Structure of PDB 1f25 Chain A Binding Site BS01
Receptor Information
>1f25 Chain A (length=399) Species:
5507
(Fusarium oxysporum) [
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APSFPFSRASGPEPPAEFAKLRATNPVSQVKLFDGSLAWLVTKHKDVCFV
ATSEKLSKVRTRQGFPELSASGKQAAKAKPTFVDMDPPEHMHQRSMVEPT
FTPEAVKNLQPYIQRTVDDLLEQMKQKGCANGPVDLVKEFALPVPSYIIY
TLLGVPFNDLEYLTQQNAIRTNGSSTAREASAANQELLDYLAILVEQRLV
EPKDDIISKLCTEQVKPGNIDKSDAVQIAFLLLVAGNANMVNMIALGVAT
LAQHPDQLAQLKANPSLAPQFVEELCRYHTASALAIKRTAKEDVMIGDKL
VRANEGIIASNQSANRDEEVFENPDEFNMNRKWPPQDPLGFGFGDHRCIA
EHLAKAELTTVFSTLYQKFPDLKVAVPLGKINYTPLNRDVGIVDLPVIF
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
1f25 Chain A Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
1f25
Mutation effects of a conserved threonine (Thr243) of cytochrome P450nor on its structure and function.
Resolution
1.4 Å
Binding residue
(original residue number in PDB)
F86 V87 R98 L236 A239 G240 N243 M244 G344 F345 G346 F347 H350 C352 I353 A354
Binding residue
(residue number reindexed from 1)
F82 V83 R94 L232 A235 G236 N239 M240 G340 F341 G342 F343 H346 C348 I349 A350
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
T175 A239 A242 N243 M244 S286 C352 I353 A354 E361 D393
Catalytic site (residue number reindexed from 1)
T171 A235 A238 N239 M240 S282 C348 I349 A350 E357 D389
Enzyme Commision number
1.7.1.14
: nitric oxide reductase [NAD(P)(+), nitrous oxide-forming].
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
GO:0102199
nitric oxide reductase (NAD(P)H) activity
View graph for
Molecular Function
External links
PDB
RCSB:1f25
,
PDBe:1f25
,
PDBj:1f25
PDBsum
1f25
PubMed
11132616
UniProt
P23295
|NOR_FUSOX NADP nitrous oxide-forming nitric oxide reductase (Gene Name=CYP55A1)
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