6nq1: Difference between revisions

Latest revision as of 15:55, 6 November 2024

Cryo-EM structure of human TPC2 channel in the apo stateCryo-EM structure of human TPC2 channel in the apo state

6nq1, resolution 3.50Å

Structural highlights

6nq1 is a 2 chain structure with sequence from Homo sapiens. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:	Electron Microscopy, Resolution 3.5Å
Experimental data:	Check
Resources:	FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

TPC2_HUMAN Nicotinic acid adenine dinucleotide phosphate (NAADP) receptor that may function as one of the major voltage-gated Ca(2+) channels (VDCC) across the lysosomal membrane. May be involved in smooth muscle contraction.^[1] ^[2]

Publication Abstract from PubMed

Mammalian two-pore channels (TPCs) regulate the physiological functions of the endolysosome. Here we present cryo-EM structures of human TPC2 (HsTPC2), a phosphatidylinositol 3,5-bisphosphate (PI(3,5)P2)-activated, Na(+) selective channel, in the ligand-bound and apo states. The apo structure captures the closed conformation, while the ligand-bound form features the channel in both open and closed conformations. Combined with functional analysis, these structures provide insights into the mechanism of PI(3,5)P2-regulated gating of TPC2, which is distinct from that of TPC1. Specifically, the endolysosome-specific PI(3,5)P2 binds at the first 6-TM and activates the channel - independently of the membrane potential - by inducing a structural change at the pore-lining inner helix (IS6), which forms a continuous helix in the open state but breaks into two segments at Gly317 in the closed state. Additionally, structural comparison to the voltage-dependent TPC1 structure allowed us to identify Ile551 as being responsible for the loss of voltage dependence in TPC2.

Structural mechanisms of phospholipid activation of the human TPC2 channel.,She J, Zeng W, Guo J, Chen Q, Bai XC, Jiang Y Elife. 2019 Mar 12;8. pii: 45222. doi: 10.7554/eLife.45222. PMID:30860481^[3]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

References

↑ Calcraft PJ, Ruas M, Pan Z, Cheng X, Arredouani A, Hao X, Tang J, Rietdorf K, Teboul L, Chuang KT, Lin P, Xiao R, Wang C, Zhu Y, Lin Y, Wyatt CN, Parrington J, Ma J, Evans AM, Galione A, Zhu MX. NAADP mobilizes calcium from acidic organelles through two-pore channels. Nature. 2009 May 28;459(7246):596-600. doi: 10.1038/nature08030. Epub 2009 Apr, 22. PMID:19387438 doi:http://dx.doi.org/10.1038/nature08030
↑ Brailoiu E, Churamani D, Cai X, Schrlau MG, Brailoiu GC, Gao X, Hooper R, Boulware MJ, Dun NJ, Marchant JS, Patel S. Essential requirement for two-pore channel 1 in NAADP-mediated calcium signaling. J Cell Biol. 2009 Jul 27;186(2):201-9. doi: 10.1083/jcb.200904073. Epub 2009 Jul , 20. PMID:19620632 doi:http://dx.doi.org/10.1083/jcb.200904073
↑ She J, Zeng W, Guo J, Chen Q, Bai XC, Jiang Y. Structural mechanisms of phospholipid activation of the human TPC2 channel. Elife. 2019 Mar 12;8. pii: 45222. doi: 10.7554/eLife.45222. PMID:30860481 doi:http://dx.doi.org/10.7554/eLife.45222

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OCA

[1] Calcraft PJ, Ruas M, Pan Z, Cheng X, Arredouani A, Hao X, Tang J, Rietdorf K, Teboul L, Chuang KT, Lin P, Xiao R, Wang C, Zhu Y, Lin Y, Wyatt CN, Parrington J, Ma J, Evans AM, Galione A, Zhu MX. NAADP mobilizes calcium from acidic organelles through two-pore channels. Nature. 2009 May 28;459(7246):596-600. doi: 10.1038/nature08030. Epub 2009 Apr, 22. PMID:19387438 doi:http://dx.doi.org/10.1038/nature08030

