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Conserved domains on  [gi|157822555|ref|NP_001101522|]
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ras and Rab interactor 3 isoform 3 [Rattus norvegicus]

Protein Classification

VPS9 domain-containing protein( domain architecture ID 13105837)

VPS9 domain-containing protein similar to Homo sapiens VPS9 domain-containing protein 1 that regulates tubular endosome formation through specific activation of Rab22A

Graphical summary

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List of domain hits

Name Accession Description Interval E-value
RA_Rin3 cd16130
Ras-associating (RA) domain found in Ras and Rab interactor 3 (Rin3); Rin3, also termed Ras ...
791-878 2.78e-48

Ras-associating (RA) domain found in Ras and Rab interactor 3 (Rin3); Rin3, also termed Ras interaction/interference protein 3, is a RAS effector and a RAB5-activating guanine nucleotide exchange factor (GEF) specifically for GTPase Rab31. It functions as a negative regulator of mast cell responses to Stem Cell Factor (SCF). Rin3 contains the Vps9p-like guanine nucleotide exchange factor and Ras-association (RA) domains.


:

Pssm-ID: 340547  Cd Length: 88  Bit Score: 165.67  E-value: 2.78e-48
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555 791 QDFICVSYLQPEQQSRTLASRADTVAQALCAQCAEKFEVAQPQDYRLFVLVDGRCFQLADEALPHRIKGYLLRSEPKRDF 870
Cdd:cd16130    1 QDFISVSFLEPGSNTRTLAIRPDTTAEDLCKQCAEKFEVLDPENYGLFVLVDGRCLQLADDALPHHIKSDLLKSEPRKDF 80

                 ....*...
gi 157822555 871 HFVYRPQD 878
Cdd:cd16130   81 HFLYKQLS 88
SH2 super family cl15255
Src homology 2 (SH2) domain; In general, SH2 domains are involved in signal transduction; they ...
1-70 1.64e-38

Src homology 2 (SH2) domain; In general, SH2 domains are involved in signal transduction; they bind pTyr-containing polypeptide ligands via two surface pockets, a pTyr and hydrophobic binding pocket, allowing proteins with SH2 domains to localize to tyrosine phosphorylated sites. They are present in a wide array of proteins including: adaptor proteins (Nck1, Crk, Grb2), scaffolds (Slp76, Shc, Dapp1), kinases (Src, Syk, Fps, Tec), phosphatases (Shp-1, Shp-2), transcription factors (STAT1), Ras signaling molecules (Ras-Gap), ubiquitination factors (c-Cbl), cytoskeleton regulators (Tensin), signal regulators (SAP), and phospholipid second messengers (PLCgamma), amongst others.


The actual alignment was detected with superfamily member cd10395:

Pssm-ID: 472789  Cd Length: 101  Bit Score: 138.36  E-value: 1.64e-38
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   1 MFLVCRDSSLKRLVLCVHFPSlKNTSTEVLEYPIKEEKSILYLEGSVLVFEDIFRLIAFYCVSRDLLPFT 70
Cdd:cd10395   33 MFLVRRDSNSKQMVLCVHFPS-NESSAEVLEYPIKEEKSILYLEGSVLVFEDIFKLIAFYCVSRDLLPFT 101
VPS9 pfam02204
Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). ...
653-756 2.94e-36

Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). It activates Rab GTPases by stimulating the release of GDP and allowing GTP to bind.


:

Pssm-ID: 460489  Cd Length: 104  Bit Score: 132.33  E-value: 2.94e-36
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  653 MEKILQKLTNMHKAYSPGKKISILLKTCKLIYDSMALGNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 732
Cdd:pfam02204   1 WEQAQQELKKLNEAKSPREKLKCLLRTCKLITEALSKSNRDESLGADDLLPILIYVLIRANPPNLYSNLQFISEFRDPDL 80
                          90       100
                  ....*....|....*....|....
gi 157822555  733 QLGEGSYYLTTTYGALEHIKNYDK 756
Cdd:pfam02204  81 LSGEEGYYLTTLEAALEFIESLDP 104
PHA03247 super family cl33720
large tegument protein UL36; Provisional
161-479 2.73e-10

large tegument protein UL36; Provisional


The actual alignment was detected with superfamily member PHA03247:

Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 64.57  E-value: 2.73e-10
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  161 DPPPLpigsYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAP--PVQPADPLPNSPTPNSH-LAPHAPG 237
Cdd:PHA03247 2550 DPPPP----LPPAAPPAAPDRSVPPPRPAPRPSEPAVTSRARRPDAPPQSARPraPVDDRGDPRGPAPPSPLpPDTHAPD 2625
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  238 PPGhsnqppmtaceslPRPSvglgPFGEEEMKPGTTPSPlhqappppLPLKKTLPAAPPRRRISERVSLESQNVGTS--T 315
Cdd:PHA03247 2626 PPP-------------PSPS----PAANEPDPHPPPTVP--------PPERPRDDPAPGRVSRPRRARRLGRAAQASspP 2680
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  316 DRDRSGISRtaslnlPPQSTVSSLGDRSPrtteQGQDTEAKASHADS-TPVPPGKAKQPpvppprkkrvsrqlaSTFPSP 394
Cdd:PHA03247 2681 QRPRRRAAR------PTVGSLTSLADPPP----PPPTPEPAPHALVSaTPLPPGPAAAR---------------QASPAL 2735
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  395 LTSPIPEVSPEKPAAPGAPWEGLSPAGQAGMQHLQV----QTSACPQSSPEFKGSLASLSDSLGVPASAADQDSYSTSSA 470
Cdd:PHA03247 2736 PAAPAPPAVPAGPATPGGPARPARPPTTAGPPAPAPpaapAAGPPRRLTRPAVASLSESRESLPSPWDPADPPAAVLAPA 2815

                  ....*....
gi 157822555  471 EEELEFSSP 479
Cdd:PHA03247 2816 AALPPAASP 2824
 
Name Accession Description Interval E-value
RA_Rin3 cd16130
Ras-associating (RA) domain found in Ras and Rab interactor 3 (Rin3); Rin3, also termed Ras ...
791-878 2.78e-48

Ras-associating (RA) domain found in Ras and Rab interactor 3 (Rin3); Rin3, also termed Ras interaction/interference protein 3, is a RAS effector and a RAB5-activating guanine nucleotide exchange factor (GEF) specifically for GTPase Rab31. It functions as a negative regulator of mast cell responses to Stem Cell Factor (SCF). Rin3 contains the Vps9p-like guanine nucleotide exchange factor and Ras-association (RA) domains.


