Entity Details

Primary name PRS56_HUMAN
Entity type UniProt
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Details

AccessionP0CW18
EntryNamePRS56_HUMAN
FullNameSerine protease 56
TaxID9606
Evidenceevidence at transcript level
Length603
SequenceStatuscomplete
DateCreated2011-05-03
DateModified2021-06-02

Ontological Relatives

GenesPRSS56

GO terms

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GOName
GO:0002690 positive regulation of leukocyte chemotaxis
GO:0004252 serine-type endopeptidase activity
GO:0005615 extracellular space
GO:0005783 endoplasmic reticulum
GO:0006508 proteolysis
GO:0007596 blood coagulation
GO:0043010 camera-type eye development

Subcellular Location

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Domains

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DomainNameCategoryType
IPR001254 Serine proteases, trypsin domainDomainDomain
IPR001314 Peptidase S1A, chymotrypsin familyFamilyFamily
IPR009003 Peptidase S1, PA clanFamilyHomologous superfamily
IPR018114 Serine proteases, trypsin family, histidine active siteSiteActive site
IPR033116 Serine proteases, trypsin family, serine active siteSiteActive site
IPR043504 Peptidase S1, PA clan, chymotrypsin-like foldFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
613517 OMIMMicrophthalmia, isolated, 6 (MCOP6)A developmental ocular disorder characterized by small malformed eyes. Clinical features are extreme hyperopia due to short axial length with essentially normal anterior segment, steep corneal curvatures, shallow anterior chamber, thick lenses, and thickened scleral wall. Palpebral fissures appear narrow because of relatively deep-set eyes, visual acuity is mildly to moderately reduced, and anisometropic or strabismic amblyopia is common. The fundus of the eye shows crowded optical disks, tortuous vessels, and an abnormal foveal avascular zone. The disease is caused by variants affecting the gene represented in this entry.

Interactions

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