Structure of PDB 1pq2 Chain B Binding Site BS02
Receptor Information
>1pq2 Chain B (length=463) Species:
9606
(Homo sapiens) [
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KLPPGPTPLPIIGNMLQIDVKDICKSFTNFSKVYGPVFTVYFGMNPIVVF
HGYEAVKEALIDNGEEFSGRGNSPISQRITKGLGIISSNGKRWKEIRRFS
LTTLRNFGMGKRSIEDRVQEEAHCLVEELRKTKASPCDPTFILGCAPCNV
ICSVVFQKRFDYKDQNFLTLMKRFNENFRILNSPWIQVCNNFPLLIDCFP
GTHNKVLKNVALTRSYIREKVKEHQASLDVNNPRDFIDCFLIKMEQEKDN
QKSEFNIENLVGTVADLFVAGTETTSTTLRYGLLLLLKHPEVTAKVQEEI
DHVIGRHRSPCMQDRSHMPYTDAVVHEIQRYSDLVPTGVPHAVTTDTKFR
NYLIPKGTTIMALLTSVLHDDKEFPNPNIFDPGHFLDKNGNFKKSDYFMP
FSAGKRICAGEGLARMELFLFLTTILQNFNLKSVDDLKNLNTTAVTKGIV
SLPPSYQICFIPV
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
1pq2 Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1pq2
Structure of human microsomal cytochrome P450 2C8. Evidence for a peripheral fatty acid binding site
Resolution
2.7 Å
Binding residue
(original residue number in PDB)
R97 W120 R124 A297 G298 T301 T302 H368 P427 F428 S429 R433 C435 A436 G437 A441
Binding residue
(residue number reindexed from 1)
R70 W93 R97 A270 G271 T274 T275 H341 P400 F401 S402 R406 C408 A409 G410 A414
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T301 F428 C435
Catalytic site (residue number reindexed from 1)
T274 F401 C408
Enzyme Commision number
1.14.14.1
: unspecific monooxygenase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0005515
protein binding
GO:0008392
arachidonate epoxygenase 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:0020037
heme binding
GO:0034875
caffeine oxidase activity
GO:0046872
metal ion binding
GO:0070330
aromatase activity
GO:0101020
estrogen 16-alpha-hydroxylase activity
Biological Process
GO:0002933
lipid hydroxylation
GO:0006082
organic acid metabolic process
GO:0006805
xenobiotic metabolic process
GO:0008202
steroid metabolic process
GO:0008210
estrogen metabolic process
GO:0019369
arachidonate metabolic process
GO:0019373
epoxygenase P450 pathway
GO:0042178
xenobiotic catabolic process
GO:0042572
retinol metabolic process
GO:0042573
retinoic acid metabolic process
GO:0042759
long-chain fatty acid biosynthetic process
GO:0046456
icosanoid biosynthetic process
GO:0070989
oxidative demethylation
GO:0097267
omega-hydroxylase P450 pathway
Cellular Component
GO:0005737
cytoplasm
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005886
plasma membrane
GO:0016020
membrane
GO:0043231
intracellular membrane-bounded organelle
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Cellular Component
External links
PDB
RCSB:1pq2
,
PDBe:1pq2
,
PDBj:1pq2
PDBsum
1pq2
PubMed
14676196
UniProt
P10632
|CP2C8_HUMAN Cytochrome P450 2C8 (Gene Name=CYP2C8)
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