NCBI Home Page NCBI Site Search page NCBI Guide that lists and describes the NCBI resources
Conserved domains on  [gi|768032511|ref|XP_011543838|]
View 

phosphate-regulating neutral endopeptidase PHEX isoform X4 [Homo sapiens]

Protein Classification

M13 family metallopeptidase( domain architecture ID 10171382)

M13 family metallopeptidase similar to neutral endopeptidase (neprilysin), which degrades and inactivates bioactive peptides, and to endothelin-converting enzyme, which catalyzes the hydrolysis of the bond between Trp-21 and Val-22 in big endothelin to form endothelin 1

EC:  3.4.24.-
MEROPS:  M13

Graphical summary

 Zoom to residue level

show extra options »

Show site features     Horizontal zoom: ×

List of domain hits

Name Accession Description Interval E-value
M13 cd08662
Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of ...
1-371 7.13e-170

Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of metallopeptidases includes neprilysin (neutral endopeptidase, NEP, enkephalinase, CD10, CALLA, EC 3.4.24.11), endothelin-converting enzyme I (ECE-1, EC 3.4.24.71), erythrocyte surface antigen KELL (ECE-3), phosphate-regulating gene on the X chromosome (PHEX), soluble secreted endopeptidase (SEP), and damage-induced neuronal endopeptidase (DINE)/X-converting enzyme (XCE). Proteins in this family fulfill a broad range of physiological roles due to the greater variation in the active site's S2' subsite allowing substrate specificity. NEP is expressed in a variety of tissues including kidney and brain, and is involved in many physiological and pathological processes, including blood pressure and inflammatory response. It degrades a wide array of substrates such as substance P, enkephalins, cholecystokinin, neurotensin and somatostatin. It is an important enzyme in the regulation of amyloid-beta (Abeta) protein that forms amyloid plaques that are associated with Alzeimers disease (AD). ECE-1 catalyzes the final rate-limiting step in the biosynthesis of endothelins via post-translational conversion of the biologically inactive big endothelins. Like NEP, it also hydrolyzes bradykinin, substance P, neurotensin, and Abeta. Endothelin-1 overproduction has been implicated in various diseases including stroke, asthma, hypertension, and cardiac and renal failure. Kell is a homolog of NEP and constitutes a major antigen on human erythrocytes; it preferentially cleaves big endothelin-3 to produce bioactive endothelin-3, but is also known to cleave substance P and neurokinin A. PHEX forms a complex interaction with fibroblast growth factor 23 (FGF23) and matrix extracellular phosphoglycoprotein, causing bone mineralization. A loss-of-function mutation in PHEX disrupts this interaction leading to hypophosphatemic rickets; X-linked hypophosphatemic (XLH) rickets is the most common form of metabolic rickets. ECEL1 is a brain metalloprotease which plays a critical role in the nervous regulation of the respiratory system, while DINE is abundantly expressed in the hypothalamus and its expression responds to nerve injury. A majority of these M13 proteases are prime therapeutic targets for selective inhibition.


:

