KEGG   ORTHOLOGY: K00497
Entry
K00497                      KO                                     
Symbol
CYP11B1
Name
steroid 11beta-monooxygenase [EC:1.14.15.4]
Pathway
map00140  Steroid hormone biosynthesis
map01100  Metabolic pathways
map04927  Cortisol synthesis and secretion
map04934  Cushing syndrome
Module
M00108  C21-Steroid hormone biosynthesis, progesterone => corticosterone/aldosterone
M00109  C21-Steroid hormone biosynthesis, progesterone => cortisol/cortisone
Reaction
R02218  progesterone,reduced ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R02725  androstenedione,reduced-adrenal-ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R02843  steroid,reduced ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R03329  steroid,reduced-adrenal-ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R03851  11-deoxycorticosterone,reduced ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R04850  17alpha,21-dihydroxypregnenolone:oxygen oxidoreductase (11-hydroxylating)
R08949  11-deoxycorticosterone,reduced-adrenal-ferredoxin:oxygen oxidoreductase (11beta,18-hydroxylating)
Disease
H00216  Congenital adrenal hyperplasia
H00602  Glucocorticoid-remediable aldosteronism (GRA)
H01603  Primary aldosteronism
H01633  High blood pressure
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09103 Lipid metabolism
   00140 Steroid hormone biosynthesis
    K00497  CYP11B1; steroid 11beta-monooxygenase
 09150 Organismal Systems
  09152 Endocrine system
   04927 Cortisol synthesis and secretion
    K00497  CYP11B1; steroid 11beta-monooxygenase
 09160 Human Diseases
  09167 Endocrine and metabolic disease
   04934 Cushing syndrome
    K00497  CYP11B1; steroid 11beta-monooxygenase
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   00199 Cytochrome P450
    K00497  CYP11B1; steroid 11beta-monooxygenase
Enzymes [BR:ko01000]
 1. Oxidoreductases
  1.14  Acting on paired donors, with incorporation or reduction of molecular oxygen
   1.14.15  With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
    1.14.15.4  steroid 11beta-monooxygenase
     K00497  CYP11B1; steroid 11beta-monooxygenase
Cytochrome P450 [BR:ko00199]
 Cytochrome P450, animal type
  CYP11 family
   K00497  CYP11B1; steroid 11beta-monooxygenase
Other DBs
GO: 0004507
Genes
HSA: 1584(CYP11B1)
PTR: 464437(CYP11B1)
PPS: 100971586(CYP11B1)
GGO: 115930159
PON: 100459910
PPYG: 129042626
NLE: 100605657
HMH: 116465197 116465198
SSYN: 129486883
MCC: 695793(CYP11B1)
MCF: 102136659(CYP11B1)
MTHB: 126961618
MNI: 105488429
CSAB: 103237546(CYP11B1)
CATY: 105581188
MLEU: 105536287
RRO: 104679773
RBB: 108536535
PTEH: 111535654
CANG: 105509013
CJC: 100415667(CYP11B1)
SBQ: 101048076
CIMI: 108291253(CYP11B1)
ANAN: 105728099(CYP11B1)
CSYR: 103276447
OGA: 100948075
MMU: 110115(Cyp11b1) 13072(Cyp11b2)
RNO: 120093683(Cyp11b2l1) 24294(Cyp11b2) 353498(Cyp11b3) 500892(Cyp11b1)
PMAV: 102924048
CNL: 130888950
HGL: 101701311
CPOC: 111755182
OCU: 100328543(CYP11B2) 100342863
OPI: 101518686
CFA: 482071(CYP11B2)
CLUD: 112662131
VVP: 112911200
VLG: 121499022
NPO: 129502591
