KEGG   ENZYME: 1.14.14.139
Entry
EC 1.14.14.139              Enzyme                                 
Name
5beta-cholestane-3alpha,7alpha-diol 12alpha-hydroxylase;
5beta-cholestane-3alpha,7alpha-diol 12alpha-monooxygenase;
sterol 12alpha-hydroxylase (ambiguous);
CYP8B1;
cytochrome P450 8B1;
7alpha-hydroxycholest-4-en-3-one 12alpha-hydroxylase;
7alpha-hydroxy-4-cholesten-3-one 12alpha-monooxygenase;
chenodeoxycholate 12alpha monooxygenase
Class
Oxidoreductases;
Acting on paired donors, with incorporation or reduction of molecular oxygen;
With reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen into the other donor
Sysname
5beta-cholestane-3alpha,7alpha-diol,[reduced NADPH---hemoprotein reductase]:oxygen oxidoreductase (12alpha-hydroxylating)
Reaction(IUBMB)
(1) 5beta-cholestane-3alpha,7alpha-diol + [reduced NADPH---hemoprotein reductase] + O2 = 5beta-cholestane-3alpha,7alpha,12alpha-triol + [oxidized NADPH---hemoprotein reductase] + H2O [RN:R07204];
(2) 7alpha-hydroxycholest-4-en-3-one + [reduced NADPH---hemoprotein reductase] + O2 = 7alpha,12alpha-dihydroxycholest-4-en-3-one + [oxidized NADPH---hemoprotein reductase] + H2O [RN:R04826];
(3) chenodeoxycholate + [reduced NADPH---hemoprotein reductase] + O2 = cholate + [oxidized NADPH---hemoprotein reductase] + H2O [RN:R12550]
Reaction(KEGG)
Substrate
5beta-cholestane-3alpha,7alpha-diol [CPD:C05452];
[reduced NADPH---hemoprotein reductase] [CPD:C03024];
O2 [CPD:C00007];
7alpha-hydroxycholest-4-en-3-one [CPD:C05455];
chenodeoxycholate [CPD:C02528]
Product
5beta-cholestane-3alpha,7alpha,12alpha-triol [CPD:C05454];
[oxidized NADPH---hemoprotein reductase] [CPD:C03161];
H2O [CPD:C00001];
7alpha,12alpha-dihydroxycholest-4-en-3-one;
cholate [CPD:C00695]
Comment
A cytochrome P-450 (heme-thiolate) protein found in mammals. This is the key enzyme in the biosynthesis of the bile acid cholate. The enzyme can also hydroxylate 5beta-cholestane-3alpha,7alpha-diol at the 25 and 26 position, but to a lesser extent [2].
History
EC 1.14.14.139 created 2005 as EC 1.14.13.96, transferred 2018 to EC 1.14.14.139 (EC 1.14.18.8 created 2005 as EC 1.14.13.95, transferred 2015 to EC 1.14.18.8, incorporated 2020) , modified 2020
Pathway
ec00120  Primary bile acid biosynthesis
ec01100  Metabolic pathways
Orthology
K07431  sterol 12-alpha-hydroxylase
Genes
HSA1582(CYP8B1)
PTR736962(CYP8B1)
PPS100969929(CYP8B1)
GGO101147556
PON100433242
NLE100605497
HMH116473602
MCC717247
MCF102132602(CYP8B1)
MTHB126948519
MNI105480287
CSAB103227471(CYP8B1)
CATY105573840
PANU101002418
TGE112618174
MLEU105542637
RRO104670956
RBB108532333
TFN117083966
PTEH111555603
CANG105518110
CJC100402181(CYP8B1)
SBQ101037790
CIMI108300032(CYP8B1)
CSYR103271067
MMUR105874433 105874434
PCOQ105806025
OGA100943894
MMU13124(Cyp8b1)
MCAL110302470
MPAH110327161
RNO81924(Cyp8b1)
MCOC116073386
ANU117693741
MUN110554660
CGE100770995
MAUA101841117
PROB127213322
PLEU114707690
MORG121464432
MFOT126501221
AAMP119810738
NGI103747146
CPOC100734566 100734845
CCAN109691739
DORD105996287
DSP122100712
PLOP125342505
NCAR124969104
MMMA107145454
OCU100009301(CYP8B1)
OPI101531078
TUP102479742
GVR103588225
CFA485619(CYP8B1)
CLUD112668685
VVP112921604
VLG121478995
NPO129507154
AML100464768
UMR103682072
UAH113253657
