Reference/PubChem-compound 6022
type: UnificationXref
id: 6022
db: PubChem-compound

O-Phosphoethanolamine
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000224
xref: Reference/BioCyc PHOSPHORYL-ETHANOLAMINE
xref: Reference/ChemSpider 990
xref: Reference/PubChem-compound 1015
xref: Reference/KEGG Compound C00346
xref: Reference/ChEBI CHEBI 17553
xref: Reference/CAS 1071-23-4
chemical formula: C2H8NO4P
molecular weight: 141.01909
structure: ChemicalStructure/PW C000149

Reference/BioCyc PHOSPHORYL-ETHANOLAMINE
type: UnificationXref
id: PHOSPHORYL-ETHANOLAMINE
db: BioCyc

Reference/KEGG Compound C02737
type: UnificationXref
id: C02737
db: KEGG Compound

Compound/PW C060746 Mitochondrial Inner Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: PS(16:0/20:3(5Z,8Z,11Z))
stoichiometric coefficient: 1.0

Reference/PubChem-compound 1014
type: UnificationXref
id: 1014
db: PubChem-compound

Reference/PubChem-compound 1015
type: UnificationXref
id: 1015
db: PubChem-compound

Reference/UniProt X5LPX5
type: UnificationXref
id: X5LPX5
db: UniProt

Reference/BioCyc L-1-PHOSPHATIDYL-ETHANOLAMINE
type: UnificationXref
id: L-1-PHOSPHATIDYL-ETHANOLAMINE
db: BioCyc

Cytidine triphosphate
type: SmallMolecule
entity reference: Cytidine triphosphate

ChemicalStructure/PW C060746
type: ChemicalStructure
structure format: SMILES

Reference/HMDB HMDB0008935
type: UnificationXref
id: HMDB0008935
db: HMDB

ChemicalStructure/PW C003161
type: ChemicalStructure
structure format: SMILES

Reference/HMDB HMDB0000095
type: UnificationXref
id: HMDB0000095
db: HMDB

Reference/HMDB HMDB0000097
type: UnificationXref
id: HMDB0000097
db: HMDB

Pyrophosphate
type: SmallMolecule
entity reference: Pyrophosphate

Compound/PW C040034/Stoichiometry/1.0
type: Stoichiometry
physical entity: Hydrogen Ion
stoichiometric coefficient: 1.0

Reference/PubChem-compound 6131
type: UnificationXref
id: 6131
db: PubChem-compound

Reference/ChEBI CHEBI 17115
type: UnificationXref
id: CHEBI:17115
db: ChEBI

Reference/ChemSpider 13207
type: UnificationXref
id: 13207
db: ChemSpider

Reference/ChemSpider 24768428
type: UnificationXref
id: 24768428
db: ChemSpider

Compound/PW C000064/Stoichiometry/1.0
type: Stoichiometry
physical entity: Cytidine monophosphate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0000538
type: UnificationXref
id: HMDB0000538
db: HMDB

Reference/BioCyc ATP
type: UnificationXref
id: ATP
db: BioCyc

ReactionCatalysis130710
type: Catalysis
controller: Putative choline kinase B3
controlled: 2.7.1.82
control type: ACTIVATION

ReactionCatalysis130711
type: Catalysis
controller: Putative choline kinase B3
controlled: Reaction140637
control type: ACTIVATION

Compound/PW C000414/Stoichiometry/1.0
type: Stoichiometry
physical entity: Adenosine triphosphate
stoichiometric coefficient: 1.0

ChemicalStructure/PW C004029
type: ChemicalStructure
structure format: SMILES
structure data: CCCCCCCCCCCCCCCC(=O)OC[C@]([H])(COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/CCCCCCCC

ReactionCatalysis130705
type: Catalysis
controller: Putative choline-phosphate cytidylyltransferase
controlled: 2.7.7.15
control type: ACTIVATION

ReactionCatalysis130706
type: Catalysis
controller: Phosphocholine CYtidylylTransferase
controlled: 2.7.7.14
control type: ACTIVATION

Reference/ChemSpider 559142
type: UnificationXref
id: 559142
db: ChemSpider

Reference/BioCyc CDP-ETHANOLAMINE
type: UnificationXref
id: CDP-ETHANOLAMINE
db: BioCyc

Reference/BioCyc ADP
type: UnificationXref
id: ADP
db: BioCyc

Reference/ChemSpider 110296
type: UnificationXref
id: 110296
db: ChemSpider

Compound/PW C000065/Stoichiometry/1.0
type: Stoichiometry
physical entity: Choline
stoichiometric coefficient: 1.0

Reference/PubChem-compound 700
type: UnificationXref
id: 700
db: PubChem-compound

Compound/PW C001034/Stoichiometry/1.0
type: Stoichiometry
physical entity: Adenosine diphosphate
stoichiometric coefficient: 1.0

Compound/PW C000149/Stoichiometry/1.0
type: Stoichiometry
physical entity: O-Phosphoethanolamine
stoichiometric coefficient: 1.0

