data_TBV
#

_chem_comp.id                                   TBV
_chem_comp.name                                 
;3-[2-[[3-(2-CARBOXYETHYL)-5-[[3-ETHENYL-4-METHYL-5-[(2-METHYLPROPAN-2-YL)OXY]-1H-PYRROL-2-YL]METHYL]-4-METHYL-1H-PYRROL
-2-YL]METHYL]-5-[(Z)-(4-ETHENYL-3-METHYL-5-OXO-PYRROL-2-YLIDENE)METHYL]-4-METHYL-1H-PYRROL-3-YL]PROPANOIC ACID
;

_chem_comp.type                                 non-polymer
_chem_comp.pdbx_type                            ?
_chem_comp.formula                              "C37 H46 N4 O6"
_chem_comp.mon_nstd_parent_comp_id              ?
_chem_comp.pdbx_synonyms                        BILIVERDIN
_chem_comp.pdbx_formal_charge                   0
_chem_comp.pdbx_initial_date                    2009-03-19
_chem_comp.pdbx_modified_date                   2020-06-17
_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                       642.784
_chem_comp.one_letter_code                      ?
_chem_comp.three_letter_code                    TBV
_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       2WD4
_chem_comp.pdbx_subcomponent_list               ?
_chem_comp.pdbx_processing_site                 EBI
#   #
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.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
TBV  CHA   CHA   C  0  1  N  N  N  13.541  57.644  20.348  -0.600   1.097  -1.276  CHA   TBV   1  
TBV  CHB   CHB   C  0  1  N  N  N  12.738  55.077  16.271  -5.001   0.850   1.061  CHB   TBV   2  
TBV  CHD   CHD   C  0  1  N  N  N  16.997  54.432  21.550   3.529   0.372   1.584  CHD   TBV   3  
TBV  NA    NA    N  0  1  Y  N  N  13.428  56.130  18.417  -2.889   0.673  -0.240  NA    TBV   4  
TBV  C1A   C1A   C  0  1  Y  N  N  13.079  57.283  19.021  -1.779   1.439  -0.402  C1A   TBV   5  
TBV  C2A   C2A   C  0  1  Y  N  N  12.002  58.036  18.363  -1.904   2.560   0.351  C2A   TBV   6  
TBV  C3A   C3A   C  0  1  Y  N  N  11.754  57.274  17.142  -3.133   2.502   1.011  C3A   TBV   7  
TBV  C4A   C4A   C  0  1  Y  N  N  12.706  56.151  17.273  -3.742   1.315   0.633  C4A   TBV   8  
TBV  CAA   CAA   C  0  1  N  N  N  11.364  59.319  18.803  -0.893   3.673   0.457  CAA   TBV   9  
TBV  CBA   CBA   C  0  1  N  N  N  12.243  60.510  18.460  -1.177   4.725  -0.617  CBA   TBV  10  
TBV  CGA   CGA   C  0  1  N  N  N  11.514  61.711  18.999  -0.166   5.837  -0.511  CGA   TBV  11  
TBV  O1A   O1A   O  0  1  N  N  N  12.014  62.328  19.961   0.694   5.793   0.337  O1A   TBV  12  
TBV  O2A   O2A   O  0  1  N  N  N  10.417  62.035  18.484  -0.221   6.877  -1.358  O2A   TBV  13  
TBV  CMA   CMA   C  0  1  N  N  N  10.790  57.569  16.017  -3.692   3.535   1.955  CMA   TBV  14  
