Structure of PDB 1a5u Chain D Binding Site BS03
Receptor Information
>1a5u Chain D (length=519) Species:
9986
(Oryctolagus cuniculus) [
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IQTQQLHAAMADTFLEHMCRLDIDSAPITARNTGIICTIGPASRSVETLK
EMIKSGMNVARMNFSHGTHEYHAETIKNVRTATESFASDPILYRPVAVAL
DTKGPEIRTGLIKGSGTAEVELKKGATLKITLDNAYMEKCDENILWLDYK
NICKVVDVGSKVYVDDGLISLQVKQKGPDFLVTEVENGGFLGSKKGVNLP
GAAVDLPAVSEKDIQDLKFGVEQDVDMVFASFIRKAADVHEVRKILGEKG
KNIKIISKIENHEGVRRFDEILEASDGIMVARGDLGIEIPAEKVFLAQKM
IIGRCNRAGKPVICATQMLESMIKKPRPTRAEGSDVANAVLDGADCIMLS
GETAKGDYPLEAVRMQHLIAREAEAAMFHRKLFEELARSSSHSTDLMEAM
AMGSVEASYKCLAAALIVLTESGRSAHQVARYRPRAPIIAVTRNHQTARQ
AHLYRGIFPVVCKDPVQEAWAEDVDLRVNLAMNVGKARGFFKKGDVVIVL
TGWRPGSGFTNTMRVVPVP
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
1a5u Chain D Residue 2335 [
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Receptor-Ligand Complex Structure
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PDB
1a5u
Structure of the bis(Mg2+)-ATP-oxalate complex of the rabbit muscle pyruvate kinase at 2.1 A resolution: ATP binding over a barrel.
Resolution
2.35 Å
Binding residue
(original residue number in PDB)
P1852 R1872 N1874 H1877 R1919 K2006 S2161
Binding residue
(residue number reindexed from 1)
P41 R61 N63 H66 R108 K195 S350
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
R1872 R1919 K2069 T2127
Catalytic site (residue number reindexed from 1)
R61 R108 K258 T316
Enzyme Commision number
2.7.10.2
: non-specific protein-tyrosine kinase.
2.7.11.1
: non-specific serine/threonine protein kinase.
2.7.1.40
: pyruvate kinase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003729
mRNA binding
GO:0003824
catalytic activity
GO:0004713
protein tyrosine kinase activity
GO:0004743
pyruvate kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0030955
potassium ion binding
GO:0046872
metal ion binding
Biological Process
GO:0006096
glycolytic process
GO:0006417
regulation of translation
GO:0016310
phosphorylation
GO:0032869
cellular response to insulin stimulus
GO:1903672
positive regulation of sprouting angiogenesis
GO:2000767
positive regulation of cytoplasmic translation
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005791
rough endoplasmic reticulum
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1a5u
,
PDBe:1a5u
,
PDBj:1a5u
PDBsum
1a5u
PubMed
9572839
UniProt
P11974
|KPYM_RABIT Pyruvate kinase PKM (Gene Name=PKM)
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