2j91

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (14:38, 13 December 2023) (edit) (undo)
 
Line 3: Line 3:
<StructureSection load='2j91' size='340' side='right'caption='[[2j91]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
<StructureSection load='2j91' size='340' side='right'caption='[[2j91]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
-
<table><tr><td colspan='2'>[[2j91]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=2j84 2j84]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2J91 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2J91 FirstGlance]. <br>
+
<table><tr><td colspan='2'>[[2j91]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=2j84 2j84]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2J91 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2J91 FirstGlance]. <br>
-
</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AMP:ADENOSINE+MONOPHOSPHATE'>AMP</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
-
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[2j84|2j84]]</div></td></tr>
+
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AMP:ADENOSINE+MONOPHOSPHATE'>AMP</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr>
-
<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Adenylosuccinate_lyase Adenylosuccinate lyase], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=4.3.2.2 4.3.2.2] </span></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=2j91 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2j91 OCA], [https://pdbe.org/2j91 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2j91 RCSB], [https://www.ebi.ac.uk/pdbsum/2j91 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2j91 ProSAT]</span></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=2j91 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2j91 OCA], [https://pdbe.org/2j91 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2j91 RCSB], [https://www.ebi.ac.uk/pdbsum/2j91 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2j91 ProSAT]</span></td></tr>
</table>
</table>
 +
== Disease ==
 +
[https://www.uniprot.org/uniprot/PUR8_HUMAN PUR8_HUMAN] Defects in ADSL are the cause of adenylosuccinase deficiency (ADSL deficiency) [MIM:[https://omim.org/entry/103050 103050]. ADSL deficiency is an autosomal recessive disorder characterized by the accumulation in the body fluids of succinylaminoimidazole-carboxamide riboside (SAICA-riboside) and succinyladenosine (S-Ado). Most children display marked psychomotor delay, often accompanied by epilepsy or autistic features, or both, although some patients may be less profoundly retarded. Occasionally, growth retardation and muscular wasting are also present.
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/PUR8_HUMAN PUR8_HUMAN]
== Evolutionary Conservation ==
== Evolutionary Conservation ==
[[Image:Consurf_key_small.gif|200px|right]]
[[Image:Consurf_key_small.gif|200px|right]]
Line 24: Line 27:
__TOC__
__TOC__
</StructureSection>
</StructureSection>
-
[[Category: Adenylosuccinate lyase]]
+
[[Category: Homo sapiens]]
-
[[Category: Human]]
+
[[Category: Large Structures]]
[[Category: Large Structures]]
-
[[Category: Arrowsmith, C]]
+
[[Category: Arrowsmith C]]
-
[[Category: Berg, S van Den]]
+
[[Category: Berglund H]]
-
[[Category: Berglund, H]]
+
[[Category: Busam R]]
-
[[Category: Busam, R]]
+
[[Category: Collins R]]
-
[[Category: Collins, R]]
+
[[Category: Edwards A]]
-
[[Category: Edwards, A]]
+
[[Category: Ericsson UB]]
-
[[Category: Ericsson, U B]]
+
[[Category: Flodin S]]
-
[[Category: Flodin, S]]
+
[[Category: Flores A]]
-
[[Category: Flores, A]]
+
[[Category: Graslund S]]
-
[[Category: Graslund, S]]
+
[[Category: Hallberg BM]]
-
[[Category: Hallberg, B M]]
+
[[Category: Hammarstrom M]]
-
[[Category: Hammarstrom, M]]
+
[[Category: Hogbom M]]
-
[[Category: Hogbom, M]]
+
[[Category: Holmberg Schiavone L]]
-
[[Category: Johansson, I]]
+
[[Category: Johansson I]]
-
[[Category: Karlberg, T]]
+
[[Category: Karlberg T]]
-
[[Category: Kosinska, U]]
+
[[Category: Kosinska U]]
-
[[Category: Kotenyova, T]]
+
[[Category: Kotenyova T]]
-
[[Category: Magnusdottir, A]]
+
[[Category: Magnusdottir A]]
-
[[Category: Moche, M]]
+
[[Category: Moche M]]
-
[[Category: Nilsson, M E]]
+
[[Category: Nilsson ME]]
-
[[Category: Nilsson-Ehle, P]]
+
[[Category: Nilsson-Ehle P]]
-
[[Category: Nordlund, P]]
+
[[Category: Nordlund P]]
-
[[Category: Nyman, T]]
+
[[Category: Nyman T]]
-
[[Category: Ogg, D]]
+
[[Category: Ogg D]]
-
[[Category: Persson, C]]
+
[[Category: Persson C]]
-
[[Category: Sagemark, J]]
+
[[Category: Sagemark J]]
-
[[Category: Schiavone, L Holmberg]]
+
[[Category: Stenmark P]]
-
[[Category: Stenmark, P]]
+
[[Category: Sundstrom M]]
-
[[Category: Sundstrom, M]]
+
[[Category: Thorsell AG]]
-
[[Category: Thorsell, A G]]
+
[[Category: Uppenberg J]]
-
[[Category: Uppenberg, J]]
+
[[Category: Uppsten M]]
-
[[Category: Uppsten, M]]
+
[[Category: Wallden K]]
-
[[Category: Wallden, K]]
+
[[Category: Weigelt J]]
-
[[Category: Weigelt, J]]
+
[[Category: Van Den Berg S]]
-
[[Category: Adenylosuccinase]]
+
-
[[Category: Adenylosuccinase deficiency]]
+
-
[[Category: Adsl]]
+
-
[[Category: Amp]]
+
-
[[Category: Disease mutation]]
+
-
[[Category: Epilepsy]]
+
-
[[Category: Lyase]]
+
-
[[Category: Purine]]
+
-
[[Category: Purine biosynthesis]]
+
-
[[Category: S-amp]]
+
-
[[Category: Saicar]]
+
-
[[Category: Succino amp-lyase]]
+

Current revision

Crystal structure of Human Adenylosuccinate Lyase in complex with AMP

PDB ID 2j91

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools