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- PDB-3vrt: VDR ligand binding domain in complex with 2-Mehylidene-19,25,26,2... -

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Basic information

Entry
Database: PDB / ID: 3vrt
TitleVDR ligand binding domain in complex with 2-Mehylidene-19,25,26,27-tetranor-1alpha,24-dihydroxyvitaminD3
Components
  • 13-meric peptide from Mediator of RNA polymerase II transcription subunit 1
  • Vitamin D3 receptor
KeywordsTRANSCRIPTION / Vitamin D3 / VDRE / RXR / co-factors / nuclear
Function / homology
Function and homology information


positive regulation of parathyroid hormone secretion / negative regulation of bone trabecula formation / Vitamin D (calciferol) metabolism / androgen biosynthetic process / regulation of RNA biosynthetic process / SUMOylation of intracellular receptors / retinal pigment epithelium development / Nuclear Receptor transcription pathway / thyroid hormone receptor signaling pathway / response to bile acid ...positive regulation of parathyroid hormone secretion / negative regulation of bone trabecula formation / Vitamin D (calciferol) metabolism / androgen biosynthetic process / regulation of RNA biosynthetic process / SUMOylation of intracellular receptors / retinal pigment epithelium development / Nuclear Receptor transcription pathway / thyroid hormone receptor signaling pathway / response to bile acid / dense fibrillar component / cellular response to vitamin D / positive regulation of apoptotic process involved in mammary gland involution / calcitriol binding / lithocholic acid binding / nuclear receptor-mediated bile acid signaling pathway / bile acid nuclear receptor activity / positive regulation of keratinocyte differentiation / ventricular trabecula myocardium morphogenesis / vitamin D binding / mediator complex / Generic Transcription Pathway / nuclear retinoic acid receptor binding / response to aldosterone / lens development in camera-type eye / cellular response to thyroid hormone stimulus / vitamin D receptor signaling pathway / positive regulation of vitamin D receptor signaling pathway / phosphate ion transmembrane transport / megakaryocyte development / negative regulation of ossification / nuclear vitamin D receptor binding / peroxisome proliferator activated receptor binding / intestinal absorption / nuclear thyroid hormone receptor binding / cellular response to steroid hormone stimulus / negative regulation of neuron differentiation / histone acetyltransferase binding / mammary gland branching involved in pregnancy / LBD domain binding / RSV-host interactions / decidualization / regulation of calcium ion transport / nuclear receptor-mediated steroid hormone signaling pathway / negative regulation of keratinocyte proliferation / keratinocyte differentiation / general transcription initiation factor binding / positive regulation of transcription initiation by RNA polymerase II / fat cell differentiation / nuclear retinoid X receptor binding / ubiquitin ligase complex / retinoic acid receptor signaling pathway / RNA polymerase II preinitiation complex assembly / erythrocyte development / intracellular receptor signaling pathway / Regulation of lipid metabolism by PPARalpha / heterochromatin / lactation / BMAL1:CLOCK,NPAS2 activates circadian expression / RORA,B,C and NR1D1 (REV-ERBA) regulate gene expression / Activation of gene expression by SREBF (SREBP) / Expression of BMAL (ARNTL), CLOCK, and NPAS2 / positive regulation of erythrocyte differentiation / T-tubule / cellular response to epidermal growth factor stimulus / animal organ morphogenesis / nuclear estrogen receptor binding / nuclear receptor binding / skeletal system development / apoptotic signaling pathway / transcription coregulator activity / Heme signaling / positive regulation of transcription elongation by RNA polymerase II / PPARA activates gene expression / promoter-specific chromatin binding / Transcriptional activation of mitochondrial biogenesis / Cytoprotection by HMOX1 / euchromatin / Nuclear Receptor transcription pathway / protein-DNA complex / Transcriptional regulation of white adipocyte differentiation / chromatin DNA binding / response to calcium ion / caveola / mRNA transcription by RNA polymerase II / cell morphogenesis / nuclear receptor activity / RNA polymerase II transcription regulator complex / transcription coactivator binding / cellular response to amyloid-beta / intracellular calcium ion homeostasis / nuclear matrix / calcium ion transport / transcription corepressor activity / response to estradiol / ubiquitin protein ligase activity / heart development / MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis / angiogenesis / Estrogen-dependent gene expression
Similarity search - Function
: / Mediator complex, subunit Med1 / Mediator of RNA polymerase II transcription subunit 1 / Vitamin D receptor / VDR, DNA-binding domain / : / Retinoid X Receptor / Retinoid X Receptor / Nuclear hormone receptor / Nuclear hormones receptors DNA-binding region signature. ...: / Mediator complex, subunit Med1 / Mediator of RNA polymerase II transcription subunit 1 / Vitamin D receptor / VDR, DNA-binding domain / : / Retinoid X Receptor / Retinoid X Receptor / Nuclear hormone receptor / Nuclear hormones receptors DNA-binding region signature. / Zinc finger, nuclear hormone receptor-type / Double treble clef zinc finger, C4 type / Nuclear hormone receptors DNA-binding domain profile. / c4 zinc finger in nuclear hormone receptors / Nuclear hormone receptor, ligand-binding domain / Nuclear hormone receptor-like domain superfamily / Ligand-binding domain of nuclear hormone receptor / Nuclear receptor (NR) ligand-binding (LBD) domain profile. / Ligand binding domain of hormone receptors / Zinc finger, NHR/GATA-type / Orthogonal Bundle / Mainly Alpha
Similarity search - Domain/homology
Chem-YS2 / Vitamin D3 receptor / Mediator of RNA polymerase II transcription subunit 1
Similarity search - Component
Biological speciesRattus norvegicus (Norway rat)
Homo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.4 Å
AuthorsNakabayashi, M. / Yoshimoto, N. / Inaba, Y. / Itoh, T. / Ito, N. / Yamamoto, K.
CitationJournal: J.Med.Chem. / Year: 2012
Title: Butyl pocket formation in the vitamin d receptor strongly affects the agonistic or antagonistic behavior of ligands
Authors: Yoshimoto, N. / Sakamaki, Y. / Haeta, M. / Kato, A. / Inaba, Y. / Itoh, T. / Nakabayashi, M. / Ito, N. / Yamamoto, K.
History
DepositionApr 14, 2012Deposition site: PDBJ / Processing site: PDBJ
Revision 1.0May 23, 2012Provider: repository / Type: Initial release
Revision 1.1Mar 20, 2024Group: Data collection / Database references / Derived calculations
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / struct_ref_seq_dif / struct_site
Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession ..._database_2.pdbx_DOI / _database_2.pdbx_database_accession / _struct_ref_seq_dif.details / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

