KEGG   ORTHOLOGY: K05713Help
Entry
K05713                      KO                                     

Name
mhpB
Definition
2,3-dihydroxyphenylpropionate 1,2-dioxygenase [EC:1.13.11.16]
Pathway
Phenylalanine metabolism
Degradation of aromatic compounds
Module
M00545  
Trans-cinnamate degradation, trans-cinnamate => acetyl-CoA
Brite
KEGG Orthology (KO) [BR:ko00001]
 Metabolism
  Overview
   01220 Degradation of aromatic compounds
    K05713  mhpB; 2,3-dihydroxyphenylpropionate 1,2-dioxygenase
  Amino acid metabolism
   00360 Phenylalanine metabolism
    K05713  mhpB; 2,3-dihydroxyphenylpropionate 1,2-dioxygenase
KEGG modules [BR:ko00002]
 Pathway module
  Nucleotide and amino acid metabolism
   Aromatic amino acid metabolism
    M00545  Trans-cinnamate degradation, trans-cinnamate => acetyl-CoA
     K05713  mhpB; 2,3-dihydroxyphenylpropionate 1,2-dioxygenase
Enzymes [BR:ko01000]
 1. Oxidoreductases
  1.13  Acting on single donors with incorporation of molecular oxygen (oxygenases)
   1.13.11  With incorporation of two atoms of oxygen
    1.13.11.16  3-carboxyethylcatechol 2,3-dioxygenase
     K05713  mhpB; 2,3-dihydroxyphenylpropionate 1,2-dioxygenase
BRITE hierarchy
Other DBs
Genes
ECO: 
b0348(mhpB)
ECJ: 
JW0339(mhpB)
ECD: 
ECOK: 
ECE: 
Z0446(mhpB)
ECS: 
ECs0403(mhpB)
ECF: 
ETW: 
ECSP_0412(mhpB)
ELX: 
EOJ: 
EOI: 
ECO111_0384(mhpB)
EOH: 
ECO103_0330(mhpB)
EOK: 
G2583_0461(mhpB)
ELR: 
ECO55CA74_02215(mhpB)
ECX: 
EcHS_A0412(mhpB)
ECW: 
EcE24377A_0372(mhpB)
ECM: 
EcSMS35_0379(mhpB)
ECY: 
ECSE_0373
ECR: 
ECIAI1_0349(mhpB)
ECQ: 
ECED1_0376(mhpB)
ECK: 
EC55989_0355(mhpB)
ECT: 
ECIAI39_0330(mhpB)
EOC: 
CE10_0316(mhpB)
EUM: 
ECUMN_0391(mhpB)
ELO: 
EC042_0385(mhpB)
ELH: 
ETEC_0404
ESE: 
ECSF_0319
ESO: 
O3O_05560(mhpB)
ESM: 
O3M_19720(mhpB)
ESL: 
O3K_19735(mhpB)
ECL: 
EcolC_3277
EBR: 
ECB_00302(mhpB)
EBD: 
ECBD_3309
EKO: 
EKO11_3494
EKF: 
KO11_21840(mhpB)
EDH: 
EcDH1_3258
EDJ: 
ECDH1ME8569_0335(mhpB)
ENA: 
ECNA114_0331(mhpB)
EUN: 
UMNK88_398
ELW: 
ECW_m0426(mhpB)
ELL: 
WFL_02095(mhpB)
ELP: 
P12B_c0308(mhpB) P12B_c0366(mhpB)
EBL: 
ECD_00302(mhpB)
EBE: 
B21_00306(mhpB)
ECOA: 
APECO78_05260(mhpB)
ECOL: 
LY180_02130(mhpB)
ECOJ: 
P423_01830(mhpB)
ECOO: 
ECRM13514_0498(mhpB)
ECOH: 
ECRM13516_0328(mhpB)
ECOS: 
EC958_0492
SSN: 
SSON_0295(mhpB)
