Structure of PDB 6zjb Chain A Binding Site BS01
Receptor Information
>6zjb Chain A (length=217) Species:
9606
(Homo sapiens) [
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SARLLRAVIMGAPGSGKGTVSSRITTHFELKHLSSGDLLRDNMLRGTEIG
VLAKAFIDQGKLIPDDVMTRLALHELKNLTQYSWLLDGFPRTLPQAEALD
RAYQIDTVINLNVPFEVIKQRLTARWIHPASGRVYNIEFNPPKTVGIDDL
TGEPLIQREDDKPETVIKRLKAYEDQTKPVLEYYQKKGVLETFSGTETNK
IWPYVYAFLQTKVPQRS
Ligand information
Ligand ID
G5P
InChI
InChI=1S/C20H29N10O23P5/c21-14-8-15(24-3-23-14)29(4-25-8)18-12(33)10(31)6(48-18)1-46-54(36,37)50-56(40,41)52-58(44,45)53-57(42,43)51-55(38,39)47-2-7-11(32)13(34)19(49-7)30-5-26-9-16(30)27-20(22)28-17(9)35/h3-7,10-13,18-19,31-34H,1-2H2,(H,36,37)(H,38,39)(H,40,41)(H,42,43)(H,44,45)(H2,21,23,24)(H3,22,27,28,35)/t6-,7-,10-,11-,12-,13-,18-,19-/m1/s1
InChIKey
CNMILLPGDWDFCZ-INFSMZHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[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
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)O[P@@](=O)(O)O[P@@](=O)(O)O[P@@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5N=C(NC6=O)N)O)O)O)O)N
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)n5cnc6c5N=C(NC6=O)N)O)O)O)O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[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
Formula
C20 H29 N10 O23 P5
Name
P1-(5'-ADENOSYL)-P5-(5'-GUANOSYL) PENTAPHOSPHATE
ChEMBL
DrugBank
ZINC
ZINC000261495500
PDB chain
6zjb Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
6zjb
Structural Basis for GTP versus ATP Selectivity in the NMP Kinase AK3.
Resolution
1.822 Å
Binding residue
(original residue number in PDB)
P16 G17 G19 K20 G21 T22 S38 I60 K64 L65 I66 M71 G91 R94 Q98 R124 R128 V137 N139 F142 R161 R172 E200 T201
Binding residue
(residue number reindexed from 1)
P13 G14 G16 K17 G18 T19 S35 I57 K61 L62 I63 M68 G88 R91 Q95 R121 R125 V134 N136 F139 R158 R169 E197 T198
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
K20 R94 R128 R161 R172
Catalytic site (residue number reindexed from 1)
K17 R91 R125 R158 R169
Enzyme Commision number
2.7.4.10
: nucleoside-triphosphate--adenylate kinase.
Gene Ontology
Molecular Function
GO:0004017
adenylate kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0005525
GTP binding
GO:0016301
kinase activity
GO:0016776
phosphotransferase activity, phosphate group as acceptor
GO:0016874
ligase activity
GO:0019205
nucleobase-containing compound kinase activity
GO:0046899
nucleoside triphosphate adenylate kinase activity
Biological Process
GO:0006139
nucleobase-containing compound metabolic process
GO:0006172
ADP biosynthetic process
GO:0007596
blood coagulation
GO:0009117
nucleotide metabolic process
GO:0009123
nucleoside monophosphate metabolic process
GO:0009142
nucleoside triphosphate biosynthetic process
GO:0016310
phosphorylation
GO:0046033
AMP metabolic process
GO:0046039
GTP metabolic process
GO:0046041
ITP metabolic process
GO:0046051
UTP metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0043231
intracellular membrane-bounded organelle
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6zjb
,
PDBe:6zjb
,
PDBj:6zjb
PDBsum
6zjb
PubMed
32822537
UniProt
Q9UIJ7
|KAD3_HUMAN GTP:AMP phosphotransferase AK3, mitochondrial (Gene Name=AK3)
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