[English] 日本語
Yorodumi
- PDB-3ofs: Dynamic conformations of the CD38-mediated NAD cyclization captur... -

+
Open data


ID or keywords:

Loading...

-
Basic information

Entry
Database: PDB / ID: 3ofs
TitleDynamic conformations of the CD38-mediated NAD cyclization captured using multi-copy crystallography
ComponentsADP-ribosyl cyclase 1Cyclic ADP-ribose
KeywordsHYDROLASE / CD38 / cyclization / hydrolysis / cADPR / ADPR / ara-2'F-NAD / ara-2'F-ADPR
Function / homology
Function and homology information


2'-phospho-ADP-ribosyl cyclase/2'-phospho-cyclic-ADP-ribose transferase / phosphorus-oxygen lyase activity / artery smooth muscle contraction / Nicotinate metabolism / NAD+ nucleosidase activity / ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase / NAD metabolic process / NAD+ nucleotidase, cyclic ADP-ribose generating / NADP+ nucleosidase activity / negative regulation of bone resorption ...2'-phospho-ADP-ribosyl cyclase/2'-phospho-cyclic-ADP-ribose transferase / phosphorus-oxygen lyase activity / artery smooth muscle contraction / Nicotinate metabolism / NAD+ nucleosidase activity / ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase / NAD metabolic process / NAD+ nucleotidase, cyclic ADP-ribose generating / NADP+ nucleosidase activity / negative regulation of bone resorption / response to hydroperoxide / long-term synaptic depression / Hydrolases; Glycosylases; Hydrolysing N-glycosyl compounds / B cell proliferation / response to retinoic acid / positive regulation of B cell proliferation / positive regulation of vasoconstriction / response to interleukin-1 / response to progesterone / female pregnancy / apoptotic signaling pathway / B cell receptor signaling pathway / positive regulation of insulin secretion / negative regulation of neuron projection development / response to estradiol / positive regulation of cytosolic calcium ion concentration / transferase activity / positive regulation of cell growth / basolateral plasma membrane / response to hypoxia / response to xenobiotic stimulus / negative regulation of DNA-templated transcription / negative regulation of apoptotic process / positive regulation of DNA-templated transcription / cell surface / signal transduction / extracellular exosome / membrane / identical protein binding / plasma membrane
Similarity search - Function
ADP Ribosyl Cyclase; Chain A, domain 1 / ADP Ribosyl Cyclase; Chain A, domain 1 / ADP-ribosyl cyclase (CD38/157) / ADP-ribosyl cyclase / NAD(P)-binding Rossmann-like Domain / Up-down Bundle / Rossmann fold / 3-Layer(aba) Sandwich / Mainly Alpha / Alpha Beta
Similarity search - Domain/homology
Chem-AVU / ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1
Similarity search - Component
Biological speciesHomo sapiens (human)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 2.2 Å
AuthorsZhang, H. / Lee, H.C. / Hao, Q.
CitationJournal: J.Mol.Biol. / Year: 2011
Title: Dynamic Conformations of the CD38-Mediated NAD Cyclization Captured in a Single Crystal
Authors: Zhang, H. / Graeff, R. / Chen, Z. / Zhang, L.R. / Zhang, L.H. / Lee, H.C. / Hao, Q.
History
DepositionAug 16, 2010Deposition site: RCSB / Processing site: PDBJ
Revision 1.0Dec 15, 2010Provider: repository / Type: Initial release
Revision 1.1Jul 13, 2011Group: Version format compliance
Revision 1.2Nov 8, 2017Group: Refinement description / Category: software
Revision 1.3Nov 1, 2023Group: Data collection / Database references ...Data collection / Database references / Derived calculations / Refinement description
Category: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model / struct_conn / 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_conn.pdbx_leaving_atom_flag / _struct_ref_seq_dif.details / _struct_site.pdbx_auth_asym_id / _struct_site.pdbx_auth_comp_id / _struct_site.pdbx_auth_seq_id

