Structure of PDB 7obt Chain A Binding Site BS02
Receptor Information
>7obt Chain A (length=235) Species:
9606
(Homo sapiens) [
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GAMGSMERASLIQKAKLAEQAERYEDMAAFMKGAVEKGEELSCEERNLLS
VAYKNVVGGQRAAWRVLSSIEQKSNEEGSEEGPEVREYREKVETELQGVC
DTVLGLLDSHLIKEAGDAESRVFYLKMKGDYYRYLAEVATGDDKKRIIDS
ARSAYQEAMDISKKEMPPTNPIRLGLALNFSVFHYEIANSPEEAISLAKT
TFDEAMADLHTLSEDSYKDSTLIMQLLRDNLTLWT
Ligand information
Ligand ID
FSC
InChI
InChI=1S/C36H56O12/c1-10-35(6,7)45-17-26-30(41)33(46-21(5)38)31(42)34(47-26)48-32-28-24(18(2)15-44-20(4)37)13-27(39)36(28,8)14-25-22(16-43-9)11-12-23(25)19(3)29(32)40/h10,14,18-19,22-23,26-27,29-34,39-42H,1,11-13,15-17H2,2-9H3/b25-14-/t18-,19-,22-,23+,26-,27+,29-,30-,31-,32-,33+,34-,36+/m1/s1
InChIKey
KXTYBXCEQOANSX-WYKQKOHHSA-N
SMILES
Software
SMILES
CACTVS 3.385
COC[CH]1CC[CH]2[CH](C)[CH](O)[CH](O[CH]3O[CH](COC(C)(C)C=C)[CH](O)[CH](OC(C)=O)[CH]3O)C4=C(C[CH](O)[C]4(C)C=C12)[CH](C)COC(C)=O
CACTVS 3.385
COC[C@H]/1CC[C@H]2[C@@H](C)[C@@H](O)[C@H](O[C@H]3O[C@H](COC(C)(C)C=C)[C@@H](O)[C@H](OC(C)=O)[C@H]3O)C4=C(C[C@H](O)[C@]4(C)\C=C/12)[C@H](C)COC(C)=O
OpenEye OEToolkits 1.7.5
C[C@@H]1[C@@H]\2CC[C@@H](/C2=C/[C@]3([C@H](CC(=C3[C@H]([C@@H]1O)O[C@@H]4[C@@H]([C@H]([C@@H]([C@H](O4)COC(C)(C)C=C)O)OC(=O)C)O)[C@H](C)COC(=O)C)O)C)COC
OpenEye OEToolkits 1.7.5
CC1C2CCC(C2=CC3(C(CC(=C3C(C1O)OC4C(C(C(C(O4)COC(C)(C)C=C)O)OC(=O)C)O)C(C)COC(=O)C)O)C)COC
ACDLabs 10.04
O=C(OCC(C3=C2C(OC1OC(C(O)C(OC(=O)C)C1O)COC(\C=C)(C)C)C(O)C(C)C4C(=CC2(C)C(O)C3)C(COC)CC4)C)C
Formula
C36 H56 O12
Name
FUSICOCCIN
ChEMBL
CHEMBL4244843
DrugBank
DB01780
ZINC
PDB chain
7obt Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
7obt
IFN alpha primes cancer cells for Fusicoccin-induced cell death via 14-3-3 PPI stabilization.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
N42 V46 F119 K122 P167 D215 L218
Binding residue
(residue number reindexed from 1)
N47 V51 F123 K126 P171 D219 L222
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008426
protein kinase C inhibitor activity
GO:0019901
protein kinase binding
GO:0042802
identical protein binding
GO:0045296
cadherin binding
GO:0050815
phosphoserine residue binding
GO:0051219
phosphoprotein binding
GO:0140311
protein sequestering activity
Biological Process
GO:0000122
negative regulation of transcription by RNA polymerase II
GO:0001836
release of cytochrome c from mitochondria
GO:0003334
keratinocyte development
GO:0006469
negative regulation of protein kinase activity
GO:0006611
protein export from nucleus
GO:0007165
signal transduction
GO:0008104
protein localization
GO:0008630
intrinsic apoptotic signaling pathway in response to DNA damage
GO:0010482
regulation of epidermal cell division
GO:0010839
negative regulation of keratinocyte proliferation
GO:0022407
regulation of cell-cell adhesion
GO:0030216
keratinocyte differentiation
GO:0030307
positive regulation of cell growth
GO:0031424
keratinization
GO:0032880
regulation of protein localization
GO:0043588
skin development
GO:0043616
keratinocyte proliferation
GO:0045606
positive regulation of epidermal cell differentiation
GO:0045785
positive regulation of cell adhesion
GO:0045824
negative regulation of innate immune response
GO:0046827
positive regulation of protein export from nucleus
GO:0051726
regulation of cell cycle
GO:0061436
establishment of skin barrier
GO:0072089
stem cell proliferation
GO:0141156
cAMP/PKA signal transduction
GO:1903077
negative regulation of protein localization to plasma membrane
GO:1903829
positive regulation of protein localization
GO:2000647
negative regulation of stem cell proliferation
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0070062
extracellular exosome
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7obt
,
PDBe:7obt
,
PDBj:7obt
PDBsum
7obt
PubMed
37130519
UniProt
P31947
|1433S_HUMAN 14-3-3 protein sigma (Gene Name=SFN)
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