MiMeDB: Showing metabocard for L-Lysyl-tRNA (MMDBc0031907)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2021-11-18 01:54:26 UTC

Update Date

2024-04-30 19:53:42 UTC

Metabolite ID

MMDBc0031907

Metabolite Identification

Common Name

L-Lysyl-tRNA

Description

L-Lysyl-tRNA is an intermediate in tRNA charging pathway in E.coli. It is a product for the enzyme lysyl-tRNA synthetase which catalyzes the reaction ATP + L-lysine + tRNALys -> AMP + diphosphate + L-lysyl-tRNALys (BioCyc class: Charged-LYS-tRNAs).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306222023482D          

 27 26  0  0  0  0            999 V2000
   -2.0863   -0.6105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3718   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0572    0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861    0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3718    0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573    1.0395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006    1.0395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0572   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9150   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6295   -0.6105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7716    1.0395    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7716   -0.6105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006   -0.6105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9150    0.6270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006    1.8645    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -3.5152   -2.2605    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.3882   -2.5625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2132   -1.1335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0863   -1.4355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573   -0.6105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8007   -1.8480    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0863    1.0395    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573    1.8645    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006    2.6895    0.0000 Mo  0  2  0  0  0  0  0  0  0  0  0  0
    5.9867    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  2  1  0  0  0  0
  6  3  1  0  0  0  0
  6  5  2  0  0  0  0
  7  4  2  0  0  0  0
  8  4  1  0  0  0  0
  9  3  1  0  0  0  0
 11 10  2  0  0  0  0
 12  3  1  0  0  0  0
 12  4  1  0  0  0  0
 13  7  1  0  0  0  0
 13  9  1  0  0  0  0
 14  7  1  0  0  0  0
 14 10  1  0  0  0  0
 15  8  2  0  0  0  0
 15 10  1  0  0  0  0
 16  8  1  0  0  0  0
 20  1  1  0  0  0  0
 21  2  1  0  0  0  0
 21  9  1  0  0  0  0
 22 17  1  0  0  0  0
 22 18  1  0  0  0  0
 22 19  2  0  0  0  0
 22 20  1  0  0  0  0
 23  5  1  0  0  0  0
 24  6  1  0  0  0  0
M  CHG  3  16  -1  17  -1  25   2
M  END


  Mrv1652306222023482D          

 27 26  0  0  0  0            999 V2000
   -2.0863   -0.6105    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3718   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0572    0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861    0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3718    0.6270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573    1.0395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4861   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006    1.0395    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0572   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9150   -0.1980    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6295   -0.6105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7716    1.0395    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7716   -0.6105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006   -0.6105    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.9150    0.6270    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006    1.8645    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -3.5152   -2.2605    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
   -2.3882   -2.5625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2132   -1.1335    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0863   -1.4355    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573   -0.6105    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8007   -1.8480    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0863    1.0395    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6573    1.8645    0.0000 S   0  0  0  0  0  0  0  0  0  0  0  0
    2.2006    2.6895    0.0000 Mo  0  2  0  0  0  0  0  0  0  0  0  0
    5.9867    0.0000    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000   -4.2125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  0  0  0  0
  5  2  1  0  0  0  0
  6  3  1  0  0  0  0
  6  5  2  0  0  0  0
  7  4  2  0  0  0  0
  8  4  1  0  0  0  0
  9  3  1  0  0  0  0
 11 10  2  0  0  0  0
 12  3  1  0  0  0  0
 12  4  1  0  0  0  0
 13  7  1  0  0  0  0
 13  9  1  0  0  0  0
 14  7  1  0  0  0  0
 14 10  1  0  0  0  0
 15  8  2  0  0  0  0
 15 10  1  0  0  0  0
 16  8  1  0  0  0  0
 20  1  1  0  0  0  0
 21  2  1  0  0  0  0
 21  9  1  0  0  0  0
 22 17  1  0  0  0  0
 22 18  1  0  0  0  0
 22 19  2  0  0  0  0
 22 20  1  0  0  0  0
 23  5  1  0  0  0  0
 24  6  1  0  0  0  0
M  CHG  3  16  -1  17  -1  25   2
M  END
> <DATABASE_ID>
MMDBc0031907

> <DATABASE_NAME>
MIME

> <SMILES>
O.O.[Mo++].OP([O-])(=O)OCC1OC2NC3=C(NC2C(S)=C1S)C([O-])=NC(=N)N3

> <INCHI_IDENTIFIER>
InChI=1S/C10H14N5O6PS2.Mo.2H2O/c11-10-14-7-4(8(16)15-10)12-3-6(24)5(23)2(21-9(3)13-7)1-20-22(17,18)19;;;/h2-3,9,12,23-24H,1H2,(H2,17,18,19)(H4,11,13,14,15,16);;2*1H2/q;+2;;/p-2

