MiMeDB: Showing metabocard for tetrahydropteroyl mono-L-glutamate (MMDBc0032180)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 02:05:46 UTC

Update Date

2022-08-31 18:32:30 UTC

Metabolite ID

MMDBc0032180

Metabolite Identification

Common Name

tetrahydropteroyl mono-L-glutamate

Description

Tetrahydropteroyl mono-L-glutamate, also known as tetrahydrofolate is a soluble coenzyme (vitamin B9) that is synthesized de novo by plants and microorganisms, and absorbed from the diet by animals. It is composed of three distinct parts: a pterin ring, a p-ABA (p-aminobenzoic acid) and a polyglutamate chain with a number of residues varying between 1 and 8. Only the tetra-reduced form of the molecule serves as a coenzyme for C1 transfer reactions. In biological systems, the C1-units exist under various oxidation states and the different tetrahydrofolate derivatives constitute a family of related molecules named indistinctly under the generic term folate. (PMID 16042593 )

Structure

MOL SDF PDB SMILES InChI


  Mrv1572008131519112D          

 32 34  0  0  0  0            999 V2000
   -2.1434   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -1.0312    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -2.6812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.6812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0012   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0012   -1.4437    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.2062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7157   -2.6812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.2062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.2687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.0312    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8578    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0012    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7157    1.4437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0012    0.2062    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    2.8578    2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723    2.6812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.6812    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  CHG  2  29  -1  32  -1
M  END


  Mrv1572008131519112D          

 32 34  0  0  0  0            999 V2000
   -2.1434   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1434   -1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -1.0312    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5723   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8578   -2.6812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -2.6812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0012   -2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0012   -1.4437    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2868   -0.2062    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7157   -2.6812    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4289   -0.2062    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7144    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7144    0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -0.2062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    2.2687    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.0312    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8578    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2868    1.4437    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0012    1.0312    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7157    1.4437    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0012    0.2062    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    2.8578    2.2687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5723    2.6812    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    2.6812    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  1  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9 10  1  0  0  0  0
  4 10  1  0  0  0  0
 10 11  2  0  0  0  0
  8 12  1  0  0  0  0
  2 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  2  0  0  0  0
 16 17  1  0  0  0  0
 17 18  2  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 15 20  1  0  0  0  0
 18 21  1  0  0  0  0
 21 22  2  0  0  0  0
 21 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  2  0  0  0  0
 27 29  1  0  0  0  0
 24 30  1  0  0  0  0
 30 31  2  0  0  0  0
 30 32  1  0  0  0  0
M  CHG  2  29  -1  32  -1
M  END
> <DATABASE_ID>
MMDBc0032180

> <DATABASE_NAME>
MIME

> <SMILES>
NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C=C3)C(=O)NC(CCC([O-])=O)C([O-])=O)N2)N1

> <INCHI_IDENTIFIER>
InChI=1S/C19H23N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4,11-12,21,23H,5-8H2,(H,24,29)(H,27,28)(H,31,32)(H4,20,22,25,26,30)/p-2

> <INCHI_KEY>
MSTNYGQPCMXVAQ-UHFFFAOYSA-L

> <FORMULA>
C19H21N7O6

> <MOLECULAR_WEIGHT>
443.421

> <EXACT_MASS>
443.156428584

> <JCHEM_ACCEPTOR_COUNT>
12

> <JCHEM_ATOM_COUNT>
53

> <JCHEM_AVERAGE_POLARIZABILITY>
43.75633139377499

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
-2

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[(4-{[(2-amino-4-oxo-1,4,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioate

> <ALOGPS_LOGP>
0.18

> <JCHEM_LOGP>
-2.2237752242087367

> <ALOGPS_LOGS>
-2.92

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
4.204005738351694

> <JCHEM_PKA_STRONGEST_ACIDIC>
3.4675958752347134

> <JCHEM_PKA_STRONGEST_BASIC>
2.796095578971363

> <JCHEM_POLAR_SURFACE_AREA>
212.92999999999998

> <JCHEM_REFRACTIVITY>
143.0608

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
5.72e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-[(4-{[(2-amino-4-oxo-5,6,7,8-tetrahydro-1H-pteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 13-AUG-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   13-AUG-15         0                                  
HETATM    1  C   UNK     0      -4.001  -4.235   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.001  -2.695   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      -5.335  -1.925   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      -6.668  -2.695   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -6.668  -4.235   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0      -5.335  -5.005   0.000  0.00  0.00           N+0
HETATM    7  N   UNK     0      -8.002  -5.005   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      -9.336  -4.235   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      -9.336  -2.695   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      -8.002  -1.925   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0      -8.002  -0.385   0.000  0.00  0.00           O+0
HETATM   12  N   UNK     0     -10.669  -5.005   0.000  0.00  0.00           N+0
HETATM   13  C   UNK     0      -2.667  -1.925   0.000  0.00  0.00           C+0
HETATM   14  N   UNK     0      -2.667  -0.385   0.000  0.00  0.00           N+0
HETATM   15  C   UNK     0      -1.334   0.385   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      -1.334   1.925   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       0.000   2.695   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       1.334   1.925   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       1.334   0.385   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.000  -0.385   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.667   2.695   0.000  0.00  0.00           C+0
HETATM   22  O   UNK     0       2.667   4.235   0.000  0.00  0.00           O+0
HETATM   23  N   UNK     0       4.001   1.925   0.000  0.00  0.00           N+0
HETATM   24  C   UNK     0       5.335   2.695   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       6.668   1.925   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       8.002   2.695   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       9.336   1.925   0.000  0.00  0.00           C+0
HETATM   28  O   UNK     0      10.669   2.695   0.000  0.00  0.00           O+0
HETATM   29  O   UNK     0       9.336   0.385   0.000  0.00  0.00           O-1
HETATM   30  C   UNK     0       5.335   4.235   0.000  0.00  0.00           C+0
HETATM   31  O   UNK     0       6.668   5.005   0.000  0.00  0.00           O+0
HETATM   32  O   UNK     0       4.001   5.005   0.000  0.00  0.00           O-1
CONECT    1    2    6                                                       
CONECT    2    1    3   13                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5   10                                                  
CONECT    5    4    6    7                                                  
CONECT    6    5    1                                                       
CONECT    7    5    8                                                       
CONECT    8    7    9   12                                                  
CONECT    9    8   10                                                       
CONECT   10    9    4   11                                                  
CONECT   11   10                                                            
CONECT   12    8                                                            
CONECT   13    2   14                                                       
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   21                                                  
CONECT   19   18   20                                                       
CONECT   20   19   15                                                       
CONECT   21   18   22   23                                                  
CONECT   22   21                                                            
CONECT   23   21   24                                                       
CONECT   24   23   25   30                                                  
CONECT   25   24   26                                                       
CONECT   26   25   27                                                       
CONECT   27   26   28   29                                                  
CONECT   28   27                                                            
CONECT   29   27                                                            
CONECT   30   24   31   32                                                  
CONECT   31   30                                                            
CONECT   32   30                                                            
MASTER        0    0    0    0    0    0    0    0   32    0   68    0
END