Pssm-ID: 341056 [Multi-domain]  Cd Length: 642  Bit Score: 488.80  E-value: 7.13e-170
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511   1 MVYSRIPNLSRRFQYRWLEFSRVIQGTTTLLPQWDKCVNFIESALPYVVGKMFVDVYFQEDKKEMMEELVEGVRWAFIDM 80
Cdd:cd08662  274 LLDSLAPYLSKEFRDARFFYGKALSGQKEPEPRWKRCVELVNGALGEALGRLYVEKYFSEEAKADVEEMVENIKEAFKER 353
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  81 LEkENEWMDAGTKRKAKEKARAVLAKVGYPEFIMNDTHVNEDLKAIKFSEaDYFGNVLQTRKYLAQSDFFWLRKAVPKTE 160
Cdd:cd08662  354 LE-NLDWMDEETKKKALEKLDAMKVKIGYPDKWRDYSALDIYYDDLNVSD-SYFENVLRLLRFETKRQLAKLGKPVDRTE 431
                        170       180       190       200       210       220       230       240
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 161 WFTNPTTVNAFYSASTNQIRFPAGELQKPFFwGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPWWSTESEE 240
Cdd:cd08662  432 WSMSPQTVNAYYNPSLNEIVFPAGILQPPFF-DPDAPDALNYGGIGAVIGHEITHGFDDQGRQYDENGNLRNWWTNEDRK 510
                        250       260       270       280       290       300       310       320
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 241 KFKEKTKCMINQYSNYYWKKaGLNVKGKRTLGENIADNGGLREAFRAYRKWINDRrqglEEPLLPGITFTNNQLFFLSYA 320
Cdd:cd08662  511 EFEERAQCLVDQYSNYEVPP-GLHVNGKLTLGENIADNGGLRLAYRAYKKWLKEN----GPELPGLEGFTPEQLFFLSFA 585
                        330       340       350       360       370
                 ....*....|....*....|....*....|....*....|....*....|.
gi 768032511 321 HVRCNSYRPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMN 371
Cdd:cd08662  586 QVWCSKYRPEALRQLLLTDPHSPGKFRVNGPLSNSPEFAEAFNCPPGSPMN 636
 
Name Accession Description Interval E-value
M13 cd08662
Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of ...
1-371 7.13e-170

Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of metallopeptidases includes neprilysin (neutral endopeptidase, NEP, enkephalinase, CD10, CALLA, EC 3.4.24.11), endothelin-converting enzyme I (ECE-1, EC 3.4.24.71), erythrocyte surface antigen KELL (ECE-3), phosphate-regulating gene on the X chromosome (PHEX), soluble secreted endopeptidase (SEP), and damage-induced neuronal endopeptidase (DINE)/X-converting enzyme (XCE). Proteins in this family fulfill a broad range of physiological roles due to the greater variation in the active site's S2' subsite allowing substrate specificity. NEP is expressed in a variety of tissues including kidney and brain, and is involved in many physiological and pathological processes, including blood pressure and inflammatory response. It degrades a wide array of substrates such as substance P, enkephalins, cholecystokinin, neurotensin and somatostatin. It is an important enzyme in the regulation of amyloid-beta (Abeta) protein that forms amyloid plaques that are associated with Alzeimers disease (AD). ECE-1 catalyzes the final rate-limiting step in the biosynthesis of endothelins via post-translational conversion of the biologically inactive big endothelins. Like NEP, it also hydrolyzes bradykinin, substance P, neurotensin, and Abeta. Endothelin-1 overproduction has been implicated in various diseases including stroke, asthma, hypertension, and cardiac and renal failure. Kell is a homolog of NEP and constitutes a major antigen on human erythrocytes; it preferentially cleaves big endothelin-3 to produce bioactive endothelin-3, but is also known to cleave substance P and neurokinin A. PHEX forms a complex interaction with fibroblast growth factor 23 (FGF23) and matrix extracellular phosphoglycoprotein, causing bone mineralization. A loss-of-function mutation in PHEX disrupts this interaction leading to hypophosphatemic rickets; X-linked hypophosphatemic (XLH) rickets is the most common form of metabolic rickets. ECEL1 is a brain metalloprotease which plays a critical role in the nervous regulation of the respiratory system, while DINE is abundantly expressed in the hypothalamus and its expression responds to nerve injury. A majority of these M13 proteases are prime therapeutic targets for selective inhibition.


