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Conserved domains on  [gi|1958776856|ref|XP_038966042|]
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membrane metallo-endopeptidase-like 1 isoform X4 [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 ...
107-506 1.18e-154

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: 447.13  E-value: 1.18e-154
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 107 PCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSEP 184
Cdd:pfam05649   1 PCDDFYQYACGGWLKNHPIPADKSSWGTFDELRERNEKQLREILEEAAASEsdPGAVEKAKDLYKSCMDTDAIEKLGLKP 80
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 185 LLNVLDMIGGWPVAMDKWnetmgpkwELERQLAVLNSqFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKED 264
Cdd:pfam05649  81 LKPLLDEIGGPLANKDKF--------DLLETLAKLRR-YGVDSLFGFGVGPDDKNSSRNILYLDQPGLGLPDRDYYLKDR 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 265 SHR---VREAYLQFMTSVATMLrrdlnlpGETDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFgl 341
Cdd:pfam05649 152 DEKsaeIREAYKAYIAKLLTLL-------GASEEAAALAEEVLAFETKLAKASLSREERRDPEKTYNPMTLAELQKLA-- 222
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 342 KGFNWTLFIQNVLssvqVELLPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRKAL 421
Cdd:pfam05649 223 PGIDWKAYLNAAG----LPDVPSDEVIVSQPEYLKALSKLLAETPLRTLKNYLIWRLVRSLAPYLSDEFRDANFEFYGTL 298
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 422 YGTTMEEvRWRECVSYVNSNMESAVGSLYIKRAFSKDSKSIVSELIEKIRSVFVDNLDELNWMDEESKKKAQEKALNIRE 501
Cdd:pfam05649 299 SGTKQRP-RWKRCVSLVNGLLGEALGRLYVKKYFPEEAKARVEELVENIKEAFRERLDELDWMDEETKKKALEKLDAMTV 377

                  ....*
gi 1958776856 502 QIGYP 506
Cdd:pfam05649 378 KIGYP 382
 
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 ...
107-506 1.18e-154

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: 447.13  E-value: 1.18e-154
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 107 PCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSEP 184
Cdd:pfam05649   1 PCDDFYQYACGGWLKNHPIPADKSSWGTFDELRERNEKQLREILEEAAASEsdPGAVEKAKDLYKSCMDTDAIEKLGLKP 80
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 185 LLNVLDMIGGWPVAMDKWnetmgpkwELERQLAVLNSqFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKED 264
Cdd:pfam05649  81 LKPLLDEIGGPLANKDKF--------DLLETLAKLRR-YGVDSLFGFGVGPDDKNSSRNILYLDQPGLGLPDRDYYLKDR 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 265 SHR---VREAYLQFMTSVATMLrrdlnlpGETDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFgl 341
Cdd:pfam05649 152 DEKsaeIREAYKAYIAKLLTLL-------GASEEAAALAEEVLAFETKLAKASLSREERRDPEKTYNPMTLAELQKLA-- 222
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 342 KGFNWTLFIQNVLssvqVELLPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRKAL 421
Cdd:pfam05649 223 PGIDWKAYLNAAG----LPDVPSDEVIVSQPEYLKALSKLLAETPLRTLKNYLIWRLVRSLAPYLSDEFRDANFEFYGTL 298
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 422 YGTTMEEvRWRECVSYVNSNMESAVGSLYIKRAFSKDSKSIVSELIEKIRSVFVDNLDELNWMDEESKKKAQEKALNIRE 501
Cdd:pfam05649 299 SGTKQRP-RWKRCVSLVNGLLGEALGRLYVKKYFPEEAKARVEELVENIKEAFRERLDELDWMDEETKKKALEKLDAMTV 377

                  ....*
gi 1958776856 502 QIGYP 506
Cdd:pfam05649 378 KIGYP 382
M13 cd08662
Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of ...
106-524 2.84e-136

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: 409.45  E-value: 2.84e-136
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 106 KPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSE 183
Cdd:cd08662     2 DPCDDFYQYACGNWLKNHPIPADKSSWGSFSELQDRNEEQLREILEEAASSAadSSAEQKAKDFYKSCMDEEAIEKLGLK 81
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 184 PLLNVLDMIGGWPVAMDKWNETmgpkwelerqLAVLNSQFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKE 263
Cdd:cd08662    82 PLKPLLDKIGGLPSLDDLAAEL----------LLALLRRLGVSLLFGLGVSPDPKNSSRNILYLGQPGLGLPDRDYYLDE 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 264 DSHRVREAYLQFMTSVATMLRRDLnlpgetDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFglKG 343
Cdd:cd08662   152 ENAEIREAYKKYIAKLLELLGADE------EEAEKLAEDVLAFETELAKISLSSEELRDPEKTYNPLTLAELQKLA--PS 223
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 344 FNWTLFIQNVLSSVQvellPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRKALYG 423
Cdd:cd08662   224 IDWKAYLKALGPPAD----DPDKVIVSQPEYLKKLDKLLASTPLRTLKNYLIWRLLDSLAPYLSKEFRDARFFYGKALSG 299
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 424 TTMEEVRWRECVSYVNSNMESAVGSLYIKRAFSKDSKSIVSELIEKIRSVFVDNLDELNWMDEESKKKAQEKALNIREQI 503
Cdd:cd08662   300 QKEPEPRWKRCVELVNGALGEALGRLYVEKYFSEEAKADVEEMVENIKEAFKERLENLDWMDEETKKKALEKLDAMKVKI 379
                         410       420
                  ....*....|....*....|.
gi 1958776856 504 GYPDYILedNNRHLDEEYSSV 524
Cdd:cd08662   380 GYPDKWR--DYSALDIYYDDL 398
PepO COG3590
Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];
98-507 1.41e-100

