KEGG   ORTHOLOGY: K09459
Entry
K09459                      KO                                     
Symbol
E4.1.1.82
Name
phosphonopyruvate decarboxylase [EC:4.1.1.82]
Pathway
map00440  Phosphonate and phosphinate metabolism
map00998  Biosynthesis of various antibiotics
map01100  Metabolic pathways
map01110  Biosynthesis of secondary metabolites
map01120  Microbial metabolism in diverse environments
Module
M00903  Fosfomycin biosynthesis, phosphoenolpyruvate => fosfomycin
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09106 Metabolism of other amino acids
   00440 Phosphonate and phosphinate metabolism
    K09459  E4.1.1.82; phosphonopyruvate decarboxylase
  09110 Biosynthesis of other secondary metabolites
   00998 Biosynthesis of various antibiotics
    K09459  E4.1.1.82; phosphonopyruvate decarboxylase
Enzymes [BR:ko01000]
 4. Lyases
  4.1  Carbon-carbon lyases
   4.1.1  Carboxy-lyases
    4.1.1.82  phosphonopyruvate decarboxylase
     K09459  E4.1.1.82; phosphonopyruvate decarboxylase
Other DBs
RN: R04053
GO: 0033980
Genes
ZNE: 110841498
CSEC: 111875044
FCD: 110847575
LGI: LOTGIDRAFT_114966
PCAN: 112559357
HRJ: 124268737
MYI: 110448928
PMAX: 117336379
MMER: 123537598
LAK: 106157387 106176585
NVE: 5511287
EPA: 110243717
ATEN: 116287539
ADF: 107333309
AMIL: 114948801
PDAM: 113684314
SPIS: 111344557
DGT: 114523267
XEN: 124452918
HMG: 100197891
SMIN: v1.2.019412.t1(symbB.v1.2.019412.t1)
TCR: 505965.50
HDE: HDEF_0202
SRL: SOD_c30100(bcpC)
FSM: CCS41_00900(aepY)
ECA: ECA0488(fom2)
PATR: EV46_02525
PATO: GZ59_05040(fom2)
PCT: PC1_0477
PEC: W5S_0591
PPUJ: E2566_02930(aepY)
PARI: I2D83_19360(aepY)
LBQ: CKQ53_06555(aepY)
LPOP: I6N93_15655(aepY)
EPE: CI789_05495(aepY)
PLF: PANA5342_2584(ppd)
PAJ: PAJ_2521
XVA: C7V42_03525(aepY)
XHY: FZ025_12105(aepY)
SDN: Sden_1162
NOC: Noc_1316
NHL: Nhal_1305
NWA: Nwat_1198
NWR: E3U44_16830(aepY)
NTT: TAO_1302
NTG: NSCAC_0557(ppd)
MPRF: J8N69_05405(aepY)
SALN: SALB1_2155
RME: Rmet_1809(ppd)
CPAU: EHF44_14445(aepY)
COX: E0W60_18820(aepY)
BMA: BMAA1769(ppd)
BMV: BMASAVP1_0759(ppd)
BMAL: DM55_4013(aepY)
BMAQ: DM76_4709(aepY)
BMAI: DM57_07160
BMAF: DM51_3462(aepY)
BMAZ: BM44_3973(aepY)
BMAB: BM45_4750(aepY)
BPD: BURPS668_A0779(aepY_2) BURPS668_A0909(aepY_1)
BPSE: BDL_3734(aepY) BDL_3836(aepY)
BPSM: BBQ_5586(aepY) BBQ_5688(aepY)
BPSU: BBN_3908(aepY) BBN_4008(aepY)
BPSD: BBX_5571(aepY) BBX_5673(aepY)
BPK: BBK_3882(aepY) BBK_5713(aepY)
BPSH: DR55_4743(aepY) DR55_4844(aepY)
BPSA: BBU_5437(aepY) BBU_5539(aepY)
