Structure of PDB 6bxn Chain B Binding Site BS01
Receptor Information
>6bxn Chain B (length=316) Species:
1392998
(Candidatus Methanoperedens nitroreducens) [
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DLERILKTIKDKNCKKVGLQFPEGLKRQAINIAREIEEKTRANVIISGNP
CFGACDIDTILAGSVDILFHFGHAGMGEYENVVFIEARSNIDIIPAVKTA
LNLLKANRIGLITTVQHVHKLEEACKVIKEYGKECVIGKGDPRAIYPGQV
LGCNFTAARVDCEEFIYIGSGIFHPLGVAIATKKRVIAADPFLNQAVEVS
PERFLRKRGGYIAKATGAKIFGIIVSTKSGQYRMKLAQKLKEIADKHGKI
GYIILMDLVTPEQLLAFKADAYVNTACPRITIDDAERFHAPVLTPQEFEI
VLGERRWENMEMDEMI
Ligand information
Ligand ID
SF4
InChI
InChI=1S/4Fe.4S
InChIKey
LJBDFODJNLIPKO-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
[S]12[Fe]3[S]4[Fe]1[S]5[Fe]2[S]3[Fe]45
CACTVS 3.385
S1[Fe]S[Fe]1.S2[Fe]S[Fe]2
Formula
Fe4 S4
Name
IRON/SULFUR CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
6bxn Chain B Residue 900 [
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Receptor-Ligand Complex Structure
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PDB
6bxn
Organometallic and radical intermediates reveal mechanism of diphthamide biosynthesis.
Resolution
2.079 Å
Binding residue
(original residue number in PDB)
C61 R149 G158 C159 C283
Binding residue
(residue number reindexed from 1)
C55 R143 G152 C153 C277
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.5.1.108
: 2-(3-amino-3-carboxypropyl)histidine synthase.
Gene Ontology
Molecular Function
GO:0016740
transferase activity
GO:0046872
metal ion binding
GO:0051539
4 iron, 4 sulfur cluster binding
GO:0090560
2-(3-amino-3-carboxypropyl)histidine synthase activity
Biological Process
GO:0017183
protein histidyl modification to diphthamide
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6bxn
,
PDBe:6bxn
,
PDBj:6bxn
PDBsum
6bxn
PubMed
29590073
UniProt
A0A062UZ78
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