Structure of PDB 6fnr Chain A Binding Site BS01
Receptor Information
>6fnr Chain A (length=321) Species:
1772
(Mycolicibacterium smegmatis) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
HMALSLANYLAADSAAEALRRDVRAGLTATQKSLPPKWFYDAGSDLFDQI
TRLPEYYPTRTEAQILRTRSAEIISAAGADTLVELGSGTSEKTRMLLDAM
RDAELLRRFIPFDVDAGVLRSAGAAIGAEYPGIEIDAVCGDFEEHLGKIP
HVGRRLVVFLGSTIGNLTPAPRAEFLSTLADTLQPGDSLLLGTDLVKDTG
RLVRAYDDAAGVTAAFNRNVLAVVNRELSADFDLDAFEHVAKWNSDEERI
EMWLRARTAQHVRVAALDLEVDFAAGEEMLTEVSCKFRPENVVAELAEAG
LRQTHWWTDPAGDFGLSLAVR
Ligand information
Ligand ID
DYT
InChI
InChI=1S/C6H7ClN2O2/c7-5(6(10)11)1-4-2-8-3-9-4/h2-3,5H,1H2,(H,8,9)(H,10,11)/t5-/m0/s1
InChIKey
JZLQYMHAXPPICX-YFKPBYRVSA-N
SMILES
Software
SMILES
CACTVS 3.385
OC(=O)[CH](Cl)Cc1[nH]cnc1
CACTVS 3.385
OC(=O)[C@@H](Cl)Cc1[nH]cnc1
OpenEye OEToolkits 2.0.6
c1c([nH]cn1)CC(C(=O)O)Cl
OpenEye OEToolkits 2.0.6
c1c([nH]cn1)C[C@@H](C(=O)O)Cl
Formula
C6 H7 Cl N2 O2
Name
(2~{S})-2-chloranyl-3-(1~{H}-imidazol-5-yl)propanoic acid
ChEMBL
DrugBank
ZINC
ZINC000001571549
PDB chain
6fnr Chain A Residue 403 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
6fnr
Inhibition and Regulation of the Ergothioneine Biosynthetic Methyltransferase EgtD.
Resolution
1.83 Å
Binding residue
(original residue number in PDB)
F47 Y56 Y206 E282 S284
Binding residue
(residue number reindexed from 1)
F47 Y56 Y206 E282 S284
Annotation score
3
Binding affinity
MOAD
: Ki=2.6uM
PDBbind-CN
: -logKd/Ki=5.59,Ki=2.6uM
Enzymatic activity
Enzyme Commision number
2.1.1.44
: L-histidine N(alpha)-methyltransferase.
Gene Ontology
Molecular Function
GO:0008168
methyltransferase activity
GO:0008276
protein methyltransferase activity
GO:0052706
L-histidine N(alpha)-methyltransferase activity
Biological Process
GO:0032259
methylation
GO:0052699
ergothioneine biosynthetic process
GO:0052704
ergothioneine biosynthesis from histidine via gamma-glutamyl-hercynylcysteine sulfoxide
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:6fnr
,
PDBe:6fnr
,
PDBj:6fnr
PDBsum
6fnr
PubMed
29658702
UniProt
A0R5M8
|EGTD_MYCS2 Histidine N-alpha-methyltransferase (Gene Name=egtD)
[
Back to BioLiP
]