MiMeDB: Showing metabocard for alpha-D-Ribose 1-methylphosphonate 5-triphosphate (MMDBc0031930)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 01:55:27 UTC

Update Date

2022-08-31 18:26:32 UTC

Metabolite ID

MMDBc0031930

Metabolite Identification

Common Name

alpha-D-Ribose 1-methylphosphonate 5-triphosphate

Description

In E. coli, alpha-D-Ribose 1-methylphosphonate 5-triphosphate is an intermediate in the transformation of Phosphonates to Phosphate. The enzyme alpha-D-ribose 1-methylphosphonate 5-triphosphate synthase (EC 2.7.8.37) catalyses the reaction ATP + methylphosphonate <=> alpha-D-ribose 1-methylphosphonate 5-triphosphate + adenine (PMID: 22089136 ).

Structure

MOL SDF PDB SMILES InChI

 
  Mrv1533006051502352D          
 
 26 26  0  0  1  0            999 V2000
    9.8357   -4.7270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0714   -5.2234    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3940   -4.7162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8144   -5.9668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7340   -5.1886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9911   -5.9668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9490   -4.9351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3341   -5.4909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5004   -5.4909    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -5.4909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4971   -6.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4971   -4.6606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8400   -5.4874    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    3.0099   -5.4874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8366   -6.3176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8366   -4.6537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1762   -5.4839    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    2.1727   -6.3141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460   -5.4770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1727   -4.6502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5238   -4.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6985   -4.7604    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   10.6985   -5.5823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6985   -3.9315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2924   -6.6374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5106   -6.6312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  2  0  0  0  0
  5  6  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
  1 22  1  0  0  0  0
  4 25  1  6  0  0  0
  6 26  1  6  0  0  0
M  END

 
  Mrv1533006051502352D          
 
 26 26  0  0  1  0            999 V2000
    9.8357   -4.7270    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.0714   -5.2234    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    8.3940   -4.7162    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.8144   -5.9668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.7340   -5.1886    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    7.9911   -5.9668    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.9490   -4.9351    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.3341   -5.4909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.5004   -5.4909    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    4.6703   -5.4909    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4971   -6.3211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.4971   -4.6606    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8400   -5.4874    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    3.0099   -5.4874    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8366   -6.3176    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8366   -4.6537    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1762   -5.4839    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    2.1727   -6.3141    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3460   -5.4770    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1727   -4.6502    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.5238   -4.7673    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.6985   -4.7604    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   10.6985   -5.5823    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.6985   -3.9315    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.2924   -6.6374    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.5106   -6.6312    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  6  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  3  5  1  0  0  0  0
  4  6  1  0  0  0  0
  5  7  1  1  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
  9 12  2  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
 13 16  2  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 17 19  1  0  0  0  0
 17 20  2  0  0  0  0
  5  6  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 22 24  2  0  0  0  0
  1 22  1  0  0  0  0
  4 25  1  6  0  0  0
  6 26  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0031930

> <DATABASE_NAME>
MIME

> <SMILES>
CP(O)(=O)O[C@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C6H16O16P4/c1-23(9,10)20-6-5(8)4(7)3(19-6)2-18-25(14,15)22-26(16,17)21-24(11,12)13/h3-8H,2H2,1H3,(H,9,10)(H,14,15)(H,16,17)(H2,11,12,13)/t3-,4-,5-,6-/m1/s1

> <INCHI_KEY>
UXNHAIRVTPGNPL-KVTDHHQDSA-N

> <FORMULA>
C6H16O16P4

> <MOLECULAR_WEIGHT>
468.073

> <EXACT_MASS>
467.938882427

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
42

> <JCHEM_AVERAGE_POLARIZABILITY>
32.87328559837629

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
({[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-{[hydroxy(methyl)phosphoryl]oxy}oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)phosphonic acid

