MiMeDB: Showing metabocard for (2R,3S)-beta-methylmalyl-CoA (MMDBc0054811)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2022-06-17 19:35:24 UTC

Update Date

2022-08-12 20:09:05 UTC

MiMeDB ID

MMDBc0054811

Metabolite Identification

Common Name

(2R,3S)-beta-methylmalyl-CoA

Description

L-erythro-3-methylmalyl-CoA(5-), also known as (2R,3S)-beta-methylmalyl-CoA or L-erythro-3-methylmalyl-coenzyme A, belongs to the class of organic compounds known as (s)-3-hydroxyacyl coas. These are organic compounds containing a (S)-3-hydroxyl acylated coenzyme A derivative. Based on a literature review very few articles have been published on L-erythro-3-methylmalyl-CoA(5-).

Structure

MOL SDF PDB SMILES InChI


  Mrv1652306172221352D          

 64 66  0  0  1  0            999 V2000
    7.2985   13.4953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7578   19.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4078   19.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117   15.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117   16.7953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4406   14.3203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1551   14.7328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5607   23.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828   20.0953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5345   26.3301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8138   23.6971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2985   14.3203    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2751   24.2203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.7262   15.5578    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7070   24.6891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.0130   14.7328    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.1683   25.2123    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.3614   25.0407    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.5828   18.4453    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.3745   25.1740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9533   25.0247    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    6.5841   14.7328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5828   19.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1281   24.8385    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.7262   14.7328    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.2972   17.2078    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2882   25.9945    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8671   25.8451    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6208   23.8686    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4013   24.4116    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.4406   15.9703    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
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   -2.5039   25.9659    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8683   18.0328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117   18.4453    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    9.4419   14.7328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7275   13.4953    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    6.5841   15.5578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2186   24.5532    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.2913   26.1225    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.8210   25.0829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2587   21.8558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5663   23.2847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   21.3328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -0.5607   22.9828    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8683   20.5078    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.9745   24.4887    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2972   18.8578    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0302   25.1897    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
 12  1  1  6  0  0  0
 13  8  1  1  0  0  0
 14  4  1  0  0  0  0
 16 12  1  0  0  0  0
 18 13  1  0  0  0  0
 18 17  1  0  0  0  0
 20 15  2  0  0  0  0
 21 15  1  0  0  0  0
 22 19  1  0  0  0  0
 23 17  1  0  0  0  0
 24 16  1  0  0  0  0
 25 12  1  0  0  0  0
 26  2  1  0  0  0  0
 26  3  1  0  0  0  0
 26  9  1  0  0  0  0
 26 19  1  0  0  0  0
 27 20  1  0  0  0  0
 28  6  1  4  0  0  0
 28 14  2  0  0  0  0
 29  5  1  4  0  0  0
 29 22  2  0  0  0  0
 30 10  2  0  0  0  0
 30 20  1  0  0  0  0
 31 10  1  0  0  0  0
 31 21  2  0  0  0  0
 32 11  2  0  0  0  0
 32 15  1  0  0  0  0
 33 11  1  0  0  0  0
 33 21  1  0  0  0  0
 23 33  1  1  0  0  0
 34 14  1  0  0  0  0
 16 35  1  1  0  0  0
 17 36  1  6  0  0  0
 19 37  1  1  0  0  0
 38 22  1  0  0  0  0
 39 24  2  0  0  0  0
 40 24  1  0  0  0  0
 41 25  2  0  0  0  0
 49  8  1  0  0  0  0
 50  9  1  0  0  0  0
 51 13  1  0  0  0  0
 51 23  1  0  0  0  0
 18 52  1  1  0  0  0
 54 42  1  0  0  0  0
 54 43  1  0  0  0  0
 54 44  2  0  0  0  0
 54 52  1  0  0  0  0
 55 45  1  0  0  0  0
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 55 53  1  0  0  0  0
 56 47  1  0  0  0  0
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 56 53  1  0  0  0  0
 57  7  1  0  0  0  0
 57 25  1  0  0  0  0
 12 58  1  1  0  0  0
 13 59  1  6  0  0  0
 16 60  1  6  0  0  0
 17 61  1  1  0  0  0
 18 62  1  1  0  0  0
 19 63  1  1  0  0  0
 23 64  1  6  0  0  0
M  CHG  5  34  -1  38  -1  40  -1  42  -1  43  -1
M  END


