1r02: Difference between revisions

New page: left|200px<br /> <applet load="1r02" size="450" color="white" frame="true" align="right" spinBox="true" caption="1r02" /> '''Solution structure of Human Orexin-A:Regula...
 
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'''Solution structure of Human Orexin-A:Regulator of Appetite and Wakefulness'''<br />


==Overview==
==Solution structure of Human Orexin-A:Regulator of Appetite and Wakefulness==
Orexin-A and orexin-B (hypocretin-1 and hypocretin-2, respectively) are, important hypothalamic neuro-peptides, which are encoded by a single mRNA, transcript and stimulate food intake as well as regulate wakefulness. Here, we determined the solution structure of orexin-A by NMR spectroscopy and, by simulated-annealing calculation. The structural features of orexin-A, involve two alpha-helices, with the hydrophobic residues disposed to on, one side of helix, and hydrophilic residues to the other. A hydrophilic, turn induced by two disulfide bonds provides the key difference between, orexin-A and -B. With previous mutagenic studies, the derived structure of, orexin-A provides us with a structure-functional view for novel drug, design.
<StructureSection load='1r02' size='340' side='right'caption='[[1r02]]' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1r02]] 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=1R02 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1R02 FirstGlance]. <br>
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 1 model</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=1r02 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1r02 OCA], [https://pdbe.org/1r02 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1r02 RCSB], [https://www.ebi.ac.uk/pdbsum/1r02 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1r02 ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/OREX_HUMAN OREX_HUMAN] Defects in HCRT are the cause of narcolepsy type 1 (NRCLP1) [MIM:[https://omim.org/entry/161400 161400]. Narcolepsy is a neurological disabling sleep disorder, characterized by excessive daytime sleepiness, sleep fragmentation, symptoms of abnormal rapid-eye-movement (REM) sleep, such as cataplexy, hypnagogic hallucinations, and sleep paralysis. Cataplexy is a sudden loss of muscle tone triggered by emotions, which is the most valuable clinical feature used to diagnose narcolepsy. Human narcolepsy is primarily a sporadically occurring disorder but familial clustering has been observed. Note=Human narcolepsy is associated with a deficient orexin system. Orexins are absent and/or greatly diminished in the brain and cerebrospinal fluid (CSF) of most narcoleptic patients.<ref>PMID:10973318</ref>
== Function ==
[https://www.uniprot.org/uniprot/OREX_HUMAN OREX_HUMAN] Neuropeptides that play a significant role in the regulation of food intake and sleep-wakefulness, possibly by coordinating the complex behavioral and physiologic responses of these complementary homeostatic functions. A broader role in the homeostatic regulation of energy metabolism, autonomic function, hormonal balance and the regulation of body fluids, is also suggested. Orexin-A binds to both OX1R and OX2R with a high affinity, whereas orexin-B binds only to OX2R with a similar high affinity.
<div style="background-color:#fffaf0;">
== Publication Abstract from PubMed ==
Orexin-A and orexin-B (hypocretin-1 and hypocretin-2, respectively) are important hypothalamic neuro-peptides, which are encoded by a single mRNA transcript and stimulate food intake as well as regulate wakefulness. Here we determined the solution structure of orexin-A by NMR spectroscopy and by simulated-annealing calculation. The structural features of orexin-A involve two alpha-helices, with the hydrophobic residues disposed to on one side of helix, and hydrophilic residues to the other. A hydrophilic turn induced by two disulfide bonds provides the key difference between orexin-A and -B. With previous mutagenic studies, the derived structure of orexin-A provides us with a structure-functional view for novel drug design.


==Disease==
Solution structure of human orexin-A: regulator of appetite and wakefulness.,Kim HY, Hong E, Kim JI, Lee W J Biochem Mol Biol. 2004 Sep 30;37(5):565-73. PMID:15479620<ref>PMID:15479620</ref>
Known diseases associated with this structure: Narcolepsy OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=602358 602358]], Porphyria variegata OMIM:[[http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=600923 600923]]


==About this Structure==
From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
1R02 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/ ]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1R02 OCA].
</div>
<div class="pdbe-citations 1r02" style="background-color:#fffaf0;"></div>


==Reference==
==See Also==
Solution structure of human orexin-A: regulator of appetite and wakefulness., Kim HY, Hong E, Kim JI, Lee W, J Biochem Mol Biol. 2004 Sep 30;37(5):565-73. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=15479620 15479620]
*[[Orexin and Orexin receptor|Orexin and Orexin receptor]]
[[Category: Single protein]]
== References ==
[[Category: Hong, E.]]
<references/>
[[Category: Kim, H.Y.]]
__TOC__
[[Category: Kim, J.I.]]
</StructureSection>
[[Category: Lee, W.]]
[[Category: Homo sapiens]]
[[Category: helix-loop-helix]]
[[Category: Large Structures]]
[[Category: turn]]
[[Category: Hong E]]
 
[[Category: Kim H-Y]]
''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 12 18:58:02 2007''
[[Category: Kim J-I]]
[[Category: Lee W]]

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