data_bmst000002 save_entry_information _Entry.Sf_category entry_information _Entry.Sf_framecode entry_information _Entry.ID bmst000002 _Entry.Title 2_deoxyguanosine _Entry.Version_type update _Entry.Submission_date 2006-02-23 _Entry.Accession_date 2006-02-23 _Entry.Last_release_date 2011-09-14 _Entry.Original_release_date 2006-02-23 _Entry.Origination author _Entry.NMR_STAR_version 3.1.1.7 _Entry.Original_NMR_STAR_version 'NMR STAR v3.1' _Entry.Experimental_method NMR _Entry.Experimental_method_subtype theoretical _Entry.Details ? _Entry.BMRB_internal_directory_name 2_deoxyguanosine loop_ _Entry_author.Ordinal _Entry_author.Given_name _Entry_author.Family_name _Entry_author.Middle_initials _Entry_author.Family_title _Entry_author.Entry_ID 1 William Westler M. ? bmst000002 2 John Markley L. ? bmst000002 stop_ loop_ _Entry_src.ID _Entry_src.Project_name _Entry_src.Organization_full_name _Entry_src.Organization_initials _Entry_src.Entry_ID 1 metabolics "Madison Metabolomics Consortium" MMC bmst000002 stop_ loop_ _Data_set.Type _Data_set.Count _Data_set.Entry_ID other_data_list 1 bmst000002 stop_ loop_ _Datum.Type _Datum.Count _Datum.Entry_ID "theoretical chemical shifts" 1 bmst000002 stop_ loop_ _Release.Release_number _Release.Date _Release.Submission_date _Release.Type _Release.Author _Release.Detail _Release.Entry_ID 1 2006-02-23 2006-02-23 original BMRB "Original theoretical calculations from NMRFAM" bmst000002 2 2008-11-20 2008-11-20 update BMRB "updated the file to match latest NMR STAR dictionary" bmst000002 3 2008-11-25 2008-11-25 update BMRB "fixed enumerations: N should be no" bmst000002 4 2010-09-16 2010-09-16 update BMRB "Removed Shielding_tensor_list_ID and Shielding_tensor_list_label from theoretical_chem_shifts" bmst000002 5 2011-09-14 2011-09-14 update BMRB "Partially brought up to date with latest Dictionary" bmst000002 stop_ save_ save_citations _Citation.Sf_category citations _Citation.Sf_framecode citations _Citation.Entry_ID bmst000002 _Citation.ID 1 _Citation.Class 'reference citation' _Citation.PubMed_ID 18940862 _Citation.Title 'Database resources of the National Center for Biotechnology Information.' _Citation.Status published _Citation.Type internet _Citation.WWW_URL http://pubchem.ncbi.nlm.nih.gov/ _Citation.Year 2006 _Citation.Details ? loop_ _Citation_author.Ordinal _Citation_author.Given_name _Citation_author.Family_name _Citation_author.First_initial _Citation_author.Middle_initials _Citation_author.Family_title _Citation_author.Entry_ID _Citation_author.Citation_ID 1 D. Wheeler D. L. ? bmst000002 1 2 T. Barrett T. ? ? bmst000002 1 3 D. Benson D. A. ? bmst000002 1 4 S. Bryant S. H. ? bmst000002 1 5 K. Canese K. ? ? bmst000002 1 6 V. Chetvenin V. ? ? bmst000002 1 7 D. Church D. M. ? bmst000002 1 8 M. DiCuccio M. ? ? bmst000002 1 9 R. Edgar R. ? ? bmst000002 1 10 S. Federhen S. ? ? bmst000002 1 11 L. Geer L. Y. ? bmst000002 1 12 W. Helmberg W. ? ? bmst000002 1 13 Y. Kapustin Y. ? ? bmst000002 1 14 D. Kenton D. L. ? bmst000002 1 15 O. Khovayko O. ? ? bmst000002 1 16 D. Lipman D. J. ? bmst000002 1 17 T. Madden T. L. ? bmst000002 1 18 D. Maglott D. R. ? bmst000002 1 19 J. Ostell J. ? ? bmst000002 1 20 