SHQ: 
A0259_05410(mhpB)
KPN: 
KPN_02121(mhpB)
KPU: 
KP1_3216(mhpB)
KPM: 
KPHS_31030 KPHS_31040
KPP: 
A79E_2123
KPK: 
A593_25660(mhpB)
KPH: 
KPNIH24_12935(mhpB)
KPZ: 
KPNIH27_14860(mhpB)
KPV: 
KPNIH29_15520(mhpB)
KPW: 
KPNIH30_15800(mhpB)
KPY: 
KPNIH31_14655(mhpB)
KPG: 
KPNIH32_15695(mhpB)
KPC: 
KPNIH10_15320(mhpB)
KPQ: 
KPR0928_15295(mhpB)
KPT: 
VK055_0340(mhpB)
KPE: 
KPK_2202(mhpB)
KPO: 
KPN2242_13560(mhpB)
KPR: 
KPR_2666(mhpB)
KPJ: 
N559_2168
KPI: 
D364_10870(mhpB)
KPA: 
KPNJ1_02341
KPS: 
KPNJ2_02301
KPX: 
PMK1_04485(mhpB)
KPB: 
FH42_06700(mhpB)
KPNE: 
KU54_010820(mhpB)
KPNU: 
LI86_10775(mhpB)
KVA: 
Kvar_2154
KVD: 
KR75_23580(mhpB)
KVQ: 
SP68_04235(mhpB)
KOX: 
KOX_22690(mhpB)
KOE: 
A225_3415
KOY: 
J415_14955
KOK: 
KONIH1_16725(mhpB)
KOC: 
AB185_19180(mhpB)
KOM: 
HR38_20985(mhpB)
KQU: 
AVR78_19685(mhpB)
CFD: 
CFNIH1_11835(mhpB)
CIF: 
AL515_06440(mhpB)
EBT: 
EBL_c20030(mhpB)
ROR: 
RORB6_04280
PGE: 
LG71_09615(mhpB)
KGO: 
CEW81_11375(mhpB)
EBF: 
D782_1983
SFW: 
WN53_15165(mhpB)
SFG: 
AV650_10705(mhpB)
SOD: 
Sant_0204
PLU: 
plu2208
PAY: 
PAU_02353(mhpB)
PTT: 
VY86_20020
VNA: 
PN96_06270(mhpB)
VEJ: 
VEJY3_06785(mhpB)
VFU: 
vfu_A01976
PPW: 
PputW619_1980
PPUH: 
B479_25885
PVR: 
PverR02_12310(mhpB)
PSV: 
PVLB_26047
PPSY: 
AOC04_16945(mhpB)
AVN: 
Avin_15050(mphB)
AVL: 
AvCA_15050(mhpB)
AVD: 
AvCA6_15050(mhpB)
ACX: 
Achr_27820(mhpB)
AEI: 
AOY20_01930
ASJ: 
AsACE_CH00362(mhpB)
GBI: 
PG2T_03950
AQL: 
BXU06_16215 BXU06_17035(mhpB)
RPJ: 
N234_23040(mhpB) N234_34800(mhpB) N234_36990
REU: 
Reut_A0271
CNC: 
CNE_1c17850(mhpB)
CBW: 
RR42_s1476
CCUP: 
BKK81_25720(mhpB)
BVI: 
Bcep1808_5387
BVE: 
AK36_3499(mhpB)
BCEW: 
DM40_5003(mhpB)
BMK: 
DM80_3369
BCON: 
NL30_34145(mhpB)
BDF: 
WI26_30215(mhpB)
BLAT: 
WK25_27495(mhpB)
BSEM: 
WJ12_26045(mhpB)
BPSL: 
WS57_02985(mhpB) WS57_14600(mhpB)
BGE: 
BC1002_4116 BC1002_4723
BUK: 
MYA_5005
BXE: 
Bxe_B2328
BXB: 
DR64_4660(mhpB)
BPH: 
Bphy_4536
BCAI: 
K788_0000440
PPNO: 
DA70_11720(mhpB)
PPNM: 
LV28_19230(mhpB)
PRB: 
X636_15110(mhpB)
PSPU: 
NA29_07815(mhpB)
PAPI: 
SG18_24445(mhpB)
PVE: 
UC34_22410(mhpB)
PFG: 
AB870_09225(mhpB)
BPA: 
BPP3697
BBR: 
BB4131
BBH: 
BN112_4272
BBX: 
BBS798_3921
AXO: 
NH44784_059111
AXN: 
AX27061_4150
AXS: 
LH59_19120
AXX: 
ERS451415_04169(mhpB)
AFA: 
UZ73_04235(mhpB)
DAC: 
