Structure of PDB 1bzl Chain A Binding Site BS02
Receptor Information
>1bzl Chain A (length=486) Species:
5693
(Trypanosoma cruzi) [
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MSKIFDLVVIGAGSGGLEAAWNAATLYKKRVAVIDVQMVHGPPFFSALGG
TCVNVGCVPKKLMVTGAQYMEHLRESAGFGWEFDRTTLRAEWKNLIAVKD
EAVLNINKSYDEMFRDTEGLEFFLGWGSLESKNVVNVRESADPASAVKER
LETEHILLASGSWPHMPNIPGIEHCISSNEAFYLPEPPRRVLTVGGGFIS
VEFAGIFNAYKPKDGQVTLCYRGEMILRGFDHTLREELTKQLTANGIQIL
TKENPAKVELNADGSKSVTFESGKKMDFDLVMMAIGRSPRTKDLQLQNAG
VMIKNGGVQVDEYSRTNVSNIYAIGDVTNRVMLTPVAINEAAALVDTVFG
TTPRKTDHTRVASAVFSIPPIGTCGLIEEVASKRYEVVAVYLSSFTPLMH
KVSGSKYKTFVAKIITNHSDGTVLGVHLLGDNAPEIIQGIGICLKLNAKI
SDFYNTIGVHPTSAEELCSMRTPSYYYVKGEKMEKP
Ligand information
Ligand ID
GCG
InChI
InChI=1S/C27H49N9O10S2/c28-16(26(43)44)4-6-20(37)35-18(14-47)24(41)33-12-22(39)31-10-2-1-8-30-9-3-11-32-23(40)13-34-25(42)19(15-48)36-21(38)7-5-17(29)27(45)46/h16-19,30,47-48H,1-15,28-29H2,(H,31,39)(H,32,40)(H,33,41)(H,34,42)(H,35,37)(H,36,38)(H,43,44)(H,45,46)/t16-,17-,18-,19-/m0/s1
InChIKey
PHDOXVGRXXAYEB-VJANTYMQSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(CCNC(=O)CNC(=O)C(CS)NC(=O)CCC(C(=O)O)N)CNCCCNC(=O)CNC(=O)C(CS)NC(=O)CCC(C(=O)O)N
OpenEye OEToolkits 1.5.0
C(CCNC(=O)CNC(=O)[C@H](CS)NC(=O)CC[C@@H](C(=O)O)N)CNCCCNC(=O)CNC(=O)[C@H](CS)NC(=O)CC[C@@H](C(=O)O)N
CACTVS 3.341
N[CH](CCC(=O)N[CH](CS)C(=O)NCC(=O)NCCCCNCCCNC(=O)CNC(=O)[CH](CS)NC(=O)CC[CH](N)C(O)=O)C(O)=O
ACDLabs 10.04
O=C(NCC(=O)NCCCNCCCCNC(=O)CNC(=O)C(NC(=O)CCC(C(=O)O)N)CS)C(NC(=O)CCC(C(=O)O)N)CS
CACTVS 3.341
N[C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(=O)NCCCCNCCCNC(=O)CNC(=O)[C@H](CS)NC(=O)CC[C@H](N)C(O)=O)C(O)=O
Formula
C27 H49 N9 O10 S2
Name
BIS(GAMMA-GLUTAMYL-CYSTEINYL-GLYCINYL)SPERMIDINE;
TRYPANOTHIONE
ChEMBL
DrugBank
DB03470
ZINC
ZINC000008217540
PDB chain
1bzl Chain A Residue 603 [
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Receptor-Ligand Complex Structure
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PDB
1bzl
Crystal structure of Trypanosoma cruzi trypanothione reductase in complex with trypanothione, and the structure-based discovery of new natural product inhibitors.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
L18 E19 V59 S110 Y111 I339
Binding residue
(residue number reindexed from 1)
L17 E18 V58 S109 Y110 I338
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
S15 L49 C53 C58 K61 R86 T87 F199 E203 I339 G459 H461 E466 E485 K486
Catalytic site (residue number reindexed from 1)
S14 L48 C52 C57 K60 R85 T86 F198 E202 I338 G458 H460 E465 E484 K485
Enzyme Commision number
1.8.1.12
: trypanothione-disulfide reductase.
Gene Ontology
Molecular Function
GO:0004362
glutathione-disulfide reductase (NADPH) activity
GO:0015036
disulfide oxidoreductase activity
GO:0015042
trypanothione-disulfide reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016668
oxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
GO:0050660
flavin adenine dinucleotide binding
Biological Process
GO:0006749
glutathione metabolic process
GO:0034599
cellular response to oxidative stress
GO:0045454
cell redox homeostasis
GO:0098869
cellular oxidant detoxification
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1bzl
,
PDBe:1bzl
,
PDBj:1bzl
PDBsum
1bzl
PubMed
10368274
UniProt
P28593
|TYTR_TRYCR Trypanothione reductase (Gene Name=TPR)
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