Structure of PDB 1z83 Chain C Binding Site BS03
Receptor Information
>1z83 Chain C (length=195) Species:
9606
(Homo sapiens) [
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SMEEKLKKTNIIFVVGGPGSGKGTQCEKIVQKYGYTHLSTGDLLRSEVSS
GSARGKKLSEIMEKGQLVPLETVLDMLRDAMVAKVNTSKGFLIDGYPREV
QQGEEFERRIGQPTLLLYVDAGPETMTQRLLKRGETSGRVDDNEETIKKR
LETYYKATEPVIAFYEKRGIVRKVNAEGSVDSVFSQVCTHLDALL
Ligand information
Ligand ID
AP5
InChI
InChI=1S/C20H29N10O22P5/c21-15-9-17(25-3-23-15)29(5-27-9)19-13(33)11(31)7(47-19)1-45-53(35,36)49-55(39,40)51-57(43,44)52-56(41,42)50-54(37,38)46-2-8-12(32)14(34)20(48-8)30-6-28-10-16(22)24-4-26-18(10)30/h3-8,11-14,19-20,31-34H,1-2H2,(H,35,36)(H,37,38)(H,39,40)(H,41,42)(H,43,44)(H2,21,23,25)(H2,22,24,26)/t7-,8-,11-,12-,13-,14-,19-,20-/m1/s1
InChIKey
OIMACDRJUANHTJ-XPWFQUROSA-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)OP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)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[P@](O)(=O)O[P@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)[C@@H](O)[C@H]3O
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[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)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[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)[CH](O)[CH]3O
Formula
C20 H29 N10 O22 P5
Name
BIS(ADENOSINE)-5'-PENTAPHOSPHATE
ChEMBL
CHEMBL437508
DrugBank
DB01717
ZINC
ZINC000096085195
PDB chain
1z83 Chain C Residue 633 [
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Receptor-Ligand Complex Structure
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PDB
1z83
Crystal structure of human AK1A in complex with AP5A
Resolution
1.9 Å
Binding residue
(original residue number in PDB)
P17 G18 S19 G20 K21 G22 T23 T39 G40 L43 R44 M61 Q65 L66 V67 G94 R97 Q101 R128 R132 R138 R149 G177
Binding residue
(residue number reindexed from 1)
P18 G19 S20 G21 K22 G23 T24 T40 G41 L44 R45 M62 Q66 L67 V68 G95 R98 Q102 R129 R133 R139 R150 G178
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
K21 R97 R132 R138 R149
Catalytic site (residue number reindexed from 1)
K22 R98 R133 R139 R150
Enzyme Commision number
2.7.4.10
: nucleoside-triphosphate--adenylate kinase.
2.7.4.3
: adenylate kinase.
2.7.4.6
: nucleoside-diphosphate kinase.
Gene Ontology
Molecular Function
GO:0004017
adenylate kinase activity
GO:0004550
nucleoside diphosphate kinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0019205
nucleobase-containing compound kinase activity
GO:0047506
(deoxy)adenylate kinase activity
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0006172
ADP biosynthetic process
GO:0009142
nucleoside triphosphate biosynthetic process
GO:0015949
nucleobase-containing small molecule interconversion
GO:0016310
phosphorylation
GO:0046033
AMP metabolic process
GO:0046034
ATP metabolic process
GO:0046940
nucleoside monophosphate phosphorylation
Cellular Component
GO:0001520
outer dense fiber
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0036126
sperm flagellum
GO:0070062
extracellular exosome
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1z83
,
PDBe:1z83
,
PDBj:1z83
PDBsum
1z83
PubMed
UniProt
P00568
|KAD1_HUMAN Adenylate kinase isoenzyme 1 (Gene Name=AK1)
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