Structure of PDB 3exf Chain H Binding Site BS01
Receptor Information
>3exf Chain H (length=329) Species:
9606
(Homo sapiens) [
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LQVTVRDAINQGMDEELERDEKVFLLGEEVAQYDGAYKVSRGLWKKYGDK
RIIDTPISEMGFAGIAVGAAMAGLRPICEFMTFNFSMQAIDQVINSAAKT
YYMSGGLQPVPIVFRGPNGASAGVAAQHSQCFAAWYGHCPGLKVVSPWNS
EDAKGLIKSAIRDNNPVVVLENELMYGVPFEFPPEAQSKDFLIPIGKAKI
ERQGTHITVVSHSRPVGHCLEAAAVLSKEGVECEVINMRTIRPMDMETIE
ASVMKTNHLVTVEGGWPQFGVGAEICARIMEGPAFNFLDAPAVRVTGADV
PMPYAKILEDNSIPQVKDIIFAIKKTLNI
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
3exf Chain E Residue 1009 [
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Receptor-Ligand Complex Structure
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PDB
3exf
Structural basis for inactivation of the human pyruvate dehydrogenase complex by phosphorylation: role of disordered phosphorylation loops.
Resolution
2.998 Å
Binding residue
(original residue number in PDB)
E28 I57 E59 F85 Q88
Binding residue
(residue number reindexed from 1)
E28 I57 E59 F85 Q88
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
E59 H128
Catalytic site (residue number reindexed from 1)
E59 H128
Enzyme Commision number
1.2.4.1
: pyruvate dehydrogenase (acetyl-transferring).
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004739
pyruvate dehydrogenase (acetyl-transferring) activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0034604
pyruvate dehydrogenase (NAD+) activity
GO:0046872
metal ion binding
Biological Process
GO:0006006
glucose metabolic process
GO:0006086
acetyl-CoA biosynthetic process from pyruvate
GO:0006099
tricarboxylic acid cycle
Cellular Component
GO:0005634
nucleus
GO:0005654
nucleoplasm
GO:0005739
mitochondrion
GO:0005759
mitochondrial matrix
GO:0045254
pyruvate dehydrogenase complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3exf
,
PDBe:3exf
,
PDBj:3exf
PDBsum
3exf
PubMed
19081061
UniProt
P11177
|ODPB_HUMAN Pyruvate dehydrogenase E1 component subunit beta, mitochondrial (Gene Name=PDHB)
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