[2] Brailoiu E, Churamani D, Cai X, Schrlau MG, Brailoiu GC, Gao X, Hooper R, Boulware MJ, Dun NJ, Marchant JS, Patel S. Essential requirement for two-pore channel 1 in NAADP-mediated calcium signaling. J Cell Biol. 2009 Jul 27;186(2):201-9. doi: 10.1083/jcb.200904073. Epub 2009 Jul , 20. PMID:19620632 doi:http://dx.doi.org/10.1083/jcb.200904073

[3] She J, Zeng W, Guo J, Chen Q, Bai XC, Jiang Y. Structural mechanisms of phospholipid activation of the human TPC2 channel. Elife. 2019 Mar 12;8. pii: 45222. doi: 10.7554/eLife.45222. PMID:30860481 doi:http://dx.doi.org/10.7554/eLife.45222

[1]

[2]

[3]

@@ Line 1: / Line 1: @@
 ==Cryo-EM structure of human TPC2 channel in the apo state==
-<StructureSection load='6nq1' size='340' side='right'caption='[[6nq1]], [[Resolution|resolution]] 3.50&Aring;' scene=''>
+<SX load='6nq1' size='340' side='right' viewer='molstar' caption='[[6nq1]], [[Resolution|resolution]] 3.50&Aring;' scene=''>
 == Structural highlights ==
-<table><tr><td colspan='2'>[[6nq1]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6NQ1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6NQ1 FirstGlance]. <br>
+<table><tr><td colspan='2'>[[6nq1]] 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=6NQ1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6NQ1 FirstGlance]. <br>
-</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">TPCN2, TPC2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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]] 3.5&#8491;</td></tr>
-<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6nq1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6nq1 OCA], [http://pdbe.org/6nq1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6nq1 RCSB], [http://www.ebi.ac.uk/pdbsum/6nq1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6nq1 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=6nq1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6nq1 OCA], [https://pdbe.org/6nq1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6nq1 RCSB], [https://www.ebi.ac.uk/pdbsum/6nq1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6nq1 ProSAT]</span></td></tr>
 </table>
 == Function ==
-[[http://www.uniprot.org/uniprot/TPC2_HUMAN TPC2_HUMAN]] Nicotinic acid adenine dinucleotide phosphate (NAADP) receptor that may function as one of the major voltage-gated Ca(2+) channels (VDCC) across the lysosomal membrane. May be involved in smooth muscle contraction.<ref>PMID:19387438</ref> <ref>PMID:19620632</ref>
+[https://www.uniprot.org/uniprot/TPC2_HUMAN TPC2_HUMAN] Nicotinic acid adenine dinucleotide phosphate (NAADP) receptor that may function as one of the major voltage-gated Ca(2+) channels (VDCC) across the lysosomal membrane. May be involved in smooth muscle contraction.<ref>PMID:19387438</ref> <ref>PMID:19620632</ref>
 <div style="background-color:#fffaf0;">
 == Publication Abstract from PubMed ==
@@ Line 24: / Line 24: @@
 <references/>
 __TOC__
-</StructureSection>
+</SX>
-[[Category: Human]]
+[[Category: Homo sapiens]]
 [[Category: Large Structures]]
-[[Category: Bai, X]]
+[[Category: Bai X]]
-[[Category: Chen, Q]]
+[[Category: Chen Q]]
-[[Category: Guo, J]]
+[[Category: Guo J]]
-[[Category: Jiang, Y]]
+[[Category: Jiang Y]]
-[[Category: She, J]]
+[[Category: She J]]
-[[Category: Zeng, W]]
+[[Category: Zeng W]]
-[[Category: Channel]]
-[[Category: Lysosome]]
-[[Category: Transport protein]]

6nq1: Difference between revisions

Latest revision as of 15:55, 6 November 2024

Cryo-EM structure of human TPC2 channel in the apo stateCryo-EM structure of human TPC2 channel in the apo state

Structural highlights

Function

Publication Abstract from PubMed

See Also

References

Contents

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6nq1: Difference between revisions

Latest revision as of 15:55, 6 November 2024

Cryo-EM structure of human TPC2 channel in the apo stateCryo-EM structure of human TPC2 channel in the apo state

Structural highlights

Function

Publication Abstract from PubMed

See Also

References

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

Navigation menu

Search