Structure of PDB 8cp2 Chain B Binding Site BS01
Receptor Information
>8cp2 Chain B (length=600) Species:
1424099
(Streptomyces sp. V2) [
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MPLSVAVVGAGPRGTSVLERLCASAPELLAPGVRLTVHVVDPAPPGPGRV
WRTAQSEDLLMNTVASQVTLFTDESVNCSGPILAGPSLHEWADGAIGPDD
YPTRALYGRYLEWVFARTLRHAPPSVRVETHRARAVRLDDAADGRQHLAL
DNGRTLTGLSAVVLAQGHLPVRPSAAVLRDTEHADRHALRHIPPANPADV
DLTVISPGEPVLLRGLGLNFFDHMALLTTGRGGTYVREDGVLRYVPSGRE
PRVYAGSRRGLPYQARGDNAKGPYGRHLPEVLTPEAVSAFRKRADSGEAP
DFLRDIWPLVAKEVETVYYTALVRHPDFAPRYLSLPYGDPQEAELLAEFG
VDADARWDWERVSRPYAQREFAHRGEWRQWLLGYLRADAAEALRGNVDGP
LKAALDVLRDLRNELRLVVDHRGLRGDSRRDHLDRWYTPLNAFLSIGPPR
RRIEELTALLEAGVVEVLGPRLEVTREDGAWLARSPDVPGSAVRVTTLIE
ARLPEPDLGQTADALLAHLRETGQCRAHVVDGYTTGGIDVSARPYHLVDR
EGVAHPRRFAFGVPTEGVHWVTAAGARPGVDSVTLSDADAVARAVLRVAG
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
8cp2 Chain B Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
8cp2
A biosynthetic aspartate N-hydroxylase performs successive oxidations by holding intermediates at a site away from the catalytic center.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
V8 G9 P12 R13 V40 D41 P42 G48 V50 W51 M61 R134 A135 Q166 G167 H168 L169 N196 A573 A574 G575
Binding residue
(residue number reindexed from 1)
V8 G9 P12 R13 V40 D41 P42 G48 V50 W51 M61 R134 A135 Q166 G167 H168 L169 N196 A573 A574 G575
Annotation score
4
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
View graph for
Molecular Function
External links
PDB
RCSB:8cp2
,
PDBe:8cp2
,
PDBj:8cp2
PDBsum
8cp2
PubMed
37302552
UniProt
A0A2V1NMV1
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