data_PIA
#
_chem_comp.id PIA
_chem_comp.name '[(4Z)-2-[(1S)-1-aminoethyl]-4-(4-hydroxybenzylidene)-5-oxo-4,5-dihydro-1H-imidazol-1-yl]acetic acid'
_chem_comp.type 'L-PEPTIDE LINKING'
_chem_comp.pdbx_type ATOMP
_chem_comp.formula 'C14 H15 N3 O4'
_chem_comp.mon_nstd_parent_comp_id ALA,TYR,GLY
_chem_comp.pdbx_synonyms ?
_chem_comp.pdbx_formal_charge 0
_chem_comp.pdbx_initial_date 2001-06-22
_chem_comp.pdbx_modified_date 2024-09-27
_chem_comp.pdbx_ambiguous_flag N
_chem_comp.pdbx_release_status REL
_chem_comp.pdbx_replaced_by ?
_chem_comp.pdbx_replaces ?
_chem_comp.formula_weight 289.287
_chem_comp.one_letter_code AYG
_chem_comp.three_letter_code PIA
_chem_comp.pdbx_model_coordinates_details ?
_chem_comp.pdbx_model_coordinates_missing_flag N
_chem_comp.pdbx_ideal_coordinates_details Corina
_chem_comp.pdbx_ideal_coordinates_missing_flag N
_chem_comp.pdbx_model_coordinates_db_code 1H6R
_chem_comp.pdbx_subcomponent_list ?
_chem_comp.pdbx_processing_site EBI
_chem_comp.pdbx_pcm Y
#
loop_
_chem_comp_atom.comp_id
_chem_comp_atom.atom_id
_chem_comp_atom.alt_atom_id
_chem_comp_atom.type_symbol
_chem_comp_atom.charge
_chem_comp_atom.pdbx_align
_chem_comp_atom.pdbx_aromatic_flag
_chem_comp_atom.pdbx_leaving_atom_flag
_chem_comp_atom.pdbx_stereo_config
_chem_comp_atom.pdbx_backbone_atom_flag
_chem_comp_atom.pdbx_n_terminal_atom_flag
_chem_comp_atom.pdbx_c_terminal_atom_flag
_chem_comp_atom.model_Cartn_x
_chem_comp_atom.model_Cartn_y
_chem_comp_atom.model_Cartn_z
_chem_comp_atom.pdbx_model_Cartn_x_ideal
_chem_comp_atom.pdbx_model_Cartn_y_ideal
_chem_comp_atom.pdbx_model_Cartn_z_ideal
_chem_comp_atom.pdbx_component_atom_id
_chem_comp_atom.pdbx_component_comp_id
_chem_comp_atom.pdbx_ordinal
PIA N1 N1 N 0 1 N N N Y Y N 21.969 22.898 18.924 -0.872 -3.026 -1.194 N1 PIA 1
PIA CA1 CA1 C 0 1 N N S Y N N 21.953 24.130 19.714 -1.828 -2.151 -0.504 CA1 PIA 2
PIA CB1 CB1 C 0 1 N N N N N N 23.173 24.179 20.665 -2.017 -2.635 0.935 CB1 PIA 3
PIA C1 C1 C 0 1 N N N Y N N 21.737 25.252 18.697 -1.301 -0.739 -0.494 C1 PIA 4
PIA N2 N2 N 0 1 N N N Y N N 22.726 26.032 18.292 -0.046 -0.428 -0.391 N2 PIA 5
PIA N3 N3 N 0 1 N N N Y N N 20.589 25.444 17.970 -2.082 0.377 -0.598 N3 PIA 6
PIA C2 C2 C 0 1 N N N Y N N 20.728 26.423 17.077 -1.281 1.464 -0.554 C2 PIA 7
PIA O2 O2 O 0 1 N N N Y N N 19.729 26.766 16.424 -1.617 2.633 -0.618 O2 PIA 8
PIA CA2 CA2 C 0 1 N N N Y N N 22.060 26.665 17.330 0.086 0.933 -0.415 CA2 PIA 9
PIA CA3 CA3 C 0 1 N N N Y N N 19.348 24.714 18.066 -3.541 0.392 -0.735 CA3 PIA 10
PIA C3 C3 C 0 1 N N N Y N Y 18.477 25.148 19.223 -4.173 0.436 0.632 C3 PIA 11
