Structure of PDB 2i5b Chain D Binding Site BS01
Receptor Information
>2i5b Chain D (length=267) Species:
1423
(Bacillus subtilis) [
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SMHKALTIAGSDSSGGAGIQADLKTFQEKNVYGMTALTVIVAMDPNNSWN
HQVFPIDTDTIRAQLATITDGIGVDAMKTGMLPTVDIIELAAKTIKEKQL
KNVVIDPVMVCKGANEVLYPEHAQALREQLAPLATVITPNLFEASQLSGM
DELKTVDDMIEAAKKIHALGAQYVVITGGGKLKHEKAVDVLYDGETAEVL
ESEMIDTPYTHGAGCTFSAAVTAELAKGAEVKEAIYAAKEFITAAIKESF
PLNQYVGPTKHSALRLN
Ligand information
Ligand ID
ADP
InChI
InChI=1S/C10H15N5O10P2/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(24-10)1-23-27(21,22)25-26(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
XTWYTFMLZFPYCI-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)O)O)N
Formula
C10 H15 N5 O10 P2
Name
ADENOSINE-5'-DIPHOSPHATE
ChEMBL
CHEMBL14830
DrugBank
DB16833
ZINC
ZINC000012360703
PDB chain
2i5b Chain D Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
2i5b
The Crystal Structure of an ADP Complex of Bacillus subtilis Pyridoxal Kinase Provides Evidence for the Parallel Emergence of Enzyme Activity During Evolution.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
N141 T178 G180 G181 K182 A188 D190 I206 G215 I247
Binding residue
(residue number reindexed from 1)
N140 T177 G179 G180 K181 A187 D189 I205 G214 I246
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
T178 T211 G213 A214 G215 C216
Catalytic site (residue number reindexed from 1)
T177 T210 G212 A213 G214 C215
Enzyme Commision number
2.7.1.35
: pyridoxal kinase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0008478
pyridoxal kinase activity
GO:0008902
hydroxymethylpyrimidine kinase activity
GO:0008972
phosphomethylpyrimidine kinase activity
GO:0016301
kinase activity
GO:0046872
metal ion binding
Biological Process
GO:0009228
thiamine biosynthetic process
GO:0016310
phosphorylation
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Cellular Component
External links
PDB
RCSB:2i5b
,
PDBe:2i5b
,
PDBj:2i5b
PDBsum
2i5b
PubMed
16978644
UniProt
P39610
|PDXK_BACSU Pyridoxine kinase (Gene Name=pdxK)
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