Structure of PDB 7nr4 Chain A Binding Site BS01
Receptor Information
>7nr4 Chain A (length=334) Species:
9606
(Homo sapiens) [
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TKRERDQLYYECYSDVSVHEEMIADRVRTDAYRLGILRNWAALRGKTVLD
VGAGTGILSIFCAQAGARRVYAVEASAIWQQAREVVRFNGLEDRVHVLPG
PVETVELPEQVDAIVSEWMGYGLLHESMLSSVLHARTKWLKEGGLLLPAS
AELFIVPISDQMLEWRLGFWSQVKQHYGVDMSCLEGFATRCLMGHSEIVV
QGLSGEDVLARPQRFAQLELSRAGLEQELEAGVGGRFRCSCYGSAPMHGF
AIWFQVTFPGEKPLVLSTSPFHPATHWKQALLYLNEPVQVEQDTDVSGEI
TLLPSRDNPRRLRVLLRYKVGDQEEKTKDFAMED
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
7nr4 Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
7nr4
Rational Design and Synthesis of Selective PRMT4 Inhibitors: A New Chemotype for Development of Cancer Therapeutics*.
Resolution
2.03 Å
Binding residue
(original residue number in PDB)
Y48 Y51 M60 R66 G90 A91 L96 E112 A113 P139 V140 E141 M166 S169
Binding residue
(residue number reindexed from 1)
Y10 Y13 M22 R28 G52 A53 L58 E74 A75 P101 V102 E103 M128 S131
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
D63 E155 E164 H317
Catalytic site (residue number reindexed from 1)
D25 E117 E126 H276
Enzyme Commision number
2.1.1.319
: type I protein arginine methyltransferase.
Gene Ontology
Molecular Function
GO:0003682
chromatin binding
GO:0005515
protein binding
GO:0008168
methyltransferase activity
GO:0008469
histone arginine N-methyltransferase activity
GO:0016274
protein-arginine N-methyltransferase activity
GO:0035241
protein-arginine omega-N monomethyltransferase activity
GO:0035242
protein-arginine omega-N asymmetric methyltransferase activity
GO:0042054
histone methyltransferase activity
GO:0042393
histone binding
GO:0044020
histone H4R3 methyltransferase activity
GO:0070611
histone H3R2 methyltransferase activity
GO:0070612
histone H2AR3 methyltransferase activity
GO:0140938
histone H3 methyltransferase activity
Biological Process
GO:0000122
negative regulation of transcription by RNA polymerase II
GO:0006281
DNA repair
GO:0006284
base-excision repair
GO:0006325
chromatin organization
GO:0006338
chromatin remodeling
GO:0010821
regulation of mitochondrion organization
GO:0018216
peptidyl-arginine methylation
GO:0032259
methylation
GO:0036211
protein modification process
GO:0045652
regulation of megakaryocyte differentiation
GO:0045892
negative regulation of DNA-templated transcription
GO:0090398
cellular senescence
GO:1901796
regulation of signal transduction by p53 class mediator
GO:2000059
negative regulation of ubiquitin-dependent protein catabolic process
Cellular Component
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005730
nucleolus
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:7nr4
,
PDBe:7nr4
,
PDBj:7nr4
PDBsum
7nr4
PubMed
33513288
UniProt
Q96LA8
|ANM6_HUMAN Protein arginine N-methyltransferase 6 (Gene Name=PRMT6)
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