Structure of PDB 3ahc Chain A Binding Site BS02
Receptor Information
>3ahc Chain A (length=802) Species:
1685
(Bifidobacterium breve) [
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VIGTPWQKLDRPVSEEAIEGMDKYWRVTNYMSIGQIYLRSNPLMKEPFTR
DDVKHRLVGHWGTTPGLNFLLAHINRLIADHQQNTVFIMGPGHGGPAGTS
QSYVDGTYTEYYPNITKDEAGLQKFFRQFSYPGGIPSHFAPETPGSIHEG
GELGYALSHAYGAVMNNPSLFVPCIIGDGEAETGPLATGWQSNKLVNPRT
DGIVLPILHLNGYKIANPTILARISDEELHDFFRGMGYHPYEFVAGFDNE
DHMSIHRRFAELFETIFDEICDIKAAAQTDDMTRPFYPMLIFRTPKGWTC
PKFIDGKKTEGSWRAHQVPLASARDTEEHFEVLKGWMESYKPEELFNADG
SIKDDVTAFMPKGELRIGANPNANGGVIREDLKLPELDQYEVTGVKEYGH
GWGQVEAPRALGAYCRDIIKNNPDSFRIFGPDETASNRLNATYEVTDKQW
DNGYLSGLVDEHMAVTGQVTEQLSEHQCEGFLEAYLLTGRHGIWSSYESF
VHVIDSMLNQHAKWLEATVREIPWRKPISSVNLLVSSHVWRQDHNGFSHQ
DPGVTSLLINKTFNNDHVTNIYFATDANMLLAISEKCFKSTNKINAIFAG
KQPAPTWVTLDEARAELEAGAAEWKWASNAENNDEVQVVLASAGDVPTQE
LMAASDALNKMGIKFKVVNVVDLLKLQSRENNDEALTDEEFTELFTADKP
VLFAYHSYAQDVRGLIYDRPNHDNFHVVGYKEQGSTTTPFDMVRVNDMDR
YALQAAALKLIDADKYADKIDELNAFRKKAFQFAVDNGYDIPEFTDWVYP
DV
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
3ahc Chain A Residue 827 [
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Receptor-Ligand Complex Structure
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PDB
3ahc
Crystal Structures of phosphoketolase: thiamine diphosphate-dependent dehydration mechanism
Resolution
1.7 Å
Binding residue
(original residue number in PDB)
T67 H97 G155 L157 G181 D182 G183 N215 Y217 K218 I219 K300 H320
Binding residue
(residue number reindexed from 1)
T63 H93 G151 L153 G177 D178 G179 N211 Y213 K214 I215 K296 H316
Annotation score
4
Enzymatic activity
Enzyme Commision number
4.1.2.-
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0016829
lyase activity
GO:0016832
aldehyde-lyase activity
GO:0046872
metal ion binding
Biological Process
GO:0005975
carbohydrate metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:3ahc
,
PDBe:3ahc
,
PDBj:3ahc
PDBsum
3ahc
PubMed
20739284
UniProt
D6PAH1
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