Structure of PDB 6v11 Chain C Binding Site BS01
Receptor Information
>6v11 Chain C (length=503) Species:
632
(Yersinia pestis) [
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ALKRKIEAAKMPKDAREKTEAELQKLKMMSPMSAEATVVRGYIDWMLQVP
WNSRSKVKKDLVKAQEVLDTDHYGLERVKDRILEYLAVQSRVSKIKGPIL
CLVGPPGVGKTSLGQSIAKATGRQYVRMALGRRTIGSMPGKLIQKMAKVG
VKNPLFLLDEIDKMPASALLEVLDPEQNVAFNDHYLEVDYDLSDVMFVAT
SNSMNIPAPLLDRMEVIRLSGYTEDEKLNIAKQHLLPKQFERNAIKKGEL
TIDDSAIMSIIYYTREAGVRSLEREISKLCRKAVKNLLMDKTVKHIEING
DNLKDFLGVQKVDYGRADTENRVGQVTGLAWTEVGGDLLTIETACVPGKG
KLTYTGSLGEVMQESIQAALTVVRARADKLGINPDFYEKRDIHVHVPEGA
TPKDGPSAGIAMCTALVSCLTGNPVRADVAMTGEITLRGLVLPIGGLKEK
LLAAHRGGIKVVLIPDDNKRDLEEIPDNVIADLEIHPVKRIDDVLAIALE
HPA
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=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)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
6v11 Chain C Residue 800 [
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Receptor-Ligand Complex Structure
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PDB
6v11
Structural basis for distinct operational modes and protease activation in AAA+ protease Lon.
Resolution
3.8 Å
Binding residue
(original residue number in PDB)
D323 H324 G359 V360 G361 K362 T363 S364 V541 R542
Binding residue
(residue number reindexed from 1)
D71 H72 G107 V108 G109 K110 T111 S112 V269 R270
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:6v11
,
PDBe:6v11
,
PDBj:6v11
PDBsum
6v11
PubMed
32490208
UniProt
A0A5P8YJ65
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