Structure of PDB 6y87 Chain B Binding Site BS01
Receptor Information
>6y87 Chain B (length=466) Species:
287
(Pseudomonas aeruginosa) [
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SINPPQRIVFVGLGTIAQSFLPLLSKVHDLSTLEIYAIDPKTPPLIEYFA
NSFGLKFINSAIDQINYRDILVPILGEGTVLINLSTDVSSLALIELCRSA
GALYLDTCIEPWKGGYDDPTIPLHKRTNYHLREQMLSLKKRLGSGVTALV
AHGANPGLVSHFVKRALLDLAEEILGDCKKPSNKEQWAILSQRLGVKVIH
VAEYDSQISQKSRERGEFVNTWSVHGFISESQQPAELGWGSHERSLPTDA
SMHTDGCGAAIYIEKPGASVRVKTWTPFNGPSLGYLVTHHEAISIADFLT
LRTADETYRPTVHYAYRPSDEAILSVHEWFGNDCMTPEKTKVLRPGDILS
GSDYLGVLLMGHEKSSYWYGSILSIEKAKELATLNTATTLQVAAGVLSGY
LWILSHPSAGIIEAEDMDHEVALSYISQYLGELKGVYSDWNPTKNNPGTF
SAIDSDSPWLFSNFVL
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
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)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)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)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]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)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
6y87 Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
6y87
Structural and catalytic characterization of Blastochloris viridis and Pseudomonas aeruginosa homospermidine synthases supports the essential role of cation-pi interaction.
Resolution
2.15 Å
Binding residue
(original residue number in PDB)
G17 T18 I19 D42 P43 I65 L87 S88 T89 V91 T110 A157 N158 P159 V395
Binding residue
(residue number reindexed from 1)
G14 T15 I16 D39 P40 I62 L84 S85 T86 V88 T107 A154 N155 P156 V392
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.5.1.44
: homospermidine synthase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016740
transferase activity
GO:0047296
homospermidine synthase activity
View graph for
Molecular Function
External links
PDB
RCSB:6y87
,
PDBe:6y87
,
PDBj:6y87
PDBsum
6y87
PubMed
34605434
UniProt
Q6X2Y9
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