Structure of PDB 4fdh Chain D Binding Site BS01
Receptor Information
>4fdh Chain D (length=465) Species:
9606
(Homo sapiens) [
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TVLPFEAMPQHPGNRWLRLLQIWREQGYEHLHLEMHQTFQELGPIFRYNL
GGPRMVCVMLPEDVEKLQQVDSLHPCRMILEPWVAYRQHRGHKCGVFLLN
GPEWRFNRLRLNPDVLSPKAVQRFLPMVDAVARDFSQALKKKVLQNARGS
LTLDVQPSIFHYTIEASNLALFGERLGLVGHSPSSASLNFLHALEVMFKS
TVQLMFMPRSLSRWISPKVWKEHFEAWDCIFQYGDNCIQKIYQELAFNRP
QHYTGIVAELLLKAELSLEAIKANSMELTAGSVDTTAFPLLMTLFELARN
PDVQQILRQESLAAAASISEHPQKATTELPLLRAALKETLRLYPVGLFLE
RVVSSDLVLQNYHIPAGTLVQVFLYSLGRNAALFPRPERYNPQRWLDIRN
FHHVPFGFGMRQCLGRRLAEAEMLLLLHHVLKHFLVETLTQEDIKMVYSF
ILRPGTSPLLTFRAI
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
4fdh Chain D Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
4fdh
Structural insights into aldosterone synthase substrate specificity and targeted inhibition.
Resolution
2.71 Å
Binding residue
(original residue number in PDB)
R110 V129 F130 R141 L311 G314 S315 T318 R384 P442 F443 R448 C450 G452 A456
Binding residue
(residue number reindexed from 1)
R77 V96 F97 R108 L278 G281 S282 T285 R351 P405 F406 R411 C413 G415 A419
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T318 F443 C450
Catalytic site (residue number reindexed from 1)
T285 F406 C413
Enzyme Commision number
1.14.15.4
: steroid 11beta-monooxygenase.
1.14.15.5
: corticosterone 18-monooxygenase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0004507
steroid 11-beta-monooxygenase activity
GO:0005506
iron ion binding
GO:0008395
steroid hydroxylase activity
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0020037
heme binding
GO:0046872
metal ion binding
GO:0047783
corticosterone 18-monooxygenase activity
Biological Process
GO:0002017
regulation of blood volume by renal aldosterone
GO:0003091
renal water homeostasis
GO:0006629
lipid metabolic process
GO:0006694
steroid biosynthetic process
GO:0006700
C21-steroid hormone biosynthetic process
GO:0006704
glucocorticoid biosynthetic process
GO:0006705
mineralocorticoid biosynthetic process
GO:0008203
cholesterol metabolic process
GO:0016125
sterol metabolic process
GO:0032342
aldosterone biosynthetic process
GO:0032870
cellular response to hormone stimulus
GO:0034650
cortisol metabolic process
GO:0034651
cortisol biosynthetic process
GO:0035865
cellular response to potassium ion
GO:0055075
potassium ion homeostasis
GO:0055078
sodium ion homeostasis
GO:0071375
cellular response to peptide hormone stimulus
GO:1901615
organic hydroxy compound metabolic process
Cellular Component
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4fdh
,
PDBe:4fdh
,
PDBj:4fdh
PDBsum
4fdh
PubMed
23322723
UniProt
P19099
|C11B2_HUMAN Cytochrome P450 11B2, mitochondrial (Gene Name=CYP11B2)
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