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2m1t

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'''Unreleased structure'''
 
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The entry 2m1t is ON HOLD until Paper Publication
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==SP-B C-terminal (residues 59-80) peptide in DPC micelles==
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<StructureSection load='2m1t' size='340' side='right'caption='[[2m1t]]' scene=''>
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Authors: Kuznetsova, A., Vanni, J., Long, J.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[2m1t]] 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=2M1T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2M1T FirstGlance]. <br>
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Description: SP-B C-terminal (residues 59-80) peptide in DPC micelles
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr>
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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=2m1t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2m1t OCA], [https://pdbe.org/2m1t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2m1t RCSB], [https://www.ebi.ac.uk/pdbsum/2m1t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2m1t ProSAT]</span></td></tr>
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/PSPB_HUMAN PSPB_HUMAN] Defects in SFTPB are the cause of pulmonary surfactant metabolism dysfunction type 1 (SMDP1) [MIM:[https://omim.org/entry/265120 265120]; also called pulmonary alveolar proteinosis due to surfactant protein B deficiency. A rare lung disorder due to impaired surfactant homeostasis. It is characterized by alveolar filling with floccular material that stains positive using the periodic acid-Schiff method and is derived from surfactant phospholipids and protein components. Excessive lipoproteins accumulation in the alveoli results in severe respiratory distress.<ref>PMID:7491219</ref> Genetic variations in SFTPB are a cause of susceptibility to respiratory distress syndrome in premature infants (RDS) [MIM:[https://omim.org/entry/267450 267450]. RDS is a lung disease affecting usually premature newborn infants. It is characterized by deficient gas exchange, diffuse atelectasis, high-permeability lung edema and fibrin-rich alveolar deposits called 'hyaline membranes'. Note=A variation Ile to Thr at position 131 influences the association between specific alleles of SFTPA1 and respiratory distress syndrome in premature infants.<ref>PMID:11063734</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/PSPB_HUMAN PSPB_HUMAN] Pulmonary surfactant-associated proteins promote alveolar stability by lowering the surface tension at the air-liquid interface in the peripheral air spaces. SP-B increases the collapse pressure of palmitic acid to nearly 70 millinewtons per meter.
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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: Kuznetsova A]]
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[[Category: Long J]]
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[[Category: Vanni J]]

Current revision

SP-B C-terminal (residues 59-80) peptide in DPC micelles

PDB ID 2m1t

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