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


Pssm-ID: 442809 [Multi-domain]  Cd Length: 674  Bit Score: 317.87  E-value: 1.41e-100
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856  98 LQNMDQSKKPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQHRPA--VE-KAKTLYRSCMNQ 174
Cdd:COG3590    30 LANMDTSVRPGDDFYRYVNGGWLKTTPIPADRSRWGSFNELRERNEARLRAILEEAAAAPAAAgsDEqKIGDLYASFMDE 109
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 175 SVIEKRDSEPLLNVLDMIggwpvamdkwnETMGPKWELERQLAVLNSQFNRrVLIDLFIWNDDQNSSRHVIYIDQPTLGM 254
Cdd:COG3590   110 AAIEALGLAPLKPDLARI-----------DAIKDKADLAALLAALHRAGVG-GLFGFGVDADLKNSTRYIAYLGQGGLGL 177
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 255 PSREYYFKEDSH--RVREAYLQFmtsVATMLRrdlnLPGETDLVQEEMAQ-VLHLETHLANATVPQEKRHDVTALYHRMG 331
Cdd:COG3590   178 PDRDYYLKDDEKsaEIRAAYVAH---VAKMLE----LAGYDEADAAAAAEaVLALETALAKAHWSRVELRDPEKTYNPMT 250
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 332 LEELQERFglKGFNWTLFiqnvLSSVQVELLpnEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFK 411
Cdd:COG3590   251 VAELAKLA--PGFDWDAY----LKALGLPAV--DEVIVGQPSFFKALDKLLASTPLEDWKAYLRWHLLDSAAPYLSKAFV 322
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 412 EARVD-YRKALYGTTMEEVRWRECVSYVNSNMESAVGSLYIKRAFSKDSKSIVSELIEKIRSVFVDNLDELNWMDEESKK 490
Cdd:COG3590   323 DANFDfYGKTLSGQKEQRPRWKRAVALVNGALGEALGQLYVERYFPPEAKARMEELVANLRAAYRERIENLDWMSPETKA 402
                         410
                  ....*....|....*..
gi 1958776856 491 KAQEKALNIREQIGYPD 507
Cdd:COG3590   403 KALEKLAAFTPKIGYPD 419
 
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 ...
107-506 1.18e-154

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: 447.13  E-value: 1.18e-154
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 107 PCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSEP 184
Cdd:pfam05649   1 PCDDFYQYACGGWLKNHPIPADKSSWGTFDELRERNEKQLREILEEAAASEsdPGAVEKAKDLYKSCMDTDAIEKLGLKP 80
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 185 LLNVLDMIGGWPVAMDKWnetmgpkwELERQLAVLNSqFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKED 264
Cdd:pfam05649  81 LKPLLDEIGGPLANKDKF--------DLLETLAKLRR-YGVDSLFGFGVGPDDKNSSRNILYLDQPGLGLPDRDYYLKDR 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 265 SHR---VREAYLQFMTSVATMLrrdlnlpGETDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFgl 341
Cdd:pfam05649 152 DEKsaeIREAYKAYIAKLLTLL-------GASEEAAALAEEVLAFETKLAKASLSREERRDPEKTYNPMTLAELQKLA-- 222
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 342 KGFNWTLFIQNVLssvqVELLPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRKAL 421
Cdd:pfam05649 223 PGIDWKAYLNAAG----LPDVPSDEVIVSQPEYLKALSKLLAETPLRTLKNYLIWRLVRSLAPYLSDEFRDANFEFYGTL 298
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 422 YGTTMEEvRWRECVSYVNSNMESAVGSLYIKRAFSKDSKSIVSELIEKIRSVFVDNLDELNWMDEESKKKAQEKALNIRE 501
Cdd:pfam05649 299 SGTKQRP-RWKRCVSLVNGLLGEALGRLYVKKYFPEEAKARVEELVENIKEAFRERLDELDWMDEETKKKALEKLDAMTV 377

