NCBI Home Page NCBI Site Search page NCBI Guide that lists and describes the NCBI resources
Conserved domains on  [gi|987437828|ref|NP_001306916|]
View 

ras and Rab interactor 3 isoform 2 [Homo sapiens]

Protein Classification

VPS9 and RA_Rin3 domain-containing protein( domain architecture ID 13105837)

protein containing domains SH2, PHA03247, VPS9, and RA_Rin3

Graphical summary

 Zoom to residue level

show extra options »

Show site features     Horizontal zoom: ×

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 ...
802-889 2.51e-49

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: 168.75  E-value: 2.51e-49
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 802 QDFICVSYLEPEQQARTLASRADTQAQALCAQCAEKFAVERPQAHRLFVLVDGRCFQLADDALPHCIKGYLLRSEPKRDF 881
Cdd:cd16130    1 QDFISVSFLEPGSNTRTLAIRPDTTAEDLCKQCAEKFEVLDPENYGLFVLVDGRCLQLADDALPHHIKSDLLKSEPRKDF 80

                 ....*...
gi 987437828 882 HFVYRPLD 889
Cdd:cd16130   81 HFLYKQLS 88
SH2 super family cl15255
Src homology 2 (SH2) domain; In general, SH2 domains are involved in signal transduction; they ...
9-78 5.71e-40

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: 142.60  E-value: 5.71e-40
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828   9 MFLVRRDSSSKQLVLCVHFPSlNESSAEVLEYTIKEEKSILYLEGSALVFEDIFRLIAFYCVSRDLLPFT 78
Cdd:cd10395   33 MFLVRRDSNSKQMVLCVHFPS-NESSAEVLEYPIKEEKSILYLEGSVLVFEDIFKLIAFYCVSRDLLPFT 101
VPS9 pfam02204
Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). ...
664-767 1.04e-35

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: 130.79  E-value: 1.04e-35
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  664 MEKILQKFTSMHKAYSPEKKISILLKTCKLIYDSMALGNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 743
Cdd:pfam02204   1 WEQAQQELKKLNEAKSPREKLKCLLRTCKLITEALSKSNRDESLGADDLLPILIYVLIRANPPNLYSNLQFISEFRDPDL 80
                          90       100
                  ....*....|....*....|....
gi 987437828  744 QLGEGSYYLTTTYGALEHIKSYDK 767
Cdd:pfam02204  81 LSGEEGYYLTTLEAALEFIESLDP 104
PHA03247 super family cl33720
large tegument protein UL36; Provisional
165-450 5.66e-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: 63.80  E-value: 5.66e-10
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  165 IEDCSSALPTDQPPLgnCPARPLPPTSDATSPTSRWAPRRPPPPPPVLPLQPCSPAQPPVLPALAPAPACPLPTSPPVPA 244
Cdd:PHA03247 2540 LEELASDDAGDPPPP--LPPAAPPAAPDRSVPPPRPAPRPSEPAVTSRARRPDAPPQSARPRAPVDDRGDPRGPAPPSPL 2617
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  245 PHvTPHAPGPPDhPNQPPMMTCERLPCPTAGLGPLREEAMKPGAASSPLQQVPAPPLPAKKNLPTAPPRRRVSErvsled 324
Cdd:PHA03247 2618 PP-DTHAPDPPP-PSPSPAANEPDPHPPPTVPPPERPRDDPAPGRVSRPRRARRLGRAAQASSPPQRPRRRAAR------ 2689
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  325 qsPGMAAEGDQLSLPPQGTSdgPEDTPRESTEQGQDTEVKASDPHSMPELPRTAkqppvppprkkrISRQLASTLPAPLE 404
Cdd:PHA03247 2690 --PTVGSLTSLADPPPPPPT--PEPAPHALVSATPLPPGPAAARQASPALPAAP------------APPAVPAGPATPGG 2753
                         250       260       270       280
                  ....*....|....*....|....*....|....*....|....*.
gi 987437828  405 NAELCTQAMALETPTPGPPREGQSPASQAGTQHPPAQATAHSQSSP 450
Cdd:PHA03247 2754 PARPARPPTTAGPPAPAPPAAPAAGPPRRLTRPAVASLSESRESLP 2799
 
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 ...
802-889 2.51e-49

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: 168.75  E-value: 2.51e-49
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 802 QDFICVSYLEPEQQARTLASRADTQAQALCAQCAEKFAVERPQAHRLFVLVDGRCFQLADDALPHCIKGYLLRSEPKRDF 881
Cdd:cd16130    1 QDFISVSFLEPGSNTRTLAIRPDTTAEDLCKQCAEKFEVLDPENYGLFVLVDGRCLQLADDALPHHIKSDLLKSEPRKDF 80

                 ....*...
gi 987437828 882 HFVYRPLD 889
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 ...
9-78 5.71e-40

