Structure of PDB 8bb4 Chain Q Binding Site BS01
Receptor Information
>8bb4 Chain Q (length=297) Species:
9606
(Homo sapiens) [
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PNYALKFTLAGHTKAVSSVKFSPNGEWLASSSADKLIKIWGAYDGKFEKT
ISGHKLGISDVAWSSDSNLLVSASDDKTLKIWDVSSGKCLKTLKGHSNYV
FCCNFNPQSNLIVSGSFDESVRIWDVKTGKCLKTLPAHSDPVSAVHFNRD
GSLIVSSSYDGLCRIWDTASGQCLKTLPPVSFVKFSPNGKYILAATLDNT
LKLWDYSKGKCLKTYTGHKNEKYCIFANFSVTGGKWIVSGSEDNLVYIWN
LQTKEIVQKLQGHTDVVISTACHPTENIIASAALENDKTIKLWKSDC
Ligand information
Ligand ID
Q3R
InChI
InChI=1S/C51H58F3N9O7S/c1-30-44(71-29-58-30)33-10-8-31(9-11-33)26-57-48(69)41-24-36(64)28-63(41)49(70)45(50(2,3)4)60-42(65)7-6-18-55-46(67)34-14-12-32(13-15-34)35-16-17-40(62-21-19-61(5)20-22-62)39(23-35)59-47(68)37-27-56-43(66)25-38(37)51(52,53)54/h8-17,23,25,27,29,36,41,45,64H,6-7,18-22,24,26,28H2,1-5H3,(H,55,67)(H,56,66)(H,57,69)(H,59,68)(H,60,65)/t36-,41+,45-/m1/s1
InChIKey
KFCLTULBYCCZBG-LTJJNQLXSA-N
SMILES
Software
SMILES
CACTVS 3.385
CN1CCN(CC1)c2ccc(cc2NC(=O)c3cnc(O)cc3C(F)(F)F)c4ccc(cc4)C(=O)NCCCC(=O)N[C@H](C(=O)N5C[C@H](O)C[C@H]5C(=O)NCc6ccc(cc6)c7scnc7C)C(C)(C)C
CACTVS 3.385
CN1CCN(CC1)c2ccc(cc2NC(=O)c3cnc(O)cc3C(F)(F)F)c4ccc(cc4)C(=O)NCCCC(=O)N[CH](C(=O)N5C[CH](O)C[CH]5C(=O)NCc6ccc(cc6)c7scnc7C)C(C)(C)C
OpenEye OEToolkits 3.1.0.0
Cc1c(scn1)c2ccc(cc2)CNC(=O)[C@@H]3C[C@H](CN3C(=O)[C@H](C(C)(C)C)NC(=O)CCCNC(=O)c4ccc(cc4)c5ccc(c(c5)NC(=O)c6cnc(cc6C(F)(F)F)O)N7CCN(CC7)C)O
OpenEye OEToolkits 3.1.0.0
Cc1c(scn1)c2ccc(cc2)CNC(=O)C3CC(CN3C(=O)C(C(C)(C)C)NC(=O)CCCNC(=O)c4ccc(cc4)c5ccc(c(c5)NC(=O)c6cnc(cc6C(F)(F)F)O)N7CCN(CC7)C)O
Formula
C51 H58 F3 N9 O7 S
Name
~{N}-[5-[4-[[4-[[(2~{S})-3,3-dimethyl-1-[(2~{S},4~{R})-2-[[4-(4-methyl-1,3-thiazol-5-yl)phenyl]methylcarbamoyl]-4-oxidanyl-pyrrolidin-1-yl]-1-oxidanylidene-butan-2-yl]amino]-4-oxidanylidene-butyl]carbamoyl]phenyl]-2-(4-methylpiperazin-1-yl)phenyl]-6-oxidanyl-4-(trifluoromethyl)pyridine-3-carboxamide
ChEMBL
CHEMBL5185035
DrugBank
ZINC
PDB chain
8bb4 Chain P Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
8bb4
Structure of human WDR5 and pVHL:ElonginC:ElonginB bound to PROTAC with C3 linker
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
S49 S50 A65 G89 S91 D107 F133 F149 Y191 C261
Binding residue
(residue number reindexed from 1)
S17 S18 A33 G57 S59 D75 F101 F117 Y159 C224
Annotation score
1
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0035064
methylated histone binding
GO:0042393
histone binding
GO:0042800
histone H3K4 methyltransferase activity
Biological Process
GO:0000122
negative regulation of transcription by RNA polymerase II
GO:0001501
skeletal system development
GO:0006094
gluconeogenesis
GO:0006325
chromatin organization
GO:0006355
regulation of DNA-templated transcription
GO:0006357
regulation of transcription by RNA polymerase II
GO:0045722
positive regulation of gluconeogenesis
GO:0045815
transcription initiation-coupled chromatin remodeling
GO:0045893
positive regulation of DNA-templated transcription
GO:0045995
regulation of embryonic development
GO:0051302
regulation of cell division
GO:0051726
regulation of cell cycle
GO:0090043
regulation of tubulin deacetylation
Cellular Component
GO:0000123
histone acetyltransferase complex
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0035097
histone methyltransferase complex
GO:0044545
NSL complex
GO:0044665
MLL1/2 complex
GO:0044666
MLL3/4 complex
GO:0048188
Set1C/COMPASS complex
GO:0071339
MLL1 complex
GO:0072686
mitotic spindle
GO:0140672
ATAC complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:8bb4
,
PDBe:8bb4
,
PDBj:8bb4
PDBsum
8bb4
PubMed
37354907
UniProt
P61964
|WDR5_HUMAN WD repeat-containing protein 5 (Gene Name=WDR5)
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