Structure of PDB 6bcx Chain B Binding Site BS01
Receptor Information
>6bcx Chain B (length=2178) Species:
9606
(Homo sapiens) [
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AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATRFYDQLNHHIFELERKG
GILAIASLIGVEGGNATRIGRFANYLRNLLPSNDPVVMEMASKAIGRLAM
AGDTFTAEYVEFEVKRALEWLEGRRHAAVLVLRELAISVPTFFFQQVQPF
FDNIFVAVWDPKQAIREGAVAALRACLILTTQRWYRHTFEEAEKGFDDDR
IHGALLILNELVRISSMEGERLREEMEEIAAAAAAAAAAAAAAAAAAAAA
AAAASLIQMTILNLLPRLAAFRPTQYLQDTMNHVLSCVKKEKERTAAFQA
LGLLSVAVRSEFKVYLPRVLDIIRAALPPKVDATVFTCISMLARIQQDIK
ELLEPMLAVGLSPALTAVLYDLSRQIPQLKKDIQDGLLKMLSLVLMAAVG
SITLALRTLGSFEFELTQFVRHCADHFLNSEHKEIRMEAARTCSRLLTPS
VSQTAVQVVADVLSKLLVVGITDPDPDIRYCVLASLDERFDAHLAQAENL
QALFVALNDQVFEIRELAICTVGRLSSMNPAFVMPFLRKMLIQILTELEH
SGIGRIKEQSARMLGHLVSNAPRLIRPYMEPILKALILKLKDPNPGVINN
VLATIGELAQVSGLEMRKWVDELFIIIMDMLQDSSLLAKRQVALWTLGQL
VASTGYVVEPYRKYPTLLEVLLNFLKTEQNQGTRREAIRVLGLLGALDPY
KHKVNIEMLVNMGNLPLDEFYPAVSMVALMRIFRDQSLSHHHTMVVQAIT
FIFKSLGLKCVQFLPQVMPTFLNVIRVCDGAIREFLFQQLGMLVSFVKSH
IRPYMDEIVTLMREFWVMNTSIQSTIILLIEQIVVALGGEFKLYLPQLIP
HMLRVFMHDNSPGRIVSIKLLAAIQLFGANLDDYLHLLLPPIVKLFDAPE
APLPSRKAALETVDRLTESLDFTDYASRIIHPIVRTLDQSPELRSTAMDT
LSSLVFQLGKKYQIFIPMVNKVLVRHRINHQRYDVLICRIVKGYTLSTIN
LQKAWGAARRVSKDDWLEWLRRLSLELLKDSSSPSLRSCWALAQAYNPMA
RDLFNAAFVSCWSELNEDQQDELIRSIELALTSQDIAEVTQTLLNLAEFM
EHSDKGPLPLRDDNGIVLLGERAAKCRAYAKALHYKELEFQKGPTPAILE
SLISINNKLQQPEAAAGVLEYAMKHFGELEIQATWYEKLHEWEDALVAYD
KKMDTNKDDPELMLGRMRCLEALGEWGQLHQQCCEKWTLVNDETQAKMAR
MAAAAAWGLGQWDSMEEYTCMIPRDTHDGAFYRAVLALHQDLFSLAQQCI
DKARDLLDAELTAMAGESYSRAYGAMVSCHMLSELEEVIQYKLVPERREI
IRQIWWERLQGCQRIVEDWQKILMVRSLVVSPHEDMRTWLKYASLCGKSG
RLALAHKTLVLLLGVDPSRQLDHPLPTVHPQVTYAYMKNMWKSARKIDAF
QHMQHFVQTMQQQAQHAIATEDQQHKQELHKLMARCFLKLGEWQLNLQGI
NESTIPKVLQYYSAATEHDRSWYKAWHAWAVMNFEAVLHYKHQNQARDEK
KKVTEDLSKTLLMYTVPAVQGFFRSISLSRGNNLQDTLRVLTLWFDYGHW
PDVNEALVEGVKAIQIDTWLQVIPQLIARIDTPRPLVGRLIHQLLTDIGR
YHPQALIYPLTVASKSTTTARHNAANKILKNMCEHSNTLVQQAMMVSEEL
IRVAILWHEMWHEGLEEASRLYFGERNVKGMFEVLEPLHAMMERGPQTLK
ETSFNQAYGRDLMEAQEWCRKYMKSGNVKDLTQAWDLYYHVFRRISKQLP
QLTSLELQYVSPKLLMCRDLELAVPGTYDPNQPIIRIQSIAPSLQVITSK
QRPRKLTLMGSNGHEFVFLLKGHEDLRQDERVMQLFGLVNTLLANDPTSL
RKNLSIQRYAVIPLSTNSGLIGWVPHCDTLHALIRDYREKKKILLNIEHR
IMLRMAPDYDHLTLMQKVEVFEHAVNNTAGDDLAKLLWLKSPSSEVWFDR
RTNYTRSLAVMSMVGYILGLGDRHPSNLMLDRLSGKILHIDFGDCFEVAM
TREKFPEKIPFRLTRMLTNAMEVTGLDGNYRITCHTVMEVLREHKDSVMA
VLEAFVYDPLLNWRLMDTNTALNKKAIQIINRVRDKLTGRDFSHDDTLDV
PTQVELLIKQATSHENLCQCYIGWCPFW
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
6bcx Chain B Residue 3000 [
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Receptor-Ligand Complex Structure
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PDB
6bcx
Mechanisms of mTORC1 activation by RHEB and inhibition by PRAS40.
Resolution
3.23 Å
Binding residue
(original residue number in PDB)
S2165 Q2167 K2187 W2239 V2240 T2245 M2345 I2356
Binding residue
(residue number reindexed from 1)
S1849 Q1851 K1871 W1923 V1924 T1929 M2029 I2040
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.7.11.1
: non-specific serine/threonine protein kinase.