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: 142.60  E-value: 5.71e-40
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828   9 MFLVRRDSSSKQLVLCVHFPSlNESSAEVLEYTIKEEKSILYLEGSALVFEDIFRLIAFYCVSRDLLPFT 78
Cdd:cd10395   33 MFLVRRDSNSKQMVLCVHFPS-NESSAEVLEYPIKEEKSILYLEGSVLVFEDIFKLIAFYCVSRDLLPFT 101
VPS9 pfam02204
Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). ...
664-767 1.04e-35

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: 130.79  E-value: 1.04e-35
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  664 MEKILQKFTSMHKAYSPEKKISILLKTCKLIYDSMALGNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 743
Cdd:pfam02204   1 WEQAQQELKKLNEAKSPREKLKCLLRTCKLITEALSKSNRDESLGADDLLPILIYVLIRANPPNLYSNLQFISEFRDPDL 80
                          90       100
                  ....*....|....*....|....
gi 987437828  744 QLGEGSYYLTTTYGALEHIKSYDK 767
Cdd:pfam02204  81 LSGEEGYYLTTLEAALEFIESLDP 104
VPS9 smart00167
Domain present in VPS9; Domain present in yeast vacuolar sorting protein 9 and other proteins.
664-780 4.15e-29

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


Pssm-ID: 128469  Cd Length: 117  Bit Score: 112.16  E-value: 4.15e-29
                           10        20        30        40        50        60        70        80
                   ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828   664 MEKILQKFTSMHKaySPEKKISILLKTCKLIYDSMALgNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 743
Cdd:smart00167   4 IEQIELKFLQLYK--SPSDKIKCLLRACKLIYTLLET-QSGEVAGADDFLPVLIYVIIKCDPRDLLLNAEYMEEFLEPSL 80
                           90       100       110
                   ....*....|....*....|....*....|....*..
gi 987437828   744 QLGEGSYYLTTTYGALEHIKSYDKITVTRQLSVEVQD 780
Cdd:smart00167  81 LTGEGGYYLTSLSAALALIKGLTEAHALPLSPEQELE 117
PHA03247 PHA03247
large tegument protein UL36; Provisional
165-450 5.66e-10

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 63.80  E-value: 5.66e-10
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  165 IEDCSSALPTDQPPLgnCPARPLPPTSDATSPTSRWAPRRPPPPPPVLPLQPCSPAQPPVLPALAPAPACPLPTSPPVPA 244
Cdd:PHA03247 2540 LEELASDDAGDPPPP--LPPAAPPAAPDRSVPPPRPAPRPSEPAVTSRARRPDAPPQSARPRAPVDDRGDPRGPAPPSPL 2617
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  245 PHvTPHAPGPPDhPNQPPMMTCERLPCPTAGLGPLREEAMKPGAASSPLQQVPAPPLPAKKNLPTAPPRRRVSErvsled 324
Cdd:PHA03247 2618 PP-DTHAPDPPP-PSPSPAANEPDPHPPPTVPPPERPRDDPAPGRVSRPRRARRLGRAAQASSPPQRPRRRAAR------ 2689
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  325 qsPGMAAEGDQLSLPPQGTSdgPEDTPRESTEQGQDTEVKASDPHSMPELPRTAkqppvppprkkrISRQLASTLPAPLE 404
Cdd:PHA03247 2690 --PTVGSLTSLADPPPPPPT--PEPAPHALVSATPLPPGPAAARQASPALPAAP------------APPAVPAGPATPGG 2753
                         250       260       270       280
                  ....*....|....*....|....*....|....*....|....*.
gi 987437828  405 NAELCTQAMALETPTPGPPREGQSPASQAGTQHPPAQATAHSQSSP 450
Cdd:PHA03247 2754 PARPARPPTTAGPPAPAPPAAPAAGPPRRLTRPAVASLSESRESLP 2799
Atrophin-1 pfam03154
Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ...
176-492 3.32e-04

Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian atrophy (DRPLA) gene. DRPLA OMIM:125370 is a progressive neurodegenerative disorder. It is caused by the expansion of a CAG repeat in the DRPLA gene on chromosome 12p. This results in an extended polyglutamine region in atrophin-1, that is thought to confer toxicity to the protein, possibly through altering its interactions with other proteins. The expansion of a CAG repeat is also the underlying defect in six other neurodegenerative disorders, including Huntington's disease. One interaction of expanded polyglutamine repeats that is thought to be pathogenic is that with the short glutamine repeat in the transcriptional coactivator CREB binding protein, CBP. This interaction draws CBP away from its usual nuclear location to the expanded polyglutamine repeat protein aggregates that are characteriztic of the polyglutamine neurodegenerative disorders. This interferes with CBP-mediated transcription and causes cytotoxicity.