Daci_0103
DEL: 
DelCs14_0105
DTS: 
BI380_22260
DHK: 
BO996_02475
VPE: 
Varpa_0244
DAR: 
Daro_0901 Daro_1353
AZO: 
azo1975(mhpB)
SAME: 
SAMCFNEI73_pB0464
XAU: 
Xaut_0932
HMC: 
HYPMC_0176(pydA)
RHZ: 
RHPLAN_32550
PSIN: 
CAK95_01470
SUAM: 
BOO69_22190
NRE: 
BES08_20375
SPHP: 
LH20_19530
SWI: 
Swit_4311
MPA: 
MAP_0695(mhpB)
MAO: 
MAP4_3169
MAVI: 
RC58_15705(mhpB)
MAVU: 
RE97_15735(mhpB)
MAV: 
MAV_1947 MAV_2652
MAVD: 
NF84_03740(mhpB)
MAVR: 
LA63_03840(mhpB)
MAVA: 
LA64_03850(mhpB)
MIT: 
OCO_07350 OCO_14340
MIA: 
OCU_07360 OCU_14800
MIE: 
LG41_03645(mhpB) LG41_07135
MIR: 
OCQ_07500 OCQ_28050
MID: 
MIP_01271
MYO: 
OEM_07430
MCHI: 
AN480_04830(mhpB)
MSM: 
MSMEG_4865(mhpB)
MSG: 
MSMEI_4740
MSB: 
LJ00_24060(mhpB)
MSN: 
LI99_24065(mhpB)
MSH: 
LI98_24070(mhpB)
MSA: 
Mycsm_01986 Mycsm_04568
MUL: 
MUL_0347(mhpB)
MVA: 
Mvan_4244
MGI: 
Mflv_2402
MSP: 
Mspyr1_18340
MAB: 
MAB_4372
MAY: 
LA62_22215(mhpB)
MABO: 
NF82_21905(mhpB)
MAZ: 
LA61_22110(mhpB)
MMC: 
Mmcs_3785
MKM: 
Mkms_3858
MJL: 
Mjls_3789 Mjls_4035
MJD: 
JDM601_3457(mhpB)
MMI: 
MMAR_4776(mhpB)
MMAE: 
MMARE11_46050(mhpB)
MRH: 
MycrhN_3919
MMM: 
W7S_03595(mhpB)
MCB: 
Mycch_3688
MKN: 
MKAN_10215(mhpB)
MKS: 
LG40_10055(mhpB)
MKI: 
LH54_10200(mhpB)
MYV: 
G155_20870(mhpB)
MYE: 
AB431_21455(mhpB)
MGO: 
AFA91_16190(mhpB)
MFT: 
XA26_42570
MPHL: 
MPHLCCUG_03810(mhpB)
MVQ: 
MYVA_4047(mhpB) MYVA_4677(pydA)
ASD: 
AS9A_0167(mhpB)
CDR: 
CDHC03_1946(mhpB)
CAZ: 
CARG_03190
CII: 
CIMIT_11780(mhpB)
CMV: 
CMUST_15055(mhpB)
NNO: 
NONO_c29000
RHA: 
RHA1_ro00518
REB: 
XU06_01795
ROP: 
ROP_70940 ROP_pROB02-01950(nimB)
ROA: 
Pd630_LPD12024 Pd630_LPD12044
REQ: 
REQ_30260 REQ_35200 REQ_43390
RPY: 
Y013_12695(mhpB) Y013_22370
RAV: 
AAT18_09070(mhpB)
SCB: 
SCAB_2101(mhpB)
SVL: 
Strvi_4245
SRC: 
M271_04215
STRF: 
ASR50_31440(mhpB)
STSI: 
A4E84_36440(mhpB)
ARZ: 
AUT26_01400 AUT26_19825(mhpB)
NAE: 
BHE16_09170(mhpB)
PSIM: 
KR76_02285
FRE: 
Franean1_2892 Franean1_4746
FRI: 
FraEuI1c_4094 FraEuI1c_5339
NML: 
Namu_1342
AMD: 
AMED_5706(mhpB)
AMN: 
RAM_29140(mhpB)
AMM: 
AMES_5632(mhpB)
AMZ: 
B737_5632(mhpB)
AMQ: 
AMETH_1850(mhpB) AMETH_2409(mhpB) AMETH_4604(mhpB)
PDX: 
Psed_0217 Psed_6036
LED: 
BBK82_32635
AFS: 
AFR_23715(mhpB)
 » show all
TaxonomyKoalaUniProt
Reference
PMID:9098055
  Authors
Ferrandez A, Garcia JL, Diaz E.
