Structure of PDB 5bot Chain B

Receptor sequence
>5botB (length=166) Species: 9606 (Homo sapiens) [Search protein sequence]
YNVFPRTLKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNF
TRLHDGIADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDD
DETWTSSSKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTGKSHFM
LPDDDVQGIQSLYGPG
3D structure
PDB5bot Fragment-based discovery of indole inhibitors of matrix metalloproteinase-13.
ChainB
Resolution1.85 Å
3D
structure
Catalytic site residues are labeled in the structure
[Spin on]
[Spin off]
[Reset orientation]

[High quality]
[Low quality]

[White background]
[Black background]

[Download]
[Download structure with residue number starting from 1]
Enzymatic activity
Catalytic site (original residue number in PDB) H222 E223 H226 H232
Catalytic site (residue number reindexed from 1) H119 E120 H123 H129
Enzyme Commision number 3.4.24.-
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 4UM B H222 A238 L239 F241 P242 I243 Y244 T245 H119 A135 L136 F138 P139 I140 Y141 T142 MOAD: ic50=39uM
BindingDB: IC50=39000nM
BS02 ZN B H222 H226 H232 H119 H123 H129
BS03 ZN B H172 D174 H187 H200 H69 D71 H84 H97
BS04 CA B D128 D203 E205 D25 D100 E102
BS05 CA B D179 G180 S182 L184 D202 E205 D76 G77 S79 L81 D99 E102
BS06 CA B D162 N194 Y195 G196 D198 D59 N91 Y92 G93 D95
Gene Ontology
Molecular Function
GO:0004222 metalloendopeptidase activity
GO:0008237 metallopeptidase activity
GO:0008270 zinc ion binding
Biological Process
GO:0006508 proteolysis
Cellular Component
GO:0031012 extracellular matrix

View graph for
Molecular Function

View graph for
Biological Process

View graph for
Cellular Component
External links
PDB RCSB:5bot, PDBe:5bot, PDBj:5bot
PDBsum5bot
PubMed22017539
UniProtP45452|MMP13_HUMAN Collagenase 3 (Gene Name=MMP13)

[Back to BioLiP]