PIA O3 O3 O 0 1 N N N Y N Y 17.385 24.600 19.396 -3.477 0.454 1.620 O3 PIA 12
PIA CB2 CB2 C 0 1 N N N N N N 22.452 27.795 16.380 1.255 1.656 -0.330 CB2 PIA 13
PIA CG2 CG2 C 0 1 Y N N N N N 23.869 28.366 16.250 2.525 0.969 -0.084 CG2 PIA 14
PIA CD1 CD1 C 0 1 Y N N N N N 24.864 27.781 16.963 2.575 -0.432 -0.060 CD1 PIA 15
PIA CD2 CD2 C 0 1 Y N N N N N 24.009 29.358 15.334 3.698 1.710 0.122 CD2 PIA 16
PIA CE1 CE1 C 0 1 Y N N N N N 26.151 28.247 16.722 3.767 -1.069 0.170 CE1 PIA 17
PIA CE2 CE2 C 0 1 Y N N N N N 25.305 29.830 15.094 4.884 1.062 0.351 CE2 PIA 18
PIA CZ CZ C 0 1 Y N N N N N 26.366 29.261 15.797 4.925 -0.328 0.379 CZ PIA 19
PIA OH OH O 0 1 N N N N N N 27.642 29.703 15.591 6.102 -0.965 0.607 OH PIA 20
PIA OXT O31 O 0 1 N Y N Y N Y 19.029 25.989 20.101 -5.510 0.457 0.753 O31 PIA 21
PIA H HN11 H 0 0 N N N Y Y N 21.176 22.881 18.315 0.042 -2.970 -0.769 HN11 PIA 22
PIA H2 HN12 H 0 0 N Y N Y Y N 22.807 22.862 18.380 -1.203 -3.979 -1.214 HN12 PIA 23
PIA HA1 HA1 H 0 1 N N N Y N N 21.058 24.103 20.353 -2.786 -2.177 -1.024 HA1 PIA 24
PIA HB11 HB11 H 0 0 N N N N N N 23.145 25.110 21.250 -1.059 -2.608 1.456 HB11 PIA 25
PIA HB12 HB12 H 0 0 N N N N N N 23.141 23.316 21.347 -2.727 -1.985 1.447 HB12 PIA 26
PIA HB13 HB13 H 0 0 N N N N N N 24.100 24.145 20.074 -2.398 -3.656 0.928 HB13 PIA 27
PIA HA31 HA31 H 0 0 N N N Y N N 18.785 24.862 17.133 -3.843 1.271 -1.304 HA31 PIA 28
PIA HA32 HA32 H 0 0 N N N Y N N 19.582 23.646 18.188 -3.866 -0.508 -1.257 HA32 PIA 29
PIA HB2 HB2 H 0 1 N N N N N N 21.679 28.221 15.758 1.235 2.730 -0.445 HB2 PIA 30
PIA HD1 HD1 H 0 1 N N N N N N 24.667 26.996 17.678 1.676 -1.008 -0.222 HD1 PIA 31
PIA HD2 HD2 H 0 1 N N N N N N 23.156 29.766 14.812 3.667 2.790 0.100 HD2 PIA 32
PIA HE1 HE1 H 0 1 N N N N N N 26.987 27.819 17.256 3.806 -2.148 0.189 HE1 PIA 33
PIA HE2 HE2 H 0 1 N N N N N N 25.479 30.620 14.378 5.788 1.631 0.510 HE2 PIA 34
PIA HH HH H 0 1 N N N N N N 27.637 30.392 14.937 6.606 -1.159 -0.196 HH PIA 35
PIA HXT "HO'" H 0 1 N Y N Y N Y 18.455 26.086 20.851 -5.869 0.485 1.651 "HO'" PIA 36
#
loop_
_chem_comp_bond.comp_id
_chem_comp_bond.atom_id_1
_chem_comp_bond.atom_id_2
_chem_comp_bond.value_order
_chem_comp_bond.pdbx_aromatic_flag
_chem_comp_bond.pdbx_stereo_config
_chem_comp_bond.pdbx_ordinal
PIA N1 CA1 SING N N 1
PIA N1 H SING N N 2
PIA N1 H2 SING N N 3
PIA CA1 CB1 SING N N 4
PIA CA1 C1 SING N N 5
PIA CA1 HA1 SING N N 6
PIA CB1 HB11 SING N N 7
PIA CB1 HB12 SING N N 8
PIA CB1 HB13 SING N N 9
PIA C1 N2 DOUB N N 10
PIA C1 N3 SING N N 11
PIA N2 CA2 SING N N 12
PIA N3 C2 SING N N 13
PIA N3 CA3 SING N N 14
