ITGA9 and PXN

Number of citations of the paper that reports this interaction (PubMedID 11598204)
34

Data Source:
HPRD (in vitro, in vivo)

		ITGA9	PXN
Description		integrin subunit alpha 9	paxillin
Image		No pdb structure
GO Annotations	Cellular Component	Plasma Membrane Integrin Complex Basal Plasma Membrane Integrin Alpha9-beta1 Complex	Stress Fiber Cytosol Microtubule Associated Complex Plasma Membrane Cell-cell Junction Focal Adhesion Cell Cortex Lamellipodium
	Molecular Function	Collagen Binding Laminin Binding Metal Ion Binding	Transcription Coregulator Activity Integrin Binding Protein Binding Beta-catenin Binding Vinculin Binding Protein Kinase Binding Protein Phosphatase Binding Ubiquitin Protein Ligase Binding Neuropilin Binding Metal Ion Binding
	Biological Process	Cell Adhesion Integrin-mediated Signaling Pathway Extracellular Matrix Organization Neutrophil Chemotaxis Wound Healing	Muscle Contraction Cell Adhesion Signal Transduction Signal Complex Assembly Transforming Growth Factor Beta Receptor Signaling Pathway Substrate Adhesion-dependent Cell Spreading Cellular Response To Reactive Oxygen Species Endothelial Cell Migration Vascular Endothelial Growth Factor Receptor Signaling Pathway Positive Regulation Of Stress Fiber Assembly Growth Hormone Receptor Signaling Pathway Regulation Of Nucleic Acid-templated Transcription
Pathways		Integrin cell surface interactions Integrin cell surface interactions ECM proteoglycans Signal transduction by L1	GAB1 signalosome VEGFA-VEGFR2 Pathway Smooth Muscle Contraction Localization of the PINCH-ILK-PARVIN complex to focal adhesions Regulation of cytoskeletal remodeling and cell spreading by IPP complex components PTK6 Regulates RHO GTPases, RAS GTPase and MAP kinases
Drugs
Diseases		Congenital muscular dystrophies (CMD/MDC), including: Merosin-deficient CMD (MDC1A); Ullrich CMD (UCMD); Integrin alpha7-deficient CMD; CMD with joint hyperlaxity (CMDH); CMD with epidermolysis bullosa; Walker-Warburg syndrome (WWS); Muscle-eye-brain disease (MEB); Fukuyama CMD (FCMD); CMD with muscle hypertrophy (MDC1C); CMD with severe intellectual impairment and abnormal glycosylation (MDC1D); Rigid spine syndrome (RSS); LMNA-deficient CMD; CMD with respiratory failure and muscle hypertrophy (MDC1B); Bethlem myopathy
GWAS		Amyotrophic lateral sclerosis (sporadic) ( 24529757) Heel bone mineral density ( 30598549) Mortality in sepsis ( 27639821) Nasopharyngeal carcinoma ( 19478819) Phospholipid levels (plasma) ( 22359512) PR interval ( 23139255) Pulse pressure ( 30224653 30578418) Response to antidepressants (symptom improvement) ( 29160301) Systolic blood pressure ( 30578418)	Bipolar disorder ( 31043756) Platelet count ( 29403010)
Interacting Genes		6 interacting genes: GPX1 ITGB1 PXN SAT1 SPP1 VEGFD	78 interacting genes: ABL1 AHCY AR ARHGEF7 ASAP1 ASAP2 BCAR1 BCL2 CASP3 CEACAM1 CLTC CREB3L2 CRK CRKL CSK DGUOK EPHB1 FYN GART GIT1 GIT2 GRB2 GSK3A GSK3B GSN HDAC6 ILK IMPDH2 ITGA4 ITGA6 ITGA9 ITGAV ITGB1 ITGB3 LCK LIMK1 MAPK1 MAPK3 MAPK8 MATK NCK1 NEDD9 NF2 PABPC1 PAK1 PAK3 PARVA PDPK1 PKD1 POLR1D PPP2CA PPP2R5C PTEN PTK2 PTK2B PTPN11 PTPN12 PTPRH RASA1 REPS2 RHOU RNF5 SCARB1 SDC4 SELE SORBS1 SRC SYK TGM2 TLN1 TRIM15 TRIP6 TUBA1B TUBA3C TUBA8 TUBG1 TUBG2 VCL
Entrez ID		3680	5829
HPRD ID		04910	03937
Ensembl ID		ENSG00000144668	ENSG00000089159
Uniprot IDs		Q13797 Q8N6H6	A0A140VJQ8 P49023
PDB IDs			1KKY 1KL0 1OW6 1OW7 1OW8 2K2R 2O9V 2VZD 2VZG 2VZI 3GM1 3PY7 3RQE 3RQF 3RQG 3U3F 4EDN 4R32 4XGZ 4XH2 5UWH 6IUI 6U4M 6U4N
Enriched GO Terms of Interacting Partners?
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