Structure of PDB 2reh Chain C Binding Site BS01
Receptor Information
>2reh Chain C (length=430) Species:
5507
(Fusarium oxysporum) [
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VDFKLSPSQLEARRHAQAFANTVLTKASAEYSTQKDQLSRFQATRPFYRE
AVRHGLIKAQVPIPLGGTMESLVHESIILEELFAVEPATSITIVATALGL
MPVILCDSPSLQEKFLKPFISGEGEPLASLMHSEPNGTANWLQKGGPGLQ
TTARKVGNEWVISGEKLWPSNSGGWDYKGADLACVVCRVSDDPSKPQDPN
VDPATQIAVLLVTRETIANNKKDAYQILGEPELAGHITTSGPHTRFTEFH
VPHENLLCTPGLKAQGLVETAFAMSAALVGAMAIGTARAAFEEALVFAKS
DTRGGSKHIIEHQSVADKLIDCKIRLETSRLLVWKAVTTLEDEALEWKVK
LEMAMQTKIYTTDVAVECVIDAMKAVGMKSYAKDMSFPRLLNEVMCYPLF
EGGNIGLRRRQMQRVMALEDYEPWAATYGS
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
2reh Chain C Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
2reh
Mechanistic and structural analyses of the roles of Arg409 and Asp402 in the reaction of the flavoprotein nitroalkane oxidase.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
L131 H133 S134 G138 A140 N141 W169 P170 S171 C397 L400 F401 E402 G403 G404 I406 G407
Binding residue
(residue number reindexed from 1)
L130 H132 S133 G137 A139 N140 W168 P169 S170 C396 L399 F400 E401 G402 G403 I405 G406
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H133 S134 S276 E402 R415
Catalytic site (residue number reindexed from 1)
H132 S133 S275 E401 R414
Enzyme Commision number
1.7.3.1
: nitroalkane oxidase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003995
acyl-CoA dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016627
oxidoreductase activity, acting on the CH-CH group of donors
GO:0050660
flavin adenine dinucleotide binding
GO:0052664
nitroalkane oxidase activity
GO:0071949
FAD binding
Biological Process
GO:0033539
fatty acid beta-oxidation using acyl-CoA dehydrogenase
GO:0046359
butyrate catabolic process
GO:0098754
detoxification
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2reh
,
PDBe:2reh
,
PDBj:2reh
PDBsum
2reh
PubMed
17994768
UniProt
Q8X1D8
|NAO_FUSOX Nitroalkane oxidase
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