Protein family
Protein sequence
Protein function
Catalytic activity
EC number
EC number description
3.4.24.24
Hydrolases;
Acting on peptide bonds (peptidases);
Metalloendopeptidases;
gelatinase A
PDB | Resolution (Å) | PDB name |
---|---|---|
1CK7 | 2.8 | GELATINASE A (FULL-LENGTH) |
1CXW | THE SECOND TYPE II MODULE FROM HUMAN MATRIX METALLOPROTEINASE 2 | |
1EAK | 2.66 | Catalytic domain of proMMP-2 E404Q mutant |
1GEN | 2.15 | C-TERMINAL DOMAIN OF GELATINASE A |
1GXD | 3.1 | proMMP-2/TIMP-2 complex |
1HOV | SOLUTION STRUCTURE OF A CATALYTIC DOMAIN OF MMP-2 COMPLEXED WITH SC-74020 | |
1J7M | The Third Fibronectin Type II Module from Human Matrix Metalloproteinase 2 | |
1KS0 | The First Fibronectin Type II Module from Human Matrix Metalloproteinase 2 | |
1QIB | 2.8 | CRYSTAL STRUCTURE OF GELATINASE A CATALYTIC DOMAIN |
1RTG | 2.6 | C-TERMINAL DOMAIN (HAEMOPEXIN-LIKE DOMAIN) OF HUMAN MATRIX METALLOPROTEINASE-2 |
3AYU | 2.0 | Crystal structure of MMP-2 active site mutant in complex with APP-drived decapeptide inhibitor |
7XGJ | 2.8 | Crystal structure of human MMP-2 catalytic domain in complex with inhibitor |
7XJO | 2.0 | Crystal structure of human MMP-2 catalytic domain in complex with inhibitor |
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0007568 | aging |
Biological Process | GO:0001525 | angiogenesis |
Biological Process | GO:0001955 | blood vessel maturation |
Biological Process | GO:0060346 | bone trabecula formation |
Biological Process | GO:0071492 | cellular response to UV-A |
Biological Process | GO:0071230 | cellular response to amino acid stimulus |
Biological Process | GO:0071392 | cellular response to estradiol stimulus |
Biological Process | GO:0071498 | cellular response to fluid shear stress |
Biological Process | GO:0071347 | cellular response to interleukin-1 |
Biological Process | GO:0034614 | cellular response to reactive oxygen species |
Biological Process | GO:0030574 | collagen catabolic process |
Biological Process | GO:0007566 | embryo implantation |
Biological Process | GO:0035987 | endodermal cell differentiation |
Biological Process | GO:0048013 | ephrin receptor signaling pathway |
Biological Process | GO:0022617 | extracellular matrix disassembly |
Biological Process | GO:0030198 | extracellular matrix organization |
Biological Process | GO:0060325 | face morphogenesis |
Biological Process | GO:0007507 | heart development |
Biological Process | GO:0001957 | intramembranous ossification |
Biological Process | GO:0001553 | luteinization |
Biological Process | GO:0048246 | macrophage chemotaxis |
Biological Process | GO:0007162 | negative regulation of cell adhesion |
Biological Process | GO:0045906 | negative regulation of vasoconstriction |
Biological Process | GO:0001541 | ovarian follicle development |
Biological Process | GO:0001542 | ovulation from ovarian follicle |
Biological Process | GO:0007567 | parturition |
Biological Process | GO:0014012 | peripheral nervous system axon regeneration |
Biological Process | GO:0043065 | positive regulation of apoptotic process |
Biological Process | GO:0030335 | positive regulation of cell migration |
Biological Process | GO:1904707 | positive regulation of vascular associated smooth muscle cell proliferation |
Biological Process | GO:0060740 | prostate gland epithelium morphogenesis |
Biological Process | GO:0030163 | protein catabolic process |
Biological Process | GO:0019538 | protein metabolic process |
Biological Process | GO:0006508 | proteolysis |
