Structure of PDB 1i41 Chain F Binding Site BS02
Receptor Information
>1i41 Chain F (length=396) Species:
4097
(Nicotiana tabacum) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
YASFLNSDGSVAIHAGERLGRGIVTDAITTPVVNTSAYFFNKTSELIDFK
EKRRASFEYGRYGNPTTVVLEEKISALEGAESTLLMASGMCASTVMLLAL
VPAGGHIVTTTDCYRKTRIFIETILPKMGITATVIDPADVGALELALNQK
KVNLFFTESPTNPFLRCVDIELVSKLCHEKGALVCIDGTFATPLNQKALA
LGADLVLHSATKFLGGHNDVLAGCISGPLKLVSEIRNLHHILGGALNPNA
AYLIIRGMKTLHLRVQQQNSTALRMAEILEAHPKVRHVYYPGLQSHPEHH
IAKKQMTGFGGAVSFEVDGDLLTTAKFVDALKIPYIAPSFGGCESIVDQP
AIMSYWDLSQSDRAKYGIMDNLVRFSFGVEDFDDLKADILQALDSI
Ligand information
Ligand ID
HEN
InChI
InChI=1S/C13H18N2O10P2/c1-8-12(16)10(9(5-14-8)7-25-27(22,23)24)6-15-11(13(17)18)3-2-4-26(19,20)21/h2-3,5,16H,4,6-7H2,1H3,(H,17,18)(H2,19,20,21)(H2,22,23,24)/b3-2+,15-11+
InChIKey
VKWJKURKEYQKKW-ZCOJICPHSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(CN=C(\C=C\C[P](O)(O)=O)C(O)=O)c1O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)C/N=C(\C=C\CP(=O)(O)O)/C(=O)O)O
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(CN=C(C=CC[P](O)(O)=O)C(O)=O)c1O
ACDLabs 10.04
O=P(O)(O)C/C=C/C(=N\Cc1c(cnc(c1O)C)COP(=O)(O)O)C(=O)O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)CN=C(C=CCP(=O)(O)O)C(=O)O)O
Formula
C13 H18 N2 O10 P2
Name
2-[(3-HYDROXY-2-METHYL-5-PHOSPHONOOXYMETHYL-PYRIDIN-4-YLMETHYL)-IMINO]-5-PHOSPHONO-PENT-3-ENOIC ACID
ChEMBL
DrugBank
DB02328
ZINC
ZINC000103544596
PDB chain
1i41 Chain H Residue 507 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
1i41
Crystal structures of cystathionine gamma-synthase inhibitor complexes rationalize the increased affinity of a novel inhibitor.
Resolution
3.2 Å
Binding residue
(original residue number in PDB)
E107 Y108 R110 Y111
Binding residue
(residue number reindexed from 1)
E58 Y59 R61 Y62
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
R110 Y163 D236 K261
Catalytic site (residue number reindexed from 1)
R61 Y114 D187 K212
Enzyme Commision number
4.2.99.9
: Transferred entry: 2.5.1.48.
Gene Ontology
Molecular Function
GO:0003962
cystathionine gamma-synthase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0009086
methionine biosynthetic process
GO:0019346
transsulfuration
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1i41
,
PDBe:1i41
,
PDBj:1i41
PDBsum
1i41
PubMed
11518531
UniProt
Q9ZPL5
[
Back to BioLiP
]