Structure of PDB 4q3d Chain B Binding Site BS02

Receptor Information
>4q3d Chain B (length=258) Species: 269797 (Methanosarcina barkeri str. Fusaro) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
ALLTPDDLININMQLQKADSAVQEVTGLDIKGICKALYGTFSSSEKVGIV
PVTSGNGIIGNFSASLHAITQYFGFDSFVTDMPDVSGYYEAVQNGAEIIL
MADDRTFLAHNLKNGKMANNQPCTGIIYAEIASRYLKADSKDVLVVGLGK
VGFPGAEHLVQKDFRVYGYDADETLLERATSNLGIIPFDPANPKKFSIIF
EATPCANTIPEAVLSENCVLSTPGIPCAISEELRDKYEVQLIAEPLGIGT
ASMLYSVL
Ligand information
Ligand IDMG
InChIInChI=1S/Mg/q+2
InChIKeyJLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341[Mg++]
FormulaMg
NameMAGNESIUM ION
ChEMBL
DrugBankDB01378
ZINC
PDB chain4q3d Chain B Residue 903 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure 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]
PDB4q3d The Formation of Pyrroline and Tetrahydropyridine Rings in Amino Acids Catalyzed by Pyrrolysine Synthase (PylD).
Resolution2.2 Å
Binding residue
(original residue number in PDB)
Y129 E245 L247 I249
Binding residue
(residue number reindexed from 1)
Y128 E244 L246 I248
Annotation score1
Enzymatic activity
Enzyme Commision number 1.4.1.-
Gene Ontology
Molecular Function
GO:0016491 oxidoreductase activity
Biological Process
GO:0008652 amino acid biosynthetic process

View graph for
Molecular Function

View graph for
Biological Process
External links
PDB RCSB:4q3d, PDBe:4q3d, PDBj:4q3d
PDBsum4q3d
PubMed24916332
UniProtQ46E80|PYLD_METBF Pyrrolysine synthase (Gene Name=pylD)

[Back to BioLiP]