> <INCHI_KEY>
VUKICSJFFDCESC-UHFFFAOYSA-L

> <FORMULA>
C10H16MoN5O8PS2

> <MOLECULAR_WEIGHT>
525.31

> <EXACT_MASS>
526.923197

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
43

> <JCHEM_AVERAGE_POLARIZABILITY>
34.17847966980008

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
7

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
molybdenum(2+) ion 8-[(hydrogen phosphonooxy)methyl]-2-imino-6,7-disulfanyl-1H,2H,5H,5aH,8H,9aH,10H-pyrano[3,2-g]pteridin-4-olate dihydrate

> <ALOGPS_LOGP>
0.86

> <JCHEM_LOGP>
-1.8514778430814034

> <ALOGPS_LOGS>
-2.74

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
5.854304600172498

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.1935424585190892

> <JCHEM_PKA_STRONGEST_BASIC>
2.905079388232262

> <JCHEM_POLAR_SURFACE_AREA>
174.17999999999998

> <JCHEM_REFRACTIVITY>
119.20759999999999

> <JCHEM_ROTATABLE_BOND_COUNT>
3

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.79e-01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
molybdenum(2+) ion 8-[(hydrogen phosphonooxy)methyl]-2-imino-6,7-disulfanyl-1H,5H,5aH,8H,9aH,10H-pyrano[3,2-g]pteridin-4-olate dihydrate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 22-JUN-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   22-JUN-20         0                                  
HETATM    1  C   UNK     0      -3.894  -1.140   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.561  -0.370   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       0.107   1.170   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.774   1.170   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -2.561   1.170   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -1.227   1.940   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.774  -0.370   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.108   1.940   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       0.107  -0.370   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       5.441  -0.370   0.000  0.00  0.00           C+0
HETATM   11  N   UNK     0       6.775  -1.140   0.000  0.00  0.00           N+0
HETATM   12  N   UNK     0       1.440   1.940   0.000  0.00  0.00           N+0
HETATM   13  N   UNK     0       1.440  -1.140   0.000  0.00  0.00           N+0
HETATM   14  N   UNK     0       4.108  -1.140   0.000  0.00  0.00           N+0
HETATM   15  N   UNK     0       5.441   1.170   0.000  0.00  0.00           N+0
HETATM   16  O   UNK     0       4.108   3.480   0.000  0.00  0.00           O-1
HETATM   17  O   UNK     0      -6.562  -4.220   0.000  0.00  0.00           O-1
HETATM   18  O   UNK     0      -4.458  -4.783   0.000  0.00  0.00           O+0
HETATM   19  O   UNK     0      -5.998  -2.116   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0      -3.894  -2.680   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      -1.227  -1.140   0.000  0.00  0.00           O+0
HETATM   22  P   UNK     0      -5.228  -3.450   0.000  0.00  0.00           P+0
HETATM   23  S   UNK     0      -3.894   1.940   0.000  0.00  0.00           S+0
HETATM   24  S   UNK     0      -1.227   3.480   0.000  0.00  0.00           S+0
HETATM   25 Mo   UNK     0       4.108   5.020   0.000  0.00  0.00          Mo+2
HETATM   26  O   UNK     0      11.175   0.000   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       0.000  -7.863   0.000  0.00  0.00           O+0
CONECT    1    2   20                                                       
CONECT    2    1    5   21                                                  
CONECT    3    6    9   12                                                  
CONECT    4    7    8   12                                                  
CONECT    5    2    6   23                                                  
CONECT    6    3    5   24                                                  
CONECT    7    4   13   14                                                  
CONECT    8    4   15   16                                                  
CONECT    9    3   13   21                                                  
CONECT   10   11   14   15                                                  
CONECT   11   10                                                            
CONECT   12    3    4                                                       
CONECT   13    7    9                                                       
CONECT   14    7   10                                                       
CONECT   15    8   10                                                       
CONECT   16    8                                                            
CONECT   17   22                                                            
CONECT   18   22                                                            
CONECT   19   22                                                            
CONECT   20    1   22                                                       
CONECT   21    2    9                                                       
CONECT   22   17   18   19   20                                             
CONECT   23    5                                                            
CONECT   24    6                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   52    0
END

Synonyms

Not Available

Molecular Formula

C₁₀H₁₆MoN₅O₈PS₂

Average Mass

525.31

Monoisotopic Mass

526.923197

IUPAC Name

molybdenum(2+) ion 8-[(hydrogen phosphonooxy)methyl]-2-imino-6,7-disulfanyl-1H,2H,5H,5aH,8H,9aH,10H-pyrano[3,2-g]pteridin-4-olate dihydrate

Traditional Name

molybdenum(2+) ion 8-[(hydrogen phosphonooxy)methyl]-2-imino-6,7-disulfanyl-1H,5H,5aH,8H,9aH,10H-pyrano[3,2-g]pteridin-4-olate dihydrate

CAS Registry Number

Not Available

SMILES

O.O.[Mo++].OP([O-])(=O)OCC1OC2NC3=C(NC2C(S)=C1S)C([O-])=NC(=N)N3

InChI Identifier

InChI=1S/C10H14N5O6PS2.Mo.2H2O/c11-10-14-7-4(8(16)15-10)12-3-6(24)5(23)2(21-9(3)13-7)1-20-22(17,18)19;;;/h2-3,9,12,23-24H,1H2,(H2,17,18,19)(H4,11,13,14,15,16);;2*1H2/q;+2;;/p-2