Reference/PubChem-compound 6323481
type: UnificationXref
id: 6323481
db: PubChem-compound

Reference/ChemSpider 5742
type: UnificationXref
id: 5742
db: ChemSpider

Compound/PW C043034/Stoichiometry/1.0
type: Stoichiometry
physical entity: CDP-Choline
stoichiometric coefficient: 1.0

Reference/PubChem-compound 1038
type: UnificationXref
id: 1038
db: PubChem-compound

Reference/KEGG Compound C00570
type: UnificationXref
id: C00570
db: KEGG Compound

Compound/PW C004983/Stoichiometry/1.0
type: Stoichiometry
physical entity: PE(16:0/20:3(5Z,8Z,11Z))
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0112347
type: UnificationXref
id: HMDB0112347
db: HMDB

Reference/ChemSpider 274
type: UnificationXref
id: 274
db: ChemSpider

PE(16:0/20:3(5Z,8Z,11Z))
type: SmallMolecule
cellular location: Mitochondrial Inner Membrane
entity reference: PE(16:0/20:3(5Z,8Z,11Z))

Reference/HMDB HMDB0007980
type: UnificationXref
id: HMDB0007980
db: HMDB

Transport9509
type: Transport
participant stoichiometry: Compound/PW C004983 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
participant stoichiometry: Compound/PW C004983 Mitochondrial Inner Membrane/Stoichiometry/1.0
right: PE(16:0/20:3(5Z,8Z,11Z))
spontaneous: false
left: PE(16:0/20:3(5Z,8Z,11Z))
name: PE(16:0/20:3(5Z,8Z,11Z)) (↔) Transport: Caenorhabditis elegans, Cell, Endoplasmic Reticulum Membrane to Caenorhabditis elegans, Cell, Mitochondrial Inner Membrane
conversion direction: LEFT_TO_RIGHT

Reference/ChemSpider 5736
type: UnificationXref
id: 5736
db: ChemSpider

Reference/ChEBI CHEBI 18303
type: UnificationXref
id: CHEBI:18303
db: ChEBI

O-Phosphoethanolamine
type: SmallMolecule
entity reference: O-Phosphoethanolamine

Reference/ChEBI CHEBI 16000
type: UnificationXref
id: CHEBI:16000
db: ChEBI

Reference/KEGG Compound C00346
type: UnificationXref
id: C00346
db: KEGG Compound

Reference/KEGG Compound C00588
type: UnificationXref
id: C00588
db: KEGG Compound

Reference/ChemSpider 1010
type: UnificationXref
id: 1010
db: ChemSpider

Reference/BioCyc SER
type: UnificationXref
id: SER
db: BioCyc

Transport9508
type: Transport
participant stoichiometry: Compound/PW C060746 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
participant stoichiometry: Compound/PW C060746 Mitochondrial Inner Membrane/Stoichiometry/1.0
right: PS(16:0/20:3(5Z,8Z,11Z))
spontaneous: false
left: PS(16:0/20:3(5Z,8Z,11Z))
name: PS(16:0/20:3(5Z,8Z,11Z)) (→) Transport: Caenorhabditis elegans, Cell, Endoplasmic Reticulum Membrane to Caenorhabditis elegans, Cell, Mitochondrial Inner Membrane
conversion direction: LEFT_TO_RIGHT

PE(16:0/20:3(5Z,8Z,11Z))
type: SmallMolecule
entity reference: PE(16:0/20:3(5Z,8Z,11Z))

PE(16:0/20:3(5Z,8Z,11Z))
type: SmallMoleculeReference
xref: Reference/BioCyc L-1-PHOSPHATIDYL-ETHANOLAMINE
xref: Reference/ChemSpider 24768428
xref: Reference/HMDB HMDB0008935
xref: Reference/KEGG Compound C00350
xref: Reference/PubChem-compound 53479587
chemical formula: C41H76NO8P
molecular weight: 741.5309
structure: ChemicalStructure/PW C004983

Reference/HMDB HMDB0001413
type: UnificationXref
id: HMDB0001413
db: HMDB

Reference/BioCyc PPI
type: UnificationXref
id: PPI
db: BioCyc

Reference/CAS 63-37-6
type: UnificationXref
id: 63-37-6
db: CAS

Reference/ChEBI CHEBI 16732
type: UnificationXref
id: CHEBI:16732
db: ChEBI

Hydrogen Ion
type: SmallMolecule
entity reference: Hydrogen Ion

Reaction140637
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001202/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000065/Stoichiometry/1.0
right: Adenosine diphosphate
right: Phosphorylcholine
spontaneous: false
left: Choline
left: Adenosine triphosphate
name: Adenosine triphosphate + Choline → Adenosine diphosphate + Phosphorylcholine
conversion direction: LEFT_TO_RIGHT

Phosphocholine CYtidylylTransferase
type: Protein
entity reference: Phosphocholine CYtidylylTransferase

Choline/EthanolaminePhosphoTransferase
type: Protein
entity reference: Choline/EthanolaminePhosphoTransferase

