Structure of PDB 6b04 Chain A Binding Site BS03

Receptor Information
>6b04 Chain A (length=341) Species: 7141 (Choristoneura fumiferana) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
TKKESFEDVLPSILNTITTNSELTEVPEVANWLKKVLEYNLAGGKKARGL
TTLFAYEMLEKPENITEETIYLAKTLGWCVEILQGFLVMLDDIMDGSTTR
RGVPCWYQLPEVGLAAVNDSSLMFSSIFYVLHAHFADKKIYTNLVELFNE
SLMHTSIGQHLDVTMERRQKSDYSLFTIERYNAIVKYKTAYYTYQLPVCL
GMLLANISDPVLHQKAEDMCLEIGKFFQIQDDYIDCYGDESLTGKMGTDI
QEAKCSWLAVMALQRCSASQKIVFTTCYGSKEPAHIERIKELYKQLQLPE
LYAQEETRMYESLIKQAHGLPSELSPALFVRLIHMIYKRNH
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain6b04 Chain A Residue 403 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB6b04 Structural characterization of a lepidopteran type-II farnesyl diphosphate synthase from the spruce budworm, Choristoneura fumiferana: Implications for inhibitor design.
Resolution1.83 Å
Binding residue
(original residue number in PDB)
D147 D151
Binding residue
(residue number reindexed from 1)
D91 D95
Annotation score4
Enzymatic activity
Catalytic site (original residue number in PDB) K101 F142 D147 D151 R156 D218 K244 F283 D287 D288
Catalytic site (residue number reindexed from 1) K45 F86 D91 D95 R100 D162 K188 F227 D231 D232
Enzyme Commision number 2.5.1.-
Gene Ontology
Molecular Function
GO:0004659 prenyltransferase activity
GO:0016765 transferase activity, transferring alkyl or aryl (other than methyl) groups
Biological Process
GO:0008299 isoprenoid biosynthetic process

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Molecular Function

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Biological Process
External links
PDB RCSB:6b04, PDBe:6b04, PDBj:6b04
PDBsum6b04
PubMed29183817
UniProtQ1XAB1

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