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Conserved domains on  [gi|1958776860|ref|XP_038966044|]
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membrane metallo-endopeptidase-like 1 isoform X7 [Rattus norvegicus]

Protein Classification

M13 family metallopeptidase N-terminal domain-containing protein( domain architecture ID 10529119)

M13 family metallopeptidase N-terminal domain-containing protein, similar to the N-termini of 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

MEROPS:  M13
PubMed:  7674922|18215274

Graphical summary

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List of domain hits

Name Accession Description Interval E-value
Peptidase_M13_N pfam05649
Peptidase family M13; M13 peptidases are well-studied proteases found in a wide range of ...
107-419 1.66e-108

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: 326.56  E-value: 1.66e-108
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 107 PCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSEP 184
Cdd:pfam05649   1 PCDDFYQYACGGWLKNHPIPADKSSWGTFDELRERNEKQLREILEEAAASEsdPGAVEKAKDLYKSCMDTDAIEKLGLKP 80
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 185 LLNVLDMIGGWPVAMDkwnetmgpKWELERQLAVLNSqFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKED 264
Cdd:pfam05649  81 LKPLLDEIGGPLANKD--------KFDLLETLAKLRR-YGVDSLFGFGVGPDDKNSSRNILYLDQPGLGLPDRDYYLKDR 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 265 SHR---VREAYLQFMTSVATMLrrdlnlpGETDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFgl 341
Cdd:pfam05649 152 DEKsaeIREAYKAYIAKLLTLL-------GASEEAAALAEEVLAFETKLAKASLSREERRDPEKTYNPMTLAELQKLA-- 222
                         250       260       270       280       290       300       310
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 1958776860 342 KGFNWTLFIQNVLssvqVELLPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRK 419
Cdd:pfam05649 223 PGIDWKAYLNAAG----LPDVPSDEVIVSQPEYLKALSKLLAETPLRTLKNYLIWRLVRSLAPYLSDEFRDANFEFYG 296
 
Name Accession Description Interval E-value
Peptidase_M13_N pfam05649
Peptidase family M13; M13 peptidases are well-studied proteases found in a wide range of ...
107-419 1.66e-108

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: 326.56  E-value: 1.66e-108
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 107 PCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSEP 184
Cdd:pfam05649   1 PCDDFYQYACGGWLKNHPIPADKSSWGTFDELRERNEKQLREILEEAAASEsdPGAVEKAKDLYKSCMDTDAIEKLGLKP 80
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 185 LLNVLDMIGGWPVAMDkwnetmgpKWELERQLAVLNSqFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKED 264
Cdd:pfam05649  81 LKPLLDEIGGPLANKD--------KFDLLETLAKLRR-YGVDSLFGFGVGPDDKNSSRNILYLDQPGLGLPDRDYYLKDR 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 265 SHR---VREAYLQFMTSVATMLrrdlnlpGETDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFgl 341
Cdd:pfam05649 152 DEKsaeIREAYKAYIAKLLTLL-------GASEEAAALAEEVLAFETKLAKASLSREERRDPEKTYNPMTLAELQKLA-- 222
                         250       260       270       280       290       300       310
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 1958776860 342 KGFNWTLFIQNVLssvqVELLPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRK 419
Cdd:pfam05649 223 PGIDWKAYLNAAG----LPDVPSDEVIVSQPEYLKALSKLLAETPLRTLKNYLIWRLVRSLAPYLSDEFRDANFEFYG 296
M13 cd08662
Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of ...
106-420 6.59e-90

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: 286.57  E-value: 6.59e-90
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 106 KPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSE 183
Cdd:cd08662     2 DPCDDFYQYACGNWLKNHPIPADKSSWGSFSELQDRNEEQLREILEEAASSAadSSAEQKAKDFYKSCMDEEAIEKLGLK 81
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 184 PLLNVLDMIGGWPVAMDKWNETmgpkwelerqLAVLNSQFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKE 263
Cdd:cd08662    82 PLKPLLDKIGGLPSLDDLAAEL----------LLALLRRLGVSLLFGLGVSPDPKNSSRNILYLGQPGLGLPDRDYYLDE 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 264 DSHRVREAYLQFMTSVATMLRRDLnlpgetDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFglKG 343
Cdd:cd08662   152 ENAEIREAYKKYIAKLLELLGADE------EEAEKLAEDVLAFETELAKISLSSEELRDPEKTYNPLTLAELQKLA--PS 223
                         250       260       270       280       290       300       310
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*..
gi 1958776860 344 FNWTLFIQNVLSSVQvellPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRKR 420
Cdd:cd08662   224 IDWKAYLKALGPPAD----DPDKVIVSQPEYLKKLDKLLASTPLRTLKNYLIWRLLDSLAPYLSKEFRDARFFYGKA 296
PepO COG3590
Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];
98-420 3.95e-67