TBV  NB    NB    N  0  1  N  N  N  14.072  53.482  17.567  -5.189  -0.734  -0.819  NB    TBV  15  
TBV  C1B   C1B   C  0  1  N  N  N  13.358  53.764  16.463  -5.639  -0.161   0.365  C1B   TBV  16  
TBV  C2B   C2B   C  0  1  N  N  N  13.305  52.697  15.444  -6.844  -0.773   0.739  C2B   TBV  17  
TBV  C3B   C3B   C  0  1  N  N  N  14.086  51.637  16.092  -7.140  -1.730  -0.221  C3B   TBV  18  
TBV  C4B   C4B   C  0  1  N  N  N  14.480  52.211  17.391  -6.061  -1.684  -1.209  C4B   TBV  19  
TBV  CMB   CMB   C  0  1  N  N  N  12.614  52.713  14.114  -7.667  -0.450   1.959  CMB   TBV  20  
TBV  CAB   CAB   C  0  1  N  N  N  14.392  50.288  15.567  -8.314  -2.621  -0.241  CAB   TBV  21  
TBV  CBB   CBB   C  0  1  N  N  N  14.321  49.258  16.391  -8.467  -3.496  -1.230  CBB   TBV  22  
TBV  NC    NC    N  0  1  Y  N  N  16.713  53.808  19.152   5.433  -1.052   0.641  NC    TBV  23  
TBV  C1C   C1C   C  0  1  Y  N  N  17.321  52.862  18.367   6.450  -0.931  -0.259  C1C   TBV  24  
TBV  C2C   C2C   C  0  1  Y  N  N  18.334  51.996  19.038   6.416   0.312  -0.789  C2C   TBV  25  
TBV  C3C   C3C   C  0  1  Y  N  N  18.301  52.559  20.397   5.286   1.003  -0.161  C3C   TBV  26  
TBV  C4C   C4C   C  0  1  Y  N  N  17.304  53.635  20.363   4.726   0.113   0.705  C4C   TBV  27  
TBV  CMC   CMC   C  0  1  N  N  N  19.168  50.870  18.477   7.355   0.877  -1.824  CMC   TBV  28  
TBV  CAC   CAC   C  0  1  N  N  N  19.083  52.199  21.607   4.844   2.390  -0.416  CAC   TBV  29  
TBV  CBC   CBC   C  0  1  N  N  N  19.525  50.987  21.858   5.722   3.383  -0.382  CBC   TBV  30  
TBV  ND    ND    N  0  1  Y  N  N  15.224  55.878  20.620   1.530   1.044   0.138  ND    TBV  31  
TBV  C1D   C1D   C  0  1  Y  N  N  16.036  55.530  21.643   2.267   0.110   0.804  C1D   TBV  32  
TBV  C2D   C2D   C  0  1  Y  N  N  15.902  56.336  22.864   1.671  -1.089   0.644  C2D   TBV  33  
TBV  C3D   C3D   C  0  1  Y  N  N  14.867  57.297  22.514   0.525  -0.888  -0.150  C3D   TBV  34  
TBV  C4D   C4D   C  0  1  Y  N  N  14.522  56.913  21.133   0.463   0.427  -0.445  C4D   TBV  35  
TBV  CMD   CMD   C  0  1  N  N  N  16.642  56.205  24.160   2.144  -2.403   1.210  CMD   TBV  36  
TBV  OC    OC    O  0  1  N  N  N  17.036  52.686  17.026   7.350  -1.900  -0.571  OC    TBV  37  
TBV  CAD   CAD   C  0  1  N  N  N  14.270  58.386  23.354  -0.454  -1.947  -0.589  CAD   TBV  38  
TBV  CBD   CBD   C  0  1  N  N  N  14.883  59.729  22.996  -1.568  -2.074   0.451  CBD   TBV  39  
TBV  C46   C46   C  0  1  N  N  N  19.096  53.962  16.528   7.353  -2.804   1.670  C46   TBV  40  