UAR123778630
ELK111158988
LLV125105604
MPUF101678059
MNP132011721
MLK131824441
NVS122910564
ORO101374077
EJU114212204
ZCA113917882
MLX117999729
NSU110570803
LWW102751180
FCA101082004(CYP8B1)
PYU121033533
PCOO112850288
PBG122492097
PVIV125174942
LRUF124526704
PTG102956513
PPAD109248827
PUC125922037
AJU106966675
HHV120243596 120243597
BTA538964(CYP8B1)
BIU109576421
BBUB102407955
BBIS104985319
CHX102173339
OAS101119853
BTAX128048202 128055603
ODA120867731
CCAD122425003
MBEZ129548099
SSC403328(CYP8B1)
CFR102524173
CBAI105061779
CDK105084606
VPC102527710
BACU103000983
BMUS118904139
LVE103085360
OOR101285967
DLE111164311
PCAD102990799
PSIU116762132
NASI112407426
ECB100054970
EPZ103559259
EAI123275565
MYB102245777
MYD102765424
MMYO118668388
MLF102440551
PKL118715531
EFUS103300174
MNA107524319
DRO112309563
SHON118976225
AJM119051535
PDIC114501955
PHAS123830673
MMF118632899
PPAM129087561
HAI109377081
RFQ117036539
PALE102877747
PGIG120581963
PVP105290391
RAY107519986
MJV108397210
TOD119258772
SARA101553886
SETR126020323
LAV100665029
TMU101356001
ETF101641635
DNM101440886
MDO100026525 100026549(CYP8B)
GAS123230807 123254771
SHR100918099 100919664 100926550 105749568
PCW110217059
OAA103166427
GGA425055(CYP8B1)
PCOC116238313
MGP100546803
CJO107308837
TPAI128086424
LMUT125696205
NMEL110395135
APLA101797490
ACYG106036789
CATA118251836
AFUL116486814
TGU100217899
LSR110474519
SCAN103812684
PMOA120510523
OTC121338124
PRUF121365741
GFR102041987
FAB101809893
OMA130249640
PHI102112501
PMAJ107201006
CCAE111925558
CCW104686389
CBRC103623922
ETL114064499
ZAB102072546
ACHL103806276
SVG106851620
MMEA130576304
HRT120761181
FPG101924073
FCH102052323
CLV102083443
EGZ104124585
NNI104021734
PCRI104033050
PLET104619451
EHS104515298
PCAO104052603
ACUN113476903
TALA104358666
PADL103924714
AFOR103896167
ACHC115338885
HALD104325797
HLE104828057
AGEN126037987
GCL127013785
CCRI104165126
CSTI104557140
CMAC104477299
MUI104544950
BREG104634046
FGA104080441
GSTE104259738
LDI104352636
MNB103770557
OHA104326246
NNT104401579
SHAB115608225
DPUB104298110
PGUU104472378
ACAR104530672
CPEA104386005
AVIT104270263
CVF104282407
RTD128906301
CUCA104056957
TEO104376951
BRHI104500507
NPD112953164
TGT104567901
DNE112980758
SCAM104150126
ASN102374897
AMJ102573091(CYP8B1)
CPOO109306069
GGN109291179
PSS102444673
CMY102934823
CCAY125630813
DCC119850697 119851812
CPIC101950173
TST117871942
CABI116819555
MRV120399358
ACS100551676 100551876 100562756 100562953 100565509 100565705 100565905 100566106
ASAO132779804 132779808 132779809 132779810
PVT110091568 110091574 110091575
SUND121932425 121934688 121935162 121935580 121935581
PBI103051222 103065731
PMUR107284342 107284343 107284344 107284346 107284348 107284362
CTIG120296691 120318053 120318058 120318065 120319285
TSR106538485 106538492
PGUT117680087 117680089
APRI131196734 131196735
PTEX113449276 113449277
NSS113422182 113422190
VKO123020905 123020984
PMUA114607583 114607705 114607796 114607915
PRAF128398296 128398297 128398298
ZVI118091758 118091759 118091944
HCG128330313 128330314 128330315 128331371 128331373 128331374 128331751 128331752
GJA107106985 107106986 107110695 107112093 107125164
STOW125440698 125441151
EMC129337237 129337817 129337819 129337820 129337853 129337869 129337928