Gene Ontology
Molecular Function
GO:0001002
RNA polymerase III type 1 promoter sequence-specific DNA binding
GO:0001003
RNA polymerase III type 2 promoter sequence-specific DNA binding
GO:0001006
RNA polymerase III type 3 promoter sequence-specific DNA binding
GO:0001156
TFIIIC-class transcription factor complex binding
GO:0004672
protein kinase activity
GO:0004674
protein serine/threonine kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0042802
identical protein binding
GO:0043022
ribosome binding
GO:0044024
histone H2AS1 kinase activity
GO:0044877
protein-containing complex binding
GO:0051219
phosphoprotein binding
GO:0106310
protein serine kinase activity
Biological Process
GO:0001558
regulation of cell growth
GO:0002296
T-helper 1 cell lineage commitment
GO:0003007
heart morphogenesis
GO:0003179
heart valve morphogenesis
GO:0006112
energy reserve metabolic process
GO:0006207
'de novo' pyrimidine nucleobase biosynthetic process
GO:0006338
chromatin remodeling
GO:0006468
protein phosphorylation
GO:0006954
inflammatory response
GO:0006974
DNA damage response
GO:0007010
cytoskeleton organization
GO:0007040
lysosome organization
GO:0007281
germ cell development
GO:0007584
response to nutrient
GO:0008361
regulation of cell size
GO:0009267
cellular response to starvation
GO:0009408
response to heat
GO:0009791
post-embryonic development
GO:0010506
regulation of autophagy
GO:0010507
negative regulation of autophagy
GO:0010592
positive regulation of lamellipodium assembly
GO:0010628
positive regulation of gene expression
GO:0010718
positive regulation of epithelial to mesenchymal transition
GO:0010831
positive regulation of myotube differentiation
GO:0016236
macroautophagy
GO:0016241
regulation of macroautophagy
GO:0016242
negative regulation of macroautophagy
GO:0016310
phosphorylation
GO:0018105
peptidyl-serine phosphorylation
GO:0019219
regulation of nucleobase-containing compound metabolic process
GO:0019228
neuronal action potential
GO:0030030
cell projection organization
GO:0030163
protein catabolic process
GO:0030307
positive regulation of cell growth
GO:0030838
positive regulation of actin filament polymerization
GO:0031295
T cell costimulation
GO:0031529
ruffle organization
GO:0031641
regulation of myelination
GO:0031648
protein destabilization
GO:0031667
response to nutrient levels
GO:0031669
cellular response to nutrient levels
GO:0031670
cellular response to nutrient
GO:0031929
TOR signaling
GO:0032868
response to insulin
GO:0032869
cellular response to insulin stimulus
GO:0032956
regulation of actin cytoskeleton organization
GO:0033173
calcineurin-NFAT signaling cascade
GO:0034198
cellular response to amino acid starvation
GO:0035264
multicellular organism growth
GO:0038202
TORC1 signaling
GO:0042752
regulation of circadian rhythm
GO:0043066
negative regulation of apoptotic process
GO:0043200
response to amino acid
GO:0043276
anoikis
GO:0045670
regulation of osteoclast differentiation
GO:0045727
positive regulation of translation
GO:0045792