  Title
Genetic characterization and expression in heterologous hosts of the 3-(3-hydroxyphenyl)propionate catabolic pathway of Escherichia coli K-12.
  Journal
J Bacteriol 179:2573-81 (1997)
DOI:10.1128/JB.179.8.2573-2581.1997
  Sequence
[eco:b0348]
LinkDB All DBs

KEGG   ENZYME: 1.13.11.16Help
Entry
EC 1.13.11.16               Enzyme                                 

Name
3-carboxyethylcatechol 2,3-dioxygenase;
2,3-dihydroxy-beta-phenylpropionic dioxygenase;
2,3-dihydroxy-beta-phenylpropionate oxygenase;
3-(2,3-dihydroxyphenyl)propanoate:oxygen 1,2-oxidoreductase;
3-(2,3-dihydroxyphenyl)propanoate:oxygen 1,2-oxidoreductase (decyclizing)
Class
Oxidoreductases;
Acting on single donors with incorporation of molecular oxygen (oxygenases);
With incorporation of two atoms of oxygen
BRITE hierarchy
Sysname
3-(2,3-dihydroxyphenyl)propanoate:oxygen 1,2-oxidoreductase (ring-opening)
Reaction(IUBMB)
(1) 3-(2,3-dihydroxyphenyl)propanoate + O2 = (2Z,4E)-2-hydroxy-6-oxonona-2,4-diene-1,9-dioate [RN:R04376];
(2) (2E)-3-(2,3-dihydroxyphenyl)prop-2-enoate + O2 = (2Z,4E,7E)-2-hydroxy-6-oxonona-2,4,7-triene-1,9-dioate [RN:R06788]
Reaction(KEGG)
Substrate
3-(2,3-dihydroxyphenyl)propanoate [CPD:C04044];
O2 [CPD:C00007];
(2E)-3-(2,3-dihydroxyphenyl)prop-2-enoate [CPD:C12623]
Product
(2Z,4E)-2-hydroxy-6-oxonona-2,4-diene-1,9-dioate [CPD:C04479];
(2Z,4E,7E)-2-hydroxy-6-oxonona-2,4,7-triene-1,9-dioate [CPD:C12624]
Comment
An iron protein. This enzyme catalyses a step in the pathway of phenylpropanoid compounds degradation.
History
EC 1.13.11.16 created 1972, modified 2011, modified 2012
Pathway
Phenylalanine metabolism
Microbial metabolism in diverse environments
Orthology
K05713  
2,3-dihydroxyphenylpropionate 1,2-dioxygenase
Genes
ECO: 
b0348(mhpB)
ECJ: 
JW0339(mhpB)
ECD: 
ECOK: 
ECE: 
Z0446(mhpB)
ECS: 
ECs0403(mhpB)
ECF: 
ETW: 
ECSP_0412(mhpB)
ELX: 
EOJ: 
EOI: 
ECO111_0384(mhpB)
EOH: 
ECO103_0330(mhpB)
EOK: 
G2583_0461(mhpB)
ELR: 
ECO55CA74_02215(mhpB)
ECX: 
EcHS_A0412(mhpB)
ECW: 
EcE24377A_0372(mhpB)
ECM: 
EcSMS35_0379(mhpB)
ECY: 
ECSE_0373
ECR: 
ECIAI1_0349(mhpB)
ECQ: 
ECED1_0376(mhpB)
ECK: 
EC55989_0355(mhpB)
ECT: 
ECIAI39_0330(mhpB)
EOC: 
CE10_0316(mhpB)
EUM: 
ECUMN_0391(mhpB)
ELO: 
