Structure of PDB 8xtg Chain E Binding Site BS01
Receptor Information
>8xtg Chain E (length=391) Species:
5074
(Penicillium brevicompactum) [
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SIIQELASAAKQYENNESGAREALIAQSRALIASLEVPSEFIQHTFWSQP
ALSAIVRLATDVNLFQYLKDAQEEGLNAEALASKTGMDVSLFARLARHLV
AMNVITSRNGVFYGTALSNGLAAENYQQSIRFCHDVSRPSFGAFPSFFKG
NGYKTPALGTTDGPFQSAHKVDISFPQWLVGNPPYLQYFNSYMSAYRAGK
PNWCDNGFYPVADRLLNGFDASVSDVLLVDVGGGRGHDIATFGSQFSPLP
GRLVLQDREQVINSIPADESRQFEATTHDIFTTQPVKHARAYYMHSVPHG
FGDEDAVKIMANLVPALAKGYSRVLLNEIVVDEERPVMSATNMDLIMLAH
MGAKERTEADWRSILTRAGLKVVNIYSYPGVAESLIEAELA
Ligand information
Ligand ID
SAH
InChI
InChI=1S/C14H20N6O5S/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6-,7+,9+,10+,13+/m0/s1
InChIKey
ZJUKTBDSGOFHSH-WFMPWKQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
N[CH](CCSC[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23)C(O)=O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)CSCCC(C(=O)O)N)O)O)N
CACTVS 3.341
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23)C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCSCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CSCC[C@@H](C(=O)O)N)O)O)N
Formula
C14 H20 N6 O5 S
Name
S-ADENOSYL-L-HOMOCYSTEINE
ChEMBL
CHEMBL418052
DrugBank
DB01752
ZINC
ZINC000004228232
PDB chain
8xtg Chain E Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
8xtg
Structural basis for substrate flexibility of the O-methyltransferase MpaG' involved in mycophenolic acid biosynthesis.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
M200 Y203 G239 H244 D264 R265 D286 I287 H302 S303
Binding residue
(residue number reindexed from 1)
M193 Y196 G232 H237 D257 R258 D279 I280 H295 S296
Annotation score
5
External links
PDB
RCSB:8xtg
,
PDBe:8xtg
,
PDBj:8xtg
PDBsum
8xtg
PubMed
39150221
UniProt
A0A0B5L781
|MPAG2_PENBR O-methyltransferase mpaG' (Gene Name=mpaG')
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