Pssm-ID: 460830 [Multi-domain]  Cd Length: 991  Bit Score: 44.76  E-value: 3.32e-04
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  176 QPPLGNCPARPLPPTSDATSPTSRWAPRRPPPPPPVLplqpcsPAQPpvlpalapapacplptSPPVPAPHVTPHAPGPP 255
Cdd:pfam03154 170 QPPVLQAQSGAASPPSPPPPGTTQAATAGPTPSAPSV------PPQG----------------SPATSQPPNQTQSTAAP 227
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  256 DH-PNQPPMMTCERLPCPTAGLGPLREEAMKPGAASSPLQQV----PAPPLPakKNLPTAPPR------RRVSERVSLED 324
Cdd:pfam03154 228 HTlIQQTPTLHPQRLPSPHPPLQPMTQPPPPSQVSPQPLPQPslhgQMPPMP--HSLQTGPSHmqhpvpPQPFPLTPQSS 305
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  325 QSPGMAAEGDQLSLPPQGTSDGPEDTPRESTEQGQDTEVKASDPHSMPEL---PRTAKQPPVPPPRKKRISR-------Q 394
Cdd:pfam03154 306 QSQVPPGPSPAAPGQSQQRIHTPPSQSQLQSQQPPREQPLPPAPLSMPHIkppPTTPIPQLPNPQSHKHPPHlsgpspfQ 385
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  395 LASTLPAP--------LEN----------AELCTQAMALETPTPGPPREGQSPA-SQAGTQHPPAQATAHSQSSPEFKGS 455
Cdd:pfam03154 386 MNSNLPPPpalkplssLSThhppsahpppLQLMPQSQQLPPPPAQPPVLTQSQSlPPPAASHPPTSGLHQVPSQSPFPQH 465
                         330       340       350
                  ....*....|....*....|....*....|....*..
gi 987437828  456 LASLSDSLGVSVMATDQDSYSTSSTEEELEQFSSPSV 492
Cdd:pfam03154 466 PFVPGGPPPITPPSGPPTSTSSAMPGIQPPSSASVSS 502
 
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 ...
802-889 2.51e-49

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: 168.75  E-value: 2.51e-49
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 802 QDFICVSYLEPEQQARTLASRADTQAQALCAQCAEKFAVERPQAHRLFVLVDGRCFQLADDALPHCIKGYLLRSEPKRDF 881
Cdd:cd16130    1 QDFISVSFLEPGSNTRTLAIRPDTTAEDLCKQCAEKFEVLDPENYGLFVLVDGRCLQLADDALPHHIKSDLLKSEPRKDF 80

                 ....*...
gi 987437828 882 HFVYRPLD 889
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 ...
9-78 5.71e-40

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: 142.60  E-value: 5.71e-40
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828   9 MFLVRRDSSSKQLVLCVHFPSlNESSAEVLEYTIKEEKSILYLEGSALVFEDIFRLIAFYCVSRDLLPFT 78
Cdd:cd10395   33 MFLVRRDSNSKQMVLCVHFPS-NESSAEVLEYPIKEEKSILYLEGSVLVFEDIFKLIAFYCVSRDLLPFT 101
VPS9 pfam02204
Vacuolar sorting protein 9 (VPS9) domain; This domain acts as a GDP-GTP exchange factor (GEF). ...
664-767 1.04e-35

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: 130.79  E-value: 1.04e-35
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  664 MEKILQKFTSMHKAYSPEKKISILLKTCKLIYDSMALGNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 743
Cdd:pfam02204   1 WEQAQQELKKLNEAKSPREKLKCLLRTCKLITEALSKSNRDESLGADDLLPILIYVLIRANPPNLYSNLQFISEFRDPDL 80
                          90       100
                  ....*....|....*....|....
gi 987437828  744 QLGEGSYYLTTTYGALEHIKSYDK 767
Cdd:pfam02204  81 LSGEEGYYLTTLEAALEFIESLDP 104
RA_Rin cd01776
Ras-associating (RA) domain of Ras and Rab interactor (Rin) protein family; Family of ...
802-889 2.17e-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: 2.17e-29
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 802 QDFICVSYLEPEQ---QARTLASRADTQAQALCAQCAEKFAVERPQAHRLFVLVDGRCFQLADDALPHCIKGYLLRsEPK 878
Cdd:cd01776    1 QGFLRVAVPDENNgsiVSKTLPVRPSMTAREVCKMIAHKFRVTNPQDYGLFLLVDGEEIQLEDNECPQLIKGELLA-TSK 79
                         90
                 ....*....|.
gi 987437828 879 RDFHFVYRPLD 889
Cdd:cd01776   80 KPCYFAYKRID 90
VPS9 smart00167
Domain present in VPS9; Domain present in yeast vacuolar sorting protein 9 and other proteins.
664-780 4.15e-29