Pssm-ID: 341056 [Multi-domain]  Cd Length: 642  Bit Score: 488.80  E-value: 7.13e-170
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511   1 MVYSRIPNLSRRFQYRWLEFSRVIQGTTTLLPQWDKCVNFIESALPYVVGKMFVDVYFQEDKKEMMEELVEGVRWAFIDM 80
Cdd:cd08662  274 LLDSLAPYLSKEFRDARFFYGKALSGQKEPEPRWKRCVELVNGALGEALGRLYVEKYFSEEAKADVEEMVENIKEAFKER 353
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  81 LEkENEWMDAGTKRKAKEKARAVLAKVGYPEFIMNDTHVNEDLKAIKFSEaDYFGNVLQTRKYLAQSDFFWLRKAVPKTE 160
Cdd:cd08662  354 LE-NLDWMDEETKKKALEKLDAMKVKIGYPDKWRDYSALDIYYDDLNVSD-SYFENVLRLLRFETKRQLAKLGKPVDRTE 431
                        170       180       190       200       210       220       230       240
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 161 WFTNPTTVNAFYSASTNQIRFPAGELQKPFFwGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPWWSTESEE 240
Cdd:cd08662  432 WSMSPQTVNAYYNPSLNEIVFPAGILQPPFF-DPDAPDALNYGGIGAVIGHEITHGFDDQGRQYDENGNLRNWWTNEDRK 510
                        250       260       270       280       290       300       310       320
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 241 KFKEKTKCMINQYSNYYWKKaGLNVKGKRTLGENIADNGGLREAFRAYRKWINDRrqglEEPLLPGITFTNNQLFFLSYA 320
Cdd:cd08662  511 EFEERAQCLVDQYSNYEVPP-GLHVNGKLTLGENIADNGGLRLAYRAYKKWLKEN----GPELPGLEGFTPEQLFFLSFA 585
                        330       340       350       360       370
                 ....*....|....*....|....*....|....*....|....*....|.
gi 768032511 321 HVRCNSYRPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMN 371
Cdd:cd08662  586 QVWCSKYRPEALRQLLLTDPHSPGKFRVNGPLSNSPEFAEAFNCPPGSPMN 636
PepO COG3590
Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];
1-380 1.14e-123

Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];


Pssm-ID: 442809 [Multi-domain]  Cd Length: 674  Bit Score: 371.41  E-value: 1.14e-123
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511   1 MVYSRIPNLSRRFQYRWLEF-SRVIQGTTTLLPQWDKCVNFIESALPYVVGKMFVDVYFQEDKKEMMEELVEGVRWAFID 79
Cdd:COG3590  309 LLDSAAPYLSKAFVDANFDFyGKTLSGQKEQRPRWKRAVALVNGALGEALGQLYVERYFPPEAKARMEELVANLRAAYRE 388
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  80 MLEKeNEWMDAGTKRKAKEKARAVLAKVGYPEfimndthVNEDLKAIKFSEADYFGNVLQTRKylaqsdFFWLR------ 153
Cdd:COG3590  389 RIEN-LDWMSPETKAKALEKLAAFTPKIGYPD-------KWRDYSGLEIKRDDLVGNVLRASA------FEYQRelaklg 454
                        170       180       190       200       210       220       230       240
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 154 KAVPKTEWFTNPTTVNAFYSASTNQIRFPAGELQKPFFwGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPW 233
Cdd:COG3590  455 KPVDRTEWGMTPQTVNAYYNPTMNEIVFPAAILQPPFF-DPKADDAVNYGGIGAVIGHEITHGFDDQGSQFDGDGNLRNW 533
                        250       260       270       280       290       300       310       320
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 234 WSTESEEKFKEKTKCMINQYSNYYWKKaGLNVKGKRTLGENIADNGGLREAFRAYRKwindRRQGLEEPLLPGitFTNNQ 313
Cdd:COG3590  534 WTPEDRAAFEARTKKLVAQYDAYEPLP-GLHVNGKLTLGENIADLGGLSIAYDAYKL----SLKGKEAPVIDG--FTGDQ 606
                        330       340       350       360       370       380
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 768032511 314 LFFLSYAHVRCNSYRPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMNR-GMDSCRLW 380
Cdd:COG3590  607 RFFLGWAQVWRSKARDEALRQRLATDPHSPGEFRVNGPVRNLDAFYEAFDVKPGDKMYLaPEDRVRIW 674
Peptidase_M13 pfam01431
Peptidase family M13; Mammalian enzymes are typically type-II membrane anchored enzymes which ...
169-379 2.24e-79

Peptidase family M13; Mammalian enzymes are typically type-II membrane anchored enzymes which are known, or believed to activate or inactivate oligopeptide (pro)-hormones such as opioid peptides. The family also contains a bacterial member believed to be involved with milk protein cleavage.