Pssm-ID: 340547  Cd Length: 88  Bit Score: 165.67  E-value: 2.78e-48
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555 791 QDFICVSYLQPEQQSRTLASRADTVAQALCAQCAEKFEVAQPQDYRLFVLVDGRCFQLADEALPHRIKGYLLRSEPKRDF 870
Cdd:cd16130    1 QDFISVSFLEPGSNTRTLAIRPDTTAEDLCKQCAEKFEVLDPENYGLFVLVDGRCLQLADDALPHHIKSDLLKSEPRKDF 80

                 ....*...
gi 157822555 871 HFVYRPQD 878
Cdd:cd16130   81 HFLYKQLS 88
SH2_RIN3 cd10395
Src homology 2 (SH2) domain found in Ras and Rab interactor 3 (RIN3)-like proteins; RIN3, a ...
1-70 1.64e-38

Src homology 2 (SH2) domain found in Ras and Rab interactor 3 (RIN3)-like proteins; RIN3, a member of the RIN (AKA Ras interaction/interference) family, have multifunctional domains including SH2 and proline-rich (PR) domains in the N-terminal region, and RIN-family homology (RH), VPS9 and Ras-association (RA) domains in the C-terminal region. RIN proteins function as Rab5-GEFs. RIN3 stimulated the formation of GTP-bound Rab31, a Rab5-subfamily GTPase, and formed enlarged vesicles and tubular structures, where it colocalized with Rab31. Transferrin appeared to be transported partly through the RIN3-positive vesicles to early endosomes. RIN3 interacts via its Pro-rich domain with amphiphysin II, which contains SH3 domain and participates in receptor-mediated endocytosis. RIN3, a Rab5 and Rab31 GEF, plays an important role in the transport pathway from plasma membrane to early endosomes. Mutations in the region between the SH2 and RH domain of RIN3 specifically abolished its GEF action on Rab31, but not Rab5. RIN3 was also found to partially translocate the cation-dependent mannose 6-phosphate receptor from the trans-Golgi network to peripheral vesicles and that this is dependent on its Rab31-GEF activity. These data indicate that RIN3 specifically acts as a GEF for Rab31. In general SH2 domains are involved in signal transduction. They typically bind pTyr-containing ligands via two surface pockets, a pTyr and hydrophobic binding pocket, allowing proteins with SH2 domains to localize to tyrosine phosphorylated sites.


Pssm-ID: 198258  Cd Length: 101  Bit Score: 138.36  E-value: 1.64e-38
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   1 MFLVCRDSSLKRLVLCVHFPSlKNTSTEVLEYPIKEEKSILYLEGSVLVFEDIFRLIAFYCVSRDLLPFT 70
Cdd:cd10395   33 MFLVRRDSNSKQMVLCVHFPS-NESSAEVLEYPIKEEKSILYLEGSVLVFEDIFKLIAFYCVSRDLLPFT 101
VPS9 pfam02204
Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). ...
653-756 2.94e-36

Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). It activates Rab GTPases by stimulating the release of GDP and allowing GTP to bind.


Pssm-ID: 460489  Cd Length: 104  Bit Score: 132.33  E-value: 2.94e-36
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  653 MEKILQKLTNMHKAYSPGKKISILLKTCKLIYDSMALGNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 732
Cdd:pfam02204   1 WEQAQQELKKLNEAKSPREKLKCLLRTCKLITEALSKSNRDESLGADDLLPILIYVLIRANPPNLYSNLQFISEFRDPDL 80
                          90       100
                  ....*....|....*....|....
gi 157822555  733 QLGEGSYYLTTTYGALEHIKNYDK 756
Cdd:pfam02204  81 LSGEEGYYLTTLEAALEFIESLDP 104
VPS9 smart00167
Domain present in VPS9; Domain present in yeast vacuolar sorting protein 9 and other proteins.
653-769 7.61e-29

Domain present in VPS9; Domain present in yeast vacuolar sorting protein 9 and other proteins.


Pssm-ID: 128469  Cd Length: 117  Bit Score: 111.39  E-value: 7.61e-29
                           10        20        30        40        50        60        70        80
                   ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   653 MEKILQKLTNMHKaySPGKKISILLKTCKLIYDSMALgNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 732
Cdd:smart00167   4 IEQIELKFLQLYK--SPSDKIKCLLRACKLIYTLLET-QSGEVAGADDFLPVLIYVIIKCDPRDLLLNAEYMEEFLEPSL 80
                           90       100       110
                   ....*....|....*....|....*....|....*..
gi 157822555   733 QLGEGSYYLTTTYGALEHIKNYDKITVTRQLSVEVQD 769
Cdd:smart00167  81 LTGEGGYYLTSLSAALALIKGLTEAHALPLSPEQELE 117
PHA03247 PHA03247
large tegument protein UL36; Provisional
161-479 2.73e-10

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 64.57  E-value: 2.73e-10
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  161 DPPPLpigsYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAP--PVQPADPLPNSPTPNSH-LAPHAPG 237
Cdd:PHA03247 2550 DPPPP----LPPAAPPAAPDRSVPPPRPAPRPSEPAVTSRARRPDAPPQSARPraPVDDRGDPRGPAPPSPLpPDTHAPD 2625
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  238 PPGhsnqppmtaceslPRPSvglgPFGEEEMKPGTTPSPlhqappppLPLKKTLPAAPPRRRISERVSLESQNVGTS--T 315
Cdd:PHA03247 2626 PPP-------------PSPS----PAANEPDPHPPPTVP--------PPERPRDDPAPGRVSRPRRARRLGRAAQASspP 2680
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  316 DRDRSGISRtaslnlPPQSTVSSLGDRSPrtteQGQDTEAKASHADS-TPVPPGKAKQPpvppprkkrvsrqlaSTFPSP 394
Cdd:PHA03247 2681 QRPRRRAAR------PTVGSLTSLADPPP----PPPTPEPAPHALVSaTPLPPGPAAAR---------------QASPAL 2735
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  395 LTSPIPEVSPEKPAAPGAPWEGLSPAGQAGMQHLQV----QTSACPQSSPEFKGSLASLSDSLGVPASAADQDSYSTSSA 470
Cdd:PHA03247 2736 PAAPAPPAVPAGPATPGGPARPARPPTTAGPPAPAPpaapAAGPPRRLTRPAVASLSESRESLPSPWDPADPPAAVLAPA 2815

                  ....*....
gi 157822555  471 EEELEFSSP 479
Cdd:PHA03247 2816 AALPPAASP 2824
DUF5585 pfam17823
Family of unknown function (DUF5585); This is a family of unknown function found in chordata.
92-464 4.34e-05

Family of unknown function (DUF5585); This is a family of unknown function found in chordata.


