Structure of PDB 8cp5 Chain A Binding Site BS01
Receptor Information
>8cp5 Chain A (length=600) Species:
1424099
(Streptomyces sp. V2) [
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PLSVAVVGAGPRGTSVLERLCASAPELLAPGVRLTVHVVDPAPPGPGRVW
RTAQSEDLLMNTVASQVTLFTDESVNCSGPILAGPSLHEWADGAIGPDDY
PTRALYGRYLEWVFARTLRHAPPSVRVETHRARAVRLDDAADGRQHLALD
NGRTLTGLSAVVLAQGHLPVRPSAAVLRDTEHADRHALRHIPPANPADVD
LTVISPGEPVLLRGLGLNFFDHMALLTTGRGGTYVREDGVLRYVPSGREP
RVYAGSRRGLPYQARGDNAKGPYGRHLPEVLTPEAVSAFRKRADSGEAPD
FLRDIWPLVAKEVETVYYTALVRHPDFAPRYLSLPYGDPQEAELLAEFGV
DADARWDWERVSRPYAQREFAHRGEWRQWLLGYLRADAAEALRGNVDGPL
KAALDVLRDLRNELRLVVDHRGLRGDSRRDHLDRWYTPLNAFLSIGPPRR
RIEELTALLEAGVVEVLGPRLEVTREDGAWLARSPDVPGSAVRVTTLIEA
RLPEPDLGQTADALLAHLRETGQCRAHVVDGYTTGGIDVSARPYHLVDRE
GVAHPRRFAFGVPTEGVHWVTAAGARPGVDSVTLSDADAVARAVLRVAGQ
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
8cp5 Chain A Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
8cp5
A biosynthetic aspartate N-hydroxylase performs successive oxidations by holding intermediates at a site away from the catalytic center.
Resolution
2.54 Å
Binding residue
(original residue number in PDB)
V8 G9 P12 R13 D41 P42 G48 R49 V50 W51 M61 N62 R104 A135 Q166 G167 H168 L169 N196 A573 A574 G575
Binding residue
(residue number reindexed from 1)
V7 G8 P11 R12 D40 P41 G47 R48 V49 W50 M60 N61 R103 A134 Q165 G166 H167 L168 N195 A572 A573 G574
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:8cp5
,
PDBe:8cp5
,
PDBj:8cp5
PDBsum
8cp5
PubMed
37302552
UniProt
A0A2V1NMV1
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