BPSO: X996_3789(aepY) X996_4594(aepY)
BUT: X994_4010(aepY) X994_4112(aepY)
BTQ: BTQ_5191(aepY)
BTJ: BTJ_3821(aepY)
BTZ: BTL_4577(aepY) BTL_4677(aepY)
BTD: BTI_5337(aepY)
BTV: BTHA_5552(aepY)
BTHE: BTN_4316(aepY)
BTHM: BTRA_4581(aepY)
BTHL: BG87_4648(aepY)
BOK: DM82_4610(aepY) DM82_4704(aepY)
BOC: BG90_5889(aepY) BG90_5981(aepY)
BVE: AK36_4233(aepY)
BCN: Bcen_4246
BCJ: BCAM1244
BCEN: DM39_3754(aepY)
BCEW: DM40_4162(aepY)
BCEO: I35_5093
BAM: Bamb_3534
BMJ: BMULJ_04038(ppd)
BMU: Bmul_4472
BMK: DM80_3633(aepY)
BMUL: NP80_4147(aepY)
BCT: GEM_4496
BCED: DM42_3847(aepY)
BDL: AK34_4231(aepY)
BCON: NL30_06375
BUB: BW23_4918(aepY)
BLAT: WK25_23145
BTEI: WS51_03915
BSEM: WJ12_26080
BPSL: WS57_07795
BMEC: WJ16_24705
BSTG: WT74_25010
BANN: JFN94_23425(aepY)
BGU: KS03_4594(aepY)
BGO: BM43_5002(aepY)
BUK: MYA_4543
BUL: BW21_5017(aepY)
BURK: DM992_19620(aepY)
BXE: Bxe_B2234
BXB: DR64_4565(aepY)
BPH: Bphy_3821
BFN: OI25_4535(aepY)
PSPW: BJG93_18655(aepY)
PARB: CJU94_32425(aepY)
PHS: C2L64_30755(aepY)
PTER: C2L65_27415(aepY)
PGP: CUJ91_19560(aepY)
PCJ: CUJ87_30245(aepY)
PTS: CUJ90_26945(aepY)
PMEG: FNZ07_08535(aepY)
PTRO: G5S35_19395(aepY)
PGIS: I6I06_19280(aepY)
PACP: FAZ97_15195(aepY)
PACS: FAZ98_20210(aepY)
PEW: KZJ38_30040(aepY)
PPNO: DA70_09040
PPNM: LV28_21765
PPUL: RO07_16155
PSPU: NA29_20995
PAPI: SG18_00145
PAND: DRB87_06675(aepY)
PFIB: PI93_020430(aepY)
CABA: SBC2_10690
AAA: Acav_2123
AZO: azo2699
AOA: dqs_2834
HWI: A0Z60_07475(aepY)
CJU: C8J_1330
CHYO: CHH_1592
CHW: A2J15_004810(aepY)
CINF: CINF_1347
DAL: Dalk_1322
DLI: dnl_05850
ARA: Arad_7868
AVI: Avi_3414
AOL: S58_09490
SIW: GH266_09710(aepY)
ROS: CTJ15_07645(aepY)
RMUC: FOB66_09670(aepY)
RMT: IAI58_18635(aepY)
LCK: HN018_01550(aepY)
AZZ: DEW08_28015(aepY)
ECOG: FIV45_08010(aepY)
BSTO: C0V70_16035(aepY)
BMQ: BMQ_0785(aepY)
BMD: BMD_0786(aepY)
BMH: BMWSH_4463(ppd)
BMEG: BG04_3079(aepY)
PTB: DER53_11740(aepY)
MEKU: HUW50_16410(aepY)
BOU: I5818_22335(aepY)
BRW: GOP56_09090(aepY)
PPOL: X809_41425
PLUT: EI981_13660(aepY)
PCHI: PC41400_18310(aepY)
CTC: CTC_01699
CBE: Cbei_4337
CBZ: Cbs_4337
CBEI: LF65_04861
CSR: Cspa_c46180(bcpC)
CSB: CLSA_c08740(bcpC)
CDY: F3K33_22180(aepY)
CCAA: KQH81_02880(aepY)
RCH: RUM_11410
BPRO: PMF13cell1_05127(mdlC)
NTP: CRH09_19450(aepY)
NOZ: DMB37_08000(aepY)
SCO: SCO6824(SC1A2.33c)
SALS: SLNWT_3224
SALW: CP975_03130(aepY)
SRJ: SRO_1309
SSEO: D0Z67_12190(aepY)
SRIM: CP984_37455(aepY)
SDW: K7C20_15035(aepY)
CELH: GXP71_14040(aepY)
SAIU: J4H86_04285(aepY)
FAL: FRAAL6378
