Structure of PDB 6tzh Chain C

Receptor sequence
>6tzhC (length=354) Species: 470 (Acinetobacter baumannii) [Search protein sequence]
DQEIKKLVDQNFKPLLEKYDVPGMAVGVIQNNKKYEMYYGLQSVQDKKAV
NSNTIFELGSVSKLFTATAGGYAKNKGKISFDDTPGKYWKELKNTPIDQV
NLLQLATYTSGNLALQFPDEVQTDQQVLTFFKDWKPKNPIGEYRQYSNPS
IGLFGKVVALSMNKPFDQVLEKTIFPALGLKHSYVNVPKTQMQNYAFGYN
QENQPIRVNPGPLDAPAYGVKSTLPDMLSFIHANLNPQKYPTDIQRAINE
THQGRYQVNTMYQALGWEEFSYPATLQTLLDSNSEQIVMKPNKVTAISKE
PSVKMYHKTGSTSGFGTYVVFIPKENIGLVMLTNKRIPNEERIKAAYVVL
NAIK
3D structure
PDB6tzh 1,2,3-Triazolylmethaneboronate: A Structure Activity Relationship Study of a Class of beta-Lactamase Inhibitors againstAcinetobacter baumanniiCephalosporinase.
ChainC
Resolution2.04 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) S64 K67 Y150 E272 K312 S315
Catalytic site (residue number reindexed from 1) S60 K63 Y146 E268 K308 S311
Enzyme Commision number 3.5.2.6: beta-lactamase.
Interaction with ligand
Site
#		 Ligand Ligand
chain		 Binding residues on receptor
(original residue number in PDB)		 Binding residues on receptor
(residue number reindexed from 1)		 Binding affinity
BS01 ERF C S64 Q120 Y150 N152 T313 G314 S315 S60 Q116 Y146 N148 T309 G310 S311
BS02 GLY C Y222 S317 Y218 S313
Gene Ontology
Molecular Function
GO:0008800 beta-lactamase activity
GO:0016787 hydrolase activity
Biological Process
GO:0017001 antibiotic catabolic process
GO:0046677 response to antibiotic
Cellular Component
GO:0030288 outer membrane-bounded periplasmic space

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Molecular Function
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Biological Process
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Cellular Component
External links
PDB RCSB:6tzh, PDBe:6tzh, PDBj:6tzh
PDBsum6tzh
PubMed32502340
UniProtQ6DRA1

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