Structure of PDB 2fzn Chain A Binding Site BS02
Receptor Information
>2fzn Chain A (length=449) Species:
562
(Escherichia coli) [
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QSVSRAAITAAYRRPETEAVSMLLEQARLPQPVAEQAHKLAYQLADKLRN
QKNASGRAGGVALMCLAEALLRIPDKATRDALIRKGVDMAMRLMGEQFVT
GETIAEALANARKLEEKGFRYSYDMLGEAALTAADAQAYMVSYQQAIHAI
GKASNGRGIYEGPGISIKLSALHPRYSRAQYDRVMEELYPRLKSLTLLAR
QYDIGINIDAEESDRLEISLDLLEKLCFEPELAGWNGIGFVIQAYQKRCP
LVIDYLIDLATRSRRRLMIRLVKGAYWDSEIKRAQMDGLEGYPVYTRKVY
TDVSYLACAKKLLAVPNLIYPQFATHNAHTLAAIYQLAGQNYYPGQYEFQ
CLHGMGEPLYEQVTGKVADGKLNRPCRIYAPVGTHETLLAYLVRRLLENG
ANTSFVNRIADTSLPLDELVADPVTAVEKLAQQEGQTGLPHPKIPLPRD
Ligand information
Ligand ID
PRO
InChI
InChI=1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)/t4-/m0/s1
InChIKey
ONIBWKKTOPOVIA-BYPYZUCNSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1C[C@H](NC1)C(=O)O
CACTVS 3.341
OC(=O)[C@@H]1CCCN1
CACTVS 3.341
OC(=O)[CH]1CCCN1
OpenEye OEToolkits 1.5.0
C1CC(NC1)C(=O)O
ACDLabs 10.04
O=C(O)C1NCCC1
Formula
C5 H9 N O2
Name
PROLINE
ChEMBL
CHEMBL54922
DrugBank
DB00172
ZINC
ZINC000000895360
PDB chain
2fzn Chain A Residue 2002 [
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Receptor-Ligand Complex Structure
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PDB
2fzn
Hydrogen Bonding Interactions of the 2-OH Ribityl Group and the N(5) Position of the FAD Cofactor Regulate PutA-membrane Associations in Escherichia coli
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
K329 L513 Y540 R555 R556
Binding residue
(residue number reindexed from 1)
K168 L352 Y379 R394 R395
Annotation score
5
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:2fzn
,
PDBe:2fzn
,
PDBj:2fzn
PDBsum
2fzn
PubMed
UniProt
P09546
|PUTA_ECOLI Bifunctional protein PutA (Gene Name=putA)
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