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Reviewed, UniProtKB/Swiss-Prot P03950 (ANGI_HUMAN)

Last modified July 22, 2008. Version 111. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (7) | Third-party data | Customize display text xml rdf/xml gff fasta
Names and origin · Protein attributes · General annotation (Comments) · Ontologies · Binary interactions · Sequence annotation (Features) · Sequences · References · Web resources · Cross-references · Entry information · Relevant documents

Names and origin

Protein namesRecommended name:
    Angiogenin
    EC=3.1.27.-
Alternative name(s):
    Ribonuclease 5
      Short name=RNase 5
Gene names
Name: ANG
Synonyms: RNASE5
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length147 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level.

General annotation (Comments)

Function

May function as a tRNA-specific ribonuclease that binds to actin on the surface of endothelial cells; once bound, angiogenin is endocytosed and translocated to the nucleus, thereby promoting the endothelial invasiveness necessary for blood vessel formation. Angiogenin induces vascularization of normal and malignant tissues. Abolishes protein synthesis by specifically hydrolyzing cellular tRNAs.

Subcellular location

Secreted.

Tissue specificity

Expressed predominantly in the liver. Also detected in endothelial cells and spinal cord neurons.

Developmental stage

Low level expression in the developing fetus, increased in the neonate, and maximal in the adult.

Involvement in disease

Defects in ANG are the cause of susceptibility to amyotrophic lateral sclerosis type 9 (ALS9) [MIM:611895]. ALS is a degenerative disorder of motor neurons in the cortex, brain stem and spinal cord. ALS is characterized by muscular weakness and atrophy.

Sequence similarities

Belongs to the pancreatic ribonuclease family.

Caution

It is uncertain whether Met-1 or Met-3 is the initiator.

Ontologies

Keywords

   Biological processAngiogenesis
Differentiation
   Cellular componentSecreted
   Coding sequence diversityPolymorphism
   DiseaseAmyotrophic lateral sclerosis
Disease mutation
   DomainSignal
   Molecular functionDevelopmental protein
Endonuclease
Hydrolase
Nuclease
Protein synthesis inhibitor
   PTMPyrrolidone carboxylic acid
   Technical term3D-structure
Direct protein sequencing

Gene Ontology (GO)

   Biological processactin filament polymerization

Inferred from sequence or structural similarity. Source: UniProtKB

activation of phospholipase A2

Inferred from mutant phenotype. Source: UniProtKB

activation of phospholipase C activity

Inferred from mutant phenotype. Source: UniProtKB

activation of protein kinase B activity

Inferred from mutant phenotype. Source: UniProtKB

angiogenesis

Inferred from mutant phenotype. Source: UniProtKB

cell migration

Inferred from mutant phenotype. Source: UniProtKB

diacylglycerol biosynthetic process

Inferred from direct assay. Source: UniProtKB

homeostatic process

Non-traceable author statement. Source: UniProtKB

negative regulation of smooth muscle cell proliferation

Inferred from direct assay. Source: UniProtKB

oocyte maturation

Non-traceable author statement. Source: UniProtKB

ovarian follicle development

Non-traceable author statement. Source: UniProtKB

placenta development

Non-traceable author statement. Source: UniProtKB

positive regulation of endothelial cell proliferation

Inferred from direct assay. Source: UniProtKB

positive regulation of phosphorylation

Inferred from direct assay. Source: UniProtKB

positive regulation of protein secretion

Inferred from direct assay. Source: UniProtKB

rRNA transcription

Inferred from mutant phenotype. Source: UniProtKB

response to hormone stimulus

Inferred from direct assay. Source: UniProtKB

response to hypoxia

Inferred from direct assay. Source: UniProtKB

   Cellular componentangiogenin-PRI complex

Inferred from physical interaction. Source: UniProtKB

basal lamina

Inferred from direct assay. Source: UniProtKB

cell soma

Inferred from sequence or structural similarity. Source: UniProtKB

extracellular space

Inferred from direct assay. Source: UniProtKB

growth cone

Inferred from sequence or structural similarity. Source: UniProtKB

nucleolus

Inferred from sequence or structural similarity. Source: UniProtKB

   Molecular functionDNA binding

Inferred by curator. Source: UniProtKB

actin binding

Inferred from direct assay. Source: UniProtKB

copper ion binding

Inferred from direct assay. Source: UniProtKB

endonuclease activity

Traceable author statement. Source: UniProtKB

heparin binding

Inferred from direct assay. Source: UniProtKB

peptide binding

Inferred from direct assay. Source: UniProtKB

rRNA binding

Traceable author statement. Source: UniProtKB

receptor binding

Inferred from direct assay. Source: UniProtKB

ribonuclease activity

Inferred from direct assay. Source: UniProtKB

Complete GO annotation...

