Structure of PDB 5ve3 Chain B Binding Site BS01

Receptor Information
>5ve3 Chain B (length=348) Species: 398527 (Paraburkholderia phytofirmans PsJN) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GSHMLIFRQLFDQQSSTYTYLLADSTTREAVLIDPVFEQVRRDAALIEEL
GLHLLYTIDTHVHADHVTGAWMLNRRIGSRIAISAASGAEGADRYLSHGD
KVEFGTRYLTVRATPGHTDGCITLVLDNETMAFTGDCLLIRGTGRTDFQR
GDAHTMFRAVHGQIFTLPTACLLYPAHDYRGLTVTSVGEERRFNPRLGGE
LCEEDFTGYMTNLHLPHPKQIDVAVPANLKCGLAEPDWAPLTCSFAGIWE
INAQWLEENLRAVEIVDVREPEEFNGPLGRIPAARLISLGELAGRTAELT
KDRPIVTVCRAGGRSAQATVMLRQAGFERVANLPGGMLRWRAEGRVVE
Ligand information
Ligand IDFE
InChIInChI=1S/Fe/q+3
InChIKeyVTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
FormulaFe
NameFE (III) ION
ChEMBL
DrugBankDB13949
ZINC
PDB chain5ve3 Chain B Residue 500 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB5ve3 Structural and biochemical analyses indicate that a bacterial persulfide dioxygenase-rhodanese fusion protein functions in sulfur assimilation.
Resolution1.793 Å
Binding residue
(original residue number in PDB)
H58 H114 D133
Binding residue
(residue number reindexed from 1)
H61 H117 D136
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) R25 H58 H60 D62 H63 H114 D133 H174
Catalytic site (residue number reindexed from 1) R28 H61 H63 D65 H66 H117 D136 H177
Enzyme Commision number '1.13.11.18
2.8.1.1'
Gene Ontology
Molecular Function
GO:0046872 metal ion binding
GO:0050313 sulfur dioxygenase activity
Biological Process
GO:0006749 glutathione metabolic process
GO:0070813 hydrogen sulfide metabolic process

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Molecular Function

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Biological Process
External links
PDB RCSB:5ve3, PDBe:5ve3, PDBj:5ve3
PDBsum5ve3
PubMed28684420
UniProtB2TEQ2

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