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


Pssm-ID: 128469  Cd Length: 117  Bit Score: 112.16  E-value: 4.15e-29
                           10        20        30        40        50        60        70        80
                   ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828   664 MEKILQKFTSMHKaySPEKKISILLKTCKLIYDSMALgNPGKPYGADDFLPVLMYVLARSNLTEMLLNVEYMMELMDPAL 743
Cdd:smart00167   4 IEQIELKFLQLYK--SPSDKIKCLLRACKLIYTLLET-QSGEVAGADDFLPVLIYVIIKCDPRDLLLNAEYMEEFLEPSL 80
                           90       100       110
                   ....*....|....*....|....*....|....*..
gi 987437828   744 QLGEGSYYLTTTYGALEHIKSYDKITVTRQLSVEVQD 780
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 ...
9-78 5.33e-27

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: 105.70  E-value: 5.33e-27
                         10        20        30        40        50        60        70
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828   9 MFLVRRDSSSKQLVLCVHFPSlNESSAEVLEYTIKEEKSILYLEGSALVFEDIFRLIAFYCVSRDLLPFT 78
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 ...
10-78 1.74e-16

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: 75.62  E-value: 1.74e-16
                         10        20        30        40        50        60
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 987437828  10 FLVRRDSSSKQLVLCVHFPslNESSAEVLEYTIKEEKSILYLEGSALVFEDIFRLIAFYCVSRDLLPFT 78
Cdd:cd10394   34 FLVRKSSKMQKKVLSLRLP--CEFGAPLKEFAIKESTYTFSLEGSGISFADLFRLIAFYCISRDVLPFT 100
SH2_RIN1 cd10393
Src homology 2 (SH2) domain found in Ras and Rab interactor 1 (RIN1)-like proteins; RIN1, a ...
10-78 5.81e-13

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: 65.64  E-value: 5.81e-13
                         10        20        30        40        50        60
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....
gi 987437828  10 FLVRRDSSSKQLVLCVHFPSLNESSAeVLEYTIKEEKSILYLEGSALVFEDIFRLIAFYCVSRDLLPFT 78
Cdd:cd10393   34 FLVRKSNTRQCQALCVRLPEASGPSF-VSSHYIQESPGGVSLEGSELTFPDLVQLICAYCHTRDILLLP 101
RA_Rin2 cd16131
Ras-associating (RA) domain found in Ras and Rab interactor 2 (Rin2); Rin2, also termed Ras ...
802-886 1.60e-10

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: 58.33  E-value: 1.60e-10
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 802 QDFICVSYLEPEQ--QARTLASRADTQAQALCAQCAEKFAVERPQAHRLFVLVDGRCFQLADDALPHCIKGYLLRSEPKR 879
Cdd:cd16131    2 QNYLRVAFQEVNSgcTAKTLLVRPYTTTEEVCQLCAQKFKVQDPENYSLFLLIDDTWQQLAEDTYPQKIKAELHSRPQPQ 81

                 ....*..
gi 987437828 880 DFHFVYR 886
Cdd:cd16131   82 IFHFVYK 88
PHA03247 PHA03247
large tegument protein UL36; Provisional
165-450 5.66e-10

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 63.80  E-value: 5.66e-10
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  165 IEDCSSALPTDQPPLgnCPARPLPPTSDATSPTSRWAPRRPPPPPPVLPLQPCSPAQPPVLPALAPAPACPLPTSPPVPA 244
Cdd:PHA03247 2540 LEELASDDAGDPPPP--LPPAAPPAAPDRSVPPPRPAPRPSEPAVTSRARRPDAPPQSARPRAPVDDRGDPRGPAPPSPL 2617
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  245 PHvTPHAPGPPDhPNQPPMMTCERLPCPTAGLGPLREEAMKPGAASSPLQQVPAPPLPAKKNLPTAPPRRRVSErvsled 324
Cdd:PHA03247 2618 PP-DTHAPDPPP-PSPSPAANEPDPHPPPTVPPPERPRDDPAPGRVSRPRRARRLGRAAQASSPPQRPRRRAAR------ 2689
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  325 qsPGMAAEGDQLSLPPQGTSdgPEDTPRESTEQGQDTEVKASDPHSMPELPRTAkqppvppprkkrISRQLASTLPAPLE 404
Cdd:PHA03247 2690 --PTVGSLTSLADPPPPPPT--PEPAPHALVSATPLPPGPAAARQASPALPAAP------------APPAVPAGPATPGG 2753
                         250       260       270       280
                  ....*....|....*....|....*....|....*....|....*.
gi 987437828  405 NAELCTQAMALETPTPGPPREGQSPASQAGTQHPPAQATAHSQSSP 450
Cdd:PHA03247 2754 PARPARPPTTAGPPAPAPPAAPAAGPPRRLTRPAVASLSESRESLP 2799
PHA03247 PHA03247
large tegument protein UL36; Provisional
107-496 3.86e-09

