8b29: Difference between revisions

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-'''Unreleased structure'''
-The entry 8b29 is ON HOLD  until Paper Publication
+==Human carbonic anhydrase II containing 6-fluorotryptophanes.==
+<StructureSection load='8b29' size='340' side='right'caption='[[8b29]], [[Resolution|resolution]] 1.70&Aring;' scene=''>
-Authors: Pham, L.B.T., Costantino, A., Barbieri, L., Calderone, V., Luchinat, E., Banci, L.
+== Structural highlights ==
+<table><tr><td colspan='2'>[[8b29]] 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=8B29 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8B29 FirstGlance]. <br>
-Description: Human carbonic anhydrase II containing 6-fluorotryptophanes.
+</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=FT6:6-FLUORO-L-TRYPTOPHAN'>FT6</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene></td></tr>
-[[Category: Unreleased Structures]]
+<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8b29 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8b29 OCA], [https://pdbe.org/8b29 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8b29 RCSB], [https://www.ebi.ac.uk/pdbsum/8b29 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8b29 ProSAT]</span></td></tr>
-[[Category: Pham, L.B.T]]
+</table>
-[[Category: Barbieri, L]]
+== Disease ==
-[[Category: Calderone, V]]
+[https://www.uniprot.org/uniprot/CAH2_HUMAN CAH2_HUMAN] Defects in CA2 are the cause of osteopetrosis autosomal recessive type 3 (OPTB3) [MIM:[https://omim.org/entry/259730 259730]; also known as osteopetrosis with renal tubular acidosis, carbonic anhydrase II deficiency syndrome, Guibaud-Vainsel syndrome or marble brain disease. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. The disorder occurs in two forms: a severe autosomal recessive form occurring in utero, infancy, or childhood, and a benign autosomal dominant form occurring in adolescence or adulthood. Autosomal recessive osteopetrosis is usually associated with normal or elevated amount of non-functional osteoclasts. OPTB3 is associated with renal tubular acidosis, cerebral calcification (marble brain disease) and in some cases with mental retardation.<ref>PMID:1928091</ref> <ref>PMID:1542674</ref> <ref>PMID:8834238</ref> <ref>PMID:9143915</ref> <ref>PMID:15300855</ref>
-[[Category: Banci, L]]
+== Function ==
-[[Category: Costantino, A]]
+[https://www.uniprot.org/uniprot/CAH2_HUMAN CAH2_HUMAN] Essential for bone resorption and osteoclast differentiation (By similarity). Reversible hydration of carbon dioxide. Can hydrate cyanamide to urea. Involved in the regulation of fluid secretion into the anterior chamber of the eye.<ref>PMID:10550681</ref> <ref>PMID:11831900</ref>
-[[Category: Luchinat, E]]
+== References ==
+<references/>
+__TOC__
+</StructureSection>
+[[Category: Homo sapiens]]
+[[Category: Large Structures]]
+[[Category: Banci L]]
+[[Category: Barbieri L]]
+[[Category: Calderone V]]
+[[Category: Costantino A]]
+[[Category: Luchinat E]]
+[[Category: Pham LBT]]