Pssm-ID: 465521 [Multi-domain]  Cd Length: 506  Bit Score: 47.26  E-value: 4.34e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   92 LGLGFWDSSLNSSR-------------------GPAEPLRSSAPGTPASSGRPATHLANCSCEIELSvgndrlwfvnpif 152
Cdd:pfam17823  72 LTKGTSAAHLNSTEvtaehtphgtdlsepatreGAADGAASRALAAAASSSPSSAAQSLPAAIAALP------------- 138
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  153 iedcTLPADPPPLPIGSYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPV----QPADPLPNSPTPN 228
Cdd:pfam17823 139 ----SEAFSAPRAAACRANASAAPRAAIAAASAPHAASPAPRTAASSTTAASSTTAASSAPTTaassAPATLTPARGIST 214
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  229 SHLAphapgpPGHSNQPPMTACESLPRPSVGLGPFGEEEMKPGTTPSPLHQAPPPPLPLKKTLPAAPPRRRISErvsles 308
Cdd:pfam17823 215 AATA------TGHPAAGTALAAVGNSSPAAGTVTAAVGTVTPAALATLAAAAGTVASAAGTINMGDPHARRLSP------ 282
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  309 qnvGTSTDRDRSGISRTASLNLPPQSTVSSLGDRSPRTTEQGQDTEAKASHADSTPVPPGKAKQPPVPPPRKKRVSRQ-L 387
Cdd:pfam17823 283 ---AKHMPSDTMARNPAAPMGAQAQGPIIQVSTDQPVHNTAGEPTPSPSNTTLEPNTPKSVASTNLAVVTTTKAQAKEpS 359
                         330       340       350       360       370       380       390
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 157822555  388 ASTFPSPLTSPIPEVSPEKPAAPGAPWEGLSPAGQAGMQHL--QVQTSACPQSSPefKGSLASLSDSLGVPASAADQDS 464
Cdd:pfam17823 360 ASPVPVLHTSMIPEVEATSPTTQPSPLLPTQGAAGPGILLApeQVATEATAGTAS--AGPTPRSSGDPKTLAMASCQLS 436
 
Name Accession Description Interval E-value
RA_Rin3 cd16130
Ras-associating (RA) domain found in Ras and Rab interactor 3 (Rin3); Rin3, also termed Ras ...
791-878 2.78e-48

Ras-associating (RA) domain found in Ras and Rab interactor 3 (Rin3); Rin3, also termed Ras interaction/interference protein 3, is a RAS effector and a RAB5-activating guanine nucleotide exchange factor (GEF) specifically for GTPase Rab31. It functions as a negative regulator of mast cell responses to Stem Cell Factor (SCF). Rin3 contains the Vps9p-like guanine nucleotide exchange factor and Ras-association (RA) domains.


Pssm-ID: 340547  Cd Length: 88  Bit Score: 165.67  E-value: 2.78e-48
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555 791 QDFICVSYLQPEQQSRTLASRADTVAQALCAQCAEKFEVAQPQDYRLFVLVDGRCFQLADEALPHRIKGYLLRSEPKRDF 870
Cdd:cd16130    1 QDFISVSFLEPGSNTRTLAIRPDTTAEDLCKQCAEKFEVLDPENYGLFVLVDGRCLQLADDALPHHIKSDLLKSEPRKDF 80

                 ....*...
gi 157822555 871 HFVYRPQD 878
Cdd:cd16130   81 HFLYKQLS 88
SH2_RIN3 cd10395
Src homology 2 (SH2) domain found in Ras and Rab interactor 3 (RIN3)-like proteins; RIN3, a ...
1-70 1.64e-38

Src homology 2 (SH2) domain found in Ras and Rab interactor 3 (RIN3)-like proteins; RIN3, a member of the RIN (AKA Ras interaction/interference) family, have multifunctional domains including SH2 and proline-rich (PR) domains in the N-terminal region, and RIN-family homology (RH), VPS9 and Ras-association (RA) domains in the C-terminal region. RIN proteins function as Rab5-GEFs. RIN3 stimulated the formation of GTP-bound Rab31, a Rab5-subfamily GTPase, and formed enlarged vesicles and tubular structures, where it colocalized with Rab31. Transferrin appeared to be transported partly through the RIN3-positive vesicles to early endosomes. RIN3 interacts via its Pro-rich domain with amphiphysin II, which contains SH3 domain and participates in receptor-mediated endocytosis. RIN3, a Rab5 and Rab31 GEF, plays an important role in the transport pathway from plasma membrane to early endosomes. Mutations in the region between the SH2 and RH domain of RIN3 specifically abolished its GEF action on Rab31, but not Rab5. RIN3 was also found to partially translocate the cation-dependent mannose 6-phosphate receptor from the trans-Golgi network to peripheral vesicles and that this is dependent on its Rab31-GEF activity. These data indicate that RIN3 specifically acts as a GEF for Rab31. In general SH2 domains are involved in signal transduction. They typically bind pTyr-containing ligands via two surface pockets, a pTyr and hydrophobic binding pocket, allowing proteins with SH2 domains to localize to tyrosine phosphorylated sites.


Pssm-ID: 198258  Cd Length: 101  Bit Score: 138.36  E-value: 1.64e-38
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   1 MFLVCRDSSLKRLVLCVHFPSlKNTSTEVLEYPIKEEKSILYLEGSVLVFEDIFRLIAFYCVSRDLLPFT 70
Cdd:cd10395   33 MFLVRRDSNSKQMVLCVHFPS-NESSAEVLEYPIKEEKSILYLEGSVLVFEDIFKLIAFYCVSRDLLPFT 101
VPS9 pfam02204
Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). ...
653-756 2.94e-36

Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). It activates Rab GTPases by stimulating the release of GDP and allowing GTP to bind.