-
Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

Downloads & links

-
Assembly

Deposited unit
A: ADP-ribosyl cyclase 1
B: ADP-ribosyl cyclase 1
C: ADP-ribosyl cyclase 1
D: ADP-ribosyl cyclase 1
E: ADP-ribosyl cyclase 1
F: ADP-ribosyl cyclase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)181,80012
Polymers178,5286
Non-polymers3,2726
Water7,062392
1
A: ADP-ribosyl cyclase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)30,3002
Polymers29,7551
Non-polymers5451
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
2
B: ADP-ribosyl cyclase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)30,3002
Polymers29,7551
Non-polymers5451
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
3
C: ADP-ribosyl cyclase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)30,3002
Polymers29,7551
Non-polymers5451
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
4
D: ADP-ribosyl cyclase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)30,3002
Polymers29,7551
Non-polymers5451
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
5
E: ADP-ribosyl cyclase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)30,3002
Polymers29,7551
Non-polymers5451
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
6
F: ADP-ribosyl cyclase 1
hetero molecules


Theoretical massNumber of molelcules
Total (without water)30,3002
Polymers29,7551
Non-polymers5451
Water181
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
MethodPISA
Unit cell
Length a, b, c (Å)56.655, 146.662, 191.086
Angle α, β, γ (deg.)90.000, 90.000, 90.000
Int Tables number19
Space group name H-MP212121

-
Components

#1: Protein
ADP-ribosyl cyclase 1 / Cyclic ADP-ribose / CD38 / Cyclic ADP-ribose hydrolase 1 / cADPr hydrolase 1 / T10


Mass: 29754.703 Da / Num. of mol.: 6 / Fragment: extracellular domain, residues 46-300 / Mutation: Q49T, N100D, E146A, N164D, N209D, N219D
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) Homo sapiens (human) / Gene: CD38 / Plasmid: pPICZalpha / Production host: Pichia pastoris (fungus) / Strain (production host): X33 / References: UniProt: P28907, NAD+ glycohydrolase
#2: Chemical
ChemComp-AVU / [(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl [(2R,3R,4R)-4-fluoro-3-hydroxytetrahydrofuran-2-yl]methyl dihydrogen diphosphate / arabinosyl-2-fluoro-deoxy-adenosine diphosphate ribose, ara-2'F-ADPR


Mass: 545.307 Da / Num. of mol.: 6 / Source method: obtained synthetically / Formula: C15H22FN5O12P2
#3: Water ChemComp-HOH / water / Water


Mass: 18.015 Da / Num. of mol.: 392 / Source method: isolated from a natural source / Formula: H2O

-
Experimental details

-
Experiment

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

-
Sample preparation

CrystalDensity Matthews: 2.22 Å3/Da / Density % sol: 44.68 % / Mosaicity: 0.516 °
Crystal growTemperature: 298 K / Method: vapor diffusion, hanging drop / pH: 4
Details: 0.1M sodium acetate pH 4.0, 15% PEG 4000, 0.2M ammonium acetate, 3% isopropanol, vapor diffusion, hanging drop, temperature 298K

-
Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: SSRF / Beamline: BL17U / Wavelength: 0.97623 Å
DetectorType: RAYONIX MX-225 / Detector: CCD / Date: Jul 16, 2009
RadiationProtocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.97623 Å / Relative weight: 1
ReflectionResolution: 2.2→100 Å / Num. obs: 79445 / % possible obs: 97.7 % / Redundancy: 7.1 % / Rmerge(I) obs: 0.095 / Χ2: 1.247 / Net I/σ(I): 12.6
Reflection shell
Resolution (Å)Redundancy (%)Rmerge(I) obsNum. unique allΧ2% possible all
2.2-2.284.60.35472080.92789.9
2.28-2.375.10.31576130.97395
2.37-2.485.70.29977491.00496.7
2.48-2.616.40.24779431.0798.6
2.61-2.777.10.21480171.199.3
2.77-2.997.70.17780571.07699.5
2.99-3.2980.12980471.08899.7
3.29-3.768.40.181641.38699.7
3.76-4.748.70.0881951.71499.6
4.74-1008.40.0684521.58298.6

