Structure of PDB 1kh2 Chain A Binding Site BS01
Receptor Information
>1kh2 Chain A (length=380) Species:
274
(Thermus thermophilus) [
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MKIVLAYSGGLDTSIILKWLKETYRAEVIAFTADIGQGEEVEEAREKALR
TGASKAIALDLKEEFVRDFVFPMMRAGAVYEGYYLLGTSIARPLIAKHLV
RIAEEEGAEAIAHGATGKGNDQVRFELTAYALKPDIKVIAPWREWSFQGR
KEMIAYAEAHGIPVPPYSMDANLLHISYEGGVLEDPWAEPPKGMFRMTQD
PEEAPDAPEYVEVEFFEGDPVAVNGERLSPAALLQRLNEIGGRHGVGRVD
IVENRFVGMKSRGVYETPGGTILYHARRAVESLTLDREVLHQRDMLSPKY
AELVYYGFWYAPEREALQAYFDHVARSVTGVARLKLYKGNVYVVGRKAPK
SLYRGYDQKDAEGFIKIQALRLRVRALVER
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=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[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
1kh2 Chain A Residue 510 [
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Receptor-Ligand Complex Structure
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PDB
1kh2
Crystal structure of argininosuccinate synthetase from Thermus thermophilus HB8. Structural basis for the catalytic action.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
A6 S8 G10 D12 T13 A33 I95 G114 F125
Binding residue
(residue number reindexed from 1)
A6 S8 G10 D12 T13 A33 I95 G114 F125
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
D12 R92 D121 S173
Catalytic site (residue number reindexed from 1)
D12 R92 D121 S168
Enzyme Commision number
6.3.4.5
: argininosuccinate synthase.
Gene Ontology
Molecular Function
GO:0004055
argininosuccinate synthase activity
GO:0005524
ATP binding
GO:0016874
ligase activity
Biological Process
GO:0000050
urea cycle
GO:0000053
argininosuccinate metabolic process
GO:0006526
L-arginine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1kh2
,
PDBe:1kh2
,
PDBj:1kh2
PDBsum
1kh2
PubMed
11844799
UniProt
P59846
|ASSY_THET8 Argininosuccinate synthase (Gene Name=argG)
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