Structure of PDB 7dl1 Chain A Binding Site BS01
Receptor Information
>7dl1 Chain A (length=351) Species:
459349
(Candidatus Cloacimonas acidaminovorans str. Evry) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
MKSNGCRYGTHRVIEPKGVLPQPAKILNNDMSEIWDNEMLIDVIRLNIDS
ASFHQIKNKLIAQGHQDLEKAFAEHAIELTNRTGKHKNEDTGSGGMFIGR
VAAIGDKFEMKEEVKVGDKIASLVSLSLTPLKINKVKKVLLDKDQMEIEG
QAILFSSGVYAKLPDDLDENLALSVLDVAGAPAQVERLVKPDDTVVIIGA
NGKSGILCNAVAKERAGICGKVIGVVRNENYIPTCKATGCDEVILAQATD
AITIQKEVSRLTNGKMADVVINVVNTEDTELPSIMAAKDRGMVYFFSMAT
SFTKAALGAGGIGADVDMMIGNSYAHHHSEIALDLLRRNSVLMKIFKERY
A
Ligand information
Ligand ID
NAP
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[CH](CO[P]([O-])(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O[P](O)(O)=O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[C@H](CO[P]([O-])(=O)O[P@@](O)(=O)OC[C@H]3O[C@H]([C@H](O[P](O)(O)=O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Formula
C21 H28 N7 O17 P3
Name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBL
CHEMBL295069
DrugBank
DB03461
ZINC
PDB chain
7dl1 Chain A Residue 401 [
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
7dl1
Crystal Structures and Catalytic Mechanism of l-erythro-3,5-Diaminohexanoate Dehydrogenase and Rational Engineering for Asymmetric Synthesis of beta-Amino Acids.
Resolution
2.72 Å
Binding residue
(original residue number in PDB)
D177 G202 K203 S204 R227 Y231 A248 V274 N275 T276 F296 S297 M298 S323
Binding residue
(residue number reindexed from 1)
D177 G202 K203 S204 R227 Y231 A248 V274 N275 T276 F296 S297 M298 S323
Annotation score
3
Enzymatic activity
Enzyme Commision number
1.4.1.11
: L-erythro-3,5-diaminohexanoate dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0016491
oxidoreductase activity
GO:0047124
L-erythro-3,5-diaminohexanoate dehydrogenase activity
View graph for
Molecular Function
External links
PDB
RCSB:7dl1
,
PDBe:7dl1
,
PDBj:7dl1
PDBsum
7dl1
PubMed
33624917
UniProt
B0VJ11
[
Back to BioLiP
]