Pssm-ID: 460489  Cd Length: 104  Bit Score: 132.33  E-value: 2.94e-36
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  653 MEKILQKLTNMHKAYSPGKKISILLKTCKLIYDSMALGNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 732
Cdd:pfam02204   1 WEQAQQELKKLNEAKSPREKLKCLLRTCKLITEALSKSNRDESLGADDLLPILIYVLIRANPPNLYSNLQFISEFRDPDL 80
                          90       100
                  ....*....|....*....|....
gi 157822555  733 QLGEGSYYLTTTYGALEHIKNYDK 756
Cdd:pfam02204  81 LSGEEGYYLTTLEAALEFIESLDP 104
RA_Rin cd01776
Ras-associating (RA) domain of Ras and Rab interactor (Rin) protein family; Family of ...
791-878 2.00e-29

Ras-associating (RA) domain of Ras and Rab interactor (Rin) protein family; Family of Ras-interaction/interference (Rin) proteins, also known as Ras and Rab interactors, is composed of Rin1, Rin2, and Rin3, which have multifunctional domains, including SH2 and proline-rich domains in the N-terminal region, and RH, VPS9, and RA domains in the C-terminal region. RA domain-containing proteins function by interacting with Ras proteins directly or indirectly and are involved in several different functions ranging from tumor suppression to being oncoproteins. Ras proteins are small GTPases that are involved in cellular signal transduction. The RA domain has the beta-grasp ubiquitin-like (Ubl) fold with low sequence similarity to ubiquitin; ubiquitin is a protein modifier in eukaryotes that is involved in various cellular processes including transcriptional regulation, cell cycle control, and DNA repair. The RA domains of Rin1, Rin2, and Rin3 are well conserved and they all have Ras binding characteristics.


Pssm-ID: 340474  Cd Length: 90  Bit Score: 112.00  E-value: 2.00e-29
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555 791 QDFICVSYLQPEQ---QSRTLASRADTVAQALCAQCAEKFEVAQPQDYRLFVLVDGRCFQLADEALPHRIKGYLLRsEPK 867
Cdd:cd01776    1 QGFLRVAVPDENNgsiVSKTLPVRPSMTAREVCKMIAHKFRVTNPQDYGLFLLVDGEEIQLEDNECPQLIKGELLA-TSK 79
                         90
                 ....*....|.
gi 157822555 868 RDFHFVYRPQD 878
Cdd:cd01776   80 KPCYFAYKRID 90
VPS9 smart00167
Domain present in VPS9; Domain present in yeast vacuolar sorting protein 9 and other proteins.
653-769 7.61e-29

Domain present in VPS9; Domain present in yeast vacuolar sorting protein 9 and other proteins.


Pssm-ID: 128469  Cd Length: 117  Bit Score: 111.39  E-value: 7.61e-29
                           10        20        30        40        50        60        70        80
                   ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   653 MEKILQKLTNMHKaySPGKKISILLKTCKLIYDSMALgNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 732
Cdd:smart00167   4 IEQIELKFLQLYK--SPSDKIKCLLRACKLIYTLLET-QSGEVAGADDFLPVLIYVIIKCDPRDLLLNAEYMEEFLEPSL 80
                           90       100       110
                   ....*....|....*....|....*....|....*..
gi 157822555   733 QLGEGSYYLTTTYGALEHIKNYDKITVTRQLSVEVQD 769
Cdd:smart00167  81 LTGEGGYYLTSLSAALALIKGLTEAHALPLSPEQELE 117
SH2_RIN_family cd10339
Src homology 2 (SH2) domain found in Ras and Rab interactor (RIN)-family; The RIN (AKA Ras ...
1-70 3.20e-28

Src homology 2 (SH2) domain found in Ras and Rab interactor (RIN)-family; The RIN (AKA Ras interaction/interference) family is composed of RIN1, RIN2 and RIN3. These proteins have multifunctional domains including SH2 and proline-rich (PR) domains in the N-terminal region, and RIN-family homology (RH), VPS9 and Ras-association (RA) domains in the C-terminal region. RIN proteins function as Rab5-GEFs, and RIN3 specifically functions as a Rab31-GEF. In general SH2 domains are involved in signal transduction. They typically bind pTyr-containing ligands via two surface pockets, a pTyr and hydrophobic binding pocket, allowing proteins with SH2 domains to localize to tyrosine phosphorylated sites.


Pssm-ID: 198202  Cd Length: 101  Bit Score: 109.16  E-value: 3.20e-28
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   1 MFLVCRDSSLKRLVLCVHFPSlKNTSTEVLEYPIKEEKSILYLEGSVLVFEDIFRLIAFYCVSRDLLPFT 70
Cdd:cd10339   33 TFLVRKSNTRQCQVLCMRLPE-ASGPAFVSEHYIKESPGGVSLEGSELMFPDLFRLIAFYCHSRDILPFT 101
SH2_RIN2 cd10394
Src homology 2 (SH2) domain found in Ras and Rab interactor 2 (RIN2)-like proteins; RIN2, a ...
2-70 3.36e-15

Src homology 2 (SH2) domain found in Ras and Rab interactor 2 (RIN2)-like proteins; RIN2, a member of the RIN (AKA Ras interaction/interference) family, have multifunctional domains including SH2 and proline-rich (PR) domains in the N-terminal region, and RIN-family homology (RH), VPS9 and Ras-association (RA) domains in the C-terminal region. RIN proteins function as Rab5-GEFs. Ras induces activation of Rab5 through RIN2, which is a direct downstream target of Ras and a direct upstream regulator of Rab5. In other words it is the binding of the GTP-bound form of Ras to the RA domain of RIN2 that enhances the GEF activity toward Rab5. It is thought that the RA domain negatively regulates the Rab5 GEF activity. In steady state, RIN2 is likely to form a closed conformation by an intramolecular interaction between the RA domain and the Vps9p-like (Rab5 GEF) domain, negatively regulating the Rab5 GEF activity. In the active state, the binding of Ras to the RA domain may reduce the intramolecular interaction and stabilize an open conformation of RIN2. In general SH2 domains are involved in signal transduction. They typically bind pTyr-containing ligands via two surface pockets, a pTyr and hydrophobic binding pocket, allowing proteins with SH2 domains to localize to tyrosine phosphorylated sites.


