Homo sapiens Protein: ANG
Summary
InnateDB Protein IDBP-234138.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol ANG
Protein Name angiogenin, ribonuclease, RNase A family, 5
Synonyms ALS9; HEL168; RAA1; RNASE4; RNASE5;
Species Homo sapiens
Ensembl Protein ENSP00000381077
InnateDB Gene IDBG-234136 (ANG)
Protein Structure
UniProt Annotation
Function Binds to actin on the surface of endothelial cells; once bound, angiogenin is endocytosed and translocated to the nucleus. Stimulates ribosomal RNA synthesis including that containing the initiation site sequences of 45S rRNA. Cleaves tRNA within anticodon loops to produce tRNA-derived stress-induced fragments (tiRNAs) which inhibit protein synthesis and triggers the assembly of stress granules (SGs). Angiogenin induces vascularization of normal and malignant tissues. Angiogenic activity is regulated by interaction with RNH1 in vivo. {ECO:0000269PubMed:12051708, ECO:0000269PubMed:1400510, ECO:0000269PubMed:19354288, ECO:0000269PubMed:21855800}.
Subcellular Localization Secreted, extracellular space, extracellular matrix, basement membrane. Nucleus, nucleolus. Note=Rapidly endocytosed by target cells and translocated to the nucleus where it accumulates in the nucleolus and binds to DNA.
Disease Associations Amyotrophic lateral sclerosis 9 (ALS9) [MIM:611895]: A neurodegenerative disorder affecting upper motor neurons in the brain and lower motor neurons in the brain stem and spinal cord, resulting in fatal paralysis. Sensory abnormalities are absent. The pathologic hallmarks of the disease include pallor of the corticospinal tract due to loss of motor neurons, presence of ubiquitin-positive inclusions within surviving motor neurons, and deposition of pathologic aggregates. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5- 10% of the cases. {ECO:0000269PubMed:15557516, ECO:0000269PubMed:16501576, ECO:0000269PubMed:17703939, ECO:0000269PubMed:17886298, ECO:0000269PubMed:18087731}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.
Tissue Specificity Expressed predominantly in the liver. Also detected in endothelial cells and spinal cord neurons. {ECO:0000269PubMed:17886298, ECO:0000269PubMed:2440105}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
Experimentally validated
Total 11 [view]
Protein-Protein 10 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003779 actin binding
GO:0004519 endonuclease activity
GO:0004540 ribonuclease activity
GO:0005102 receptor binding
GO:0005507 copper ion binding
GO:0005515 protein binding
GO:0008201 heparin binding
GO:0016892 endoribonuclease activity, producing 3'-phosphomonoesters
GO:0019843 rRNA binding
GO:0042277 peptide binding
Biological Process
GO:0001525 angiogenesis
GO:0001541 ovarian follicle development
GO:0001556 oocyte maturation
GO:0001666 response to hypoxia
GO:0001890 placenta development
GO:0001938 positive regulation of endothelial cell proliferation
GO:0006651 diacylglycerol biosynthetic process
GO:0007154 cell communication
GO:0007202 activation of phospholipase C activity
GO:0008219 cell death
GO:0009303 rRNA transcription
GO:0009725 response to hormone
GO:0016477 cell migration
GO:0017148 negative regulation of translation
GO:0030041 actin filament polymerization
GO:0032148 activation of protein kinase B activity
GO:0032431 activation of phospholipase A2 activity
GO:0042327 positive regulation of phosphorylation
GO:0042592 homeostatic process
GO:0048662 negative regulation of smooth muscle cell proliferation
GO:0050714 positive regulation of protein secretion
GO:0090305 nucleic acid phosphodiester bond hydrolysis
GO:0090501 RNA phosphodiester bond hydrolysis
GO:0090502 RNA phosphodiester bond hydrolysis, endonucleolytic
Cellular Component
GO:0005605 basal lamina
GO:0005615 extracellular space
GO:0005634 nucleus
GO:0005730 nucleolus
GO:0030426 growth cone
GO:0032311 angiogenin-PRI complex
GO:0043025 neuronal cell body
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR001427 Pancreatic ribonuclease
IPR023412 Ribonuclease A-domain
PFAM PF00074
PRINTS PR00794
PIRSF
SMART SM00092
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P03950
PhosphoSite PhosphoSite-P03950
TrEMBL W0UV28
UniProt Splice Variant
Entrez Gene 283
UniGene Hs.743472
RefSeq NP_001091046
HUGO HGNC:483
OMIM 105850
CCDS CCDS9554
HPRD 00105
IMGT
EMBL AF449647 AF449648 AF449649 AF449650 AF449651 AK313989 BC020704 BC054880 BC062698 CH471078 CR407633 FJ236304 HG328835 M11567
GenPept AAA51678 AAH20704 AAH54880 AAH62698 AAL67710 AAL67711 AAL67712 AAL67713 AAL67714 ACI45236 BAG36701 CAG28561 CDG31911 EAW66450 EAW66451