5H7V,1YC0,4ISL,4ISN,4ISO,5EZD


Conserved Protein Domain Family
Kunitz_HAI1_1-like

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cd22623: Kunitz_HAI1_1-like 
Click on image for an interactive view with Cn3D
Kunitz domain 1 of hepatocyte growth factor activator inhibitor-1 (HAI-1)
This model includes Kunitz domain 1 (KD1) of hepatocyte growth factor activator inhibitor type 1 (HAI1 or HAI-1, also known as Kunitz-type protease inhibitor 1), a membrane-bound multidomain protein essential to the integrity of the basement membrane during placental development. HAI-1 contains an extracellular region and several internal domains that include two Kunitz domains separated in sequence but spatially closed to each other, and their interdomain interactions have evolved to stimulate the inhibitory activity of an integrated Kunitz. KD1, the major inhibitory domain of HAI-1, is involved in auto-inhibition of the extracellular region via steric blockage of its active site in the HAI-1 compact tertiary structure; presence of the target protease causes changes in the HAI-1 structure to an extended conformation. HAI-1 has been shown to inhibit several serine proteases such as matripase, hepsin, trypsin, hepatocyte growth factor activator (HGFA), and prostasin. It is also important in maintaining postnatal homeostasis in many tissues, including keratinization of the epidermis, hair development, colonic epithelium integrity, proliferation and cell fate of neural progenitor cells, and tissue injury and repair. The interaction between HAI-1 and matriptase is critical for tissue morphogenesis and cellular biology. HAI-1:matriptase ratio imbalance results in tumorigenesis; slight overexpression of matriptase relative to HAI-1 causes spontaneous squamous cell carcinoma, a phenotype that can be effectively reversed back to wild type by additional expression of HAI-1, indicating the need for a tight functional relationship between the two to maintain homeostasis. The structures of these domains are similar to those of Kunitz-type proteinase inhibitors such as BPTI (bovine pancreatic trypsin inhibitor), showing an alpha/beta fold with irregular secondary structure stabilized by three disulfide bonds.
Statistics
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PSSM-Id: 438666
Aligned: 72 rows
Threshold Bit Score: 108.399
Created: 8-Jul-2020
Updated: 17-Oct-2022
Structure
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Program:
Drawing:
Aligned Rows:
 
serine protease
Conserved site includes 17 residues -Click on image for an interactive view with Cn3D
Feature 1:serine protease binding site [polypeptide binding site]
Evidence:
  • Structure:4ISL: Homo sapiens hepatocyte growth factor activator inhibitor-1 (HAI-1) binds matriptase; contacts at 4.0A

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1                    ##########             # # ## #  # #            
5H7V_A        215 QTEDYCLASNKVGRCRGSFPRWYYDPteQICKSFVYGGCLGNKNNYLREEECILACRGV 273  Homo sapiens
4ISL_B          1 QTEDYCLASNKVGRCRGSFPRWYYDPteQICKSFVYGGCLGNKNNYLREEECILACRGV 59   human
5EZD_A         80 QTEDYCLASNKVGRCRGSFPRWYYDPteQICKSFVYGGCLGNKNNYLREEECILACRGV 138  Homo sapiens
XP_001381154  323 QTEEHCLAPKKVGRCRGSFPRWYYDPteQQCKQYVYGGCLGNKNNYIREEECKMACKDV 381  gray short-tailed opossum
XP_421130     241 QTEEHCLTPKKVGWCRGSFPRWFYDPtlQQCQEFIFGGCKPNKNNYLREEECKLACRNV 299  chicken
XP_014340918  238 DSELYCNAPKKVGHCRGSFERWYYVPatLKCEKFIYGGCKGNKNNYLEEWECMQACKHY 296  coelacanth
KRZ68849      504 VCADPCMLPKKVGRCRGAFQRWYYDSsaNKCRKFIYGGCDANENNFVGEEECISACVRG 562  Trichinella papuae
XP_018086738  237 ETEEHCFAPYKVGRCRGSFTRWYYNPeaNECLEFIYGGCKPNKNNYLRIEDCRQTCMNN 295  African clawed frog
XP_018420861  231 QTEEYCLAPKKVGRCRGSFTRWYYNSdvNDCEEFVFGGCKPNKNNYVQQEDCRQACVNL 289  Nanorana parkeri
XP_692207      95 AENERCLMPKKVGPCRGAIPRWHFNPvtKKCENFIFGGCKENHNNFLTLEECSKACHTV 153  zebrafish

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