negative regulation of cell size
GO:0045821
positive regulation of glycolytic process
GO:0045945
positive regulation of transcription by RNA polymerase III
GO:0045948
positive regulation of translational initiation
GO:0046777
protein autophosphorylation
GO:0046889
positive regulation of lipid biosynthetic process
GO:0048266
behavioral response to pain
GO:0048511
rhythmic process
GO:0048709
oligodendrocyte differentiation
GO:0048714
positive regulation of oligodendrocyte differentiation
GO:0048738
cardiac muscle tissue development
GO:0050731
positive regulation of peptidyl-tyrosine phosphorylation
GO:0050882
voluntary musculoskeletal movement
GO:0051128
regulation of cellular component organization
GO:0051247
positive regulation of protein metabolic process
GO:0051496
positive regulation of stress fiber assembly
GO:0051549
positive regulation of keratinocyte migration
GO:0051647
nucleus localization
GO:0051896
regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
GO:0051897
positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
GO:0055006
cardiac cell development
GO:0055013
cardiac muscle cell development
GO:0060048
cardiac muscle contraction
GO:0061431
cellular response to methionine
GO:0070885
negative regulation of calcineurin-NFAT signaling cascade
GO:0071230
cellular response to amino acid stimulus
GO:0071233
cellular response to L-leucine
GO:0071456
cellular response to hypoxia
GO:0071470
cellular response to osmotic stress
GO:0080135
regulation of cellular response to stress
GO:0090559
regulation of membrane permeability
GO:1900034
regulation of cellular response to heat
GO:1900181
negative regulation of protein localization to nucleus
GO:1901796
regulation of signal transduction by p53 class mediator
GO:1901838
positive regulation of transcription of nucleolar large rRNA by RNA polymerase I
GO:1903691
positive regulation of wound healing, spreading of epidermal cells
GO:1904059
regulation of locomotor rhythm
GO:1904690
positive regulation of cytoplasmic translational initiation
GO:1905672
negative regulation of lysosome organization
GO:1905857
positive regulation of pentose-phosphate shunt
GO:1990253
cellular response to leucine starvation
GO:2000785
regulation of autophagosome assembly
Cellular Component
GO:0000139
Golgi membrane
GO:0005634
nucleus
GO:0005635
nuclear envelope
GO:0005654
nucleoplasm
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005741
mitochondrial outer membrane
GO:0005764
lysosome
GO:0005765
lysosomal membrane
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005794
Golgi apparatus
GO:0005829
cytosol
GO:0012505
endomembrane system
GO:0016020
membrane
GO:0016605
PML body
GO:0030425
dendrite
GO:0031410
cytoplasmic vesicle
GO:0031931
TORC1 complex
GO:0031932
TORC2 complex
GO:0045335
phagocytic vesicle
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:6bcx
,
PDBe:6bcx
,
PDBj:6bcx
PDBsum
6bcx
PubMed
29236692
UniProt
P42345
|MTOR_HUMAN Serine/threonine-protein kinase mTOR (Gene Name=MTOR)
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