Structure of PDB 6qb8 Chain q Binding Site BS01
Receptor Information
>6qb8 Chain q (length=483) Species:
9606
(Homo sapiens) [
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VYRNIQACKELAQTTRTAYGPNGMNKMVINHLEKLFVTNDAATILRELEV
QHPAAKMIVMASHMQEQEVGDGTNFVLVFAGALLELAEELLRIGLSVSEV
IEGYEIACRKAHEILPNLVCCSAKNLRDIDEVSSLLRTSIMSKQYGNEVF
LAKLIAQACVSIFPDSGHFNVDNIRVCKILGSGISSSSVLHGMVFKKETE
GDVTSVKDAKIAVYSCPFAEELMNFSKGEENLMDAQVKAIADTGANVVVT
GGKVADMALHYANKYNIMLVRLNSKWDLRRLCKTVGATALPRLTPPVLEE
MGHCDSVYLSEVGDTQVVVFKHEKEDGAISTIVLRGSTDNLMDDIERAVD
DGVNTFKVLTRDKRLVPGGGATEIELAKQITSYGETCPGLEQYAIKKFAE
AFEAIPRALAENSGVKANEVISKLYAVHQEGNKNVGLDIEAEVPAVKDML
EAGILDTYLGKYWAIKLATNAAVTVLRVDQIIM
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
6qb8 Chain q Residue 5000 [
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Receptor-Ligand Complex Structure
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PDB
6qb8
Structural and functional analysis of the role of the chaperonin CCT in mTOR complex assembly.
Resolution
3.97 Å
Binding residue
(original residue number in PDB)
Y47 P49 D99 G100 M169 S170 K171 G411 G412 I497 D499
Binding residue
(residue number reindexed from 1)
Y19 P21 D71 G72 M141 S142 K143 G368 G369 I454 D456
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
D68 T101 N102 D394
Catalytic site (residue number reindexed from 1)
D40 T73 N74 D351
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0044183
protein folding chaperone
GO:0045296
cadherin binding
GO:0051082
unfolded protein binding
GO:0140662
ATP-dependent protein folding chaperone
Biological Process
GO:0006457
protein folding
GO:0007339
binding of sperm to zona pellucida
GO:0032212
positive regulation of telomere maintenance via telomerase
GO:0050821
protein stabilization
GO:0051086
chaperone mediated protein folding independent of cofactor
GO:0061077
chaperone-mediated protein folding
GO:1904871
positive regulation of protein localization to Cajal body
GO:1904874
positive regulation of telomerase RNA localization to Cajal body
Cellular Component
GO:0002199
zona pellucida receptor complex
GO:0005576
extracellular region
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005813
centrosome
GO:0005829
cytosol
GO:0005832
chaperonin-containing T-complex
GO:0005856
cytoskeleton
GO:0005874
microtubule
GO:0005929
cilium
GO:0034774
secretory granule lumen
GO:0035578
azurophil granule lumen
GO:0044297
cell body
GO:0045111
intermediate filament cytoskeleton
GO:0070062
extracellular exosome
GO:1904813
ficolin-1-rich granule lumen
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6qb8
,
PDBe:6qb8
,
PDBj:6qb8
PDBsum
6qb8
PubMed
31253771
UniProt
P50990
|TCPQ_HUMAN T-complex protein 1 subunit theta (Gene Name=CCT8)
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