Structure of PDB 5w19 Chain D Binding Site BS01
Receptor Information
>5w19 Chain D (length=466) Species:
585
(Proteus vulgaris) [
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AKRIVEPFRIKMVEKIRVPSREEREAALKEAGYNPFLLPSSAVYIDLLTD
SGTNAMSDHQWAAMITGDEAYAGSRNYYDLKDKAKELFNYDYIIPAHQGR
GAENILFPVLLKYKQKEGKAKNPVFISNFHFDTTAAHVELNGCKAINIVT
EKAFDSETYDDWKGDFDIKKLKENIAQHGADNIVAIVSTVTCNSAGGQPV
SMSNLKEVYEIAKQHGIFVVMDSARFCENAYFIKARDPKYKNATIKEVIF
DMYKYADALTMSAKKDPLLNIGGLVAIRDNEEIFTLARQRCVPMEGFVTY
GGLAGRDMAAMVQGLEEGTEEEYLHYRIGQVKYLGDRLREAGIPIQYPTG
GHAVFVDCKKLVPQIPGDQFPAQAVINALYLESGVRAVEIGSFLLGRDPA
TGEQKHADMEFMRLTIARRVYTNDHMDYIADALIGLKEKFATLKGLEFEY
EPPVLRHFTARLKPIE
Ligand information
Ligand ID
9TD
InChI
InChI=1S/C19H20N3O8P/c1-10-17(23)14(11(7-20-10)9-30-31(27,28)29)8-21-16(19(25)26)6-13-12-4-2-3-5-15(12)22-18(13)24/h2-5,7-8,13,21,23H,6,9H2,1H3,(H,22,24)(H,25,26)(H2,27,28,29)/t13-/m1/s1
InChIKey
QWYZKAZTPCEUQJ-CYBMUJFWSA-N
SMILES
Software
SMILES
CACTVS 3.385
Cc1ncc(CO[P](O)(O)=O)c(C=[NH+][C-](C[C@H]2C(=O)Nc3ccccc23)C(O)=O)c1O
OpenEye OEToolkits 2.0.6
Cc1c(c(c(cn1)COP(=O)(O)O)C=[NH+][C-](CC2c3ccccc3NC2=O)C(=O)O)O
OpenEye OEToolkits 2.0.6
Cc1c(c(c(cn1)COP(=O)(O)O)/C=[NH+]/[C-](C[C@@H]2c3ccccc3NC2=O)C(=O)O)O
CACTVS 3.385
Cc1ncc(CO[P](O)(O)=O)c(C=[NH+][C-](C[CH]2C(=O)Nc3ccccc23)C(O)=O)c1O
ACDLabs 12.01
C(c1cnc(c(c1\C=[NH+]\[C-](C(O)=O)CC2c3c(NC2=O)cccc3)O)C)OP(O)(=O)O
Formula
C19 H20 N3 O8 P
Name
1-carboxy-1-{[(E)-{3-hydroxy-2-methyl-5-[(phosphonooxy)methyl]pyridin-4-yl}methylidene]azaniumyl}-2-[(3R)-2-oxo-2,3-dihydro-1H-indol-3-yl]ethan-1-ide
ChEMBL
DrugBank
ZINC
PDB chain
5w19 Chain D Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5w19
The crystal structure of Proteus vulgaris tryptophan indole-lyase complexed with oxindolyl-L-alanine: implications for the reaction mechanism.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
F37 T50 Q99 G100 R101 F132 D133 T134 N194 D223 R226 S263 K266 R414 F459
Binding residue
(residue number reindexed from 1)
F36 T49 Q98 G99 R100 F131 D132 T133 N193 D222 R225 S262 K265 R413 F458
Annotation score
1
Binding affinity
MOAD
: Ki~5uM
Enzymatic activity
Catalytic site (original residue number in PDB)
Y72 F132 D133 D223 A225 K266 I391 H458
Catalytic site (residue number reindexed from 1)
Y71 F131 D132 D222 A224 K265 I390 H457
Enzyme Commision number
4.1.99.1
: tryptophanase.
Gene Ontology
Molecular Function
GO:0009034
tryptophanase activity
GO:0016829
lyase activity
GO:0016830
carbon-carbon lyase activity
Biological Process
GO:0006520
amino acid metabolic process
GO:0006568
tryptophan metabolic process
GO:0006569
tryptophan catabolic process
GO:0009072
aromatic amino acid metabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5w19
,
PDBe:5w19
,
PDBj:5w19
PDBsum
5w19
PubMed
30082510
UniProt
P28796
|TNAA_PROVU Tryptophanase (Gene Name=tnaA)
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