PIA C2 O2 DOUB N N 15
PIA C2 CA2 SING N N 16
PIA CA2 CB2 DOUB N Z 17
PIA CA3 C3 SING N N 18
PIA CA3 HA31 SING N N 19
PIA CA3 HA32 SING N N 20
PIA C3 O3 DOUB N N 21
PIA C3 OXT SING N N 22
PIA CB2 CG2 SING N N 23
PIA CB2 HB2 SING N N 24
PIA CG2 CD1 DOUB Y N 25
PIA CG2 CD2 SING Y N 26
PIA CD1 CE1 SING Y N 27
PIA CD1 HD1 SING N N 28
PIA CD2 CE2 DOUB Y N 29
PIA CD2 HD2 SING N N 30
PIA CE1 CZ DOUB Y N 31
PIA CE1 HE1 SING N N 32
PIA CE2 CZ SING Y N 33
PIA CE2 HE2 SING N N 34
PIA CZ OH SING N N 35
PIA OH HH SING N N 36
PIA OXT HXT SING N N 37
#
loop_
_pdbx_chem_comp_descriptor.comp_id
_pdbx_chem_comp_descriptor.type
_pdbx_chem_comp_descriptor.program
_pdbx_chem_comp_descriptor.program_version
_pdbx_chem_comp_descriptor.descriptor
PIA SMILES ACDLabs 12.01 'O=C1C(\N=C(N1CC(=O)O)C(N)C)=C\c2ccc(O)cc2'
PIA InChI InChI 1.03 'InChI=1S/C14H15N3O4/c1-8(15)13-16-11(14(21)17(13)7-12(19)20)6-9-2-4-10(18)5-3-9/h2-6,8,18H,7,15H2,1H3,(H,19,20)/b11-6-/t8-/m0/s1'
PIA InChIKey InChI 1.03 UMPNJELZAAOGQG-OITNDJBGSA-N
PIA SMILES_CANONICAL CACTVS 3.370 'C[C@H](N)C1=N\C(=C/c2ccc(O)cc2)C(=O)N1CC(O)=O'
PIA SMILES CACTVS 3.370 'C[CH](N)C1=NC(=Cc2ccc(O)cc2)C(=O)N1CC(O)=O'
PIA SMILES_CANONICAL 'OpenEye OEToolkits' 1.7.6 'C[C@@H](C1=N/C(=C\c2ccc(cc2)O)/C(=O)N1CC(=O)O)N'
PIA SMILES 'OpenEye OEToolkits' 1.7.6 'CC(C1=NC(=Cc2ccc(cc2)O)C(=O)N1CC(=O)O)N'
#
loop_
_pdbx_chem_comp_identifier.comp_id
_pdbx_chem_comp_identifier.type
_pdbx_chem_comp_identifier.program
_pdbx_chem_comp_identifier.program_version
_pdbx_chem_comp_identifier.identifier
PIA 'SYSTEMATIC NAME' ACDLabs 12.01 '[(4Z)-2-[(1S)-1-aminoethyl]-4-(4-hydroxybenzylidene)-5-oxo-4,5-dihydro-1H-imidazol-1-yl]acetic acid'
PIA 'SYSTEMATIC NAME' 'OpenEye OEToolkits' 1.7.6 '2-[(4Z)-2-[(1S)-1-azanylethyl]-4-[(4-hydroxyphenyl)methylidene]-5-oxidanylidene-imidazol-1-yl]ethanoic acid'
#
loop_
_pdbx_chem_comp_audit.comp_id
_pdbx_chem_comp_audit.action_type
_pdbx_chem_comp_audit.date
_pdbx_chem_comp_audit.processing_site
PIA 'Create component' 2001-06-22 EBI
PIA 'Modify descriptor' 2011-06-04 RCSB
PIA 'Modify name' 2012-02-03 RCSB
PIA 'Modify leaving atom flag' 2021-08-16 PDBE
PIA 'Modify backbone' 2023-11-03 PDBE
PIA 'Modify PCM' 2024-09-27 PDBE
#
_pdbx_chem_comp_pcm.pcm_id 1
_pdbx_chem_comp_pcm.comp_id PIA
_pdbx_chem_comp_pcm.modified_residue_id 'ALA, TYR, GLY'
_pdbx_chem_comp_pcm.type None
_pdbx_chem_comp_pcm.category Chromophore/chromophore-like
_pdbx_chem_comp_pcm.position 'Amino-acid side chain and backbone'
_pdbx_chem_comp_pcm.polypeptide_position 'Any position'
_pdbx_chem_comp_pcm.comp_id_linking_atom ?
