Structure of PDB 4u0o Chain B Binding Site BS01

Receptor Information
>4u0o Chain B (length=273) Species: 197221 (Thermosynechococcus vestitus BP-1) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
PSWLRISTVQRLVRQYGIHTICEEGRCPNRGECYGQKTATFLLLGPTCTR
ACAFCQVEKGHAPAAVDPEEPTKIAAAVATLGLRYVVLTSVARDDLPDQG
AGQFVATMAAIRQRCPGTEIEVLSPDFRMDRGRLSQRDCIAQIVAAQPAC
YNHNLETVRRLQGPVRRGATYESSLRVLATVKELNPDIPTKSGLMLGLGE
TEAEIIETLKDLRRVGCDRLTLGQYLPPSLSHLPVVKYWTPEEFNTLGNI
ARELGFSHVRSGPLVRSSYHAAE
Ligand information
Ligand IDSF4
InChIInChI=1S/4Fe.4S
InChIKeyLJBDFODJNLIPKO-UHFFFAOYSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 2.0.7[S]12[Fe]3[S]4[Fe]1[S]5[Fe]2[S]3[Fe]45
CACTVS 3.385S1[Fe]S[Fe]1.S2[Fe]S[Fe]2
FormulaFe4 S4
NameIRON/SULFUR CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain4u0o Chain B Residue 301 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB4u0o Structures of lipoyl synthase reveal a compact active site for controlling sequential sulfur insertion reactions.
Resolution1.6 Å
Binding residue
(original residue number in PDB)
C63 C67 C70
Binding residue
(residue number reindexed from 1)
C48 C52 C55
Annotation score1
Enzymatic activity
Enzyme Commision number 2.8.1.8: lipoyl synthase.
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0016740 transferase activity
GO:0016992 lipoate synthase activity
GO:0046872 metal ion binding
GO:0051536 iron-sulfur cluster binding
GO:0051539 4 iron, 4 sulfur cluster binding
Biological Process
GO:0009107 lipoate biosynthetic process
GO:0009249 protein lipoylation
Cellular Component
GO:0005737 cytoplasm

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:4u0o, PDBe:4u0o, PDBj:4u0o
PDBsum4u0o
PubMed25100160
UniProtQ8DLC2|LIPA2_THEVB Lipoyl synthase 2 (Gene Name=lipA2)

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