Structure of PDB 5fdo Chain B Binding Site BS01
Receptor Information
>5fdo Chain B (length=150) Species:
9606
(Homo sapiens) [
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GDELYRQSLEIISRYLREQATGAKDTKPMGRSGATSRKALETLRRVGDGV
QRNHETAFQGMLRKLDIKNEDDVKSLSRVMIHVFSDGVTNWGRIVTLISF
GAFVAKHLKTINQESCIEPLAESITDVLVRTKRDWLVKQRGWDGFVEFFH
Ligand information
Ligand ID
5X2
InChI
InChI=1S/C26H25ClN2O4S/c1-17-15-19(16-18(2)24(17)27)33-14-8-12-22-21-11-6-7-13-23(21)28-25(22)26(30)29-34(31,32)20-9-4-3-5-10-20/h3-7,9-11,13,15-16,28H,8,12,14H2,1-2H3,(H,29,30)
InChIKey
SMGRUAFEHILHHU-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.4
Cc1cc(cc(c1Cl)C)OCCCc2c3ccccc3[nH]c2C(=O)NS(=O)(=O)c4ccccc4
CACTVS 3.385
Cc1cc(OCCCc2c([nH]c3ccccc23)C(=O)N[S](=O)(=O)c4ccccc4)cc(C)c1Cl
Formula
C26 H25 Cl N2 O4 S
Name
3-[3-(4-chloranyl-3,5-dimethyl-phenoxy)propyl]-~{N}-(phenylsulfonyl)-1~{H}-indole-2-carboxamide
ChEMBL
CHEMBL3785312
DrugBank
ZINC
ZINC000222400502
PDB chain
5fdo Chain B Residue 400 [
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Receptor-Ligand Complex Structure
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PDB
5fdo
Discovery of 2-Indole-acylsulfonamide Myeloid Cell Leukemia 1 (Mcl-1) Inhibitors Using Fragment-Based Methods.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
F228 M231 L246 V249 M250 G262 R263 T266 F270 G271
Binding residue
(residue number reindexed from 1)
F58 M61 L76 V79 M80 G92 R93 T96 F100 G101
Annotation score
1
Binding affinity
BindingDB: Ki=361nM,IC50=400nM
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Biological Process
GO:0042981
regulation of apoptotic process
View graph for
Biological Process
External links
PDB
RCSB:5fdo
,
PDBe:5fdo
,
PDBj:5fdo
PDBsum
5fdo
PubMed
26878343
UniProt
Q07820
|MCL1_HUMAN Induced myeloid leukemia cell differentiation protein Mcl-1 (Gene Name=MCL1)
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