Structure of PDB 1zak Chain A Binding Site BS01
Receptor Information
>1zak Chain A (length=220) Species:
4577
(Zea mays) [
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ADPLKVMISGAPASGKGTQCELIKTKYQLAHISAGDLLRAEIAAGSENGK
RAKEFMEKGQLVPDEIVVNMVKERLRQPDAQENGWLLDGYPRSYSQAMAL
ETLEIRPDTFILLDVPDELLVERVVGRRLDPVTGKIYHLKYSPPENEEIA
SRLTQRFDDTEEKVKLRLETYYQNIESLLSTYENIIVKVQGDATVDAVFA
KIDELLGSILEKKNEMVSST
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
1zak Chain A Residue 223 [
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Receptor-Ligand Complex Structure
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PDB
1zak
Structure, catalysis and supramolecular assembly of adenylate kinase from maize.
Resolution
3.5 Å
Binding residue
(original residue number in PDB)
P14 A15 S16 G17 K18 G19 T20 L40 R41 M58 Q62 V64 G91 R94 Q98 R125 R129 I138 H140 Y143 R158 A195 V197
Binding residue
(residue number reindexed from 1)
P12 A13 S14 G15 K16 G17 T18 L38 R39 M56 Q60 V62 G89 R92 Q96 R123 R127 I136 H138 Y141 R156 A193 V195
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
K18 R94 R129 R158 R169
Catalytic site (residue number reindexed from 1)
K16 R92 R127 R156 R167
Enzyme Commision number
2.7.4.3
: adenylate kinase.
Gene Ontology
Molecular Function
GO:0004017
adenylate kinase activity
GO:0004127
(d)CMP kinase activity
GO:0004550
nucleoside diphosphate kinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016776
phosphotransferase activity, phosphate group as acceptor
GO:0019205
nucleobase-containing compound kinase activity
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0016310
phosphorylation
GO:0046940
nucleoside monophosphate phosphorylation
Cellular Component
GO:0005737
cytoplasm
GO:0009507
chloroplast
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1zak
,
PDBe:1zak
,
PDBj:1zak
PDBsum
1zak
PubMed
9428681
UniProt
P43188
|KADC_MAIZE Adenylate kinase, chloroplastic (Gene Name=ADK1)
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