AML: 100478197
UMR: 103680551
ELK: 111146729
MNP: 132013308
ORO: 101364874
MLX: 118015252
MANO: 123858670
NSU: 110578976
LWW: 102732818
FCA: 101097790(CYP11B1)
PCOO: 112859405
PVIV: 125156496
PTG: 102972244
PPAD: 109258417
PUC: 125924912
PLEZ: 122210855
HHV: 120227687
CCRU: 144226680
BTA: 282422(CYP11B1) 787628
BOM: 102272939
BBIS: 104997957
OAS: 101102377 767576(CYP11B1)
ODA: 120859420
CCAD: 122451091
MREE: 136144977
MBEZ: 129560226
SSC: 110260194
CFR: 102517728
CBAI: 105077899
CDK: 105106427
VPC: 102532708
BACU: 103009357
BMUS: 118883237
LVE: 103089121
OOR: 101286768
LALB: 132507857
GMF: 115863290
DDP: 132440410
DLE: 111165107
PCAD: 102988484
PSIU: 116742421
PPHC: 136136821
NASI: 112397123
MYD: 102752229
MMYO: 118670722
MDT: 132219835
MYUM: 138993306
PKL: 118718613
EFUS: 103302673
MNA: 107542744
DRO: 112315587
SHON: 118988945
AJM: 119064760
PDIC: 114514446
PHAS: 123833011
MMF: 118643316
PPAM: 129084099
HAI: 109390820
RFQ: 117033759
PALE: 102881458
PGIG: 120588772
RAY: 107507877
MJV: 108400067(CYP11B2)
TOD: 119232024
SARA: 101544036
SFUM: 130033610
SETR: 126008743
LAV: 100654178
TMU: 101354125
ETF: 101664498
DNM: 101424711
MDO: 100032885
GAS: 123255806
SHR: 100930767
AFZ: 127544520
PCW: 110214194
TVP: 118833874
PBRV: 138155881(CYP11B2)
OAA: 100082065
TACU: 119939998
AACU: 137849090
TGU: 116807520
LSR: 110479458
ATRC: 139587191
PHI: 102113159
ACOE: 138101691
CCIC: 134057549
FPG: 101918505
FCH: 102046275
BBUT: 142028520
PPUS: 135181278
CBOY: 140646799(SCRT1)
CNIC: 135985062
AROW: 112976664
ASN: 102375758
AMJ: 102575737(CYP11B1)
CPOO: 109310774
CIZ: 142009015
CMY: 102933677
CCAY: 125630881
LKP: 140905827
NDS: 141981237
DCC: 119851557
CPIC: 101950678
TST: 117873891
CABI: 116833743
MRV: 120396417
ACS: 100560890
ASAO: 132773556
PVT: 110084842
SUND: 121929727
PBI: 103058342
PMUR: 107300041
CTIG: 120298053
TSR: 106545562
PGUT: 117666942
PCAE: 139314526
APRI: 131196363
VKO: 123035256
PMUA: 114600140
PRAF: 128416955
ZVI: 118089700
HCG: 128322106
GJA: 107116366
STOW: 125425154
EMC: 129333751
XLA: 108718624
XTR: 101731070
RTEM: 120921857
PADS: 140330394
BBUF: 121001585
BGAR: 122938238
DTC: 141060323
PWL: 138274973
MUO: 115481511
GSH: 117353600
DRE: 791124(cyp11c1)
SRX: 107745157
SANH: 107698185
SGH: 107570796
CCAR: 109110857
CAUA: 113059430
CGIB: 128030261
PTET: 122357920
LROH: 127178203
GRF: 141342427(cyp11c1)
OMC: 131521331
PPRM: 120491104
RKG: 130103912
MAMB: 125243223
CIDE: 127497506
CERY: 137002098
MASI: 127453357
TDW: 130432709
MANU: 129448943(cyp11c1)
PDAB: 135752178(cyp11c1)
IPU: 108263488
PHYP: 113525473
SMEO: 124384380
TFD: 113647799
TVC: 132846065
CGAR: 128520287
NGRA: 132886340
TRN: 134310851
AMEX: 103026652
CMAO: 118813895
EEE: 113574779
CHAR: 105912980
SPIL: 134082421
ASAD: 121720838
TRU: 101075863
TFS: 130532956
LCO: 104920541
NCC: 104944920
TBEN: 117480465
CGOB: 115021232
PGEO: 117460921(cyp11c1)
GACU: 117541005
EMAC: 134861593
ELY: 117265363
EFO: 125893014
PLEP: 121945728
SLUC: 116049596
ECRA: 117946724
ESP: 116691100
PFLV: 114556971
GAT: 120810783
AFB: 129110285
CLUM: 117745803
PSWI: 130213196
