Structure of PDB 2fzm Chain A Binding Site BS01
Receptor Information
>2fzm Chain A (length=450) Species:
562
(Escherichia coli) [
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QSVSRAAITAAYRRPETEAVSMLLEQARLPQPVAEQAHKLAYQLADKLRN
QKNASGRAGMGVALMCLAEALLRIPDKATRDALIRKGVDMAMRLMGEQFV
TGETIAEALANARKLEEKGFRYSYDMLGEAALTAADAQAYMVSYQQAIHA
IGKASNGRGIYEGPGISIKLSALHPRYSRAQYDRVMEELYPRLKSLTLLA
RQYDIGINIDAEESDRLEISLDLLEKLCFEPELAGWNGIGFVIQAYQKRC
PLVIDYLIDLATRSRRRLMIRLVKGAYWDSEIKRAQMDGLEGYPVYTRKV
YTDVSYLACAKKLLAVPNLIYPQFATHNAHTLAAIYQLAGQNYYPGQYEF
QCLHGMGEPLYEQVTGKVADGKLNRPCRIYAPVGTHETLLAYLVRRLLEN
GANTSFVNRIADTSLPLDELVADPVTAVEKLAQQEGQTGLPHPKIPLPRD
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
2fzm Chain A Residue 2001 [
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Receptor-Ligand Complex Structure
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PDB
2fzm
Redox-induced changes in flavin structure and roles of flavin N(5) and the ribityl 2'-OH group in regulating PutA--membrane binding.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
D370 A371 V402 Q404 R431 V433 K434 G435 A436 W438 Y456 T457 R458 K459 T462 A485 T486 H487 N488 Q511 C512 L513 Y540 E559 S565
Binding residue
(residue number reindexed from 1)
D210 A211 V242 Q244 R271 V273 K274 G275 A276 W278 Y296 T297 R298 K299 T302 A325 T326 H327 N328 Q351 C352 L353 Y380 E399 S405
Annotation score
2
Enzymatic activity
Enzyme Commision number
1.2.1.88
: L-glutamate gamma-semialdehyde dehydrogenase.
1.5.5.2
: proline dehydrogenase.
Gene Ontology
Molecular Function
GO:0003842
1-pyrroline-5-carboxylate dehydrogenase activity
GO:0004657
proline dehydrogenase activity
Biological Process
GO:0006562
proline catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:2fzm
,
PDBe:2fzm
,
PDBj:2fzm
PDBsum
2fzm
PubMed
17209558
UniProt
P09546
|PUTA_ECOLI Bifunctional protein PutA (Gene Name=putA)
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