-
Processing

Software
NameVersionClassificationNB
DENZOdata reduction
SCALEPACKdata scaling
REFMACrefinement
PDB_EXTRACT3.1data extraction
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: PDB ENTRY 1YH3
Resolution: 2.2→48.73 Å / Cor.coef. Fo:Fc: 0.949 / Cor.coef. Fo:Fc free: 0.922 / WRfactor Rfree: 0.2579 / WRfactor Rwork: 0.2077 / Occupancy max: 1 / Occupancy min: 1 / FOM work R set: 0.8284 / SU B: 14.383 / SU ML: 0.17 / SU R Cruickshank DPI: 0.3024 / SU Rfree: 0.2246 / Cross valid method: THROUGHOUT / σ(F): 0 / ESU R Free: 0.225 / Stereochemistry target values: MAXIMUM LIKELIHOOD
Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS U VALUES
RfactorNum. reflection% reflectionSelection details
Rfree0.2496 3969 5 %RANDOM
Rwork0.2033 ---
obs0.2057 79380 97.25 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.4 Å / Solvent model: BABINET MODEL WITH MASK
Displacement parametersBiso max: 69.13 Å2 / Biso mean: 47.9 Å2 / Biso min: 2 Å2
Baniso -1Baniso -2Baniso -3
1-0.59 Å20 Å20 Å2
2--1.99 Å20 Å2
3----2.58 Å2
Refinement stepCycle: LAST / Resolution: 2.2→48.73 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms11346 0 210 392 11948
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0090.02211898
X-RAY DIFFRACTIONr_bond_other_d0.0010.028047
X-RAY DIFFRACTIONr_angle_refined_deg1.171.95416190
X-RAY DIFFRACTIONr_angle_other_deg0.8223.00119431
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.50151396
X-RAY DIFFRACTIONr_dihedral_angle_2_deg37.47624.007554
X-RAY DIFFRACTIONr_dihedral_angle_3_deg13.316152003
X-RAY DIFFRACTIONr_dihedral_angle_4_deg15.111573
X-RAY DIFFRACTIONr_chiral_restr0.0680.21774
X-RAY DIFFRACTIONr_gen_planes_refined0.0050.02112881
X-RAY DIFFRACTIONr_gen_planes_other0.0010.022398
X-RAY DIFFRACTIONr_mcbond_it0.4451.57026
X-RAY DIFFRACTIONr_mcbond_other0.0951.52800
X-RAY DIFFRACTIONr_mcangle_it0.861211436
X-RAY DIFFRACTIONr_scbond_it1.48934872
X-RAY DIFFRACTIONr_scangle_it2.3464.54754
LS refinement shellResolution: 2.202→2.259 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.321 246 -
Rwork0.24 4700 -
all-4946 -
obs--82.99 %
Refinement TLS params.

