1hll: Difference between revisions

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 ==NMR STRUCTURE OF T3-I2, A 32 RESIDUE PEPTIDE FROM THE ALPHA-2A ADRENERGIC RECEPTOR==
-<StructureSection load='1hll' size='340' side='right'caption='[[1hll]], [[NMR_Ensembles_of_Models | 1 NMR models]]' scene=''>
+<StructureSection load='1hll' size='340' side='right'caption='[[1hll]]' scene=''>
 == Structural highlights ==
-<table><tr><td colspan='2'>[[1hll]] is a 1 chain structure. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HLL OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1HLL FirstGlance]. <br>
+<table><tr><td colspan='2'>[[1hll]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1HLL OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1HLL FirstGlance]. <br>
-</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1hof|1hof]], [[1hod|1hod]], [[1ho9|1ho9]]</td></tr>
+</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=1hll FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1hll OCA], [http://pdbe.org/1hll PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=1hll RCSB], [http://www.ebi.ac.uk/pdbsum/1hll PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=1hll 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=1hll FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1hll OCA], [https://pdbe.org/1hll PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1hll RCSB], [https://www.ebi.ac.uk/pdbsum/1hll PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1hll ProSAT]</span></td></tr>
 </table>
 == Function ==
-[[http://www.uniprot.org/uniprot/ADA2A_HUMAN ADA2A_HUMAN]] Alpha-2 adrenergic receptors mediate the catecholamine-induced inhibition of adenylate cyclase through the action of G proteins. The rank order of potency for agonists of this receptor is oxymetazoline > clonidine > epinephrine > norepinephrine > phenylephrine > dopamine > p-synephrine > p-tyramine > serotonin = p-octopamine. For antagonists, the rank order is yohimbine > phentolamine = mianserine > chlorpromazine = spiperone = prazosin > propanolol > alprenolol = pindolol.<ref>PMID:23105096</ref>
+[https://www.uniprot.org/uniprot/ADA2A_HUMAN ADA2A_HUMAN] Alpha-2 adrenergic receptors mediate the catecholamine-induced inhibition of adenylate cyclase through the action of G proteins. The rank order of potency for agonists of this receptor is oxymetazoline > clonidine > epinephrine > norepinephrine > phenylephrine > dopamine > p-synephrine > p-tyramine > serotonin = p-octopamine. For antagonists, the rank order is yohimbine > phentolamine = mianserine > chlorpromazine = spiperone = prazosin > propanolol > alprenolol = pindolol.<ref>PMID:23105096</ref>
 == Evolutionary Conservation ==
 [[Image:Consurf_key_small.gif|200px|right]]
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 __TOC__
 </StructureSection>
+[[Category: Homo sapiens]]
 [[Category: Large Structures]]
-[[Category: Chung, D A]]
+[[Category: Chung DA]]
-[[Category: Neubig, R R]]
+[[Category: Neubig RR]]
-[[Category: Zuiderweg, E R.P]]
+[[Category: Zuiderweg ERP]]
-[[Category: Helix-linker-helix]]
-[[Category: Membrane protein]]