EC042_0385(mhpB)
ELH: 
ETEC_0404
ESE: 
ECSF_0319
ESO: 
O3O_05560(mhpB)
ESM: 
O3M_19720(mhpB)
ESL: 
O3K_19735(mhpB)
ECL: 
EcolC_3277
EBR: 
ECB_00302(mhpB)
EBD: 
ECBD_3309
EKO: 
EKO11_3494
EKF: 
KO11_21840(mhpB)
EDH: 
EcDH1_3258
EDJ: 
ECDH1ME8569_0335(mhpB)
ENA: 
ECNA114_0331(mhpB)
EUN: 
UMNK88_398
ELW: 
ECW_m0426(mhpB)
ELL: 
WFL_02095(mhpB)
ELP: 
P12B_c0308(mhpB) P12B_c0366(mhpB)
EBL: 
ECD_00302(mhpB)
EBE: 
B21_00306(mhpB)
ECOA: 
APECO78_05260(mhpB)
ECOL: 
LY180_02130(mhpB)
ECOJ: 
P423_01830(mhpB)
ECOO: 
ECRM13514_0498(mhpB)
ECOH: 
ECRM13516_0328(mhpB)
ECOS: 
EC958_0492
SSN: 
SSON_0295(mhpB)
SHQ: 
A0259_05410(mhpB)
KPN: 
KPN_02121(mhpB)
KPU: 
KP1_3216(mhpB)
KPM: 
KPHS_31030 KPHS_31040
KPP: 
A79E_2123
KPK: 
A593_25660(mhpB)
KPH: 
KPNIH24_12935(mhpB)
KPZ: 
KPNIH27_14860(mhpB)
KPV: 
KPNIH29_15520(mhpB)
KPW: 
KPNIH30_15800(mhpB)
KPY: 
KPNIH31_14655(mhpB)
KPG: 
KPNIH32_15695(mhpB)
KPC: 
KPNIH10_15320(mhpB)
KPQ: 
KPR0928_15295(mhpB)
KPT: 
VK055_0340(mhpB)
KPE: 
KPK_2202(mhpB)
KPO: 
KPN2242_13560(mhpB)
KPR: 
KPR_2666(mhpB)
KPJ: 
N559_2168
KPI: 
D364_10870(mhpB)
KPA: 
KPNJ1_02341
KPS: 
KPNJ2_02301
KPX: 
PMK1_04485(mhpB)
KPB: 
FH42_06700(mhpB)
KPNE: 
KU54_010820(mhpB)
KPNU: 
LI86_10775(mhpB)
KVA: 
Kvar_2154
KVD: 
KR75_23580(mhpB)
KVQ: 
SP68_04235(mhpB)
KOX: 
KOX_22690(mhpB)
KOE: 
A225_3415
KOY: 
J415_14955
KOK: 
KONIH1_16725(mhpB)
KOC: 
AB185_19180(mhpB)
KOM: 
HR38_20985(mhpB)
KQU: 
AVR78_19685(mhpB)
CFD: 
CFNIH1_11835(mhpB)
CIF: 
AL515_06440(mhpB)
EBT: 
EBL_c20030(mhpB)
ROR: 
RORB6_04280
PGE: 
LG71_09615(mhpB)
KGO: 
CEW81_11375(mhpB)
EBF: 
D782_1983
SFW: 
WN53_15165(mhpB)
SFG: 
AV650_10705(mhpB)
SOD: 
Sant_0204
PLU: 
plu2208
PAY: 
PAU_02353(mhpB)
PTT: 
VY86_20020
VNA: 
PN96_06270(mhpB)
VEJ: 
VEJY3_06785(mhpB)
VFU: 
vfu_A01976
PPW: 
PputW619_1980
PPUH: 
B479_25885
PVR: 
PverR02_12310(mhpB)
PSV: 
PVLB_26047
PPSY: 
AOC04_16945(mhpB)
AVN: 
Avin_15050(mphB)
AVL: 
AvCA_15050(mhpB)
AVD: 
AvCA6_15050(mhpB)
ACX: 
Achr_27820(mhpB)
AEI: 
AOY20_01930
ASJ: 
AsACE_CH00362(mhpB)
GBI: 
PG2T_03950
AQL: 
BXU06_16215 BXU06_17035(mhpB)
RPJ: 
N234_23040(mhpB) N234_34800(mhpB) N234_36990
REU: 
Reut_A0271
CNC: 
CNE_1c17850(mhpB)
CBW: 
RR42_s1476
CCUP: 
BKK81_25720(mhpB)
BVI: 
Bcep1808_5387
BVE: 
AK36_3499(mhpB)