Pssm-ID: 279739 [Multi-domain]  Cd Length: 205  Bit Score: 242.32  E-value: 2.24e-79
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  169 NAFYSASTNQIRFPAGELQKPFFwGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPWWSTESEEKFKEKTKC 248
Cdd:pfam01431   1 NAYYQPNRNEIVFPAAILQPPFF-DPNYPRAVNYGGIGNVIAHEITHGFDDQGAQFDKDGNLRSWWTDEDAEEFKDRAQC 79
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  249 MINQYSNYYWKKAGLNVKGKRTLGENIADNGGLREAFRAYRKwindrRQGLEEPLLPGI-TFTNNQLFFLSYAHVRCNSY 327
Cdd:pfam01431  80 LIEQYSEYTPPDGTKCANGTLTLGENIADLGGLTIALRAYKK-----LLSANETVLPGFeNLTPDQLFFRGAAQIWCMKQ 154
                         170       180       190       200       210
                  ....*....|....*....|....*....|....*....|....*....|..
gi 768032511  328 RPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMNRGmDSCRL 379
Cdd:pfam01431 155 SPAEVLRQLLVDPHSPPEFRVNGVMSNMPAFYEAFNCPEGDKMNPE-PRCRL 205
 
Name Accession Description Interval E-value
M13 cd08662
Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of ...
1-371 7.13e-170

Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of metallopeptidases includes neprilysin (neutral endopeptidase, NEP, enkephalinase, CD10, CALLA, EC 3.4.24.11), endothelin-converting enzyme I (ECE-1, EC 3.4.24.71), erythrocyte surface antigen KELL (ECE-3), phosphate-regulating gene on the X chromosome (PHEX), soluble secreted endopeptidase (SEP), and damage-induced neuronal endopeptidase (DINE)/X-converting enzyme (XCE). Proteins in this family fulfill a broad range of physiological roles due to the greater variation in the active site's S2' subsite allowing substrate specificity. NEP is expressed in a variety of tissues including kidney and brain, and is involved in many physiological and pathological processes, including blood pressure and inflammatory response. It degrades a wide array of substrates such as substance P, enkephalins, cholecystokinin, neurotensin and somatostatin. It is an important enzyme in the regulation of amyloid-beta (Abeta) protein that forms amyloid plaques that are associated with Alzeimers disease (AD). ECE-1 catalyzes the final rate-limiting step in the biosynthesis of endothelins via post-translational conversion of the biologically inactive big endothelins. Like NEP, it also hydrolyzes bradykinin, substance P, neurotensin, and Abeta. Endothelin-1 overproduction has been implicated in various diseases including stroke, asthma, hypertension, and cardiac and renal failure. Kell is a homolog of NEP and constitutes a major antigen on human erythrocytes; it preferentially cleaves big endothelin-3 to produce bioactive endothelin-3, but is also known to cleave substance P and neurokinin A. PHEX forms a complex interaction with fibroblast growth factor 23 (FGF23) and matrix extracellular phosphoglycoprotein, causing bone mineralization. A loss-of-function mutation in PHEX disrupts this interaction leading to hypophosphatemic rickets; X-linked hypophosphatemic (XLH) rickets is the most common form of metabolic rickets. ECEL1 is a brain metalloprotease which plays a critical role in the nervous regulation of the respiratory system, while DINE is abundantly expressed in the hypothalamus and its expression responds to nerve injury. A majority of these M13 proteases are prime therapeutic targets for selective inhibition.


