Structure of PDB 5kne Chain B Binding Site BS01
Receptor Information
>5kne Chain B (length=711) Species:
4932
(Saccharomyces cerevisiae) [
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QFTERALTILTLAQKLASDHQHPQLQPIHILAAFIETPEDGSVPYLQNLI
EKGRYDYDLFKKVVNRNLVRIPQQQPAPAEITPSYALGKVLQDAAKIQKQ
QKDSFIAQDHILFALFNDSSIQQIFKEAQVDIEAIKQQALELRGNTRIDS
RGADTNTPLEYLSKYAIDMTEQARQGKLDPVIGREEEIRSTIRVLARRIK
SNPCLIGEPGIGKTAIIEGVAQRIIDDDVPTILQGAKLFSLDLAALTGDF
EERFKGVLKEIEESKTLIVLFIDEIHMLMGAANILKPALSRGQLKVIGAT
TNNEYRSIVEKDGAFERRFQKIEVAEPSVRQTVAILRGLQPKYEIHHGVR
ILDSALVTAAQLAKRYLPYRRLPDSALDLVDISCAGVAVARDSSMIQNVV
DSDTISETAARLTGIPVKKLSESENEKLIHMERDLSSEVVGQMDAIKAVS
NAVRLSRSGLANPRQPASFLFLGLSGSGKTELAKKVAGFLFNDEDMMIRV
DCSELSEKYAVSKLLGTTYDEGGFLTNQLQYKPYSVLLFDEVEKAHPDVL
TVMLQMLDDGRITSGQGKTIDCSNCIVIMTSNLGAEFINSQQGSKIQEST
KNLVMGAVRQHFRPEFLNRISSIVIFNKLSRKAIHKIVDIRLKEIEERFE
QNDKHYKLNLTQEAKDFLAKYGYSDDMGARPLNRLIQNEILNKLALRILK
NEIKDKETVNV
Ligand information
Ligand ID
ANP
InChI
InChI=1S/C10H17N6O12P3/c11-8-5-9(13-2-12-8)16(3-14-5)10-7(18)6(17)4(27-10)1-26-31(24,25)28-30(22,23)15-29(19,20)21/h2-4,6-7,10,17-18H,1H2,(H,24,25)(H2,11,12,13)(H4,15,19,20,21,22,23)/t4-,6-,7-,10-/m1/s1
InChIKey
PVKSNHVPLWYQGJ-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(NP(=O)(O)O)O)O)O)N
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)N[P](O)(O)=O)[CH](O)[CH]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(=O)N[P](O)(O)=O)[C@@H](O)[C@H]3O
ACDLabs 12.01
O=P(O)(O)NP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.7.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@@](=O)(NP(=O)(O)O)O)O)O)N
Formula
C10 H17 N6 O12 P3
Name
PHOSPHOAMINOPHOSPHONIC ACID-ADENYLATE ESTER
ChEMBL
CHEMBL1230989
DrugBank
ZINC
ZINC000008660410
PDB chain
5kne Chain B Residue 901 [
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Receptor-Ligand Complex Structure
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PDB
5kne
Spiral architecture of the Hsp104 disaggregase reveals the basis for polypeptide translocation.
Resolution
5.64 Å
Binding residue
(original residue number in PDB)
V186 I187 G215 I216 G217 K218 T219 A220
Binding residue
(residue number reindexed from 1)
V181 I182 G210 I211 G212 K213 T214 A215
Annotation score
3
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:5kne
,
PDBe:5kne
,
PDBj:5kne
PDBsum
5kne
PubMed
27478928
UniProt
P31539
|HS104_YEAST Heat shock protein 104 (Gene Name=HSP104)
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