Home Research COVID-19 Services Publications People Teaching Job Opening News Forum Lab Only
Online Services

I-TASSER I-TASSER-MTD C-I-TASSER CR-I-TASSER QUARK C-QUARK LOMETS MUSTER CEthreader SEGMER DeepFold DeepFoldRNA FoldDesign COFACTOR COACH MetaGO TripletGO IonCom FG-MD ModRefiner REMO DEMO DEMO-EM SPRING COTH Threpp PEPPI BSpred ANGLOR EDock BSP-SLIM SAXSTER FUpred ThreaDom ThreaDomEx EvoDesign BindProf BindProfX SSIPe GPCR-I-TASSER MAGELLAN ResQ STRUM DAMpred

TM-score TM-align US-align MM-align RNA-align NW-align LS-align EDTSurf MVP MVP-Fit SPICKER HAAD PSSpred 3DRobot MR-REX I-TASSER-MR SVMSEQ NeBcon ResPRE TripletRes DeepPotential WDL-RF ATPbind DockRMSD DeepMSA FASPR EM-Refiner GPU-I-TASSER

BioLiP E. coli GLASS GPCR-HGmod GPCR-RD GPCR-EXP Tara-3D TM-fold DECOYS POTENTIAL RW/RWplus EvoEF HPSF THE-DB ADDRESS Alpaca-Antibody CASP7 CASP8 CASP9 CASP10 CASP11 CASP12 CASP13 CASP14

BioLiP

Structure of PDB 3g5n Chain C

Receptor sequence
>3g5nC (length=452) Species: 9986 (Oryctolagus cuniculus) [Search protein sequence]
SKGKLPPGPSPLPVLGNLLQMDRKGLLRSFLRLREKYGDVFTVYLGSRPV
VVLCGTDAIREALVDQAEAFSGRGKIAVVDPIFQGYGVIFANGERWRALR
RFSLATMRDKRSVEERIQEEARCLVEELRKSKGALLDNTLLFHSITSNII
CSIVFGKRFDYKDPVFLRLLDLFFQSFSLISSFSSQVFELFSGFLKYFPG
THRQIYRNLQEINTFIGQSVEKHRATLDPSNPRDFIDVYLLRMEHQNLIL
TVLSLFFAGTETTSTTLRYGFLLMLKYPHVTERVQKEIEQVIGSHRPPAL
DDRAKMPYTDAVIHEIQRLGDLIPFGVPHTVTKDTQFRGYVIPKNTEVFP
VLSSALHDPRYFETPNTFNPGHFLDANGALKRNEGFMPFSLGKRICLGEG
IARTELFLFFTTILQNFSIASPVPPEDIDLTPRESGVGNVPPSYQIRFLA
RH
3D structure
PDB3g5n Crystal structures of cytochrome P450 2B4 in complex with the inhibitor 1-biphenyl-4-methyl-1H-imidazole: ligand-induced structural response through alpha-helical repositioning.
ChainC
Resolution2.5 Å
3D
structure
Catalytic site residues are labeled in the structure
[Spin on]
[Spin off]
[Reset orientation]

[High quality]
[Low quality]

[White background]
[Black background]

[Download]
[Download structure with residue number starting from 1]
Enzymatic activity
Catalytic site (original residue number in PDB) T302 F429 C436
Catalytic site (residue number reindexed from 1) T262 F389 C396
Enzyme Commision number 1.14.14.1: unspecific monooxygenase.
Interaction with ligand
Site
#
Ligand Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01 HEM C R98 W121 R125 F296 G299 T302 T303 I363 V367 H369 P428 F429 S430 R434 C436 L437 G438 R73 W96 R100 F256 G259 T262 T263 I323 V327 H329 P388 F389 S390 R394 C396 L397 G398
BS02 PB2 C A298 G299 I363 P368 A258 G259 I323 P328 MOAD: ic50=0.035uM
BS03 PB2 C L43 L51 Y69 L70 V477 L18 L26 Y44 L45 V437 MOAD: ic50=0.035uM
BS04 PB2 C R73 E387 R48 E347 MOAD: ic50=0.035uM
BS05 CM5 C R98 N117 L288 R73 N92 L248
BS06 PB2 C F217 E218 F188 E189 MOAD: ic50=0.035uM
BS07 PB2 C P228 T230 P199 T201 MOAD: ic50=0.035uM
Gene Ontology
Molecular Function
GO:0004497 monooxygenase activity
GO:0005506 iron ion binding
GO:0008392 arachidonate epoxygenase activity
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0016712 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen
GO:0020037 heme binding
GO:0046872 metal ion binding
GO:0070330 aromatase activity
Biological Process
GO:0006805 xenobiotic metabolic process
GO:0019373 epoxygenase P450 pathway
Cellular Component
GO:0005737 cytoplasm
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0016020 membrane
GO:0043231 intracellular membrane-bounded organelle

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:3g5n, PDBe:3g5n, PDBj:3g5n
PDBsum3g5n
PubMed19397311
UniProtP00178|CP2B4_RABIT Cytochrome P450 2B4 (Gene Name=CYP2B4)

[Back to BioLiP]

zhanglabzhanggroup.org | +65-6601-1241 | Computing 1, 13 Computing Drive, Singapore 117417