Pssm-ID: 198257  Cd Length: 100  Bit Score: 72.15  E-value: 3.36e-15
                         10        20        30        40        50        60
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 157822555   2 FLVCRDSSLKRLVLCVHFPSlkNTSTEVLEYPIKEEKSILYLEGSVLVFEDIFRLIAFYCVSRDLLPFT 70
Cdd:cd10394   34 FLVRKSSKMQKKVLSLRLPC--EFGAPLKEFAIKESTYTFSLEGSGISFADLFRLIAFYCISRDVLPFT 100
RA_Rin2 cd16131
Ras-associating (RA) domain found in Ras and Rab interactor 2 (Rin2); Rin2, also termed Ras ...
805-875 2.25e-11

Ras-associating (RA) domain found in Ras and Rab interactor 2 (Rin2); Rin2, also termed Ras association domain family 4, or Ras inhibitor JC265, or Ras interaction/interference protein 2, is a Rab5 GDP/GTP exchange factor with the Vps9p-like guanine nucleotide exchange factor and Ras-association (RA) domains. Rin2 connects three GTPases, R-Ras, Rab5 and Rac1, to promote endothelial cell adhesion through the regulation of integrin internalization and Rac1 activation. Rin2 is involved in the regulation of Rab5-mediated early endocytosis. The deficiency of Rin2 can cause the RIN2 syndrome, an autosomal recessive connective tissue disorder.


Pssm-ID: 340548  Cd Length: 91  Bit Score: 60.64  E-value: 2.25e-11
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|..
gi 157822555 805 SRTLASRADTVAQALCAQCAEKFEVAQPQDYRLFVLVDGRCFQLADEALPHRIKGYlLRSEPK-RDFHFVYR 875
Cdd:cd16131   18 AKTLLVRPYTTTEEVCQLCAQKFKVQDPENYSLFLLIDDTWQQLAEDTYPQKIKAE-LHSRPQpQIFHFVYK 88
SH2_RIN1 cd10393
Src homology 2 (SH2) domain found in Ras and Rab interactor 1 (RIN1)-like proteins; RIN1, a ...
2-70 1.59e-10

Src homology 2 (SH2) domain found in Ras and Rab interactor 1 (RIN1)-like proteins; RIN1, a member of the RIN (AKA Ras interaction/interference) family, have multifunctional domains including SH2 and proline-rich (PR) domains in the N-terminal region, and RIN-family homology (RH), VPS9 and Ras-association (RA) domains in the C-terminal region. RIN proteins function as Rab5-GEFs. Previous studies showed that RIN1 interacts with EGF receptors via its SH2 domain and regulates trafficking and degradation of EGF receptors via its interaction with STAM, indicating a vital role for RIN1 in regulating endosomal trafficking of receptor tyrosine kinases (RTKs). RIN1 was first identified as a Ras-binding protein that suppresses the activated RAS2 allele in S. cerevisiae. RIN1 binds to the activated Ras through its carboxyl-terminal domain and this Ras-binding domain also binds to 14-3-3 proteins as Raf-1 does. The SH2 domain of RIN1 are thought to interact with the phosphotyrosine-containing proteins, but the physiological partners for this domain are unknown. The proline-rich domain in RIN1 is similar to the consensus SH3 binding regions. In general SH2 domains are involved in signal transduction. They typically bind pTyr-containing ligands via two surface pockets, a pTyr and hydrophobic binding pocket, allowing proteins with SH2 domains to localize to tyrosine phosphorylated sites.


Pssm-ID: 198256  Cd Length: 101  Bit Score: 58.71  E-value: 1.59e-10
                         10        20        30        40        50        60
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 157822555   2 FLVCRDSSLKRLVLCVHFPSLKNTSTeVLEYPIKEEKSILYLEGSVLVFEDIFRLIAFYCVSRDLLPFT 70
Cdd:cd10393   34 FLVRKSNTRQCQALCVRLPEASGPSF-VSSHYIQESPGGVSLEGSELTFPDLVQLICAYCHTRDILLLP 101
PHA03247 PHA03247
large tegument protein UL36; Provisional
161-479 2.73e-10

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 64.57  E-value: 2.73e-10
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  161 DPPPLpigsYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAP--PVQPADPLPNSPTPNSH-LAPHAPG 237
Cdd:PHA03247 2550 DPPPP----LPPAAPPAAPDRSVPPPRPAPRPSEPAVTSRARRPDAPPQSARPraPVDDRGDPRGPAPPSPLpPDTHAPD 2625
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  238 PPGhsnqppmtaceslPRPSvglgPFGEEEMKPGTTPSPlhqappppLPLKKTLPAAPPRRRISERVSLESQNVGTS--T 315
Cdd:PHA03247 2626 PPP-------------PSPS----PAANEPDPHPPPTVP--------PPERPRDDPAPGRVSRPRRARRLGRAAQASspP 2680
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  316 DRDRSGISRtaslnlPPQSTVSSLGDRSPrtteQGQDTEAKASHADS-TPVPPGKAKQPpvppprkkrvsrqlaSTFPSP 394
Cdd:PHA03247 2681 QRPRRRAAR------PTVGSLTSLADPPP----PPPTPEPAPHALVSaTPLPPGPAAAR---------------QASPAL 2735
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  395 LTSPIPEVSPEKPAAPGAPWEGLSPAGQAGMQHLQV----QTSACPQSSPEFKGSLASLSDSLGVPASAADQDSYSTSSA 470
Cdd:PHA03247 2736 PAAPAPPAVPAGPATPGGPARPARPPTTAGPPAPAPpaapAAGPPRRLTRPAVASLSESRESLPSPWDPADPPAAVLAPA 2815

                  ....*....
gi 157822555  471 EEELEFSSP 479
Cdd:PHA03247 2816 AALPPAASP 2824
RA_Rin1 cd17215
Ras-associating (RA) domain found in Ras and Rab interactor 1 (Rin1); Rin1, also termed Ras ...
791-878 4.08e-10

