Structure of PDB 8blf Chain F Binding Site BS01
Receptor Information
>8blf Chain F (length=525) Species:
562
(Escherichia coli) [
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AAKDVKFGNDARVKMLRGVNVLADAVKVTLGPKGRNVVLDKSFGAPTITK
DGVSVAREIELEDKFENMGAQMVKEVASKANDAAGDGTTTATVLAQAIIT
EGLKAVAAGMNPMDLKRGIDKAVTAAVEELKALSVPCSDSKAIAQVGTIS
ANSDETVGKLIAEAMDKVGKEGVITVEDGTGLQDELDVVEGMQFDRGYLS
PYFINKPETGAVELESPFILLADKKISNIREMLPVLEAVAKAGKPLLIIA
EDVEGEALATLVVNTMRGIVKVAAVKAPGFGDRRKAMLQDIATLTGGTVI
SEEIGMELEKATLEDLGQAKRVVINKDTTTIIDGVGEEAAIQGRVAQIRQ
QIEEATSDYDREKLQERVAKLAGGVAVIKVGAATEVEMKEKKARVEDALH
ATRAAVEEGVVAGGGVALIRVASKLADLRGQNEDQNVGIKVALRAMEAPL
RQIVLNCGEEPSVVANTVKGGDGNYGYNAATEEYGNMIDMGILDPTKVTR
SALQYAASVAGLMITTECMVTDLPK
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
8blf Chain F Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
8blf
Time-resolved cryo-EM using a combination of droplet microfluidics with on-demand jetting.
Resolution
3.9 Å
Binding residue
(original residue number in PDB)
G32 P33 G53 D87 G88 T89 T90 T91 G414 G415 I454 A480 A481 I493 D495
Binding residue
(residue number reindexed from 1)
G31 P32 G52 D86 G87 T88 T89 T90 G413 G414 I453 A479 A480 I492 D494
Annotation score
5
Enzymatic activity
Enzyme Commision number
5.6.1.7
: chaperonin ATPase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016853
isomerase activity
GO:0016887
ATP hydrolysis activity
GO:0042802
identical protein binding
GO:0051082
unfolded protein binding
GO:0140662
ATP-dependent protein folding chaperone
Biological Process
GO:0006457
protein folding
GO:0009314
response to radiation
GO:0009408
response to heat
GO:0019068
virion assembly
GO:0042026
protein refolding
GO:0051085
chaperone cofactor-dependent protein refolding
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0016020
membrane
GO:1990220
GroEL-GroES complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8blf
,
PDBe:8blf
,
PDBj:8blf
PDBsum
8blf
PubMed
37592181
UniProt
P0A6F5
|CH60_ECOLI Chaperonin GroEL (Gene Name=groEL)
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