K. Pruitt K. D. ? bmst000002 1 21 G. Schuler G. D. ? bmst000002 1 22 L. Schriml L. M. ? bmst000002 1 23 E. Sequeira E. ? ? bmst000002 1 24 S. Sherry S. T. ? bmst000002 1 25 K. Sirotkin K. ? ? bmst000002 1 26 A. Souvorov A. ? ? bmst000002 1 27 G. Starchenko G. ? ? bmst000002 1 28 T. Suzek T. O. ? bmst000002 1 29 R. Tatusov R. ? ? bmst000002 1 30 T. Tatusova T. A. ? bmst000002 1 31 L. Bagner L. ? ? bmst000002 1 32 E. Yaschenko E. ? ? bmst000002 1 stop_ save_ save_assembly _Assembly.Sf_category assembly _Assembly.Sf_framecode assembly _Assembly.Entry_ID bmst000002 _Assembly.ID 1 _Assembly.Name ASSEMBLY_NAME _Assembly.Number_of_components 1 _Assembly.Organic_ligands 0 _Assembly.Metal_ions ? _Assembly.Non_standard_bonds no _Assembly.Paramagnetic no _Assembly.Thiol_state 'not reported' loop_ _Entity_assembly.ID _Entity_assembly.Entity_assembly_name _Entity_assembly.Entity_ID _Entity_assembly.Entity_label _Entity_assembly.Experimental_data_reported _Entity_assembly.Physical_state _Entity_assembly.Conformational_isomer _Entity_assembly.Chemical_exchange_state _Entity_assembly.Magnetic_equivalence_group_code _Entity_assembly.Role _Entity_assembly.Details _Entity_assembly.Entry_ID _Entity_assembly.Assembly_ID 1 ENT_NAME 1 $2_deoxyguanosine yes native no no ? ? ? bmst000002 1 stop_ save_ save_2_deoxyguanosine _Entity.Sf_category entity _Entity.Sf_framecode 2_deoxyguanosine _Entity.Entry_ID bmst000002 _Entity.ID 1 _Entity.BMRB_code ? _Entity.Name "2'-Deoxyguanosine" _Entity.Type non-polymer _Entity.Ambiguous_conformational_states no _Entity.Ambiguous_chem_comp_sites no _Entity.Nstd_monomer no _Entity.Nstd_chirality no _Entity.Nstd_linkage no _Entity.Paramagnetic no _Entity.Thiol_state 'not reported' loop_ _Entity_comp_index.ID _Entity_comp_index.Comp_ID _Entity_comp_index.Comp_label _Entity_comp_index.Entry_ID _Entity_comp_index.Entity_ID 1 1 $chem_comp_1 bmst000002 1 stop_ save_ save_chem_comp_1 _Chem_comp.Sf_category chem_comp _Chem_comp.Sf_framecode chem_comp_1 _Chem_comp.Entry_ID bmst000002 _Chem_comp.ID 1 _Chem_comp.Provenance PubChem _Chem_comp.Name "2'-Deoxyguanosine" _Chem_comp.Type non-polymer _Chem_comp.BMRB_code ? _Chem_comp.PDB_code ? _Chem_comp.InCHi_code ; InChI=1/C10H13N5O4/c11-10-13-8-7(9(18)14-10)12-3-15(8)6-1-4(17)5(2-16)19-6/h3-6,16-17H,1-2H2,(H3,11,13,14,18)/t4-,5+,6+/m0/s1/f/h13H,11H2 ; _Chem_comp.Mon_nstd_flag ? _Chem_comp.Std_deriv_one_letter_code ? _Chem_comp.Std_deriv_three_letter_code ? _Chem_comp.Std_deriv_BMRB_code ? _Chem_comp.Std_deriv_PDB_code ? _Chem_comp.Formal_charge ? _Chem_comp.Paramagnetic no _Chem_comp.Aromatic yes _Chem_comp.Formula 'C10 H13 N5 O4' _Chem_comp.Formula_weight 267.2413200000 _Chem_comp.Formula_mono_iso_wt_nat 267.096753932 _Chem_comp.Formula_mono_iso_wt_13C 277.13030231 _Chem_comp.Formula_mono_iso_wt_15N 272.081928398 _Chem_comp.Formula_mono_iso_wt_13C_15N 277.13030231 _Chem_comp.Image_file_name standards/2_deoxyguanosine/lit/3624.png _Chem_comp.Image_file_format png _Chem_comp.Topo_file_name ? _Chem_comp.Topo_file_format ? _Chem_comp.Struct_file_name standards/2_deoxyguanosine/lit/3624.mol _Chem_comp.Struct_file_format mol _Chem_comp.Stereochem_param_file_name ? _Chem_comp.Details ? _Chem_comp.DB_query_date ? _Chem_comp.DB_last_query_revised_last_date ? loop_ _Chem_comp_common_name.Name _Chem_comp_common_name.Type _Chem_comp_common_name.Entry_ID _Chem_comp_common_name.Comp_ID 961-07-9 synonym bmst000002 1 Deoxyguanosine synonym bmst000002 1 "2'-Deoxyguanosine" synonym bmst000002 1 stop_ loop_ _Chem_comp_systematic_name.Name _Chem_comp_systematic_name.Naming_system _Chem_comp_systematic_name.Entry_ID _Chem_comp_systematic_name.Comp_ID 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one IUPAC bmst000002 1 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-methylol-tetrahydrofuran-2-yl]-3H-purin-6-one IUPAC_TRADITIONAL bmst000002 1 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-3H-purin-6-one IUPAC_CAS bmst000002 1 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-3H-purin-6-one IUPAC_OPENEYE bmst000002 1 2-amino-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one IUPAC_SYSTEMATIC bmst000002 1 stop_ loop_ _Chem_comp_SMILES.Type _Chem_comp_SMILES.String _Chem_comp_SMILES.Entry_ID _Chem_comp_SMILES.Comp_ID Isomeric C1[C@@H]([C@H](O[C@H]1N2C=NC3=C2NC(=NC3=O)N)CO)O bmst000002 1 Canonical C1C(C(OC1N2C=NC3=C2NC(=NC3=O)N)CO)O bmst000002 1 stop_ loop_ _Chem_comp_atom.Atom_ID _Chem_comp_atom.Type_symbol _Chem_comp_atom.Stereo_config _Chem_comp_atom.Charge _Chem_comp_atom.Oxidation_number _Chem_comp_atom.Unpaired_electron_number _Chem_comp_atom.Drawing_2D_coord_x _Chem_comp_atom.Drawing_2D_coord_y _Chem_comp_atom.Model_Cartn_x _Chem_comp_atom.Model_Cartn_y _Chem_comp_atom.Model_Cartn_z _Chem_comp_atom.Entry_ID _Chem_comp_atom.Comp_ID O1 O ? ? ? ? 6.7577 3.2384 -1.822 1.870 1.761 bmst000002 1 O2 O ? ? ? ? 8.1552 1.8206 1.919 4.013 -0.460 bmst000002 1 O3 O ? ? ? ? 5.8055 0.7369 0.732 1.521 0.918 bmst000002 1 O4 O ? ? ? ? 4.2690 -3.8284 -0.297 -4.573 -0.888 bmst000002 1 N5 N ? ? ? ? 2.5369 -0.8284 -2.912 -1.550 1.428 bmst000002 1 N6 N ? ? ? ? 6.0812 -1.0237 1.344 -0.301 -0.407 bmst000002 1 N7 N ? ? ? ? 4.2690 -0.8284 -0.913 -0.785 0.519 bmst000002 1 N8 N ? ? ? ? 3.4030 -2.3284 -1.631 -3.043 0.194 bmst000002 1 N9 N ? ? ? ? 6.0812 -2.6332 1.787 -2.354 -1.225 bmst000002 1 C10 C ? ? ? ? 6.0873 2.4965 -1.411 2.642 0.633 bmst000002 1 C11 C ? ? ? ? 6.3919 -0.0732 1.513 1.128 -0.207 bmst000002 1 C12 C ? ? ? ? 6.3947 1.5449 0.109 2.794 0.684 bmst000002 1 C13 C ? ? ? ? 7.3452 1.2342 0.694 3.317 -0.647 bmst000002 1 C14 C ? ? ? ? 7.3435 0.2342 1.035 2.014 -1.368 bmst000002 1 C15 C ? ? ? ? 3.4030 -1.3284 -1.793 -1.849 0.668 bmst000002 1 C16 C ? ? ? ? 5.1350 -1.3284 0.258 -1.097 -0.132 bmst000002 1 C17 C ? ? ? ? 4.2690 -2.8284 -0.445 -3.433 -0.480 bmst000002 1 C18 C ? ? ? ? 5.1350 -2.3284 0.535 -2.350 -0.636 bmst000002 1 C19 C ? ? ? ? 6.6648 -1.8284 2.239 -1.140 -1.072 bmst000002 1 H20 H ? ? ? ? 6.5672 3.8284 -2.762 2.038 1.924 bmst000002 1 H21 H ? ? ? ? 8.7212 1.5674 1.751 4.799 0.085 bmst000002 1 H22 H ? ? ? ? 2.0000 -1.1384 -3.281 -0.613 1.327 bmst000002 1 H23 H ? ? ? ? 2.5369 -0.2084 -3.614 -2.278 1.363 bmst000002 1 H24 H ? ? ? ? 4.2690 -0.2084 -0.977 0.030 1.127 bmst000002 1 H25 H ? ? ? ? 5.7065 2.9857 -1.863 3.645 0.651 bmst000002 1 H26 H ? ? ? ? 5.5394 2.2063 -1.715 2.150 -0.303 bmst000002 1 H27 H ? ? ? ? 