Structure of PDB 5ve3 Chain B Binding Site BS01
Receptor Information
>5ve3 Chain B (length=348) Species:
398527
(Paraburkholderia phytofirmans PsJN) [
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GSHMLIFRQLFDQQSSTYTYLLADSTTREAVLIDPVFEQVRRDAALIEEL
GLHLLYTIDTHVHADHVTGAWMLNRRIGSRIAISAASGAEGADRYLSHGD
KVEFGTRYLTVRATPGHTDGCITLVLDNETMAFTGDCLLIRGTGRTDFQR
GDAHTMFRAVHGQIFTLPTACLLYPAHDYRGLTVTSVGEERRFNPRLGGE
LCEEDFTGYMTNLHLPHPKQIDVAVPANLKCGLAEPDWAPLTCSFAGIWE
INAQWLEENLRAVEIVDVREPEEFNGPLGRIPAARLISLGELAGRTAELT
KDRPIVTVCRAGGRSAQATVMLRQAGFERVANLPGGMLRWRAEGRVVE
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
5ve3 Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
5ve3
Structural and biochemical analyses indicate that a bacterial persulfide dioxygenase-rhodanese fusion protein functions in sulfur assimilation.
Resolution
1.793 Å
Binding residue
(original residue number in PDB)
H58 H114 D133
Binding residue
(residue number reindexed from 1)
H61 H117 D136
Annotation score
1
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
PDBsum
5ve3
PubMed
28684420
UniProt
B2TEQ2
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