KEGG   ENZYME: 5.5.1.9
Entry
EC 5.5.1.9                  Enzyme                                 
Name
cycloeucalenol cycloisomerase;
cycloeucalenol---obtusifoliol isomerase;
cycloeucalenol lyase (cyclopropane-decyclizing)
Class
Isomerases;
Intramolecular lyases;
Intramolecular lyases (only sub-subclass identified to date)
Sysname
cycloeucalenol lyase (cyclopropane-ring opening)
Reaction(IUBMB)
cycloeucalenol = obtusifoliol [RN:R03775]
Reaction(KEGG)
R03775
Substrate
cycloeucalenol [CPD:C02141]
Product
obtusifoliol [CPD:C01943]
Comment
Opens the cyclopropane ring of a number of related 4alpha-methyl-9beta-19-cyclosterols, but not those with a 4beta-methyl group, with formation of an 8(9) double bond. Involved in the synthesis of plant sterols.
History
EC 5.5.1.9 created 1986
Pathway
ec00100  Steroid biosynthesis
ec01100  Metabolic pathways
ec01110  Biosynthesis of secondary metabolites
Orthology
K08246  cycloeucalenol cycloisomerase
Genes
ATHAT5G50375(CPI1)
ALY9301866
CRB17875827
CSAT104725142 104725553 104761032
EUSEUTSA_v10014300mg
BRP103842220 103858451
BNA106368587 106388428 106388470 106395079
BOE106311073 106334665
RSZ108807455 108844331
THJ104803145
CPAP110820324
CIT102630846
CICCICLE_v10021465mg
PVY116116762 116120803
MINC123210580
TCC18605081
GRA105786328
GHI107941049 121232048
GAB108469977
HSYR120140161 120172208
DZI111289822
EGR104426171 120286014
GMX100777966 100780309
GSJ114409933 114416235
PVUPHAVU_009G167500g
VRA106752757
VAR108322558
VUN114196069
VUM124842371
CCAJ109797244
APRC113852402
MTR11427814
TPRA123897010
CAM101498621
PSAT127084734
VVO131661577
LJALj6g3v0984700.1(Lj6g3v0984700.1)
ADU107463495
AIP107612057 107623410
AHF112708166 112772166 112783263
LANG109326998
PCIN129320683
QSAO6P43_022565 O6P43_030741
FVE101310407
RCN112175496
PPER18777316
PMUM103338046
PAVI110762938
PDUL117629408
MDM103437547 103455012
MSYL126599463 126627368
PXB103938239 103950025
ZJU107404400
MNT21385761
CSAV115711204
CSV101215719
CMO103484362
BHJ120082504
MCHA111008866
CMAX111490163 111495263
CMOS111431284 111456735
CPEP111782922 111802556
RCU8266323
JCU105640216
HBR110665271 110671892
MESC110631103
POP7454702
PEU105125341
PALZ118057574
JRE108993469 108994421
CILL122282764 122290375
CAVE132176586
QSU112022579 112035543
QLO115962575 115964043
TWL119985894 120003718
VVI100262783
VRI117905013
SLY100301930(CPI)
SPEN107007161
SOT102603067
SSTN125862621
SDUL129883130
CANN107851175
LBB132604434
NTA107797131 107802648
NSY104212751
NTO104106158
NAU109235692
INI109158212
ITR115998497
SIND105171061
OEU111382474
EGT105970513
SSPL121753221 121785358
SMIL131010494 131010544
SHIS125213808
APAN127244057
HAN110879898
ECAD122588625
LSV111877353
CCAV112509434
DCR108220910 108226853
CSIN114309622
RVL131335147
AEW130767397 130796454
BVG104894046
SOE110787305
CQI110704787 110707516 110709473
ATRI130797692
MOF131159640
NNU104591683
MING122071920
TSS122656929 122671169
PSOM113274262 113278392 113281490 113316791
OSA9270960
DOSAOs11t0302500-01(Os11g0302500)
OBR102700845
OGL127755003
BDI100834141
ATS109737590 109737950 109767330 109785596
TDC119286681 119295069 119318216 119324494
TAES123086881 123091100 123096100 123123551 123128693 123134769 123145824
TUA125515008 125550622
LPER127293914
LRD124681258 124699553
SBI8071249 8071275
ZMA100283632
SITA101757137
SVS117850911
PVIR120664159 120697355
PHAI112886950
PDA103708538
EGU105038657 105043283 105051400
MUS103988675 103996747
ZOF122004862 122022485 122036588 122053448
DCT110108578
PEQ110028193 110039207
AOF109844540
MSIN131246316
NCOL116260419
ATR18423006
SMOSELMODRAFT_135190 SELMODRAFT_83343
PPP112291331
CRECHLRE_16g657300v5
VCNVOLCADRAFT_109265
CSLCOCSUDRAFT_65481
CVRCHLNCDRAFT_11379
APROF751_6325
OLUOSTLU_6401
OTAOT_ostta04g04690
BPGBathy08g04310
MISMICPUN_76248
MPPMICPUCDRAFT_60333(JGI:MicpuC2_60333)
CMECYME_CMO369C
GSLGasu_41820
CCPCHC_T00002985001
PBELQC761_302790
FPOAFPOAC1_010342
FVNFVRRES_11328
FKRNCS57_01483300
FMUJ7337_002278
SREPTSG_06238
DDIDDB_G0268970
DFADFA_11434
ACANACA1_220570
PTIPHATRDRAFT_49447
FCYFRACYDRAFT_189108
TPSTHAPSDRAFT_7708
AAFAURANDRAFT_23404
EHXEMIHUDRAFT_432676 EMIHUDRAFT_444727
GTTGUITHDRAFT_85507
NGRNAEGRDRAFT_81142
 » show all
Reference
1  [PMID:4369016]
  Authors
Heintz R, Benveniste P.
  Title
Plant sterol metabolism. Enzymatic cleavage of the 9beta, 19beta-cyclopropane ring of cyclopropyl sterols in bramble tissue cultures.
  Journal
J Biol Chem 249:4267-74 (1974)
Reference
2
  Authors
Rahier, A., Schmitt, P. and Benveniste, P.
  Title
7-oxo-24xi(28)-dihydrocycloeucalenol, a potent inhibitor of plant sterol biosynthesis.
  Journal
Phytochemistry 21:1969-1974 (1982)
Other DBs
ExplorEnz - The Enzyme Database: 5.5.1.9
IUBMB Enzyme Nomenclature: 5.5.1.9
ExPASy - ENZYME nomenclature database: 5.5.1.9
BRENDA, the Enzyme Database: 5.5.1.9
CAS: 60496-19-7

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