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Assembly

Deposited unit
A: Vitamin D3 receptor
C: 13-meric peptide from Mediator of RNA polymerase II transcription subunit 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)32,5403
Polymers32,1662
Non-polymers3751
Water72140
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area1030 Å2
ΔGint-9 kcal/mol
Surface area11250 Å2
MethodPISA
Unit cell
Length a, b, c (Å)152.988, 43.867, 42.428
Angle α, β, γ (deg.)90.00, 95.94, 90.00
Int Tables number5
Space group name H-MC121

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Components

#1: Protein Vitamin D3 receptor / VDR / 1 / 25-dihydroxyvitamin D3 receptor / Nuclear receptor subfamily 1 group I member 1


Mass: 30595.037 Da / Num. of mol.: 1 / Fragment: Ligand binding domain, residues 116-423 / Mutation: deletion mutant, residues 165-211
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Rattus norvegicus (Norway rat) / Gene: Vdr, Nr1i1 / Production host: Escherichia coli (E. coli) / References: UniProt: P13053
#2: Protein/peptide 13-meric peptide from Mediator of RNA polymerase II transcription subunit 1


Mass: 1570.898 Da / Num. of mol.: 1 / Fragment: DRIP205 NR2 BOX peptide, UNP residues 640-652 / Source method: obtained synthetically / Source: (synth.) Homo sapiens (human) / References: UniProt: Q15648
#3: Chemical ChemComp-YS2 / (1R,3R,7E,17beta)-17-[(2R)-5-hydroxypentan-2-yl]-2-methylidene-9,10-secoestra-5,7-diene-1,3-diol


Mass: 374.557 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C24H38O3
#4: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 40 / Source method: isolated from a natural source / Formula: H2O

