Structure of PDB 3r5f Chain A

Receptor sequence
>3r5fA (length=343) Species: 291331 (Xanthomonas oryzae pv. oryzae KACC 10331) [Search protein sequence]
KIRVGLIFGGKSAEHEVSLQSARNILDALDPQRFEPVLIGIDKQGQWHVN
DPDSFLLHADDPARIALHRSGRGVALLPGAQQQQLRPIQALAQIDVVFPI
VHGTLGEDGSLQGLLRMANLPFVGSGVLGSAVAMDKDMAKRVLRDARLAV
APFVCFDRHTAAHADVDTLIAQLGLPLFVKPANQGSSVGVSQVRTADAFA
AALALALAYDHKVLVEAAVAGREIECAVLGNAVPHASVCGEVVVEIVIPA
DIDAQTQQRIQQIAVQAYQALGCAGMARVDVFLCADGRIVINEVNTLPGF
TRISVYPKLWQASGLDYRGLITRLIELALERHTDDQLLRSAVE
3D structure
PDB3r5f Crystal structure of D-alanine-D-alanine ligase A from Xanthomonas oryzae pathovar oryzae with ATP
ChainA
Resolution2.07 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) Q22 H107 S191 R300 D302 E315 N317 G321 I325
Catalytic site (residue number reindexed from 1) Q20 H102 S186 R278 D280 E293 N295 G299 I303
Enzyme Commision number 6.3.2.4: D-alanine--D-alanine ligase.
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 ATP A F183 K185 S192 A223 V224 E228 F304 E315 F178 K180 S187 A218 V219 E223 F282 E293
BS02 MG A D302 E315 D280 E293
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0005524 ATP binding
GO:0008716 D-alanine-D-alanine ligase activity
GO:0016874 ligase activity
GO:0046872 metal ion binding
Biological Process
GO:0008360 regulation of cell shape
GO:0009252 peptidoglycan biosynthetic process
GO:0071555 cell wall organization
Cellular Component
GO:0005737 cytoplasm
GO:0005829 cytosol

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:3r5f, PDBe:3r5f, PDBj:3r5f
PDBsum3r5f
PubMed
UniProtQ5H614

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