  Mrv1652306172221352D          

 64 66  0  0  1  0            999 V2000
    7.2985   13.4953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7578   19.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4078   19.2703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117   15.9703    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117   16.7953    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4406   14.3203    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1551   14.7328    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5607   23.8078    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -4.5345   26.3301    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8138   23.6971    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2985   14.3203    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2751   24.2203    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -4.7070   24.6891    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.3614   25.0407    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
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   -5.3745   25.1740    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    3.7262   14.7328    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.4013   24.4116    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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    0.8683   18.0328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.0117   18.4453    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    9.4419   14.7328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7275   13.4953    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    6.5841   15.5578    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2186   24.5532    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.2913   26.1225    0.0000 O   0  5  0  0  0  0  0  0  0  0  0  0
    0.8210   25.0829    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2587   21.8558    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.5663   23.2847    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433   21.3328    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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    8.0130   13.9078    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5832   24.6696    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -1.6491   25.8534    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
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    2.2972   18.8578    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0302   25.1897    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  5  4  1  0  0  0  0
  7  6  1  0  0  0  0
 12  1  1  6  0  0  0
 13  8  1  1  0  0  0
 14  4  1  0  0  0  0
 16 12  1  0  0  0  0
 18 13  1  0  0  0  0
 18 17  1  0  0  0  0
 20 15  2  0  0  0  0
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 22 19  1  0  0  0  0
 23 17  1  0  0  0  0
 24 16  1  0  0  0  0
 25 12  1  0  0  0  0
 26  2  1  0  0  0  0
 26  3  1  0  0  0  0
 26  9  1  0  0  0  0
 26 19  1  0  0  0  0
 27 20  1  0  0  0  0
 28  6  1  4  0  0  0
 28 14  2  0  0  0  0
 29  5  1  4  0  0  0
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 23 33  1  1  0  0  0
 34 14  1  0  0  0  0
 16 35  1  1  0  0  0
 17 36  1  6  0  0  0
 19 37  1  1  0  0  0
 38 22  1  0  0  0  0
 39 24  2  0  0  0  0
 40 24  1  0  0  0  0
 41 25  2  0  0  0  0
 49  8  1  0  0  0  0
 50  9  1  0  0  0  0
 51 13  1  0  0  0  0
 51 23  1  0  0  0  0
 18 52  1  1  0  0  0
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 55 49  1  0  0  0  0
 55 53  1  0  0  0  0
 56 47  1  0  0  0  0
 56 48  2  0  0  0  0
 56 50  1  0  0  0  0
 56 53  1  0  0  0  0
 57  7  1  0  0  0  0
 57 25  1  0  0  0  0
 12 58  1  1  0  0  0
 13 59  1  6  0  0  0
 16 60  1  6  0  0  0
 17 61  1  1  0  0  0
 18 62  1  1  0  0  0
 19 63  1  1  0  0  0
 23 64  1  6  0  0  0
M  CHG  5  34  -1  38  -1  40  -1  42  -1  43  -1
M  END
> <DATABASE_ID>
MMDBc0054811

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@](C)(C(=O)SCCN=C([O-])CCN=C([O-])[C@]([H])(O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@@]1([H])O[C@@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])OP([O-])([O-])=O)[C@@]([H])(O)C([O-])=O

> <INCHI_IDENTIFIER>
InChI=1S/C26H42N7O20P3S/c1-12(16(35)24(39)40)25(41)57-7-6-28-14(34)4-5-29-22(38)19(37)26(2,3)9-50-56(47,48)53-55(45,46)49-8-13-18(52-54(42,43)44)17(36)23(51-13)33-11-32-15-20(27)30-10-31-21(15)33/h10-13,16-19,23,35-37H,4-9H2,1-3H3,(H,28,34)(H,29,38)(H,39,40)(H,45,46)(H,47,48)(H2,27,30,31)(H2,42,43,44)/p-5/t12-,13+,16+,17+,18+,19-,23+/m0/s1

> <INCHI_KEY>
OTENCPQKSBPYCM-IGVLTWCCSA-I

> <FORMULA>
C26H37N7O20P3S

> <MOLECULAR_WEIGHT>
892.6

> <EXACT_MASS>
892.105436687

> <JCHEM_ACCEPTOR_COUNT>
22

> <JCHEM_ATOM_COUNT>
94

> <JCHEM_AVERAGE_POLARIZABILITY>
77.0194354884401

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
-5

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,3S)-4-({2-[(3-{[(2R)-4-({[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-2-hydroxy-3,3-dimethyl-1-oxidobutylidene]amino}-1-oxidopropylidene)amino]ethyl}sulfanyl)-2-hydroxy-3-methyl-4-oxobutanoate