CANA: 137780999(cyp11c1)
CVE: 137891513(cyp11c1)
MSAM: 119897544
SCHU: 122881607
EARM: 139289734(cyp11c1)
CUD: 121514148
SPUL: 138584179(cyp11c1)
LMIX: 132983189
HTC: 141800409(cyp11c1)
ALAT: 119006071
ASTR: 137601281(cyp11c1)
PKLU: 139204982(cyp11c1)
MZE: 101463871(cyp11c1)
ONL: 100533461(cyp11b)
OAU: 116320943
OLA: 100125822(cyp11b)
OML: 112143274
CSAI: 133432964
XMA: 102236274
XCO: 114139300
XHE: 116715552
PRET: 103478110
PFOR: 103136813
PLAI: 106957061
PMEI: 106922010
GAF: 122830567
PPRL: 129371107
CVG: 107088793
CTUL: 119783082
GMU: 124865602
NFU: 107379700
KMR: 108235361
ALIM: 106515094
NWH: 119410002
EJA: 138192094(cyp11c1)
BFRE: 138619392(cyp11c1)
MCEP: 125015727
CSEM: 103388284
POV: 109633048
SSEN: 122774868
SSOE: 131471413
HHIP: 117777191
HSP: 118113534
PPLT: 128449257
SMAU: 118299793
LCF: 108885901
SDU: 111230014
SLAL: 111652162
XGL: 120784322
HCQ: 109522775
SSCV: 125975714
SBIA: 133500663
PEE: 133401343
PTAO: 133479217
BPEC: 110163163
ENY: 140374293(cyp11c1)
MALB: 109970182
BSPL: 114842551
SJO: 128366469
SSCO: 133982928
TTY: 137191355(cyp11c1)
GMH: 115553949
SASA: 100136945
OTW: 121840636
OMY: 100135891(cyp11b) 110534298
ONE: 115122985
OKI: 109881262
SALP: 112074060
SNH: 120047273
SFON: 129841898
ELS: 105018961
OEP: 134023661
SFM: 108925533
PKI: 111853322
AANG: 118210794
AROT: 135233515
CCOG: 133133540
LOC: 102683152
PSPA: 121306922
PSEX: 120518870
LCM: 102345423
CPUN: 140453886
HAKA: 140736351
 » show all
Reference
PMID:2592361
  Authors
Mornet E, Dupont J, Vitek A, White PC
  Title
Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta).
  Journal
J Biol Chem 264:20961-7 (1989)
  Sequence
[hsa:1584]
Reference
PMID:3485096
  Authors
Yanagibashi K, Haniu M, Shively JE, Shen WH, Hall P
  Title
The synthesis of aldosterone by the adrenal cortex. Two zones (fasciculata and glomerulosa) possess one enzyme for 11 beta-, 18-hydroxylation, and aldehyde synthesis.
  Journal
J Biol Chem 261:3556-62 (1986)
LinkDB

KEGG   ORTHOLOGY: K07433
Entry
K07433                      KO                                     
Symbol
CYP11B2
Name
steroid 11beta-monooxygenase / corticosterone 18-monooxygenase [EC:1.14.15.4 1.14.15.5]
Pathway
map00140  Steroid hormone biosynthesis
map01100  Metabolic pathways
map04925  Aldosterone synthesis and secretion
Module
M00108  C21-Steroid hormone biosynthesis, progesterone => corticosterone/aldosterone
Reaction
R02218  progesterone,reduced ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R02725  androstenedione,reduced-adrenal-ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R02843  steroid,reduced ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R03262  corticosterone,reduced-adrenal-ferredoxin:oxygen oxidoreductase (18-hydroxylating)
R03263  
R03329  steroid,reduced-adrenal-ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R03851  11-deoxycorticosterone,reduced ferredoxin:oxygen oxidoreductase (11-hydroxylating)
R04850  17alpha,21-dihydroxypregnenolone:oxygen oxidoreductase (11-hydroxylating)
Disease
H00258  Aldosterone synthase deficiency
H00602  Glucocorticoid-remediable aldosteronism (GRA)
