data Source:
HPRD (in vivo)

		DPM2	DPM1
Gene Name		dolichyl-phosphate mannosyltransferase polypeptide 2, regulatory subunit	dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit
Image		No pdb structure	No pdb structure
Gene Ontology Annotations	Cellular Component	Glycosylphosphatidylinositol-N-acetylglucosaminyltransferase (GPI-GnT) Complex Endoplasmic Reticulum Membrane Integral Component Of Endoplasmic Reticulum Membrane Dolichol-phosphate-mannose Synthase Complex Perinuclear Region Of Cytoplasm	Nucleus Endoplasmic Reticulum Endoplasmic Reticulum Membrane Membrane Dolichol-phosphate-mannose Synthase Complex
	Molecular Function	Dolichyl-phosphate Beta-D-mannosyltransferase Activity Protein Binding Enzyme Regulator Activity	Dolichyl-phosphate-mannose-protein Mannosyltransferase Activity Dolichyl-phosphate Beta-D-mannosyltransferase Activity Protein Binding Mannose Binding Alcohol Binding
	Biological Process	Dolichol-linked Oligosaccharide Biosynthetic Process C-terminal Protein Lipidation GPI Anchor Biosynthetic Process Preassembly Of GPI Anchor In ER Membrane Protein N-linked Glycosylation Via Asparagine Dolichol Metabolic Process Regulation Of Protein Stability Protein O-linked Mannosylation Post-translational Protein Modification Cellular Protein Metabolic Process Regulation Of Catalytic Activity	Dolichol-linked Oligosaccharide Biosynthetic Process C-terminal Protein Lipidation GPI Anchor Biosynthetic Process Protein N-linked Glycosylation Via Asparagine Dolichol Metabolic Process GDP-mannose Metabolic Process Protein Mannosylation Protein O-linked Mannosylation Post-translational Protein Modification Cellular Protein Metabolic Process
Pathways		Diseases of glycosylation Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Defective ALG1 causes ALG1-CDG (CDG-1k) Defective MGAT2 causes MGAT2-CDG (CDG-2a) Defective MOGS causes MOGS-CDG (CDG-2b) Synthesis of glycosylphosphatidylinositol (GPI) Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Defective ALG9 causes ALG9-CDG (CDG-1l) Synthesis of dolichyl-phosphate mannose Defective MAN1B1 causes MRT15 Defective ALG11 causes ALG11-CDG (CDG-1p) Defective ALG2 causes ALG2-CDG (CDG-1i) Defective ALG3 causes ALG3-CDG (CDG-1d) Post-translational protein modification Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 Synthesis of substrates in N-glycan biosythesis Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Post-translational modification: synthesis of GPI-anchored proteins Defective ALG6 causes ALG6-CDG (CDG-1c) Defective RFT1 causes RFT1-CDG (CDG-1n) Asparagine N-linked glycosylation Defective ALG8 causes ALG8-CDG (CDG-1h) Defective MPDU1 causes MPDU1-CDG (CDG-1f) Defective ALG12 causes ALG12-CDG (CDG-1g) Synthesis of dolichyl-phosphate mannose Diseases associated with N-glycosylation of proteins	Diseases of glycosylation Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Defective ALG1 causes ALG1-CDG (CDG-1k) Defective MGAT2 causes MGAT2-CDG (CDG-2a) Defective MOGS causes MOGS-CDG (CDG-2b) Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Defective ALG9 causes ALG9-CDG (CDG-1l) Synthesis of dolichyl-phosphate mannose Defective MAN1B1 causes MRT15 Defective ALG11 causes ALG11-CDG (CDG-1p) Defective ALG2 causes ALG2-CDG (CDG-1i) Defective ALG3 causes ALG3-CDG (CDG-1d) Post-translational protein modification Defective DPAGT1 causes DPAGT1-CDG (CDG-1j) and CMSTA2 Synthesis of substrates in N-glycan biosythesis Defective B4GALT1 causes B4GALT1-CDG (CDG-2d) Post-translational modification: synthesis of GPI-anchored proteins Defective ALG6 causes ALG6-CDG (CDG-1c) Defective RFT1 causes RFT1-CDG (CDG-1n) Asparagine N-linked glycosylation Defective ALG8 causes ALG8-CDG (CDG-1h) Defective MPDU1 causes MPDU1-CDG (CDG-1f) Defective ALG12 causes ALG12-CDG (CDG-1g) Synthesis of dolichyl-phosphate mannose Diseases associated with N-glycosylation of proteins