Synonyms

Value	Source
Tetrahydropteroyl mono-L-glutamic acid	Generator

Molecular Formula

C₁₉H₂₁N₇O₆

Average Mass

443.421

Monoisotopic Mass

443.156428584

IUPAC Name

2-[(4-{[(2-amino-4-oxo-1,4,5,6,7,8-hexahydropteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioate

Traditional Name

2-[(4-{[(2-amino-4-oxo-5,6,7,8-tetrahydro-1H-pteridin-6-yl)methyl]amino}phenyl)formamido]pentanedioate

CAS Registry Number

Not Available

SMILES

NC1=NC(=O)C2=C(NCC(CNC3=CC=C(C=C3)C(=O)NC(CCC([O-])=O)C([O-])=O)N2)N1

InChI Identifier

InChI=1S/C19H23N7O6/c20-19-25-15-14(17(30)26-19)23-11(8-22-15)7-21-10-3-1-9(2-4-10)16(29)24-12(18(31)32)5-6-13(27)28/h1-4,11-12,21,23H,5-8H2,(H,24,29)(H,27,28)(H,31,32)(H4,20,22,25,26,30)/p-2

InChI Key

MSTNYGQPCMXVAQ-UHFFFAOYSA-L

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as polyprenyl phospho carbohydrates. These are polyprenyl phosphates with a carbohydrate moiety attached to it.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Polyprenols

Direct Parent

Polyprenyl phospho carbohydrates

Alternative Parents

Substituents

Polyterpenoid
Polyprenyl phospho carbohydrate
Bactoprenol diphosphate
Polyprenyl monophosphate
Polyprenyl phosphate skeleton
N-acyl-alpha-hexosamine
Hexose monosaccharide
Isoprenoid phosphate
Monosaccharide phosphate
Organic pyrophosphate
Monoalkyl phosphate
Monosaccharide
Organic phosphoric acid derivative
Oxane
Phosphoric acid ester
Alkyl phosphate
Acetamide
Carboxamide group
Secondary carboxylic acid amide
Secondary alcohol
Oxacycle
Carboxylic acid derivative
Organoheterocyclic compound
Carbonyl group
Organic oxide
Alcohol
Organopnictogen compound
Organic oxygen compound
Organic nitrogen compound
Hydrocarbon derivative
Primary alcohol
Organonitrogen compound
Organooxygen compound
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic compounds

External Descriptors

polyprenyl glycosyl phosphate (CHEBI:16511 )
N-acyl-D-glucosamine 1-phosphate (CHEBI:16511 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.57 g/L	ALOGPS
logP	0.18	ALOGPS
logP	-2.2	ChemAxon
logS	-2.9	ALOGPS
pKa (Strongest Acidic)	3.47	ChemAxon
pKa (Strongest Basic)	2.8	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	12	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	212.93 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	143.06 m³·mol⁻¹	ChemAxon
Polarizability	43.76 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-0006-0000900000-86711adedb4c17c5f407	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-0005-0000900000-47891bd2186d7759bb7e	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-00fr-9211500000-e36c75aa18884d23d714	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-0006-0000900000-7cacc4b456840684186c	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-0006-2000900000-9a45cd85179831331550	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-0006-9100100000-a8f7d7cabba4464375e3	2015-09-15	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	1	Human ; Human feces; Human feces; pleural fluid plaque; bal; Human stool	Unknown
Eukaryota/Fungi	Ascomycota	1	Human feces; Human saliva	Unknown

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference

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

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

135956778

PDB ID

Not Available

ChEBI ID

Not Available

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 ]

Showing metabocard for tetrahydropteroyl mono-L-glutamate (MMDBc0032180)

MOL for #<Metabolite:0x00007fecea856d88>

3D MOL for #<Metabolite:0x00007fecea856d88>

3D SDF for #<Metabolite:0x00007fecea856d88>

3D-SDF for #<Metabolite:0x00007fecea856d88>

PDB for #<Metabolite:0x00007fecea856d88>

3D PDB for #<Metabolite:0x00007fecea856d88>

SMILES for #<Metabolite:0x00007fecea856d88>

INCHI for #<Metabolite:0x00007fecea856d88>

Structure for #<Metabolite:0x00007fecea856d88>

3D Structure for #<Metabolite:0x00007fecea856d88>