XLA108718630(cyp8b1.2.L) 379482(cyp8b1.1.S)
XTR100488015(cyp8b1.2) 100488168(cyp8b1.1)
NPR108788787
RTEM120939823
BBUF121000933
BGAR122929107 122929108
MUO115466283 115466290 115466320 115466327 115466341 115466365
GSH117355598
DRE100004274(cyp8b1.2) 445281(cyp8b1.1) 447848(cyp8b1.3)
SRX107711691 107727542
SANH107661909 107671665
SGH107558014 107580338 107593879
CCAR109056773 109056779 109056788
CAUA113038725 113038733 113046101
CGIB127950969 128024980 128024994
PTET122324044
LROH127152816
OMC131525180
PPRM120477644 120479271
RKG130098852
MAMB125254255
CIDE127504066
MASI127440947 127441950
TROS130554573
TDW130417464
MANU129442789 129442794 129442795
IPU108261592 108268189 108268197
IFU128610594 128610595 128610596 128610597 128610598 128610762
PHYP113524124 113524125
SMEO124387147
TFD113636597
TVC132849183
AMEX103039627
CMAO118826322 118826323
EEE113582944 113590803
CHAR105900586
TRU101070868 101071841 101080232 115248012 115248013
TFS130538329 130538331 130538332 130539269
TNGGSTEN00016125G001 GSTEN00016134G001
LCO104917693 104924020
NCC104940932 104941058
TBEN117488443 117490710
CGOB115022806
PGEO117462682
GACU117558328
EMAC134866467
ELY117269563 117272242 117272243
EFO125898267 125901748
PLEP121939385 121952022
SLUC116045967
ECRA117954895
ESP116699759
PFLV114565114 114570013
GAT120816014
PPUG119206272
AFB129114977
CLUM117746545
PSWI130189685 130198009
MSAM119901973
SCHU122887207 122887208
CUD121519631
ALAT119011762
MZE101474730 106675939 106676194
ONL100693750 109195682 109195683 109195699
OAU116316201 116316225 120434437
OLA101157008
OML112147054
CSAI133452788
XMA102227191
XCO114147167
XHE116722321
PRET103479711
PFOR103135748
PLAI106948855
PMEI106914255
GAF122841414
PPRL129362291
CVG107081670
CTUL119794200
GMU124869592
NFU107383849
KMR108241650 108241654
ALIM106533255 106533266
NWH119414670
AOCE111568649 111568654
MCEP125010344
CSEM103396384
POV109625444 109637167 109638123
SSEN122767875 122767883 122767892 122767898 122767900 122768649 122768658 122779511
HHIP117777688 117777689
HSP118117221 118118273
SMAU118310554 118311576
LCF108883349 108893535
SDU111231161
SLAL111653251
XGL120798539 120802087
HCQ109521313
SSCV125984634 125984635
SBIA133510826
PEE133411474
PTAO133488702
BPEC110154953 110159864
BSPL114843905 114845031 114845073
SJO128368941
SASA106569335 106599887 106599889
STRU115157201 115169574 115169575
OTW112226785 112226786 112260644
OMY110508572 110530492
OGO124010151 124040889 124041735
ONE115102943 115102944 115114571
OKI109872203 109872381 109875004
OKE118394819 118401954 127907637
SALP111956862
SNH120019994 120020264 120055983
CCLU121535363 121581051 121581540
ELS105019795 105019804 106024913
SFM108919335 108937621 114910968 114910986
PKI111845862 111845867
AANG118232872
LOC102682983 102694619 102694818
PSPA121311421 121311422 121312642 121312643 121312849 121314286 121314287 121314288 121314311 121314312
ARUT117394306 117394549 117394961 117399933
PSEX120529851 120529852 120529853
LCM102357417 102361952
CMK103188298
RTP109923397
CPLA122550148
HOC132815858
LERI129714125
PMRN116946580 116946581 116946582 116946700
LRJ133353068 133353069 133353070
MMER123529448
RPHI132742682
MOREE1B28_009492
 » show all
Reference
1  [PMID:6766451]
  Authors
Hansson R, Wikvall K.