Ras-associating (RA) domain found in Ras and Rab interactor 1 (Rin1); Rin1, also termed Ras inhibitor JC99, or Ras interaction/interference protein 1, is a downstream Ras effector that represents a unique class of Ras effector connected to two independent signaling pathways. The first effector pathway is the direct activation of RAB5-mediated endocytosis and the second pathway involves direct activation of ABL tyrosine kinase activity. Rin1 functions as a guanine nucleotide exchange factor (GEF) for RAB5 GTPases. The RAB5 GEF activity of Rin1 promotes early endosome fusion, an early event in transit to the lysosome. Rin1 binds the SH3 and SH2 domains of ABL proteins, ABL1 and ABL2, and activates their tyrosine kinase activity. Rin1 contains SH2 and proline-rich domains in the N-terminal region, and RH, VPS9, and RA domains in the C-terminal region. The RA domain has the beta-grasp ubiquitin-like (Ubl) fold with low sequence similarity to ubiquitin; ubiquitin is a protein modifier in eukaryotes that is involved in various cellular processes including transcriptional regulation, cell cycle control, and DNA repair.


Pssm-ID: 340735  Cd Length: 88  Bit Score: 57.30  E-value: 4.08e-10
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555 791 QDFICVSYLQPEQ--QSRTLASRADTVAQALCAQCAEKFEVAQPQDYRLFVLVDGRCFQLADEALPHRIKGYLlrSEPKR 868
Cdd:cd17215    1 QNFLRVAYQDPSSgcTSKTLAVPPSATVADLNQLCATKFKVTQPETYGIFLYKEQGYQRLPPDALPQRIKAQL--KEKGS 78
                         90
                 ....*....|
gi 157822555 869 DFHFVYRPQD 878
Cdd:cd17215   79 TFYFVYQRAE 88
PHA03247 PHA03247
large tegument protein UL36; Provisional
103-441 1.51e-07

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 55.71  E-value: 1.51e-07
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  103 SSRGPAEPLRSSA-PGTPASSGRPATHLANCSCEIELSVGNDRLWFVNPifiedctlPADPPPLPIGSYPTRPAPAAPDA 181
Cdd:PHA03247 2687 AARPTVGSLTSLAdPPPPPPTPEPAPHALVSATPLPPGPAAARQASPAL--------PAAPAPPAVPAGPATPGGPARPA 2758
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  182 TSLTSKGSPRRPPPPppvptvpptGPAWPPAPPVQPADPLPNSPTPNSHLAPHAPGPPGHSNQPPMTACESLPRPSVGLG 261
Cdd:PHA03247 2759 RPPTTAGPPAPAPPA---------APAAGPPRRLTRPAVASLSESRESLPSPWDPADPPAAVLAPAAALPPAASPAGPLP 2829
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  262 PfgEEEMKPGTTPSPLHQAPPPPLPLKKTLPAAPPRRRISERvslesQNVGTSTDRDRSGISRTASLNLPPQSTVSSLGD 341
Cdd:PHA03247 2830 P--PTSAQPTAPPPPPGPPPPSLPLGGSVAPGGDVRRRPPSR-----SPAAKPAAPARPPVRRLARPAVSRSTESFALPP 2902
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  342 RSPRTTEQGQdteakashADSTPVPPGKAKQPPVPPPRKKRVSRQLASTFPSPLTSPIPEVSPEKPaapgAPWEGLSPAG 421
Cdd:PHA03247 2903 DQPERPPQPQ--------APPPPQPQPQPPPPPQPQPPPPPPPRPQPPLAPTTDPAGAGEPSGAVP----QPWLGALVPG 2970
                         330       340
                  ....*....|....*....|
gi 157822555  422 QAGMQHLQVQTSACPQSSPE 441
Cdd:PHA03247 2971 RVAVPRFRVPQPAPSREAPA 2990
PHA03307 PHA03307
transcriptional regulator ICP4; Provisional
159-479 2.84e-06

transcriptional regulator ICP4; Provisional


Pssm-ID: 223039 [Multi-domain]  Cd Length: 1352  Bit Score: 51.33  E-value: 2.84e-06
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  159 PADPPPlpiGSYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPVQPADPLPNSPTPNSHL------- 231
Cdd:PHA03307   68 PTGPPP---GPGTEAPANESRSTPTWSLSTLAPASPAREGSPTPPGPSSPDPPPPTPPPASPPPSPAPDLSEMlrpvgsp 144
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  232 --APHAPGPPGHSNQPPMTACESLPRPSVGLGPFGEEEMKPGTTPSPlhqapPPPLPLKKTLPAAPPRRRISERVSLESQ 309
Cdd:PHA03307  145 gpPPAASPPAAGASPAAVASDAASSRQAALPLSSPEETARAPSSPPA-----EPPPSTPPAAASPRPPRRSSPISASASS 219
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  310 NVGTSTDRDRSGISRTASLNLPPQSTVSslgdrsprttEQGQDTEAKASHADSTPVPPGKAKQPPVPPPRKKRVSRQLAS 389
Cdd:PHA03307  220 PAPAPGRSAADDAGASSSDSSSSESSGC----------GWGPENECPLPRPAPITLPTRIWEASGWNGPSSRPGPASSSS 289
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  390 TFPSPLTSPIPEVSPEKPAAPGAP----WEGLSPAGqagmqhlqvqtSACPQSSPEfkgslasLSDSLGVPASAADQDSY 465
Cdd:PHA03307  290 SPRERSPSPSPSSPGSGPAPSSPRasssSSSSRESS-----------SSSTSSSSE-------SSRGAAVSPGPSPSRSP 351
                         330
                  ....*....|....
gi 157822555  466 STSSAEEELEFSSP 479
Cdd:PHA03307  352 SPSRPPPPADPSSP 365
PHA03247 PHA03247
large tegument protein UL36; Provisional
106-421 5.43e-06