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Experimental details

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Experiment

ExperimentMethod: X-RAY DIFFRACTION / Number of used crystals: 1

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Sample preparation

CrystalDensity Matthews: 2.2 Å3/Da / Density % sol: 44.12 %
Crystal growTemperature: 293 K / Method: vapor diffusion, hanging drop / pH: 7
Details: MOPS-Na, Na-Formate, PEG 4000, Ethyleneglycol, pH 7, VAPOR DIFFUSION, HANGING DROP, temperature 293.0K

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: Photon Factory / Beamline: BL-6A / Wavelength: 0.978 Å
DetectorType: ADSC QUANTUM 4 / Detector: CCD / Date: Feb 25, 2009
RadiationMonochromator: TRIANGULAR SI(111) / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.978 Å / Relative weight: 1
ReflectionResolution: 2.4→38.04 Å / Num. obs: 11168 / % possible obs: 99.5 % / Observed criterion σ(I): -3
Reflection shellResolution: 2.4→2.49 Å / % possible all: 99.6

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Processing

Software
NameVersionClassification
HKL-2000data collection
CNSrefinement
REFMAC5.5.0110refinement
HKL-2000data reduction
HKL-2000data scaling
CNSphasing
RefinementMethod to determine structure: MOLECULAR REPLACEMENT / Resolution: 2.4→38.04 Å / Cor.coef. Fo:Fc: 0.944 / Cor.coef. Fo:Fc free: 0.918 / Cross valid method: THROUGHOUT / ESU R: 0.487 / ESU R Free: 0.291 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
RfactorNum. reflection% reflectionSelection details
Rfree0.27302 528 4.8 %RANDOM
Rwork0.22516 ---
obs0.22736 10550 99.27 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å / Solvent model: MASK
Displacement parametersBiso mean: 76.029 Å2
Baniso -1Baniso -2Baniso -3
1--0.09 Å20 Å2-0.02 Å2
2--0.1 Å20 Å2
3----0.01 Å2
Refinement stepCycle: LAST / Resolution: 2.4→38.04 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms1932 0 27 40 1999
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0140.0222001
X-RAY DIFFRACTIONr_bond_other_d
X-RAY DIFFRACTIONr_angle_refined_deg1.4621.9962718
X-RAY DIFFRACTIONr_angle_other_deg
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.5925245
X-RAY DIFFRACTIONr_dihedral_angle_2_deg38.41425.0683
X-RAY DIFFRACTIONr_dihedral_angle_3_deg19.69615345
X-RAY DIFFRACTIONr_dihedral_angle_4_deg12.518157
X-RAY DIFFRACTIONr_chiral_restr0.0870.2317
X-RAY DIFFRACTIONr_gen_planes_refined0.0080.0211474
X-RAY DIFFRACTIONr_gen_planes_other
X-RAY DIFFRACTIONr_nbd_refined
X-RAY DIFFRACTIONr_nbd_other
X-RAY DIFFRACTIONr_nbtor_refined
X-RAY DIFFRACTIONr_nbtor_other
X-RAY DIFFRACTIONr_xyhbond_nbd_refined
X-RAY DIFFRACTIONr_xyhbond_nbd_other
X-RAY DIFFRACTIONr_metal_ion_refined
X-RAY DIFFRACTIONr_metal_ion_other
X-RAY DIFFRACTIONr_symmetry_vdw_refined
X-RAY DIFFRACTIONr_symmetry_vdw_other
X-RAY DIFFRACTIONr_symmetry_hbond_refined
X-RAY DIFFRACTIONr_symmetry_hbond_other
X-RAY DIFFRACTIONr_symmetry_metal_ion_refined
X-RAY DIFFRACTIONr_symmetry_metal_ion_other
X-RAY DIFFRACTIONr_mcbond_it4.0771.51244
X-RAY DIFFRACTIONr_mcbond_other
X-RAY DIFFRACTIONr_mcangle_it5.90922011
X-RAY DIFFRACTIONr_scbond_it4.0933757
X-RAY DIFFRACTIONr_scangle_it6.6894.5707
X-RAY DIFFRACTIONr_rigid_bond_restr
X-RAY DIFFRACTIONr_sphericity_free
X-RAY DIFFRACTIONr_sphericity_bonded
LS refinement shellResolution: 2.4→2.462 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.402 47 -
Rwork0.341 752 -
obs--98.89 %

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