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


Pssm-ID: 442809 [Multi-domain]  Cd Length: 674  Bit Score: 227.34  E-value: 3.95e-67
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860  98 LQNMDQSKKPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQHRPA--VE-KAKTLYRSCMNQ 174
Cdd:COG3590    30 LANMDTSVRPGDDFYRYVNGGWLKTTPIPADRSRWGSFNELRERNEARLRAILEEAAAAPAAAgsDEqKIGDLYASFMDE 109
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 175 SVIEKRDSEPLLNVLDMIggwpvamdkwnETMGPKWELERQLAVLNSQFNrRVLIDLFIWNDDQNSSRHVIYIDQPTLGM 254
Cdd:COG3590   110 AAIEALGLAPLKPDLARI-----------DAIKDKADLAALLAALHRAGV-GGLFGFGVDADLKNSTRYIAYLGQGGLGL 177
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 255 PSREYYFKEDSH--RVREAYLQFmtsVATMLRrdlnLPGETDLVQEEMAQ-VLHLETHLANATVPQEKRHDVTALYHRMG 331
Cdd:COG3590   178 PDRDYYLKDDEKsaEIRAAYVAH---VAKMLE----LAGYDEADAAAAAEaVLALETALAKAHWSRVELRDPEKTYNPMT 250
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 332 LEELQERFglKGFNWTLFiqnvLSSVQVELLpnEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFK 411
Cdd:COG3590   251 VAELAKLA--PGFDWDAY----LKALGLPAV--DEVIVGQPSFFKALDKLLASTPLEDWKAYLRWHLLDSAAPYLSKAFV 322

                  ....*....
gi 1958776860 412 EARVDYRKR 420
Cdd:COG3590   323 DANFDFYGK 331
 
Name Accession Description Interval E-value
Peptidase_M13_N pfam05649
Peptidase family M13; M13 peptidases are well-studied proteases found in a wide range of ...
107-419 1.66e-108

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: 326.56  E-value: 1.66e-108
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 107 PCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSEP 184
Cdd:pfam05649   1 PCDDFYQYACGGWLKNHPIPADKSSWGTFDELRERNEKQLREILEEAAASEsdPGAVEKAKDLYKSCMDTDAIEKLGLKP 80
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 185 LLNVLDMIGGWPVAMDkwnetmgpKWELERQLAVLNSqFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKED 264
Cdd:pfam05649  81 LKPLLDEIGGPLANKD--------KFDLLETLAKLRR-YGVDSLFGFGVGPDDKNSSRNILYLDQPGLGLPDRDYYLKDR 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 265 SHR---VREAYLQFMTSVATMLrrdlnlpGETDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFgl 341
Cdd:pfam05649 152 DEKsaeIREAYKAYIAKLLTLL-------GASEEAAALAEEVLAFETKLAKASLSREERRDPEKTYNPMTLAELQKLA-- 222
                         250       260       270       280       290       300       310
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*...
gi 1958776860 342 KGFNWTLFIQNVLssvqVELLPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRK 419
Cdd:pfam05649 223 PGIDWKAYLNAAG----LPDVPSDEVIVSQPEYLKALSKLLAETPLRTLKNYLIWRLVRSLAPYLSDEFRDANFEFYG 296
M13 cd08662
Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of ...
106-420 6.59e-90

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: 286.57  E-value: 6.59e-90
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 106 KPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSE 183
Cdd:cd08662     2 DPCDDFYQYACGNWLKNHPIPADKSSWGSFSELQDRNEEQLREILEEAASSAadSSAEQKAKDFYKSCMDEEAIEKLGLK 81
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 184 PLLNVLDMIGGWPVAMDKWNETmgpkwelerqLAVLNSQFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKE 263
Cdd:cd08662    82 PLKPLLDKIGGLPSLDDLAAEL----------LLALLRRLGVSLLFGLGVSPDPKNSSRNILYLGQPGLGLPDRDYYLDE 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 264 DSHRVREAYLQFMTSVATMLRRDLnlpgetDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFglKG 343
Cdd:cd08662   152 ENAEIREAYKKYIAKLLELLGADE------EEAEKLAEDVLAFETELAKISLSSEELRDPEKTYNPLTLAELQKLA--PS 223
                         250       260       270       280       290       300       310
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*..
gi 1958776860 344 FNWTLFIQNVLSSVQvellPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRKR 420
Cdd:cd08662   224 IDWKAYLKALGPPAD----DPDKVIVSQPEYLKKLDKLLASTPLRTLKNYLIWRLLDSLAPYLSKEFRDARFFYGKA 296
PepO COG3590
Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];
98-420 3.95e-67

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


Pssm-ID: 442809 [Multi-domain]  Cd Length: 674  Bit Score: 227.34  E-value: 3.95e-67
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860  98 LQNMDQSKKPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQHRPA--VE-KAKTLYRSCMNQ 174
Cdd:COG3590    30 LANMDTSVRPGDDFYRYVNGGWLKTTPIPADRSRWGSFNELRERNEARLRAILEEAAAAPAAAgsDEqKIGDLYASFMDE 109
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 175 SVIEKRDSEPLLNVLDMIggwpvamdkwnETMGPKWELERQLAVLNSQFNrRVLIDLFIWNDDQNSSRHVIYIDQPTLGM 254
Cdd:COG3590   110 AAIEALGLAPLKPDLARI-----------DAIKDKADLAALLAALHRAGV-GGLFGFGVDADLKNSTRYIAYLGQGGLGL 177
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 255 PSREYYFKEDSH--RVREAYLQFmtsVATMLRrdlnLPGETDLVQEEMAQ-VLHLETHLANATVPQEKRHDVTALYHRMG 331
Cdd:COG3590   178 PDRDYYLKDDEKsaEIRAAYVAH---VAKMLE----LAGYDEADAAAAAEaVLALETALAKAHWSRVELRDPEKTYNPMT 250
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776860 332 LEELQERFglKGFNWTLFiqnvLSSVQVELLpnEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFK 411
Cdd:COG3590   251 VAELAKLA--PGFDWDAY----LKALGLPAV--DEVIVGQPSFFKALDKLLASTPLEDWKAYLRWHLLDSAAPYLSKAFV 322

                  ....*....
gi 1958776860 412 EARVDYRKR 420
Cdd:COG3590   323 DANFDFYGK 331
 
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.
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