2fs4
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2fs4]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FS4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2FS4 FirstGlance]. <br> | <table><tr><td colspan='2'>[[2fs4]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2FS4 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2FS4 FirstGlance]. <br> | ||
- | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=PZ1:(6R)-6-({[1-(3-HYDROXYPROPYL)-1,7-DIHYDROQUINOLIN-7-YL]OXY}METHYL)-1-(4-{3-[(2-METHOXYBENZYL)OXY]PROPOXY}PHENYL)PIPERAZIN-2-ONE'>PZ1</scene>< | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=PZ1:(6R)-6-({[1-(3-HYDROXYPROPYL)-1,7-DIHYDROQUINOLIN-7-YL]OXY}METHYL)-1-(4-{3-[(2-METHOXYBENZYL)OXY]PROPOXY}PHENYL)PIPERAZIN-2-ONE'>PZ1</scene></td></tr> |
- | <tr><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">REN ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr> | + | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">REN ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</td></tr> |
- | <tr><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Renin Renin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.15 3.4.23.15] </span></td></tr> | + | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Renin Renin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.15 3.4.23.15] </span></td></tr> |
- | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2fs4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2fs4 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2fs4 RCSB], [http://www.ebi.ac.uk/pdbsum/2fs4 PDBsum]</span></td></tr> | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2fs4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2fs4 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2fs4 RCSB], [http://www.ebi.ac.uk/pdbsum/2fs4 PDBsum]</span></td></tr> |
- | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/RENI_HUMAN RENI_HUMAN]] Defects in REN are a cause of renal tubular dysgenesis (RTD) [MIM:[http://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:[http://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> | [[http://www.uniprot.org/uniprot/RENI_HUMAN RENI_HUMAN]] Defects in REN are a cause of renal tubular dysgenesis (RTD) [MIM:[http://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:[http://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> | ||
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[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Renin]] | [[Category: Renin]] | ||
- | [[Category: Bryant, J | + | [[Category: Bryant, J]] |
- | [[Category: Cai, C | + | [[Category: Cai, C]] |
- | [[Category: Cheng, X M | + | [[Category: Cheng, X M]] |
- | [[Category: Cody, W L | + | [[Category: Cody, W L]] |
- | [[Category: Downing, D M | + | [[Category: Downing, D M]] |
- | [[Category: Edmunds, J J | + | [[Category: Edmunds, J J]] |
- | [[Category: Erasga, N | + | [[Category: Erasga, N]] |
- | [[Category: Hall, E | + | [[Category: Hall, E]] |
- | [[Category: Holsworth, D D | + | [[Category: Holsworth, D D]] |
- | [[Category: Jalaie, M | + | [[Category: Jalaie, M]] |
- | [[Category: Kasani, A | + | [[Category: Kasani, A]] |
- | [[Category: Lee, C | + | [[Category: Lee, C]] |
- | [[Category: Li, T | + | [[Category: Li, T]] |
- | [[Category: Maiti, S | + | [[Category: Maiti, S]] |
- | [[Category: McConnell, P | + | [[Category: McConnell, P]] |
- | [[Category: Powell, N A | + | [[Category: Powell, N A]] |
- | [[Category: Rahim, M | + | [[Category: Rahim, M]] |
- | [[Category: Ryan, M J | + | [[Category: Ryan, M J]] |
- | [[Category: Stier, M | + | [[Category: Stier, M]] |
- | [[Category: Subedi, R | + | [[Category: Subedi, R]] |
- | [[Category: Zhang, E | + | [[Category: Zhang, E]] |
[[Category: Hydrolase]] | [[Category: Hydrolase]] | ||
[[Category: Protein-ligand complex]] | [[Category: Protein-ligand complex]] |
Revision as of 08:36, 16 January 2015
Ketopiperazine-Based Renin Inhibitors: Optimization of the C ring
|
Categories: Homo sapiens | Renin | Bryant, J | Cai, C | Cheng, X M | Cody, W L | Downing, D M | Edmunds, J J | Erasga, N | Hall, E | Holsworth, D D | Jalaie, M | Kasani, A | Lee, C | Li, T | Maiti, S | McConnell, P | Powell, N A | Rahim, M | Ryan, M J | Stier, M | Subedi, R | Zhang, E | Hydrolase | Protein-ligand complex