BCEW: 
DM40_5003(mhpB)
BMK: 
DM80_3369
BCON: 
NL30_34145(mhpB)
BDF: 
WI26_30215(mhpB)
BLAT: 
WK25_27495(mhpB)
BSEM: 
WJ12_26045(mhpB)
BPSL: 
WS57_02985(mhpB) WS57_14600(mhpB)
BGE: 
BC1002_4116 BC1002_4723
BUK: 
MYA_5005
BXE: 
Bxe_B2328
BXB: 
DR64_4660(mhpB)
BPH: 
Bphy_4536
BCAI: 
K788_0000440
PPNO: 
DA70_11720(mhpB)
PPNM: 
LV28_19230(mhpB)
PRB: 
X636_15110(mhpB)
PSPU: 
NA29_07815(mhpB)
PAPI: 
SG18_24445(mhpB)
PVE: 
UC34_22410(mhpB)
PFG: 
AB870_09225(mhpB)
BPA: 
BPP3697
BBR: 
BB4131
BBH: 
BN112_4272
BBX: 
BBS798_3921
AXO: 
NH44784_059111
AXN: 
AX27061_4150
AXS: 
LH59_19120
AXX: 
ERS451415_04169(mhpB)
AFA: 
UZ73_04235(mhpB)
DAC: 
Daci_0103
DEL: 
DelCs14_0105
DTS: 
BI380_22260
DHK: 
BO996_02475
VPE: 
Varpa_0244
DAR: 
Daro_0901 Daro_1353
AZO: 
azo1975(mhpB)
SAME: 
SAMCFNEI73_pB0464
XAU: 
Xaut_0932
HMC: 
HYPMC_0176(pydA)
RHZ: 
RHPLAN_32550
PSIN: 
CAK95_01470
SUAM: 
BOO69_22190
NRE: 
BES08_20375
SPHP: 
LH20_19530
SWI: 
Swit_4311
MPA: 
MAP_0695(mhpB)
MAO: 
MAP4_3169
MAVI: 
RC58_15705(mhpB)
MAVU: 
RE97_15735(mhpB)
MAV: 
MAV_1947 MAV_2652
MAVD: 
NF84_03740(mhpB)
MAVR: 
LA63_03840(mhpB)
MAVA: 
LA64_03850(mhpB)
MIT: 
OCO_07350 OCO_14340
MIA: 
OCU_07360 OCU_14800
MIE: 
LG41_03645(mhpB) LG41_07135
MIR: 
OCQ_07500 OCQ_28050
MID: 
MIP_01271
MYO: 
OEM_07430
MCHI: 
AN480_04830(mhpB)
MSM: 
MSMEG_4865(mhpB)
MSG: 
MSMEI_4740
MSB: 
LJ00_24060(mhpB)
MSN: 
LI99_24065(mhpB)
MSH: 
LI98_24070(mhpB)
MSA: 
Mycsm_01986 Mycsm_04568
MUL: 
MUL_0347(mhpB)
MVA: 
Mvan_4244
MGI: 
Mflv_2402
MSP: 
Mspyr1_18340
MAB: 
MAB_4372
MAY: 
LA62_22215(mhpB)
MABO: 
NF82_21905(mhpB)
MAZ: 
LA61_22110(mhpB)
MMC: 
Mmcs_3785
MKM: 
Mkms_3858
MJL: 
Mjls_3789 Mjls_4035
MJD: 
JDM601_3457(mhpB)
MMI: 
MMAR_4776(mhpB)
MMAE: 
MMARE11_46050(mhpB)
MRH: 
MycrhN_3919
MMM: 
W7S_03595(mhpB)
MCB: 
Mycch_3688
MKN: 
MKAN_10215(mhpB)
MKS: 
LG40_10055(mhpB)
MKI: 
LH54_10200(mhpB)
MYV: 
G155_20870(mhpB)
MYE: 
AB431_21455(mhpB)
MGO: 
AFA91_16190(mhpB)
MFT: 
XA26_42570
MPHL: 
MPHLCCUG_03810(mhpB)
MVQ: 
MYVA_4047(mhpB) MYVA_4677(pydA)
ASD: 
AS9A_0167(mhpB)
CDR: 
CDHC03_1946(mhpB)
CAZ: 
CARG_03190
CII: 
CIMIT_11780(mhpB)
CMV: 
CMUST_15055(mhpB)
NNO: 
NONO_c29000
RHA: 
RHA1_ro00518
REB: 
XU06_01795
ROP: 
ROP_70940 ROP_pROB02-01950(nimB)
ROA: 