Reference/KEGG Compound C00350
type: UnificationXref
id: C00350
db: KEGG Compound

Putative choline-phosphate cytidylyltransferase
type: Protein
entity reference: Putative choline-phosphate cytidylyltransferase

Reference/KEGG Compound C00114
type: UnificationXref
id: C00114
db: KEGG Compound

Phosphatidylserine decarboxylase proenzyme, mitochondrial
type: Protein
entity reference: Phosphatidylserine decarboxylase proenzyme, mitochondrial

Reference/BioCyc PHOSPHATIDYLCHOLINE
type: UnificationXref
id: PHOSPHATIDYLCHOLINE
db: BioCyc

2.7.1.82
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000414/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000149/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000096/Stoichiometry/1.0
right: Adenosine diphosphate
right: Hydrogen Ion
right: O-Phosphoethanolamine
spontaneous: false
EC number: 2.7.1.82
left: Ethanolamine
left: Adenosine triphosphate
name: Adenosine triphosphate + Ethanolamine → Adenosine diphosphate + Hydrogen Ion + O-Phosphoethanolamine
conversion direction: LEFT_TO_RIGHT

Adenosine triphosphate
type: SmallMolecule
entity reference: Adenosine triphosphate

Reference/CAS 1071-23-4
type: UnificationXref
id: 1071-23-4
db: CAS

Ethanolamine
type: SmallMolecule
entity reference: Ethanolamine

2.7.7.15
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001202/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000057/Stoichiometry/1.0
participant stoichiometry: Compound/PW C043034/Stoichiometry/1.0
right: CDP-Choline
right: Pyrophosphate
spontaneous: false
EC number: 2.7.7.15
left: Cytidine triphosphate
left: Phosphorylcholine
name: Cytidine triphosphate + Phosphorylcholine → CDP-Choline + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

2.7.7.14
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000170/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001201/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000057/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000149/Stoichiometry/1.0
right: CDP-ethanolamine
right: Pyrophosphate
spontaneous: false
EC number: 2.7.7.14
left: Cytidine triphosphate
left: O-Phosphoethanolamine
name: Cytidine triphosphate + O-Phosphoethanolamine → CDP-ethanolamine + Pyrophosphate
conversion direction: LEFT_TO_RIGHT

Compound/PW C000057/Stoichiometry/1.0
type: Stoichiometry
physical entity: Cytidine triphosphate
stoichiometric coefficient: 1.0

Reference/CAS 124-38-9
type: UnificationXref
id: 124-38-9
db: CAS

Reference/KEGG Compound C00008
type: UnificationXref
id: C00008
db: KEGG Compound

Reference/BioCyc CDP-CHOLINE
type: UnificationXref
id: CDP-CHOLINE
db: BioCyc

Reference/PubChem-compound 53478028
type: UnificationXref
id: 53478028
db: PubChem-compound

Reference/BioCyc CTP
type: UnificationXref
id: CTP
db: BioCyc

Reference/ChEBI CHEBI 18361
type: UnificationXref
id: CHEBI:18361
db: ChEBI

PS(16:0/20:3(5Z,8Z,11Z))
type: SmallMolecule
cellular location: Mitochondrial Inner Membrane
entity reference: PS(16:0/20:3(5Z,8Z,11Z))

PhosphatidylSerine SYnthase
type: Protein
entity reference: PhosphatidylSerine SYnthase

Reference/UniProt P46560
type: UnificationXref
id: P46560
db: UniProt

Reference/KEGG Compound C00002
type: UnificationXref
id: C00002
db: KEGG Compound

Reference/HMDB HMDB0000224
type: UnificationXref
id: HMDB0000224
db: HMDB

Reference/ChemSpider 13835336
type: UnificationXref
id: 13835336
db: ChemSpider

ChemicalStructure/PW C004983
type: ChemicalStructure
structure format: SMILES

Mitochondrial Inner Membrane
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005743

ChemicalStructure/PW C043034
type: ChemicalStructure
structure format: SMILES

Reference/UniProt G5EC09
type: UnificationXref
id: G5EC09
db: UniProt

Compound/PW C000120/Stoichiometry/1.0
type: Stoichiometry
physical entity: L-Serine
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 17361
type: UnificationXref
id: CHEBI:17361
db: ChEBI

Reference/KEGG Compound C00011
type: UnificationXref
id: C00011
db: KEGG Compound

ChemicalStructure/PW C001316
type: ChemicalStructure
structure format: SMILES
structure data: O=C=O

Reference/PubChem-compound 5951
type: UnificationXref
id: 5951
db: PubChem-compound

Compound/PW C000096/Stoichiometry/1.0
type: Stoichiometry
physical entity: Ethanolamine
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00013
type: UnificationXref
id: C00013
db: KEGG Compound

Reference/HMDB HMDB0001564
type: UnificationXref
id: HMDB0001564
db: HMDB

Pyrophosphate
type: SmallMoleculeReference
xref: Reference/PubChem-compound 644102
xref: Reference/BioCyc PPI
xref: Reference/ChemSpider 559142
xref: Reference/ChEBI CHEBI 18361
xref: Reference/HMDB HMDB0000250
xref: Reference/CAS 14000-31-8
xref: Reference/KEGG Compound C00013
chemical formula: O7P2
molecular weight: 173.91193
structure: ChemicalStructure/PW C000170

