Structure of PDB 4zfk Chain B Binding Site BS01
Receptor Information
>4zfk Chain B (length=231) Species:
246196
(Mycolicibacterium smegmatis MC2 155) [
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CRHVAWLGAPRSLADLVLDPPQGLLVQSYAPRRQKHGLMNADGWGAGFFD
DDGVARRWRSDKPLWGDASFASVAPALRSRCVVAAVRSATIGMPIEPSAS
APFSDGQWLLSHNGLVDRGVLPLTGAAESTVDSAILAALIFSRGLDALGA
TIAEVGELDPNARLNILAANGSRLLATTWGDTLSVLRRPDGVVLASEPYD
DDPGWSDIPDRHLVDVRDAHVVVTPLLEHHH
Ligand information
Ligand ID
GLN
InChI
InChI=1S/C5H10N2O3/c6-3(5(9)10)1-2-4(7)8/h3H,1-2,6H2,(H2,7,8)(H,9,10)/t3-/m0/s1
InChIKey
ZDXPYRJPNDTMRX-VKHMYHEASA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(CC(=O)N)C(C(=O)O)N
OpenEye OEToolkits 1.5.0
C(CC(=O)N)[C@@H](C(=O)O)N
ACDLabs 10.04
O=C(N)CCC(N)C(=O)O
CACTVS 3.341
N[CH](CCC(N)=O)C(O)=O
CACTVS 3.341
N[C@@H](CCC(N)=O)C(O)=O
Formula
C5 H10 N2 O3
Name
GLUTAMINE
ChEMBL
CHEMBL930
DrugBank
DB00130
ZINC
ZINC000001532526
PDB chain
4zfk Chain B Residue 311 [
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Receptor-Ligand Complex Structure
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PDB
4zfk
Structure of the Ergothioneine-Biosynthesis Amidohydrolase EgtC.
Resolution
1.82 Å
Binding residue
(original residue number in PDB)
C2 R88 S89 T91 N114 G115 V132 D133
Binding residue
(residue number reindexed from 1)
C1 R87 S88 T90 N113 G114 V131 D132
Annotation score
2
Enzymatic activity
Enzyme Commision number
3.5.1.118
: gamma-glutamyl hercynylcysteine S-oxide hydrolase.
Gene Ontology
Molecular Function
GO:0016787
hydrolase activity
GO:0016811
hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides
Biological Process
GO:0006541
glutamine metabolic process
GO:0052699
ergothioneine biosynthetic process
GO:0052704
ergothioneine biosynthesis from histidine via gamma-glutamyl-hercynylcysteine sulfoxide
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Molecular Function
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Biological Process
External links
PDB
RCSB:4zfk
,
PDBe:4zfk
,
PDBj:4zfk
PDBsum
4zfk
PubMed
26079795
UniProt
A0R5M9
|EGTC_MYCS2 Gamma-glutamyl-hercynylcysteine sulfoxide hydrolase (Gene Name=egtC)
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