[English] 日本語
Yorodumi- PDB-2kve: C-terminal domain of mesencephalic astrocyte-derived neurotrophic... -
+Open data
-Basic information
Entry | Database: PDB / ID: 2kve | ||||||
---|---|---|---|---|---|---|---|
Title | C-terminal domain of mesencephalic astrocyte-derived neurotrophic factor (MANF) | ||||||
Components | Mesencephalic astrocyte-derived neurotrophic factor | ||||||
Keywords | HORMONE / Disulfide bond / Glycoprotein / Growth factor / Secreted / Sialic acid / Unfolded protein response | ||||||
Function / homology | Function and homology information vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure / regulation of response to endoplasmic reticulum stress / sulfatide binding / sarcoplasmic reticulum lumen / dopaminergic neuron differentiation / response to unfolded protein / growth factor activity / neuron projection development / Platelet degranulation / endoplasmic reticulum lumen ...vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure / regulation of response to endoplasmic reticulum stress / sulfatide binding / sarcoplasmic reticulum lumen / dopaminergic neuron differentiation / response to unfolded protein / growth factor activity / neuron projection development / Platelet degranulation / endoplasmic reticulum lumen / endoplasmic reticulum / RNA binding / extracellular space / extracellular region / nucleus / cytosol Similarity search - Function | ||||||
Biological species | Homo sapiens (human) | ||||||
Method | SOLUTION NMR / TORSION ANGLE DYNAMICS, simulated annealing, TORSION ANGLE DYNAMICS | ||||||
Model details | fewest violations, model 1 | ||||||
Authors | Hellman, M.H. / Saarma, M. / Permi, P. | ||||||
Citation | Journal: J.Biol.Chem. / Year: 2011 Title: Mesencephalic Astrocyte-derived Neurotrophic Factor (MANF) Has a Unique Mechanism to Rescue Apoptotic Neurons Authors: Hellman, M.H. / Arumae, U. / Yu, L.-Y. / Lindholm, P. / Peranen, J. / Saarma, M. / Permi, P. | ||||||
History |
|
-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
---|
-Downloads & links
-Download
PDBx/mmCIF format | 2kve.cif.gz | 320.2 KB | Display | PDBx/mmCIF format |
---|---|---|---|---|
PDB format | pdb2kve.ent.gz | 266.9 KB | Display | PDB format |
PDBx/mmJSON format | 2kve.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Summary document | 2kve_validation.pdf.gz | 347.1 KB | Display | wwPDB validaton report |
---|---|---|---|---|
Full document | 2kve_full_validation.pdf.gz | 392.3 KB | Display | |
Data in XML | 2kve_validation.xml.gz | 14.5 KB | Display | |
Data in CIF | 2kve_validation.cif.gz | 25.4 KB | Display | |
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/kv/2kve ftp://data.pdbj.org/pub/pdb/validation_reports/kv/2kve | HTTPS FTP |
-Related structure data
-Links
-Assembly
Deposited unit |
| |||||||||
---|---|---|---|---|---|---|---|---|---|---|
1 |
| |||||||||
NMR ensembles |
|
-Components
#1: Protein | Mass: 7476.777 Da / Num. of mol.: 1 / Fragment: C-terminal domain, UNP Residues 117-179 Source method: isolated from a genetically manipulated source Source: (gene. exp.) Homo sapiens (human) / Production host: Escherichia coli (E. coli) / Strain (production host): OrigamiB(DE3) / References: UniProt: P55145 |
---|---|
Has protein modification | Y |
-Experimental details
-Experiment
Experiment | Method: SOLUTION NMR | ||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
NMR experiment |
|
-Sample preparation
Details | Contents: 1mM [U-99% 13C; U-99% 15N] C-MANF; 93% H2O/7% D2O / Solvent system: 93% H2O/7% D2O |
---|---|
Sample | Conc.: 1 mM / Component: C-MANF-1 / Isotopic labeling: [U-99% 13C; U-99% 15N] |
Sample conditions | Ionic strength: 50 / pH: 6.5 / Pressure: AMBIENT / Temperature: 298 K |
-NMR measurement
NMR spectrometer |
|
---|
-Processing
NMR software |
| ||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Refinement | Method: TORSION ANGLE DYNAMICS, simulated annealing, TORSION ANGLE DYNAMICS Software ordinal: 1 | ||||||||||||||||
NMR constraints | NOE constraints total: 845 / NOE intraresidue total count: 272 / NOE long range total count: 141 / NOE medium range total count: 217 / NOE sequential total count: 215 | ||||||||||||||||
NMR representative | Selection criteria: fewest violations | ||||||||||||||||
NMR ensemble | Conformer selection criteria: structures with the least restraint violations Conformers calculated total number: 400 / Conformers submitted total number: 15 / Representative conformer: 1 |