Structure of PDB 4j0b Chain A Binding Site BS01
Receptor Information
>4j0b Chain A (length=594) Species:
7955
(Danio rerio) [
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TLHNIITDTENVQGSFSKHEFQAETKKLLDIVARSLYSEKEVFIRELISN
GSDALEKLRHRMITAGGDTAPMEIHLQTDSVKGTFTIQDTGVGMNKEDLV
SNLGTIARSGSKAFLDALQNQAEASSSIIGQFGVGFYSAFMVADKVEVYS
QSAEADAPGYKWSSDGSGVFEVAEASGVRQGTKIVLHLKDDCKEFSSEDR
VKEVVTKYSNFVSFPIFLNGRRLNTLQALWMMEPKDISEWQHEEFYRYVA
QAYDKPRYTLHYRADAPLNIRSIFYVPEMKPMGSSVALYSRKILIQTKAT
DILPKWLRFLRGVVDSEDIPLNLSRELLQESALIRKLRDVLQQRVIRFLL
DQSKKDPEKYARFFEDYGLFMREGIVTTGEQSVKEDIAKLLRFESSALPA
GQQTSLMEYSSRMKAGTRNIYYLCAPNRHLAEHSPYFEAMKDMEVLFCFE
QFDELTLLHLREFDRKKLISAETRLSSEQAEDLLAWMRNALVQRVTNIKV
TPRLDTHPAMITVLEMGAARHFLRTQQILQPTLEINTGHDLIKKLHALKD
SNPELAQLLLEQIYDNAMIAAGLNEDPRPMISRLNQLLTRALEK
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
4j0b Chain A Residue 803 [
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Receptor-Ligand Complex Structure
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PDB
4j0b
Structural asymmetry in the closed state of mitochondrial Hsp90 (TRAP1) supports a two-step ATP hydrolysis mechanism.
Resolution
2.352 Å
Binding residue
(original residue number in PDB)
N134 A138 M178 N186 S193 G194 S195 G214 G217 V218 F220 T266
Binding residue
(residue number reindexed from 1)
N50 A54 M94 N102 S109 G110 S111 G130 G133 V134 F136 T182
Annotation score
5
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0005509
calcium ion binding
GO:0005524
ATP binding
GO:0016887
ATP hydrolysis activity
GO:0019901
protein kinase binding
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
Cellular Component
GO:0005739
mitochondrion
GO:0005743
mitochondrial inner membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4j0b
,
PDBe:4j0b
,
PDBj:4j0b
PDBsum
4j0b
PubMed
24462206
UniProt
A8WFV1
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