Reference/HMDB HMDB0001565
type: UnificationXref
id: HMDB0001565
db: HMDB

Compound/PW C001202/Stoichiometry/1.0
type: Stoichiometry
physical entity: Phosphorylcholine
stoichiometric coefficient: 1.0

ChemicalStructure/PW C001202
type: ChemicalStructure
structure format: SMILES
structure data: C[N+](C)(C)CCOP(O)(O)=O

ChemicalStructure/PW C001201
type: ChemicalStructure
structure format: SMILES

Reference/PubChem-compound 5957
type: UnificationXref
id: 5957
db: PubChem-compound

Reference/GENE ONTOLOGY GO 0005743
type: UnificationXref
id: GO:0005743
db: GENE ONTOLOGY

Cytidine triphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 17677
xref: Reference/CAS 65-47-4
xref: Reference/PubChem-compound 6176
xref: Reference/KEGG Compound C00063
xref: Reference/ChemSpider 5941
xref: Reference/HMDB HMDB0000082
xref: Reference/BioCyc CTP
chemical formula: C9H16N3O14P3
molecular weight: 482.9845
structure: ChemicalStructure/PW C000057

Reference/SMPDB SMP0100165
type: UnificationXref
id: SMP0100165
db: SMPDB

Hydrogen Ion
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00080
xref: Reference/ChEBI CHEBI 15378
xref: Reference/HMDB HMDB0059597
xref: Reference/PubChem-compound 1038
xref: Reference/ChemSpider 1010
chemical formula: H
molecular weight: 1.007825
structure: ChemicalStructure/PW C040034

Reference/ChemSpider 24765933
type: UnificationXref
id: 24765933
db: ChemSpider

Reference/BioCyc CPD-563
type: UnificationXref
id: CPD-563
db: BioCyc

Reference/CAS 56-65-5
type: UnificationXref
id: 56-65-5
db: CAS

Reaction164475
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000064/Stoichiometry/1.0
participant stoichiometry: Compound/PW C004983/Stoichiometry/1.0
participant stoichiometry: Compound/PW C001201/Stoichiometry/1.0
participant stoichiometry: Compound/PW C003161/Stoichiometry/1.0
right: Cytidine monophosphate
right: PE(16:0/20:3(5Z,8Z,11Z))
spontaneous: false
left: CDP-ethanolamine
left: DG(16:0/20:3(5Z,8Z,11Z)/0:0)
name: CDP-ethanolamine + DG(16:0/20:3(5Z,8Z,11Z)/0:0) → Cytidine monophosphate + PE(16:0/20:3(5Z,8Z,11Z))
conversion direction: LEFT_TO_RIGHT

Cytidine monophosphate
type: SmallMolecule
entity reference: Cytidine monophosphate

Adenosine diphosphate
type: SmallMolecule
entity reference: Adenosine diphosphate

ChemicalStructure/PW C000120
type: ChemicalStructure
structure format: SMILES
structure data: N[C@@H](CO)C(O)=O

Reaction164476
type: BiochemicalReaction
participant stoichiometry: Compound/PW C000064/Stoichiometry/1.0
participant stoichiometry: Compound/PW C043034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C003161/Stoichiometry/1.0
participant stoichiometry: Compound/PW C040034/Stoichiometry/1.0
participant stoichiometry: Compound/PW C004029/Stoichiometry/1.0
right: Cytidine monophosphate
right: Hydrogen Ion
right: PC(16:0/20:3(5Z,8Z,11Z))
spontaneous: false
left: CDP-Choline
left: DG(16:0/20:3(5Z,8Z,11Z)/0:0)
name: CDP-Choline + DG(16:0/20:3(5Z,8Z,11Z)/0:0) → Cytidine monophosphate + Hydrogen Ion + PC(16:0/20:3(5Z,8Z,11Z))
conversion direction: LEFT_TO_RIGHT

2.7.8.-
type: BiochemicalReaction
participant stoichiometry: Compound/PW C060746/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000065/Stoichiometry/1.0
participant stoichiometry: Compound/PW C004029/Stoichiometry/1.0
participant stoichiometry: Compound/PW C000120/Stoichiometry/1.0
right: Choline
right: PS(16:0/20:3(5Z,8Z,11Z))
spontaneous: false
EC number: 2.7.8.-
left: L-Serine
left: PC(16:0/20:3(5Z,8Z,11Z))
name: L-Serine + PC(16:0/20:3(5Z,8Z,11Z)) → Choline + PS(16:0/20:3(5Z,8Z,11Z))
conversion direction: LEFT_TO_RIGHT

