Structure of PDB 1qpb Chain B Binding Site BS02
Receptor Information
>1qpb Chain B (length=555) Species:
520522
(Saccharomyces pastorianus Weihenstephan 34/70) [
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SEITLGKYLFERLKQVNVNTVFGLPGDFNLSLLDKIYEVEGMRWAGNANE
LNAAYAADGYARIKGMSCIITTFGVGELSALNGIAGSYAEHVGVLHVVGV
PSISAQAKQLLLHHTLGNGDFTVFHRMSANISETTAMITDIATAPAEIDR
CIRTTYVTQRPVYLGLPANLVDLNVPAKLLQTPIDMSLKPNDAESEKEVI
DTILVLIKDAKNPVILADACCSRHDVKAETKKLIDLTQFPAFVTPMGKGS
IDEQHPRYGGVYVGTLSKPEVKEAVESADLILSVGALLSDFNTGSFSYSY
KTKNIVEFHSDHMKIRNATFPGVQMKFVLQKLLTAIADAAKGYKPVAVPA
RTPANAAVPASTPLKQEWMWNQLGNFLQEGDVVIAETGTSAFGINQTTFP
NNTYGISQVLWGSIGFTTGATLGAAFAAEEIDPKKRVILFIGDGSLQLTV
QEISTMIRWGLKPYLFVLNNDGYTIEKLIHGPKAQYNEIQGWDHLSLLPT
FGAKDYETHRVATTGEWDKLTQDKSFNDNSKIRMIEVMLPVFDAPQNLVE
QAKLT
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
1qpb Chain B Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1qpb
The Structural Basis of Substrate Activation in Yeast Pyruvate Decarboxylase a Crystallographic and Kinetic Study
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
G389 T390 I415 G443 G445 S446 N471 G473 Y474 T475 I476
Binding residue
(residue number reindexed from 1)
G388 T389 I414 G442 G444 S445 N470 G472 Y473 T474 I475
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L25 G27 D28 F29 N30 E51 T73 H114 H115 L117 G118 A169 T266 N293 T388 G413 I415 D444 N471 G473 Y474 I476 E477 I480 V542
Catalytic site (residue number reindexed from 1)
L24 G26 D27 F28 N29 E50 T72 H113 H114 L116 G117 A168 T265 N292 T387 G412 I414 D443 N470 G472 Y473 I475 E476 I479 V541
Enzyme Commision number
4.1.1.-
4.1.1.43
: phenylpyruvate decarboxylase.
4.1.1.72
: branched-chain-2-oxoacid decarboxylase.
4.1.1.74
: indolepyruvate decarboxylase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0003824
catalytic activity
GO:0004737
pyruvate decarboxylase activity
GO:0005515
protein binding
GO:0016831
carboxy-lyase activity
GO:0030976
thiamine pyrophosphate binding
GO:0046872
metal ion binding
GO:0047433
branched-chain-2-oxoacid decarboxylase activity
GO:0047434
indolepyruvate decarboxylase activity
GO:0050177
phenylpyruvate decarboxylase activity
Biological Process
GO:0000949
aromatic amino acid family catabolic process to alcohol via Ehrlich pathway
GO:0000955
amino acid catabolic process via Ehrlich pathway
GO:0006090
pyruvate metabolic process
GO:0006559
L-phenylalanine catabolic process
GO:0006569
tryptophan catabolic process
GO:0009083
branched-chain amino acid catabolic process
GO:0019655
glycolytic fermentation to ethanol
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1qpb
,
PDBe:1qpb
,
PDBj:1qpb
PDBsum
1qpb
PubMed
10651824
UniProt
P06169
|PDC1_YEAST Pyruvate decarboxylase isozyme 1 (Gene Name=PDC1)
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