Structure of PDB 7uiy Chain F Binding Site BS01
Receptor Information
>7uiy Chain F (length=575) Species:
562
(Escherichia coli) [
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ENFTTNLNQLARVGGIDPLIGREKELERAIQVLCRRRKNNPLLVGESGVG
KTAIAEGLAWRIVQGDVPEVMADCTIYSLDIGSLLAGTKYRGDFEKRFKA
LLKQLEQDTNSILFIDEIHTIIGAGAAVDAANLIKPLLSSGKIRVIGSTT
YQEFSNIFEKDRALARRFQKIDITEPSIEETVQIINGLKPKYEAHHDVRY
TAKAVRAAVELAVKYINDRHLPDKAIDVIDEAGARARLMPVSKRKKTVNV
ADIESVVARIARIPEKSVSQSDRDTLKNLGDRLKMLVFGQDKAIEALTEA
IKMARAGLGHEHKPVGSFLFAGPTGVGKTEVTVQLSKALGIELLRFDMSE
YMERHTVSRLIGAPPGYVGFDQGGLLTDAVIKHPHAVLLLDEIEKAHPDV
FNILLQVMDNGTLTDNNGRKADFRNVVLVMTTNAGVRETERKSIGLIHQD
NSTDAMEEIKKIFTPEFRNRLDNIIWFDHLSTDVIHQVVDKFIVELQVQL
DQKGVSLEVSQEARNWLAEKGYDRAMGARPMARVIQDNLKKPLANELLFG
SLVDGGQVTVALDKEKNELTYGFQS
Ligand information
Ligand ID
AGS
InChI
InChI=1S/C10H16N5O12P3S/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(25-10)1-24-28(18,19)26-29(20,21)27-30(22,23)31/h2-4,6-7,10,16-17H,1H2,(H,18,19)(H,20,21)(H2,11,12,13)(H2,22,23,31)/t4-,6-,7-,10-/m1/s1
InChIKey
NLTUCYMLOPLUHL-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=S)(O)O)O)O)N
CACTVS 3.370
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=S)[C@@H](O)[C@H]3O
CACTVS 3.370
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=S)[CH](O)[CH]3O
OpenEye OEToolkits 1.7.6
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)OP(=O)(O)OP(=S)(O)O)O)O)N
ACDLabs 12.01
O=P(O)(OP(=S)(O)O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C10 H16 N5 O12 P3 S
Name
PHOSPHOTHIOPHOSPHORIC ACID-ADENYLATE ESTER;
ATP-GAMMA-S;
ADENOSINE 5'-(3-THIOTRIPHOSPHATE);
ADENOSINE 5'-(GAMMA-THIOTRIPHOSPHATE);
ADENOSINE-5'-DIPHOSPHATE MONOTHIOPHOSPHATE
ChEMBL
CHEMBL131890
DrugBank
DB02930
ZINC
ZINC000008295128
PDB chain
7uiy Chain F Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
7uiy
AAA+ protease-adaptor structures reveal altered conformations and ring specialization.
Resolution
3.22 Å
Binding residue
(original residue number in PDB)
D186 L188 S216 G217 V218 G219 K220 T221 I399
Binding residue
(residue number reindexed from 1)
D17 L19 S47 G48 V49 G50 K51 T52 I226
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0004176
ATP-dependent peptidase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
Biological Process
GO:0006508
proteolysis
GO:0006515
protein quality control for misfolded or incompletely synthesized proteins
GO:0006979
response to oxidative stress
GO:0034605
cellular response to heat
GO:0043335
protein unfolding
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0009368
endopeptidase Clp complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7uiy
,
PDBe:7uiy
,
PDBj:7uiy
PDBsum
7uiy
PubMed
36329286
UniProt
P0ABH9
|CLPA_ECOLI ATP-dependent Clp protease ATP-binding subunit ClpA (Gene Name=clpA)
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