_pdbx_chem_comp_pcm.modified_residue_id_linking_atom ?
_pdbx_chem_comp_pcm.uniprot_specific_ptm_accession ?
_pdbx_chem_comp_pcm.uniprot_generic_ptm_accession ?
#
loop_
_software.name
_software.version
_software.description
rdkit 2023.09.6 'Core functionality.'
pdbeccdutils 0.8.6 'Wrapper to provide 2D templates and molecular fragments.'
#
loop_
_pdbe_chem_comp_atom_depiction.comp_id
_pdbe_chem_comp_atom_depiction.atom_id
_pdbe_chem_comp_atom_depiction.element
_pdbe_chem_comp_atom_depiction.model_Cartn_x
_pdbe_chem_comp_atom_depiction.model_Cartn_y
_pdbe_chem_comp_atom_depiction.pdbx_ordinal
PIA N1 N 10.074 -0.670 1
PIA CA1 C 9.464 0.700 2
PIA CB1 C 10.345 1.914 3
PIA C1 C 7.972 0.857 4
PIA N2 N 6.968 -0.258 5
PIA N3 N 7.222 2.156 6
PIA C2 C 5.755 1.844 7
PIA O2 O 4.640 2.848 8
PIA CA2 C 5.598 0.352 9
PIA CA3 C 7.832 3.526 10
PIA C3 C 6.950 4.740 11
PIA O3 O 7.561 6.110 12
PIA CB2 C 4.299 -0.398 13
PIA CG2 C 4.299 -1.898 14
PIA CD1 C 3.000 -2.648 15
PIA CD2 C 5.598 -2.648 16
PIA CE1 C 3.000 -4.148 17
PIA CE2 C 5.598 -4.148 18
PIA CZ C 4.299 -4.898 19
PIA OH O 4.299 -6.398 20
PIA OXT O 5.459 4.583 21
#
loop_
_pdbe_chem_comp_bond_depiction.comp_id
_pdbe_chem_comp_bond_depiction.atom_id_1
_pdbe_chem_comp_bond_depiction.atom_id_2
_pdbe_chem_comp_bond_depiction.value_order
_pdbe_chem_comp_bond_depiction.bond_dir
_pdbe_chem_comp_bond_depiction.pdbx_ordinal
PIA N1 CA1 SINGLE NONE 1
PIA CA1 CB1 SINGLE BEGINDASH 2
PIA CA1 C1 SINGLE NONE 3
PIA C1 N2 DOUBLE NONE 4
PIA C1 N3 SINGLE NONE 5
PIA N2 CA2 SINGLE ENDUPRIGHT 6
PIA N3 C2 SINGLE NONE 7
PIA N3 CA3 SINGLE NONE 8
PIA C2 O2 DOUBLE NONE 9
PIA C2 CA2 SINGLE ENDDOWNRIGHT 10
PIA CA2 CB2 DOUBLE NONE 11
PIA CA3 C3 SINGLE NONE 12
PIA C3 O3 DOUBLE NONE 13
PIA C3 OXT SINGLE NONE 14
PIA CB2 CG2 SINGLE ENDDOWNRIGHT 15
PIA CG2 CD1 DOUBLE NONE 16
PIA CG2 CD2 SINGLE NONE 17
PIA CD1 CE1 SINGLE NONE 18
PIA CD2 CE2 DOUBLE NONE 19
PIA CE1 CZ DOUBLE NONE 20
PIA CE2 CZ SINGLE NONE 21
PIA CZ OH SINGLE NONE 22
#
loop_
_pdbe_chem_comp_substructure.comp_id
_pdbe_chem_comp_substructure.substructure_name
_pdbe_chem_comp_substructure.id
_pdbe_chem_comp_substructure.substructure_type
_pdbe_chem_comp_substructure.substructure_smiles
_pdbe_chem_comp_substructure.substructure_inchis
_pdbe_chem_comp_substructure.substructure_inchikeys
PIA MurckoScaffold S1 scaffold O=C1NC=N/C1=C\c1ccccc1 InChI=1S/C10H8N2O/c13-10-9(11-7-12-10)6-8-4-2-1-3-5-8/h1-7H,(H,11,12,13)/b9-6- CQGIJPFYWRPMRO-TWGQIWQCSA-N