AMYY: YIM_29485
SSYI: EKG83_20795(aepY)
NHY: JQS43_02330(aepY)
SNA: Snas_5664
NAV: JQS30_13660(aepY)
OLS: Olsu_0592
NED: HUN01_29210(aepY)
TOQ: HCG51_21870(aepY)
OTE: Oter_2977
TDE: TDE_1414
TAZ: TREAZ_2215(aepY)
TPI: TREPR_2365(aepY)
TPHG: FUT81_06850(aepY)
TRI: DYE50_04585(aepY)
TPAV: HRQ91_06195(aepY)
BHC: JFL75_01535(aepY)
BIP: Bint_1238
FSC: FSU_1438
BTH: BT_1719
BTHO: Btheta7330_01296(ilvB)
BFS: BF9343_1815(aepY)
BSTE: K6V31_00390(aepY)
PARC: CI960_12855(aepY)
PCOI: LK433_14485(aepY)
DRC: G0Q07_19265(aepY)
FUV: JR347_10755(aepY)
PROC: Ptc2401_00815(ilvB_1)
NDE: NIDE2902(ppd)
PSYT: DSAG12_01621(comE_1)
AG: BAA07055(bcpC) BAA32496(fom2)
 » show all
Reference
PMID:9127192
  Authors
Nakashita H, Watanabe K, Hara O, Hidaka T, Seto H
  Title
Studies on the biosynthesis of bialaphos. Biochemical mechanism of C-P bond formation: discovery of phosphonopyruvate decarboxylase which catalyzes the formation of phosphonoacetaldehyde from phosphonopyruvate.
  Journal
J Antibiot (Tokyo) 50:212-9 (1997)
DOI:10.7164/antibiotics.50.212
Reference
  Authors
Nakashita H, Kozuka K, Hidaka T, Hara O, Seto H
  Title
Identification and expression of the gene encoding phosphonopyruvate decarboxylase of Streptomyces hygroscopicus.
  Journal
Biochim Biophys Acta 1490:159-62 (2000)
DOI:10.1016/s0167-4781(99)00249-3
  Sequence
LinkDB

KEGG   ENZYME: 4.1.1.82
Entry
EC 4.1.1.82                 Enzyme                                 
Name
phosphonopyruvate decarboxylase;
3-phosphonopyruvate carboxy-lyase
Class
Lyases;
Carbon-carbon lyases;
Carboxy-lyases
Sysname
3-phosphonopyruvate carboxy-lyase (2-phosphonoacetaldehyde-forming)
Reaction(IUBMB)
3-phosphonopyruvate = 2-phosphonoacetaldehyde + CO2 [RN:R04053]
Reaction(KEGG)
R04053
Substrate
3-phosphonopyruvate [CPD:C02798]
Product
2-phosphonoacetaldehyde [CPD:C03167];
CO2 [CPD:C00011]
Comment
The enzyme catalyses a step in the biosynthetic pathway of 2-aminoethylphosphonate, a component of the capsular polysaccharide complex of Bacteroides fragilis. Requires thiamine diphosphate and Mg2+ as cofactors. The enzyme is activated by the divalent cations Mg2+, Ca2+ and Mn2+. Pyruvate and sulfopyruvate can also act as substrates, but more slowly. This enzyme drives the reaction catalysed by EC 5.4.2.9, phosphoenolpyruvate mutase, in the thermodynamically unfavourable direction of 3-phosphonopyruvate formation [2]. It is the initial step in all of the major biosynthetic pathways of phosphonate natural products [3].