Reaction164474
type: BiochemicalReaction
participant stoichiometry: Compound/PW C001316/Stoichiometry/1.0
participant stoichiometry: Compound/PW C004983/Stoichiometry/1.0
participant stoichiometry: Compound/PW C060746/Stoichiometry/1.0
right: PE(16:0/20:3(5Z,8Z,11Z))
right: Carbon dioxide
spontaneous: false
left: PS(16:0/20:3(5Z,8Z,11Z))
name: PS(16:0/20:3(5Z,8Z,11Z)) → Carbon dioxide + PE(16:0/20:3(5Z,8Z,11Z))
conversion direction: LEFT_TO_RIGHT

Adenosine diphosphate
type: SmallMoleculeReference
xref: Reference/KEGG Compound C00008
xref: Reference/PubChem-compound 6022
xref: Reference/ChemSpider 5800
xref: Reference/CAS 58-64-0
xref: Reference/BioCyc ADP
xref: Reference/ChEBI CHEBI 16761
xref: Reference/HMDB HMDB0001341
chemical formula: C10H15N5O10P2
molecular weight: 427.02942
structure: ChemicalStructure/PW C001034

Choline
type: SmallMolecule
entity reference: Choline

Reference/BioCyc PHOSPHORYL-CHOLINE
type: UnificationXref
id: PHOSPHORYL-CHOLINE
db: BioCyc

Choline
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15354
xref: Reference/ChemSpider 299
xref: Reference/BioCyc CPD-563
xref: Reference/PubChem-compound 305
xref: Reference/CAS 62-49-7
xref: Reference/HMDB HMDB0000097
xref: Reference/KEGG Compound C00114
chemical formula: C5H14NO
molecular weight: 104.10754
structure: ChemicalStructure/PW C000065

Cytidine monophosphate
type: SmallMoleculeReference
xref: Reference/BioCyc CMP
xref: Reference/ChemSpider 5901
xref: Reference/PubChem-compound 6131
xref: Reference/ChEBI CHEBI 17361
xref: Reference/KEGG Compound C00055
xref: Reference/HMDB HMDB0000095
xref: Reference/CAS 63-37-6
chemical formula: C9H14N3O8P
molecular weight: 323.05185
structure: ChemicalStructure/PW C000064

Reference/BioCyc DIACYLGLYCEROL
type: UnificationXref
id: DIACYLGLYCEROL
db: BioCyc

Endoplasmic Reticulum Membrane
type: CellularLocationVocabulary
xref: Reference/GENE ONTOLOGY GO 0005789

Reference/UniProt P49583
type: UnificationXref
id: P49583
db: UniProt

Reference/KEGG Compound C00157
type: UnificationXref
id: C00157
db: KEGG Compound

Putative choline kinase B3
type: Protein
entity reference: Putative choline kinase B3

ChemicalStructure/PW C000057
type: ChemicalStructure
structure format: SMILES

PhosphatidylSerine SYnthase
type: ProteinReference
xref: Reference/UniProt Q09643

DG(16:0/20:3(5Z,8Z,11Z)/0:0)
type: SmallMolecule
entity reference: DG(16:0/20:3(5Z,8Z,11Z)/0:0)

Reference/HMDB HMDB0000250
type: UnificationXref
id: HMDB0000250
db: HMDB

ChemicalStructure/PW C000170
type: ChemicalStructure
structure format: SMILES
structure data: [O-]P([O-])(=O)OP([O-])([O-])=O

PE(16:0/20:3(5Z,8Z,11Z))
type: SmallMolecule
cellular location: Endoplasmic Reticulum Membrane
entity reference: PE(16:0/20:3(5Z,8Z,11Z))

Reference/HMDB HMDB0001341
type: UnificationXref
id: HMDB0001341
db: HMDB

Reference/CAS 14000-31-8
type: UnificationXref
id: 14000-31-8
db: CAS

Phosphocholine CYtidylylTransferase
type: ProteinReference
xref: Reference/UniProt X5LPX5

Putative choline-phosphate cytidylyltransferase
type: ProteinReference
xref: Reference/UniProt P49583

Phosphatidylserine decarboxylase proenzyme, mitochondrial
type: ProteinReference
xref: Reference/UniProt Q10949

Reference/KEGG Compound C00165
type: UnificationXref
id: C00165
db: KEGG Compound

ReactionCatalysis154616
type: Catalysis
controller: Phosphatidylserine decarboxylase proenzyme, mitochondrial
controlled: Reaction164474
control type: ACTIVATION

ChemicalStructure/PW C001034
type: ChemicalStructure
structure format: SMILES

ChemicalStructure/PW C000065
type: ChemicalStructure
structure format: SMILES
structure data: C[N+](C)(C)CCO

ChemicalStructure/PW C000064
type: ChemicalStructure
structure format: SMILES

Compound/PW C004983 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: PE(16:0/20:3(5Z,8Z,11Z))
stoichiometric coefficient: 1.0

Compound/PW C000170/Stoichiometry/1.0
type: Stoichiometry
physical entity: Pyrophosphate
stoichiometric coefficient: 1.0

