KEGG   ENZYME: 1.14.19.28
Entry
EC 1.14.19.28               Enzyme                                 
Name
sn-1 stearoyl-lipid 9-desaturase;
desC (gene name)
Class
Oxidoreductases;
Acting on paired donors, with incorporation or reduction of molecular oxygen;
With oxidation of a pair of donors resulting in the reduction of O2 to two molecules of water
Sysname
1-stearoyl-2-acyl-[glycerolipid],ferredoxin:oxygen oxidoreductase (9,10 cis-dehydrogenating)
Reaction(IUBMB)
a 1-stearoyl-2-acyl-[glycerolipid] + 2 reduced ferredoxin [iron-sulfur] cluster + O2 + 2 H+ = a 1-oleoyl-2-acyl-[glycerolipid] + 2 oxidized ferredoxin [iron-sulfur] cluster + 2 H2O
Substrate
1-stearoyl-2-acyl-[glycerolipid];
reduced ferredoxin [iron-sulfur] cluster [CPD:C00138];
O2 [CPD:C00007];
H+ [CPD:C00080]
Product
1-oleoyl-2-acyl-[glycerolipid];
oxidized ferredoxin [iron-sulfur] cluster [CPD:C00139];
H2O [CPD:C00001]
Comment
The enzyme, characterized from cyanobacteria, introduces a cis double bond at carbon 9 of stearoyl groups (18:0) attached to the sn-1 position of glycerolipids. The enzyme is nonspecific with respect to the polar head group of the glycerolipid.
History
EC 1.14.19.28 created 2015
Orthology
K23054  sn-1 stearoyl-lipid 9-desaturase
Genes
LABLA76x_3785
LAQGLA29479_942
LCPLC55x_3788
LGULG3211_1428
LAEGL2Y94_00175
PFVPsefu_1593
HJABST95_06850
MNRACZ75_23535
BEBABWI17_00040
AAKAA2016_5347
AMISAmn_08870
RLTRleg2_0069
RHNAMJ98_CH00444
RHXAMK02_CH00445
REZAMJ99_CH00444
RADCO657_00350
RHIDFFM81_018930
RBQJ2J99_02345
RLNJ0663_11120
BROSQUH67_30345
TRBHB776_22640
MDIMETDI0702
MCHMchl_0732
MPOMpop_2228
MZAB2G69_10360
LABRCHH27_00670
BRDJL11_04570
BMEDGYM46_08745
OCDFHY55_14745
MALUKU6B_40580(desC3)
SNJA7E77_02965
SPAPH3Z74_01420
SPAIFPZ24_07960
SPHYCHN51_01825
SPHSETR14_04680
CCXCOCOR_04747
MFULILAB_00410
MMASMYMAC_001780
SCLsce0690
MRMA7982_01170
NANNO0S08_17565
BEXA11Q_2549
HAXBALOs_0899
SBFJCM31447_01880
PIJQEJ31_08215
SAQIAXG55_01020
MKNMKAN_26240
NFANFA_22050
NFRERS450000_01893
AMNRAM_28475
AMMAMES_5512
AMZB737_5512
BSOLFSW04_08395
SYNsll0541(desC(des9))
SYZMYO_125630(desC(des9))
SYYSYNGTS_2538(desC)
SYTSYNGTI_2537(desC)
SYSSYNPCCN_2536(desC)
SYQSYNPCCP_2536(desC)
SYJD082_16540(desC)
SYOC7I86_13285
SYCsyc1549_d(desC)
SYUM744_03400
SYFSynpcc7942_2561
SYDSyncc9605_2541
SYESyncc9902_2191 Syncc9902_2192
SYGsync_2791 sync_2793
SYRSynRCC307_2393 SynRCC307_2395
