Structure of PDB 4a7b Chain A

Receptor sequence
>4a7bA (length=169) Species: 9606 (Homo sapiens) [Search protein sequence]
YNVFPRTLKWSKMNLTYRIVNYTPDMTHSEVEKAFKKAFKVWSDVTPLNF
TRLHDGIADIMISFGIKEHGDFYPFDGPSGLLAHAFPPGPNYGGDAHFDD
DETWTSSSKGYNLFLVAAHEFGHSLGLDHSKDPGALMFPIYTYTGKSHFM
LPDDDVQGIQSLYGPGDED
3D structure
PDB4a7b Lead Optimisation of Selective Non-Zinc Binding Inhibitors of Mmp13. Part 2.
ChainA
Resolution2.2 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 3W5 A G183 L184 L185 V219 H222 E223 G237 L239 F241 P242 I243 Y244 T245 T247 G80 L81 L82 V116 H119 E120 G134 L136 F138 P139 I140 Y141 T142 T144 PDBbind-CN: -logKd/Ki=7.40,IC50=39.8nM
BS02 ZN A H222 H226 H232 H119 H123 H129
BS03 CA A D162 N194 G196 D198 D59 N91 G93 D95
BS04 ZN A H172 D174 H187 H200 H69 D71 H84 H97
BS05 CA A D179 G180 S182 L184 D202 E205 D76 G77 S79 L81 D99 E102
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:4a7b, PDBe:4a7b, PDBj:4a7b
PDBsum4a7b
PubMed22153941
UniProtP45452|MMP13_HUMAN Collagenase 3 (Gene Name=MMP13)

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