Reference/HMDB HMDB0000149
type: UnificationXref
id: HMDB0000149
db: HMDB

Caenorhabditis elegans
type: BioSource
xref: Reference/TAXONOMY 6239

ReactionCatalysis154621
type: Catalysis
controller: PhosphatidylSerine SYnthase
controlled: 2.7.8.-
control type: ACTIVATION

ReactionCatalysis154620
type: Catalysis
controller: Choline/EthanolaminePhosphoTransferase
controlled: Reaction164476
control type: ACTIVATION

Choline/EthanolaminePhosphoTransferase
type: ProteinReference
xref: Reference/UniProt G5EC09

Reference/ChemSpider 5901
type: UnificationXref
id: 5901
db: ChemSpider

Reference/TAXONOMY 6239
type: UnificationXref
id: 6239
db: TAXONOMY

Reference/ChEBI CHEBI 15422
type: UnificationXref
id: CHEBI:15422
db: ChEBI

Reference/PubChem-compound 305
type: UnificationXref
id: 305
db: PubChem-compound

Reference/ChEBI CHEBI 18132
type: UnificationXref
id: CHEBI:18132
db: ChEBI

Reference/ChemSpider 24766651
type: UnificationXref
id: 24766651
db: ChemSpider

Reference/KEGG Compound C00055
type: UnificationXref
id: C00055
db: KEGG Compound

ChemicalStructure/PW C000149
type: ChemicalStructure
structure format: SMILES
structure data: NCCOP(O)(O)=O

PS(16:0/20:3(5Z,8Z,11Z))
type: SmallMolecule
entity reference: PS(16:0/20:3(5Z,8Z,11Z))

Compound/PW C060746/Stoichiometry/1.0
type: Stoichiometry
physical entity: PS(16:0/20:3(5Z,8Z,11Z))
stoichiometric coefficient: 1.0

Reference/PubChem-compound 53479587
type: UnificationXref
id: 53479587
db: PubChem-compound

ReactionCatalysis154615
type: Catalysis
controller: Choline/EthanolaminePhosphoTransferase
controlled: Reaction164475
control type: ACTIVATION

Compound/PW C001316/Stoichiometry/1.0
type: Stoichiometry
physical entity: Carbon dioxide
stoichiometric coefficient: 1.0

Reference/KEGG Compound C00063
type: UnificationXref
id: C00063
db: KEGG Compound

Reference/GENE ONTOLOGY GO 0005789
type: UnificationXref
id: GO:0005789
db: GENE ONTOLOGY

PS(16:0/20:3(5Z,8Z,11Z))
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 18303
xref: Reference/ChemSpider 13628254
xref: Reference/BioCyc L-1-PHOSPHATIDYL-SERINE
xref: Reference/HMDB HMDB0112347
xref: Reference/KEGG Compound C02737
xref: Reference/PubChem-compound 6323481
chemical formula: C42H76NO10P
molecular weight: 785.5207
structure: ChemicalStructure/PW C060746

Reference/BioCyc ETHANOL-AMINE
type: UnificationXref
id: ETHANOL-AMINE
db: BioCyc

Reference/UniProt Q10949
type: UnificationXref
id: Q10949
db: UniProt

Compound/PW C003161/Stoichiometry/1.0
type: Stoichiometry
physical entity: DG(16:0/20:3(5Z,8Z,11Z)/0:0)
stoichiometric coefficient: 1.0

Ethanolamine
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0000149
xref: Reference/ChemSpider 13835336
xref: Reference/PubChem-compound 700
xref: Reference/CAS 141-43-5
xref: Reference/BioCyc ETHANOL-AMINE
xref: Reference/ChEBI CHEBI 16000
xref: Reference/KEGG Compound C00189
chemical formula: C2H7NO
molecular weight: 61.052765
structure: ChemicalStructure/PW C000096

Reference/ChemSpider 13628254
type: UnificationXref
id: 13628254
db: ChemSpider

Adenosine triphosphate
type: SmallMoleculeReference
xref: Reference/ChEBI CHEBI 15422
xref: Reference/PubChem-compound 5957
xref: Reference/HMDB HMDB0000538
xref: Reference/CAS 56-65-5
xref: Reference/ChemSpider 5742
xref: Reference/BioCyc ATP
xref: Reference/KEGG Compound C00002
chemical formula: C10H16N5O13P3
molecular weight: 506.99576
structure: ChemicalStructure/PW C000414

Compound/PW C001201/Stoichiometry/1.0
type: Stoichiometry
physical entity: CDP-ethanolamine
stoichiometric coefficient: 1.0