History
EC 4.1.1.82 created 2005
Pathway
ec00440  Phosphonate and phosphinate metabolism
ec00998  Biosynthesis of various antibiotics
ec01100  Metabolic pathways
ec01110  Biosynthesis of secondary metabolites
ec01120  Microbial metabolism in diverse environments
Orthology
K09459  phosphonopyruvate decarboxylase
Genes
ZNE110841498
CSEC111875044
FCD110847575
LGILOTGIDRAFT_114966
PCAN112559357
HRJ124268737
MYI110448928
PMAX117336379
MMER123537598
LAK106157387 106176585
NVE5511287
EPA110243717
ATEN116287539
ADF107333309
AMIL114948801
PDAM113684314
SPIS111344557
DGT114523267
XEN124452918
HMG100197891
TETTTHERM_01287980
PTMGSPATT00025990001 GSPATT00026172001
SMINv1.2.019412.t1(symbB.v1.2.019412.t1)
TBRTb11.01.1120
TBGTbgDal_XI10470
TCR505965.50
HDEHDEF_0202
SRLSOD_c30100(bcpC)
SRYM621_16410
FSMCCS41_00900(aepY)
ECAECA0488(fom2)
PATREV46_02525
PATOGZ59_05040(fom2)
PCTPC1_0477
PCCPCC21_005020
PWAPecwa_0573
PPARA8F97_15525
PECW5S_0591
PPOABJK05_19420
PPUJE2566_02930(aepY)
PARII2D83_19360(aepY)
LBQCKQ53_06555(aepY)
LPOPI6N93_15655(aepY)
EPECI789_05495(aepY)
PLFPANA5342_2584(ppd)
PAJPAJ_2521
PAQPAGR_g3819
EICNT01EI_2702
XVAC7V42_03525(aepY)
XHYFZ025_12105(aepY)
PPZH045_01955
SDNSden_1162
OSGBST96_06900
NOCNoc_1316
NHLNhal_1305
NWANwat_1198
NWRE3U44_16830(aepY)
NTTTAO_1302
NTGNSCAC_0557(ppd)
ZPLZBT109_1639
MPRFJ8N69_05405(aepY)
SALNSALB1_2155
RPJN234_04635
RMERmet_1809(ppd)
CBWRR42_s0340
CPAUEHF44_14445(aepY)
COXE0W60_18820(aepY)
BMABMAA1769(ppd)
BMVBMASAVP1_0759(ppd)
BMALDM55_4013(aepY)
BMAQDM76_4709(aepY)
BMAIDM57_07160
BMAFDM51_3462(aepY)
BMAZBM44_3973(aepY)
BMABBM45_4750(aepY)
BPSBPSS0508 BPSS0609
BPMBURPS1710b_A2064(ppd) BURPS1710b_A2172(fom2)
BPLBURPS1106A_A0690(ppd) BURPS1106A_A0817(ppd)
BPDBURPS668_A0779(aepY_2) BURPS668_A0909(aepY_1)
BPSEBDL_3734(aepY) BDL_3836(aepY)
BPSMBBQ_5586(aepY) BBQ_5688(aepY)
BPSUBBN_3908(aepY) BBN_4008(aepY)
BPSDBBX_5571(aepY) BBX_5673(aepY)
BPZBP1026B_II0563 BP1026B_II0673
BPQBPC006_II0734 BPC006_II0865
BPKBBK_3882(aepY) BBK_5713(aepY)
BPSHDR55_4743(aepY) DR55_4844(aepY)
BPSABBU_5437(aepY) BBU_5539(aepY)
BPSOX996_3789(aepY) X996_4594(aepY)
BUTX994_4010(aepY) X994_4112(aepY)
BTEBTH_II1909
BTQBTQ_5191(aepY)
BTJBTJ_3821(aepY)
BTZBTL_4577(aepY) BTL_4677(aepY)
BTDBTI_5337(aepY)
BTVBTHA_5552(aepY)
BTHEBTN_4316(aepY)
BTHMBTRA_4581(aepY)
BTHADR62_4262 DR62_4365
BTHLBG87_4648(aepY)
BOKDM82_4610(aepY) DM82_4704(aepY)
BOCBG90_5889(aepY) BG90_5981(aepY)
BUUWS70_20050
BSAVWS86_21235 WS86_21650
BVIBcep1808_4686
BVEAK36_4233(aepY)
BURBcep18194_B1915
BCNBcen_4246
BCHBcen2424_4120
BCMBcenmc03_3399
BCJBCAM1244
BCENDM39_3754(aepY)
BCEWDM40_4162(aepY)
BCEOI35_5093
BAMBamb_3534
BACBamMC406_4015
BMJBMULJ_04038(ppd)
BMUBmul_4472
BMKDM80_3633(aepY)
BMULNP80_4147(aepY)
BCTGEM_4496
BCEDDM42_3847(aepY)
BCEPAPZ15_18455
BDLAK34_4231(aepY)
