Structure of PDB 6n8v Chain E Binding Site BS02
Receptor Information
>6n8v Chain E (length=709) Species:
559292
(Saccharomyces cerevisiae S288C) [
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QFTERALTILTLAQKLASDHQHPQLQPIHILAAFIETPEDGSVPYLQNLI
EKGRYDYDLFKKVVNRNLVRIPQQQPAPAEITPSYALGKVLQDAAKIQKQ
QKDSFIAQDHILFALFNDSSIQQIFKEAQVDIEAIKQQALELRGNTRIDS
RGADTEYLSKYAIDMTEQARQGKLDPVIGREEEIRSTIRVLARRIKSNPC
LIGEPGIGKTAIIEGVAQRIIDDDVPTILQGAKLFSLDLAALGDFEERFK
GVLKEIEESKTLIVLFIDEIHMLMGNAANILKPALSRGQLKVIGATTNNE
YRSIVEKDGAFERRFQKIEVAEPSVRQTVAILRGLQPKYEIHHGVRILDS
ALVTAAQLAKRYLPYRRLPDSALDLVDISCAGVAVARDSKPSMIQNVVDS
DTISETAARLTGIPVKKLSESENEKLIHMERDLSSEVVGQMDAIKAVSNA
VRLSRSGLANPRQPASFLFLGLSGSGKTELAKKVAGFLFNDEDMMIRVDC
SELSEKYAVSKLLGTTYDEGGFLTNQLQYKPYSVLLFDEVEKAHPDVLTV
MLQMLDDGRITSGQGKTIDCSNCIVIMTSNLGAEFINSQQGSKIQESTKN
LVMGAVRQHFRPEFLNRISSIVIFNKLSRKAIHKIVDIRLKEIEERFEQN
DKHYKLNLTQEAKDFLAKYGYSDDMGARPLNRLIQNEILNKLALRILKNE
IKDKETVNV
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
6n8v Chain E Residue 902 [
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Receptor-Ligand Complex Structure
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PDB
6n8v
Cryo-EM Structures of the Hsp104 Protein Disaggregase Captured in the ATP Conformation.
Resolution
9.3 Å
Binding residue
(original residue number in PDB)
V580 V581 S616 G617 S618 G619 K620 T621
Binding residue
(residue number reindexed from 1)
V437 V438 S473 G474 S475 G476 K477 T478
Annotation score
5
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0042802
identical protein binding
GO:0043531
ADP binding
GO:0051082
unfolded protein binding
GO:0051087
protein-folding chaperone binding
Biological Process
GO:0006620
post-translational protein targeting to endoplasmic reticulum membrane
GO:0034605
cellular response to heat
GO:0034975
protein folding in endoplasmic reticulum
GO:0035617
stress granule disassembly
GO:0042026
protein refolding
GO:0043335
protein unfolding
GO:0051085
chaperone cofactor-dependent protein refolding
GO:0070370
cellular heat acclimation
GO:0070414
trehalose metabolism in response to heat stress
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0034399
nuclear periphery
GO:0072380
TRC complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6n8v
,
PDBe:6n8v
,
PDBj:6n8v
PDBsum
6n8v
PubMed
30605683
UniProt
P31539
|HS104_YEAST Heat shock protein 104 (Gene Name=HSP104)
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