5.7794 -0.1691 2.576 1.302 -0.000 bmst000002 1 H28 H ? ? ? ? 5.7825 1.6429 0.376 3.445 1.526 bmst000002 1 H29 H ? ? ? ? 7.2493 1.8467 -0.031 3.932 -1.201 bmst000002 1 H30 H ? ? ? ? 7.4713 -0.3725 1.798 2.163 -2.135 bmst000002 1 H31 H ? ? ? ? 7.9602 0.2979 0.146 1.575 -1.832 bmst000002 1 H32 H ? ? ? ? 7.2848 -1.8284 3.203 -0.771 -1.401 bmst000002 1 stop_ loop_ _Atom_nomenclature.Atom_ID _Atom_nomenclature.Atom_name _Atom_nomenclature.Naming_system _Atom_nomenclature.Entry_ID _Atom_nomenclature.Comp_ID O1 O1 ? bmst000002 1 O2 O2 ? bmst000002 1 O3 O3 ? bmst000002 1 O4 O4 ? bmst000002 1 N5 N5 ? bmst000002 1 N6 N6 ? bmst000002 1 N7 N7 ? bmst000002 1 N8 N8 ? bmst000002 1 N9 N9 ? bmst000002 1 C10 C10 ? bmst000002 1 C11 C11 ? bmst000002 1 C12 C12 ? bmst000002 1 C13 C13 ? bmst000002 1 C14 C14 ? bmst000002 1 C15 C15 ? bmst000002 1 C16 C16 ? bmst000002 1 C17 C17 ? bmst000002 1 C18 C18 ? bmst000002 1 C19 C19 ? bmst000002 1 H20 H20 ? bmst000002 1 H21 H21 ? bmst000002 1 H22 H22 ? bmst000002 1 H23 H23 ? bmst000002 1 H24 H24 ? bmst000002 1 H25 H25 ? bmst000002 1 H26 H26 ? bmst000002 1 H27 H27 ? bmst000002 1 H28 H28 ? bmst000002 1 H29 H29 ? bmst000002 1 H30 H30 ? bmst000002 1 H31 H31 ? bmst000002 1 H32 H32 ? bmst000002 1 stop_ loop_ _Chem_comp_bond.ID _Chem_comp_bond.Type _Chem_comp_bond.Value_order _Chem_comp_bond.Atom_ID_1 _Chem_comp_bond.Atom_ID_2 _Chem_comp_bond.Details _Chem_comp_bond.Entry_ID _Chem_comp_bond.Comp_ID 1 covalent SING O1 C10 ? bmst000002 1 2 covalent SING O1 H20 ? bmst000002 1 3 covalent SING C13 O2 ? bmst000002 1 4 covalent SING O2 H21 ? bmst000002 1 5 covalent SING O3 C11 ? bmst000002 1 6 covalent SING O3 C12 ? bmst000002 1 7 covalent DOUB O4 C17 ? bmst000002 1 8 covalent SING N5 C15 ? bmst000002 1 9 covalent SING N5 H22 ? bmst000002 1 10 covalent SING N5 H23 ? bmst000002 1 11 covalent SING C11 N6 ? bmst000002 1 12 covalent SING N6 C16 ? bmst000002 1 13 covalent SING N6 C19 ? bmst000002 1 14 covalent SING N7 C15 ? bmst000002 1 15 covalent SING N7 C16 ? bmst000002 1 16 covalent SING N7 H24 ? bmst000002 1 17 covalent DOUB N8 C15 ? bmst000002 1 18 covalent SING N8 C17 ? bmst000002 1 19 covalent SING N9 C18 ? bmst000002 1 20 covalent DOUB N9 C19 ? bmst000002 1 21 covalent SING C12 C10 ? bmst000002 1 22 covalent SING C10 H25 ? bmst000002 1 23 covalent SING C10 H26 ? bmst000002 1 24 covalent SING C11 C14 ? bmst000002 1 25 covalent SING C11 H27 ? bmst000002 1 26 covalent SING C12 C13 ? bmst000002 1 27 covalent SING C12 H28 ? bmst000002 1 28 covalent SING C13 C14 ? bmst000002 1 29 covalent SING C13 H29 ? bmst000002 1 30 covalent SING C14 H30 ? bmst000002 1 31 covalent SING C14 H31 ? bmst000002 1 32 covalent DOUB C16 C18 ? bmst000002 1 33 covalent SING C17 C18 ? bmst000002 1 34 covalent SING C19 H32 ? bmst000002 1 stop_ loop_ _Chem_comp_db_link.Author_supplied _Chem_comp_db_link.Database_code _Chem_comp_db_link.Accession_code _Chem_comp_db_link.Accession_code_type _Chem_comp_db_link.Entry_mol_code _Chem_comp_db_link.Entry_mol_name _Chem_comp_db_link.Entry_experimental_method _Chem_comp_db_link.Entry_relation_type _Chem_comp_db_link.Entry_details _Chem_comp_db_link.Entry_ID _Chem_comp_db_link.Comp_ID no PubChem 765278 sid ? "2'-Deoxyguanosine" ? "matching entry" ? bmst000002 1 no PubChem 187790 cid ? "2'-Deoxyguanosine" ? "matching entry" ? bmst000002 1 no PubChem 3624 sid ? "2'-Deoxyguanosine" ? "matching entry" ? bmst000002 1 no KEGG C00330 "compound ID" ? "2'-Deoxyguanosine" ? "matching entry" ? bmst000002 1 no "CAS Registry" 38559-49-8 "registry number" ? "2'-Deoxyguanosine" ? "matching entry" ? bmst000002 1 no CHEBI 17172 ? ? "2'-Deoxyguanosine" ? "matching entry" ? bmst000002 1 stop_ loop_ _Chem_comp_citation.Citation_ID _Chem_comp_citation.Citation_label _Chem_comp_citation.Entry_ID _Chem_comp_citation.Comp_ID 1 $citations bmst000002 1 stop_ save_ save_software_1 _Software.Sf_category software _Software.Sf_framecode software_1 _Software.Entry_ID bmst000002 _Software.ID 1 _Software.Name Gaussian _Software.Version ? _Software.Details ? loop_ _Vendor.Name _Vendor.Address _Vendor.Electronic_address _Vendor.Entry_ID _Vendor.Software_ID "Gaussian, Inc." ? http://www.gaussian.com/home.htm bmst000002 1 stop_ loop_ _Task.Task _Task.Entry_ID _Task.Software_ID "geometry optimization" bmst000002 1 "chemical shift calculation" bmst000002 1 stop_ save_ save_chem_shift_reference _Chem_shift_reference.Sf_category chem_shift_reference _Chem_shift_reference.Sf_framecode chem_shift_reference _Chem_shift_reference.Entry_ID bmst000002 _Chem_shift_reference.ID 1 _Chem_shift_reference.Details ? loop_ _Chem_shift_ref.Atom_type _Chem_shift_ref.Atom_isotope_number _Chem_shift_ref.Mol_common_name _Chem_shift_ref.Atom_group _Chem_shift_ref.Chem_shift_units _Chem_shift_ref.Chem_shift_val _Chem_shift_ref.Ref_method _Chem_shift_ref.Ref_type _Chem_shift_ref.Indirect_shift_ratio _Chem_shift_ref.Entry_ID _Chem_shift_ref.Chem_shift_reference_ID H 1 TMS "methyl protons" ppm 0.00 na direct ? bmst000002 1 C 13 TMS "methyl carbons" ppm 0.00 na direct ? bmst000002 1 N 15 "ammonia pentamer" nitrogen ppm 0.00 na direct ? bmst000002 1 P 31 "phosphoric acid" phosphorus ppm 0.00 na direct ? bmst000002 1 stop_ save_ save_chem_shifts_calc_type _Chem_shifts_calc_type.Sf_category chem_shifts_calc_type _Chem_shifts_calc_type.Sf_framecode chem_shifts_calc_type _Chem_shifts_calc_type.Entry_ID bmst000002 _Chem_shifts_calc_type.ID 1 _Chem_shifts_calc_type.Calculation_level 'Density Functional Theory' _Chem_shifts_calc_type.Quantum_mechanical_method GIAO _Chem_shifts_calc_type.Quantum_mechanical_theory_level B3LYP _Chem_shifts_calc_type.Quantum_mechanical_basis_set 3-21g** _Chem_shifts_calc_type.Chem_shift_nucleus ? _Chem_shifts_calc_type.Chem_shift_reference_ID 1 _Chem_shifts_calc_type.Chem_shift_reference_label $chem_shift_reference _Chem_shifts_calc_type.Details ; Theoretical Chemical shift referencing and correction: 1H chemical shifts Tetramethylsilane (TMS) was geometry optimized at the B3LYP/6-311+g* level of theory. The chemical shielding of TMS was calculated at the pbe1pbe/3-21g* level of theory using the GIAO method. The chemical shielding of TMS was used as the reference (0 ppm) to obtain all other chemical shifts. A series of small organic molecules were optimized and the chemical shieldings were calculated in the same manner as that for TMS. To correct for biases arising from