Structure of PDB 2bqz Chain E Binding Site BS02
Receptor Information
>2bqz Chain E (length=161) Species:
9606
(Homo sapiens) [
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RKSKAELQSEERKRIDELIESGKEEGMKIDLIDGKGRGVIATKQFSRGDF
VVEYHGDLIEITDAKKREALYAQDPSTGCYMYYFQYLSKTYCVDATRETN
RLGRLINHSKCGNCQTKLHDIDGVPHLILIASRDIAAGEELLYDYGDRSK
ASIEAHPWLKH
Ligand information
Ligand ID
SAH
InChI
InChI=1S/C14H20N6O5S/c15-6(14(23)24)1-2-26-3-7-9(21)10(22)13(25-7)20-5-19-8-11(16)17-4-18-12(8)20/h4-7,9-10,13,21-22H,1-3,15H2,(H,23,24)(H2,16,17,18)/t6-,7+,9+,10+,13+/m0/s1
InChIKey
ZJUKTBDSGOFHSH-WFMPWKQPSA-N
SMILES
Software
SMILES
CACTVS 3.341
N[CH](CCSC[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23)C(O)=O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)CSCCC(C(=O)O)N)O)O)N
CACTVS 3.341
N[C@@H](CCSC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23)C(O)=O
ACDLabs 10.04
O=C(O)C(N)CCSCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CSCC[C@@H](C(=O)O)N)O)O)N
Formula
C14 H20 N6 O5 S
Name
S-ADENOSYL-L-HOMOCYSTEINE
ChEMBL
CHEMBL418052
DrugBank
DB01752
ZINC
ZINC000004228232
PDB chain
2bqz Chain E Residue 1354 [
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Receptor-Ligand Complex Structure
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PDB
2bqz
Specificity and Mechanism of the Histone Methyltransferase Pr-Set7
Resolution
1.5 Å
Binding residue
(original residue number in PDB)
K226 R228 Y271 R295 L296 N298 H299 Y336 W349
Binding residue
(residue number reindexed from 1)
K35 R37 Y80 R104 L105 N107 H108 Y145 W158
Annotation score
5
Enzymatic activity
Enzyme Commision number
2.1.1.-
2.1.1.361
: [histone H4]-lysine(20) N-methyltransferase.
Gene Ontology
Molecular Function
GO:0042799
histone H4K20 methyltransferase activity
View graph for
Molecular Function
External links
PDB
RCSB:2bqz
,
PDBe:2bqz
,
PDBj:2bqz
PDBsum
2bqz
PubMed
15933069
UniProt
Q9NQR1
|KMT5A_HUMAN N-lysine methyltransferase KMT5A (Gene Name=KMT5A)
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