SYXSynWH7803_2415(desC) SynWH7803_2417(desC)
SYNESyn6312_0622 Syn6312_1743
SYNKKR100_15525
SYNRKR49_08200
SYNDKR52_03225
SYHSyncc8109_2618(desC)
SYNWSynWH8103_02736
SYNCCB0101_00320 CB0101_07525 CB0101_07535
SYNYBM449_04770 BM449_04780
DSLDacsa_0829
SYWSYNW2377(desC)
CGCCyagr_2709 Cyagr_2711
CYICBM981_2126
PMAPro_1833(OLE1)
PMMPMM1672(des9)
PMTPMT_2172 PMT_2174
PMNPMN2A_1271
PMIPMT9312_1764
PMBA9601_18811(ole1)
PMCP9515_18621(ole1)
PMFP9303_28931 P9303_28951(ole1)
PMGP9301_18621(ole1)
PMHP9215_19451(ole1)
PMJP9211_17991(ole1)
PMENATL1_21421(ole1)
PRCEW14_2040
PRMEW15_2227
WNAKA717_26905
CMPCha6605_5134
CYNCyan7425_4812
CEPCri9333_0221
TVNNIES2134_107740(desC1) NIES2134_115680(desC2)
SLWBRW62_06125 BRW62_12340
AMRAM1_1527
ACAMHRE53_05710
TELtlr1653(desC2) tlr2380(desC1)
THNNK55_04900(desC2) NK55_11555(desC)
THECFFX45_01530 FFX45_05765
TSZOOK60_14860
LENLEP3755_06760
LETO77CONTIG1_03274 O77CONTIG1_03680
LBOLBWT_2260 LBWT_42500
KOVK9N68_01010
LSCKIK02_08760
LSKJ5X98_20855
HHGXM38_043120
THEUHPC62_15085 HPC62_17785
TOGHNI00_15240 HNI00_21800
TSINOXH18_19075 OXH18_19080
GLPGlo7428_0047
CHONNIES4102_12720(desC)
GDUP0S91_09120
GENGM3709_1645
GEEGM3708_530
CANCyan10605_0014
CSNCyast_0516
CYLAA637_05810(desC)
SYPSYNPCC7002_A2198(desC)
SYVAWQ23_10980
SYLAWQ21_11125
LEPLepto7376_2492
SYNNNIES970_19270(desC)
MARMAE_50330(desC)
MPKVL20_2979
MIQB5D77_11225
MVZmyaer102_23510(desC)
HAOPCC7418_1242
ENNFRE64_04400
CYUUCYN_05530
CYTcce_3100(desC1)
CWACwatDRAFT_1377
CYPPCC8801_0640
CYHCyan8802_0662
CYCPCC7424_3349
CYJCyan7822_5588
TERTery_1437
ARPNIES39_L02040(desC)
PAGHNIES204_34440(desC)
PPSUNO713_03226(ADS3)
PRUNPCC7821_00426(ADS3)
OXYHCG48_25280
MVAGD0A34_03095 D0A34_03105
LFSHFV01_07745
OACOscil6304_5631
ONIOsc7112_3803 Osc7112_3804
MPROBJP34_22970
PHORJWS08_21245
PYHNEA10_10950
MICMic7113_1889
GEIGEI7407_0446
GVIglr1235(desC)
GLJGKIL_3522(desC)
GMLISF26_05595
ANAall1599(desC)
NPUNpun_R6232
NOSNos7107_0618
NOPNos7524_4756
NONNOS3756_14550
NFLCOO91_07296
NOECLI64_08225
NSHGXM_01593
NEDHUN01_29395
NPZACX27_26500
AVAAva_4212
NAZAazo_3554
ANBANA_C20202
ACYAnacy_4776
AWAAA650_16770
ANNEH233_10965
CSGCylst_2676
RSINB6N60_02677
HBQQI031_00950
CALOCal7507_2593
CALTCal6303_1443
CALHIJ00_05005
CALNNIES2098_27900
CALSNIES3974_19210
RIVRiv7116_4397 Riv7116_5894
FISFIS3754_37630
NSPHBDGGKGIB_02541
DOUBMF77_00179
DFSHGD76_17205
DHTNG743_21970
CCURIAR63_05425
CRKL3I90_06320
AFLOHEQ12_18915
