Structure of PDB 5dxj Chain B Binding Site BS01
Receptor Information
>5dxj Chain B (length=344) Species:
9606
(Homo sapiens) [
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RSVFSERTEESSAVQYFQFYGYLSQQQNMMQDYVRTGTYQRAILQNHTDF
KDKIVLDVGCGSGILSFFAAQAGARKIYAVEASTMAQHAEVLVKSNNLTD
RIVVIPGKVEEVSLPEQVDIIISEPMGYMLFNERMLESYLHAKKYLKPSG
NMFPTIGDVHLAPFTDEQLYMEQFTKANFWYQPSFHGVDLSALRGAAVDE
YFRQPVVDTFDIRILMAKSVKYTVNFLEAKEGDLHRIEIPFKFHMLHSGL
VHGLAFWFDVAFIGSIMTVWLSTAPTEPLTHWYQVRCLFQSPLFAKAGDT
LSGTCLLIANKRQSYDISIVAQVDQTGSKSSNLLDLKNPFFRYT
Ligand information
Ligand ID
SFG
InChI
InChI=1S/C15H23N7O5/c16-6(1-2-7(17)15(25)26)3-8-10(23)11(24)14(27-8)22-5-21-9-12(18)19-4-20-13(9)22/h4-8,10-11,14,23-24H,1-3,16-17H2,(H,25,26)(H2,18,19,20)/t6-,7-,8+,10+,11+,14+/m0/s1
InChIKey
LMXOHSDXUQEUSF-YECHIGJVSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)C[C@H](CC[C@@H](C(=O)O)N)N)O)O)N
OpenEye OEToolkits 1.7.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)CC(CCC(C(=O)O)N)N)O)O)N
CACTVS 3.370
N[CH](CC[CH](N)C(O)=O)C[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23
CACTVS 3.370
N[C@@H](CC[C@H](N)C(O)=O)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23
ACDLabs 12.01
O=C(O)C(N)CCC(N)CC3OC(n2cnc1c(ncnc12)N)C(O)C3O
Formula
C15 H23 N7 O5
Name
SINEFUNGIN;
ADENOSYL-ORNITHINE
ChEMBL
CHEMBL1214186
DrugBank
DB01910
ZINC
ZINC000004217451
PDB chain
5dxj Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5dxj
Structural Insights into Ternary Complex Formation of Human CARM1 with Various Substrates.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
Y149 F150 Y153 M162 R168 G192 C193 I197 L198 E214 A215 K241 V242 E243 E257 M268 S271
Binding residue
(residue number reindexed from 1)
Y16 F17 Y20 M29 R35 G59 C60 I64 L65 E81 A82 K108 V109 E110 E124 M135 S138
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
D165 E257 E266 H414
Catalytic site (residue number reindexed from 1)
D32 E124 E133 H281
Enzyme Commision number
2.1.1.319
: type I protein arginine methyltransferase.
Gene Ontology
Molecular Function
GO:0016274
protein-arginine N-methyltransferase activity
Biological Process
GO:0018216
peptidyl-arginine methylation
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5dxj
,
PDBe:5dxj
,
PDBj:5dxj
PDBsum
5dxj
PubMed
26551522
UniProt
Q86X55
|CARM1_HUMAN Histone-arginine methyltransferase CARM1 (Gene Name=CARM1)
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