Structure of PDB 6x0i Chain A Binding Site BS01
Receptor Information
>6x0i Chain A (length=443) Species:
330879
(Aspergillus fumigatus Af293) [
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RLRSTPQDELHDLLCVGFGPASLAIAIALHDALDPRLNQPKICFLERQKQ
FAWHSGMLVPGSKMQISFIKDLATLRDPRSSFTFLNYLHQKGRLIHFTNL
STFLPARLEFEDYMRWCAQQFSDVVAYGEEVVEVIPGKSDPSSSVVDFFT
VRSRNVETGEISARRTRKVVIAIGGTAKMPSGLPQDPRIIHSSKYCTTLP
ALLKDKSKPYNIAVLGSGQSAAEIFHDLQKRYPNSRTTLIMRDSAMRPSD
DSPFVNEIFNPERVDKFYSQSAAERQRSLLADKATNYSVVRLELIEEIYN
DMYLQRVKNPDETQWQHRILPERKITRVEHHGPQSRMRIHLKSSKPKETL
EVDALMVATGYNRNAHERLLSKVQHLRPTGQDQWKPHRDYRVEMDPSKVS
SEAGIWLQGCNERTHGLSDSLLSVLAVRGGEMVQSIFGEQLER
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
6x0i Chain A Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
6x0i
Trapping conformational states of a flavin-dependent N -monooxygenase in crystallo reveals protein and flavin dynamics.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
G48 P49 A50 E83 R84 Q85 W90 H91 M94 M101 I103 V168 I210 G211 Y407 S466 L468
Binding residue
(residue number reindexed from 1)
G19 P20 A21 E46 R47 Q48 W53 H54 M57 M64 I66 V131 I173 G174 Y361 S420 L422
Annotation score
2
Enzymatic activity
Enzyme Commision number
1.14.13.196
: L-ornithine N(5)-monooxygenase [NAD(P)H].
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0004497
monooxygenase activity
GO:0004499
N,N-dimethylaniline monooxygenase activity
GO:0005506
iron ion binding
GO:0031172
ornithine N5-monooxygenase activity
GO:0070401
NADP+ binding
Biological Process
GO:0006696
ergosterol biosynthetic process
GO:0006879
intracellular iron ion homeostasis
GO:0009058
biosynthetic process
GO:0010106
cellular response to iron ion starvation
GO:0019290
siderophore biosynthetic process
GO:0031169
ferrichrome biosynthetic process
GO:0033214
siderophore-dependent iron import into cell
GO:0044550
secondary metabolite biosynthetic process
Cellular Component
GO:0005575
cellular_component
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6x0i
,
PDBe:6x0i
,
PDBj:6x0i
PDBsum
6x0i
PubMed
32723870
UniProt
E9QYP0
|SIDA_ASPFU L-ornithine N(5)-monooxygenase (Gene Name=sidA)
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