Structure of PDB 5uap Chain A Binding Site BS01
Receptor Information
>5uap Chain A (length=464) Species:
9606
(Homo sapiens) [
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GKLPPGPRPLPLLGNLLQMDRRGLLKSFLRFREKYGDVFTVHLGPRPVVM
LCGVEAIREALVDKAEAFSGRGKIAMVDPFFRGYGVIFANGNRWKVLRRF
SVTTMRDFGMGKRSVEERIQEEAQCLIEELRKSKGALMDPTFLFQSITAN
IICSIVFGKRFHYQDQEFLKMLNLFYQTFSLISSVFGQLFELFSGFLKHF
PGAHRQVYKNLQEINAYIGHSVEKHRETLDPSAPRDLIDTYLLHMEKEKS
NAHSEFSHQNLNLNTLSLFFAGTETTSTTLRYGFLLMLKYPHVAERVYRE
IEQVIGPHRPPELHDRAKMPYTEAVIYEIQRFSDLLPMGVPHIVTQHTSF
RGYIIPKDTEVFLILSTALHDPHYFEKPDAFNPDHFLDANGALKKTEAFI
PFSLGKRICLGEGIARAELFLFFTTILQNFSMASPVAPEDIDLTPQECGV
GKIPPTYQIRFLPR
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
5uap Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5uap
Halogen-pi Interactions in the Cytochrome P450 Active Site: Structural Insights into Human CYP2B6 Substrate Selectivity.
Resolution
2.03 Å
Binding residue
(original residue number in PDB)
R98 R125 A298 G299 T302 L362 L363 V367 H369 P428 F429 S430 R434 C436 L437 G438 A442
Binding residue
(residue number reindexed from 1)
R71 R98 A271 G272 T275 L335 L336 V340 H342 P401 F402 S403 R407 C409 L410 G411 A415
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T302 F429 C436
Catalytic site (residue number reindexed from 1)
T275 F402 C409
Enzyme Commision number
1.14.13.-
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0008390
testosterone 16-alpha-hydroxylase activity
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:0062184
testosterone 16-beta-hydroxylase activity
GO:0062187
anandamide 8,9 epoxidase activity
GO:0062188
anandamide 11,12 epoxidase activity
GO:0062189
anandamide 14,15 epoxidase activity
GO:0101021
estrogen 2-hydroxylase activity
Biological Process
GO:0006629
lipid metabolic process
GO:0006805
xenobiotic metabolic process
GO:0008202
steroid metabolic process
GO:0019373
epoxygenase P450 pathway
GO:0042178
xenobiotic catabolic process
GO:0042180
cellular ketone metabolic process
Cellular Component
GO:0005737
cytoplasm
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:5uap
,
PDBe:5uap
,
PDBj:5uap
PDBsum
5uap
PubMed
28368100
UniProt
P20813
|CP2B6_HUMAN Cytochrome P450 2B6 (Gene Name=CYP2B6)
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