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 61.11  E-value: 3.86e-09
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  107 SSLNPPQERGKPAEPPRDRAPGFPL--VSSLRPTAHDANCACEIELSVGNDRLWFVNPIfiedcssalPTDQPPLGNCPA 184
Cdd:PHA03247 2697 SLADPPPPPPTPEPAPHALVSATPLppGPAAARQASPALPAAPAPPAVPAGPATPGGPA---------RPARPPTTAGPP 2767
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  185 RPLPPTSDATSPTSRWAPRRPPPPPPVLPLQPCSPAQPPVLPALAPAPACPLPTSPPV----PAPHVTPHAPGPPDHPNQ 260
Cdd:PHA03247 2768 APAPPAAPAAGPPRRLTRPAVASLSESRESLPSPWDPADPPAAVLAPAAALPPAASPAgplpPPTSAQPTAPPPPPGPPP 2847
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  261 PPMMTCERLpcptAGLGPLREEAmkpgaassplqqvPAPPLPAKKNLPTAPPRRRVSErvsledqsPGMAAEGDQLSLPP 340
Cdd:PHA03247 2848 PSLPLGGSV----APGGDVRRRP-------------PSRSPAAKPAAPARPPVRRLAR--------PAVSRSTESFALPP 2902
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  341 qgtsDGPEDTPR-ESTEQGQDTEVKASDPHSMPELPRTAK-QPPVPPPRKKRISRQLASTLPAPLENAELCTQAMA--LE 416
Cdd:PHA03247 2903 ----DQPERPPQpQAPPPPQPQPQPPPPPQPQPPPPPPPRpQPPLAPTTDPAGAGEPSGAVPQPWLGALVPGRVAVprFR 2978
                         330       340       350       360       370       380       390       400
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  417 TPTPGPPREGQSPASQAGTQHPPAQATAHSQS---SPEFKGSLASLSDSLGVSvmATDQDSYSTSSTEEELEQFSSPSVK 493
Cdd:PHA03247 2979 VPQPAPSREAPASSTPPLTGHSLSRVSSWASSlalHEETDPPPVSLKQTLWPP--DDTEDSDADSLFDSDSERSDLEALD 3056

                  ...
gi 987437828  494 KKP 496
Cdd:PHA03247 3057 PLP 3059
PHA03247 PHA03247
large tegument protein UL36; Provisional
111-454 1.21e-07

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 56.10  E-value: 1.21e-07
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  111 PPQERGKPAEPPRDRAPGFPLVSSLRPTAHDANCACEIELSVGNDRLWFVNPIFIEDCSSALPTDQPPLGNCPA-RPLPP 189
Cdd:PHA03247 2607 DPRGPAPPSPLPPDTHAPDPPPPSPSPAANEPDPHPPPTVPPPERPRDDPAPGRVSRPRRARRLGRAAQASSPPqRPRRR 2686
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  190 TS-DATSPTSRWAPRRPPPPPPVLPLQPCSPAQPPVLPALAPAPACPLPT-SPPVPAPHVTPHAPGPPDHPNQPPMMTCE 267
Cdd:PHA03247 2687 AArPTVGSLTSLADPPPPPPTPEPAPHALVSATPLPPGPAAARQASPALPaAPAPPAVPAGPATPGGPARPARPPTTAGP 2766
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  268 RLPCPTAGLGPLREEAMKPGAASSPLQQVPAPPLPAKKNLPTAPPRRRVSERVSLEDQSPGMAAEGDQLSLPPQGTSDGP 347
Cdd:PHA03247 2767 PAPAPPAAPAAGPPRRLTRPAVASLSESRESLPSPWDPADPPAAVLAPAAALPPAASPAGPLPPPTSAQPTAPPPPPGPP 2846
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  348 ED--TPRESTEQGQDTEVKASdPHSMPELPRTAKQPPVPPPRKKRISRQLASTLPAPLENAELCT---QAMALETPTPGP 422
Cdd:PHA03247 2847 PPslPLGGSVAPGGDVRRRPP-SRSPAAKPAAPARPPVRRLARPAVSRSTESFALPPDQPERPPQpqaPPPPQPQPQPPP 2925
                         330       340       350
                  ....*....|....*....|....*....|..
gi 987437828  423 PREGQSPASQAGTQHPPAQATAHSQSSPEFKG 454
Cdd:PHA03247 2926 PPQPQPPPPPPPRPQPPLAPTTDPAGAGEPSG 2957
PHA03247 PHA03247
large tegument protein UL36; Provisional
106-450 2.45e-07