TBV  CGD   CGD   C  0  1  N  N  N  14.373  60.820  23.916  -2.546  -3.133   0.012  CGD   TBV  41  
TBV  O2D   O2D   O  0  1  N  N  N  13.806  60.525  24.992  -2.370  -3.725  -1.026  O2D   TBV  42  
TBV  O1D   O1D   O  0  1  N  N  N  14.566  61.994  23.547  -3.613  -3.419   0.775  O1D   TBV  43  
TBV  C47   C47   C  0  1  N  N  N  17.061  54.208  15.158   5.957  -3.825  -0.133  C47   TBV  44  
TBV  C44   C44   C  0  1  N  N  N  17.880  53.223  15.985   7.278  -3.117   0.174  C44   TBV  45  
TBV  OB    OB    O  0  1  N  N  N  15.200  51.561  18.239  -5.968  -2.380  -2.206  OB    TBV  46  
TBV  C45   C45   C  0  1  N  N  N  18.407  52.085  15.119   8.446  -4.024  -0.217  C45   TBV  47  
TBV  HHA1  HHA1  H  0  0  N  N  N  13.983  58.643  20.221  -0.920   0.423  -2.070  HHA1  TBV  48  
TBV  HHA2  HHA2  H  0  0  N  N  N  12.631  57.456  20.937  -0.197   2.010  -1.714  HHA2  TBV  49  
TBV  HHB   HHB   H  0  1  N  N  N  12.268  55.271  15.318  -5.468   1.282   1.934  HHB   TBV  50  
TBV  HHD1  HHD1  H  0  0  N  N  N  16.632  53.695  22.280   3.565  -0.289   2.450  HHD1  TBV  51  
TBV  HHD2  HHD2  H  0  0  N  N  N  17.938  54.993  21.652   3.541   1.410   1.918  HHD2  TBV  52  
TBV  HAA1  HAA1  H  0  0  N  N  N  10.396  59.430  18.293  -0.961   4.133   1.443  HAA1  TBV  53  
TBV  HAA2  HAA2  H  0  0  N  N  N  11.226  59.287  19.894   0.109   3.268   0.313  HAA2  TBV  54  
TBV  HMA1  HMA1  H  0  0  N  N  N   9.768  57.641  16.418  -4.274   4.265   1.393  HMA1  TBV  55  
TBV  HMA2  HMA2  H  0  0  N  N  N  11.064  58.521  15.540  -4.333   3.047   2.689  HMA2  TBV  56  
TBV  HMA3  HMA3  H  0  0  N  N  N  10.836  56.760  15.274  -2.873   4.040   2.468  HMA3  TBV  57  
TBV  HBA1  HBA1  H  0  0  N  N  N  13.235  60.412  18.925  -1.109   4.265  -1.603  HBA1  TBV  58  
TBV  HBA2  HBA2  H  0  0  N  N  N  12.416  60.590  17.377  -2.179   5.129  -0.473  HBA2  TBV  59  
TBV  H2A   H2A   H  0  1  N  N  N  10.064  62.791  18.938   0.449   7.566  -1.251  H2A   TBV  60  
TBV  HB    HB    H  0  1  N  N  N  14.258  54.082  18.345  -4.379  -0.487  -1.291  HB    TBV  61  
TBV  HMB1  HMB1  H  0  0  N  N  N  11.525  52.717  14.266  -8.389   0.330   1.715  HMB1  TBV  62  
TBV  HMB2  HMB2  H  0  0  N  N  N  12.910  53.615  13.558  -8.196  -1.344   2.288  HMB2  TBV  63  
TBV  HMB3  HMB3  H  0  0  N  N  N  12.901  51.819  13.541  -7.011  -0.101   2.758  HMB3  TBV  64  
TBV  HC    HC    H  0  1  N  N  N  16.005  54.466  18.895   5.238  -1.850   1.157  HC    TBV  65  
TBV  HMC1  HMC1  H  0  0  N  N  N  19.371  51.058  17.412   6.960   0.677  -2.820  HMC1  TBV  66  
TBV  HMC2  HMC2  H  0  0  N  N  N  20.119  50.810  19.026   7.450   1.953  -1.679  HMC2  TBV  67  
