Structure of PDB 5ldq Chain C Binding Site BS01
Receptor Information
>5ldq Chain C (length=175) Species:
469008
(Escherichia coli BL21(DE3)) [
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SEPQRLFFAIDLPAEIREQIIHWRAKHFPPEAGRPVAADNLHLTLAFLGE
VSAEKEKALSLLAGRIRQPGFTLTLDDAGQWLRSRVVWLGMRQPPRGLIQ
LANMLRSQAARSGCFQSNRPFHPHITLLRDASEAVTIPPPGFNWSYAVTE
FTLYASSFARGRTRYTPLKRWALTQ
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
5ldq Chain C Residue 201 [
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Receptor-Ligand Complex Structure
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PDB
5ldq
Structural aspects of nucleotide ligand binding by a bacterial 2H phosphoesterase.
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
R6 F8 H43 F48 F116 R130 S157 F159 Y166
Binding residue
(residue number reindexed from 1)
R5 F7 H42 F47 F115 R129 S156 F158 Y165
Annotation score
1
Binding affinity
MOAD
: Kd=40uM
Enzymatic activity
Enzyme Commision number
3.1.4.58
: RNA 2',3'-cyclic 3'-phosphodiesterase.
Gene Ontology
Molecular Function
GO:0004113
2',3'-cyclic-nucleotide 3'-phosphodiesterase activity
GO:0005524
ATP binding
GO:0008081
phosphoric diester hydrolase activity
GO:0008664
RNA 2',3'-cyclic 3'-phosphodiesterase activity
GO:0016787
hydrolase activity
GO:0016874
ligase activity
View graph for
Molecular Function
External links
PDB
RCSB:5ldq
,
PDBe:5ldq
,
PDBj:5ldq
PDBsum
5ldq
PubMed
28141848
UniProt
A0A140NFI1
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