Structure of PDB 8gk3 Chain H Binding Site BS01
Receptor Information
>8gk3 Chain H (length=458) Species:
9606
(Homo sapiens) [
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THGLFKKLGIPGPTPLPFLGNALSFRKGYWTFDMECYKKYGKVWGIYDGQ
QPMLAITDPDMIKTVLVKECYSVFTNRRPFGPVGFMKNAISIAEDEEWKR
IRSLLSPTFTSGKLKEMVPIIAQYGDVLVRNLRREAETGKPVTLKHVFGA
YSMDVITSTSFGVSIDSLNNPQDPFVENTKKLLRFNPLDPFVLSIKVFPF
LTPILEALNITVFPREVISFLTKSVKQIKEGRLKVDFLQLMIDSQNTHKA
LSDLELMAQSIIFIFAGYETTSSVLSFIIYELATHPDVQQKVQKEIDTVL
PNKAPPTYDTVLQLEYLDMVVNETLRLFPVAMRLERVCKKDVEINGMFIP
KGVVVMIPSYVLHHDPKYWTEPEKFLPERFSAANADNIDPYIYTPFGSGP
RNCIGMRFALVNMKLALVRVLQNFSFKPCKETQIPLKLRFGGLLLTEKPI
VLKAESRD
Ligand information
Ligand ID
HEM
InChI
InChI=1S/C34H34N4O4.Fe/c1-7-21-17(3)25-13-26-19(5)23(9-11-33(39)40)31(37-26)16-32-24(10-12-34(41)42)20(6)28(38-32)15-30-22(8-2)18(4)27(36-30)14-29(21)35-25;/h7-8,13-16H,1-2,9-12H2,3-6H3,(H4,35,36,37,38,39,40,41,42);/q;+2/p-2/b25-13-,26-13-,27-14-,28-15-,29-14-,30-15-,31-16-,32-16-;
InChIKey
KABFMIBPWCXCRK-RGGAHWMASA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1c2n3c(c1CCC(=O)O)C=C4C(=C(C5=[N]4[Fe]36[N]7=C(C=C8N6C(=C5)C(=C8C)C=C)C(=C(C7=C2)C)C=C)C)CCC(=O)O
CACTVS 3.385
CC1=C(CCC(O)=O)C2=Cc3n4[Fe]5|6|N2=C1C=c7n5c(=CC8=N|6C(=Cc4c(C)c3CCC(O)=O)C(=C8C=C)C)c(C)c7C=C
ACDLabs 12.01
C=1c3c(c(c4C=C5C(=C(C=6C=C7C(=C(C8=CC=2C(=C(C=1N=2[Fe](n34)(N5=6)N78)CCC(=O)O)C)\C=C)C)\C=C)C)C)CCC(=O)O
Formula
C34 H32 Fe N4 O4
Name
PROTOPORPHYRIN IX CONTAINING FE;
HEME
ChEMBL
DrugBank
DB18267
ZINC
PDB chain
8gk3 Chain H Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
8gk3
Human cytochrome P450 3A7 binding four copies of its native substrate dehydroepiandrosterone 3-sulfate.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
R105 I118 S119 W126 R130 F137 A305 G306 T309 L373 R375 P434 F435 R440 C442 I443 A448
Binding residue
(residue number reindexed from 1)
R77 I90 S91 W98 R102 F109 A266 G267 T270 L334 R336 P395 F396 R401 C403 I404 A409
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.14.14.1
: unspecific monooxygenase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0008395
steroid hydroxylase activity
GO:0008401
retinoic acid 4-hydroxylase 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:0019825
oxygen binding
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0050649
testosterone 6-beta-hydroxylase activity
GO:0062183
all-trans retinoic acid 18-hydroxylase activity
GO:0070330
aromatase activity
GO:0101020
estrogen 16-alpha-hydroxylase activity
GO:0101021
estrogen 2-hydroxylase activity
Biological Process
GO:0002933
lipid hydroxylation
GO:0006694
steroid biosynthetic process
GO:0006805
xenobiotic metabolic process
GO:0008202
steroid metabolic process
GO:0008210
estrogen metabolic process
GO:0042572
retinol metabolic process
GO:0042573
retinoic acid metabolic process
GO:0070989
oxidative demethylation
Cellular Component
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0016020
membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8gk3
,
PDBe:8gk3
,
PDBj:8gk3
PDBsum
8gk3
PubMed
37392852
UniProt
P24462
|CP3A7_HUMAN Cytochrome P450 3A7 (Gene Name=CYP3A7)
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