> <JCHEM_LOGP>
-4.595345054360501

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-5

> <JCHEM_PKA>
1.8768589339351287

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.818249366972478

> <JCHEM_PKA_STRONGEST_BASIC>
4.213594481229809

> <JCHEM_POLAR_SURFACE_AREA>
442.2900000000001

> <JCHEM_REFRACTIVITY>
219.75170000000008

> <JCHEM_ROTATABLE_BOND_COUNT>
23

> <JCHEM_RULE_OF_FIVE>
0

> <JCHEM_TRADITIONAL_IUPAC>
(2R,3S)-4-({2-[(3-{[(2R)-4-[({[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-2-hydroxy-3,3-dimethyl-1-oxidobutylidene]amino}-1-oxidopropylidene)amino]ethyl}sulfanyl)-2-hydroxy-3-methyl-4-oxobutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 17-JUN-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   17-JUN-22         0                                  
HETATM    1  C   UNK     0      13.624  25.191   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.414  35.971   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.494  35.971   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       5.622  29.811   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       5.622  31.351   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       8.289  26.731   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.623  27.501   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      -1.047  44.441   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.954  37.511   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      -8.464  49.149   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      -7.119  44.235   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      13.624  26.731   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      -2.380  45.211   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.956  29.041   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      -8.786  46.086   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      14.958  27.501   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      -4.048  47.063   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      -2.541  46.743   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.954  34.431   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0     -10.032  46.992   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -7.380  46.713   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       4.288  33.661   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.818  45.729   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      16.291  26.731   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      12.290  27.501   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       2.954  35.971   0.000  0.00  0.00           C+0
HETATM   27  N   UNK     0     -11.439  46.365   0.000  0.00  0.00           N+0
HETATM   28  N   UNK     0       6.956  27.501   0.000  0.00  0.00           N+0
HETATM   29  N   UNK     0       4.288  32.121   0.000  0.00  0.00           N+0
HETATM   30  N   UNK     0      -9.871  48.523   0.000  0.00  0.00           N+0
HETATM   31  N   UNK     0      -7.219  48.244   0.000  0.00  0.00           N+0
HETATM   32  N   UNK     0      -8.625  44.555   0.000  0.00  0.00           N+0
HETATM   33  N   UNK     0      -6.349  45.568   0.000  0.00  0.00           N+0
HETATM   34  O   UNK     0       8.289  29.811   0.000  0.00  0.00           O-1
HETATM   35  O   UNK     0      14.958  29.041   0.000  0.00  0.00           O+0
HETATM   36  O   UNK     0      -4.674  48.470   0.000  0.00  0.00           O+0
HETATM   37  O   UNK     0       1.621  33.661   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0       5.622  34.431   0.000  0.00  0.00           O-1
HETATM   39  O   UNK     0      17.625  27.501   0.000  0.00  0.00           O+0
HETATM   40  O   UNK     0      16.291  25.191   0.000  0.00  0.00           O-1
HETATM   41  O   UNK     0      12.290  29.041   0.000  0.00  0.00           O+0
HETATM   42  O   UNK     0      -0.408  45.833   0.000  0.00  0.00           O-1
HETATM   43  O   UNK     0       0.544  48.762   0.000  0.00  0.00           O-1
HETATM   44  O   UNK     0       1.532  46.821   0.000  0.00  0.00           O+0
HETATM   45  O   UNK     0      -0.483  40.797   0.000  0.00  0.00           O+0
HETATM   46  O   UNK     0       1.057  43.465   0.000  0.00  0.00           O+0
HETATM   47  O   UNK     0       0.081  39.821   0.000  0.00  0.00           O+0
HETATM   48  O   UNK     0       3.161  39.821   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      -1.047  42.901   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0       1.621  38.281   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      -3.787  44.585   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      -1.397  47.773   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0       1.621  41.361   0.000  0.00  0.00           O+0
HETATM   54  P   UNK     0       0.068  47.297   0.000  0.00  0.00           P+0
HETATM   55  P   UNK     0       0.287  42.131   0.000  0.00  0.00           P+0
HETATM   56  P   UNK     0       1.621  39.821   0.000  0.00  0.00           P+0
HETATM   57  S   UNK     0      10.957  26.731   0.000  0.00  0.00           S+0
HETATM   58  H   UNK     0      14.958  25.961   0.000  0.00  0.00           H+0
HETATM   59  H   UNK     0      -1.089  46.050   0.000  0.00  0.00           H+0
HETATM   60  H   UNK     0      13.624  28.271   0.000  0.00  0.00           H+0
HETATM   61  H   UNK     0      -3.078  48.260   0.000  0.00  0.00           H+0
HETATM   62  H   UNK     0      -3.686  45.712   0.000  0.00  0.00           H+0
HETATM   63  H   UNK     0       4.288  35.201   0.000  0.00  0.00           H+0
HETATM   64  H   UNK     0      -5.656  47.021   0.000  0.00  0.00           H+0
CONECT    1   12                                                            
CONECT    2   26                                                            
CONECT    3   26                                                            
CONECT    4    5   14                                                       
CONECT    5    4   29                                                       
CONECT    6    7   28                                                       
CONECT    7    6   57                                                       
CONECT    8   13   49                                                       
CONECT    9   26   50                                                       
CONECT   10   30   31                                                       
CONECT   11   32   33                                                       
CONECT   12    1   16   25   58                                             
CONECT   13    8   18   51   59                                             
CONECT   14    4   28   34                                                  
CONECT   15   20   21   32                                                  
CONECT   16   12   24   35   60                                             
CONECT   17   18   23   36   61                                             
CONECT   18   13   17   52   62                                             
CONECT   19   22   26   37   63                                             
CONECT   20   15   27   30                                                  
CONECT   21   15   31   33                                                  
CONECT   22   19   29   38                                                  
CONECT   23   17   33   51   64                                             
CONECT   24   16   39   40                                                  
CONECT   25   12   41   57                                                  
CONECT   26    2    3    9   19                                             
CONECT   27   20                                                            
CONECT   28    6   14                                                       
CONECT   29    5   22                                                       
CONECT   30   10   20                                                       
CONECT   31   10   21                                                       
CONECT   32   11   15                                                       
CONECT   33   11   21   23                                                  
CONECT   34   14                                                            
CONECT   35   16                                                            
CONECT   36   17                                                            
CONECT   37   19                                                            
CONECT   38   22                                                            
CONECT   39   24                                                            
CONECT   40   24                                                            
CONECT   41   25                                                            
CONECT   42   54                                                            
CONECT   43   54                                                            
CONECT   44   54                                                            
CONECT   45   55                                                            
CONECT   46   55                                                            
CONECT   47   56                                                            
CONECT   48   56                                                            
CONECT   49    8   55                                                       
CONECT   50    9   56                                                       
CONECT   51   13   23                                                       
CONECT   52   18   54                                                       
CONECT   53   55   56                                                       
CONECT   54   42   43   44   52                                             
CONECT   55   45   46   49   53                                             
CONECT   56   47   48   50   53                                             
CONECT   57    7   25                                                       
CONECT   58   12                                                            
CONECT   59   13                                                            
CONECT   60   16                                                            
CONECT   61   17                                                            
CONECT   62   18                                                            
CONECT   63   19                                                            
CONECT   64   23                                                            
MASTER        0    0    0    0    0    0    0    0   64    0  132    0
END