InChI Key

VUKICSJFFDCESC-UHFFFAOYSA-L

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pyranopterins and derivatives. These are pterin derivatives in which a pyran ring is fused either to the pyrimidine ring or the pyrazine ring of the pterin moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Pteridines and derivatives

Sub Class

Pterins and derivatives

Direct Parent

Pyranopterins and derivatives

Alternative Parents

Substituents

Pyranopterin
Secondary aliphatic/aromatic amine
Organic phosphoric acid derivative
Phosphoric acid ester
Pyran
Pyrimidine
Alkyl phosphate
Heteroaromatic compound
Alkylthiol
Oxacycle
Secondary amine
Thioenol
Azacycle
Organic transition metal salt
Amine
Hydrocarbon derivative
Organic oxide
Organopnictogen compound
Organic oxygen compound
Organosulfur compound
Organic nitrogen compound
Organonitrogen compound
Organic zwitterion
Organic salt
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.98 g/L	ALOGPS
logP	0.86	ALOGPS
logP	-1.9	ChemAxon
logS	-2.7	ALOGPS
pKa (Strongest Acidic)	1.19	ChemAxon
pKa (Strongest Basic)	2.91	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	7	ChemAxon
Polar Surface Area	174.18 Å²	ChemAxon
Rotatable Bond Count	3	ChemAxon
Refractivity	119.21 m³·mol⁻¹	ChemAxon
Polarizability	34.18 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	No	ChemAxon

Spectra

Spectrum Type	Description	Splash Key	Deposition Date	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Positive	splash10-00di-0001490000-bf4dfec34731bf10ebad	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Positive	splash10-00di-1606490000-e83ef8869348bf49af28	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Positive	splash10-020r-4982200000-b29a94b7f07e6ea22651	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 10V, Negative	splash10-05e9-9606040000-926bcbb9296f4a9cd5e0	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 20V, Negative	splash10-004i-9101010000-2dd652c6c798de5919fb	2015-09-15	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - 40V, Negative	splash10-004i-9000000000-58324c83b689024dc935	2015-09-15	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)		2022-08-20	View Spectrum

Biological Properties

Cellular Locations

Not Available

Biospecimen Locations

Fibroblasts

Tissue Locations

Fibroblasts

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

Not Available

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

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
Human Fibroblasts	Detected but not Quantified						Not Specified	Not Specified	Normal	HMDB	34986597

External Links

HMDB ID

HMDB0002206

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

Molybdopterin

METLIN ID

Not Available

PubChem Compound

131750325

PDB ID

Not Available

ChEBI ID

Not Available

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Bamforth FJ, Johnson JL, Davidson AG, Wong LT, Lockitch G, Applegarth DA: Biochemical investigation of a child with molybdenum cofactor deficiency. Clin Biochem. 1990 Dec;23(6):537-42. doi: 10.1016/0009-9120(90)80046-l. [PubMed:2289312 ]
Mize C, Johnson JL, Rajagopalan KV: Defective molybdopterin biosynthesis: clinical heterogeneity associated with molybdenum cofactor deficiency. J Inherit Metab Dis. 1995;18(3):283-90. doi: 10.1007/BF00710416. [PubMed:7474893 ]
Reiss J, Gross-Hardt S, Christensen E, Schmidt P, Mendel RR, Schwarz G: A mutation in the gene for the neurotransmitter receptor-clustering protein gephyrin causes a novel form of molybdenum cofactor deficiency. Am J Hum Genet. 2001 Jan;68(1):208-13. doi: 10.1086/316941. Epub 2000 Nov 28. [PubMed:11095995 ]
Schwarz G: Molybdenum cofactor biosynthesis and deficiency. Cell Mol Life Sci. 2005 Dec;62(23):2792-810. doi: 10.1007/s00018-005-5269-y. [PubMed:16261263 ]
Macaya A, Brunso L, Fernandez-Castillo N, Arranz JA, Ginjaar HB, Cuenca-Leon E, Corominas R, Roig M, Cormand B: Molybdenum cofactor deficiency presenting as neonatal hyperekplexia: a clinical, biochemical and genetic study. Neuropediatrics. 2005 Dec;36(6):389-94. doi: 10.1055/s-2005-872877. [PubMed:16429380 ]

Showing metabocard for L-Lysyl-tRNA (MMDBc0031907)

MOL for #<Metabolite:0x00005634be77ee28>

3D MOL for #<Metabolite:0x00005634be77ee28>

3D SDF for #<Metabolite:0x00005634be77ee28>

3D-SDF for #<Metabolite:0x00005634be77ee28>

PDB for #<Metabolite:0x00005634be77ee28>

3D PDB for #<Metabolite:0x00005634be77ee28>

SMILES for #<Metabolite:0x00005634be77ee28>

INCHI for #<Metabolite:0x00005634be77ee28>

Structure for #<Metabolite:0x00005634be77ee28>

3D Structure for #<Metabolite:0x00005634be77ee28>