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- PDB-3i9l: Crystal structure of ADP ribosyl cyclase complexed with N1-cIDPR -

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Basic information

Entry
Database: PDB / ID: 3i9l
TitleCrystal structure of ADP ribosyl cyclase complexed with N1-cIDPR
ComponentsADP-ribosyl cyclase
KeywordsHYDROLASE / Homodimer / enzyme-product analog complex / ADP-ribosyl cyclase / Disulfide bond / Fertilization / NAD
Function / homology
Function and homology information


2'-phospho-ADP-ribosyl cyclase/2'-phospho-cyclic-ADP-ribose transferase / phosphorus-oxygen lyase activity / NAD+ nucleosidase activity / NAD+ nucleotidase, cyclic ADP-ribose generating / Hydrolases; Glycosylases; Hydrolysing N-glycosyl compounds / single fertilization / positive regulation of B cell proliferation / transferase activity / cytoplasmic vesicle / 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
N1-CYCLIC INOSINE 5'-DIPHOSPHORIBOSE / ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase
Similarity search - Component
Biological speciesAPLYSIA CALIFORNICA (California sea hare)
MethodX-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.75 Å
AuthorsLiu, Q. / Graeff, R. / Kriksunov, I.A. / Jiang, H. / Zhang, B. / Oppenheimer, N. / Lin, H. / Potter, B.V.L. / Lee, H.C. / Hao, Q.
CitationJournal: J.Biol.Chem. / Year: 2009
Title: Structural basis for enzymatic evolution from a dedicated ADP-ribosyl cyclase to a multifunctional NAD hydrolase
Authors: Liu, Q. / Graeff, R. / Kriksunov, I.A. / Jiang, H. / Zhang, B. / Oppenheimer, N. / Lin, H. / Potter, B.V.L. / Lee, H.C. / Hao, Q.
History
DepositionJul 12, 2009Deposition site: RCSB / Processing site: PDBJ
Revision 1.0Jul 28, 2009Provider: repository / Type: Initial release
Revision 1.1Jul 13, 2011Group: Advisory / Version format compliance
Revision 1.2Nov 10, 2021Group: Database references / Derived calculations / Category: 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
Revision 1.3Nov 1, 2023Group: Data collection / Refinement description
Category: chem_comp_atom / chem_comp_bond / pdbx_initial_refinement_model
Revision 1.4Oct 30, 2024Group: Structure summary / Category: pdbx_entry_details / pdbx_modification_feature

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Structure visualization

Structure viewerMolecule:
MolmilJmol/JSmol

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Assembly

Deposited unit
A: ADP-ribosyl cyclase
B: ADP-ribosyl cyclase
hetero molecules


Theoretical massNumber of molelcules
Total (without water)59,5583
Polymers59,0162
Non-polymers5421
Water11,079615
1


  • Idetical with deposited unit
  • defined by author&software
TypeNameSymmetry operationNumber
identity operation1_555x,y,z1
Buried area3570 Å2
ΔGint-13 kcal/mol
Surface area22950 Å2
MethodPISA
Unit cell
Length a, b, c (Å)69.627, 58.303, 71.651
Angle α, β, γ (deg.)90.00, 101.37, 90.00
Int Tables number4
Space group name H-MP1211

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Components

#1: Protein ADP-ribosyl cyclase / ADRC / NAD(+) nucleosidase / NADase / NAD glycohydrolase


Mass: 29507.883 Da / Num. of mol.: 2 / Mutation: E179G
Source method: isolated from a genetically manipulated source
Source: (gene. exp.) APLYSIA CALIFORNICA (California sea hare)
Plasmid: PPICZ(ALPHA)A / Production host: Pichia Pastoris (fungus) / Strain (production host): X-33 (INVITROGEN) / References: UniProt: P29241, NAD+ glycohydrolase
#2: Chemical ChemComp-N1C / N1-CYCLIC INOSINE 5'-DIPHOSPHORIBOSE


Mass: 542.285 Da / Num. of mol.: 1 / Source method: obtained synthetically / Formula: C15H20N4O14P2
#3: Water ChemComp-HOH / water


Mass: 18.015 Da / Num. of mol.: 615 / Source method: isolated from a natural source / Formula: H2O
Has protein modificationY

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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: 2.42 Å3/Da / Density % sol: 49.09 %
Crystal growTemperature: 298 K / Method: vapor diffusion, hanging drop / pH: 7.5
Details: 0.1M imidazole, pH 7.5, 12-24% PEG 4000, VAPOR DIFFUSION, HANGING DROP, temperature 298K

