Structure of PDB 3haz Chain A Binding Site BS01
Receptor Information
>3haz Chain A (length=983) Species:
224911
(Bradyrhizobium diazoefficiens USDA 110) [
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MPNIPPPFTAPYAPDDAEIAARLLPASHLSPPQEARIHRTATRLIEAIRK
RRLGGVEDMLREFALSTKEGLALMVLAEALLRVPDARTADQFIEDKLGEG
DFIHHETKSTAFLVNASAWAARVIQPGETPDGTIGRLVKRLGAPAVRTAT
RQAMRLMGNHFVLGETIEQALERGKPRSGQKTRYSFDMLGEGARTAADAR
RYFDAYASAIETIGKAAGNHALPDRPGISVKLSALHPRFEAISRARVMVE
LVPQLLDLAQRAKAHDLNFTVDAEEADRLELSLDVIAATLADPSLKGWDG
FGLAIQAYQKRASAVIDYVDALARAHDRKLMVRLVKGAYWDTEIKRAQER
GLDGYPVFTRKAMTDLNYVACASKLLALRPRIFPQFATHNALTVATVLEM
AEGSSGFEFQRLHGMGEALYEQLAKDHADIAYRTYAPVGSHRDLLAYLVR
RLLENGANSSFVAQAADYRVPVPALLQRPADAIVRPQAAAHPRIPLPCDL
FAPERRNSRGVEFGARTALDQLLTDVKAETGDLKPIADATPDQAHAAVAA
ARAGFAGWSRTPAGIRAAALEQAAHLLESRSAHFIALLQREGGKTLDDAL
SELREAADFCRYYAAQGRKLFGSETAMPGPTGESNALTMRGRGVFVAISP
WNFPLAIFLGQVTAALMAGNSVVAKPAEQTPRIAREAVALLHEAGIPKSA
LYLVTGDGRIGAALTAHPDIAGVVFTGSTEVARSINRALAAKDGPIVPLI
AETGGINAMIADATALPEQVADDVVTSAFRSAGQRCSALRLLFVQEDVAD
RMIEMVAGAARELKIGDPSDVATHVGPVIDVEAKQRLDAHIARMKTEARL
HFAGPAPEGCFVAPHIFELTEAGQLTEEVFGPILHVVRYRPENLERVLRA
IERTGYGLTLGVHSRIDDSIEAIIDRVQVGNIYVNRNMIGAVVGVQPFGG
NGLSGTGPKAGGPHYLARFATEQTVTINTAAAG
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
3haz Chain A Residue 2001 [
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Receptor-Ligand Complex Structure
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PDB
3haz
Crystal structure of the bifunctional proline utilization A flavoenzyme from Bradyrhizobium japonicum
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
D278 A279 Q312 R339 V341 K342 G343 A344 Y345 W346 F364 T365 R366 K367 T370 A393 T394 H395 N396 Y441 S466 F467
Binding residue
(residue number reindexed from 1)
D272 A273 Q306 R333 V335 K336 G337 A338 Y339 W340 F358 T359 R360 K361 T364 A387 T388 H389 N390 Y435 S460 F461
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
N658 K681 E758 C792 E884 A966
Catalytic site (residue number reindexed from 1)
N652 K675 E752 C786 E878 A960
Enzyme Commision number
1.2.1.88
: L-glutamate gamma-semialdehyde dehydrogenase.
1.5.5.2
: proline dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0003677
DNA binding
GO:0003700
DNA-binding transcription factor activity
GO:0003842
1-pyrroline-5-carboxylate dehydrogenase activity
GO:0004657
proline dehydrogenase activity
GO:0016491
oxidoreductase activity
GO:0016620
oxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
GO:0042802
identical protein binding
Biological Process
GO:0006355
regulation of DNA-templated transcription
GO:0006560
proline metabolic process
GO:0006561
proline biosynthetic process
GO:0006562
proline catabolic process
GO:0010133
proline catabolic process to glutamate
Cellular Component
GO:0009898
cytoplasmic side of plasma membrane
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Molecular Function
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Cellular Component
External links
PDB
RCSB:3haz
,
PDBe:3haz
,
PDBj:3haz
PDBsum
3haz
PubMed
20133651
UniProt
Q89E26
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