Structure of PDB 3hwx Chain A Binding Site BS03
Receptor Information
>3hwx Chain A (length=555) Species:
83333
(Escherichia coli K-12) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MSVSAFNRRWAAVILEALTRHGVRHICIAPGSRSTLLTLAAAENSAFIHH
THFDERGLGHLALGLAKVSKQPVAVIVTSGTAVANLYPALIEAGLTGEKL
ILLTADRPPELIDCGANQAIRQPGMFASHPTHSISLPRPTQDIPARWLVS
TIDHALGTLHAGGVHINCPFAEPLYGMDDTGLSWQQRLGDWWQDDKPWLR
EAPRLESEKQRDWFFWRQKRGVVVAGRMSAEEGKKVALWAQTLGWPLIGD
VLSQTGQPLPCADLWLGNAKATSELQQAQIVVQLGSSLTGKRLLQWQASC
EPEEYWIVDDIEGRLDPAHHRGRRLIANIADWLELHPAEKRQPWCVEIPR
LAEQAMQAVIARRDAFGEAQLAHRICDYLPEQGQLFVGNSLVVRLIDALS
QLPAGYPVYSNRGASGIDGLLSTAAGVQRASGKPTLAIVGDLSALYDLNA
LALLRQVSAPLVLIVVNNNGGQIFSLLPTPQSERERFYLMPQNVHFEHAA
AMFELKYHRPQNWQELETAFADAWRTPTTTVIEMVVNDTDGAQTLQQLLA
QVSHL
Ligand information
Ligand ID
TPP
InChI
InChI=1S/C12H18N4O7P2S/c1-8-11(3-4-22-25(20,21)23-24(17,18)19)26-7-16(8)6-10-5-14-9(2)15-12(10)13/h5,7H,3-4,6H2,1-2H3,(H4-,13,14,15,17,18,19,20,21)/p+1
InChIKey
AYEKOFBPNLCAJY-UHFFFAOYSA-O
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(C[n+]2csc(CCO[P@@](O)(=O)O[P](O)(O)=O)c2C)c(N)n1
OpenEye OEToolkits 1.5.0
Cc1c(sc[n+]1Cc2cnc(nc2N)C)CCO[P@](=O)(O)OP(=O)(O)O
OpenEye OEToolkits 1.5.0
Cc1c(sc[n+]1Cc2cnc(nc2N)C)CCOP(=O)(O)OP(=O)(O)O
CACTVS 3.341
Cc1ncc(C[n+]2csc(CCO[P](O)(=O)O[P](O)(O)=O)c2C)c(N)n1
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCCc1sc[n+](c1C)Cc2c(nc(nc2)C)N
Formula
C12 H19 N4 O7 P2 S
Name
THIAMINE DIPHOSPHATE
ChEMBL
CHEMBL1236376
DrugBank
ZINC
ZINC000008215517
PDB chain
3hwx Chain B Residue 601 [
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
3hwx
Structural and functional analysis of Vitamin K2 synthesis protein MenD.
Resolution
2.6 Å
Binding residue
(original residue number in PDB)
E55 A82
Binding residue
(residue number reindexed from 1)
E55 A82
Annotation score
1
Binding affinity
PDBbind-CN
: -logKd/Ki=7.86,Kd=13.9nM
Enzymatic activity
Enzyme Commision number
2.2.1.9
: 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0016740
transferase activity
GO:0030145
manganese ion binding
GO:0030976
thiamine pyrophosphate binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:0070204
2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylic-acid synthase activity
Biological Process
GO:0009234
menaquinone biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3hwx
,
PDBe:3hwx
,
PDBj:3hwx
PDBsum
3hwx
PubMed
19703421
UniProt
P17109
|MEND_ECOLI 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate synthase (Gene Name=menD)
[
Back to BioLiP
]