Structure of PDB 4gr0 Chain A

Receptor sequence

>4gr0A (length=159) Species: 9606 (Homo sapiens)

MGPVWRKHYITYRINNYTPDMNREDVDYAIRKAFQVWSNVTPLKFSKINT
GMADILVVFARGAHGDDHAFDGKGGILAHAFGPGSGIGGDAHFDEDEFWT
THSGGTNLFLTAVHEIGHSLGLGHSSDPKAVMFPTYKYVDINTFRLSADD
IRGIQSLYG

3D structure

• PDB: 4gr0 Molecular determinants of a selective matrix metalloprotease-12 inhibitor: insights from crystallography and thermodynamic studies.
• Chain: A
• Resolution: 1.497 Å

Enzymatic activity

• Catalytic site (original residue number in PDB): H218 E219 H222 H228
• Catalytic site (residue number reindexed from 1): H114 E115 H118 H124
• Enzyme Commision number: 3.4.24.65: macrophage elastase.

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	H218 H222 H228	H114 H118 H124
BS02	ZN	A	H168 D170 H183 H196	H64 D66 H79 H92
BS03	CA	A	D158 G190 G192 D194	D54 G86 G88 D90
BS04	CA	A	D124 E199 E201	D20 E95 E97
BS05	CA	A	D175 G176 G178 I180 D198 E201	D71 G72 G74 I76 D94 E97
BS06	R4B	A	G179 I180 L181 A182 H183 T215 H218 E219 H222 H228 K233 A234 V235 F237 T239 Y240 K241 V243 F248	G75 I76 L77 A78 H79 T111 H114 E115 H118 H124 K129 A130 V131 F133 T135 Y136 K137 V139 F144	MOAD: Ki=0.28nM PDBbind-CN: -logKd/Ki=9.55,Ki=0.28nM BindingDB: Ki=0.280000nM

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

External links

• PDB: RCSB:4gr0, PDBe:4gr0, PDBj:4gr0
• PDBsum: 4gr0
• PubMed: 23343195
• UniProt: P39900|MMP12_HUMAN Macrophage metalloelastase (Gene Name=MMP12)