> <ALOGPS_LOGP>
-0.04

> <JCHEM_LOGP>
-3.1815276599999995

> <ALOGPS_LOGS>
-1.59

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-4

> <JCHEM_PKA>
1.427661052231115

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.7545435439600032

> <JCHEM_PKA_STRONGEST_BASIC>
-3.68085352899627

> <JCHEM_POLAR_SURFACE_AREA>
256.03999999999996

> <JCHEM_REFRACTIVITY>
75.97859999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.19e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
({[(2R,3S,4R,5R)-3,4-dihydroxy-5-{[hydroxy(methyl)phosphoryl]oxy}oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 05-JUN-15   NONE
TITLE     NULL                                                        
COMPND    MOLECULE:                                                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   05-JUN-15         0                                  
HETATM    1  O   UNK     0      18.360  -8.824   0.000  0.00  0.00           O+0
HETATM    2  C   UNK     0      16.933  -9.750   0.000  0.00  0.00           C+0
HETATM    3  O   UNK     0      15.669  -8.804   0.000  0.00  0.00           O+0
HETATM    4  C   UNK     0      16.454 -11.138   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      14.437  -9.685   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      14.917 -11.138   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      12.971  -9.212   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0      11.824 -10.250   0.000  0.00  0.00           O+0
HETATM    9  P   UNK     0      10.267 -10.250   0.000  0.00  0.00           P+0
HETATM   10  O   UNK     0       8.718 -10.250   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      10.261 -11.799   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      10.261  -8.700   0.000  0.00  0.00           O+0
HETATM   13  P   UNK     0       7.168 -10.243   0.000  0.00  0.00           P+0
HETATM   14  O   UNK     0       5.618 -10.243   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0       7.162 -11.793   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0       7.162  -8.687   0.000  0.00  0.00           O+0
HETATM   17  P   UNK     0       4.062 -10.237   0.000  0.00  0.00           P+0
HETATM   18  O   UNK     0       4.056 -11.786   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0       2.512 -10.224   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0       4.056  -8.680   0.000  0.00  0.00           O+0
HETATM   21  C   UNK     0      21.511  -8.899   0.000  0.00  0.00           C+0
HETATM   22  P   UNK     0      19.970  -8.886   0.000  0.00  0.00           P+0
HETATM   23  O   UNK     0      19.970 -10.420   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      19.970  -7.339   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      17.346 -12.390   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0      14.020 -12.378   0.000  0.00  0.00           O+0
CONECT    1    2   22                                                       
CONECT    2    1    3    4                                                  
CONECT    3    2    5                                                       
CONECT    4    2    6   25                                                  
CONECT    5    3    7    6                                                  
CONECT    6    4    5   26                                                  
CONECT    7    5    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   11   12                                             
CONECT   10    9   13                                                       
CONECT   11    9                                                            
CONECT   12    9                                                            
CONECT   13   10   14   15   16                                             
CONECT   14   13   17                                                       
CONECT   15   13                                                            
CONECT   16   13                                                            
CONECT   17   14   18   19   20                                             
CONECT   18   17                                                            
CONECT   19   17                                                            
CONECT   20   17                                                            
CONECT   21   22                                                            
CONECT   22   21   23   24    1                                             
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25    4                                                            
CONECT   26    6                                                            
MASTER        0    0    0    0    0    0    0    0   26    0   52    0
END

Synonyms

Value	Source
a-D-Ribose 1-methylphosphonate 5-triphosphate	Generator
a-D-Ribose 1-methylphosphonic acid 5-triphosphoric acid	Generator
alpha-D-Ribose 1-methylphosphonic acid 5-triphosphoric acid	Generator
Α-D-ribose 1-methylphosphonate 5-triphosphate	Generator
Α-D-ribose 1-methylphosphonic acid 5-triphosphoric acid	Generator

Molecular Formula

C₆H₁₆O₁₆P₄

Average Mass

468.073

Monoisotopic Mass

467.938882427

IUPAC Name

({[({[(2R,3S,4R,5R)-3,4-dihydroxy-5-{[hydroxy(methyl)phosphoryl]oxy}oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)phosphonic acid

Traditional Name

({[(2R,3S,4R,5R)-3,4-dihydroxy-5-{[hydroxy(methyl)phosphoryl]oxy}oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxyphosphonic acid

CAS Registry Number

Not Available

SMILES

CP(O)(=O)O[C@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O

InChI Identifier

InChI=1S/C6H16O16P4/c1-23(9,10)20-6-5(8)4(7)3(19-6)2-18-25(14,15)22-26(16,17)21-24(11,12)13/h3-8H,2H2,1H3,(H,9,10)(H,14,15)(H,16,17)(H2,11,12,13)/t3-,4-,5-,6-/m1/s1