Biological Process | GO:0014823 | response to activity |
Biological Process | GO:1904645 | response to amyloid-beta |
Biological Process | GO:0051602 | response to electrical stimulus |
Biological Process | GO:0043627 | response to estrogen |
Biological Process | GO:0042542 | response to hydrogen peroxide |
Biological Process | GO:0055093 | response to hyperoxia |
Biological Process | GO:0001666 | response to hypoxia |
Biological Process | GO:0009612 | response to mechanical stimulus |
Biological Process | GO:0035094 | response to nicotine |
Biological Process | GO:0032526 | response to retinoic acid |
Biological Process | GO:0009410 | response to xenobiotic stimulus |
Biological Process | GO:0048771 | tissue remodeling |
Molecular Function | GO:0004175 | endopeptidase activity |
Molecular Function | GO:0001968 | fibronectin binding |
Molecular Function | GO:0004222 | metalloendopeptidase activity |
Molecular Function | GO:0008237 | metallopeptidase activity |
Molecular Function | GO:0004252 | serine-type endopeptidase activity |
Molecular Function | GO:0008270 | zinc ion binding |
Cellular Component | GO:0062023 | collagen-containing extracellular matrix |
Cellular Component | GO:0005576 | extracellular region |
Cellular Component | GO:0005615 | extracellular space |
Cellular Component | GO:0005739 | mitochondrion |
Cellular Component | GO:0005634 | nucleus |
Cellular Component | GO:0005886 | plasma membrane |
Cellular Component | GO:0030017 | sarcomere |
InterPro | InterPro name |
---|---|
IPR000562 | Fibronectin type II domain |
IPR000585 | Hemopexin-like domain |
IPR001818 | Peptidase M10, metallopeptidase |
IPR002477 | Peptidoglycan binding-like |
IPR006026 | Peptidase, metallopeptidase |
IPR013806 | Kringle-like fold |
IPR018486 | Hemopexin, conserved site |
IPR018487 | Hemopexin-like repeats |
IPR021158 | Peptidase M10A, cysteine switch, zinc binding site |
IPR021190 | Peptidase M10A |
IPR024079 | Metallopeptidase, catalytic domain superfamily |
IPR033739 | Peptidase M10A, catalytic domain |
IPR036365 | PGBD-like superfamily |
IPR036375 | Hemopexin-like domain superfamily |
IPR036943 | Fibronectin type II domain superfamily |
Pfam | Pfam name |
---|---|
PF00040 | Fibronectin type II domain |
PF00045 | Hemopexin |
PF00413 | Matrixin |
PF01471 | Putative peptidoglycan binding domain |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-1442490 | Collagen degradation | Leaf | R-HSA-1474244 | Extracellular matrix organization |
R-HSA-1474228 | Degradation of the extracellular matrix | Internal node | R-HSA-1474244 | Extracellular matrix organization |
R-HSA-1592389 | Activation of Matrix Metalloproteinases | Leaf | R-HSA-1474244 | Extracellular matrix organization |
R-HSA-381426 | Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | Leaf | R-HSA-392499 | Metabolism of proteins |
R-HSA-3928665 | EPH-ephrin mediated repulsion of cells | Leaf | R-HSA-1266738 | Developmental Biology |
R-HSA-6785807 | Interleukin-4 and Interleukin-13 signaling | Leaf | R-HSA-168256 | Immune System |
R-HSA-9009391 | Extra-nuclear estrogen signaling | Internal node | R-HSA-162582 | Signal Transduction |
Location | ECO term | Pubmed |
---|---|---|
Cytoplasm | ||
Membrane | ||
Mitochondrion | ||
Nucleus | ||
Secreted, extracellular space, extracellular matrix | ECO:0000305 | PubMed:2834383 |
HPO ID | HPO name |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000147 | Polycystic ovaries |
HP:0000212 | Gingival overgrowth |