PIA amide F1 fragment CC(N)=O InChI=1S/C2H5NO/c1-2(3)4/h1H3,(H2,3,4) DLFVBJFMPXGRIB-UHFFFAOYSA-N
PIA peptide F2 fragment NCC=O InChI=1S/C2H5NO/c3-1-2-4/h2H,1,3H2 LYIIBVSRGJSHAV-UHFFFAOYSA-N
PIA phenyl F3 fragment c1ccccc1 InChI=1S/C6H6/c1-2-4-6-5-3-1/h1-6H UHOVQNZJYSORNB-UHFFFAOYSA-N
#
loop_
_pdbe_chem_comp_substructure_mapping.comp_id
_pdbe_chem_comp_substructure_mapping.atom_id
_pdbe_chem_comp_substructure_mapping.substructure_id
_pdbe_chem_comp_substructure_mapping.substructure_ordinal
PIA C1 S1 1
PIA N2 S1 1
PIA N3 S1 1
PIA C2 S1 1
PIA O2 S1 1
PIA CA2 S1 1
PIA CB2 S1 1
PIA CG2 S1 1
PIA CD1 S1 1
PIA CD2 S1 1
PIA CE1 S1 1
PIA CE2 S1 1
PIA CZ S1 1
PIA N3 F1 1
PIA C2 F1 1
PIA O2 F1 1
PIA CA2 F1 1
PIA O2 F2 1
PIA C2 F2 1
PIA CA2 F2 1
PIA N2 F2 1
PIA O3 F2 2
PIA C3 F2 2
PIA CA3 F2 2
PIA N3 F2 2
PIA CG2 F3 1
PIA CD1 F3 1
PIA CE1 F3 1
PIA CZ F3 1
PIA CE2 F3 1
PIA CD2 F3 1
#
_pdbe_chem_comp_rdkit_properties.comp_id PIA
_pdbe_chem_comp_rdkit_properties.exactmw 289.106
_pdbe_chem_comp_rdkit_properties.amw 289.291
_pdbe_chem_comp_rdkit_properties.lipinskiHBA 7
_pdbe_chem_comp_rdkit_properties.lipinskiHBD 4
_pdbe_chem_comp_rdkit_properties.NumRotatableBonds 7
_pdbe_chem_comp_rdkit_properties.NumHBD 3
_pdbe_chem_comp_rdkit_properties.NumHBA 6
_pdbe_chem_comp_rdkit_properties.NumHeavyAtoms 21
_pdbe_chem_comp_rdkit_properties.NumAtoms 36
_pdbe_chem_comp_rdkit_properties.NumHeteroatoms 7
_pdbe_chem_comp_rdkit_properties.NumAmideBonds 1
_pdbe_chem_comp_rdkit_properties.FractionCSP3 0.214
_pdbe_chem_comp_rdkit_properties.NumRings 2
_pdbe_chem_comp_rdkit_properties.NumAromaticRings 1
_pdbe_chem_comp_rdkit_properties.NumAliphaticRings 1
_pdbe_chem_comp_rdkit_properties.NumSaturatedRings 0
_pdbe_chem_comp_rdkit_properties.NumHeterocycles 1
_pdbe_chem_comp_rdkit_properties.NumAromaticHeterocycles 0
_pdbe_chem_comp_rdkit_properties.NumSaturatedHeterocycles 0
_pdbe_chem_comp_rdkit_properties.NumAliphaticHeterocycles 1
_pdbe_chem_comp_rdkit_properties.NumSpiroAtoms 0
_pdbe_chem_comp_rdkit_properties.NumBridgeheadAtoms 0
_pdbe_chem_comp_rdkit_properties.NumAtomStereoCenters 1
_pdbe_chem_comp_rdkit_properties.NumUnspecifiedAtomStereoCenters 0
_pdbe_chem_comp_rdkit_properties.labuteASA 141.926
_pdbe_chem_comp_rdkit_properties.tpsa 116.220
_pdbe_chem_comp_rdkit_properties.CrippenClogP -0.112
_pdbe_chem_comp_rdkit_properties.CrippenMR 75.641
_pdbe_chem_comp_rdkit_properties.chi0v 9.975
_pdbe_chem_comp_rdkit_properties.chi1v 5.158
_pdbe_chem_comp_rdkit_properties.chi2v 2.096