Synonyms

Value	Source
(2R,3S)-beta-Methylmalyl-CoA	ChEBI
L-Erythro-3-methylmalyl-coenzyme A	ChEBI
(2R,3S)-b-Methylmalyl-CoA	Generator
(2R,3S)-Β-methylmalyl-CoA	Generator

Chemical Formula

C₂₆H₃₇N₇O₂₀P₃S

Average Molecular Weight

892.6

Monoisotopic Molecular Weight

892.105436687

IUPAC Name

(2R,3S)-4-({2-[(3-{[(2R)-4-({[({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy](hydroxy)phosphoryl}oxy)-2-hydroxy-3,3-dimethyl-1-oxidobutylidene]amino}-1-oxidopropylidene)amino]ethyl}sulfanyl)-2-hydroxy-3-methyl-4-oxobutanoate

Traditional Name

(2R,3S)-4-({2-[(3-{[(2R)-4-[({[(2R,3S,4R,5R)-5-(6-aminopurin-9-yl)-4-hydroxy-3-(phosphonooxy)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxy]-2-hydroxy-3,3-dimethyl-1-oxidobutylidene]amino}-1-oxidopropylidene)amino]ethyl}sulfanyl)-2-hydroxy-3-methyl-4-oxobutanoate

CAS Registry Number

Not Available

SMILES

[H][C@@](C)(C(=O)SCCN=C([O-])CCN=C([O-])[C@]([H])(O)C(C)(C)COP(O)(=O)OP(O)(=O)OC[C@@]1([H])O[C@@]([H])(N2C=NC3=C(N)N=CN=C23)[C@]([H])(O)[C@]1([H])OP([O-])([O-])=O)[C@@]([H])(O)C([O-])=O

