9tpp: Difference between revisions

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'''Unreleased structure'''


The entry 9tpp is ON HOLD  until Paper Publication
==Antibody-antigen complex==
 
<StructureSection load='9tpp' size='340' side='right'caption='[[9tpp]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
Authors: Alzari, P.M., Vulliez-Le Normand, B.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9tpp]] is a 3 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Mus_musculus Mus musculus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9TPP OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9TPP FirstGlance]. <br>
Description: Antibody-antigen complex
</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>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACE:ACETYL+GROUP'>ACE</scene>, <scene name='pdbligand=NIY:META-NITRO-TYROSINE'>NIY</scene></td></tr>
[[Category: Vulliez-Le Normand, B]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9tpp FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9tpp OCA], [https://pdbe.org/9tpp PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9tpp RCSB], [https://www.ebi.ac.uk/pdbsum/9tpp PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9tpp ProSAT]</span></td></tr>
[[Category: Alzari, P.M]]
</table>
== Disease ==
[https://www.uniprot.org/uniprot/NGF_HUMAN NGF_HUMAN] Defects in NGF are the cause of hereditary sensory and autonomic neuropathy type 5 (HSAN5) [MIM:[https://omim.org/entry/608654 608654]. The hereditary sensory and autonomic neuropathies are a genetically and clinically heterogeneous group of disorders characterized by degeneration of dorsal root and autonomic ganglion cells, and by sensory and/or autonomic abnormalities. HSAN5 patients manifest loss of pain perception and impaired temperature sensitivity, ulcers, and in some cases self-mutilation. The autonomic involvement is variable.<ref>PMID:14976160</ref> <ref>PMID:20978020</ref> <ref>PMID:22302274</ref>
== Function ==
[https://www.uniprot.org/uniprot/NGF_HUMAN NGF_HUMAN] Nerve growth factor is important for the development and maintenance of the sympathetic and sensory nervous systems. Extracellular ligand for the NTRK1 and NGFR receptors, activates cellular signaling cascades through those receptor tyrosine kinase to regulate neuronal proliferation, differentiation and survival.
== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Homo sapiens]]
[[Category: Large Structures]]
[[Category: Mus musculus]]
[[Category: Alzari PM]]
[[Category: Vulliez-Le Normand B]]

Latest revision as of 05:03, 27 May 2026

Antibody-antigen complex

9tpp, resolution 1.80Å

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