Structure of PDB 3f9x Chain A Binding Site BS03
Receptor Information
>3f9x Chain A (length=160) Species:
9606
(Homo sapiens) [
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KSKAELQSEERKRIDELIESGKEEGMKIDLIDGKGRGVIATKQFSRGDFV
VEYHGDLIEITDAKKREALYAQDPSTGCYMYYFQYLSKTYCVDATRETNR
LGRLINHSKCGNCQTKLHDIDGVPHLILIASRDIAAGEELLFDYGDRSKA
SIEAHPWLKH
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
3f9x Chain A Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
3f9x
Structural origins for the product specificity of SET domain protein methyltransferases.
Resolution
1.25 Å
Binding residue
(original residue number in PDB)
K226 R228 Y271 L296 N298 H299 Y336 W349
Binding residue
(residue number reindexed from 1)
K34 R36 Y79 L104 N106 H107 Y144 W157
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:3f9x
,
PDBe:3f9x
,
PDBj:3f9x
PDBsum
3f9x
PubMed
19088188
UniProt
Q9NQR1
|KMT5A_HUMAN N-lysine methyltransferase KMT5A (Gene Name=KMT5A)
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