Conserved Protein Domain Family
serpinB9_CAP-3

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cd19568: serpinB9_CAP-3 
serpin family B member 9, cytoplasmic antiproteinase 3
Cytoplasmic antiproteinase 3 (CAP-3; peptidase inhibitor 9/PI-9, Spi6, or testicular tissue protein Li 180) is an intracellular inhibitor of granzyme B (grB) that protects cytotoxic lymphocytes from grB-mediated death. It is also thought to be expressed in accessory immune cells, including dendritic cells (DCs), although there is some debate about this. Overexpression of serpin B9 may prevent cytotoxic T-lymphocytes from eliminating certain tumor cells. A pseudogene of this gene is found on chromosome 6. Diseases associated with serpin B9 include chronic obstructive pulmonary disease (COPD) and oral squamous cell carcinoma (OSCC). The ovalbumin family of serpins (ov-serpins) is a family of closely related proteins, whose members can be secreted (ovalbumin), cytosolic (leukocyte elastase inhibitor, LEI), or targeted to both compartments (plasminogen activator inhibitor 2, PAI-2). It also characterized by N- and C-terminal extensions, the absence of a signal peptide, and a Ser rather than an Asn residue at the penultimate position. The ov-serpins corresponds to clade B of the serpin superfamily. In general, SERine Proteinase INhibitors (serpins) exhibit conformational polymorphism shifting from native to cleaved, latent, delta, or polymorphic forms. Many serpins, such as antitrypsin and antichymotrypsin, function as serine protease inhibitors which regulate blood coagulation cascades. Non-inhibitory serpins perform many diverse functions such as chaperoning proteins or transporting hormones. Serpins are of medical interest because mutants can cause blood clotting disorders, emphysema, cirrhosis, and dementia. A classification based on evolutionary relatedness has resulted in the assignment of serpins to 16 clades designated A-P along with some orphans.
Statistics
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PSSM-Id: 381034
Aligned: 5 rows
Threshold Bit Score: 661.951
Created: 18-Apr-2018
Updated: 2-Oct-2020
Structure
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Aligned Rows:
 
reactive center
Feature 1:reactive center loop (RCL)
Evidence:
  • Comment:depending on the conformational state, the RC loop is surface accessible in the active form or buried and inserted as the central beta strand in the inactive form.