                  ....*
gi 1958776856 502 QIGYP 506
Cdd:pfam05649 378 KIGYP 382
M13 cd08662
Peptidase family M13 includes neprilysin and endothelin-converting enzyme I; The M13 family of ...
106-524 2.84e-136

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: 409.45  E-value: 2.84e-136
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 106 KPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQH--RPAVEKAKTLYRSCMNQSVIEKRDSE 183
Cdd:cd08662     2 DPCDDFYQYACGNWLKNHPIPADKSSWGSFSELQDRNEEQLREILEEAASSAadSSAEQKAKDFYKSCMDEEAIEKLGLK 81
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 184 PLLNVLDMIGGWPVAMDKWNETmgpkwelerqLAVLNSQFNRRVLIDLFIWNDDQNSSRHVIYIDQPTLGMPSREYYFKE 263
Cdd:cd08662    82 PLKPLLDKIGGLPSLDDLAAEL----------LLALLRRLGVSLLFGLGVSPDPKNSSRNILYLGQPGLGLPDRDYYLDE 151
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 264 DSHRVREAYLQFMTSVATMLRRDLnlpgetDLVQEEMAQVLHLETHLANATVPQEKRHDVTALYHRMGLEELQERFglKG 343
Cdd:cd08662   152 ENAEIREAYKKYIAKLLELLGADE------EEAEKLAEDVLAFETELAKISLSSEELRDPEKTYNPLTLAELQKLA--PS 223
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 344 FNWTLFIQNVLSSVQvellPNEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFKEARVDYRKALYG 423
Cdd:cd08662   224 IDWKAYLKALGPPAD----DPDKVIVSQPEYLKKLDKLLASTPLRTLKNYLIWRLLDSLAPYLSKEFRDARFFYGKALSG 299
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 424 TTMEEVRWRECVSYVNSNMESAVGSLYIKRAFSKDSKSIVSELIEKIRSVFVDNLDELNWMDEESKKKAQEKALNIREQI 503
Cdd:cd08662   300 QKEPEPRWKRCVELVNGALGEALGRLYVEKYFSEEAKADVEEMVENIKEAFKERLENLDWMDEETKKKALEKLDAMKVKI 379
                         410       420
                  ....*....|....*....|.
gi 1958776856 504 GYPDYILedNNRHLDEEYSSV 524
Cdd:cd08662   380 GYPDKWR--DYSALDIYYDDL 398
PepO COG3590
Predicted metalloendopeptidase [Posttranslational modification, protein turnover, chaperones];
98-507 1.41e-100

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


Pssm-ID: 442809 [Multi-domain]  Cd Length: 674  Bit Score: 317.87  E-value: 1.41e-100
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856  98 LQNMDQSKKPCDNFYQYACGGWLRHHVIPETNSRYSVFDILRDELEVILKGVLEDSSVQHRPA--VE-KAKTLYRSCMNQ 174
Cdd:COG3590    30 LANMDTSVRPGDDFYRYVNGGWLKTTPIPADRSRWGSFNELRERNEARLRAILEEAAAAPAAAgsDEqKIGDLYASFMDE 109
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 175 SVIEKRDSEPLLNVLDMIggwpvamdkwnETMGPKWELERQLAVLNSQFNRrVLIDLFIWNDDQNSSRHVIYIDQPTLGM 254
Cdd:COG3590   110 AAIEALGLAPLKPDLARI-----------DAIKDKADLAALLAALHRAGVG-GLFGFGVDADLKNSTRYIAYLGQGGLGL 177
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 255 PSREYYFKEDSH--RVREAYLQFmtsVATMLRrdlnLPGETDLVQEEMAQ-VLHLETHLANATVPQEKRHDVTALYHRMG 331
Cdd:COG3590   178 PDRDYYLKDDEKsaEIRAAYVAH---VAKMLE----LAGYDEADAAAAAEaVLALETALAKAHWSRVELRDPEKTYNPMT 250
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 332 LEELQERFglKGFNWTLFiqnvLSSVQVELLpnEEVVVYGIPYLENLEEIIDVFPAQTLQNYLVWRLVLDRIGSLSQRFK 411
Cdd:COG3590   251 VAELAKLA--PGFDWDAY----LKALGLPAV--DEVIVGQPSFFKALDKLLASTPLEDWKAYLRWHLLDSAAPYLSKAFV 322
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 1958776856 412 EARVD-YRKALYGTTMEEVRWRECVSYVNSNMESAVGSLYIKRAFSKDSKSIVSELIEKIRSVFVDNLDELNWMDEESKK 490
Cdd:COG3590   323 DANFDfYGKTLSGQKEQRPRWKRAVALVNGALGEALGQLYVERYFPPEAKARMEELVANLRAAYRERIENLDWMSPETKA 402
                         410
                  ....*....|....*..
gi 1958776856 491 KAQEKALNIREQIGYPD 507
Cdd:COG3590   403 KALEKLAAFTPKIGYPD 419
 
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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