_pdbe_chem_comp_rdkit_properties.chi3v 2.096
_pdbe_chem_comp_rdkit_properties.chi4v 1.323
_pdbe_chem_comp_rdkit_properties.chi0n 24.975
_pdbe_chem_comp_rdkit_properties.chi1n 12.369
_pdbe_chem_comp_rdkit_properties.chi2n 2.096
_pdbe_chem_comp_rdkit_properties.chi3n 2.096
_pdbe_chem_comp_rdkit_properties.chi4n 1.323
_pdbe_chem_comp_rdkit_properties.hallKierAlpha -2.670
_pdbe_chem_comp_rdkit_properties.kappa1 4.671
_pdbe_chem_comp_rdkit_properties.kappa2 5.758
_pdbe_chem_comp_rdkit_properties.kappa3 3.263
_pdbe_chem_comp_rdkit_properties.Phi 1.281
#
loop_
_pdbe_chem_comp_external_mappings.comp_id
_pdbe_chem_comp_external_mappings.source
_pdbe_chem_comp_external_mappings.resource
_pdbe_chem_comp_external_mappings.resource_id
PIA UniChem ZINC ZINC000006929402
PIA UniChem PubChem 49866657
#
loop_
_pdbe_chem_comp_rdkit_conformer.comp_id
_pdbe_chem_comp_rdkit_conformer.atom_id
_pdbe_chem_comp_rdkit_conformer.Cartn_x_rdkit
_pdbe_chem_comp_rdkit_conformer.Cartn_y_rdkit
_pdbe_chem_comp_rdkit_conformer.Cartn_z_rdkit
_pdbe_chem_comp_rdkit_conformer.rdkit_method
_pdbe_chem_comp_rdkit_conformer.rdkit_ordinal
PIA N1 -1.812 -2.682 0.879 ETKDGv3 1
PIA CA1 -2.388 -1.375 0.561 ETKDGv3 2
PIA CB1 -2.579 -0.560 1.843 ETKDGv3 3
PIA C1 -1.480 -0.633 -0.386 ETKDGv3 4
PIA N2 -0.210 -0.480 -0.138 ETKDGv3 5
PIA N3 -1.926 0.010 -1.595 ETKDGv3 6
PIA C2 -0.754 0.635 -2.088 ETKDGv3 7
PIA O2 -0.701 1.370 -3.110 ETKDGv3 8
PIA CA2 0.333 0.308 -1.195 ETKDGv3 9
PIA CA3 -3.297 0.308 -2.004 ETKDGv3 10
PIA C3 -3.874 1.384 -1.141 ETKDGv3 11
PIA O3 -4.891 1.152 -0.435 ETKDGv3 12
PIA CB2 1.597 0.744 -1.280 ETKDGv3 13
PIA CG2 2.660 0.409 -0.305 ETKDGv3 14
PIA CD1 2.757 -0.807 0.270 ETKDGv3 15
PIA CD2 3.695 1.430 -0.011 ETKDGv3 16
PIA CE1 3.855 -1.100 1.215 ETKDGv3 17
PIA CE2 4.692 1.160 0.841 ETKDGv3 18
PIA CZ 4.775 -0.168 1.490 ETKDGv3 19
PIA OH 5.806 -0.454 2.381 ETKDGv3 20
PIA OXT -3.285 2.644 -1.120 ETKDGv3 21
PIA H -1.737 -3.231 -0.008 ETKDGv3 22
PIA H2 -2.490 -3.203 1.483 ETKDGv3 23
PIA HA1 -3.384 -1.525 0.092 ETKDGv3 24
PIA HB11 -2.988 0.444 1.605 ETKDGv3 25
PIA HB12 -3.295 -1.076 2.518 ETKDGv3 26
PIA HB13 -1.611 -0.438 2.376 ETKDGv3 27
PIA HA31 -3.309 0.648 -3.062 ETKDGv3 28
PIA HA32 -3.916 -0.612 -1.949 ETKDGv3 29
PIA HB2 1.848 1.438 -2.073 ETKDGv3 30
PIA HD1 2.061 -1.599 0.030 ETKDGv3 31
PIA HD2 3.645 2.404 -0.481 ETKDGv3 32
PIA HE1 3.912 -2.077 1.679 ETKDGv3 33
PIA HE2 5.439 1.914 1.053 ETKDGv3 34
PIA HH 6.514 0.236 2.603 ETKDGv3 35
PIA HXT -3.661 3.383 -0.538 ETKDGv3 36
#