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1                                                                                        
XP_004628459   1 MNPLSEANGTFAIRLLKLLGQEDPARNVFFSPVSISSALGMVLLGAKGSTAAQIAEVLALNAQRDIHLGFQSLLTQVRRP 80  degu
XP_012369507  14 MSILLEASGAFATSILKVLGQEDPVCSVFFSLVSISFAMGMVLLGAKGSLVAEMAQARALNTEKDIHGGFQSLLTQVHKS 93  degu
NP_004146      1 METLSNASGTFAIRLLKILCQDNPSHNVFCSPVSISSALAMVLLGAKGNTATQMAQALSLNTEEDIHRAFQSLLTEVNKA 80  human
OWK13291       1 MDALCEANGTFALRLLKALCEDDPSGNVFFSPVSLSSVLAMVLLGAKGDTAAQVAQALSLNTEKEFHQDFQQLLAELNKP 80  Cervus elaphus ...
P50453         1 METLSNASGTFAIRLLKILCQDNPSHNVFCSPVSISSALAMVLLGAKGNTATQMAQALSLNTEEDIHRAFQSLLTEVNKA 80  human
Feature 1                                                                                        
XP_004628459  81 GAPFSLSIANRLFGEESCQFLSPFQQSCQNYYEAELEQLPFIKAPERSRKHINAWVSTKTAGKIEELLAQNSIDEfCRLL 160 degu
XP_012369507  94 GDPFSFSIANKLFSTESFELLSSFQESCLTFYQGKQEQLSFAQAPESSRKHINVWVFRKTGGKIYELLEKHSVHGvCRLV 173 degu
NP_004146     81 GTQYLLRTANRLFGEKTCQFLSTFKESCLQFYHAELKELSFIRAAEESRKHINTWVSKKTEGKIEELLPGSSIDAeTRLV 160 human
OWK13291      81 DAQYLLTTANRIFGEKTYEFLSTFKESCLRFYYAELEQLSFAEAAEPSRKQINAWVSKKTEGKIPELLPANSINAeTRLI 160 Cervus elaphus ...
P50453        81 GTQYLLRTANRLFGEKTCQFLSTFKESCLQFYHAELKELSFIRAAEESRKHINTWVSKKTEGKIEELLPGSSIDAeTRLV 160 human
Feature 1                                                                                        
XP_004628459 161 LINAVYFKGTWKETFLKQSTRTVPFKMNKNEQRPVQMMFQKDTFPWAHVsevpAQVLELPYQgQELSMVLVLPDEGV--- 237 degu
XP_012369507 174 LINVVYFKGRWQEQFEKSSTMGLSFKINQQEQRPVQMMCEEAMYPCAQE----REVLELPYKgQGLSMVLLRLDKCV--- 246 degu
NP_004146    161 LVNAIYFKGKWNEPFDETYTREMPFKINQEEQRPVQMMYQEATFKLAHVgevrAQLLELPYArKELSLLVLLPDDGV--- 237 human
OWK13291     161 LVNAVYFKGRWSEKFDKEYTREMPFRINQKEQRPVQMMFQDGVFRLARIqevqAQVLELPYAdEELSMLVLLPNDHVpls 240 Cervus elaphus ...
P50453       161 LVNAIYFKGKWNEPFDETYTREMPFKINQEEQRPVQMMYQEATFKLAHVgevrAQLLELPYArKELSLLVLLPDDGV--- 237 human
Feature 1                                                                                        
XP_004628459 238 ----------------------------------------DLSTVEKTLTLEKFQTWTSPEHMKRTDVQVSLPRFKLQED 277 degu
XP_012369507 247 ----------------------------------------DLSKVEKALTFEQFQIWTSPEFMKRNEVQVCLPRFKLEEE 286 degu
NP_004146    238 ----------------------------------------ELSTVEKSLTFEKLTAWTKPDCMKSTEVEVLLPKFKLQED 277 human
OWK13291     241 svsvlrvlparlalepllllwgvlarvperemahlsssriLAFQVEKHLTWEKFLAWTQPHSMKKTQVEVFLPKFKLEMT 320 Cervus elaphus ...
P50453       238 ----------------------------------------ELSTVEKSLTFEKLTAWTKPDCMKSTEVEVLLPKFKLQED 277 human
Feature 1                                                        ############# ###############   
XP_004628459 278 YDMVSVLQGLGVVDVFDpHKADLSGMLADRNLCVSMFVHKSVVEVNEEGTEAAAASACKIG-YCCARYWKVFCADHPFLF 356 degu
XP_012369507 287 YDMGSVLWALGILDVFHlGKADLSGMSPDSDLCLSKFMHKSVVEVNGEGMEVAAVSSCMVEnYCDNKGRPEFCTDRPFLF 366 degu
NP_004146    278 YDMESVLRHLGIVDAFQqGKADLSAMSAERDLCLSKFVHKSFVEVNEEGTEAAAASSCFVVaECCMESGPRFCADHPFLF 357 human
OWK13291     321 YDMVSVLQGLGVLEAFQsGRADFSAMSPSEGLCLSALAHKSVVEVDEEGTEAAAASAMLQV-DSCMVNQPRFCADHPFLF 399 Cervus elaphus ...
P50453       278 YDMESVLRHLGIVDAFQqGKADLSAMSAERDLCLSKFVHKSFVEVNEEGTEAAAASSCFVVaECCMESGPRFCADHPFLF 357 human
Feature 1                            
XP_004628459 357 FIRHNKT-NSLLFCGRFSSP 375 degu
XP_012369507 367 FIRHNRTdQSLLCCGRFSSH 386 degu
NP_004146    358 FIRHNRA-NSILFCGRFSSP 376 human
OWK13291     400 FIRHNGS-RSTLFCGRFSSP 418 Cervus elaphus hippelaphus
P50453       358 FIRHNRA-NSILFCGRFSSP 376 human

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