InChI Identifier

InChI=1S/C26H42N7O20P3S/c1-12(16(35)24(39)40)25(41)57-7-6-28-14(34)4-5-29-22(38)19(37)26(2,3)9-50-56(47,48)53-55(45,46)49-8-13-18(52-54(42,43)44)17(36)23(51-13)33-11-32-15-20(27)30-10-31-21(15)33/h10-13,16-19,23,35-37H,4-9H2,1-3H3,(H,28,34)(H,29,38)(H,39,40)(H,45,46)(H,47,48)(H2,27,30,31)(H2,42,43,44)/p-5/t12-,13+,16+,17+,18+,19-,23+/m0/s1

InChI Key

OTENCPQKSBPYCM-IGVLTWCCSA-I

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as (s)-3-hydroxyacyl coas. These are organic compounds containing a (S)-3-hydroxyl acylated coenzyme A derivative.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acyl thioesters

Direct Parent

(S)-3-hydroxyacyl CoAs

Alternative Parents

Substituents

Coenzyme a or derivatives
Purine ribonucleoside 3',5'-bisphosphate
Purine ribonucleoside bisphosphate
Purine ribonucleoside diphosphate
Pentose phosphate
Pentose-5-phosphate
Ribonucleoside 3'-phosphate
Beta amino acid or derivatives
Glycosyl compound
N-glycosyl compound
6-aminopurine
Monosaccharide phosphate
Organic pyrophosphate
Imidazopyrimidine
Purine
Aminopyrimidine
Hydroxy fatty acid
Thia fatty acid
Imidolactam
Fatty amide
Alkyl phosphate
Monosaccharide
N-acyl-amine
N-substituted imidazole
Organic phosphoric acid derivative
Phosphoric acid ester
Pyrimidine
Tetrahydrofuran
Heteroaromatic compound
Imidazole
Azole
Secondary carboxylic acid amide
Secondary alcohol
Thiocarboxylic acid ester
Amino acid
Carboxamide group
Carbothioic s-ester
Amino acid or derivatives
Sulfenyl compound
Organoheterocyclic compound
Carboxylic acid derivative
Carboxylic acid
Oxacycle
Thiocarboxylic acid or derivatives
Monocarboxylic acid or derivatives
Azacycle
Organic oxygen compound
Organic nitrogen compound
Organosulfur compound
Organonitrogen compound
Carbonyl group
Organic oxide
Alcohol
Amine
Organopnictogen compound
Organooxygen compound
Primary amine
Hydrocarbon derivative
Organic anion
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

acyl-CoA oxoanion (CHEBI:75634 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
logP	-4.6	ChemAxon
pKa (Strongest Acidic)	0.82	ChemAxon
pKa (Strongest Basic)	4.21	ChemAxon
Physiological Charge	-5	ChemAxon
Hydrogen Acceptor Count	22	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	442.29 Å²	ChemAxon
Rotatable Bond Count	23	ChemAxon
Refractivity	219.75 m³·mol⁻¹	ChemAxon
Polarizability	77.02 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

Not Available

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

Proteins

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Related Health Condition	Evidence Type	Measured in Matrix	Data Source	Reference

Microbial Sources

Kingdom	Phylum	Total species	Hosts and Body Sites
	Proteobacteria	6	Human
Archaea	Euryarchaeota	2
	Chloroflexi	2

Exposure Sources

Source Type	Source Sub-type	Species	Data Source	Reference	Details

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

30785661

KEGG Compound ID

Not Available

BioCyc ID

CPD-9409

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

71728455

PDB ID

Not Available

ChEBI ID

75634

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

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 (2R,3S)-beta-methylmalyl-CoA (MMDBc0054811)

MOL for #<Metabolite:0x0000564abe0a81b0>

3D MOL for #<Metabolite:0x0000564abe0a81b0>

3D SDF for #<Metabolite:0x0000564abe0a81b0>

3D-SDF for #<Metabolite:0x0000564abe0a81b0>

PDB for #<Metabolite:0x0000564abe0a81b0>

3D PDB for #<Metabolite:0x0000564abe0a81b0>

SMILES for #<Metabolite:0x0000564abe0a81b0>

INCHI for #<Metabolite:0x0000564abe0a81b0>

Structure for #<Metabolite:0x0000564abe0a81b0>

3D Structure for #<Metabolite:0x0000564abe0a81b0>