TBV  HMC3  HMC3  H  0  0  N  N  N  18.622  49.921  18.583   8.334   0.408  -1.720  HMC3  TBV  68  
TBV  HAC   HAC   H  0  1  N  N  N  19.301  52.978  22.322   3.805   2.595  -0.630  HAC   TBV  69  
TBV  HBC1  HBC1  H  0  0  N  N  N  20.063  50.984  22.795   6.760   3.178  -0.168  HBC1  TBV  70  
TBV  HBC2  HBC2  H  0  0  N  N  N  19.374  50.126  21.224   5.398   4.397  -0.569  HBC2  TBV  71  
TBV  HD    HD    H  0  1  N  N  N  15.159  55.471  19.709   1.730   1.992   0.090  HD    TBV  72  
TBV  HMD1  HMD1  H  0  0  N  N  N  17.724  56.173  23.963   1.700  -2.556   2.194  HMD1  TBV  73  
TBV  HMD2  HMD2  H  0  0  N  N  N  16.412  57.068  24.802   1.845  -3.214   0.546  HMD2  TBV  74  
TBV  HMD3  HMD3  H  0  0  N  N  N  16.334  55.278  24.666   3.230  -2.390   1.300  HMD3  TBV  75  
TBV  HAD1  HAD1  H  0  0  N  N  N  13.185  58.426  23.176  -0.884  -1.667  -1.551  HAD1  TBV  76  
TBV  HAD2  HAD2  H  0  0  N  N  N  14.474  58.172  24.413   0.064  -2.901  -0.687  HAD2  TBV  77  
TBV  HBD1  HBD1  H  0  0  N  N  N  15.977  59.661  23.094  -1.138  -2.354   1.413  HBD1  TBV  78  
TBV  HBD2  HBD2  H  0  0  N  N  N  14.601  59.980  21.963  -2.085  -1.120   0.549  HBD2  TBV  79  
TBV  H1D   H1D   H  0  1  N  N  N  14.221  62.592  24.199  -4.213  -4.106   0.452  H1D   TBV  80  
TBV  H471  H471  H  0  0  N  N  N  16.864  55.112  15.753   5.969  -4.187  -1.161  H471  TBV  81  
TBV  H472  H472  H  0  0  N  N  N  17.622  54.481  14.252   5.829  -4.667   0.547  H472  TBV  82  
TBV  H473  H473  H  0  0  N  N  N  16.106  53.742  14.873   5.131  -3.125  -0.005  H473  TBV  83  
TBV  H461  H461  H  0  0  N  N  N  19.812  54.140  15.712   6.479  -2.222   1.964  H461  TBV  84  
TBV  H462  H462  H  0  0  N  N  N  18.779  54.925  16.954   7.375  -3.736   2.235  H462  TBV  85  
TBV  H463  H463  H  0  0  N  N  N  19.575  53.354  17.310   8.257  -2.232   1.877  H463  TBV  86  
TBV  H451  H451  H  0  0  N  N  N  18.534  52.439  14.085   9.387  -3.520   0.002  H451  TBV  87  
TBV  H452  H452  H  0  0  N  N  N  19.377  51.744  15.512   8.391  -4.953   0.352  H452  TBV  88  
TBV  H453  H453  H  0  0  N  N  N  17.691  51.250  15.135   8.392  -4.247  -1.282  H453  TBV  89  
TBV  HAB   HAB   H  0  1  N  N  N  14.668  50.148  14.532  -9.049  -2.564   0.548  HAB   TBV  90  
TBV  HBB1  HBB1  H  0  0  N  N  N  14.574  48.362  15.844  -9.327  -4.149  -1.245  HBB1  TBV  91  
TBV  HBB2  HBB2  H  0  0  N  N  N  14.055  49.305  17.437  -7.732  -3.553  -2.019  HBB2  TBV  92  
TBV  HA1   HA1   H  0  1  N  N  N  14.066  55.429  18.737  -3.056  -0.180  -0.670  HA1   TBV  93  