Binary interactions

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical view

Molecule processing

Signal peptide1 – 2424
Chain25 – 147123Angiogenin

Regions

Region64 – 685Substrate binding

Sites

Active site371Proton acceptor
Active site1381Proton donor

Amino acid modifications

Modified residue251Pyrrolidone carboxylic acid
Disulfide bond50 ↔ 105
Disulfide bond63 ↔ 116
Disulfide bond81 ↔ 131

Natural variations

Natural variant121F → S in ALS9.
Natural variant201P → S in ALS9.
Natural variant361Q → L in ALS9; reduced ribonucleolytic activity; low angiogenic activity; reduced mitogenic activity; wild type far-UV CD spectra.
Natural variant411K → E in ALS9; reduced ribonucleolytic activity.
Natural variant411K → I in ALS9; loss of angiogenic activity; reduced ribonucleolytic activity; retains nuclear translocation.
Natural variant521S → N in ALS9; loss of angiogenic activity; reduced ribonucleolytic activity; unable to translocate to the nucleus.
Natural variant551R → K in ALS9; marginally reduced ribonucleolytic activity; wild type far-UV CD spectra.
Natural variant631C → W in ALS9; reduced ribonucleolytic activity; low angiogenic activity; reduced mitogenic activity; reduced thermal stability.
Natural variant641K → I in ALS9; reduced ribonucleolytic activity; low angiogenic activity; reduced mitogenic activity; moderate reduction of thermal stability.
Natural variant701I → V in some ALS9 patients; pathogenicity uncertain; reduced ribonucleolytic activity; moderate reduction of thermal stability.
Natural variant841K → E: dbSNP rs17560.
Natural variant1361P → L in ALS9; loss of angiogenic activity; reduced ribonucleolytic activity; unable to translocate to the nucleus.
Natural variant1371V → I in ALS9.
Natural variant1381H → R in ALS9.

Experimental info

Mutagenesis1401D → H, S or A: 15- to 18-fold increase in RNase activity
Mutagenesis1411Q → G: Over 18-fold increase in RNase activity
Mutagenesis143 – 1442IF → AA: 3- to 5-fold increase in RNase activity

Secondary structure

.......................... 147
Helix Strand Turn

Details...

Sequences

Sequence LengthMass (Da)Tools
P03950-1 [UniParc].

Last modified October 23, 1986. Version 1.
Checksum: 9C462DA3C8D39ACC

FASTA14716,550
        10         20         30         40         50         60 
MVMGLGVLLL VFVLGLGLTP PTLAQDNSRY THFLTQHYDA KPQGRDDRYC ESIMRRRGLT 

        70         80         90        100        110        120 
SPCKDINTFI HGNKRSIKAI CENKNGNPHR ENLRISKSSF QVTTCKLHGG SPWPPCQYRA 