Method: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
14.1006-0.0154-1.10572.73570.50255.7186-0.1521-0.2644-0.0530.068-0.05080.1387-0.5105-0.15580.2030.101-0.0376-0.04880.24270.01570.1738-38.6514.913-1.408
26.7477-5.8977-2.161911.81872.00966.2358-0.31470.0563-1.00340.6128-0.08571.06190.5519-0.80790.40030.2381-0.04720.05020.30680.02810.3303-30.82-3.48817.513
33.84570.93630.77832.4390.83247.7982-0.21860.2132-0.3484-0.0326-0.0288-0.3276-0.09870.57430.24750.0481-0.0799-0.00010.23980.03570.2129-30.5051.847-3.365
46.5454-1.86110.7198.1455-0.45554.3828-0.2795-0.0917-0.26530.15230.0071-0.5074-0.04310.46560.27250.1179-0.0185-0.00130.30120.10310.1991-17.437-1.63818.238
54.4481-0.97990.77872.9294-0.34666.9934-0.01910.25380.0649-0.2392-0.10940.3313-0.0361-1.00710.12860.17270.0482-0.00520.33230.00670.2597-10.19218.143.348
65.51984.68672.25067.2766-0.94877.4089-0.44930.14420.80420.01910.13481.0096-1.2724-0.75350.31450.4484-0.0121-0.09230.31510.05160.2911-1.79526.537-15.96
73.365-0.6067-0.93892.55021.12189.3361-0.0015-0.08550.3401-0.0579-0.0679-0.2124-0.6395-0.03780.06930.20440.0363-0.00830.10930.03960.1994-2.19421.2345.252
83.64021.6777-0.58288.7669-3.32826.5228-0.2365-0.09550.07080.0675-0.3721-0.6933-0.45390.90650.60850.2276-0.1648-0.08210.35520.12340.210711.45524.224-16.618
95.5780.0679-1.1044.10131.30994.7494-0.15610.1413-0.00280.0288-0.01680.043-0.4179-0.09270.17290.1748-0.0235-0.01290.0965-0.03690.2065-8.56422.961-46.745
108.0121.08362.02435.9984-0.4763.358-0.2468-0.53090.52530.3195-0.01670.6666-0.2348-0.84370.26350.157-0.0220.04180.2796-0.05010.2538-18.75713.114-30.447
114.2272-1.67610.24843.40930.17888.9657-0.14350.7471-0.5737-0.3527-0.13260.25080.1751-0.41760.27610.0838-0.06640.02480.204-0.13080.2692-10.73715.782-51.804
125.18431.0418-1.28833.6342-0.67262.9745-0.1564-0.052-0.3638-0.0406-0.0957-0.08660.3393-0.47110.25210.1783-0.10860.03650.1906-0.04640.2149-14.3710.108-29.302
134.11270.5008-2.19893.8674-1.81537.73160.29340.0910.267-0.2088-0.181-0.1289-0.5153-0.0604-0.11240.20910.0210.07990.01330.00790.2189.062-0.112-46.183
1411.87470.54370.39843.68852.05062.6662-0.17410.60590.7099-0.1170.1419-0.522-0.25830.78210.03230.3003-0.0150.04560.3870.16930.268819.512-9.8-62.944
152.88531.5989-1.71192.3742-0.419612.4418-0.0146-0.2848-0.20560.102-0.1875-0.28040.62720.45370.20220.16270.04850.06210.04630.05350.199611.352-7.345-41.29
166.6643-1.5772-1.67963.29560.48254.751-0.27370.0799-0.90070.3504-0.01710.24050.61570.02450.29090.33730.02120.09350.0670.03770.277514.399-22.658-63.747
176.32750.75570.73524.5859-1.13746.5853-0.35320.41140.1865-0.36360.25350.25720.6283-0.92150.09960.1426-0.16010.00760.2644-0.03440.1452-10.843-29.9383.017
187.01326.4909-1.600313.72261.82445.0155-0.22670.8281.0067-0.79960.27840.97140.2326-1.5072-0.05170.2814-0.2314-0.08610.62760.13810.2544-2.821-20.603-15.782
195.46071.1164-0.61564.4122-2.66712.2638-0.5307-0.03270.4001-0.06090.1978-0.33810.16570.0080.33290.0898-0.0386-0.02670.0727-0.05670.1716-3.06-26.8725.295
203.27931.1143-1.7116.4371.19896.161-0.20450.179-0.0725-0.09670.065-0.34090.6556-0.19760.13950.1934-0.1118-0.01910.2110.02770.124410.364-23.01-16.391
212.9360.00210.13767.68253.931810.4451-0.006-0.12760.30210.1834-0.48180.3316-1.0141-0.5930.48770.34530.0482-0.07970.0777-0.04010.2727-11.808-24.097-50.034
223.12470.93190.995512.63913.269510.3454-0.035-0.0328-0.03750.1347-0.2577-0.4537-0.67560.57230.29270.1668-0.0897-0.05150.06580.06310.185-1.693-29.099-50.422
231.61213.913-3.285610.2542-9.02958.16980.6017-0.14650.47772.13220.14260.9805-2.0842-0.4671-0.74430.99340.170.18320.5073-0.25890.2974-16.082-32.643-35.674
249.30561.41321.531913.5952.4416.76350.22130.4155-0.4093-0.1929-0.43350.26350.2991-0.25010.21220.2566-0.0056-0.04730.1407-0.06440.1686-10.12-34.839-60.724
251.69112.3496-4.30614.7837-6.429111.11180.0065-0.2083-0.3020.4233-0.7132-0.2724-0.11330.6950.70670.2461-0.12050.00460.2476-0.04090.2143-9.8-42.617-37.675
2610.75680.5606-0.30234.6756-1.63069.4731-0.0586-0.3021-0.58060.2333-0.20870.13820.0579-0.10680.26740.3231-0.1290.14690.1287-0.10780.1671-18.204-50.689-27.567
Refinement TLS group
IDRefine-IDRefine TLS-IDAuth asym-IDAuth seq-ID
1X-RAY DIFFRACTION1A46 - 114
2X-RAY DIFFRACTION2A115 - 145
3X-RAY DIFFRACTION3A146 - 194
4X-RAY DIFFRACTION4A195 - 281
5X-RAY DIFFRACTION5B46 - 114
6X-RAY DIFFRACTION6B115 - 144
7X-RAY DIFFRACTION7B145 - 194
8X-RAY DIFFRACTION8B195 - 281
9X-RAY DIFFRACTION9C46 - 115
10X-RAY DIFFRACTION10C116 - 147
11X-RAY DIFFRACTION11C148 - 192
12X-RAY DIFFRACTION12C193 - 281
13X-RAY DIFFRACTION13D46 - 116
14X-RAY DIFFRACTION14D117 - 147
15X-RAY DIFFRACTION15D148 - 192
16X-RAY DIFFRACTION16D193 - 280
17X-RAY DIFFRACTION17E46 - 114
18X-RAY DIFFRACTION18E115 - 144
19X-RAY DIFFRACTION19E145 - 192
20X-RAY DIFFRACTION20E193 - 281
21X-RAY DIFFRACTION21F46 - 81
22X-RAY DIFFRACTION22F82 - 114
23X-RAY DIFFRACTION23F115 - 159
24X-RAY DIFFRACTION24F160 - 179
25X-RAY DIFFRACTION25F180 - 235
26X-RAY DIFFRACTION26F236 - 280