Pssm-ID: 341056 [Multi-domain]  Cd Length: 642  Bit Score: 488.80  E-value: 7.13e-170
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511   1 MVYSRIPNLSRRFQYRWLEFSRVIQGTTTLLPQWDKCVNFIESALPYVVGKMFVDVYFQEDKKEMMEELVEGVRWAFIDM 80
Cdd:cd08662  274 LLDSLAPYLSKEFRDARFFYGKALSGQKEPEPRWKRCVELVNGALGEALGRLYVEKYFSEEAKADVEEMVENIKEAFKER 353
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  81 LEkENEWMDAGTKRKAKEKARAVLAKVGYPEFIMNDTHVNEDLKAIKFSEaDYFGNVLQTRKYLAQSDFFWLRKAVPKTE 160
Cdd:cd08662  354 LE-NLDWMDEETKKKALEKLDAMKVKIGYPDKWRDYSALDIYYDDLNVSD-SYFENVLRLLRFETKRQLAKLGKPVDRTE 431
                        170       180       190       200       210       220       230       240
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 161 WFTNPTTVNAFYSASTNQIRFPAGELQKPFFwGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPWWSTESEE 240
Cdd:cd08662  432 WSMSPQTVNAYYNPSLNEIVFPAGILQPPFF-DPDAPDALNYGGIGAVIGHEITHGFDDQGRQYDENGNLRNWWTNEDRK 510
                        250       260       270       280       290       300       310       320
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 241 KFKEKTKCMINQYSNYYWKKaGLNVKGKRTLGENIADNGGLREAFRAYRKWINDRrqglEEPLLPGITFTNNQLFFLSYA 320
Cdd:cd08662  511 EFEERAQCLVDQYSNYEVPP-GLHVNGKLTLGENIADNGGLRLAYRAYKKWLKEN----GPELPGLEGFTPEQLFFLSFA 585
                        330       340       350       360       370
                 ....*....|....*....|....*....|....*....|....*....|.
gi 768032511 321 HVRCNSYRPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMN 371
Cdd:cd08662  586 QVWCSKYRPEALRQLLLTDPHSPGKFRVNGPLSNSPEFAEAFNCPPGSPMN 636
PepO COG3590
Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];
1-380 1.14e-123

Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];


Pssm-ID: 442809 [Multi-domain]  Cd Length: 674  Bit Score: 371.41  E-value: 1.14e-123
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511   1 MVYSRIPNLSRRFQYRWLEF-SRVIQGTTTLLPQWDKCVNFIESALPYVVGKMFVDVYFQEDKKEMMEELVEGVRWAFID 79
Cdd:COG3590  309 LLDSAAPYLSKAFVDANFDFyGKTLSGQKEQRPRWKRAVALVNGALGEALGQLYVERYFPPEAKARMEELVANLRAAYRE 388
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  80 MLEKeNEWMDAGTKRKAKEKARAVLAKVGYPEfimndthVNEDLKAIKFSEADYFGNVLQTRKylaqsdFFWLR------ 153
Cdd:COG3590  389 RIEN-LDWMSPETKAKALEKLAAFTPKIGYPD-------KWRDYSGLEIKRDDLVGNVLRASA------FEYQRelaklg 454
                        170       180       190       200       210       220       230       240
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 154 KAVPKTEWFTNPTTVNAFYSASTNQIRFPAGELQKPFFwGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPW 233
Cdd:COG3590  455 KPVDRTEWGMTPQTVNAYYNPTMNEIVFPAAILQPPFF-DPKADDAVNYGGIGAVIGHEITHGFDDQGSQFDGDGNLRNW 533
                        250       260       270       280       290       300       310       320
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511 234 WSTESEEKFKEKTKCMINQYSNYYWKKaGLNVKGKRTLGENIADNGGLREAFRAYRKwindRRQGLEEPLLPGitFTNNQ 313
Cdd:COG3590  534 WTPEDRAAFEARTKKLVAQYDAYEPLP-GLHVNGKLTLGENIADLGGLSIAYDAYKL----SLKGKEAPVIDG--FTGDQ 606
                        330       340       350       360       370       380
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 768032511 314 LFFLSYAHVRCNSYRPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMNR-GMDSCRLW 380
Cdd:COG3590  607 RFFLGWAQVWRSKARDEALRQRLATDPHSPGEFRVNGPVRNLDAFYEAFDVKPGDKMYLaPEDRVRIW 674
Peptidase_M13 pfam01431
Peptidase family M13; Mammalian enzymes are typically type-II membrane anchored enzymes which ...
169-379 2.24e-79

