Structure of PDB 8kbg Chain H Binding Site BS02
Receptor Information
>8kbg Chain H (length=124) Species:
1491
(Clostridium botulinum) [
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MKELSTIQKREKLNTVERIGSEGPGGAYHEYVIKSNSMDSQGNYDVYETI
KFQKGARKEEKSQHGVIDSDLLEIVRDRLKSFQAGPFSSRENACALTHVE
EALMWMNRRVEDRIERNVLGTNTK
Ligand information
Ligand ID
1SY
InChI
InChI=1S/C20H24N10O13P2/c21-14-8-15(24-3-23-14)29(4-25-8)18-11(32)12-7(41-18)2-39-45(36,37)43-13-10(31)6(1-38-44(34,35)42-12)40-19(13)30-5-26-9-16(30)27-20(22)28-17(9)33/h3-7,10-13,18-19,31-32H,1-2H2,(H,34,35)(H,36,37)(H2,21,23,24)(H3,22,27,28,33)/t6-,7-,10-,11-,12-,13-,18-,19-/m1/s1
InChIKey
XRILCFTWUCUKJR-INFSMZHSSA-N
SMILES
Software
SMILES
ACDLabs 12.01
O=C7N=C(N)Nc1c7ncn1C5OC6COP(=O)(O)OC4C(OC(n2c3ncnc(N)c3nc2)C4O)COP(=O)(OC5C6O)O
CACTVS 3.370
NC1=NC(=O)c2ncn([CH]3O[CH]4CO[P](O)(=O)O[CH]5[CH](O)[CH](O[CH]5CO[P](O)(=O)O[CH]3[CH]4O)n6cnc7c(N)ncnc67)c2N1
CACTVS 3.370
NC1=NC(=O)c2ncn([C@@H]3O[C@@H]4CO[P](O)(=O)O[C@H]5[C@@H](O)[C@@H](O[C@@H]5CO[P](O)(=O)O[C@@H]3[C@@H]4O)n6cnc7c(N)ncnc67)c2N1
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)C3C(C4C(O3)COP(=O)(OC5C(C(COP(=O)(O4)O)OC5n6cnc7c6NC(=NC7=O)N)O)O)O)N
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@H]4[C@H](O3)COP(=O)(O[C@@H]5[C@@H]([C@@H](COP(=O)(O4)O)O[C@H]5n6cnc7c6NC(=NC7=O)N)O)O)O)N
Formula
C20 H24 N10 O13 P2
Name
cGAMP;
2',3' cGAMP;
c-GMP-AMP;
c[G(2',5')pA(3',5')p]
ChEMBL
CHEMBL4465054
DrugBank
ZINC
ZINC000096095421
PDB chain
8kbg Chain I Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
8kbg
Structure of CbTad1 complexed with 2',3'-cGAMP
Resolution
2.37 Å
Binding residue
(original residue number in PDB)
E11 L13 F82 F87 N92
Binding residue
(residue number reindexed from 1)
E11 L13 F82 F87 N92
Annotation score
4
External links
PDB
RCSB:8kbg
,
PDBe:8kbg
,
PDBj:8kbg
PDBsum
8kbg
PubMed
UniProt
P0DW58
|TAD1_CLOBO Thoeris anti-defense 1 (Gene Name=tad1)
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