Structure of PDB 9ema Chain B Binding Site BS01
Receptor Information
>9ema Chain B (length=326) Species:
9606
(Homo sapiens) [
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QRIASHSHVKGLGLDESGLAKQAASGLVGQENAREACGVIVELIKSKKMA
GRAVLLAGPPGTGKTALALAIAQELGSKVPFCPMVGSEVYSTEIKKTEVL
MENFRRAIGLRIKIQDVTLHDLDVANARPMGQLMKPKKTEITDKLRGEIN
KVVNKYIDQGIAELVPGVLFVDEVHMLDIECFTYLHRALESSIAPIVIFA
SNRGNCVIRGTEDITSPHGIPLDLLDRVMIIRTMLYTPQEMKQIIKIRAQ
TEGINISEEALNHLGEIGTKTTLRYSVQLLTPANLLAKINGKDSIEKEHV
EEISELFYDAKSSAKILADQQDKYMK
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=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[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
9ema Chain B Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
9ema
Mechanism of allosteric inhibition of RUVBL1-RUVBL2 by the small-molecule CB-6644
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
S17 H18 H20 V40 P72 G73 G75 K76 T77 Y366 I374 R404
Binding residue
(residue number reindexed from 1)
S5 H6 H8 V28 P60 G61 G63 K64 T65 Y236 I244 R274
Annotation score
5
Enzymatic activity
Enzyme Commision number
3.6.4.12
: DNA helicase.
Gene Ontology
Molecular Function
GO:0001094
TFIID-class transcription factor complex binding
GO:0003678
DNA helicase activity
GO:0003713
transcription coactivator activity
GO:0004386
helicase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0008094
ATP-dependent activity, acting on DNA
GO:0016787
hydrolase activity
GO:0016887
ATP hydrolysis activity
GO:0017025
TBP-class protein binding
GO:0043531
ADP binding
GO:0045296
cadherin binding
GO:0051117
ATPase binding
Biological Process
GO:0000492
box C/D snoRNP assembly
GO:0000723
telomere maintenance
GO:0006275
regulation of DNA replication
GO:0006281
DNA repair
GO:0006282
regulation of DNA repair
GO:0006310
DNA recombination
GO:0006325
chromatin organization
GO:0006338
chromatin remodeling
GO:0006355
regulation of DNA-templated transcription
GO:0006357
regulation of transcription by RNA polymerase II
GO:0007283
spermatogenesis
GO:0032508
DNA duplex unwinding
GO:0033044
regulation of chromosome organization
GO:0042981
regulation of apoptotic process
GO:0045739
positive regulation of DNA repair
GO:0045893
positive regulation of DNA-templated transcription
GO:0045995
regulation of embryonic development
GO:0050821
protein stabilization
GO:0051276
chromosome organization
GO:0051301
cell division
GO:0051726
regulation of cell cycle
GO:0060382
regulation of DNA strand elongation
GO:0090263
positive regulation of canonical Wnt signaling pathway
GO:0090671
telomerase RNA localization to Cajal body
GO:1904507
positive regulation of telomere maintenance in response to DNA damage
GO:1905168
positive regulation of double-strand break repair via homologous recombination
GO:2000779
regulation of double-strand break repair
Cellular Component
GO:0000786
nucleosome
GO:0000812
Swr1 complex
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005813
centrosome
GO:0005829
cytosol
GO:0005856
cytoskeleton
GO:0016020
membrane
GO:0016363
nuclear matrix
GO:0031011
Ino80 complex
GO:0035267
NuA4 histone acetyltransferase complex
GO:0070062
extracellular exosome
GO:0071339
MLL1 complex
GO:0097255
R2TP complex
GO:0101031
protein folding chaperone complex
GO:0120293
dynein axonemal particle
GO:1990062
RPAP3/R2TP/prefoldin-like complex
GO:1990904
ribonucleoprotein complex
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:9ema
,
PDBe:9ema
,
PDBj:9ema
PDBsum
9ema
PubMed
UniProt
Q9Y265
|RUVB1_HUMAN RuvB-like 1 (Gene Name=RUVBL1)
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