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 50.71  E-value: 5.43e-06
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  106 GPAEPLRSSAPGTPASSGRPATHlancsceielsvGNDRlwfvnpifiEDCTLPADPPPLPIGSYPTRPAPAAPDATSLT 185
Cdd:PHA03247 2579 EPAVTSRARRPDAPPQSARPRAP------------VDDR---------GDPRGPAPPSPLPPDTHAPDPPPPSPSPAANE 2637
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  186 SKGSPRRPPPPPPVPTVPPTGP-------AWPPAPPVQPADPlPNSPTPNSHLAPHA-------PGPPGHSNQPPmtace 251
Cdd:PHA03247 2638 PDPHPPPTVPPPERPRDDPAPGrvsrprrARRLGRAAQASSP-PQRPRRRAARPTVGsltsladPPPPPPTPEPA----- 2711
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  252 slPRPSVglgpfgeeemkPGTTPSPLHQAPPPPLPLKKTLPAAPPrrriserVSLESQNVGTSTDRDRSGISRTASLNLP 331
Cdd:PHA03247 2712 --PHALV-----------SATPLPPGPAAARQASPALPAAPAPPA-------VPAGPATPGGPARPARPPTTAGPPAPAP 2771
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  332 PQSTVSSLGDRSPRTteqgqdteAKASHADSTPVPPGKAKQPPVPPPRKKRVSRQLASTFPSPLTSPIPEVSPEKPAAPG 411
Cdd:PHA03247 2772 PAAPAAGPPRRLTRP--------AVASLSESRESLPSPWDPADPPAAVLAPAAALPPAASPAGPLPPPTSAQPTAPPPPP 2843
                         330
                  ....*....|
gi 157822555  412 APWEGLSPAG 421
Cdd:PHA03247 2844 GPPPPSLPLG 2853
PHA03307 PHA03307
transcriptional regulator ICP4; Provisional
103-421 8.84e-06

transcriptional regulator ICP4; Provisional


Pssm-ID: 223039 [Multi-domain]  Cd Length: 1352  Bit Score: 49.78  E-value: 8.84e-06
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  103 SSRGPAEPLRSSAPGTPASSGRPATHLANCSCEIELSVGNDRlwfvnpifIEDCTLPADPPPLPIGSYPTRPAPAAPDAT 182
Cdd:PHA03307   93 STLAPASPAREGSPTPPGPSSPDPPPPTPPPASPPPSPAPDL--------SEMLRPVGSPGPPPAASPPAAGASPAAVAS 164
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  183 SLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPVQPADPLPNSPTPNSHLAPHA----PGPPGHSNQPP------MTACES 252
Cdd:PHA03307  165 DAASSRQAALPLSSPEETARAPSSPPAEPPPSTPPAAASPRPPRRSSPISASAsspaPAPGRSAADDAgasssdSSSSES 244
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  253 ------------LPRPSVGLGPFGEEEMKPGTTPSPLHQAPPPPLPLKKT----------LPAAPPRRRISERVSLeSQN 310
Cdd:PHA03307  245 sgcgwgpenecpLPRPAPITLPTRIWEASGWNGPSSRPGPASSSSSPRERspspspsspgSGPAPSSPRASSSSSS-SRE 323
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  311 VGTSTDRDRSGISRTASLNLP--------PQSTVSSLGDRSPRTTEQGQDTEAKASHADSTPVPPGKAKQppvppPRKKR 382
Cdd:PHA03307  324 SSSSSTSSSSESSRGAAVSPGpspsrspsPSRPPPPADPSSPRKRPRPSRAPSSPAASAGRPTRRRARAA-----VAGRA 398
                         330       340       350
                  ....*....|....*....|....*....|....*....
gi 157822555  383 VSRQLASTFPSPLTSPIPEVSPEKPAAPGAPWEGLSPAG 421
Cdd:PHA03307  399 RRRDATGRFPAGRPRPSPLDAGAASGAFYARYPLLTPSG 437
DUF5585 pfam17823
Family of unknown function (DUF5585); This is a family of unknown function found in chordata.
92-464 4.34e-05

Family of unknown function (DUF5585); This is a family of unknown function found in chordata.


Pssm-ID: 465521 [Multi-domain]  Cd Length: 506  Bit Score: 47.26  E-value: 4.34e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555   92 LGLGFWDSSLNSSR-------------------GPAEPLRSSAPGTPASSGRPATHLANCSCEIELSvgndrlwfvnpif 152
Cdd:pfam17823  72 LTKGTSAAHLNSTEvtaehtphgtdlsepatreGAADGAASRALAAAASSSPSSAAQSLPAAIAALP------------- 138
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  153 iedcTLPADPPPLPIGSYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPV----QPADPLPNSPTPN 228
Cdd:pfam17823 139 ----SEAFSAPRAAACRANASAAPRAAIAAASAPHAASPAPRTAASSTTAASSTTAASSAPTTaassAPATLTPARGIST 214
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  229 SHLAphapgpPGHSNQPPMTACESLPRPSVGLGPFGEEEMKPGTTPSPLHQAPPPPLPLKKTLPAAPPRRRISErvsles 308
Cdd:pfam17823 215 AATA------TGHPAAGTALAAVGNSSPAAGTVTAAVGTVTPAALATLAAAAGTVASAAGTINMGDPHARRLSP------ 282
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  309 qnvGTSTDRDRSGISRTASLNLPPQSTVSSLGDRSPRTTEQGQDTEAKASHADSTPVPPGKAKQPPVPPPRKKRVSRQ-L 387
Cdd:pfam17823 283 ---AKHMPSDTMARNPAAPMGAQAQGPIIQVSTDQPVHNTAGEPTPSPSNTTLEPNTPKSVASTNLAVVTTTKAQAKEpS 359
                         330       340       350       360       370       380       390
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 157822555  388 ASTFPSPLTSPIPEVSPEKPAAPGAPWEGLSPAGQAGMQHL--QVQTSACPQSSPefKGSLASLSDSLGVPASAADQDS 464
Cdd:pfam17823 360 ASPVPVLHTSMIPEVEATSPTTQPSPLLPTQGAAGPGILLApeQVATEATAGTAS--AGPTPRSSGDPKTLAMASCQLS 436
PHA03307 PHA03307
transcriptional regulator ICP4; Provisional
159-452 4.86e-05

