Structure of PDB 7pxc Chain F Binding Site BS03
Receptor Information
>7pxc Chain F (length=483) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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PPSGYGVLLATHDDDTVDVFTSGRKMRLTCSPNIDAASLKKGQTVRLNEA
LTVVEAGTFEAVGEISTLREILADGHRALVVGHADEERVVWLADPLIPRK
LRPGDSLLVDTKAGYAFERIPKAEVEDLVLEEVPDVSYADIGGLSRQIEQ
IRDAVELPFLHKELYREYSLRPPKGVLLYGPPGCGKTLIAKAVANSLAKK
MAEVRGDDAHEAKSYFLNIKGPELLNKFVGETERHIRLIFQRAREKASEG
TPVIVFFDEMDSIFRTRGTGVSSDVETTVVPQLLSEIDGVEGLENVIVIG
ASNREDMIDPAILRPGRLDVKIKIERPDAEAAQDIYSKYLTEFLPVHADD
LAEFDGDRSACIKAMIEKVVDRMYAEIDDNRFLEVTYANGDKEVMYFKDF
NSGAMIQNVVDRAKKNAIKSVLETGQPGLRIQHLLDSIVDEFAENEDLPN
TTNPDDWARISGKKGERIVYIRTLVTGNLGQYL
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
7pxc Chain F Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
7pxc
Structural basis of prokaryotic ubiquitin-like protein engagement and translocation by the mycobacterial Mpa-proteasome complex.
Resolution
3.84 Å
Binding residue
(original residue number in PDB)
G255 P295 C297 G298 K299 T300 L301 N416 Y452 G516 A517 Q520
Binding residue
(residue number reindexed from 1)
G142 P182 C184 G185 K186 T187 L188 N303 Y339 G403 A404 Q407
Annotation score
5
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
GO:0042802
identical protein binding
GO:0140035
ubiquitin-like protein reader activity
Biological Process
GO:0010498
proteasomal protein catabolic process
GO:0010499
proteasomal ubiquitin-independent protein catabolic process
GO:0019941
modification-dependent protein catabolic process
GO:0030682
symbiont-mediated perturbation of host defenses
GO:0043335
protein unfolding
GO:0051409
response to nitrosative stress
GO:0052164
symbiont defense to host-produced reactive oxygen species
GO:0071732
cellular response to nitric oxide
Cellular Component
GO:0000502
proteasome complex
GO:0005886
plasma membrane
GO:0009274
peptidoglycan-based cell wall
GO:0022623
proteasome-activating nucleotidase complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7pxc
,
PDBe:7pxc
,
PDBj:7pxc
PDBsum
7pxc
PubMed
35022401
UniProt
P9WQN5
|ARC_MYCTU Proteasome-associated ATPase (Gene Name=mpa)
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