Structure of PDB 8ebc Chain C Binding Site BS01

Receptor Information
>8ebc Chain C (length=355) Species: 169963 (Listeria monocytogenes EGD-e) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
AFYFEEPSRTFSEFLLVPCVPTNVSLKTPIVKFKKGEESAITMNIPLVSA
IMQAVSDDNMGIALATEGGVSFIFGSQSIESEAAMVSRVKNHKLELLDSS
KRYVVGAGINTRDYEERVPALVEAGADILCIDSSEGYSEWQKRTLDYVRG
KYGDTVKVGAGNVVDRDGFRYLAEAGADFVKVGVGGGSICITREQKGIGR
GQATALIDVAKARDEYFEETGVYIPICSDGGIVYDYHMTLALAMGADFIM
LGRYFSRFDESPTNKVNLNGTYMKEYWGEGANRARNWQRYDLGGDKKLSF
EEGVDSYVPYAGSLKDNVAISLSKVRSTMCNCGALNIPELQQKAKITLVS
STSIV
Ligand information
Ligand IDIMP
InChIInChI=1S/C10H13N4O8P/c15-6-4(1-21-23(18,19)20)22-10(7(6)16)14-3-13-5-8(14)11-2-12-9(5)17/h2-4,6-7,10,15-16H,1H2,(H,11,12,17)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKeyGRSZFWQUAKGDAV-KQYNXXCUSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.7.5c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)N=CNC2=O
ACDLabs 10.04O=C1c2ncn(c2N=CN1)C3OC(C(O)C3O)COP(=O)(O)O
OpenEye OEToolkits 1.7.5c1nc2c(n1C3C(C(C(O3)COP(=O)(O)O)O)O)N=CNC2=O
CACTVS 3.385O[CH]1[CH](O)[CH](O[CH]1CO[P](O)(O)=O)n2cnc3C(=O)NC=Nc23
CACTVS 3.385O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CO[P](O)(O)=O)n2cnc3C(=O)NC=Nc23
FormulaC10 H13 N4 O8 P
NameINOSINIC ACID
ChEMBLCHEMBL1207374
DrugBankDB04566
ZINCZINC000004228242
PDB chain8ebc Chain C Residue 401 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB8ebc Crystal Structure of the Catalytic Domain of the Inosine Monophosphate Dehydrogenase from Listeria monocytogenes in the complex with IMP
Resolution2.5 Å
Binding residue
(original residue number in PDB)
M58 I211 T212 R213 E214 Q215 D249 G250 G251 L271 G272 R273 G298 E299 G300
Binding residue
(residue number reindexed from 1)
M52 I191 T192 R193 E194 Q195 D229 G230 G231 L251 G252 R253 G278 E279 G280
Annotation score4
Enzymatic activity
Enzyme Commision number 1.1.1.205: IMP dehydrogenase.
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0003938 IMP dehydrogenase activity
GO:0016491 oxidoreductase activity
Biological Process
GO:0006164 purine nucleotide biosynthetic process

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Molecular Function

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Biological Process
External links
PDB RCSB:8ebc, PDBe:8ebc, PDBj:8ebc
PDBsum8ebc
PubMed
UniProtQ8YAJ3

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