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 54.94  E-value: 2.45e-07
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  106 DSSLNPPQERGKPAEPP---RDRAPGFPlVSSLRPTAHdancaceielsvGNDRLWFVNPIfiedCSSALPTDQPPLgnc 182
Cdd:PHA03247 2565 DRSVPPPRPAPRPSEPAvtsRARRPDAP-PQSARPRAP------------VDDRGDPRGPA----PPSPLPPDTHAP--- 2624
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  183 parPLPPTSDATSPTSRWAPRRPPPPPPVLPLQPCSPAQPPVLPALAPAPACPLPTSPPV-PAPHVTPHAPGP----PDH 257
Cdd:PHA03247 2625 ---DPPPPSPSPAANEPDPHPPPTVPPPERPRDDPAPGRVSRPRRARRLGRAAQASSPPQrPRRRAARPTVGSltslADP 2701
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  258 PNQPPmmTCERLPCPTAGLGPLREEAMKPGAASSPLQQVPAPPLPAKKNLPTAPPRRRVSERVSLEDQSPGmaaegdqls 337
Cdd:PHA03247 2702 PPPPP--TPEPAPHALVSATPLPPGPAAARQASPALPAAPAPPAVPAGPATPGGPARPARPPTTAGPPAPA--------- 2770
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  338 lPPQGTSDGPedtPRESTEQGQDTEVKASDPHSMPELPRTAKQPPVPPPRKKRISRQLASTLPAPlenaelCTQAMALET 417
Cdd:PHA03247 2771 -PPAAPAAGP---PRRLTRPAVASLSESRESLPSPWDPADPPAAVLAPAAALPPAASPAGPLPPP------TSAQPTAPP 2840
                         330       340       350       360       370
                  ....*....|....*....|....*....|....*....|....*....|...
gi 987437828  418 PTPGPPRE--------------------GQSPASQAGTQHPPAQATAHSQSSP 450
Cdd:PHA03247 2841 PPPGPPPPslplggsvapggdvrrrppsRSPAAKPAAPARPPVRRLARPAVSR 2893
RA_Rin1 cd17215
Ras-associating (RA) domain found in Ras and Rab interactor 1 (Rin1); Rin1, also termed Ras ...
802-889 3.70e-07

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: 48.82  E-value: 3.70e-07
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 802 QDFICVSYLEPEQ--QARTLASRADTQAQALCAQCAEKFAVERPQAHRLFVLVDGRCFQLADDALPHCIKGYLlrSEPKR 879
Cdd:cd17215    1 QNFLRVAYQDPSSgcTSKTLAVPPSATVADLNQLCATKFKVTQPETYGIFLYKEQGYQRLPPDALPQRIKAQL--KEKGS 78
                         90
                 ....*....|
gi 987437828 880 DFHFVYRPLD 889
Cdd:cd17215   79 TFYFVYQRAE 88
PHA03247 PHA03247
large tegument protein UL36; Provisional
183-377 1.03e-04

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 46.47  E-value: 1.03e-04
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  183 PARPlPPTSDATSPTSRWAPRRPPPPPPVLPLQPCSPAQPPVLPALAPAPACPLPTSPPVPA-PHVTPHAPGPPDHPNQP 261
Cdd:PHA03247 2867 PSRS-PAAKPAAPARPPVRRLARPAVSRSTESFALPPDQPERPPQPQAPPPPQPQPQPPPPPqPQPPPPPPPRPQPPLAP 2945
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  262 PMMTcERLPCPTAGLGPLREEAMKPGAASSPLQQVP--APPLPAKKNlPTAPPRRRVSERVSLEDQSPGMAAEGD----- 334
Cdd:PHA03247 2946 TTDP-AGAGEPSGAVPQPWLGALVPGRVAVPRFRVPqpAPSREAPAS-STPPLTGHSLSRVSSWASSLALHEETDpppvs 3023
                         170       180       190       200       210
                  ....*....|....*....|....*....|....*....|....*....|.
gi 987437828  335 --QLSLPPQGTSDGPEDTPRESTEQGQDTEV------KASDPHSMPELPRT 377
Cdd:PHA03247 3024 lkQTLWPPDDTEDSDADSLFDSDSERSDLEAldplppEPHDPFAHEPDPAT 3074
PRK12323 PRK12323
DNA polymerase III subunit gamma/tau;
218-442 1.71e-04

DNA polymerase III subunit gamma/tau;


