PlantSME Plant secondary metabolism enzyme database
Rosmarinic acid portable pathway

Rosmarinic acid portable pathway

Category：Rosmarinic acid pathway

Rosmarinic acid pathway definition imported from the 2026-05-17 portable BLAST/HMM package.

Representative Rosmarinic Acid Reaction Route
Phenylalanine donor branch plus tyrosine acceptor branch. This pathway merges two aromatic amino-acid branches; after RAS condensation, CYP98A-type hydroxylases form rosmarinic acid with CPR electron-transfer support. The page displays annotatable members in the current reference library.
7 curated steps/modules
Phenylalanine Donor Branch
01
Substrate
L-Phenylalanine
C9H11NO2
C6H5-CH2-CH(NH2)-COOH
Deamination into the phenylpropanoid donor branch
PAL1925
Product
trans-Cinnamic acid
C9H8O2
C6H5-CH=CH-COOH
PAL converts L-phenylalanine to cinnamate as the entry step toward the 4-coumaroyl-CoA donor.
02
Substrate
trans-Cinnamic acid
C9H8O2
C6H5-CH=CH-COOH
Cinnamate 4-hydroxylation
C4H8972
Product
4-Coumaric acid
C9H8O3
4-HO-C6H4-CH=CH-COOH
C4H/CYP73A forms 4-coumaric acid for downstream CoA activation.
03
Substrate
4-Coumaric acid
C9H8O3
4-HO-C6H4-CH=CH-COOH
Substrate
CoA
C21H36N7O16P3S
CoA-SH
CoA ligation to form the RAS acyl donor
4CL3447
Product
4-Coumaroyl-CoA
C30H38N7O18P3S
4-HO-C6H4-CH=CH-C(=O)-SCoA
4CL generates 4-coumaroyl-CoA as the acyl donor for the RAS condensation reaction.
Tyrosine Acceptor Branch And Condensation
04
Substrate
L-Tyrosine
C9H11NO3
4-HO-C6H4-CH2-CH(NH2)-COOH
Transamination to 4-hydroxyphenylpyruvate
TAT2437
Product
4-Hydroxyphenylpyruvate
C9H8O4
4-HO-C6H4-CH2-C(=O)-COOH
TAT routes L-tyrosine into the 4-hydroxyphenylpyruvate acceptor branch.
05
Substrate
4-Hydroxyphenylpyruvate
C9H8O4
4-HO-C6H4-CH2-C(=O)-COOH
Reduction to the HPLA acceptor
HPPR2553
Product
4-Hydroxyphenyllactate
C9H10O4
4-HO-C6H4-CH2-CH(OH)-COOH
HPPR reduces 4-hydroxyphenylpyruvate to 4-hydroxyphenyllactate.
06
Substrate
4-Coumaroyl-CoA
C30H38N7O18P3S
4-HO-C6H4-CH=CH-C(=O)-SCoA
Substrate
4-Hydroxyphenyllactate
C9H10O4
4-HO-C6H4-CH2-CH(OH)-COOH
Ester-forming condensation
RAS3381
Product
4-Coumaroyl-4'-hydroxyphenyllactate
C18H16O7
4-HO-C6H4-CH=CH-C(=O)-O-CH(COOH)-CH2-Ar-OH
RAS couples the acyl donor with the HPLA acceptor to form the direct rosmarinic-acid precursor.
07
Substrate
4-Coumaroyl-4'-hydroxyphenyllactate
C18H16O7
mono-catechol ester precursor
CYP98A14-type hydroxylation with CPR electron-transfer support
CPR1984
Product
Rosmarinic acid
C18H16O8
caffeoyl-O-3,4-dihydroxyphenyllactate
CYP98A14 or close CYP98A enzymes catalyse 3/3' hydroxylation; CPR in the current reference library represents electron-transfer support for this P450 reaction and should not be interpreted as CPR alone performing hydroxylation.
Lineage Distribution
Assignments under this module are distributed across the following plant lineages.
All Lineages Bryophytes (24699)
Current lineage filter: Bryophytes. All species, family, module, and gene statistics below have been narrowed to this lineage.
Algae
Hits0
Bryophytes
Hits24699
Lycophytes/Ferns
Hits0
Gymnosperms
Hits0
Basal angiosperms
Hits0
Monocots
Hits0
Eudicots
Hits0
Species Distribution
Anthoceros agrestis Oxford
Bryum knowltonii
Anthoceros punctatus
Archidium alternifolium
Calliergon cordifolium
Buxbaumia aphylla
Fossombronia
Bryoxiphium norvegicum
Funaria hygrometrica
Acrobolbus urvilleanus
Lineage Summary
Bryophytes
24699
Module Gene List
Reset
GeneSpeciesProtein ID
AagrBONNSc2ySwM_344G0053380 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053380
AagrBONNSc2ySwM_344G0053390 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053390
AagrBONNSc2ySwM_344G0053400 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053400
AagrBONNSc2ySwM_344G0053410 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053410
AagrBONNSc2ySwM_344G0053420 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053420
AagrBONNSc2ySwM_344G0053430 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053430
AagrBONNSc2ySwM_344G0053440 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053440
AagrBONNSc2ySwM_344G0053530 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053530
AagrBONNSc2ySwM_344G0053560 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053560
AagrBONNSc2ySwM_344G0053580 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053580
AagrBONNSc2ySwM_344G0053640 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053640
AagrBONNSc2ySwM_344G0053660 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053660
AagrBONNSc2ySwM_344G0053670 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053670
AagrBONNSc2ySwM_344G0053700 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053700
AagrBONNSc2ySwM_344G0053810 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0053810
AagrBONNSc2ySwM_344G0054240 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0054240
AagrBONNSc2ySwM_344G0054250 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0054250
AagrBONNSc2ySwM_344G0054260 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0054260
AagrBONNSc2ySwM_344G0054270 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0054270
AagrBONNSc2ySwM_344G0054320 anthoceros_agrestis_bonn AagrBONNSc2ySwM_344G0054320
AagrBONNSc2ySwM_362G0003180 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0003180
AagrBONNSc2ySwM_362G0003220 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0003220
AagrBONNSc2ySwM_362G0005040 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0005040
AagrBONNSc2ySwM_362G0005870 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0005870
AagrBONNSc2ySwM_362G0007060 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0007060
AagrBONNSc2ySwM_362G0008870 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0008870
AagrBONNSc2ySwM_362G0009120 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0009120
AagrBONNSc2ySwM_362G0009190 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0009190
AagrBONNSc2ySwM_362G0009410 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0009410
AagrBONNSc2ySwM_362G0009550 anthoceros_agrestis_bonn AagrBONNSc2ySwM_362G0009550