#   #
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
TBV  CHA  C1A   SING  N  N   1  
TBV  CHA  C4D   SING  N  N   2  
TBV  CHB  C4A   SING  N  N   3  
TBV  CHB  C1B   DOUB  N  N   4  
TBV  CHD  C4C   SING  N  N   5  
TBV  CHD  C1D   SING  N  Z   6  
TBV  NA   C1A   SING  Y  N   7  
TBV  NA   C4A   SING  Y  N   8  
TBV  NA   HA1   SING  N  N   9  
TBV  C1A  C2A   DOUB  Y  N  10  
TBV  C2A  C3A   SING  Y  N  11  
TBV  C2A  CAA   SING  N  N  12  
TBV  C3A  C4A   DOUB  Y  N  13  
TBV  C3A  CMA   SING  N  N  14  
TBV  CAA  CBA   SING  N  N  15  
TBV  CBA  CGA   SING  N  N  16  
TBV  CGA  O1A   DOUB  N  N  17  
TBV  CGA  O2A   SING  N  N  18  
TBV  NB   C1B   SING  N  N  19  
TBV  NB   C4B   SING  N  N  20  
TBV  C1B  C2B   SING  N  N  21  
TBV  C2B  CMB   SING  N  N  22  
TBV  C2B  C3B   DOUB  N  N  23  
TBV  NC   C1C   SING  Y  N  24  
TBV  NC   C4C   SING  Y  N  25  
TBV  C1C  C2C   DOUB  Y  N  26  
TBV  C1C  OC    SING  N  N  27  
TBV  C2C  C3C   SING  Y  N  28  
TBV  C2C  CMC   SING  N  N  29  
TBV  C3C  C4C   DOUB  Y  N  30  
TBV  C3C  CAC   SING  N  N  31  
TBV  CAC  CBC   DOUB  N  N  32  
TBV  ND   C1D   SING  Y  N  33  
TBV  ND   C4D   SING  Y  N  34  
TBV  C1D  C2D   DOUB  Y  N  35  
TBV  C2D  C3D   SING  Y  N  36  
TBV  C2D  CMD   SING  N  N  37  
TBV  C3D  C4D   DOUB  Y  N  38  
TBV  C3D  CAD   SING  N  N  39  
TBV  CAD  CBD   SING  N  N  40  
TBV  CBD  CGD   SING  N  N  41  
TBV  CGD  O1D   SING  N  N  42  
TBV  CGD  O2D   DOUB  N  N  43  
TBV  OC   C44   SING  N  N  44  
TBV  C44  C47   SING  N  N  45  
TBV  C44  C46   SING  N  N  46  
TBV  C44  C45   SING  N  N  47  
TBV  C3B  CAB   SING  N  N  48  
TBV  C3B  C4B   SING  N  N  49  
TBV  CAB  CBB   DOUB  N  N  50  
TBV  C4B  OB    DOUB  N  N  51  
TBV  CHA  HHA1  SING  N  N  52  
TBV  CHA  HHA2  SING  N  N  53  
TBV  CHB  HHB   SING  N  N  54  
TBV  CHD  HHD1  SING  N  N  55  
TBV  CHD  HHD2  SING  N  N  56  
TBV  CAA  HAA1  SING  N  N  57  
TBV  CAA  HAA2  SING  N  N  58  
TBV  CMA  HMA1  SING  N  N  59  
TBV  CMA  HMA2  SING  N  N  60  
TBV  CMA  HMA3  SING  N  N  61  
TBV  CBA  HBA1  SING  N  N  62  
TBV  CBA  HBA2  SING  N  N  63  
TBV  O2A  H2A   SING  N  N  64  
TBV  NB   HB    SING  N  N  65  
TBV  CMB  HMB1  SING  N  N  66  
TBV  CMB  HMB2  SING  N  N  67  
TBV  CMB  HMB3  SING  N  N  68  
TBV  NC   HC    SING  N  N  69  
TBV  CMC  HMC1  SING  N  N  70  
TBV  CMC  HMC2  SING  N  N  71  
TBV  CMC  HMC3  SING  N  N  72  
TBV  CAC  HAC   SING  N  N  73  
TBV  CBC  HBC1  SING  N  N  74  
TBV  CBC  HBC2  SING  N  N  75  
TBV  ND   HD    SING  N  N  76  
TBV  CMD  HMD1  SING  N  N  77  
TBV  CMD  HMD2  SING  N  N  78  
