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Yorodumi- PDB-2lly: NMR structures of the transmembrane domains of the nAChR a4 subunit -
+Open data
-Basic information
Entry | Database: PDB / ID: 2lly | ||||||
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Title | NMR structures of the transmembrane domains of the nAChR a4 subunit | ||||||
Components | Neuronal acetylcholine receptor subunit alpha-4 | ||||||
Keywords | TRANSPORT PROTEIN / Acetylcholine receptor / Transmembrane domain | ||||||
Function / homology | Function and homology information Highly sodium permeable postsynaptic acetylcholine nicotinic receptors / Highly calcium permeable nicotinic acetylcholine receptors / Highly calcium permeable postsynaptic nicotinic acetylcholine receptors / acetylcholine receptor activity / acetylcholine-gated channel complex / behavioral response to nicotine / acetylcholine-gated monoatomic cation-selective channel activity / inhibitory postsynaptic potential / nervous system process / acetylcholine binding ...Highly sodium permeable postsynaptic acetylcholine nicotinic receptors / Highly calcium permeable nicotinic acetylcholine receptors / Highly calcium permeable postsynaptic nicotinic acetylcholine receptors / acetylcholine receptor activity / acetylcholine-gated channel complex / behavioral response to nicotine / acetylcholine-gated monoatomic cation-selective channel activity / inhibitory postsynaptic potential / nervous system process / acetylcholine binding / synaptic transmission, cholinergic / acetylcholine receptor signaling pathway / regulation of dopamine secretion / action potential / B cell activation / membrane depolarization / ligand-gated monoatomic ion channel activity / monoatomic ion transport / sensory perception of pain / regulation of membrane potential / response to nicotine / cognition / calcium ion transport / chemical synaptic transmission / postsynaptic membrane / response to oxidative stress / response to hypoxia / neuron projection / external side of plasma membrane / DNA repair / neuronal cell body / dendrite / synapse / signal transduction / membrane / plasma membrane Similarity search - Function | ||||||
Biological species | Homo sapiens (human) | ||||||
Method | SOLUTION NMR / simulated annealing | ||||||
Model details | closest to the average, model 11 | ||||||
Authors | Bondarenko, V. / Mowrey, D. / Tillman, T. / Cui, T. / Liu, L.T. / Xu, Y. / Tang, P. | ||||||
Citation | Journal: Biochim.Biophys.Acta / Year: 2012 Title: NMR structures of the transmembrane domains of the a4b2 nAChR. Authors: Bondarenko, V. / Mowrey, D. / Tillman, T. / Cui, T. / Liu, L.T. / Xu, Y. / Tang, P. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 2lly.cif.gz | 951 KB | Display | PDBx/mmCIF format |
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PDB format | pdb2lly.ent.gz | 819.3 KB | Display | PDB format |
PDBx/mmJSON format | 2lly.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 2lly_validation.pdf.gz | 471.9 KB | Display | wwPDB validaton report |
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Full document | 2lly_full_validation.pdf.gz | 772.8 KB | Display | |
Data in XML | 2lly_validation.xml.gz | 91.1 KB | Display | |
Data in CIF | 2lly_validation.cif.gz | 84.3 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/ll/2lly ftp://data.pdbj.org/pub/pdb/validation_reports/ll/2lly | HTTPS FTP |
-Related structure data
-Links
-Assembly
Deposited unit |
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1 |
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NMR ensembles |
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-Components
#1: Protein | Mass: 15020.915 Da / Num. of mol.: 1 Fragment: Helical transmembrane region, residues 242-339 and residues 598-625 Mutation: R240E, R241E, L301S, I303S, L305S, R336E, M626E Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Gene: CHRNA4, NACRA4 / Production host: Escherichia coli (E. coli) / References: UniProt: P43681 |
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-Experimental details
-Experiment
Experiment | Method: SOLUTION NMR | ||||||||||||||||||||||||||||||||||||
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NMR experiment |
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-Sample preparation
Details | Contents: 0.25 mM [U-100% 13C; U-100% 15N] protein, 5 mM sodium acetate, 1.5 % LDAO, 10 mM sodium chloride, 5 % [U-100% 2H] D2O, 0.1 mM DSS, 10 mM sodium chloride, 20 mM beta-mercaptoethanol, 95% H2O/5% D2O Solvent system: 95% H2O/5% D2O | ||||||||||||||||||||||||||||||||||||
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Sample |
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Sample conditions | pH: 4.65 / Pressure: ambient / Temperature: 318 K |
-NMR measurement
NMR spectrometer |
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-Processing
NMR software |
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Refinement | Method: simulated annealing / Software ordinal: 1 | ||||||||||||
NMR constraints | NOE constraints total: 1070 / NOE intraresidue total count: 362 / NOE long range total count: 28 / NOE medium range total count: 259 / NOE sequential total count: 421 / Hydrogen bond constraints total count: 296 / Protein chi angle constraints total count: 0 / Protein other angle constraints total count: 0 / Protein phi angle constraints total count: 90 / Protein psi angle constraints total count: 90 | ||||||||||||
NMR representative | Selection criteria: closest to the average | ||||||||||||
NMR ensemble | Conformer selection criteria: structures with the lowest energy Conformers calculated total number: 100 / Conformers submitted total number: 20 |