SFTPC and PQBP1

Number of citations of the paper that reports this interaction (PubMedID 19366705)
56

Data Source:
BioGRID (pull down)

		SFTPC	PQBP1
Description		surfactant protein C	polyglutamine binding protein 1
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GO Annotations	Cellular Component	Extracellular Region Extracellular Space Endoplasmic Reticulum Membrane Lamellar Body Clathrin-coated Endocytic Vesicle Alveolar Lamellar Body Multivesicular Body Lumen	Nucleus Nucleoplasm Cytoplasm Cytosol Cilium Cytoplasmic Stress Granule Microtubule Cytoskeleton Nuclear Body Nuclear Speck Ciliary Basal Body Neuronal Ribonucleoprotein Granule Plasma Membrane Bounded Cell Projection
	Molecular Function	Protein Binding Identical Protein Binding	DNA Binding Double-stranded DNA Binding Transcription Coactivator Activity Protein Binding Ribonucleoprotein Complex Binding
	Biological Process	Respiratory Gaseous Exchange By Respiratory System	Alternative MRNA Splicing, Via Spliceosome Activation Of Innate Immune Response Positive Regulation Of Defense Response To Virus By Host Immune System Process Regulation Of DNA-templated Transcription MRNA Processing RNA Splicing Neuron Projection Development Positive Regulation Of Type I Interferon Production Regulation Of RNA Splicing Innate Immune Response Positive Regulation Of DNA-templated Transcription Regulation Of Dendrite Morphogenesis Defense Response To Virus Cellular Response To Exogenous DsRNA
Pathways		Surfactant metabolism Defective pro-SFTPC causes SMDP2 and RDS Defective CSF2RB causes SMDP5 Defective CSF2RA causes SMDP4	mRNA Splicing - Major Pathway
Drugs
Diseases		Pulmonary surfactant metabolism dysfunction (SMDP)	Non-syndromic X-linked mental retardation Syndromic X-linked mental retardation with epilepsy or seizures, including: West syndrome (WS); Partington syndrome (PRTS); Proud syndrome (ACCAG); XMR and epilepsy (XMRE); MRXHF1; XMR OPHN1-related (MRXSO) ; XELBD; XMR, Christianson type (MRXSC); Creatine deficiency syndrome (XL-CDS); Renpenning syndrome (RENS1); Epilepsy and mental retardation limited to females (EFMR); Periventricular nodular heterotopia (PVNH); Hydrocephalus (XLH); XMR, JARID1C related (MRXSJ); Boerjeson-Forssman syndrome (BFLS); CK syndrome (CKS)
GWAS		Coronary artery disease ( 29212778) Hypertriglyceridemia ( 23505323)
Interacting Genes		35 interacting genes: BSCL2 CD200R1 CD79A CLDN5 CPLX4 CREB3 CXCL9 FAM209A FNDC9 GJA8 GOLM1 GPR152 GPX8 HPN ICAM3 IFNGR2 KLRC1 LMNA LSMEM2 MUC1 NEDD4 PDZK1IP1 PQBP1 SEC22A SEC61G SIGLEC9 SMIM3 SYNE4 TMEM106C TMEM139 TMEM30B TMEM79 TMPRSS2 WWP1 WWP2	27 interacting genes: APBB1 APP AQR ATXN1 CEBPA CLTB CPSF7 EEF1A1 ERG28 ESR1 GOLGA2 HNRNPH2 LNX1 LRIF1 LZTS2 MAPRE1 MED31 POLR2A POU3F2 RAB8A RBM22 RCVRN SFTPC TLX3 TXNL4A WBP11 WDR77
Entrez ID		6440	10084
HPRD ID		01520	02354
Ensembl ID		ENSG00000168484	ENSG00000102103
Uniprot IDs		A0A0S2Z4Q0 E5RI64 P11686	A0A0S2Z4V5 O60828
PDB IDs		2YAD 8OVI 8OX2	4BWQ 4BWS 4CDO
Enriched GO Terms of Interacting Partners?		Membrane Negative Regulation Of Potassium Ion Export Across Plasma Membrane	Nucleoplasm Positive Regulation Of RNA Splicing
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