HP:0000248 | Brachycephaly |
HP:0000280 | Coarse facial features |
HP:0000315 | Abnormality of the orbital region |
HP:0000316 | Hypertelorism |
HP:0000327 | Hypoplasia of the maxilla |
HP:0000347 | Micrognathia |
HP:0000414 | Bulbous nose |
HP:0000446 | Narrow nasal bridge |
HP:0000520 | Proptosis |
HP:0000612 | Iris coloboma |
HP:0000684 | Delayed eruption of teeth |
HP:0000822 | Hypertension |
HP:0000916 | Broad clavicles |
HP:0000938 | Osteopenia |
HP:0000939 | Osteoporosis |
HP:0001007 | Hirsutism |
HP:0001034 | Hypermelanotic macule |
HP:0001059 | Pterygium |
HP:0001072 | Thickened skin |
HP:0001085 | Papilledema |
HP:0001171 | Split hand |
HP:0001220 | Interphalangeal joint contracture of finger |
HP:0001230 | Broad metacarpals |
HP:0001239 | Wrist flexion contracture |
HP:0001249 | Intellectual disability |
HP:0001288 | Gait disturbance |
HP:0001369 | Arthritis |
HP:0001473 | Metatarsal osteolysis |
HP:0001476 | Delayed closure of the anterior fontanelle |
HP:0001482 | Subcutaneous nodule |
HP:0001495 | Carpal osteolysis |
HP:0001504 | Metacarpal osteolysis |
HP:0001539 | Omphalocele |
HP:0001626 | Abnormality of the cardiovascular system |
HP:0001629 | Ventricular septal defect |
HP:0001631 | Atrial septal defect |
HP:0001634 | Mitral valve prolapse |
HP:0001647 | Bicuspid aortic valve |
HP:0001678 | Atrioventricular block |
HP:0001680 | Coarctation of aorta |
HP:0001719 | Double outlet right ventricle |
HP:0001761 | Pes cavus |
HP:0001763 | Pes planus |
HP:0001783 | Broad metatarsal |
HP:0001836 | Camptodactyly of toe |
HP:0001999 | Abnormal facial shape |
HP:0002007 | Frontal bossing |
HP:0002659 | Increased susceptibility to fractures |
HP:0002751 | Kyphoscoliosis |
HP:0002753 | Thin bony cortex |
HP:0002797 | Osteolysis |
HP:0002829 | Arthralgia |
HP:0002953 | Vertebral compression fracture |
HP:0003016 | Metaphyseal widening |
HP:0003040 | Arthropathy |
HP:0003179 | Protrusio acetabuli |
HP:0003273 | Hip contracture |
HP:0003312 | Abnormal form of the vertebral bodies |
HP:0003320 | C1-C2 subluxation |
HP:0003493 | Antinuclear antibody positivity |
HP:0003593 | Infantile onset |
HP:0003621 | Juvenile onset |
HP:0004322 | Short stature |
HP:0005441 | Sclerotic cranial sutures |
HP:0005922 | Abnormal hand morphology |
HP:0005994 | Nodular goiter |
HP:0006012 | Widened metacarpal shaft |
HP:0006086 | Thin metacarpal cortices |
HP:0006234 | Osteolysis involving tarsal bones |
HP:0006252 | Interphalangeal joint erosions |
HP:0006466 | Ankle flexion contracture |
HP:0007957 | Corneal opacity |
HP:0008011 | Peripheral opacification of the cornea |
HP:0008078 | Thin metatarsal cortices |
HP:0008090 | Ankylosis of feet small joints |
HP:0008133 | Distal tapering of metatarsals |
HP:0009139 | Osteolysis involving bones of the lower limbs |
HP:0010314 | Premature thelarche |
HP:0010537 | Wide cranial sutures |
HP:0011355 | Localized skin lesion |
HP:0011463 | Childhood onset |
HP:0025131 | Finger swelling |
HP:0045039 | Osteolysis involving bones of the upper limbs |
HP:0100651 | Type I diabetes mellitus |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
multicentric osteolysis- nodulosis- and arthropathy | MONDO:0009809 | M89 | chapter13, Diseases of the musculoskeletal system and connective tissue | OMIM:259600 | |
multicentric osteolysis-nodulosis-arthropathy spectrum | MONDO:0018298 | Q85 | chapter17, Congenital malformations, deformations and chromosomal abnormalities | Orphanet:371428 |