7pnr
From Proteopedia
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==Human Angiogenin mutant-S28AT36AS37A== | ==Human Angiogenin mutant-S28AT36AS37A== | ||
| - | <StructureSection load='7pnr' size='340' side='right'caption='[[7pnr]]' scene=''> | + | <StructureSection load='7pnr' size='340' side='right'caption='[[7pnr]], [[Resolution|resolution]] 1.60Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7PNR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7PNR FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7pnr]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7PNR OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7PNR FirstGlance]. <br> |
</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7pnr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7pnr OCA], [https://pdbe.org/7pnr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7pnr RCSB], [https://www.ebi.ac.uk/pdbsum/7pnr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7pnr ProSAT]</span></td></tr> | </td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7pnr FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7pnr OCA], [https://pdbe.org/7pnr PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7pnr RCSB], [https://www.ebi.ac.uk/pdbsum/7pnr PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7pnr ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/ANGI_HUMAN ANGI_HUMAN] Defects in ANG are the cause of susceptibility to amyotrophic lateral sclerosis type 9 (ALS9) [MIM:[https://omim.org/entry/611895 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.<ref>PMID:17886298</ref> <ref>PMID:15557516</ref> <ref>PMID:16501576</ref> <ref>PMID:17900154</ref> <ref>PMID:18087731</ref> <ref>PMID:17703939</ref> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/ANGI_HUMAN ANGI_HUMAN] May function as a tRNA-specific ribonuclease that abolishes protein synthesis by specifically hydrolyzing cellular tRNAs. Binds to actin on the surface of endothelial cells; once bound, angiogenin is endocytosed and translocated to the nucleus. Angiogenin induces vascularization of normal and malignant tissues. Angiogenic activity is regulated by interaction with RNH1 in vivo.<ref>PMID:1400510</ref> <ref>PMID:19354288</ref> | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Ribonuclease 3D structures|Ribonuclease 3D structures]] | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Leonidas DD]] | [[Category: Leonidas DD]] | ||
[[Category: Papaioannou OSE]] | [[Category: Papaioannou OSE]] | ||
Revision as of 05:49, 31 May 2023
Human Angiogenin mutant-S28AT36AS37A
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