8pod

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Current revision (05:49, 19 June 2024) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8pod is ON HOLD until Paper Publication
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==Crystal structure of the kinase domain of ACVR1 (ALK2) in complex with FKBP12 and MU1700==
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<StructureSection load='8pod' size='340' side='right'caption='[[8pod]], [[Resolution|resolution]] 2.59&Aring;' scene=''>
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Authors: Cros, J., Baltanas-Copado, J., Knapp, S., Paruch, K., Nemec, N., Bullock, A.N.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8pod]] is a 2 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=8POD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8POD FirstGlance]. <br>
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Description: Crystal structure of the kinase domain of ACVR1 (ALK2) in complex with FKBP12 and MU1700
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.59&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=7IO:6-(4-piperazin-1-ylphenyl)-3-quinolin-4-yl-furo[3,2-b]pyridine'>7IO</scene>, <scene name='pdbligand=F:FLUORIDE+ION'>F</scene></td></tr>
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[[Category: Baltanas-Copado, J]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8pod FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8pod OCA], [https://pdbe.org/8pod PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8pod RCSB], [https://www.ebi.ac.uk/pdbsum/8pod PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8pod ProSAT]</span></td></tr>
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[[Category: Cros, J]]
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</table>
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[[Category: Nemec, N]]
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== Disease ==
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[[Category: Bullock, A.N]]
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[https://www.uniprot.org/uniprot/ACVR1_HUMAN ACVR1_HUMAN] Fibrodysplasia ossificans progressiva. Defects in ACVR1 are a cause of fibrodysplasia ossificans progressiva (FOP) [MIM:[https://omim.org/entry/135100 135100]. FOP is a rare autosomal dominant disorder of skeletal malformations and progressive extraskeletal ossification. Heterotopic ossification in FOP begins in childhood and can be induced by trauma or may occur without warning. Bone formation is episodic and progressive, leading to extra-articular ankylosis of all major joints of the axial and appendicular skeleton, rendering movement impossible.<ref>PMID:16642017</ref> <ref>PMID:19085907</ref> <ref>PMID:19330033</ref>
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[[Category: Knapp, S]]
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== Function ==
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[[Category: Paruch, K]]
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[https://www.uniprot.org/uniprot/ACVR1_HUMAN ACVR1_HUMAN] On ligand binding, forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. Type II receptors phosphorylate and activate type I receptors which autophosphorylate, then bind and activate SMAD transcriptional regulators. Receptor for activin. May be involved for left-right pattern formation during embryogenesis (By similarity).
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Baltanas-Copado J]]
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[[Category: Bullock AN]]
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[[Category: Cros J]]
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[[Category: Knapp S]]
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[[Category: Nemec N]]
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[[Category: Paruch K]]

Current revision

Crystal structure of the kinase domain of ACVR1 (ALK2) in complex with FKBP12 and MU1700

PDB ID 8pod

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