Drugs
Diseases
GWAS
Protein-Protein Interactions		6 interactors: DPM1 DPM3 HLA-DMB PIGA PIGC VKORC1	5 interactors: DPM2 DPM3 MTNR1A TDO2 ZBTB16
Entrez ID		8818	8813
HPRD ID		16028	04613
Ensembl ID		ENSG00000136908	ENSG00000000419
Uniprot IDs		O94777	O60762 Q5QPK2
PDB IDs
Enriched GO Terms of Interacting Partners?		C-terminal Protein Lipidation Post-translational Protein Modification GPI Anchor Biosynthetic Process GPI Anchor Metabolic Process Glycolipid Biosynthetic Process Protein Lipidation Lipoprotein Biosynthetic Process Phosphatidylinositol Biosynthetic Process Glycolipid Metabolic Process Lipoprotein Metabolic Process Glycerophospholipid Biosynthetic Process Phosphatidylinositol Metabolic Process Membrane Lipid Metabolic Process Phospholipid Biosynthetic Process Glycerophospholipid Metabolic Process Glycerolipid Metabolic Process Phospholipid Metabolic Process Protein O-linked Mannosylation Lipid Biosynthetic Process Preassembly Of GPI Anchor In ER Membrane Protein Mannosylation Mannosylation Cellular Lipid Metabolic Process Organophosphate Metabolic Process Dolichol-linked Oligosaccharide Biosynthetic Process Lipid Metabolic Process Protein O-linked Glycosylation Cellular Protein Modification Process Positive Regulation Of T Cell Activation Via T Cell Receptor Contact With Antigen Bound To MHC Molecule On Antigen Presenting Cell Protein N-linked Glycosylation Via Asparagine Protein N-linked Glycosylation Dolichol Metabolic Process Cellular Protein Metabolic Process Peptidyl-amino Acid Modification Protein C-linked Glycosylation Via 2'-alpha-mannosyl-L-tryptophan Peptide Antigen Assembly With MHC Class II Protein Complex MHC Class II Protein Complex Assembly Vitamin K Metabolic Process Phosphate-containing Compound Metabolic Process Macromolecule Glycosylation Protein Glycosylation Glycosylation Protein Metabolic Process Peptidyl-glutamic Acid Carboxylation Glycoprotein Biosynthetic Process Glycoprotein Metabolic Process Cellular Macromolecule Biosynthetic Process Macromolecule Biosynthetic Process GDP-mannose Metabolic Process Quinone Metabolic Process	Protein O-linked Mannosylation Protein Mannosylation C-terminal Protein Lipidation Mannosylation Dolichol-linked Oligosaccharide Biosynthetic Process GPI Anchor Biosynthetic Process GPI Anchor Metabolic Process Glycolipid Biosynthetic Process Protein O-linked Glycosylation Protein N-linked Glycosylation Via Asparagine Protein Lipidation Lipoprotein Biosynthetic Process Protein N-linked Glycosylation Phosphatidylinositol Biosynthetic Process Glycolipid Metabolic Process Regulation Of Protein Stability Tryptophan Catabolic Process To Acetyl-CoA Lipoprotein Metabolic Process Glycerophospholipid Biosynthetic Process Post-translational Protein Modification Dolichol Metabolic Process Phosphatidylinositol Metabolic Process Membrane Lipid Metabolic Process Positive Regulation Of NK T Cell Differentiation Protein C-linked Glycosylation Via 2'-alpha-mannosyl-L-tryptophan Phospholipid Biosynthetic Process Male Germ-line Stem Cell Asymmetric Division Glycerophospholipid Metabolic Process Macromolecule Glycosylation Protein Glycosylation Tryptophan Catabolic Process To Kynurenine Glycosylation Kynurenine Metabolic Process Glycerolipid Metabolic Process Phospholipid Metabolic Process Glycoprotein Biosynthetic Process Preassembly Of GPI Anchor In ER Membrane Glycoprotein Metabolic Process Tryptophan Catabolic Process Posttranscriptional Regulation Of Gene Expression Positive Regulation Of CGMP Biosynthetic Process Tryptophan Metabolic Process Positive Regulation Of CGMP Metabolic Process Acetyl-CoA Metabolic Process Regulation Of CGMP Biosynthetic Process Lipid Biosynthetic Process Positive Regulation Of Chondrocyte Differentiation Regulation Of CGMP Metabolic Process Mating Behavior Stem Cell Division
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