H01633  High blood pressure
Brite
KEGG Orthology (KO) [BR:ko00001]
 09100 Metabolism
  09103 Lipid metabolism
   00140 Steroid hormone biosynthesis
    K07433  CYP11B2; steroid 11beta-monooxygenase / corticosterone 18-monooxygenase
 09150 Organismal Systems
  09152 Endocrine system
   04925 Aldosterone synthesis and secretion
    K07433  CYP11B2; steroid 11beta-monooxygenase / corticosterone 18-monooxygenase
 09180 Brite Hierarchies
  09181 Protein families: metabolism
   00199 Cytochrome P450
    K07433  CYP11B2; steroid 11beta-monooxygenase / corticosterone 18-monooxygenase
Enzymes [BR:ko01000]
 1. Oxidoreductases
  1.14  Acting on paired donors, with incorporation or reduction of molecular oxygen
   1.14.15  With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
    1.14.15.4  steroid 11beta-monooxygenase
     K07433  CYP11B2; steroid 11beta-monooxygenase / corticosterone 18-monooxygenase
    1.14.15.5  corticosterone 18-monooxygenase
     K07433  CYP11B2; steroid 11beta-monooxygenase / corticosterone 18-monooxygenase
Cytochrome P450 [BR:ko00199]
 Cytochrome P450, animal type
  CYP11 family
   K07433  CYP11B2; steroid 11beta-monooxygenase / corticosterone 18-monooxygenase
Other DBs
GO: 0004507 0047783
Genes
HSA: 1585(CYP11B2)
PTR: 745937(CYP11B2)
PPS: 100971238(CYP11B2)
GGO: 101142418
PON: 100461139
PPYG: 129042640
NLE: 115830633
SSYN: 129486882
MCC: 695914(CYP11B2)
MCF: 102137301(CYP11B2)
CSAB: 103237547(CYP11B2)
CATY: 105581294
PANU: 101002842
MLEU: 105536288
RRO: 104679775
RBB: 108536550
TFN: 117078861
CANG: 105509012
CJC: 100415304(CYP11B2)
CIMI: 108291254(CYP11B2)
ANAN: 105728086(CYP11B2)
CSYR: 103276450
HGL: 101700701
CPOC: 100379213(Cyp11b2) 100727186
 » show all
Reference
PMID:2592361
  Authors
Mornet E, Dupont J, Vitek A, White PC
  Title
Characterization of two genes encoding human steroid 11 beta-hydroxylase (P-450(11) beta).
  Journal
J Biol Chem 264:20961-7 (1989)
  Sequence
[hsa:1585]
Reference
  Authors
Bureik M, Lisurek M, Bernhardt R
  Title
The human steroid hydroxylases CYP1B1 and CYP11B2.
  Journal
Biol Chem 383:1537-51 (2002)
DOI:10.1515/BC.2002.174
LinkDB

KEGG   ENZYME: 1.14.15.4
Entry
EC 1.14.15.4                Enzyme                                 
Name
steroid 11beta-monooxygenase;
steroid 11beta-hydroxylase;
steroid 11beta/18-hydroxylase
Class
Oxidoreductases;
Acting on paired donors, with incorporation or reduction of molecular oxygen;
With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
Sysname
steroid,reduced-adrenodoxin:oxygen oxidoreductase (11beta-hydroxylating)
Reaction(IUBMB)
a steroid + 2 reduced adrenodoxin + O2 + 2 H+ = an 11beta-hydroxysteroid + 2 oxidized adrenodoxin + H2O [RN:R02726]
Reaction(KEGG)
Substrate
steroid [CPD:C00377];
reduced adrenodoxin [CPD:C00662];
O2 [CPD:C00007];
H+ [CPD:C00080]
Product
11beta-hydroxysteroid [CPD:C01058];
oxidized adrenodoxin [CPD:C00667];
H2O [CPD:C00001]
Comment
A heme-thiolate protein (P-450). Also hydroxylates steroids at the 18-position, and converts 18-hydroxycorticosterone into aldosterone.