Pssm-ID: 237057 [Multi-domain]  Cd Length: 700  Bit Score: 45.25  E-value: 1.71e-04
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 218 SPAQPPVLPALAPAPACPLPTSPPVPAPHVTPHAPGPPDHPNQPPMMTCERLPCPTAGLGPLREEAMKPGAASSPLQQVP 297
Cdd:PRK12323 376 TAAAAPVAQPAPAAAAPAAAAPAPAAPPAAPAAAPAAAAAARAVAAAPARRSPAPEALAAARQASARGPGGAPAPAPAPA 455
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 298 APPLPAKKNLPTAPPRRRVSERVSLEDQSPGMAAEGDQLSLPPQgtsdgpEDTPRESTEQGQDTEVKASDPHSMPELPRT 377
Cdd:PRK12323 456 AAPAAAARPAAAGPRPVAAAAAAAPARAAPAAAPAPADDDPPPW------EELPPEFASPAPAQPDAAPAGWVAESIPDP 529
                        170       180       190       200       210       220
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*
gi 987437828 378 AKQPPVPPPRKKRISRQLASTLPAPLENAELctqamaletPTPGPPREGQSPASQAGTQHPPAQA 442
Cdd:PRK12323 530 ATADPDDAFETLAPAPAAAPAPRAAAATEPV---------VAPRPPRASASGLPDMFDGDWPALA 585
Atrophin-1 pfam03154
Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian ...
176-492 3.32e-04

Atrophin-1 family; Atrophin-1 is the protein product of the dentatorubral-pallidoluysian atrophy (DRPLA) gene. DRPLA OMIM:125370 is a progressive neurodegenerative disorder. It is caused by the expansion of a CAG repeat in the DRPLA gene on chromosome 12p. This results in an extended polyglutamine region in atrophin-1, that is thought to confer toxicity to the protein, possibly through altering its interactions with other proteins. The expansion of a CAG repeat is also the underlying defect in six other neurodegenerative disorders, including Huntington's disease. One interaction of expanded polyglutamine repeats that is thought to be pathogenic is that with the short glutamine repeat in the transcriptional coactivator CREB binding protein, CBP. This interaction draws CBP away from its usual nuclear location to the expanded polyglutamine repeat protein aggregates that are characteriztic of the polyglutamine neurodegenerative disorders. This interferes with CBP-mediated transcription and causes cytotoxicity.


Pssm-ID: 460830 [Multi-domain]  Cd Length: 991  Bit Score: 44.76  E-value: 3.32e-04
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  176 QPPLGNCPARPLPPTSDATSPTSRWAPRRPPPPPPVLplqpcsPAQPpvlpalapapacplptSPPVPAPHVTPHAPGPP 255
Cdd:pfam03154 170 QPPVLQAQSGAASPPSPPPPGTTQAATAGPTPSAPSV------PPQG----------------SPATSQPPNQTQSTAAP 227
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  256 DH-PNQPPMMTCERLPCPTAGLGPLREEAMKPGAASSPLQQV----PAPPLPakKNLPTAPPR------RRVSERVSLED 324
Cdd:pfam03154 228 HTlIQQTPTLHPQRLPSPHPPLQPMTQPPPPSQVSPQPLPQPslhgQMPPMP--HSLQTGPSHmqhpvpPQPFPLTPQSS 305
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  325 QSPGMAAEGDQLSLPPQGTSDGPEDTPRESTEQGQDTEVKASDPHSMPEL---PRTAKQPPVPPPRKKRISR-------Q 394
Cdd:pfam03154 306 QSQVPPGPSPAAPGQSQQRIHTPPSQSQLQSQQPPREQPLPPAPLSMPHIkppPTTPIPQLPNPQSHKHPPHlsgpspfQ 385
                         250       260       270       280       290       300       310       320
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  395 LASTLPAP--------LEN----------AELCTQAMALETPTPGPPREGQSPA-SQAGTQHPPAQATAHSQSSPEFKGS 455
Cdd:pfam03154 386 MNSNLPPPpalkplssLSThhppsahpppLQLMPQSQQLPPPPAQPPVLTQSQSlPPPAASHPPTSGLHQVPSQSPFPQH 465
                         330       340       350
                  ....*....|....*....|....*....|....*..
gi 987437828  456 LASLSDSLGVSVMATDQDSYSTSSTEEELEQFSSPSV 492
Cdd:pfam03154 466 PFVPGGPPPITPPSGPPTSTSSAMPGIQPPSSASVSS 502
PHA03307 PHA03307
transcriptional regulator ICP4; Provisional
168-470 8.97e-04