       130        140 
TAGFRNVVVA CENGLPVHLD QSIFRRP 

« Hide

References

« Hide 'large scale' references
[1]"Sequence of the cDNA and gene for angiogenin, a human angiogenesis factor."
Kurachi K., Davie E.W., Strydom D.J., Riordan J.F., Vallee B.L.
Biochemistry 24:5494-5499(1985) [PubMed: 2866795] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [GENOMIC DNA].
[2]"Diversifying selection of the tumor-growth promoter angiogenin in primate evolution."
Zhang J., Rosenberg H.F.
Mol. Biol. Evol. 19:438-445(2002) [PubMed: 11919285] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE, VARIANT GLU-84.
[3]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
[4]"Amino acid sequence of human tumor derived angiogenin."
Strydom D.J., Fett J.W., Lobb R.R., Alderman E.M., Bethune J.L., Riordan J.F., Vallee B.L.
Biochemistry 24:5486-5494(1985) [PubMed: 2866794] [Abstract]
Cited for: PROTEIN SEQUENCE OF 25-147, DISULFIDE BONDS.
[5]"Tissue distribution and developmental expression of the messenger RNA encoding angiogenin."
Weiner H.L., Weiner L.H., Swain J.L.
Science 237:280-282(1987) [PubMed: 2440105] [Abstract]
Cited for: TISSUE SPECIFICITY.
[6]"Angiogenin is a cytotoxic, tRNA-specific ribonuclease in the RNase A superfamily."
Saxena S.K., Rybak S.M., Davey R.T. Jr., Youle R.J., Ackerman E.J.
J. Biol. Chem. 267:21982-21986(1992) [PubMed: 1400510] [Abstract]
Cited for: FUNCTION.
[7]"Crystal structure of human angiogenin reveals the structural basis for its functional divergence from ribonuclease."
Acharya K.R., Shapiro R., Allen S.C., Riordan J.F., Vallee B.L.
Proc. Natl. Acad. Sci. U.S.A. 91:2915-2919(1994) [PubMed: 8159679] [Abstract]
Cited for: X-RAY CRYSTALLOGRAPHY (2.4 ANGSTROMS).
[8]"Molecular recognition of human angiogenin by placental ribonuclease inhibitor -- an X-ray crystallographic study at 2.0-A resolution."
Papageorgiou A.C., Shapiro R., Acharya K.R.
EMBO J. 16:5162-5177(1997) [PubMed: 9311977] [Abstract]
Cited for: X-RAY CRYSTALLOGRAPHY (2.0 ANGSTROMS) OF COMPLEX WITH INHIBITOR.
[9]"Refined crystal structures of native human angiogenin and two active site variants: implications for the unique functional properties of an enzyme involved in neovascularisation during tumour growth."
Leonidas D.D., Shapiro R., Allen S.C., Subbarao G.V., Veluraja K., Acharya K.R.
J. Mol. Biol. 285:1209-1233(1999) [PubMed: 9918722] [Abstract]
Cited for: X-RAY CRYSTALLOGRAPHY (2.0 ANGSTROMS).
[10]"Binding of phosphate and pyrophosphate ions at the active site of human angiogenin as revealed by X-ray crystallography."
Leonidas D.D., Chavali G.B., Jardine A.M., Li S., Shapiro R., Acharya K.R.
Protein Sci. 10:1669-1676(2001) [PubMed: 11468363] [Abstract]
Cited for: X-RAY CRYSTALLOGRAPHY (2.0 ANGSTROMS) OF MUTANT GLY-141 IN COMPLEX WITH PHOSPHATE AND PYROPHOSPHATE.
[11]"Crystallographic studies on the role of the C-terminal segment of human angiogenin in defining enzymatic potency."
Leonidas D.D., Shapiro R., Subbarao G.V., Russo A., Acharya K.R.
Biochemistry 41:2552-2562(2002) [PubMed: 11851402] [Abstract]
Cited for: X-RAY CRYSTALLOGRAPHY (2.0 ANGSTROMS), MUTAGENESIS OF ASP-140; GLN-141 AND 143-ILE-PHE-144.
[12]"The crystal structure of human angiogenin in complex with an antitumor neutralizing antibody."
Chavali G.B., Papageorgiou A.C., Olson K.A., Fett J.W., Hu G., Shapiro R., Acharya K.R.
Structure 11:875-885(2003) [PubMed: 12842050] [Abstract]
Cited for: X-RAY CRYSTALLOGRAPHY (2.0 ANGSTROMS).
[13]"Crystallographic studies on structural features that determine the enzymatic specificity and potency of human angiogenin: Thr44, Thr80, and residues 38-41."
Holloway D.E., Chavali G.B., Hares M.C., Baker M.D., Subbarao G.V., Shapiro R., Acharya K.R.
Biochemistry 43:1230-1241(2004) [PubMed: 14756559] [Abstract]
Cited for: X-RAY CRYSTALLOGRAPHY (2.1 ANGSTROMS) OF MUTANTS ASP-68 AND ALA-104.
[14]"Three-dimensional solution structure of human angiogenin determined by 1H,15N-NMR spectroscopy -- characterization of histidine protonation states and pKa values."
Lequin O., Thuering H., Robin M., Lallemand J.-Y.
Eur. J. Biochem. 250:712-726(1997) [PubMed: 9461294] [Abstract]
Cited for: STRUCTURE BY NMR.
[15]"A novel candidate region for ALS on chromosome 14q11.2."
Greenway M.J., Alexander M.D., Ennis S., Traynor B.J., Corr B., Frost E., Green A., Hardiman O.
Neurology 63:1936-1938(2004) [PubMed: 15557516] [Abstract]
Cited for: VARIANT ALS9 ILE-64.
[16]"ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis."
Greenway M.J., Andersen P.M., Russ C., Ennis S., Cashman S., Donaghy C., Patterson V., Swingler R., Kieran D., Prehn J., Morrison K.E., Green A., Acharya K.R., Brown R.H. Jr., Hardiman O.
Nat. Genet. 38:411-413(2006) [PubMed: 16501576] [Abstract]
Cited for: VARIANTS ALS9 LEU-36; ILE-41; GLU-41; LYS-55; TRP-63 AND ILE-64, VARIANT VAL-70.
[17]"Angiogenin loss-of-function mutations in amyotrophic lateral sclerosis."
Wu D., Yu W., Kishikawa H., Folkerth R.D., Iafrate A.J., Shen Y., Xin W., Sims K., Hu G.-F.
Ann. Neurol. 62:609-617(2007) [PubMed: 17886298] [Abstract]
Cited for: VARIANTS ALS9 SER-20; ILE-41; ASN-52 AND LEU-136, CHARACTERIZATION OF VARIANTS ALS9 ILE-41; ASN-52 AND LEU-136, TISSUE SPECIFICITY.
[18]"Characterization of human angiogenin variants implicated in amyotrophic lateral sclerosis."
Crabtree B., Thiyagarajan N., Prior S.H., Wilson P., Iyer S., Ferns T., Shapiro R., Brew K., Subramanian V., Acharya K.R.
Biochemistry 46:11810-11818(2007) [PubMed: 17900154] [Abstract]
Cited for: CHARACTERIZATION OF VARIANTS ALS9 LEU-36; ILE-41; GLU-41; LYS-55; TRP-63 AND ILE-64, CHARACTERIZATION OF VARIANT VAL-70.
[19]"Identification of new ANG gene mutations in a large cohort of Italian patients with amyotrophic lateral sclerosis."
Gellera C., Colombrita C., Ticozzi N., Castellotti B., Bragato C., Ratti A., Taroni F., Silani V.
Neurogenetics 9:33-40(2008) [PubMed: 18087731] [Abstract]
Cited for: VARIANTS ALS9 SER-12; SER-20; ILE-137 AND ARG-138, VARIANT VAL-70.
[20]"A novel angiogenin gene mutation in a sporadic patient with amyotrophic lateral sclerosis from southern Italy."
Conforti F.L., Sprovieri T., Mazzei R., Ungaro C., La Bella V., Tessitore A., Patitucci A., Magariello A., Gabriele A.L., Tedeschi G., Simone I.L., Majorana G., Valentino P., Condino F., Bono F., Monsurro M.R., Muglia M., Quattrone A.
Neuromuscul. Disord. 18:68-70(2008) [PubMed: 17703939] [Abstract]
Cited for: INVOLVEMENT IN ALS9.
+Additional computationally mapped references.