InChI Key

UXNHAIRVTPGNPL-KVTDHHQDSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentose phosphates. These are carbohydrate derivatives containing a pentose substituted by one or more phosphate groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Pentose phosphates

Alternative Parents

Substituents

Pentose phosphate
Pentose-5-phosphate
Monosaccharide phosphate
Monoalkyl phosphate
Organic phosphoric acid derivative
Phosphoric acid ester
Phosphonic acid ester
Alkyl phosphate
Organophosphonic acid derivative
Organophosphonic acid
Tetrahydrofuran
Secondary alcohol
1,2-diol
Oxacycle
Organoheterocyclic compound
Alcohol
Hydrocarbon derivative
Organic oxide
Organophosphorus compound
Organopnictogen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

organic phosphonate (CHEBI:68824 )
ribose triphosphate (CHEBI:68824 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	11.9 g/L	ALOGPS
logP	-0.04	ALOGPS
logP	-3.2	ChemAxon
logS	-1.6	ALOGPS
pKa (Strongest Acidic)	0.75	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-4	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	256.04 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	75.98 m³·mol⁻¹	ChemAxon
Polarizability	32.87 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted GC-MS	Predicted GC-MS Spectrum - GC-MS (TMS_5_11) - 70eV, Positive	Not Available	2022-08-08	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0002-9113200000-0281d4d58743ac3e86f2	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-03kd-8797100000-c8d7c9854872d0386784	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-0002-9210000000-162633a48b446e3d4360	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-00or-9020600000-139809b27af9f7963786	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-9120000000-49f2e4c84949bce8c2c7	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9100000000-ca51af04e235c66ccc2d	2015-09-15	View Spectrum
MS	Mass Spectrum (Electron Ionization)	Not Available	2022-08-06	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-17	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria	Proteobacteria	2	Human ; Human feces; Human feces; pleural fluid plaque; bal; Human stool	Unknown

Exposure Sources

Host Biospecimen and Location

Host and Biospecimen	Status	Mean	Std	Min	Max	Units	Age	Sex	Health Condition	Data Source	Reference

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

C20422

BioCyc ID

CPD0-2479

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

70678978

PDB ID

Not Available

ChEBI ID

68824

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Wishart DS, Li C, Marcu A, Badran H, Pon A, Budinski Z, Patron J, Lipton D, Cao X, Oler E, Li K, Paccoud M, Hong C, Guo AC, Chan C, Wei W, Ramirez-Gaona M: PathBank: a comprehensive pathway database for model organisms. Nucleic Acids Res. 2020 Jan 8;48(D1):D470-D478. doi: 10.1093/nar/gkz861. [PubMed:31602464 ]
Bansal P, Morgat A, Axelsen KB, Muthukrishnan V, Coudert E, Aimo L, Hyka-Nouspikel N, Gasteiger E, Kerhornou A, Neto TB, Pozzato M, Blatter MC, Ignatchenko A, Redaschi N, Bridge A: Rhea, the reaction knowledgebase in 2022. Nucleic Acids Res. 2022 Jan 7;50(D1):D693-D700. doi: 10.1093/nar/gkab1016. [PubMed:34755880 ]

Showing metabocard for alpha-D-Ribose 1-methylphosphonate 5-triphosphate (MMDBc0031930)

MOL for #<Metabolite:0x00007fdb0a9bc638>

3D MOL for #<Metabolite:0x00007fdb0a9bc638>

3D SDF for #<Metabolite:0x00007fdb0a9bc638>

3D-SDF for #<Metabolite:0x00007fdb0a9bc638>

PDB for #<Metabolite:0x00007fdb0a9bc638>

3D PDB for #<Metabolite:0x00007fdb0a9bc638>

SMILES for #<Metabolite:0x00007fdb0a9bc638>

INCHI for #<Metabolite:0x00007fdb0a9bc638>

Structure for #<Metabolite:0x00007fdb0a9bc638>

3D Structure for #<Metabolite:0x00007fdb0a9bc638>