BPYRABD05_29920
BCONNL30_06375
BUBBW23_4918(aepY)
BDFWI26_19320
BLATWK25_23145
BTEIWS51_03915
BSEMWJ12_26080
BPSLWS57_07795
BMECWJ16_24705
BSTGWT74_25010
BSTLBBJ41_19210
BANNJFN94_23425(aepY)
BGLbglu_2g13470
BGUKS03_4594(aepY)
BUGBC1001_5204
BGFBC1003_4279
BGDbgla_2g13350
BGOBM43_5002(aepY)
BYIBYI23_A006820
BUKMYA_4543
BUEBRPE67_ACDS06760
BULBW21_5017(aepY)
BUQAC233_24005
BGPBGL_2c11760
BPLAbpln_2g12600
BUDAQ610_28105
BUMAXG89_10165
BUIAX768_03890
BURKDM992_19620(aepY)
BXEBxe_B2234
BXBDR64_4565(aepY)
BPHBphy_3821
BGEBC1002_3394
BPXBUPH_05877
BPYBphyt_5998
BUZAYM40_23415
BFNOI25_4535(aepY)
BCAIK788_0000150
PSPWBJG93_18655(aepY)
PARABTO02_27440
PARBCJU94_32425(aepY)
PHSC2L64_30755(aepY)
PTERC2L65_27415(aepY)
PGPCUJ91_19560(aepY)
PCJCUJ87_30245(aepY)
PTSCUJ90_26945(aepY)
PCAFDSC91_002023
PMEGFNZ07_08535(aepY)
PTROG5S35_19395(aepY)
PGISI6I06_19280(aepY)
PACPFAZ97_15195(aepY)
PACSFAZ98_20210(aepY)
PEWKZJ38_30040(aepY)
PPKU875_16970
PPNODA70_09040
PPNMLV28_21765
PRBX636_17450
PPULRO07_16155
PSPUNA29_20995
PAPISG18_00145
PVEUC34_07415
POXMB84_11755
PFGAB870_18105
PNRAT302_26650
PANDDRB87_06675(aepY)
PFIBPI93_020430(aepY)
CABASBC2_10690
BUOBRPE64_ACDS07740
AAAAcav_2123
MEUACJ67_08965
AZOazo2699
AOAdqs_2834
HWIA0Z60_07475(aepY)
CJUC8J_1330
CHYOCHH_1592
CHWA2J15_004810(aepY)
CINFCINF_1347
ANTArnit_2942
DAKDaAHT2_1859
DALDalk_1322
DLIdnl_05850
LLUAKJ09_10388
DAODesac_2269
ARAArad_7868
AVIAvi_3414
REPIE4803_PB00124
AOLS58_09490
SIWGH266_09710(aepY)
RGIRGI145_09785
ROSCTJ15_07645(aepY)
RMUCFOB66_09670(aepY)
RMTIAI58_18635(aepY)
LCKHN018_01550(aepY)
AZZDEW08_28015(aepY)
ECOGFIV45_08010(aepY)
BSTOC0V70_16035(aepY)
BACIB1NLA3E_03310
BMQBMQ_0785(aepY)
BMDBMD_0786(aepY)
BMHBMWSH_4463(ppd)
BMEGBG04_3079(aepY)
PTBDER53_11740(aepY)
PCALBV455_03447
MEKUHUW50_16410(aepY)
BOUI5818_22335(aepY)
BLRBRLA_c034000
BRWGOP56_09090(aepY)
PPYPPE_04395 PPE_04790
PPOLX809_41425
PTAHPL003_06760
PIHUB51_20095 UB51_20635
PPEOABE82_25175
PKBB4V02_00180 B4V02_16730
PAIHASL14_12570
PLUTEI981_13660(aepY)
PCHIPC41400_18310(aepY)
EFFskT53_29660
PABSJIR001_16500
CTCCTC_01699
CTETBN906_01841
CBJH04402_02797
CBECbei_4337
CBZCbs_4337
CBEILF65_04861
CSRCspa_c46180(bcpC)
CSBCLSA_c08740(bcpC)
CBUTATN24_05945
CARGRSJ17_12815
CDYF3K33_22180(aepY)
CCAAKQH81_02880(aepY)
RALRumal_1341
RCHRUM_11410
CLEClole_3575
BPROPMF13cell1_05127(mdlC)
HASHalsa_0039
SSGSelsp_0558
SELEADJ74_04655
SELOAXE86_05285
SELTBCS37_10940
LCGL3BBH23_02730
MBJKQ51_00728
NBRO3I_021400
NTPCRH09_19450(aepY)
NOZDMB37_08000(aepY)
NAHF5544_23985
SCOSCO6824(SC1A2.33c)
SALSSLNWT_3224
STRCAA958_29495
STRTA8713_00490
SGSAVL59_02545
SALWCP975_03130(aepY)
SALFSMD44_04408
SRJSRO_1309
SGDELQ87_04605
SGFHEP81_01275
SSEOD0Z67_12190(aepY)
SRIMCP984_37455(aepY)
STSUB7R87_30295
SDWK7C20_15035(aepY)
LSEF1C12_11065
RTCAPU90_00560