Cross-references

Sequence databases

M11567 Genomic DNA. Translation: AAA51678.1.
AF449647 Genomic DNA. Translation: AAL67710.1.
AF449648 Genomic DNA. Translation: AAL67711.1.
AF449649 Genomic DNA. Translation: AAL67712.1.
AF449650 Genomic DNA. Translation: AAL67713.1.
AF449651 Genomic DNA. Translation: AAL67714.1.
BC054880 mRNA. Translation: AAH54880.1.
PIRNRHUAG. A90498.
RefSeqNP_001091046.1.
NP_001136.1.
UniGeneHs.283749
Hs.706192

3D structure databases

EntryMethodResolution (Å)ChainPositionsPDBsum
1A4YX-ray2.00B/E25-147[»]
1ANGX-ray2.40A25-147[»]
1AWZNMR-A25-147[»]
1B1EX-ray2.00A25-147[»]
1B1IX-ray1.80A25-147[»]
1B1JX-ray2.00A25-147[»]
1GV7X-ray2.10A26-145[»]
1H0DX-ray2.00C25-147[»]
1H52X-ray2.00A25-147[»]
1H53X-ray2.00A25-147[»]
1HBYX-ray2.00A25-147[»]
1K58X-ray2.70A25-147[»]
1K59X-ray1.80A25-147[»]