Structure of PDB 1n97 Chain A Binding Site BS01
Receptor Information
>1n97 Chain A (length=385) Species:
262724
(Thermus thermophilus HB27) [
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MKRLSLREAWPYLKDLQQDPLAVLLAWGRAHPRLFLPLPRFPLALIFDPE
GVEGALLAEGTTKATFQYRALSRLTGRGLLTDWGESWKEARKALKDPFLP
KNVRGYREAMEEEARAFFGEWRGEERDLDHEMLALSLRLLGRALFGKPLS
PSLAEHALKALDRIMAQTRSPLALLDLAAEARFRKDRGALYREAEALIVH
PPLSHLPRERALSEAVTLLVAGHETVASALTWSFLLLSHRPDWQKRVAES
EEAALAAFQEALRLYPPAWILTRRLERPLLLGEDRLPPGTTLVLSPYVTQ
RLHFPDGEAFRPERFLEERGTPSGRYFPFGLGQRLCLGRDFALLEGPIVL
RAFFRRFRLDPLPFPRVLAQVTLRPEGGLPARPRE
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
1n97 Chain A Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
1n97
Preliminary Characterization and Crystal Structure of a Thermostable Cytochrome P450 from Thermus thermophilus
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
K63 Y68 L79 W87 R91 A221 G222 T225 V226 R273 P328 F329 R334 C336 G338
Binding residue
(residue number reindexed from 1)
K63 Y68 L79 W87 R91 A221 G222 T225 V226 R273 P328 F329 R334 C336 G338
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
T225 F329 C336
Catalytic site (residue number reindexed from 1)
T225 F329 C336
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0016705
oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0020037
heme binding
GO:0046872
metal ion binding
View graph for
Molecular Function
External links
PDB
RCSB:1n97
,
PDBe:1n97
,
PDBj:1n97
PDBsum
1n97
PubMed
12401810
UniProt
Q746J6
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