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4amt
From Proteopedia
(Difference between revisions)
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<StructureSection load='4amt' size='340' side='right'caption='[[4amt]], [[Resolution|resolution]] 2.60Å' scene=''> | <StructureSection load='4amt' size='340' side='right'caption='[[4amt]], [[Resolution|resolution]] 2.60Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[4amt]] is a 1 chain structure | + | <table><tr><td colspan='2'>[[4amt]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4AMT OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4AMT FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand= | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=BMA:BETA-D-MANNOSE'>BMA</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=FUC:ALPHA-L-FUCOSE'>FUC</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></td></tr> |
| - | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1bbs|1bbs]], [[1bil|1bil]], [[1bim|1bim]], [[1hrn|1hrn]], [[1rne|1rne]], [[2bks|2bks]], [[2bkt|2bkt]], [[2fs4|2fs4]], [[2g1n|2g1n]], [[2g1o|2g1o]], [[2g1r|2g1r]], [[2g1s|2g1s]], [[2g1y|2g1y]], [[2g20|2g20]], [[2g21|2g21]], [[2g22|2g22]], [[2g24|2g24]], [[2g26|2g26]], [[2g27|2g27]], [[2ren|2ren]], [[2v0z|2v0z]], [[2v10|2v10]], [[2v11|2v11]], [[2v12|2v12]], [[2v13|2v13]], [[2v16|2v16]], [[2x0b|2x0b]]</td></tr> | + | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[1bbs|1bbs]], [[1bil|1bil]], [[1bim|1bim]], [[1hrn|1hrn]], [[1rne|1rne]], [[2bks|2bks]], [[2bkt|2bkt]], [[2fs4|2fs4]], [[2g1n|2g1n]], [[2g1o|2g1o]], [[2g1r|2g1r]], [[2g1s|2g1s]], [[2g1y|2g1y]], [[2g20|2g20]], [[2g21|2g21]], [[2g22|2g22]], [[2g24|2g24]], [[2g26|2g26]], [[2g27|2g27]], [[2ren|2ren]], [[2v0z|2v0z]], [[2v10|2v10]], [[2v11|2v11]], [[2v12|2v12]], [[2v13|2v13]], [[2v16|2v16]], [[2x0b|2x0b]]</div></td></tr> |
| - | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Renin Renin], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.15 3.4.23.15] </span></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4amt FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4amt OCA], [https://pdbe.org/4amt PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4amt RCSB], [https://www.ebi.ac.uk/pdbsum/4amt PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4amt ProSAT]</span></td></tr> |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [[ | + | [[https://www.uniprot.org/uniprot/RENI_HUMAN RENI_HUMAN]] Defects in REN are a cause of renal tubular dysgenesis (RTD) [MIM:[https://omim.org/entry/267430 267430]]. RTD is an autosomal recessive severe disorder of renal tubular development characterized by persistent fetal anuria and perinatal death, probably due to pulmonary hypoplasia from early-onset oligohydramnios (the Potter phenotype).<ref>PMID:16116425</ref> Defects in REN are the cause of familial juvenile hyperuricemic nephropathy type 2 (HNFJ2) [MIM:[https://omim.org/entry/613092 613092]]. It is a renal disease characterized by juvenile onset of hyperuricemia, slowly progressive renal failure and anemia.<ref>PMID:19664745</ref> |
== Function == | == Function == | ||
| - | [[ | + | [[https://www.uniprot.org/uniprot/RENI_HUMAN RENI_HUMAN]] Renin is a highly specific endopeptidase, whose only known function is to generate angiotensin I from angiotensinogen in the plasma, initiating a cascade of reactions that produce an elevation of blood pressure and increased sodium retention by the kidney. |
==See Also== | ==See Also== | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Large Structures]] |
[[Category: Renin]] | [[Category: Renin]] | ||
[[Category: Zhou, A]] | [[Category: Zhou, A]] | ||
[[Category: Hormone]] | [[Category: Hormone]] | ||
[[Category: Hydrolase]] | [[Category: Hydrolase]] | ||
Revision as of 05:39, 25 August 2022
Crystal structure at 2.6A of human prorenin
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Categories: Large Structures | Renin | Zhou, A | Hormone | Hydrolase
