Structure of PDB 3zr4 Chain D Binding Site BS01
Receptor Information
>3zr4 Chain D (length=200) Species:
2336
(Thermotoga maritima) [
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MRIGIISVGPGNIMNLYRGVKRASENFEDVSIELVESPRNDLYDLLFIPG
VGHFGEGMRRLRENDLIDFVRKHVEDERYVVGVCLGMQLLFEESEEAPGV
KGLSLIEGNVVKLRSRRLPHMGWNEVIFKDTFPNGYYYFVHTYRAVCEEE
HVLGTTEYDGEIFPSAVRKGRILGFQFHPEKSSKIGRKLLEKVIECSLSR
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
3zr4 Chain D Residue 1205 [
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Receptor-Ligand Complex Structure
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PDB
3zr4
Catalysis Uncoupling in a Glutamine Amidotransferase Bienzyme by Unblocking the Glutaminase Active Site.
Resolution
2.41 Å
Binding residue
(original residue number in PDB)
G52 Q88 E96 H141 T142 Y143
Binding residue
(residue number reindexed from 1)
G52 Q88 E96 H141 T142 Y143
Annotation score
5
Enzymatic activity
Enzyme Commision number
3.5.1.2
: glutaminase.
4.3.2.10
: imidazole glycerol-phosphate synthase.
Gene Ontology
Molecular Function
GO:0000107
imidazoleglycerol-phosphate synthase activity
GO:0004359
glutaminase activity
GO:0005515
protein binding
GO:0016763
pentosyltransferase activity
GO:0016787
hydrolase activity
GO:0016829
lyase activity
Biological Process
GO:0000105
L-histidine biosynthetic process
GO:0006541
glutamine metabolic process
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:3zr4
,
PDBe:3zr4
,
PDBj:3zr4
PDBsum
3zr4
PubMed
23261602
UniProt
Q9X0C8
|HIS5_THEMA Imidazole glycerol phosphate synthase subunit HisH (Gene Name=hisH)
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