Entry
Name
2-oxo-3-hexenedioate decarboxylase;
4-oxalocrotonate carboxy-lyase (misleading);
4-oxalocrotonate decarboxylase (misleading);
cnbF (gene name);
praD (gene name);
amnE (gene name);
nbaG (gene name);
xylI (gene name)
Class
Lyases;
Carbon-carbon lyases;
Carboxy-lyases
BRITE hierarchy
Sysname
(3E)-2-oxohex-3-enedioate carboxy-lyase (2-oxopent-4-enoate-forming)
Reaction(IUBMB)
(3E)-2-oxohex-3-enedioate = 2-oxopent-4-enoate + CO2 [RN:
R02602 ]
Reaction(KEGG)
Substrate
(3E)-2-oxohex-3-enedioate
Product
Comment
Involved in the meta-cleavage pathway for the degradation of phenols, modified phenols and catechols. The enzyme has been reported to accept multiple tautomeric forms [1-4]. However, careful analysis of the stability of the different tautomers, as well as characterization of the enzyme that produces its substrate, EC
5.3.2.6 , 2-hydroxymuconate tautomerase, showed that the actual substrate for the enzyme is (3E)-2-oxohex-3-enedioate [4].
History
EC 4.1.1.77 created 1999, modified 2011, modified 2012
Pathway
ec01120 Microbial metabolism in diverse environments
Orthology
K01617 2-oxo-3-hexenedioate decarboxylase
Genes
PFUW : KF707C_15590(bzaI) KF707C_16040(SalI)
PKC : PKB_3258(amne1) PKB_3606(amne3)
PALL : UYA_06735 UYA_06965 UYA_20140
PTAE : NCTC10697_02308(amnE)
AVN : Avin_08680(xylI) Avin_30600(lapH)
AVL : AvCA_08680(xylI) AvCA_30600(lapH)
AVD : AvCA6_08680(xylI) AvCA6_30600(lapH)
HPEG : EAO82_00540(dmpH) EAO82_09440(dmpH)
MSR : AU15_09345 AU15_21065 AU15_22100
MSHE : MAALD49_03420 MAALD49_03890
SALH : HMF8227_02737(hpaH)
MGEO : CFI10_00440(dmpH) CFI10_04975(dmpH)
NIK : F5I99_10090(dmpH) F5I99_10505(dmpH)
NZO : SAMEA4504057_0445(mhpD)
NCI : NCTC10296_00916(xylJ_2)
RPJ : N234_08155 N234_12210
REH : H16_B0549(h16_B0549)
CNC : CNE_2c04950(dmpH) CNE_BB1p11980(xylI) CNE_BB1p13270(dmpH)
REU : Reut_B5500 Reut_B5692
RME : Rmet_1318(dmpH) Rmet_5210(amnE)
CBW : RR42_m1052 RR42_s2483
CCUP : BKK81_23320 BKK81_27095
CUP : BKK80_29225 BKK80_32995
CUU : BKK79_23880 BKK79_35175
COX : E0W60_03750 E0W60_07780(dmpH)
BUR : Bcep18194_B2958 Bcep18194_C7643
BSTL : BBJ41_10525 BBJ41_33955
PARB : CJU94_37885(dmpH) CJU94_38130(dmpH)
PPK : U875_01885 U875_18215
PRB : X636_07585 X636_15900
BOJ : CBF45_01485 CBF45_04495 CBF45_06950 CBF45_16995
APES : FOC84_00280 FOC84_00315(dmpH)
CDN : BN940_01171 BN940_04311
KGY : EHF36_01670(dmpH) EHF36_04880(dmpH) EHF36_16935
RLH : MIZ03_0647 MIZ03_1027
HPSE : HPF_01820(tesE2) HPF_01865(tesE3)
HTN : KI616_01940 KI616_01960(dmpH)
DIH : G7047_01665(dmpH) G7047_06945
DRG : H9K76_11650(dmpH) H9K76_22950
METP : C1M51_06455(dmpH) C1M51_15395(dmpH)
SMIO : CATMQ487_04100 CATMQ487_17570
JAJ : EKL02_01820(dmpH) EKL02_15560
RBU : PG1C_09715 PG1C_14085
DEY : HYN24_14125(dmpH) HYN24_14195(dmpH)
FLE : KI610_08580(dmpH) KI610_13440(dmpH) KI610_15445(dmpH)
AZO : azo1854(lapH) azo2430(nahK)
AZD : CDA09_10340(dmpH) CDA09_10445(dmpH)
