Structure of PDB 7bmc Chain A Binding Site BS02
Receptor Information
>7bmc Chain A (length=234) Species:
9606
(Homo sapiens) [
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GAMGSMERASLIQKAKLAEQAERYEDMAAFMKGAVEKGEELSCEERNLLS
VAYKNVVGGQRAAWRVLSSIEQKSNEGSEEGPEVREYREKVETELQGVCD
TVLGLLDSHLIKEAGDAESRVFYLKMKGDYYRYLAEVATGDDKKRIIDSA
RSAYQEAMDISKKEMPPTNPIRLGLALNFSVFHYEIANSPEEAISLAKTT
FDEAMADLHTLSEDSYKDSTLIMQLLRDNLTLWT
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
7bmc Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
7bmc
Fusicoccin-A Targets Cancerous Inhibitor of Protein Phosphatase 2A by Stabilizing a C-Terminal Interaction with 14-3-3.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
N42 V46 F119 K122 P167 D215 L218 I219
Binding residue
(residue number reindexed from 1)
N47 V51 F122 K125 P170 D218 L221 I222
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:7bmc
,
PDBe:7bmc
,
PDBj:7bmc
PDBsum
7bmc
PubMed
36255265
UniProt
P31947
|1433S_HUMAN 14-3-3 protein sigma (Gene Name=SFN)
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