Structure of PDB 3ta1 Chain C Binding Site BS02
Receptor Information
>3ta1 Chain C (length=103) Species:
224325
(Archaeoglobus fulgidus DSM 4304) [
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MKMVVAVIRPEKLECVKKALEERGFVGMTVTEVKGRGEQKGIEVDLLQKT
KVEVVVSDDAVDEVVEAIVSSARTGKFGDGRIFVIPVEKSVKIRTGDEEV
AAA
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
3ta1 Chain C Residue 119 [
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Receptor-Ligand Complex Structure
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PDB
3ta1
Mechanism of disruption of the Amt-GlnK complex by P(II)-mediated sensing of 2-oxoglutarate.
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
G35 R36 G37 E38 K58 F86 G87 G89 R90
Binding residue
(residue number reindexed from 1)
G35 R36 G37 E38 K49 F77 G78 G80 R81
Annotation score
4
Binding affinity
PDBbind-CN
: -logKd/Ki=3.25,Kd=568uM
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0030234
enzyme regulator activity
Biological Process
GO:0006808
regulation of nitrogen utilization
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3ta1
,
PDBe:3ta1
,
PDBj:3ta1
PDBsum
3ta1
PubMed
22039461
UniProt
O28524
|GLNK3_ARCFU Nitrogen regulatory protein GlnK3 (Gene Name=glnK3)
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