Structure of PDB 5ynn Chain A Binding Site BS02
Receptor Information
>5ynn Chain A (length=295) Species:
1235996
(Human betacoronavirus 2c EMC/2012) [
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ASADWKPGHAMPSLFKVQNVNLERCELANYKQSIPMPRGVHMNIAKYMQL
CQYLNTCTLAVPANMRVIHFGAGSDKGIAPGTSVLRQWLPTDAIIIDNDL
NEFVSDADITLFGDCVTVRVGQQVDLVISDMYDPTTKNVTGSNESKALFF
TYLCNLINNNLALGGSVAIKITEHSWSVELYELMGKFAWWTVFCTNANAS
SSEGFLLGINYLGTIKENIDGGAMHANYIFWRNSTPMNLSTYSLFDLSKF
QLKLKGTPVLQLKESQINELVISLLSQGKLLIRDNDTLSVSTDVL
Ligand information
Ligand ID
GTG
InChI
InChI=1S/C21H29N10O18P3/c1-29-5-31(15-9(29)17(37)28-21(23)26-15)19-13(35)11(33)7(47-19)3-45-51(40,41)49-52(42,43)48-50(38,39)44-2-6-10(32)12(34)18(46-6)30-4-24-8-14(30)25-20(22)27-16(8)36/h4-7,10-13,18-19,32-35H,2-3H2,1H3,(H8-,22,23,25,26,27,28,36,37,38,39,40,41,42,43)/p+1/t6-,7-,10-,11-,12-,13-,18-,19-/m1/s1
InChIKey
FHHZHGZBHYYWTG-INFSMZHSSA-O
SMILES
Software
SMILES
CACTVS 3.385
C[n+]1cn([C@@H]2O[C@H](CO[P](O)(=O)O[P](O)(=O)O[P](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5C(=O)NC(=Nc45)N)[C@@H](O)[C@H]2O)c6N=C(N)NC(=O)c16
CACTVS 3.385
C[n+]1cn([CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5C(=O)NC(=Nc45)N)[CH](O)[CH]2O)c6N=C(N)NC(=O)c16
OpenEye OEToolkits 1.7.5
C[n+]1cn(c2c1C(=O)NC(=N2)N)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)OP(=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5N=C(NC6=O)N)O)O)O)O
ACDLabs 10.04
O=C1NC(=Nc2c1[n+](cn2C3OC(C(O)C3O)COP(=O)(O)OP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c5N=C(N)NC4=O)C(O)C6O)C)N
OpenEye OEToolkits 1.7.5
C[n+]1cn(c2c1C(=O)NC(=N2)N)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5N=C(NC6=O)N)O)O)O)O
Formula
C21 H30 N10 O18 P3
Name
7-METHYL-GUANOSINE-5'-TRIPHOSPHATE-5'-GUANOSINE;
MRNA CAP ANALOG N7-METHYL GPPPG
ChEMBL
DrugBank
DB03958
ZINC
ZINC000085547903
PDB chain
5ynn Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
5ynn
Structural insights into the molecular mechanism of MERS Coronavirus RNA ribose 2'-O-methylation by nsp16/nsp10 protein complex
Resolution
1.86 Å
Binding residue
(original residue number in PDB)
C25 E26 L27 Y30 Y132 P134 K137 T172 E173 H174 S201 S202
Binding residue
(residue number reindexed from 1)
C25 E26 L27 Y30 Y132 P134 K137 T172 E173 H174 S201 S202
Annotation score
2
Enzymatic activity
Enzyme Commision number
2.1.1.57
: methyltransferase cap1.
3.4.19.12
: ubiquitinyl hydrolase 1.
3.6.4.12
: DNA helicase.
3.6.4.13
: RNA helicase.
Gene Ontology
Molecular Function
GO:0004483
mRNA (nucleoside-2'-O-)-methyltransferase activity
View graph for
Molecular Function
External links
PDB
RCSB:5ynn
,
PDBe:5ynn
,
PDBj:5ynn
PDBsum
5ynn
PubMed
UniProt
K0BWD0
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