History
EC 1.14.15.4 created 1961 as EC 1.99.1.7, transferred 1965 to EC 1.14.1.6, transferred 1972 to EC 1.14.15.4, modified 1989, modified 2014
Pathway
ec00140  Steroid hormone biosynthesis
ec01100  Metabolic pathways
Orthology
K00497  steroid 11beta-monooxygenase
K07433  steroid 11beta-monooxygenase / corticosterone 18-monooxygenase
Genes
HSA1584(CYP11B1) 1585(CYP11B2)
PTR464437(CYP11B1) 745937(CYP11B2)
PPS100971238(CYP11B2) 100971586(CYP11B1)
GGO101142418 115930159
PON100459910 100461139
PPYG129042626 129042640
NLE100605657 115830633
HMH116465197 116465198
SSYN129486882 129486883
MCC695793(CYP11B1) 695914(CYP11B2)
MCF102136659(CYP11B1) 102137301(CYP11B2)
MTHB126961020 126961026 126961618
MNI105483796 105488428 105488429
CSAB103237546(CYP11B1) 103237547(CYP11B2)
CATY105581188 105581294
PANU101002490 101002842 116276421
TGE112630213 112630247
MLEU105536287 105536288
RRO104679773 104679775
RBB108536535 108536550
TFN117078861 117079172 117079174
PTEH111535654
CANG105509012 105509013
CJC100415304(CYP11B2) 100415667(CYP11B1)
SBQ101048076
CIMI108291253(CYP11B1) 108291254(CYP11B2)
ANAN105728086(CYP11B2) 105728099(CYP11B1)
CSYR103276447 103276450
MMUR105867373 105867374
LCAT123644516 123644520
ERUF138381591 138381592
PCOQ105813307 105813360
OGA100948075 100948396 100958146
MMU110115(Cyp11b1) 13072(Cyp11b2)
MCAL110310257 110310258
MPAH110334511 110335023
RNO120093683(Cyp11b2l1) 24294(Cyp11b2) 353498(Cyp11b3) 500892(Cyp11b1)
MCOC116073894 116082436
ANU117719036 117719092
ASYL127667342 127667824
MUN110544545 110562757
CGE100771648 107977023
MAUA101823339 101823606
PROB127225603 127225649 127225650
PLEU114684742 114684743
PMAV102924048
MORG121461414 121461416
MFOT126503589 126503590
AAMP119823440 119823447
CNL130888950
NGI103748431 103748432
HGL101700701 101701311
CPOC100379213(Cyp11b2) 100727186 111755182
CCAN109681807 109681816
DORD105992320 106002066
DSP122125332 122125344
PLOP125360501 125361022
NCAR124991075 124991346
MMMA107142805 107143071
ITI101963849 101968373
OCU100328543(CYP11B2) 100342863
OPI101518686
OCZ121163853 121163854
TUP102471986 102492986
GVR103599088 103604864 103604866
CFA482071(CYP11B2)
CLUD112662131
VVP112911200
VLG121499022
NPO129502591
AML100478197
UMR103680551
UAH125281062 125281076
UAR123779294 123796461
ELK111146729
LLV125098158 125099244
MNP132013308
MLK131827767 131827768
NVS122905498 122905499
ORO101364874
EJU114204069 114204070
ZCA113911085 118356903
MLX118015252
MANO123858670
NSU110578976
LWW102732818
FCA101097790(CYP11B1)
PYU121024468 121043245
PCOO112859405
PBG122496110 122496111
PVIV125156496
LRUF124507499 124507515
LGF123586547 123586550
AJU106989683 128312793
PTG102972244
PPAD109258417
PUC125924912
PLEZ122210855
HHV120227687
CCRU144226680
BTA282422(CYP11B1) 787628
BOM102272939
BIU109568177 109568372 109568377
BBUB112577757 112579063
BKE129627167 129627169
BBIS104997957
CHX102188238 102188517
OAS101102377 767576(CYP11B1)
BTAX128059464 128059476
CSUM138088413 138088750
ODA120859420
CCAD122451091
MREE136144977
MBEZ129560226
SSC110260194
CFR102517728
CBAI105077899
CDK105106427
VPC102532708
BACU103009357
BMUS118883237
LVE103089121
OOR101286768
LALB132507857
GMF115863290
DDP132440410
DLE111165107
PCAD102988484
PSIU116742421
PPHC136136821
NASI112397123
ECB100063612 100063645
EPZ103543718 103544682
EAI106827552 123275604
MYD102752229
MMYO118670722
MDT132219835
MYUM138993306
PKL118718613
EFUS103302673
MNA107542744
DRO112315587
SHON118988945
AJM119064760