transcriptional regulator ICP4; Provisional


Pssm-ID: 223039 [Multi-domain]  Cd Length: 1352  Bit Score: 47.47  E-value: 4.86e-05
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  159 PADPPPLPIGSYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPVQPADPLPNSPTPNSHlaPHAPGP 238
Cdd:PHA03307  111 PSSPDPPPPTPPPASPPPSPAPDLSEMLRPVGSPGPPPAASPPAAGASPAAVASDAASSRQAALPLSSPEET--ARAPSS 188
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  239 PGHSNqPPMTACESLPRPsvglgpfgeeemkPGTTPSPLHQAPPPPLPLKKTLPAAPPRRRISERVSLESQNVGtSTDRD 318
Cdd:PHA03307  189 PPAEP-PPSTPPAAASPR-------------PPRRSSPISASASSPAPAPGRSAADDAGASSSDSSSSESSGCG-WGPEN 253
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  319 RSGISRTASLNLPPQSTVSSLGD--------RSPRTTEQGQDTEAKASHADSTPVPPGKAKQPPVPPPRKKRVSRQLAST 390
Cdd:PHA03307  254 ECPLPRPAPITLPTRIWEASGWNgpssrpgpASSSSSPRERSPSPSPSSPGSGPAPSSPRASSSSSSSRESSSSSTSSSS 333
                         250       260       270       280       290       300
                  ....*....|....*....|....*....|....*....|....*....|....*....|....
gi 157822555  391 FPS--PLTSPIPEVSPEKPAAPGAPWEGLSPAGQAGMQHLQVQTSACPQSSPEFKGSLASLSDS 452
Cdd:PHA03307  334 ESSrgAAVSPGPSPSRSPSPSRPPPPADPSSPRKRPRPSRAPSSPAASAGRPTRRRARAAVAGR 397
PHA03247 PHA03247
large tegument protein UL36; Provisional
100-397 1.75e-04

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 45.70  E-value: 1.75e-04
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  100 SLNSSRGPAEPLRSSAPGTPA--SSGRPATHLANCSCEIELSVGNDRLWFVNPIFIEDCTLPADPPPLPIGSYPTRPAPA 177
Cdd:PHA03247 2797 SLPSPWDPADPPAAVLAPAAAlpPAASPAGPLPPPTSAQPTAPPPPPGPPPPSLPLGGSVAPGGDVRRRPPSRSPAAKPA 2876
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  178 APdATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPVqPADPLPNSPTPNSHLAPHAPGPPGHSNQP--PMTACESLPR 255
Cdd:PHA03247 2877 AP-ARPPVRRLARPAVSRSTESFALPPDQPERPPQPQA-PPPPQPQPQPPPPPQPQPPPPPPPRPQPPlaPTTDPAGAGE 2954
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  256 PSVGLGPFGEEEMKPGTTPSPLHQAPPPPLPLKKTLPAAPPRRRIS-ERVSLESQNVGTSTDRDRSGISRTASLnLPPQS 334
Cdd:PHA03247 2955 PSGAVPQPWLGALVPGRVAVPRFRVPQPAPSREAPASSTPPLTGHSlSRVSSWASSLALHEETDPPPVSLKQTL-WPPDD 3033
                         250       260       270       280       290       300
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 157822555  335 TVSSLGDRSPRTTEQGQDTEAkashADSTPVPPGKAKQPPVPPPRKKRVSRQLASTF--PSPLTS 397
Cdd:PHA03247 3034 TEDSDADSLFDSDSERSDLEA----LDPLPPEPHDPFAHEPDPATPEAGARESPSSQfgPPPLSA 3094
PHA03307 PHA03307
transcriptional regulator ICP4; Provisional
150-479 2.15e-03

transcriptional regulator ICP4; Provisional


Pssm-ID: 223039 [Multi-domain]  Cd Length: 1352  Bit Score: 42.08  E-value: 2.15e-03
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  150 PIFIEDCTLPADPPPLPI-GSYPTRPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPVQPADPLPNSPTPN 228
Cdd:PHA03307   19 EFFPRPPATPGDAADDLLsGSQGQLVSDSAELAAVTVVAGAAACDRFEPPTGPPPGPGTEAPANESRSTPTWSLSTLAPA 98
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  229 SHLAPHAPGPPGHSNQ--PPMTACESLPRPSVGLGPFGEEEMKPGTTPSPLHQAPPPPLPLKKTLPAAPPRRRISERVSL 306
Cdd:PHA03307   99 SPAREGSPTPPGPSSPdpPPPTPPPASPPPSPAPDLSEMLRPVGSPGPPPAASPPAAGASPAAVASDAASSRQAALPLSS 178
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  307 ESQNVGTSTdrdrsgisrtaslnlPPQSTVSSLGDRSPRT-TEQGQDTEAKASHADSTPVPPGKAKQPPVPPPRKKRVSR 385
Cdd:PHA03307  179 PEETARAPS---------------SPPAEPPPSTPPAAASpRPPRRSSPISASASSPAPAPGRSAADDAGASSSDSSSSE 243
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555  386 QLASTFPSPLTSPIPevSPEKPAAPGAPWEGlSPAGQAGMQHLQVQTSAcpqSSPEFKGSLASLSDSLGVPASAADQDSY 465
Cdd:PHA03307  244 SSGCGWGPENECPLP--RPAPITLPTRIWEA-SGWNGPSSRPGPASSSS---SPRERSPSPSPSSPGSGPAPSSPRASSS 317
                         330
                  ....*....|....
gi 157822555  466 STSSAEEELEFSSP 479
Cdd:PHA03307  318 SSSSRESSSSSTSS 331
PHA02682 PHA02682
ORF080 virion core protein; Provisional
156-242 5.88e-03

ORF080 virion core protein; Provisional


Pssm-ID: 177464 [Multi-domain]  Cd Length: 280  Bit Score: 39.84  E-value: 5.88e-03
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 157822555 156 CTLPADPPPLPIGSYPTrPAPAAPDATSLTSKGSPRRPPPPPPVPTVPPTGPAWPPAPPVQPADPLPNSPTPNSHLAPHA 235
Cdd:PHA02682  95 CPACAPAAPAPAVTCPA-PAPACPPATAPTCPPPAVCPAPARPAPACPPSTRQCPPAPPLPTPKPAPAAKPIFLHNQLPP 173

                 ....*..
gi 157822555 236 PGPPGHS 242
Cdd:PHA02682 174 PDYPAAS 180
 
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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