Reference/ChEBI CHEBI 16526
type: UnificationXref
id: CHEBI:16526
db: ChEBI

Phosphatidylcholine/Phosphatidylethanolamine Biosynthesis PC(16:0/20:3(5Z,8Z,11Z)) | PE(16:0/20:3(5Z,8Z,11Z))
type: Pathway
pathway order: PathwayEnzymeReaction/1914537
pathway order: PathwayEnzymeReaction/1914532
pathway order: PathwayEnzymeReaction/1914531
pathway order: PathwayTransport/1914518
pathway order: PathwayTransport/1914529
pathway order: PathwayEnzymeReaction/1914530
pathway order: PathwayEnzymeReaction/1914536
pathway order: PathwayEnzymeReaction/1914535
pathway order: PathwayEnzymeReaction/1914534
pathway order: PathwayEnzymeReaction/1914533
pathway component: Transport9509
pathway component: Reaction140637
pathway component: ReactionCatalysis130710
pathway component: Transport9508
pathway component: 2.7.1.82
pathway component: ReactionCatalysis130711
pathway component: ReactionCatalysis154616
pathway component: Reaction164475
pathway component: ReactionCatalysis154615
pathway component: Reaction164476
pathway component: 2.7.8.-
pathway component: 2.7.7.15
pathway component: ReactionCatalysis130705
pathway component: Reaction164474
pathway component: 2.7.7.14
pathway component: ReactionCatalysis154621
pathway component: ReactionCatalysis130706
pathway component: ReactionCatalysis154620
xref: Reference/SMPDB SMP0100165
xref: Reference/PathWhiz PW101192
organism: Caenorhabditis elegans

Reference/KEGG Compound C00065
type: UnificationXref
id: C00065
db: KEGG Compound

Reference/ChEBI CHEBI 16761
type: UnificationXref
id: CHEBI:16761
db: ChEBI

Reference/KEGG Compound C00189
type: UnificationXref
id: C00189
db: KEGG Compound

PS(16:0/20:3(5Z,8Z,11Z))
type: SmallMolecule
cellular location: Endoplasmic Reticulum Membrane
entity reference: PS(16:0/20:3(5Z,8Z,11Z))

Reference/CAS 107-73-3
type: UnificationXref
id: 107-73-3
db: CAS

Reference/CAS 65-47-4
type: UnificationXref
id: 65-47-4
db: CAS

Reference/CAS 3036-18-8
type: UnificationXref
id: 3036-18-8
db: CAS

Reference/CAS 987-78-0
type: UnificationXref
id: 987-78-0
db: CAS

Reference/HMDB HMDB0007110
type: UnificationXref
id: HMDB0007110
db: HMDB

Reference/ChemSpider 5800
type: UnificationXref
id: 5800
db: ChemSpider

Carbon dioxide
type: SmallMoleculeReference
xref: Reference/PubChem-compound 280
xref: Reference/ChEBI CHEBI 16526
xref: Reference/ChemSpider 274
xref: Reference/HMDB HMDB0001967
xref: Reference/CAS 124-38-9
xref: Reference/KEGG Compound C00011
chemical formula: CO2
molecular weight: 43.98983
structure: ChemicalStructure/PW C001316

Reference/BioCyc CMP
type: UnificationXref
id: CMP
db: BioCyc

Reference/KEGG Compound C00080
type: UnificationXref
id: C00080
db: KEGG Compound

ChemicalStructure/PW C000096
type: ChemicalStructure
structure format: SMILES
structure data: NCCO

Reference/ChemSpider 299
type: UnificationXref
id: 299
db: ChemSpider

CDP-ethanolamine
type: SmallMoleculeReference
xref: Reference/HMDB HMDB0001564
xref: Reference/ChEBI CHEBI 16732
xref: Reference/PubChem-compound 123727
xref: Reference/CAS 3036-18-8
xref: Reference/BioCyc CDP-ETHANOLAMINE
xref: Reference/KEGG Compound C00570
xref: Reference/ChemSpider 110296
chemical formula: C11H20N4O11P2
molecular weight: 446.0604
structure: ChemicalStructure/PW C001201

Phosphorylcholine
type: SmallMoleculeReference
xref: Reference/CAS 107-73-3
xref: Reference/HMDB HMDB0001565
xref: Reference/BioCyc PHOSPHORYL-CHOLINE
xref: Reference/PubChem-compound 1014
xref: Reference/ChEBI CHEBI 18132
xref: Reference/KEGG Compound C00588
xref: Reference/ChemSpider 989
chemical formula: C5H15NO4P
molecular weight: 184.07387
structure: ChemicalStructure/PW C001202

Reference/ChEBI CHEBI 17677
type: UnificationXref
id: CHEBI:17677
db: ChEBI

Reference/PathWhiz PW101192
type: UnificationXref
id: PW101192
db: PathWhiz

Reference/ChEBI CHEBI 15378
type: UnificationXref
id: CHEBI:15378
db: ChEBI

ChemicalStructure/PW C040034
type: ChemicalStructure
structure format: SMILES
structure data: [H+]

Reference/PubChem-compound 6176
type: UnificationXref
id: 6176
db: PubChem-compound

Reference/BioCyc L-1-PHOSPHATIDYL-SERINE
type: UnificationXref
id: L-1-PHOSPHATIDYL-SERINE
db: BioCyc

Reference/CAS 58-64-0
type: UnificationXref
id: 58-64-0
db: CAS

ChemicalStructure/PW C000414
type: ChemicalStructure
structure format: SMILES

Reference/CAS 56-45-1
type: UnificationXref
id: 56-45-1
db: CAS

Reference/ChEBI CHEBI 17553
type: UnificationXref
id: CHEBI:17553
db: ChEBI

Reference/PubChem-compound 123727
type: UnificationXref
id: 123727
db: PubChem-compound