PDIC114514446
PHAS123833011
MMF118643316
PPAM129084099
HAI109390820
RFQ117033759
PALE102881458
PGIG120588772
PVP105302023 105310134
RAY107507877
MJV108400067(CYP11B2)
TOD119232024
SARA101544036
SFUM130033610
SETR126008743
LAV100654178
TMU101354125
ETF101664498
DNM101424711
MDO100032885
GAS123255806
SHR100930767
AFZ127544520
PCW110214194
TVP118833874
PBRV138155881(CYP11B2)
OAA100082065
TACU119939998
AACU137849090
TGU116807520
LSR110479458
ATRC139587191
PHI102113159
ACOE138101691
CCIC134057549
FPG101918505
FCH102046275
BBUT142028520
PPUS135181278
CBOY140646799(SCRT1)
CNIC135985062
AROW112976664
ASN102375758
AMJ102575737(CYP11B1)
CPOO109310774
CIZ142009015
CMY102933677
CCAY125630881
LKP140905827
NDS141981237
DCC119851557
CPIC101950678
TST117873891
CABI116833743
MRV120396417
ACS100560890
ASAO132773556
PVT110084842
SUND121929727
PBI103058342
PMUR107300041
CTIG120298053
TSR106545562
PGUT117666942
PCAE139314526
APRI131196363
VKO123035256
PMUA114600140
PRAF128416955
ZVI118089700
HCG128322106
GJA107116366
STOW125425154
EMC129333751
XLA108718624
XTR101731070
RTEM120921857
PADS140330394
BBUF121001585
BGAR122938238
DTC141060323
PWL138274973
MUO115481511
GSH117353600
DRE791124(cyp11c1)
SRX107745157
SANH107698185
SGH107570796
CCAR109110857
CAUA113059430
CGIB128030261
PTET122357920
LROH127178203
GRF141342427(cyp11c1)
OMC131521331
PPRM120491104
RKG130103912
MAMB125243223
CIDE127497506
CERY137002098
MASI127453357
TDW130432709
MANU129448943(cyp11c1)
PDAB135752178(cyp11c1)
IPU108263488
PHYP113525473
SMEO124384380
TFD113647799
TVC132846065
CGAR128520287
NGRA132886340
TRN134310851
AMEX103026652
CMAO118813895
EEE113574779
CHAR105912980
SPIL134082421
ASAD121720838
TRU101075863
TFS130532956
TNGGSTEN00015374G001
LCO104920541
NCC104944920
TBEN117480465
CGOB115021232
PGEO117460921(cyp11c1)
GACU117541005
EMAC134861593
ELY117265363
EFO125893014
PLEP121945728
SLUC116049596
ECRA117946724
ESP116691100
PFLV114556971
GAT120810783
AFB129110285
CLUM117745803
PSWI130213196
CANA137780999(cyp11c1)
CVE137891513(cyp11c1)
MSAM119897544
SCHU122881607
EARM139289734(cyp11c1)
CUD121514148
SPUL138584179(cyp11c1)
LMIX132983189
HTC141800409(cyp11c1)
ALAT119006071
ASTR137601281(cyp11c1)
PKLU139204982(cyp11c1)
MZE101463871(cyp11c1)
ONL100533461(cyp11b)
OAU116320943
OLA100125822(cyp11b)
OML112143274
CSAI133432964
XMA102236274
XCO114139300
XHE116715552
PRET103478110
PFOR103136813
PLAI106957061
PMEI106922010
GAF122830567
PPRL129371107
CVG107088793
CTUL119783082
GMU124865602
NFU107379700
KMR108235361
ALIM106515094
NWH119410002
EJA138192094(cyp11c1)
BFRE138619392(cyp11c1)
MCEP125015727
CSEM103388284
POV109633048
SSEN122774868
SSOE131471413
HHIP117777191
HSP118113534
PPLT128449257
SMAU118299793
LCF108885901
SDU111230014
SLAL111652162
XGL120784322
HCQ109522775
SSCV125975714
SBIA133500663
PEE133401343
PTAO133479217
BPEC110163163
ENY140374293(cyp11c1)
MALB109970182
BSPL114842551
SJO128366469
SSCO133982928
TTY137191355(cyp11c1)
GMH115553949
SASA100136945
OTW121840636
OMY100135891(cyp11b) 110534298
OGO123998350 124004644
ONE115122985
OKI109881262
OKE118373241 127915287
OMM135519772 135523001
OCLA139379416 139405974
SALP112074060
SNH120047273
SFON129841898
CCLU121543144 123481512
ELS105018961
OEP134023661
SFM108925533
PKI111853322
AANG118210794
AROT135233515
CCOG133133540
LOC102683152
PSPA121306922
ARUT117395226 117969833
PSEX120518870
LCM102345423
CPUN140453886
HAKA140736351
 » show all
Reference
1  [PMID:13276417]
  Authors
GRANT JK, BROWNIE AC.
