Structure of PDB 6kqp Chain A Binding Site BS01
Receptor Information
>6kqp Chain A (length=220) Species:
9606
(Homo sapiens) [
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DKKPPPYKHIKVNRPIGRVQIFTADLSEIPRCNCKATDENPCGIDSECIN
RMLLYECHPTVCPAGGRCQNQCFSKRQYPEVEIFRTLQRGWGLRTKTDIK
KGEFVNEYVGELIDEEECRARIRYAQEHDITNFYMLTLDKDRIIDAGPKG
NYARFMNHCCQPNCETQKWSVNGDTRVGLFALSDIKAGTELTFNYNLECL
GNGKTVCKCGAPNCSGFLGV
Ligand information
Ligand ID
SAM
InChI
InChI=1S/C15H22N6O5S/c1-27(3-2-7(16)15(24)25)4-8-10(22)11(23)14(26-8)21-6-20-9-12(17)18-5-19-13(9)21/h5-8,10-11,14,22-23H,2-4,16H2,1H3,(H2-,17,18,19,24,25)/t7-,8+,10+,11+,14+,27-/m0/s1
InChIKey
MEFKEPWMEQBLKI-FCKMPRQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
C[S@@+](CC[C@H](N)C([O-])=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S+](CCC(C(=O)[O-])N)CC1C(C(C(O1)n2cnc3c2ncnc3N)O)O
CACTVS 3.341
C[S+](CC[CH](N)C([O-])=O)C[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
OpenEye OEToolkits 1.5.0
C[S@@+](CC[C@@H](C(=O)[O-])N)C[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)O
ACDLabs 10.04
[O-]C(=O)C(N)CC[S+](C)CC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C15 H22 N6 O5 S
Name
S-ADENOSYLMETHIONINE
ChEMBL
CHEMBL1235831
DrugBank
ZINC
PDB chain
6kqp Chain A Residue 2101 [
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Receptor-Ligand Complex Structure
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PDB
6kqp
Covalent inhibition of NSD1 histone methyltransferase.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
R1952 W1954 T1994 N1995 F1996 Y1997 R2017 N2020 H2021 Y2058 N2065 C2070 K2071 L2081
Binding residue
(residue number reindexed from 1)
R89 W91 T131 N132 F133 Y134 R154 N157 H158 Y195 N202 C207 K208 L218
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.1.357
: [histone H3]-lysine(36) N-dimethyltransferase.
Gene Ontology
Molecular Function
GO:0042054
histone methyltransferase activity
Cellular Component
GO:0005634
nucleus
View graph for
Molecular Function
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Cellular Component
External links
PDB
RCSB:6kqp
,
PDBe:6kqp
,
PDBj:6kqp
PDBsum
6kqp
PubMed
32868895
UniProt
Q96L73
|NSD1_HUMAN Histone-lysine N-methyltransferase, H3 lysine-36 specific (Gene Name=NSD1)
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