Reference/PubChem-compound 280
type: UnificationXref
id: 280
db: PubChem-compound

L-Serine
type: SmallMolecule
entity reference: L-Serine

Reference/PubChem-compound 11583971
type: UnificationXref
id: 11583971
db: PubChem-compound

Reference/PubChem-compound 24778715
type: UnificationXref
id: 24778715
db: PubChem-compound

L-Serine
type: SmallMoleculeReference
xref: Reference/ChemSpider 5736
xref: Reference/ChEBI CHEBI 17115
xref: Reference/CAS 56-45-1
xref: Reference/KEGG Compound C00065
xref: Reference/PubChem-compound 5951
xref: Reference/HMDB HMDB0000187
xref: Reference/BioCyc SER
chemical formula: C3H7NO3
molecular weight: 105.042595
structure: ChemicalStructure/PW C000120

Reference/HMDB HMDB0000187
type: UnificationXref
id: HMDB0000187
db: HMDB

Reference/PubChem-compound 644102
type: UnificationXref
id: 644102
db: PubChem-compound

Reference/ChemSpider 5941
type: UnificationXref
id: 5941
db: ChemSpider

Reference/ChEBI CHEBI 16436
type: UnificationXref
id: CHEBI:16436
db: ChEBI

Compound/PW C004983 Mitochondrial Inner Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: PE(16:0/20:3(5Z,8Z,11Z))
stoichiometric coefficient: 1.0

Phosphorylcholine
type: SmallMolecule
entity reference: Phosphorylcholine

CDP-ethanolamine
type: SmallMolecule
entity reference: CDP-ethanolamine

Putative choline kinase B3
type: ProteinReference
xref: Reference/UniProt P46560

Reference/ChemSpider 990
type: UnificationXref
id: 990
db: ChemSpider

Compound/PW C060746 Endoplasmic Reticulum Membrane/Stoichiometry/1.0
type: Stoichiometry
physical entity: PS(16:0/20:3(5Z,8Z,11Z))
stoichiometric coefficient: 1.0

DG(16:0/20:3(5Z,8Z,11Z)/0:0)
type: SmallMoleculeReference
xref: Reference/ChemSpider 24765933
xref: Reference/BioCyc DIACYLGLYCEROL
xref: Reference/PubChem-compound 53478028
xref: Reference/KEGG Compound C00165
xref: Reference/HMDB HMDB0007110
chemical formula: C39H70O5
molecular weight: 618.52234
structure: ChemicalStructure/PW C003161

Reference/ChEBI CHEBI 15354
type: UnificationXref
id: CHEBI:15354
db: ChEBI

Reference/HMDB HMDB0059597
type: UnificationXref
id: HMDB0059597
db: HMDB

Reference/CAS 141-43-5
type: UnificationXref
id: 141-43-5
db: CAS

Reference/KEGG Compound C00307
type: UnificationXref
id: C00307
db: KEGG Compound

Reference/UniProt Q09643
type: UnificationXref
id: Q09643
db: UniProt

Carbon dioxide
type: SmallMolecule
entity reference: Carbon dioxide

Reference/HMDB HMDB0001967
type: UnificationXref
id: HMDB0001967
db: HMDB

Reference/CAS 62-49-7
type: UnificationXref
id: 62-49-7
db: CAS

Reference/ChemSpider 989
type: UnificationXref
id: 989
db: ChemSpider

PC(16:0/20:3(5Z,8Z,11Z))
type: SmallMolecule
entity reference: PC(16:0/20:3(5Z,8Z,11Z))

PC(16:0/20:3(5Z,8Z,11Z))
type: SmallMoleculeReference
xref: Reference/ChemSpider 24766651
xref: Reference/PubChem-compound 24778715
xref: Reference/HMDB HMDB0007980
xref: Reference/KEGG Compound C00157
xref: Reference/BioCyc PHOSPHATIDYLCHOLINE
chemical formula: C44H82NO8P
molecular weight: 783.5778
structure: ChemicalStructure/PW C004029

Reference/HMDB HMDB0000082
type: UnificationXref
id: HMDB0000082
db: HMDB

CDP-Choline
type: SmallMolecule
entity reference: CDP-Choline

Compound/PW C004029/Stoichiometry/1.0
type: Stoichiometry
physical entity: PC(16:0/20:3(5Z,8Z,11Z))
stoichiometric coefficient: 1.0

CDP-Choline
type: SmallMoleculeReference
xref: Reference/BioCyc CDP-CHOLINE
xref: Reference/ChemSpider 13207
xref: Reference/HMDB HMDB0001413
xref: Reference/ChEBI CHEBI 16436
xref: Reference/KEGG Compound C00307
xref: Reference/PubChem-compound 11583971
xref: Reference/CAS 987-78-0
chemical formula: C14H26N4O11P2
molecular weight: 488.10733
structure: ChemicalStructure/PW C043034