Structure of PDB 6ht7 Chain N Binding Site BS01
Receptor Information
>6ht7 Chain N (length=528) Species:
9606
(Homo sapiens) [
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GSAKDVKFGADARALMLQGVDLLADAVAVTMGPKGRTVIIEQSWGSPKVT
KDGVTVAKSIDLKDKYKNIGAKLVQDVANNTNEEAGDGTTTATVLARSIA
KEGFEKISKGANPVEIRRGVMLAVDAVIAELKKQSKPVTTPEEIAQVATI
SANGDKEIGNIISDAMKKVGRKGVITVKDGKTLNDELEIIEGMKFDRGYI
SPYFINTSKGQKCEFQDAYVLLSEKKISSIQSIVPALEIANAHRKPLVII
AEDVDGEALSTLVLNRLKVGLQVVAVKAPGFGDNRKNQLKDMAIATGGAV
FGEEGLTLNLEDVQPHDLGKVGEVIVTKDDAMLLKGKGDKAQIEKRIQEI
IEQLDVTTSEYEKEKLNERLAKLSDGVAVLKVGGTSDVEVNEKKDRVTDA
LNATRAAVEEGIVLGGGCALLRCIPALDSLTPANEDQKIGIEIIKRTLKI
PAMTIAKNAGVEGSLIVEKIMQSSSEVGYDAMAGDFVNMVEKGIIDPTKV
VRTALLDAAGVASLLTTAEVVVTEIPKE
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
6ht7 Chain N Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
6ht7
Crystal structure of the WT human mitochondrial football Hsp60-Hsp10(ADPBeFx)14 complex
Resolution
3.7 Å
Binding residue
(original residue number in PDB)
T30 P33 D87 G415 G416 A481 I494 D496
Binding residue
(residue number reindexed from 1)
T30 P33 D87 G415 G416 A481 I494 D496
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
D52 T89 T90 D399
Catalytic site (residue number reindexed from 1)
D52 T89 T90 D399
Enzyme Commision number
5.6.1.7
: chaperonin ATPase.
Gene Ontology
Molecular Function
GO:0001530
lipopolysaccharide binding
GO:0002039
p53 binding
GO:0003688
DNA replication origin binding
GO:0003697
single-stranded DNA binding
GO:0003723
RNA binding
GO:0003725
double-stranded RNA binding
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0008035
high-density lipoprotein particle binding
GO:0016853
isomerase activity
GO:0016887
ATP hydrolysis activity
GO:0019899
enzyme binding
GO:0031625
ubiquitin protein ligase binding
GO:0034185
apolipoprotein binding
GO:0034186
apolipoprotein A-I binding
GO:0051082
unfolded protein binding
GO:0051087
protein-folding chaperone binding
GO:0140662
ATP-dependent protein folding chaperone
Biological Process
GO:0002755
MyD88-dependent toll-like receptor signaling pathway
GO:0002842
positive regulation of T cell mediated immune response to tumor cell
GO:0006457
protein folding
GO:0006458
'de novo' protein folding
GO:0006919
activation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0006986
response to unfolded protein
GO:0008637
apoptotic mitochondrial changes
GO:0009409
response to cold
GO:0032727
positive regulation of interferon-alpha production
GO:0032729
positive regulation of type II interferon production
GO:0032733
positive regulation of interleukin-10 production
GO:0032735
positive regulation of interleukin-12 production
GO:0032755
positive regulation of interleukin-6 production
GO:0034514
mitochondrial unfolded protein response
GO:0042026
protein refolding
GO:0042100
B cell proliferation
GO:0042110
T cell activation
GO:0042113
B cell activation
GO:0043032
positive regulation of macrophage activation
GO:0043065
positive regulation of apoptotic process
GO:0043066
negative regulation of apoptotic process
GO:0044406
adhesion of symbiont to host
GO:0045041
protein import into mitochondrial intermembrane space
GO:0048291
isotype switching to IgG isotypes
GO:0050821
protein stabilization
GO:0050870
positive regulation of T cell activation
GO:0051131
chaperone-mediated protein complex assembly
GO:0051604
protein maturation
GO:0051702
biological process involved in interaction with symbiont
GO:0098761
cellular response to interleukin-7
Cellular Component
GO:0005615
extracellular space
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
GO:0005759
mitochondrial matrix
GO:0005769
early endosome
GO:0005829
cytosol
GO:0005886
plasma membrane
GO:0005905
clathrin-coated pit
GO:0009986
cell surface
GO:0016020
membrane
GO:0030135
coated vesicle
GO:0030141
secretory granule
GO:0032991
protein-containing complex
GO:0043231
intracellular membrane-bounded organelle
GO:0046696
lipopolysaccharide receptor complex
GO:0070062
extracellular exosome
GO:0097225
sperm midpiece
GO:0097524
sperm plasma membrane
GO:0140494
migrasome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6ht7
,
PDBe:6ht7
,
PDBj:6ht7
PDBsum
6ht7
PubMed
UniProt
P10809
|CH60_HUMAN 60 kDa heat shock protein, mitochondrial (Gene Name=HSPD1)
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