Structure of PDB 4w5j Chain C Binding Site BS01
Receptor Information
>4w5j Chain C (length=211) Species:
373153
(Streptococcus pneumoniae D39) [
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MNLLIMGLPGAGKGTQAAKIVEQFHVAHISTGDMFRAAMANQTEMGVLAK
SYIDKGELVPDEVTNGIVKERLSQDDIKETGFLLDGYPRTIEQAHALDKT
LAELGIELEGIINIEVNPDSLLERLSGRIIHRVTGETFHKVFNPPVYKEE
DYYQREDDKPETVKRRLDVNIAQGEPIIAHYRAKGLVHDIEGNQDINDVF
SDIEKVLTNLK
Ligand information
Ligand ID
AP5
InChI
InChI=1S/C20H29N10O22P5/c21-15-9-17(25-3-23-15)29(5-27-9)19-13(33)11(31)7(47-19)1-45-53(35,36)49-55(39,40)51-57(43,44)52-56(41,42)50-54(37,38)46-2-8-12(32)14(34)20(48-8)30-6-28-10-16(22)24-4-26-18(10)30/h3-8,11-14,19-20,31-34H,1-2H2,(H,35,36)(H,37,38)(H,39,40)(H,41,42)(H,43,44)(H2,21,23,25)(H2,22,24,26)/t7-,8-,11-,12-,13-,14-,19-,20-/m1/s1
InChIKey
OIMACDRJUANHTJ-XPWFQUROSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)O[P@](O)(=O)O[P@](O)(=O)O[P@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@](=O)(O)OP(=O)(O)O[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(=O)O[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)[CH](O)[CH]3O
Formula
C20 H29 N10 O22 P5
Name
BIS(ADENOSINE)-5'-PENTAPHOSPHATE
ChEMBL
CHEMBL437508
DrugBank
DB01717
ZINC
ZINC000096085195
PDB chain
4w5j Chain C Residue 302 [
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Receptor-Ligand Complex Structure
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PDB
4w5j
New crystal structures of adenylate kinase from Streptococcus pneumoniae D39 in two conformations.
Resolution
1.65 Å
Binding residue
(original residue number in PDB)
P9 G10 G12 K13 G14 T15 T31 G32 F35 R36 I53 E57 L58 V59 T64 R89 Q93 R124 R128 T137 F138 H139 F142 R156 R167 I197
Binding residue
(residue number reindexed from 1)
P9 G10 G12 K13 G14 T15 T31 G32 F35 R36 I53 E57 L58 V59 T64 R89 Q93 R124 R128 T137 F138 H139 F142 R155 R166 I196
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
K13 R89 R128 R156 R167
Catalytic site (residue number reindexed from 1)
K13 R89 R128 R155 R166
Enzyme Commision number
2.7.4.3
: adenylate kinase.
Gene Ontology
Molecular Function
GO:0004017
adenylate kinase activity
GO:0004550
nucleoside diphosphate kinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016776
phosphotransferase activity, phosphate group as acceptor
GO:0019205
nucleobase-containing compound kinase activity
GO:0050145
nucleoside monophosphate kinase activity
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0009123
nucleoside monophosphate metabolic process
GO:0009132
nucleoside diphosphate metabolic process
GO:0009165
nucleotide biosynthetic process
GO:0016310
phosphorylation
GO:0044209
AMP salvage
GO:0046940
nucleoside monophosphate phosphorylation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4w5j
,
PDBe:4w5j
,
PDBj:4w5j
PDBsum
4w5j
PubMed
25372811
UniProt
Q04ML5
|KAD_STRP2 Adenylate kinase (Gene Name=adk)
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