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 IDNAP
InChIInChI=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
InChIKeyXJLXINKUBYWONI-NNYOXOHSSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.5.0c1cc(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 3.341NC(=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 3.341NC(=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 1.5.0c1cc(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
FormulaC21 H28 N7 O17 P3
NameNADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE;
2'-MONOPHOSPHOADENOSINE 5'-DIPHOSPHORIBOSE
ChEMBLCHEMBL295069
DrugBankDB03461
ZINC
PDB chain7dl1 Chain A Residue 401 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB7dl1 Crystal Structures and Catalytic Mechanism of l-erythro-3,5-Diaminohexanoate Dehydrogenase and Rational Engineering for Asymmetric Synthesis of beta-Amino Acids.
Resolution2.72 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 score3
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
PDBsum7dl1
PubMed33624917
UniProtB0VJ11

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