Structure of PDB 3wqp Chain J Binding Site BS01

Receptor Information
>3wqp Chain J (length=437) Species: 69014 (Thermococcus kodakarensis KOD1) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
IYDYYVDKGYEPSKKRDIIAVFRVTPAEGYTIEQAAGAVAAESSTGTWTT
LYPWYEQERWADLSAKAYDFHDMGDGSWIVRIAYPFHAFEEANLPGLLAS
IAGNIFGMKRVKGLRLEDLYFPEKLIREFDGPAFGIEGVRKMLEIKDRPI
YGVVPKPKVGYSPEEFEKLAYDLLSNGADYMKDDENLTSPWYNRFEERAE
IMAKIIDKVENETGEKKTWFANITADLLEMEQRLEVLADLGLKHAMVDVV
ITGWGALRYIRDLAADYGLAIHGHRAMHAAFDRNPYHGISMFVLAKLYRL
IGIDQLHVGTAGAGKLEGGKWDVIQNARILRESHYKPDENDVFHLEQKFY
SIKAAFPTSSGGLHPGNIQPVIEALGTDIVLQLGGGTLGHPDGPAAGARA
VRQAIDAIMQGIPLDEYAKTHKELARALEKWGHVTPV
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 chain3wqp Chain J Residue 501 [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]
PDB3wqp Mutation design of thermophilic Rubisco based on the three-dimensional structure enhances its activity at ambient temperature
Resolution2.25 Å
Binding residue
(original residue number in PDB)		K189 D191 E192
Binding residue
(residue number reindexed from 1)		K182 D184 E185
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) K163 K189 D190 D191 E192 H281 H314 K322
Catalytic site (residue number reindexed from 1) K156 K182 D183 D184 E185 H274 H307 K315
Enzyme Commision number 4.1.1.39: ribulose-bisphosphate carboxylase.
Gene Ontology
Molecular Function
GO:0000287 magnesium ion binding
GO:0016491 oxidoreductase activity
GO:0016829 lyase activity
GO:0016984 ribulose-bisphosphate carboxylase activity
GO:0046872 metal ion binding
Biological Process
GO:0006196 AMP catabolic process
GO:0015977 carbon fixation

View graph for
Molecular Function
View graph for
Biological Process
External links
PDB RCSB:3wqp, PDBe:3wqp, PDBj:3wqp
PDBsum3wqp
PubMed
UniProtO93627|RBL_THEKO Ribulose bisphosphate carboxylase (Gene Name=rbcL)

[Back to BioLiP]