the applied level of theory, especially the bias from the small basis set size, a linear regression analysis was used. The slope and intercept from this regression was used to correct the calculated chemical shifts. The chemical shift was calculated by subtracting the chemical shielding value of the compound of interest from that of TMS and applying the slope and intercept corrections obtained from the regression analysis. corrected_shift=((TMS_shielding - uncorrected_shielding)+1.006)/0.963 13C chemical shifts: Tetramethylsilane (TMS) was geometry optimized at the B3LYP/6-311+g* level of theory. The chemical shielding of TMS was calculated at the pbe1pbe/3-21g* level of theory using the GIAO method. The chemical shielding of TMS was used as the reference (0 ppm) to obtain all other chemical shifts. A series of small organic molecules were optimized and the chemical shieldings were calculated in the same manner as that for TMS. To correct for biases arising from the applied level of theory, especially the bias from the small basis set size, a linear regression analysis of theoretical versus experimental chemical shifts was used. The slope and intercept from this regression was used to correct the calculated chemical shifts. The chemical shift was calculated by subtracting the chemical shielding value of the compound of interest from that of TMS and applying the slope and intercept corrections obtained from the regression analysis. Corrected_shift=((TMS_shielding - uncorrected shielding) -4.53)/0.85 15N chemical shifts: A cyclic pentamer of ammonia (NH3_5) was geometry optimized at the B3LYP/6-311+g* level of theory. The chemical shielding of NH3_5 was calculated at the pbe1pbe/3-21g* level of theory using the GIAO method. The chemical shielding of NH3_5 was used as the reference (0 ppm) to obtain all other chemical shifts. A series of small organic molecules were optimized and the chemical shieldings were calculated in the same manner as that for NH3_5. To correct for biases arising from the applied level of theory, especially the bias from the small basis set size, a linear regression analysis was used. The slope and intercept from this regression was used to correct the calculated chemical shifts. The chemical shift was calculated by subtracting the chemical shielding value of the compound of interest from that of NH3_5 and applying the slope and intercept corrections obtained from the regression analysis. Corrected_shift=((NH_3_5_shielding - uncorrected_shielding)+10.2)/0.9088 31P chemical shifts: Phosphoric acid (H3PO4) was geometry optimized at the B3LYP/6-311+g* level of theory. The chemical shielding of H3PO4 was calculated at the pbe1pbe/3-21g* level of theory using the GIAO method. The chemical shielding of H3PO4 was used as the reference (0 ppm) to obtain all other chemical shifts. No correction for linear bias or offset was applied to calculated 31P chemical shifts. The chemical shift was calculated by subtracting the chemical shielding value of the compound of interest from that of H3PO4. Shift=(H3PO4_shielding - shielding) ; loop_ _Chem_shifts_calc_software.Software_ID _Chem_shifts_calc_software.Software_label _Chem_shifts_calc_software.Entry_ID _Chem_shifts_calc_software.Chem_shifts_calc_type_ID 1 $software_1 bmst000002 1 stop_ save_ save_theoretical_chem_shifts _Theoretical_chem_shift_list.Sf_category theoretical_chem_shifts _Theoretical_chem_shift_list.Sf_framecode theoretical_chem_shifts _Theoretical_chem_shift_list.Entry_ID bmst000002 _Theoretical_chem_shift_list.ID 1 _Theoretical_chem_shift_list.Data_file_name 2_deoxyguanosine_3624.g03.shifts _Theoretical_chem_shift_list.Chem_shifts_calc_type_ID 1 _Theoretical_chem_shift_list.Chem_shifts_calc_type_label $chem_shifts_calc_type _Theoretical_chem_shift_list.Model_atomic_coordinates_ID 1 _Theoretical_chem_shift_list.Model_atomic_coordinates_label $conformer_family_coord_set_1 _Theoretical_chem_shift_list.Fermi_contact_spin_density_units ? _Theoretical_chem_shift_list.Chem_shift_1H_err ? _Theoretical_chem_shift_list.Chem_shift_2H_err ? _Theoretical_chem_shift_list.Chem_shift_13C_err ? _Theoretical_chem_shift_list.Chem_shift_15N_err ? _Theoretical_chem_shift_list.Chem_shift_19F_err ? _Theoretical_chem_shift_list.Chem_shift_31P_err ? _Theoretical_chem_shift_list.Details ? _Theoretical_chem_shift_list.Text_data_format ? _Theoretical_chem_shift_list.Text_data ? loop_ _Theoretical_chem_shift.ID _Theoretical_chem_shift.Entity_assembly_ID _Theoretical_chem_shift.Entity_ID _Theoretical_chem_shift.Comp_index_ID _Theoretical_chem_shift.Comp_ID _Theoretical_chem_shift.Atom_ID _Theoretical_chem_shift.Atom_type _Theoretical_chem_shift.Fermi_contact_spin_density _Theoretical_chem_shift.Val _Theoretical_chem_shift.Val_err _Theoretical_chem_shift.Auth_seq_ID _Theoretical_chem_shift.Auth_comp_ID _Theoretical_chem_shift.Auth_atom_ID _Theoretical_chem_shift.Entry_ID _Theoretical_chem_shift.Theoretical_chem_shift_list_ID 1 1 1 1 1 N5 N ? 76.129 ? 2_deoxyguanosine ? ? bmst000002 1 2 1 1 1 1 N6 N ? 163.488 ? 2_deoxyguanosine ? ? bmst000002 1 3 1 1 1 1 N7 N ? 107.722 ? 2_deoxyguanosine ? ? bmst000002 1 4 1 1 1 1 N8 N ? 246.294 ? 2_deoxyguanosine ? ? bmst000002 1 5 1 1 1 1 N9 N ? 292.531 ? 2_deoxyguanosine ? ? bmst000002 1 6 1 1 1 1 C10 C ? 63.794 ? 2_deoxyguanosine ? ? bmst000002 1 7 1 1 1 1 C11 C ? 91.787 ? 2_deoxyguanosine ? ? bmst000002 1 8 1 1 1 1 C12 C ? 87.844 ? 2_deoxyguanosine ? ? bmst000002 1 9 1 1 1 1 C13 C ? 74.836 ? 2_deoxyguanosine ? ? bmst000002 1 10 1 1 1 1 C14 C ? 40.717 ? 2_deoxyguanosine ? ? bmst000002 1 11 1 1 1 1 C15 C ? 145.585 ? 2_deoxyguanosine ? ? bmst000002 1 12 1 1 1 1 C16 C ? 135.173 ? 2_deoxyguanosine ? ? bmst000002 1 13 1 1 1 1 C17 C ? 161.870 ? 2_deoxyguanosine ? ? bmst000002 1 14 1 1 1 1 C18 C ? 124.911 ? 2_deoxyguanosine ? ? bmst000002 1 15 1 1 1 1 C19 C ? 128.031 ? 2_deoxyguanosine ? ? bmst000002 1 16 1 1 1 1 H20 H ? 1.004 ? 2_deoxyguanosine ? ? bmst000002 1 17 1 1 1 1 H21 H ? 0.483 ? 2_deoxyguanosine ? ? bmst000002 1 18 1 1 1 1 H22 H ? 3.474 ? 2_deoxyguanosine ? ? bmst000002 1 19 1 1 1 1 H23 H ? 4.249 ? 2_deoxyguanosine ? ? bmst000002 1 20 1 1 1 1 H24 H ? 9.526 ? 2_deoxyguanosine ? ? bmst000002 1 21 1 1 1 1 H25 H ? 4.754 ? 2_deoxyguanosine ? ? bmst000002 1 22 1 1 1 1 H26 H ? 4.756 ? 2_deoxyguanosine ? ? bmst000002 1 23 1 1 1 1 H27 H ? 7.575 ? 