Structure of PDB 6ht7 Chain L Binding Site BS01
Receptor Information
>6ht7 Chain L (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 L 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 G88 T90 G416 D496
Binding residue
(residue number reindexed from 1)
T30 P33 D87 G88 T90 G416 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
View graph for
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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