Structure of PDB 3i7i Chain A

Receptor sequence
>3i7iA (length=165) Species: 9606 (Homo sapiens) [Search protein sequence]
YNVFPRTLKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNF
TRLHDGIADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDD
DETWTSSSKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTFMLPDD
DVQGIQSLYGPGDED
3D structure
PDB3i7i Improving potency and selectivity of a new class of non-Zn-chelating MMP-13 inhibitors.
ChainA
Resolution2.208 Å
3D
structure
Catalytic site residues are labeled in the structure
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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 ZN A H222 H226 H232 H119 H123 H129
BS02 ZN A H172 D174 H187 H200 H69 D71 H84 H97
BS03 CA A D128 D203 E205 D25 D100 E102
BS04 CA A D179 G180 S182 L184 D202 E205 D76 G77 S79 L81 D99 E102
BS05 CA A D162 N194 Y195 G196 D198 D59 N91 Y92 G93 D95
BS06 518 A G183 L185 H222 E223 L239 F241 P242 I243 Y244 T245 T247 F252 P255 G80 L82 H119 E120 L136 F138 P139 I140 Y141 T142 T144 F145 P148 MOAD: ic50=620nM
PDBbind-CN: -logKd/Ki=6.21,IC50=620nM
BindingDB: IC50=620nM
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

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:3i7i, PDBe:3i7i, PDBj:3i7i
PDBsum3i7i
PubMed19692239
UniProtP45452|MMP13_HUMAN Collagenase 3 (Gene Name=MMP13)

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