Structure of PDB 5ise Chain C Binding Site BS01
Receptor Information
>5ise Chain C (length=343) Species:
10090
(Mus musculus) [
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SVFSERTEESSAVQYFQFYGYLSQQQNMMQDYVRTGTYQRAILQNHTDFK
DKIVLDVGCGSGILSFFAAQAGARKIYAVEASTMAQHAEVLVKSNNLTDR
IVVIPGKVEEVSLPEQVDIIISEPMGYMLFNERMLESYLHAKKYLKPSGN
MFPTIGDVHLAPFTDEQLYMEQFTKANFWYQPSFHGVDLSALRGAAVDEY
FRQPVVDTFDIRILMAKSVKYTVNFLEAKEGDLHRIEIPFKFHMLHSGLV
HGLAFWFDVAFIGSIMTVWLSTAPTEPLTHWYQVRCLFQSPLFAKAGDTL
SGTCLLIANKRQSYDISIVAQVDQTGSKSSNLLDLKNPFFRYT
Ligand information
Ligand ID
6D2
InChI
InChI=1S/C18H30N10O5/c19-9(17(31)32)2-5-27(4-1-3-23-18(21)22)6-10-12(29)13(30)16(33-10)28-8-26-11-14(20)24-7-25-15(11)28/h7-10,12-13,16,29-30H,1-6,19H2,(H,31,32)(H2,20,24,25)(H4,21,22,23)/t9-,10+,12+,13+,16+/m0/s1
InChIKey
XBMZCXWGTKEJNB-UOYPZJKHSA-N
SMILES
Software
SMILES
ACDLabs 12.01
C(CN(CCC(C(O)=O)N)CC1C(O)C(O)C(O1)n3c2c(c(ncn2)N)nc3)CNC(=N)\N
OpenEye OEToolkits 2.0.4
[H]/N=C(/N)\NCCCN(CC[C@@H](C(=O)O)N)C[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)O
CACTVS 3.385
N[C@@H](CCN(CCCNC(N)=N)C[C@H]1O[C@H]([C@H](O)[C@@H]1O)n2cnc3c(N)ncnc23)C(O)=O
OpenEye OEToolkits 2.0.4
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)CN(CCCNC(=N)N)CCC(C(=O)O)N)O)O)N
CACTVS 3.385
N[CH](CCN(CCCNC(N)=N)C[CH]1O[CH]([CH](O)[CH]1O)n2cnc3c(N)ncnc23)C(O)=O
Formula
C18 H30 N10 O5
Name
5'-{[(3S)-3-amino-3-carboxypropyl](3-carbamimidamidopropyl)amino}-5'-deoxyadenosine
ChEMBL
CHEMBL1199364
DrugBank
ZINC
ZINC000049113375
PDB chain
5ise Chain C Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5ise
Crystal structure of mouse CARM1 in complex with SAH at 1.8 Angstroms resolution
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
Y150 Y154 M163 R169 G193 C194 I198 L199 E215 A216 K242 V243 E244 E258 M260 E267 M269 S272 H415
Binding residue
(residue number reindexed from 1)
Y15 Y19 M28 R34 G58 C59 I63 L64 E80 A81 K107 V108 E109 E123 M125 E132 M134 S137 H280
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
D166 E258 E267 H415
Catalytic site (residue number reindexed from 1)
D31 E123 E132 H280
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:5ise
,
PDBe:5ise
,
PDBj:5ise
PDBsum
5ise
PubMed
UniProt
Q9WVG6
|CARM1_MOUSE Histone-arginine methyltransferase CARM1 (Gene Name=Carm1)
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