Structure of PDB 6on2 Chain B Binding Site BS02
Receptor Information
>6on2 Chain B (length=524) Species:
632
(Yersinia pestis) [
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ALKRKIEAAKMPKDAREKTEAELQKLKMMSPMSAEATVVRGYIDWMLQVP
WNSRSKVKKDLVKAQEVLDTDHYGLERVKDRILEYLAVQSRVSKIKGPIL
CLVGPPGVGKTSLGQSIAKATGRQYVRMALGGVRDEAEIRGHRRTYIGSM
PGKLIQKMAKVGVKNPLFLLDQIDKMASDMRGDPASALLEVLDPEQNVAF
NDHYLEVDYDLSDVMFVATSNSMNIPAPLLDRMEVIRLSGYTEDEKLNIA
KQHLLPKQFERNAIKKGELTIDDSAIMSIIRYYTREAGVRSLEREISKLC
RKAVKNLLMDKTVKHIEINGDNLKDFLGVQKVDYGRADTENRVGQVTGLA
WTEVGGDLLTIETACVPGKGKLTYTGSLGEVMQESIQAALTVVRARADKL
GINPDFYEKRDIHVHVPEGATPKDGPSAGIAMCTALVSCLTGNPVRADVA
MTGEITLRGLVLPIGGLKEKLLAAHRGGIKVVLIPDDNKRDLEEIPDNVI
ADLEIHPVKRIDDVLAIALEHPAF
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
6on2 Chain B Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
6on2
Structural basis for distinct operational modes and protease activation in AAA+ protease Lon.
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
H324 Y325 P358 G359 V360 G361 K362 T363 S364 Y493 I501 H505 K509 R542
Binding residue
(residue number reindexed from 1)
H72 Y73 P106 G107 V108 G109 K110 T111 S112 Y241 I249 H253 K257 R290
Annotation score
5
Enzymatic activity
Enzyme Commision number
3.4.21.53
: endopeptidase La.
Gene Ontology
Molecular Function
GO:0004176
ATP-dependent peptidase activity
GO:0004252
serine-type endopeptidase activity
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
Biological Process
GO:0006508
proteolysis
GO:0030163
protein catabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:6on2
,
PDBe:6on2
,
PDBj:6on2
PDBsum
6on2
PubMed
32490208
UniProt
A0A5P8YJ65
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