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2Q85

Crystal Structure of E. Coli Mur B bound to a Naphthyl Tetronic Acid inihibitor

Functional Information from GO Data
ChainGOidnamespacecontents
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0007049biological_processcell cycle
A0008360biological_processregulation of cell shape
A0008762molecular_functionUDP-N-acetylmuramate dehydrogenase activity
A0009252biological_processpeptidoglycan biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0050660molecular_functionflavin adenine dinucleotide binding
A0051301biological_processcell division
A0071555biological_processcell wall organization
A0071949molecular_functionFAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues12
DetailsBINDING SITE FOR RESIDUE 973 A 401
ChainResidue
ATYR190
ALEU290
AVAL291
AFAD402
ALEU218
AGLY228
ASER229
AASN233
APRO252
ATYR254
ALYS262
AGLN288

site_idAC2
Number of Residues30
DetailsBINDING SITE FOR RESIDUE FAD A 402
ChainResidue
AILE45
ALEU46
AGLY47
AGLU48
AGLY49
ASER50
AASN51
AVAL52
AASN65
AILE110
APRO111
AGLY112
ACYS113
ASER116
AILE119
AILE122
AGLY123
AARG159
AALA172
AILE173
AARG214
AASN226
AALA227
AGLY228
AARG327
AGLU334
A973401
AHOH481
AHOH500
AHOH529

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE:
ChainResidueDetails
AARG159
AGLU325

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor
ChainResidueDetails
ASER229

site_idSWS_FT_FI3
Number of Residues1
DetailsBINDING:
ChainResidueDetails
ATYR190

Catalytic Information from CSA
site_idMCSA1
Number of Residues3
DetailsM-CSA 353
ChainResidueDetails
AARG159attractive charge-charge interaction, electrostatic stabiliser, increase electrophilicity
ASER229activator, proton acceptor, proton donor
AGLU325activator, attractive charge-charge interaction, electrostatic stabiliser, increase basicity, increase electrophilicity, proton acceptor, proton donor

218500

PDB entries from 2024-04-17

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