Pd630_LPD12024 Pd630_LPD12044
REQ: 
REQ_30260 REQ_35200 REQ_43390
RPY: 
Y013_12695(mhpB) Y013_22370
RAV: 
AAT18_09070(mhpB)
SCB: 
SCAB_2101(mhpB)
SVL: 
Strvi_4245
SRC: 
M271_04215
STRF: 
ASR50_31440(mhpB)
STSI: 
A4E84_36440(mhpB)
ARZ: 
AUT26_01400 AUT26_19825(mhpB)
NAE: 
BHE16_09170(mhpB)
PSIM: 
KR76_02285
FRE: 
Franean1_2892 Franean1_4746
FRI: 
FraEuI1c_4094 FraEuI1c_5339
NML: 
Namu_1342
AMD: 
AMED_5706(mhpB)
AMN: 
RAM_29140(mhpB)
AMM: 
AMES_5632(mhpB)
AMZ: 
B737_5632(mhpB)
AMQ: 
AMETH_1850(mhpB) AMETH_2409(mhpB) AMETH_4604(mhpB)
PDX: 
Psed_0217 Psed_6036
LED: 
BBK82_32635
AFS: 
AFR_23715(mhpB)
 » show all
Taxonomy
Reference
1  [PMID:5881653]
  Authors
Dagley S, Chapman PJ, Gibson DT.
  Title
The metabolism of beta-phenylpropionic acid by an Achromobacter.
  Journal
Biochem. J. 97 (1965) 643-50.
Reference
2
  Authors
Lam, W. W. Y and Bugg, T. D. H.
  Title
Chemistry of extradiol aromatic ring cleavage: isolation of a stable dienol ring fission intermediate and stereochemistry of its enzymatic hydrolytic clevage.
  Journal
J. Chem. Soc., Chem. Commun. 10 (1994) 1163-1164.
Reference
3  [PMID:9603882]
  Authors
Diaz E, Ferrandez A, Garcia JL.
  Title
Characterization of the hca cluster encoding the dioxygenolytic pathway for initial catabolism of 3-phenylpropionic acid in Escherichia coli K-12.
  Journal
J. Bacteriol. 180 (1998) 2915-23.
  Sequence
[eco:b0348]
Other DBs
ExplorEnz - The Enzyme Database: 
IUBMB Enzyme Nomenclature: 
ExPASy - ENZYME nomenclature database: 
UM-BBD (Biocatalysis/Biodegradation Database): 
BRENDA, the Enzyme Database: 
CAS: 
105503-63-7
LinkDB All DBs

KEGG   REACTION: R04376Help
Entry
R04376                      Reaction                               

Name
3-(2,3-dihydroxyphenyl)propanoate:oxygen 1,2-oxidoreductase (decyclizing)
Definition
3-(2,3-Dihydroxyphenyl)propanoate + Oxygen <=> 2-Hydroxy-6-oxonona-2,4-diene-1,9-dioate
Equation
Reaction class
C04044_C04479
Enzyme
Pathway
Phenylalanine metabolism
Microbial metabolism in diverse environments
Degradation of aromatic compounds
Orthology
K05713  
2,3-dihydroxyphenylpropionate 1,2-dioxygenase [EC:1.13.11.16]
Other DBs
RHEA: 
LinkDB All DBs

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