TBV  CMD  HMD3  SING  N  N  79  
TBV  CAD  HAD1  SING  N  N  80  
TBV  CAD  HAD2  SING  N  N  81  
TBV  CBD  HBD1  SING  N  N  82  
TBV  CBD  HBD2  SING  N  N  83  
TBV  O1D  H1D   SING  N  N  84  
TBV  C47  H471  SING  N  N  85  
TBV  C47  H472  SING  N  N  86  
TBV  C47  H473  SING  N  N  87  
TBV  C46  H461  SING  N  N  88  
TBV  C46  H462  SING  N  N  89  
TBV  C46  H463  SING  N  N  90  
TBV  C45  H451  SING  N  N  91  
TBV  C45  H452  SING  N  N  92  
TBV  C45  H453  SING  N  N  93  
TBV  CAB  HAB   SING  N  N  94  
TBV  CBB  HBB1  SING  N  N  95  
TBV  CBB  HBB2  SING  N  N  96  
#   #
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
TBV  SMILES_CANONICAL  CACTVS                3.352  "Cc1c(Cc2[nH]c(OC(C)(C)C)c(C)c2C=C)[nH]c(Cc3[nH]c(\C=C4/NC(=O)C(=C4C)C=C)c(C)c3CCC(O)=O)c1CCC(O)=O"  
TBV  SMILES            CACTVS                3.352  "Cc1c(Cc2[nH]c(OC(C)(C)C)c(C)c2C=C)[nH]c(Cc3[nH]c(C=C4NC(=O)C(=C4C)C=C)c(C)c3CCC(O)=O)c1CCC(O)=O"  
TBV  SMILES_CANONICAL  "OpenEye OEToolkits"  1.6.1  "Cc1c(c([nH]c1Cc2c(c(c([nH]2)OC(C)(C)C)C)C=C)Cc3c(c(c([nH]3)\C=C/4\C(=C(C(=O)N4)C=C)C)C)CCC(=O)O)CCC(=O)O"  
TBV  SMILES            "OpenEye OEToolkits"  1.6.1  "Cc1c(c([nH]c1Cc2c(c(c([nH]2)OC(C)(C)C)C)C=C)Cc3c(c(c([nH]3)C=C4C(=C(C(=O)N4)C=C)C)C)CCC(=O)O)CCC(=O)O"  
TBV  InChI             InChI                 1.03   "InChI=1S/C37H46N4O6/c1-10-23-22(6)36(47-37(7,8)9)41-30(23)17-28-21(5)26(13-15-34(44)45)32(39-28)18-31-25(12-14-33(42)43)20(4)27(38-31)16-29-19(3)24(11-2)35(46)40-29/h10-11,16,38-39,41H,1-2,12-15,17-18H2,3-9H3,(H,40,46)(H,42,43)(H,44,45)/b29-16-"  
TBV  InChIKey          InChI                 1.03   JDQNAGCTUKHXGS-MWLSYYOVSA-N  
#
_pdbx_chem_comp_identifier.comp_id          TBV
_pdbx_chem_comp_identifier.type             "SYSTEMATIC NAME"
_pdbx_chem_comp_identifier.program          "OpenEye OEToolkits"
_pdbx_chem_comp_identifier.program_version  1.6.1
_pdbx_chem_comp_identifier.identifier       "3-[2-[[3-(2-carboxyethyl)-5-[[3-ethenyl-4-methyl-5-[(2-methylpropan-2-yl)oxy]-1H-pyrrol-2-yl]methyl]-4-methyl-1H-pyrrol-2-yl]methyl]-5-[(Z)-(4-ethenyl-3-methyl-5-oxo-pyrrol-2-ylidene)methyl]-4-methyl-1H-pyrrol-3-yl]propanoic 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
TBV  "Create component"      2009-03-19  EBI   
TBV  "Modify aromatic_flag"  2011-06-04  RCSB  
TBV  "Modify descriptor"     2011-06-04  RCSB  
TBV  "Modify synonyms"       2020-06-05  PDBE  
#
_pdbx_chem_comp_synonyms.ordinal     1
_pdbx_chem_comp_synonyms.comp_id     TBV
_pdbx_chem_comp_synonyms.name        BILIVERDIN
_pdbx_chem_comp_synonyms.provenance  ?
_pdbx_chem_comp_synonyms.type        ?
##