  Title
The role of fumarate and TPN in steroid enzymic 11beta-hydroxylation.
  Journal
Biochim Biophys Acta 18:433-4 (1955)
DOI:10.1016/0006-3002(55)90111-6
Reference
2  [PMID:13211659]
  Authors
HAYANO M, DORFMAN RI.
  Title
On the mechanism of the C11 beta-hydroxylation of steroids.
  Journal
J Biol Chem 211:227-35 (1954)
Reference
3  [PMID:13426185]
  Authors
TOMKINS GM, MICHAEL PJ, CURRAN JF.
  Title
Studies on the nature of steroid 11-beta hydroxylation.
  Journal
Biochim Biophys Acta 23:655-6 (1957)
DOI:10.1016/0006-3002(57)90396-7
Reference
4  [PMID:3485096]
  Authors
Yanagibashi K, Haniu M, Shively JE, Shen WH, Hall P
  Title
The synthesis of aldosterone by the adrenal cortex. Two zones (fasciculata and glomerulosa) possess one enzyme for 11 beta-, 18-hydroxylation, and aldehyde synthesis.
  Journal
J Biol Chem 261:3556-62 (1986)
Reference
5  [PMID:4967077]
  Authors
Zuidweg MH.
  Title
Hydroxylation of Reichstein's compound S with cell-free preparations from Curvularia lunata.
  Journal
Biochim Biophys Acta 152:144-58 (1968)
DOI:10.1016/0005-2760(68)90016-7
Other DBs
ExplorEnz - The Enzyme Database: 1.14.15.4
IUBMB Enzyme Nomenclature: 1.14.15.4
ExPASy - ENZYME nomenclature database: 1.14.15.4
BRENDA, the Enzyme Database: 1.14.15.4
CAS: 9029-66-7
LinkDB

KEGG   REACTION: R02843
Entry
R02843                      Reaction                               
Name
steroid,reduced ferredoxin:oxygen oxidoreductase (11-hydroxylating)
Definition
11-Deoxycortisol + 2 Reduced ferredoxin + Oxygen + 2 H+ <=> Cortisol + 2 Oxidized ferredoxin + H2O
Equation
Reaction class
RC00661  C00735_C05488
Enzyme
Pathway
rn00140  Steroid hormone biosynthesis
rn01100  Metabolic pathways
Module
M00109  C21-Steroid hormone biosynthesis, progesterone => cortisol/cortisone
Brite
Enzymatic reactions [BR:br08201]
 1. Oxidoreductase reactions
  1.14  Acting on paired donors, with incorporation or reduction of molecular oxygen
   1.14.15  With reduced iron-sulfur protein as one donor, and incorporation of one atom of oxygen into the other donor
    1.14.15.4
     R02843  11-Deoxycortisol + 2 Reduced ferredoxin + Oxygen + 2 H+ <=> Cortisol + 2 Oxidized ferredoxin + H2O
Orthology
K00497  steroid 11beta-monooxygenase [EC:1.14.15.4]
K07433  steroid 11beta-monooxygenase / corticosterone 18-monooxygenase [EC:1.14.15.4 1.14.15.5]
LinkDB

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