Structure of PDB 6v11 Chain E Binding Site BS01
Receptor Information
>6v11 Chain E (length=464) Species:
632
(Yersinia pestis) [
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ALKRKIEAAKMPKDAREKTEAELQKLKMMSPMSAEATVVRGYIDWMLQAQ
EVLDTDHYGLERVKDRILEYLAVQSRVSKIKGPILCLVGPPGVGKTSLGQ
SIAKATGRQYVRMALGPGKLIQKMAKVGVKNPLFLLDEIDKASALLEVLD
PEQSDVMFVATSNSMNIPAPLLDRMEVIRLSGYTEDEKLNIAKQHLLPKQ
FERNAIKKGELTIDDSAIMSIIRYYTREAGVRSLEREISKLCRKAVKNLL
MDKTVKHIEINGDNLKDFLGVQKVDGRADTENRVGQVTGLAWTEVGGDLL
TIETACVPGKGKLTYTGSLGEVMQESIQAALTVVRARADKLGINPDFYEK
RDIHVHVPEGATPKDGPSAGIAMCTALVSCLTGNPVRADVAMTGEITLRG
LVLPIGGLKEKLLAAHRGGIKVVLIPDDNKRDLEEIPDNVIADLEIHPVK
RIDDVLAIALEHPA
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 E 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)
H324 Y325 V360 G361 T363 S364 Y493 I501 V541 R542
Binding residue
(residue number reindexed from 1)
H57 Y58 V93 G94 T96 S97 Y183 I191 V231 R232
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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