CELHGXP71_14040(aepY)
TESBW730_00190
SAIUJ4H86_04285(aepY)
FALFRAAL6378
AMYYYIM_29485
SSYIEKG83_20795(aepY)
NHYJQS43_02330(aepY)
SNASnas_5664
NAVJQS30_13660(aepY)
AYMYM304_30160
OLSOlsu_0592
ARPNIES39_A00300
MPROBJP34_15510
NEDHUN01_29210(aepY)
TOQHCG51_21870(aepY)
NCNBZZ01_05230
OTEOter_2977
OBGVerru16b_03221
TDETDE_1414
TBETrebr_0278
TAZTREAZ_2215(aepY)
TPITREPR_2365(aepY)
SCDSpica_1332
TPKJO40_09720
TPHGFUT81_06850(aepY)
TRIDYE50_04585(aepY)
TPAVHRQ91_06195(aepY)
SSMSpirs_4229
STASTHERM_c15600
SBUSpiBuddy_0273
SGPSpiGrapes_1559
BHCJFL75_01535(aepY)
TPXTurpa_2339
BIPBint_1238
FSUFisuc_0992
FSCFSU_1438
BTHBT_1719
BTHOBtheta7330_01296(ilvB)
BFRBF1833 BF2577
BFSBF9343_1815(aepY)
BFGBF638R_1868
BUNBun01g_29030
BEGINE88_02863
BSTEK6V31_00390(aepY)
BDOEL88_10430
PARCCI960_12855(aepY)
PCOILK433_14485(aepY)
DRCG0Q07_19265(aepY)
PCMAY601_0433
FUVJR347_10755(aepY)
PROCPtc2401_00815(ilvB_1)
NDENIDE2902(ppd)
NKFNkreftii_003418
METBAW729_03840
TARTALC_00082
PSYTDSAG12_01621(comE_1)
 » show all
Reference
1  [PMID:12904299]
  Authors
Zhang G, Dai J, Lu Z, Dunaway-Mariano D.
  Title
The phosphonopyruvate decarboxylase from Bacteroides fragilis.
  Journal
J Biol Chem 278:41302-8 (2003)
DOI:10.1074/jbc.M305976200
Reference
2  [PMID:8180189]
  Authors
Seidel HM, Knowles JR.
  Title
Interaction of inhibitors with phosphoenolpyruvate mutase: implications for the reaction mechanism and the nature of the active site.
  Journal
Biochemistry 33:5641-6 (1994)
DOI:10.1021/bi00184a037
Reference
3  [PMID:9127192]
  Authors
Nakashita H, Watanabe K, Hara O, Hidaka T, Seto H
  Title
Studies on the biosynthesis of bialaphos. Biochemical mechanism of C-P bond formation: discovery of phosphonopyruvate decarboxylase which catalyzes the formation of phosphonoacetaldehyde from phosphonopyruvate.
  Journal
J Antibiot (Tokyo) 50:212-9 (1997)
DOI:10.7164/antibiotics.50.212
Other DBs
ExplorEnz - The Enzyme Database: 4.1.1.82
IUBMB Enzyme Nomenclature: 4.1.1.82
ExPASy - ENZYME nomenclature database: 4.1.1.82
BRENDA, the Enzyme Database: 4.1.1.82
CAS: 151662-34-9
LinkDB

KEGG   REACTION: R04053
Entry
R04053                      Reaction                               
Name
3-phosphonopyruvate carboxy-lyase
Definition
3-Phosphonopyruvate <=> Phosphonoacetaldehyde + CO2
Equation
Reaction class
RC00506  C02798_C03167
Enzyme
Pathway
rn00440  Phosphonate and phosphinate metabolism
rn00998  Biosynthesis of various antibiotics
rn01100  Metabolic pathways
rn01110  Biosynthesis of secondary metabolites
rn01120  Microbial metabolism in diverse environments
Module
M00903  Fosfomycin biosynthesis, phosphoenolpyruvate => fosfomycin
Orthology
K09459  phosphonopyruvate decarboxylase [EC:4.1.1.82]
Other DBs
RHEA: 20771
LinkDB

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