Structure of PDB 6tmw Chain L Binding Site BS01
Receptor Information
>6tmw Chain L (length=545) Species:
273133
(Pseudomonas phage EL) [
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SQTLLVHGKDAQGIIKQVLSEVYDAVTSTMGPNGQLVMIKNGVSTKTTKD
GVTVARSIRFADEAHELVNRVITEPATKTDEECGDGTTTTIMLTHALYHL
FKDFPGFQHHRNIEDLVERVIQRLESMAIRVEVDDPRLYQVALTSSNQDE
KLARLVSELYANNKGSYPDIELKEGVNFEDQIEQTTGRTIRMFYANPWFA
KGHQGGVTELTGFTAFVIDRRIDKEDTQKLIDGVNHLVKTHKQHLALPIL
LIARSFEEAANSTLMQLNAAHPTLVEDGRPWLIPLSTPGTSELQDIAVML
NAPMLSDVADLTKLDTHSINGQHGQLELGGNRSILKSTTPKDEDRIEQHA
RGIEELLEGFSLSDKFSVRARYNERRIRTLRGKLITISVGGETYSEVKER
VDRYEDVVKAIRSALENGILPGGGVSLVKAVFGTIKEGLEDKDQSAEFAK
RYINSGIANELMRLSTIQHKLLFKDTALYKENGSFHFNDDWLNTPTVMNL
ATGEIGTPEGLGIYDTAYASITALKGGLQTAKILATTKTLILGEK
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
6tmw Chain L Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
6tmw
Structure and conformational cycle of a bacteriophage-encoded chaperonin.
Resolution
5.91 Å
Binding residue
(original residue number in PDB)
P33 D86 G87 T89 T90 G429 L478 N505 I519 D521
Binding residue
(residue number reindexed from 1)
P32 D85 G86 T88 T89 G423 L472 N499 I513 D515
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0140662
ATP-dependent protein folding chaperone
Biological Process
GO:0006457
protein folding
GO:0042026
protein refolding
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6tmw
,
PDBe:6tmw
,
PDBj:6tmw
PDBsum
6tmw
PubMed
32339190
UniProt
Q2Z0T5
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