Structure of PDB 5cku Chain A Binding Site BS02
Receptor Information
>5cku Chain A (length=451) Species:
330879
(Aspergillus fumigatus Af293) [
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LSLDPPRLRSTPQDELHDLLCVGFGPASLAIAIALHDALDPRLNKSAAQP
KICFLERQKQFAWHSGMLVPGSKMQISFIKDLATLRDPRSSFTFLNYLHQ
KGRLIHFTNLSTFLPARLEFEDYMRWCAQQFSDVVAYGEEVVEVIPGKSD
PSSSVVDFFTVRSRNVETGEISARRTRKVVIAIGGTAKMPSGLPQDPRII
HSSKYCTTLPALLKDKSKPYNIAVLGSGQSAAEIFHDLQKRYPNSRTTLI
MRDSAMRPSDDSPFVNEIFNPERVDKFYSQSAAERQRSLLADKATAYSVV
RLELIEEIYNDMYLQRVKNPDETQWQHRILPERKITRVEHHGPQSRMRIH
LKSSKPETLEVDALMVATGYNRNAHERLLSKVQHLRPTGQDQWKPHRDYR
VEMDPSKVSSEAGIWLQGCNERTHGLSDSLLSVLAVRGGEMVQSIFGEQL
E
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
5cku Chain A Residue 602 [
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Receptor-Ligand Complex Structure
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PDB
5cku
Contribution to catalysis of ornithine binding residues in ornithine N5-monooxygenase.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
P217 S254 G255 S257 R279 S325 A404 T405
Binding residue
(residue number reindexed from 1)
P190 S227 G228 S230 R252 S298 A367 T368
Annotation score
4
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
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5cku
,
PDBe:5cku
,
PDBj:5cku
PDBsum
5cku
PubMed
26375201
UniProt
E9QYP0
|SIDA_ASPFU L-ornithine N(5)-monooxygenase (Gene Name=sidA)
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