Peptidase family M13; Mammalian enzymes are typically type-II membrane anchored enzymes which are known, or believed to activate or inactivate oligopeptide (pro)-hormones such as opioid peptides. The family also contains a bacterial member believed to be involved with milk protein cleavage.


Pssm-ID: 279739 [Multi-domain]  Cd Length: 205  Bit Score: 242.32  E-value: 2.24e-79
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  169 NAFYSASTNQIRFPAGELQKPFFwGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPWWSTESEEKFKEKTKC 248
Cdd:pfam01431   1 NAYYQPNRNEIVFPAAILQPPFF-DPNYPRAVNYGGIGNVIAHEITHGFDDQGAQFDKDGNLRSWWTDEDAEEFKDRAQC 79
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511  249 MINQYSNYYWKKAGLNVKGKRTLGENIADNGGLREAFRAYRKwindrRQGLEEPLLPGI-TFTNNQLFFLSYAHVRCNSY 327
Cdd:pfam01431  80 LIEQYSEYTPPDGTKCANGTLTLGENIADLGGLTIALRAYKK-----LLSANETVLPGFeNLTPDQLFFRGAAQIWCMKQ 154
                         170       180       190       200       210
                  ....*....|....*....|....*....|....*....|....*....|..
gi 768032511  328 RPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMNRGmDSCRL 379
Cdd:pfam01431 155 SPAEVLRQLLVDPHSPPEFRVNGVMSNMPAFYEAFNCPEGDKMNPE-PRCRL 205
Peptidase_M13_N pfam05649
Peptidase family M13; M13 peptidases are well-studied proteases found in a wide range of ...
1-110 5.91e-35

Peptidase family M13; M13 peptidases are well-studied proteases found in a wide range of organizms including mammals and bacteria. In mammals they participate in processes such as cardiovascular development, blood-pressure regulation, nervous control of respiration, and regulation of the function of neuropeptides in the central nervous system. In bacteria they may be used for digestion of milk.


Pssm-ID: 461703  Cd Length: 382  Bit Score: 132.04  E-value: 5.91e-35
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 768032511    1 MVYSRIPNLSRRFQYRWLEFSRVIQGTTTLlPQWDKCVNFIESALPYVVGKMFVDVYFQEDKKEMMEELVEGVRWAFIDM 80
Cdd:pfam05649 275 LVRSLAPYLSDEFRDANFEFYGTLSGTKQR-PRWKRCVSLVNGLLGEALGRLYVKKYFPEEAKARVEELVENIKEAFRER 353
                          90       100       110
                  ....*....|....*....|....*....|
gi 768032511   81 LEkENEWMDAGTKRKAKEKARAVLAKVGYP 110
Cdd:pfam05649 354 LD-ELDWMDEETKKKALEKLDAMTVKIGYP 382
 
Blast search parameters
Data Source: Precalculated data, version = cdd.v.3.21
Preset Options:Database: CDSEARCH/cdd   Low complexity filter: no  Composition Based Adjustment: yes   E-value threshold: 0.01

References:

  • Wang J et al. (2023), "The conserved domain database in 2023", Nucleic Acids Res.51(D)384-8.
  • Lu S et al. (2020), "The conserved domain database in 2020", Nucleic Acids Res.48(D)265-8.
  • Marchler-Bauer A et al. (2017), "CDD/SPARCLE: functional classification of proteins via subfamily domain architectures.", Nucleic Acids Res.45(D)200-3.
Help | Disclaimer | Write to the Help Desk
NCBI | NLM | NIH