+
About Yorodumi

-
News

-
Feb 9, 2022. New format data for meta-information of EMDB entries

New format data for meta-information of EMDB entries

  • Version 3 of the EMDB header file is now the official format.
  • The previous official version 1.9 will be removed from the archive.

Related info.:EMDB header

External links:wwPDB to switch to version 3 of the EMDB data model

-
Aug 12, 2020. Covid-19 info

Covid-19 info

URL: https://pdbj.org/emnavi/covid19.php

New page: Covid-19 featured information page in EM Navigator.

Related info.:Covid-19 info / Mar 5, 2020. Novel coronavirus structure data

+
Mar 5, 2020. Novel coronavirus structure data

Novel coronavirus structure data

Related info.:Yorodumi Speices / Aug 12, 2020. Covid-19 info

External links:COVID-19 featured content - PDBj / Molecule of the Month (242):Coronavirus Proteases

+
Jan 31, 2019. EMDB accession codes are about to change! (news from PDBe EMDB page)

EMDB accession codes are about to change! (news from PDBe EMDB page)

  • The allocation of 4 digits for EMDB accession codes will soon come to an end. Whilst these codes will remain in use, new EMDB accession codes will include an additional digit and will expand incrementally as the available range of codes is exhausted. The current 4-digit format prefixed with “EMD-” (i.e. EMD-XXXX) will advance to a 5-digit format (i.e. EMD-XXXXX), and so on. It is currently estimated that the 4-digit codes will be depleted around Spring 2019, at which point the 5-digit format will come into force.
  • The EM Navigator/Yorodumi systems omit the EMD- prefix.

Related info.:Q: What is EMD? / ID/Accession-code notation in Yorodumi/EM Navigator

External links:EMDB Accession Codes are Changing Soon! / Contact to PDBj

+
Jul 12, 2017. Major update of PDB

Major update of PDB

  • wwPDB released updated PDB data conforming to the new PDBx/mmCIF dictionary.
  • This is a major update changing the version number from 4 to 5, and with Remediation, in which all the entries are updated.
  • In this update, many items about electron microscopy experimental information are reorganized (e.g. em_software).
  • Now, EM Navigator and Yorodumi are based on the updated data.

External links:wwPDB Remediation / Enriched Model Files Conforming to OneDep Data Standards Now Available in the PDB FTP Archive

-
Yorodumi

Thousand views of thousand structures

  • Yorodumi is a browser for structure data from EMDB, PDB, SASBDB, etc.
  • This page is also the successor to EM Navigator detail page, and also detail information page/front-end page for Omokage search.
  • The word "yorodu" (or yorozu) is an old Japanese word meaning "ten thousand". "mi" (miru) is to see.

Related info.:EMDB / PDB / SASBDB / Comparison of 3 databanks / Yorodumi Search / Aug 31, 2016. New EM Navigator & Yorodumi / Yorodumi Papers / Jmol/JSmol / Function and homology information / Changes in new EM Navigator and Yorodumi

Read more