Structure of PDB 5tfu Chain B Binding Site BS02
Receptor Information
>5tfu Chain B (length=451) Species:
9606
(Homo sapiens) [
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GKLPPGPLPQNTPYCFDQLRRRFGDVFSLQLAWTPVVVLNGLAAVREALV
THGEDTADRPPVPITQILGFGPRSQGVFLARYGPAWREQRRFSVSTLRNL
KSLEQWVTEEAACLCAAFANHSGRPFRPNGLLDKAVSNVIASLTCGRRFE
YDDPRFLRLLDLAQEGLKEESGFLREVLNAVPVLLHIPALAGKVLRFQKA
FLTQLDELLTEHRMTWDPAQPPRDLTEAFLAEMEKAKGNPESSFNDENLR
IVVADLFSAGMVTTSTTLAWGLLLMILHPDVQRRVQQEIDDVIGQVRRPE
MGDQAHMPYTTAVIHEVQRFGDIVPLGVTHMTSRDIEVQGFRIPKGTTLI
TNLSSVLKDEAVWEKPFRFHPEHFLDAQGHFVKPEAFLPFSAGRRACLGE
PLARMELFLFFTSLLQHFSFSVPTGQPRPSHHGVFAFLVSPSPYELCAVP
R
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
5tfu Chain B Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
5tfu
Aminomethyl-Derived Beta Secretase (BACE1) Inhibitors: Engaging Gly230 without an Anilide Functionality.
Resolution
2.75 Å
Binding residue
(original residue number in PDB)
R101 F120 R132 G306 T309 V374 H376 P435 F436 S437 R441 C443 L444 G445
Binding residue
(residue number reindexed from 1)
R59 F78 R90 G260 T263 V328 H330 P389 F390 S391 R395 C397 L398 G399
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T309 F436 C443
Catalytic site (residue number reindexed from 1)
T263 F390 C397
Enzyme Commision number
1.14.14.-
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0016491
oxidoreductase 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:0062187
anandamide 8,9 epoxidase activity
GO:0062188
anandamide 11,12 epoxidase activity
GO:0062189
anandamide 14,15 epoxidase activity
Biological Process
GO:0006631
fatty acid metabolic process
GO:0006805
xenobiotic metabolic process
GO:0008202
steroid metabolic process
GO:0008203
cholesterol metabolic process
GO:0008210
estrogen metabolic process
GO:0009804
coumarin metabolic process
GO:0009820
alkaloid metabolic process
GO:0009822
alkaloid catabolic process
GO:0016098
monoterpenoid metabolic process
GO:0019369
arachidonate metabolic process
GO:0033076
isoquinoline alkaloid metabolic process
GO:0042178
xenobiotic catabolic process
GO:0042572
retinol metabolic process
GO:0042759
long-chain fatty acid biosynthetic process
GO:0051100
negative regulation of binding
GO:0070989
oxidative demethylation
GO:0090350
negative regulation of cellular organofluorine metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0016020
membrane
GO:0043231
intracellular membrane-bounded organelle
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5tfu
,
PDBe:5tfu
,
PDBj:5tfu
PDBsum
5tfu
PubMed
27997172
UniProt
P10635
|CP2D6_HUMAN Cytochrome P450 2D6 (Gene Name=CYP2D6)
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