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| | <SX load='6s59' size='340' side='right' viewer='molstar' caption='[[6s59]], [[Resolution|resolution]] 3.70Å' scene=''> | | <SX load='6s59' size='340' side='right' viewer='molstar' caption='[[6s59]], [[Resolution|resolution]] 3.70Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[6s59]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Ovis_aries Ovis aries]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6S59 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6S59 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6s59]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Ovis_aries Ovis aries]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6S59 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6S59 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PC1:1,2-DIACYL-SN-GLYCERO-3-PHOSPHOCHOLINE'>PC1</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.7Å</td></tr> |
| - | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[6qti|6qti]], [[6que|6que]]</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PC1:1,2-DIACYL-SN-GLYCERO-3-PHOSPHOCHOLINE'>PC1</scene></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6s59 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6s59 OCA], [http://pdbe.org/6s59 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6s59 RCSB], [http://www.ebi.ac.uk/pdbsum/6s59 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6s59 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=6s59 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6s59 OCA], [https://pdbe.org/6s59 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6s59 RCSB], [https://www.ebi.ac.uk/pdbsum/6s59 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6s59 ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | == Function == | | == Function == |
| - | [[http://www.uniprot.org/uniprot/NNTM_SHEEP NNTM_SHEEP]] The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity). May play a role in reactive oxygen species (ROS) detoxification in the adrenal gland (By similarity).[UniProtKB:P07001][UniProtKB:Q13423] | + | [https://www.uniprot.org/uniprot/NNTM_SHEEP NNTM_SHEEP] The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity). May play a role in reactive oxygen species (ROS) detoxification in the adrenal gland (By similarity).[UniProtKB:P07001][UniProtKB:Q13423] |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | [[Category: Large Structures]] | | [[Category: Large Structures]] |
| | [[Category: Ovis aries]] | | [[Category: Ovis aries]] |
| - | [[Category: Kampjut, D]] | + | [[Category: Kampjut D]] |
| - | [[Category: Sazanov, L A]] | + | [[Category: Sazanov LA]] |
| - | [[Category: Membrane protein]]
| + | |
| - | [[Category: Mitochondrial]]
| + | |
| - | [[Category: Nicotinamide nucleotide transhydrogenase]]
| + | |
| - | [[Category: Proton-translocating]]
| + | |
| Structural highlights
Function
NNTM_SHEEP The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane (By similarity). May play a role in reactive oxygen species (ROS) detoxification in the adrenal gland (By similarity).[UniProtKB:P07001][UniProtKB:Q13423]
Publication Abstract from PubMed
Proton-translocating transhydrogenase (also known as nicotinamide nucleotide transhydrogenase (NNT)) is found in the plasma membranes of bacteria and the inner mitochondrial membranes of eukaryotes. NNT catalyses the transfer of a hydride between NADH and NADP(+), coupled to the translocation of one proton across the membrane. Its main physiological function is the generation of NADPH, which is a substrate in anabolic reactions and a regulator of oxidative status; however, NNT may also fine-tune the Krebs cycle(1,2). NNT deficiency causes familial glucocorticoid deficiency in humans and metabolic abnormalities in mice, similar to those observed in type II diabetes(3,4). The catalytic mechanism of NNT has been proposed to involve a rotation of around 180 degrees of the entire NADP(H)-binding domain that alternately participates in hydride transfer and proton-channel gating. However, owing to the lack of high-resolution structures of intact NNT, the details of this process remain unclear(5,6). Here we present the cryo-electron microscopy structure of intact mammalian NNT in different conformational states. We show how the NADP(H)-binding domain opens the proton channel to the opposite sides of the membrane, and we provide structures of these two states. We also describe the catalytically important interfaces and linkers between the membrane and the soluble domains and their roles in nucleotide exchange. These structures enable us to propose a revised mechanism for a coupling process in NNT that is consistent with a large body of previous biochemical work. Our results are relevant to the development of currently unavailable NNT inhibitors, which may have therapeutic potential in ischaemia reperfusion injury, metabolic syndrome and some cancers(7-9).
Structure and mechanism of mitochondrial proton-translocating transhydrogenase.,Kampjut D, Sazanov LA Nature. 2019 Sep;573(7773):291-295. doi: 10.1038/s41586-019-1519-2. Epub 2019 Aug, 28. PMID:31462775[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
See Also
References
- ↑ Kampjut D, Sazanov LA. Structure and mechanism of mitochondrial proton-translocating transhydrogenase. Nature. 2019 Sep;573(7773):291-295. doi: 10.1038/s41586-019-1519-2. Epub 2019 Aug, 28. PMID:31462775 doi:http://dx.doi.org/10.1038/s41586-019-1519-2
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