2_deoxyguanosine ? ? bmst000002 1 24 1 1 1 1 H28 H ? 5.247 ? 2_deoxyguanosine ? ? bmst000002 1 25 1 1 1 1 H29 H ? 4.890 ? 2_deoxyguanosine ? ? bmst000002 1 26 1 1 1 1 H30 H ? 3.618 ? 2_deoxyguanosine ? ? bmst000002 1 27 1 1 1 1 H31 H ? 2.815 ? 2_deoxyguanosine ? ? bmst000002 1 28 1 1 1 1 H32 H ? 8.085 ? 2_deoxyguanosine ? ? bmst000002 1 stop_ save_ save_conformer_family_coord_set_1 _Conformer_family_coord_set.Sf_category conformer_family_coord_set _Conformer_family_coord_set.Sf_framecode conformer_family_coord_set_1 _Conformer_family_coord_set.Entry_ID bmst000002 _Conformer_family_coord_set.ID 1 _Conformer_family_coord_set.File_name 2_deoxyguanosine_3624_opt.pdb _Conformer_family_coord_set.Details ? loop_ _Conformer_family_software.Software_ID _Conformer_family_software.Software_label _Conformer_family_software.Entry_ID _Conformer_family_software.Conformer_family_coord_set_ID 1 $software_1 bmst000002 1 stop_ loop_ _Atom_site.Model_ID _Atom_site.ID _Atom_site.Label_entity_assembly_ID _Atom_site.Label_entity_ID _Atom_site.Label_comp_index_ID _Atom_site.Label_comp_ID _Atom_site.Label_atom_ID _Atom_site.Auth_seq_ID _Atom_site.Auth_comp_ID _Atom_site.Auth_atom_ID _Atom_site.Type_symbol _Atom_site.Cartn_x _Atom_site.Cartn_y _Atom_site.Cartn_z _Atom_site.Entry_ID _Atom_site.Conformer_family_coord_set_ID 1 1 1 1 1 1 O1 1 1 O1 O -1.822 1.870 1.761 bmst000002 1 1 2 1 1 1 1 O2 1 1 O2 O 1.919 4.013 -0.460 bmst000002 1 1 3 1 1 1 1 O3 1 1 O3 O 0.732 1.521 0.918 bmst000002 1 1 4 1 1 1 1 O4 1 1 O4 O -0.297 -4.573 -0.888 bmst000002 1 1 5 1 1 1 1 N5 1 1 N5 N -2.912 -1.550 1.428 bmst000002 1 1 6 1 1 1 1 N6 1 1 N6 N 1.344 -0.301 -0.407 bmst000002 1 1 7 1 1 1 1 N7 1 1 N7 N -0.913 -0.785 0.519 bmst000002 1 1 8 1 1 1 1 N8 1 1 N8 N -1.631 -3.043 0.194 bmst000002 1 1 9 1 1 1 1 N9 1 1 N9 N 1.787 -2.354 -1.225 bmst000002 1 1 10 1 1 1 1 C10 1 1 C10 C -1.411 2.642 0.633 bmst000002 1 1 11 1 1 1 1 C11 1 1 C11 C 1.513 1.128 -0.207 bmst000002 1 1 12 1 1 1 1 C12 1 1 C12 C 0.109 2.794 0.684 bmst000002 1 1 13 1 1 1 1 C13 1 1 C13 C 0.694 3.317 -0.647 bmst000002 1 1 14 1 1 1 1 C14 1 1 C14 C 1.035 2.014 -1.368 bmst000002 1 1 15 1 1 1 1 C15 1 1 C15 C -1.793 -1.849 0.668 bmst000002 1 1 16 1 1 1 1 C16 1 1 C16 C 0.258 -1.097 -0.132 bmst000002 1 1 17 1 1 1 1 C17 1 1 C17 C -0.445 -3.433 -0.480 bmst000002 1 1 18 1 1 1 1 C18 1 1 C18 C 0.535 -2.350 -0.636 bmst000002 1 1 19 1 1 1 1 C19 1 1 C19 C 2.239 -1.140 -1.072 bmst000002 1 1 20 1 1 1 1 H20 1 1 H20 H -2.762 2.038 1.924 bmst000002 1 1 21 1 1 1 1 H21 1 1 H21 H 1.751 4.799 0.085 bmst000002 1 1 22 1 1 1 1 H22 1 1 H22 H -3.281 -0.613 1.327 bmst000002 1 1 23 1 1 1 1 H23 1 1 H23 H -3.614 -2.278 1.363 bmst000002 1 1 24 1 1 1 1 H24 1 1 H24 H -0.977 0.030 1.127 bmst000002 1 1 25 1 1 1 1 H25 1 1 H25 H -1.863 3.645 0.651 bmst000002 1 1 26 1 1 1 1 H26 1 1 H26 H -1.715 2.150 -0.303 bmst000002 1 1 27 1 1 1 1 H27 1 1 H27 H 2.576 1.302 -0.000 bmst000002 1 1 28 1 1 1 1 H28 1 1 H28 H 0.376 3.445 1.526 bmst000002 1 1 29 1 1 1 1 H29 1 1 H29 H -0.031 3.932 -1.201 bmst000002 1 1 30 1 1 1 1 H30 1 1 H30 H 1.798 2.163 -2.135 bmst000002 1 1 31 1 1 1 1 H31 1 1 H31 H 0.146 1.575 -1.832 bmst000002 1 1 32 1 1 1 1 H32 1 1 H32 H 3.203 -0.771 -1.401 bmst000002 1 stop_ save_