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Data collection

DiffractionMean temperature: 100 K
Diffraction sourceSource: SYNCHROTRON / Site: CHESS / Beamline: A1 / Wavelength: 0.9771 Å
DetectorType: ADSC QUANTUM 210 / Detector: CCD / Date: Mar 31, 2007
RadiationMonochromator: Si 111 CHANNEL / Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray
Radiation wavelengthWavelength: 0.9771 Å / Relative weight: 1
ReflectionResolution: 1.75→30 Å / Num. all: 56813 / Num. obs: 56813 / % possible obs: 99.8 % / Observed criterion σ(F): 0 / Observed criterion σ(I): 0
Reflection shellResolution: 1.75→1.81 Å / % possible all: 97.7

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Processing

Software
NameVersionClassification
ADSCQuantumdata collection
MOLREPphasing
REFMAC5.4.0067refinement
HKL-2000data reduction
HKL-2000data scaling
RefinementMethod to determine structure: MOLECULAR REPLACEMENT
Starting model: PDB ENTRY 1LBE

1lbe


Resolution: 1.75→20 Å / Cor.coef. Fo:Fc: 0.963 / Cor.coef. Fo:Fc free: 0.952 / Occupancy max: 1 / Occupancy min: 1 / SU B: 4.045 / SU ML: 0.068 / TLS residual ADP flag: LIKELY RESIDUAL / Cross valid method: THROUGHOUT / σ(F): 0 / σ(I): 0 / ESU R: 0.108 / ESU R Free: 0.103 / Stereochemistry target values: MAXIMUM LIKELIHOOD / Details: HYDROGENS HAVE BEEN ADDED IN THE RIDING POSITIONS
RfactorNum. reflection% reflectionSelection details
Rfree0.19634 2873 5.1 %RANDOM
Rwork0.16564 53804 --
all0.16725 ---
obs0.16725 56677 100 %-
Solvent computationIon probe radii: 0.8 Å / Shrinkage radii: 0.8 Å / VDW probe radii: 1.2 Å / Solvent model: BABINET MODEL WITH MASK
Displacement parametersBiso max: 65.56 Å2 / Biso mean: 25.496 Å2 / Biso min: 13.65 Å2
Baniso -1Baniso -2Baniso -3
1--0.19 Å20 Å2-0.09 Å2
2--0.04 Å20 Å2
3---0.11 Å2
Refinement stepCycle: LAST / Resolution: 1.75→20 Å
ProteinNucleic acidLigandSolventTotal
Num. atoms4014 0 35 615 4664
Refine LS restraints
Refine-IDTypeDev idealDev ideal targetNumber
X-RAY DIFFRACTIONr_bond_refined_d0.0160.0224168
X-RAY DIFFRACTIONr_angle_refined_deg1.9711.9715660
X-RAY DIFFRACTIONr_dihedral_angle_1_deg5.9335500
X-RAY DIFFRACTIONr_dihedral_angle_2_deg28.84423.505194
X-RAY DIFFRACTIONr_dihedral_angle_3_deg14.11615696
X-RAY DIFFRACTIONr_dihedral_angle_4_deg20.7141528
X-RAY DIFFRACTIONr_chiral_restr0.2120.2598
X-RAY DIFFRACTIONr_gen_planes_refined0.0090.0213183
X-RAY DIFFRACTIONr_mcbond_it0.8871.52506
X-RAY DIFFRACTIONr_mcangle_it1.69724040
X-RAY DIFFRACTIONr_scbond_it2.91231662
X-RAY DIFFRACTIONr_scangle_it4.6444.51617
LS refinement shellResolution: 1.75→1.795 Å / Total num. of bins used: 20
RfactorNum. reflection% reflection
Rfree0.227 216 -
Rwork0.196 3719 -
all-3935 -
obs--100 %
Refinement TLS params.

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

IDL11 (°2)L12 (°2)L13 (°2)L22 (°2)L23 (°2)L33 (°2)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T11 (Å2)T12 (Å2)T13 (Å2)T22 (Å2)T23 (Å2)T33 (Å2)Origin x (Å)Origin y (Å)Origin z (Å)
11.18390.708-0.40141.0896-0.48310.5166-0.00530.0952-0.036-0.0391-0.00850.1605-0.0072-0.08020.0138-0.04110.0193-0.0221-0.0234-0.0282-0.0684-11.4641.39215.528
21.0333-0.36290.46141.1236-0.88091.2514-0.00350.0761-0.0501-0.0192-0.0316-0.06330.04530.04430.0352-0.08890.0028-0.004-0.1008-0.0151-0.069518.006-1.10124.546
Refinement TLS group
IDRefine-IDRefine TLS-IDAuth asym-IDAuth seq-ID
1X-RAY DIFFRACTION1A1 - 250
2X-RAY DIFFRACTION2B1 - 250

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