STOQK2F26_06480
AEEIM676_07015
RCSNIES932_16810
TOQHCG51_19365
ALAXNIES50_15180
NCNBZZ01_14795 BZZ01_18245
CTHEChro_4139
PLPPle7327_0060 Ple7327_0061
SCSSta7437_3027
STANSTA3757_26310(desC)
GLTGlitD10_0158(desC)
GCYLQF76_11620
CEOETSB_1681(desC)
CERRGRSB_1326(desC)
CEECP3F56_08610
VABWPS_03440(desC)
ROLCA51_19930
RUVEC9_09030 EC9_18170 EC9_35390
AAGGETAA8_48240
BVOPan97_23020
BREMPSR63_23125 PSR63_27955
RLCK227x_15260 K227x_24310 K227x_57240
SMAMMal15_52760
SNEPEnr13x_18080
LLHI41_49260
BMEISpa11_08300
PBSPlabr_0643 Plabr_4622
SDYNMal52_04350
CHYAV22_30460
CCOPMal65_09750
SACISinac_3004
PBORBSF38_00549
AGVOJF2_65440
PHMPSMK_25950
PCORKS4_06540
ABAAcid345_4171
ACMAciX9_1688
GRWFTO74_12200
TSAAciPR4_2160 AciPR4_2410
TRSTerro_0105
TALBFTW19_22055
ABASACPOL_1636 ACPOL_5501
ADINH7849_02630 H7849_23410
ABACLuPra_01032
LUBTBR22_A09820(desC_1)
MCOSGM418_06960
CHIHGWR21_03985
FGGFSB75_04860
AGIFSB73_10810
ARACE0W69_013520
FLNFLA_5482
SHGSph21_4486
SPHNBV902_21835
SPDRG6053_08660
STHANCTC11429_00217
MUCMuYL_3330
MUHHYN43_005540 HYN43_007955
MGINFRZ54_16340
MGKFSB76_02760
MRUBDEO27_005735
MGOSDIU38_005555
MMABHQ865_12340
MGIKGO620_007170
MDJLLH06_09345
OLIFKG96_20355
DCNMUK70_15775
HSWHsw_2919
FEKC1H87_16940
MGELG5B37_12475
NLIG3M70_17875
NWTNSPWAT_1991
NVAG3M78_09040
 » show all
Reference
1  [PMID:8419301]
  Authors
Wada H, Schmidt H, Heinz E, Murata N
  Title
In vitro ferredoxin-dependent desaturation of fatty acids in cyanobacterial thylakoid membranes.
  Journal
J Bacteriol 175:544-7 (1993)
DOI:10.1128/JB.175.2.544-547.1993
Reference
2  [PMID:12231903]
  Authors
Higashi S, Murata N
  Title
An in Vivo Study of Substrate Specificities of Acyl-Lipid Desaturases and Acyltransferases in Lipid Synthesis in Synechocystis PCC6803.
  Journal
Plant Physiol 102:1275-1278 (1993)
DOI:10.1104/pp.102.4.1275
Reference
3  [PMID:7929259]
  Authors
Sakamoto T, Wada H, Nishida I, Ohmori M, Murata N
  Title
delta 9 Acyl-lipid desaturases of cyanobacteria. Molecular cloning and substrate specificities in terms of fatty acids, sn-positions, and polar head groups.
  Journal
J Biol Chem 269:25576-80 (1994)
  Sequence
[syn:sll0541] [ana:all1599]
Other DBs
ExplorEnz - The Enzyme Database: 1.14.19.28
IUBMB Enzyme Nomenclature: 1.14.19.28
ExPASy - ENZYME nomenclature database: 1.14.19.28
BRENDA, the Enzyme Database: 1.14.19.28

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