transcriptional regulator ICP4; Provisional


Pssm-ID: 223039 [Multi-domain]  Cd Length: 1352  Bit Score: 43.24  E-value: 8.97e-04
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  168 CSSALPTDQPPLGNCPARPLPPTSDATSPTSRWAPrrppppppvlplqpcsPAQPPVLPALAPAPACPLPTSPPVPAPHV 247
Cdd:PHA03307   62 CDRFEPPTGPPPGPGTEAPANESRSTPTWSLSTLA----------------PASPAREGSPTPPGPSSPDPPPPTPPPAS 125
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  248 TPHAPGPPDHPNQPPMMT-----CERLPCPTAGLGPLREEAMKPGAASSPLQQVPA---PPLPAKKNLPTAPPRRRVSER 319
Cdd:PHA03307  126 PPPSPAPDLSEMLRPVGSpgpppAASPPAAGASPAAVASDAASSRQAALPLSSPEEtarAPSSPPAEPPPSTPPAAASPR 205
                         170       180       190       200       210       220       230       240
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  320 VSLEDqSPGMAAEGDQLSLPPQGTSDGPE-----DTPRESTEQGQDTEVKASDPH-SMPELPRTAKQPPVPPPRKKRISR 393
Cdd:PHA03307  206 PPRRS-SPISASASSPAPAPGRSAADDAGasssdSSSSESSGCGWGPENECPLPRpAPITLPTRIWEASGWNGPSSRPGP 284
                         250       260       270       280       290       300       310
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*..
gi 987437828  394 QLASTLPAPlenaelctqamalETPTPGPPREGQSPASqagtqhPPAQATAHSQSSPEfKGSLASLSDSLGVSVMAT 470
Cdd:PHA03307  285 ASSSSSPRE-------------RSPSPSPSSPGSGPAP------SSPRASSSSSSSRE-SSSSSTSSSSESSRGAAV 341
PRK12323 PRK12323
DNA polymerase III subunit gamma/tau;
169-375 1.27e-03

DNA polymerase III subunit gamma/tau;


Pssm-ID: 237057 [Multi-domain]  Cd Length: 700  Bit Score: 42.56  E-value: 1.27e-03
                         10        20        30        40        50        60        70        80
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 169 SSALPTDQPPLGNCPARPLPPTSDATSPTSRWAPRRPPPPPPVLPLQPCS-PAQPPVLPALAPAPACPLPTSPPVPAPHV 247
Cdd:PRK12323 383 AQPAPAAAAPAAAAPAPAAPPAAPAAAPAAAAAARAVAAAPARRSPAPEAlAAARQASARGPGGAPAPAPAPAAAPAAAA 462
                         90       100       110       120       130       140       150       160
                 ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828 248 TPHAPGPPDHPN----QPPMMTCERLPCPTAGLGPLREEAMKPGAASSPLQQVPAPPLPAKKNLPTAPPRRRVSERVSLE 323
Cdd:PRK12323 463 RPAAAGPRPVAAaaaaAPARAAPAAAPAPADDDPPPWEELPPEFASPAPAQPDAAPAGWVAESIPDPATADPDDAFETLA 542
                        170       180       190       200       210
                 ....*....|....*....|....*....|....*....|....*....|..
gi 987437828 324 DQSPGMAAEGDQLSLPPQgtsdgPEDTPRESTEQGQDTEVKASDPHSMPELP 375
Cdd:PRK12323 543 PAPAAAPAPRAAAATEPV-----VAPRPPRASASGLPDMFDGDWPALAARLP 589
PHA03247 PHA03247
large tegument protein UL36; Provisional
241-451 7.88e-03

large tegument protein UL36; Provisional


Pssm-ID: 223021 [Multi-domain]  Cd Length: 3151  Bit Score: 40.31  E-value: 7.88e-03
                          10        20        30        40        50        60        70        80
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  241 PVPAPHVTPHAPGPPdhpnQPPMMTCERLPCPTAGlGPLREEAMKPGAASSPLQQVPaPPLPAKKNLPTAPPRRRVSErv 320
Cdd:PHA03247  255 PAPPPVVGEGADRAP----ETARGATGPPPPPEAA-APNGAAAPPDGVWGAALAGAP-LALPAPPDPPPPAPAGDAEE-- 326
                          90       100       110       120       130       140       150       160
                  ....*....|....*....|....*....|....*....|....*....|....*....|....*....|....*....|
gi 987437828  321 slEDQSPGMAAEGDQLSLPPQGTSDG------PEDTPRESTEQ---GQDTEVKASDPHSMPELPRTAKQ---PPVPPPRK 388
Cdd:PHA03247  327 --EDDEDGAMEVVSPLPRPRQHYPLGfpkrrrPTWTPPSSLEDlsaGRHHPKRASLPTRKRRSARHAATpfaRGPGGDDQ 404
                         170       180       190       200       210       220
                  ....*....|....*....|....*....|....*....|....*....|....*....|....
gi 987437828  389 KRISRQLASTLPAPLENAELCTQAMALETPTPGP-PREGQSPASQAGTQhPPAQATAHSQSSPE 451
Cdd:PHA03247  405 TRPAAPVPASVPTPAPTPVPASAPPPPATPLPSAePGSDDGPAPPPERQ-PPAPATEPAPDDPD 467
 
Blast search parameters
Data Source: Precalculated data, version = cdd.v.3.21
Preset Options:Database: CDSEARCH/cdd   Low complexity filter: no  Composition Based Adjustment: yes   E-value threshold: 0.01

References:

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