Structure of PDB 6qqw Chain A Binding Site BS01
Receptor Information
>6qqw Chain A (length=212) Species:
36809
(Mycobacteroides abscessus) [
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SMKIDVVTIFPEYLQPVRQSLPGKAIDAGLVDVAVHDLRRWTHDVHKSVD
DSPYGGGPGMVMKPTVWGDALDEICTSETLLVVPTPAGYPFTQETAWQWS
TEDHLVIACGRYEGIDQRVADDAATRMRVREVSIGDYVLNGGEAAALVII
EAVLRLVPGVLSLLEGPSYTRPPSWRGMDVPPVLLSGDHAKIAAWRAEQS
RQRTIERRPDLL
Ligand information
Ligand ID
JDQ
InChI
InChI=1S/C18H16N4/c19-18-11-16(20-21-18)15-7-6-14-8-9-22(17(14)10-15)12-13-4-2-1-3-5-13/h1-11H,12H2,(H3,19,20,21)
InChIKey
IXGUTMYAJBKSPV-UHFFFAOYSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 2.0.7
c1ccc(cc1)Cn2ccc3c2cc(cc3)c4cc([nH]n4)N
CACTVS 3.385
Nc1[nH]nc(c1)c2ccc3ccn(Cc4ccccc4)c3c2
Formula
C18 H16 N4
Name
3-[1-(phenylmethyl)indol-6-yl]-1~{H}-pyrazol-5-amine
ChEMBL
CHEMBL4537315
DrugBank
ZINC
PDB chain
6qqw Chain A Residue 301 [
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Receptor-Ligand Complex Structure
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PDB
6qqw
Development of Inhibitors againstMycobacterium abscessustRNA (m1G37) Methyltransferase (TrmD) Using Fragment-Based Approaches.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
P83 T84 P85 G109 R110 Y111 E112 I133 G134 Y136 L138 N139 G140 G141
Binding residue
(residue number reindexed from 1)
P84 T85 P86 G110 R111 Y112 E113 I134 G135 Y137 L139 N140 G141 G142
Annotation score
1
Binding affinity
MOAD
: Kd=19uM
PDBbind-CN
: -logKd/Ki=4.72,Kd=19uM
Enzymatic activity
Catalytic site (original residue number in PDB)
P85 E112 R154
Catalytic site (residue number reindexed from 1)
P86 E113 R155
Enzyme Commision number
2.1.1.228
: tRNA (guanine(37)-N(1))-methyltransferase.
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0052906
tRNA (guanine(37)-N1)-methyltransferase activity
Biological Process
GO:0002939
tRNA N1-guanine methylation
GO:0006400
tRNA modification
GO:0008033
tRNA processing
GO:0032259
methylation
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6qqw
,
PDBe:6qqw
,
PDBj:6qqw
PDBsum
6qqw
PubMed
31282680
UniProt
B1MDI3
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