Structure of PDB 5w74 Chain D Binding Site BS01
Receptor Information
>5w74 Chain D (length=477) Species:
39152
(Methanococcus maripaludis) [
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DAQRMNILAGRIIAETVRSTLGPKGMDKMLVDDLGDVVVTNDGVTILREM
SVEHPAAKMLIEVAKTQEKEVGDGTTTAVVVAGELLRKAEELLDQNVHPT
IVVKGYQAAAQKAQELLKTIACEVGAQDKEILTKIAMTSITGKGAEKAKE
KLAEIIVEAVSAVVDDEGKVDKDLIKIEKKSGASIDDTELIKGVLVDKER
VSAQMPKKVTDAKIALLNCAIEMLKDMVAEIKASGANVLFCQKGIDDLAQ
HYLAKEGIVAARRVKKSDMEKLAKATGANVITNIKDLSAQDLGDAGLVEE
RKISGDSMIFVEECKHPKAVTMLIRGTTEHVIEEVARAVDAAVGVVGCTI
EDGRIVSGGGSTEVELSMKLREYAEGISGREQLAVRAFADALEVIPRTLA
ENAGLDAIEILVKVRAAHASNGNKCAGLNVFTGAVEDMCENGVVEPLRVK
TQAIQSAAESTEMLLRIDDVIAAEKLR
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
5w74 Chain D Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
5w74
The Conformational Cycle of the Group II Chaperonin Termini
Resolution
3.65 Å
Binding residue
(original residue number in PDB)
L39 G40 P41 D91 G92 T94 T95 T156 G160 G404 E490
Binding residue
(residue number reindexed from 1)
L21 G22 P23 D73 G74 T76 T77 T138 G142 G359 E445
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
D60 T93 T94 A386
Catalytic site (residue number reindexed from 1)
D42 T75 T76 A341
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0051082
unfolded protein binding
GO:0140662
ATP-dependent protein folding chaperone
Biological Process
GO:0006457
protein folding
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5w74
,
PDBe:5w74
,
PDBj:5w74
PDBsum
5w74
PubMed
UniProt
Q877G8
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