Structure of PDB 4nmf Chain B Binding Site BS01
Receptor Information
>4nmf Chain B (length=979) Species:
243231
(Geobacter sulfurreducens PCA) [
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ELNTKIVNRGKEFFGSISGEKPSLFNKGAWMGKAMDWSMQNEQFKIQMFR
FVDVFPSLTTSKLLTEHIREYFGNEQDMPAFMAVLNKVLTSNIEEMARQF
IVGETTKEAVKNLEKLRKDGFAAVVDVLGEATLSEEEAEVYTNTYLELLE
ALKKEQGSWKGLPGKGGDPGLDWGHAPKVNIAVKPTALFCLANPQDFEGS
VVAILDRMRRIFKKVMELNGFLCIDMESYRHKEIILEVFRRLKLEYRDYP
HLGIVLQAYLKDNDKDLDDLLAWAKEHKVQISVRLVKGAYWDYETVKAKQ
NDWEVPVWTIKAESDAAYERQARKILENHQICHFACASHNIRTISAVMEM
ARELNVPEDRYEFQVLYGMAEPVRKGILKVAGRIRLYAPYGNMVPGMGYL
VRRLLENTANESFLRQSFAEDAQIERLLEDPAVTVERERAARAARKGLGG
LPPFNNEAMVDFTRADHRAAFPKHIAQVRTQLGKTYPLFINGKEVRTNDL
IPTVNPNKPSEVLGQICQAGTTEVGDAIAAAKAAFPAWRDTDPRTRAEYL
LKAAQAARKRLFELSAWQVLEIGKQWDQAYADVTEAIDFLEYYAREMIRL
GQPQRVGHAPGELNHYFYEPKGVAAVIAPWNFPLAISMGMASAAIVTGNC
VVFKPSGITSIIGWHLVELFREAGLPEGVFNFTPGRGSVMGDYLVDHPDI
SLIAFTGSMETGLRIIERAAKVHPGQANVKKIISEMGGKNAIIIDDDADL
DEAVPHVLYSAFGFQGQKCSACSRVIVLDAVYDKFIERLVSMAKATKVGP
SEDPANYMGAVADDKAMKSIKEYAEIGKREGHVLYESPVPAGEGYFVPMT
IIGGIKPEHRIAQEEIFGPVLAVMRAKDFDQAIEWANSTQFALTGGIFSR
SPEHLAKARREFRVGNLYINRNNTGALVERQPFGGARMSGVGTKAGGPDY
LLHFMDPRVVTENTMRRGFAPIEEDDDWV
Ligand information
Ligand ID
P5F
InChI
InChI=1S/C32H40N10O17P2/c1-14-6-16-17(7-15(14)2)41(29-23(30(50)39-32(51)38-29)40(16)5-3-4-34-8-21(45)46)9-18(43)24(47)19(44)10-56-60(52,53)59-61(54,55)57-11-20-25(48)26(49)31(58-20)42-13-37-22-27(33)35-12-36-28(22)42/h3-7,12-13,18-20,24-26,31,43-44,47-49H,8-11H2,1-2H3,(H,45,46)(H,52,53)(H,54,55)(H2,33,35,36)(H2,38,39,50,51)/b5-3+,34-4?/t18-,19+,20+,24-,25+,26+,31+/m0/s1
InChIKey
IRSTVKNHNHEQIM-RDJFLKOLSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
CC1=CC2=[N](C3=C(C(=O)NC(=O)N3)[N](=C2C=C1C)C=CC=NCC(=O)O)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.7.6
CC1=CC2=[N](C3=C(C(=O)NC(=O)N3)[N](=C2C=C1C)C=CC=NCC(=O)O)C[C@@H]([C@@H]([C@@H](COP(=O)(O)OP(=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.385
Cc1cc2c(cc1C)n(C=CC=NCC(O)=O)c3C(=O)NC(=O)Nc3n2C[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
CACTVS 3.385
Cc1cc2c(cc1C)n(\C=C\C=NCC(O)=O)c3C(=O)NC(=O)Nc3n2C[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
Formula
C32 H40 N10 O17 P2
Name
N-propargylglycine-modified flavin adenine dinucleotide
ChEMBL
DrugBank
ZINC
PDB chain
4nmf Chain B Residue 1101 [
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Receptor-Ligand Complex Structure
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PDB
4nmf
Structures of the PutA peripheral membrane flavoenzyme reveal a dynamic substrate-channeling tunnel and the quinone-binding site.
Resolution
1.95 Å
Binding residue
(original residue number in PDB)
K203 D244 M245 V274 Q276 R303 V305 K306 G307 A308 W310 W327 T328 I329 K330 S333 A356 S357 H358 N359 Q383 L385 Y406 E425 E430 S431 F432
Binding residue
(residue number reindexed from 1)
K184 D225 M226 V255 Q257 R284 V286 K287 G288 A289 W291 W308 T309 I310 K311 S314 A337 S338 H339 N340 Q364 L366 Y387 E406 E411 S412 F413
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
N655 K678 E759 C793 E889 A969
Catalytic site (residue number reindexed from 1)
N631 K654 E735 C769 E865 A945
Enzyme Commision number
1.2.1.88
: L-glutamate gamma-semialdehyde dehydrogenase.
Gene Ontology
Molecular Function
GO:0000166
nucleotide 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
Biological Process
GO:0006355
regulation of DNA-templated transcription
GO:0006562
proline catabolic process
GO:0010133
proline catabolic process to glutamate
Cellular Component
GO:0005737
cytoplasm
GO:0009898
cytoplasmic side of plasma membrane
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4nmf
,
PDBe:4nmf
,
PDBj:4nmf
PDBsum
4nmf
PubMed
24550478
UniProt
Q746X3
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