Structure of PDB 3tsd Chain B Binding Site BS01
Receptor Information
>3tsd Chain B (length=426) Species:
198094
(Bacillus anthracis str. Ames) [
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TENLYFQSNAMWESKFVKEGLTFDDVLLVPAKSDVLPREVSVKTVLSESL
QLNIPLISAGMDTVTEADMAIAMARQGGLGIIHKNMSIEQQAEQVDKVKR
SESTPEHQHLMGKYRISGVPVVRKLVIITNRDMRFISIKISDVMTKEITA
PVGTTLSEAEKILQKYKIEKLPLVDNNGVLQGLITIKDIEKVIEFPNSAK
DKQGRLLVGAAVGVTADAMTRIDALVKASVDAIVLDTAHGHSQGVIDKVK
EVRAKYPSLNIIAGNVATAEATKALIEAGANVVKVGIGPGSICTTRVVAG
VGVPQLTAVYDCATEARKHGIPVIADGGIKYSGDMVKALAAGAHVVMLGS
MFAGVAESPGEGRQFKVYRGMIEGRVPYKGPLADTVHQLVGGLRAGMGYC
GAQDLEFLRENAQFIRMSGAGLLESH
Ligand information
Ligand ID
XMP
InChI
InChI=1S/C10H13N4O9P/c15-5-3(1-22-24(19,20)21)23-9(6(5)16)14-2-11-4-7(14)12-10(18)13-8(4)17/h2-3,5-6,9,15-16H,1H2,(H2,19,20,21)(H2,12,13,17,18)/p+1/t3-,5-,6-,9-/m1/s1
InChIKey
DCTLYFZHFGENCW-UUOKFMHZSA-O
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1[nH+]c2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)O)O)O)NC(=O)NC2=O
CACTVS 3.341
O[C@H]1[C@@H](O)[C@@H](O[C@@H]1CO[P](O)(O)=O)n2c[nH+]c3C(=O)NC(=O)Nc23
OpenEye OEToolkits 1.5.0
c1[nH+]c2c(n1C3C(C(C(O3)COP(=O)(O)O)O)O)NC(=O)NC2=O
ACDLabs 10.04
O=C3Nc1c([nH+]cn1C2OC(C(O)C2O)COP(=O)(O)O)C(=O)N3
CACTVS 3.341
O[CH]1[CH](O)[CH](O[CH]1CO[P](O)(O)=O)n2c[nH+]c3C(=O)NC(=O)Nc23
Formula
C10 H14 N4 O9 P
Name
XANTHOSINE-5'-MONOPHOSPHATE;
5-MONOPHOSPHATE-9-BETA-D-RIBOFURANOSYL XANTHINE
ChEMBL
DrugBank
ZINC
PDB chain
3tsd Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
3tsd
Bacillus anthracis inosine 5'-monophosphate dehydrogenase in action: the first bacterial series of structures of phosphate ion-, substrate-, and product-bound complexes.
Resolution
2.653 Å
Binding residue
(original residue number in PDB)
M51 S306 C308 D341 S365 Y388 G390 M391
Binding residue
(residue number reindexed from 1)
M61 S291 C293 D326 S350 Y368 G370 M371
Annotation score
2
Enzymatic activity
Enzyme Commision number
1.1.1.205
: IMP dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003824
catalytic activity
GO:0003938
IMP dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0046872
metal ion binding
Biological Process
GO:0006164
purine nucleotide biosynthetic process
GO:0006177
GMP biosynthetic process
GO:0006183
GTP biosynthetic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3tsd
,
PDBe:3tsd
,
PDBj:3tsd
PDBsum
3tsd
PubMed
22788966
UniProt
A0A6L8P2U9
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