Structure of PDB 8wuw Chain K Binding Site BS01
Receptor Information
>8wuw Chain K (length=529) Species:
608538
(Hydrogenobacter thermophilus TK-6) [
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AAKKVIYGEDARARLKAGVDKLANAVKVTLGPRGREVIIEKKWGTPVVTK
DGVTVAKEIEFKDPYENMGAQLVKEVASKTSDVAGDGTTTATVLAQAIFN
EGLRAIASGANPMDIKRGIDKAVETVVNEIKKLSIPVSGRKEIEQVATIS
ANNDATIGKIIADAMEAVGKDGVITVEESKSAETTLETVQGMQFDRGYLS
PYFVTNPDKMEAVLEDPFILIYEKKISNVKDLLPVLENVVRAGKPLLIIA
EDVEAEALATLVVNHIKGVIRACAVKAPGFGQRRKDYLQDIAILTGGTAI
TEELGIKLESVTLDMLGRADKVIVDKDNTTIVGGKGSKEAIQARIEQIKR
QILETTSDYDREKLQERLAKLSGGVAIIRVGAATEAELKEKKARVEDAVH
ATKAAVEEGIVPGGGVALVRASEALDNLKVDNADQQLGIDIIKKACRTPI
RQIAANSGFEGYVVLEKVLQLGKEKGKNWGFDAGVGDYKDMVEAGIIDPT
KVVRVAIQNAASVAGTMLTAEALVAEIPE
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
8wuw Chain K Residue 603 [
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Receptor-Ligand Complex Structure
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PDB
8wuw
Structural insights into thermophilic chaperonin complexes.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
L31 G32 P33 V54 D87 G88 T89 T90 T91 G414 G415 D483 A484 I497 D499
Binding residue
(residue number reindexed from 1)
L30 G31 P32 V53 D86 G87 T88 T89 T90 G413 G414 D482 A483 I496 D498
Annotation score
4
Enzymatic activity
Enzyme Commision number
5.6.1.7
: chaperonin ATPase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016853
isomerase activity
GO:0051082
unfolded protein binding
GO:0140662
ATP-dependent protein folding chaperone
Biological Process
GO:0006457
protein folding
GO:0009408
response to heat
GO:0042026
protein refolding
GO:0051085
chaperone cofactor-dependent protein refolding
Cellular Component
GO:0005737
cytoplasm
GO:1990220
GroEL-GroES complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8wuw
,
PDBe:8wuw
,
PDBj:8wuw
PDBsum
8wuw
PubMed
38492570
UniProt
D3DK86
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