Structure of PDB 3ldp Chain A Binding Site BS01
Receptor Information
>3ldp Chain A (length=381) Species:
9606
(Homo sapiens) [
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DVGTVVGIDLGTTYSCVGVFKNGRVEIIANDQGNRITPSYVAFTPEGERL
IGDAAKNQLTSNPENTVFDAKRLIGRTWNDPSVQQDIKFLPFKVVEKKTK
PYIQVDIGGGQTKTFAPEEISAMVLTKMKETAEAYLGKKVTHAVVTVPAY
FNDAQRQATKDAGTIAGLNVMRIINEPTAAAIAYGLDKREGEKNILVFDL
GGGTFDVSLLTIDNGVFEVVATNGDTHLGGEDFDQRVMEHFIKLYKKKTG
KDVRKDNRAVQKLRREVEKAKRALSSQHQARIEIESFYEGEDFSETLTRA
KFEELNMDLFRSTMKPVQKVLEDSDLKKSDIDEIVLVGGSTRIPKIQQLV
KEFFNGKEPSRGINPDEAVAYGAAVQAGVLS
Ligand information
Ligand ID
3P1
InChI
InChI=1S/C20H21N7O4/c21-17-14-18(24-9-23-17)27(19-16(30)15(29)13(8-28)31-19)20(26-14)22-7-11-6-5-10-3-1-2-4-12(10)25-11/h1-6,9,13,15-16,19,28-30H,7-8H2,(H,22,26)(H2,21,23,24)/t13-,15-,16-,19-/m1/s1
InChIKey
NAHSCHKAPXMNFP-NVQRDWNXSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
c1ccc2c(c1)ccc(n2)CNc3nc4c(ncnc4n3C5C(C(C(O5)CO)O)O)N
CACTVS 3.352
Nc1ncnc2n([CH]3O[CH](CO)[CH](O)[CH]3O)c(NCc4ccc5ccccc5n4)nc12
OpenEye OEToolkits 1.7.0
c1ccc2c(c1)ccc(n2)CNc3nc4c(ncnc4n3[C@H]5[C@@H]([C@@H]([C@H](O5)CO)O)O)N
CACTVS 3.352
Nc1ncnc2n([C@@H]3O[C@H](CO)[C@@H](O)[C@H]3O)c(NCc4ccc5ccccc5n4)nc12
Formula
C20 H21 N7 O4
Name
8-[(quinolin-2-ylmethyl)amino]adenosine
ChEMBL
CHEMBL1614768
DrugBank
ZINC
ZINC000064490880
PDB chain
3ldp Chain A Residue 408 [
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Receptor-Ligand Complex Structure
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PDB
3ldp
Adenosine-Derived Inhibitors of 78 kDa Glucose Regulated Protein (Grp78) ATPase: Insights into Isoform Selectivity.
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
Y39 G227 G255 E293 K296 R297 S300 G364 R367 D391
Binding residue
(residue number reindexed from 1)
Y14 G202 G230 E268 K271 R272 S275 G339 R342 D366
Annotation score
1
Binding affinity
MOAD
: Kd=2.41uM
PDBbind-CN
: -logKd/Ki=5.62,Kd=2.41uM
BindingDB: koff=0.4s-1,Kd=2.41e+3nM
Enzymatic activity
Catalytic site (original residue number in PDB)
D34 K96 E201 D224
Catalytic site (residue number reindexed from 1)
D9 K71 E176 D199
Enzyme Commision number
3.6.4.10
: non-chaperonin molecular chaperone ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0140662
ATP-dependent protein folding chaperone
View graph for
Molecular Function
External links
PDB
RCSB:3ldp
,
PDBe:3ldp
,
PDBj:3ldp
PDBsum
3ldp
PubMed
21526763
UniProt
P11021
|BIP_HUMAN Endoplasmic reticulum chaperone BiP (Gene Name=HSPA5)
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