  Title
Hydroxylations in biosynthesis and metabolism of bile acids. Catalytic properties of different forms of cytochrome P-450.
  Journal
J Biol Chem 255:1643-9 (1980)
Reference
2  [PMID:6811268]
  Authors
Hansson R, Wikvall K.
  Title
Hydroxylations in biosynthesis of bile acids. Cytochrome P-450 LM4 and 12alpha-hydroxylation of 5beta-cholestane-3alpha, 7alpha-diol.
  Journal
Eur J Biochem 125:423-9 (1982)
DOI:10.1111/j.1432-1033.1982.tb06700.x
Reference
3  [PMID:1400444]
  Authors
Ishida H, Noshiro M, Okuda K, Coon MJ
  Title
Purification and characterization of 7 alpha-hydroxy-4-cholesten-3-one 12 alpha-hydroxylase.
  Journal
J Biol Chem 267:21319-23 (1992)
Reference
4  [PMID:8943286]
  Authors
Eggertsen G, Olin M, Andersson U, Ishida H, Kubota S, Hellman U, Okuda KI, Bjorkhem I.
  Title
Molecular cloning and expression of rabbit sterol 12alpha-hydroxylase.
  Journal
J Biol Chem 271:32269-75 (1996)
DOI:10.1074/jbc.271.50.32269
  Sequence
[ocu:100009301]
Reference
5  [PMID:14643796]
  Authors
Lundell K, Wikvall K.
  Title
Gene structure of pig sterol 12alpha-hydroxylase (CYP8B1) and expression in fetal liver: comparison with expression of taurochenodeoxycholic acid 6alpha-hydroxylase (CYP4A21).
  Journal
Biochim Biophys Acta 1634:86-96 (2003)
DOI:10.1016/j.bbalip.2003.09.002
  Sequence
[ssc:403328]
Reference
6  [PMID:10747975]
  Authors
del Castillo-Olivares A, Gil G.
  Title
Alpha 1-fetoprotein transcription factor is required for the expression of sterol 12alpha -hydroxylase, the specific enzyme for cholic acid synthesis. Potential role in the bile acid-mediated regulation of gene transcription.
  Journal
J Biol Chem 275:17793-9 (2000)
DOI:10.1074/jbc.M000996200
Reference
7  [PMID:12069850]
  Authors
Yang Y, Zhang M, Eggertsen G, Chiang JY.
  Title
On the mechanism of bile acid inhibition of rat sterol 12alpha-hydroxylase gene (CYP8B1) transcription: roles of alpha-fetoprotein transcription factor and hepatocyte nuclear factor 4alpha.
  Journal
Biochim Biophys Acta 1583:63-73 (2002)
DOI:10.1016/S1388-1981(02)00186-5
Reference
8  [PMID:12543708]
  Authors
Russell DW
  Title
The enzymes, regulation, and genetics of bile acid synthesis.
  Journal
Annu Rev Biochem 72:137-74 (2003)
DOI:10.1146/annurev.biochem.72.121801.161712
  Sequence
[hsa:1582] [mmu:13124]
Reference
9  [PMID:30465713]
  Authors
Fan L, Joseph JF, Durairaj P, Parr MK, Bureik M.
  Title
Conversion of chenodeoxycholic acid to cholic acid by human CYP8B1.
  Journal
Biol Chem 400:625-628 (2019)
DOI:10.1515/hsz-2018-0379
Other DBs
ExplorEnz - The Enzyme Database: 1.14.14.139
IUBMB Enzyme Nomenclature: 1.14.14.139
ExPASy - ENZYME nomenclature database: 1.14.14.139
BRENDA, the Enzyme Database: 1.14.14.139

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