AZR : CJ010_12255(dmpH) CJ010_15200(dmpH)
THK : CCZ27_10765(dmpH) CCZ27_16280(dmpH)
THAG : CKCBHOJB_03305(hpcG)
AZQ : G3580_00540(dmpH) G3580_08285(dmpH)
MTUN : MTUNDRAET4_3891(amnE)
MAAD : AZF01_08270 AZF01_21095
NPP : PP1Y_AT15722 PP1Y_AT31571
SPHD : HY78_06675 HY78_22125
SJP : SJA_C1-11880(hpaH_xylI)
SYB : TZ53_09015 TZ53_23460
SBAR : H5V43_20650 H5V43_22345
SPAG : sphantq_04471(amnE)
ERY : CP97_03155 CP97_14235
BSON : S101395_00392(dmpH)
BFD : NCTC4823_00794(xylJ)
BACI : B1NLA3E_08440 B1NLA3E_09300
PCAL : BV455_00226(tesE_1)
PARG : PspKH34_14930 PspKH34_15490
RUE : DT065_12670 DT065_13795 DT065_15120 DT065_15210
NDT : L1999_11900 L1999_17840
NNV : QNH39_12250 QNH39_24865
HYI : K2M58_09700 K2M58_09725
BAYD : BSPP4475_07470(dmpH)
PNP : IJ22_00700 IJ22_32390 IJ22_48600
ADAU : NZD86_00710 NZD86_06140
KYR : CVV65_10340 CVV65_11285
SPAE : E2C16_04465 E2C16_12275
MYV : G155_08390 G155_08470
MFT : XA26_16790 XA26_16950
MMAT : MMAGJ_45260 MMAGJ_45420
NFR : ERS450000_00296(xylJ_1) ERS450000_01021(xylJ_2)
RPSK : JWS13_12560 JWS13_18955
RHOJ : JVH1_17120 JVH1_20175 JVH1_39410
STUD : STRTU_001643 STRTU_001677
AMAU : DSM26151_04170(amnE)
OCP : NF557_14855 NF557_15600
AGRA : AGRA3207_000779 AGRA3207_003642
AMAZ : LUW76_22725 LUW76_47885
ACIR : OG979_20775 OG979_41955
AMYC : CU254_17665 CU254_35760
AROO : NQK81_00865 NQK81_28575
ARHD : VSH64_19090 VSH64_30305 VSH64_35370
ACOR : LCL61_08955 LCL61_24560
PBRO : HOP40_26620 HOP40_31750
KUT : JJ691_102210 JJ691_11960
ACTY : OG774_08010 OG774_09250
VMA : VAB18032_17780 VAB18032_28741
MCRA : ID554_21670 ID554_30890
VER : HUT12_13555 HUT12_26050
MICF : QQG74_13325 QQG74_25585
PRY : Prubr_10590 Prubr_59260
DACT : KZZ52_26440 KZZ52_45190
» show all
Taxonomy
Reference
Authors
Shingler V, Powlowski J, Marklund U
Title
Nucleotide sequence and functional analysis of the complete phenol/3,4-dimethylphenol catabolic pathway of Pseudomonas sp. strain CF600.
Journal
Sequence
Reference
Authors
Takenaka S, Murakami S, Shinke R, Aoki K
Title
Metabolism of 2-aminophenol by Pseudomonas sp. AP-3: modified meta-cleavage pathway.
Journal
Reference
Authors
Stanley TM, Johnson WH Jr, Burks EA, Whitman CP, Hwang CC, Cook PF
Title
Expression and stereochemical and isotope effect studies of active 4-oxalocrotonate decarboxylase.
Journal
Reference
Authors
Wang SC, Johnson WH Jr, Czerwinski RM, Stamps SL, Whitman CP
Title
Kinetic and stereochemical analysis of YwhB, a 4-oxalocrotonate tautomerase homologue in Bacillus subtilis: mechanistic implications for the YwhB- and 4-oxalocrotonate tautomerase-catalyzed reactions.
Journal
Reference
Authors
Kasai D, Fujinami T, Abe T, Mase K, Katayama Y, Fukuda M, Masai E
Title
Uncovering the protocatechuate 2,3-cleavage pathway genes.
Journal
Other DBs
ExplorEnz - The Enzyme Database: 4.1.1.77
ExPASy - ENZYME nomenclature database: 4.1.1.77
UM-BBD (Biocatalysis/Biodegradation Database): 4.1.1.77
LinkDB
All DBs