Structure of PDB 7fbo Chain B Binding Site BS01
Receptor Information
>7fbo Chain B (length=281) Species:
1507734,1894972
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RIVGQYYDDKTAKLVRKYGPGPRIHYHVGYYPSSEAPRHTRDVTPDAFRR
SIRLHQEGLLRYAAKIWGAEHRLSGRILDVGCGLGGGSLFWAQEYGADVT
AVTNAPEHAPIVEGFARECGVGGRVRTLVCDAMHLPLDGGPYDAAVAIES
SGYFDRPVWFERLAHVLRPGGSVCIEEVFTTRPHGADVWAEYFYTKPATV
LDYAEAAKAAGFELVDDVDATSETLPFWEESTAWTKAVLDSDSTLSAVDR
RQLRISLMANQALGAEWQAGGLRLGFLRFER
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
7fbo Chain B Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
7fbo
Structural and Molecular Basis of the Catalytic Mechanism of Geranyl Pyrophosphate C6-Methyltransferase: Creation of an Unprecedented Farnesyl Pyrophosphate C6-Methyltransferase.
Resolution
2.56 Å
Binding residue
(original residue number in PDB)
Y28 Y47 H48 G102 G104 N125 D152 A153 I169 Y174
Binding residue
(residue number reindexed from 1)
Y7 Y26 H27 G81 G83 N104 D131 A132 I148 Y153
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
Biological Process
GO:0009058
biosynthetic process
GO:0032259
methylation
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:7fbo
,
PDBe:7fbo
,
PDBj:7fbo
PDBsum
7fbo
PubMed
34626048
UniProt
A0A1V4D079
;
A0A2Z5X7B9
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