Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S7X0L2
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 11 |
GO:0004518 | nuclease activity | 4 | 1 |
GO:0004527 | exonuclease activity | 5 | 1 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 225 | 229 | PF00656 | 0.382 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.254 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.223 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.237 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.254 |
CLV_PCSK_KEX2_1 | 328 | 330 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.237 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.237 |
CLV_PCSK_PC1ET2_1 | 315 | 317 | PF00082 | 0.279 |
CLV_PCSK_PC1ET2_1 | 374 | 376 | PF00082 | 0.263 |
CLV_PCSK_PC7_1 | 74 | 80 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 285 | 289 | PF00082 | 0.223 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 374 | 378 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.281 |
DEG_APCC_DBOX_1 | 77 | 85 | PF00400 | 0.481 |
DOC_CKS1_1 | 7 | 12 | PF01111 | 0.520 |
DOC_CYCLIN_yCln2_LP_2 | 187 | 193 | PF00134 | 0.437 |
DOC_MAPK_gen_1 | 78 | 86 | PF00069 | 0.517 |
DOC_MAPK_MEF2A_6 | 147 | 155 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 24 | 31 | PF00149 | 0.257 |
DOC_PP1_RVXF_1 | 283 | 289 | PF00149 | 0.463 |
DOC_PP2B_LxvP_1 | 187 | 190 | PF13499 | 0.437 |
DOC_PP4_FxxP_1 | 94 | 97 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.519 |
DOC_WW_Pin1_4 | 349 | 354 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 79 | 85 | PF00244 | 0.480 |
LIG_APCC_ABBA_1 | 114 | 119 | PF00400 | 0.458 |
LIG_eIF4E_1 | 75 | 81 | PF01652 | 0.481 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.318 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.563 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.423 |
LIG_FHA_2 | 246 | 252 | PF00498 | 0.531 |
LIG_FHA_2 | 349 | 355 | PF00498 | 0.484 |
LIG_LIR_Apic_2 | 93 | 97 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 161 | 169 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 208 | 218 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 291 | 302 | PF02991 | 0.437 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 208 | 213 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 22 | 28 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 291 | 297 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 37 | 43 | PF02991 | 0.500 |
LIG_PDZ_Class_2 | 374 | 379 | PF00595 | 0.454 |
LIG_SH2_GRB2like | 370 | 373 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 162 | 166 | PF00017 | 0.445 |
LIG_SH2_PTP2 | 42 | 45 | PF00017 | 0.382 |
LIG_SH2_SRC | 162 | 165 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 162 | 166 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 302 | 305 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 342 | 345 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.427 |
LIG_SH3_3 | 110 | 116 | PF00018 | 0.509 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.478 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.486 |
LIG_SUMO_SIM_par_1 | 139 | 146 | PF11976 | 0.438 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.436 |
LIG_TRAF2_1 | 248 | 251 | PF00917 | 0.443 |
LIG_TYR_ITIM | 160 | 165 | PF00017 | 0.429 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.454 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.517 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.445 |
MOD_CK2_1 | 245 | 251 | PF00069 | 0.457 |
MOD_CK2_1 | 348 | 354 | PF00069 | 0.469 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.297 |
MOD_GlcNHglycan | 228 | 232 | PF01048 | 0.199 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.229 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.303 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.429 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.329 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.459 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.527 |
MOD_N-GLC_1 | 18 | 23 | PF02516 | 0.296 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.237 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.129 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.468 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.387 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.465 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.423 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.471 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.448 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.517 |
MOD_Plk_1 | 361 | 367 | PF00069 | 0.536 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.517 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.496 |
MOD_ProDKin_1 | 349 | 355 | PF00069 | 0.512 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.527 |
TRG_DiLeu_BaEn_1 | 251 | 256 | PF01217 | 0.437 |
TRG_DiLeu_BaEn_1 | 331 | 336 | PF01217 | 0.479 |
TRG_DiLeu_BaLyEn_6 | 76 | 81 | PF01217 | 0.537 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 261 | 264 | PF00928 | 0.449 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.382 |
TRG_ER_diArg_1 | 73 | 75 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 78 | 80 | PF00400 | 0.437 |
TRG_NLS_MonoCore_2 | 314 | 319 | PF00514 | 0.503 |
TRG_NLS_MonoExtC_3 | 314 | 319 | PF00514 | 0.517 |
TRG_NLS_MonoExtN_4 | 312 | 319 | PF00514 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 96 | 101 | PF00026 | 0.245 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3Q2 | Leptomonas seymouri | 30% | 100% |
A0A0N1IL51 | Leptomonas seymouri | 69% | 100% |
A0A0S4IY84 | Bodo saltans | 31% | 100% |
A0A0S4JNN8 | Bodo saltans | 49% | 100% |
A0A1X0NWJ2 | Trypanosomatidae | 29% | 100% |
A0A1X0P426 | Trypanosomatidae | 48% | 97% |
A0A3R7K0P4 | Trypanosoma rangeli | 51% | 100% |
A0A3R7LLG2 | Trypanosoma rangeli | 31% | 100% |
A0A3S5H6J9 | Leishmania donovani | 30% | 96% |
A4H6P9 | Leishmania braziliensis | 30% | 87% |
A4HFM3 | Leishmania braziliensis | 83% | 100% |
A4HV34 | Leishmania infantum | 30% | 96% |
A4I2Q1 | Leishmania infantum | 100% | 100% |
A4WFX9 | Enterobacter sp. (strain 638) | 27% | 100% |
A7MQN1 | Cronobacter sakazakii (strain ATCC BAA-894) | 28% | 100% |
A8ACY8 | Citrobacter koseri (strain ATCC BAA-895 / CDC 4225-83 / SGSC4696) | 28% | 100% |
A8G8C4 | Serratia proteamaculans (strain 568) | 28% | 100% |
B1JP69 | Yersinia pseudotuberculosis serotype O:3 (strain YPIII) | 26% | 100% |
B2VG45 | Erwinia tasmaniensis (strain DSM 17950 / CFBP 7177 / CIP 109463 / NCPPB 4357 / Et1/99) | 27% | 100% |
B7LTZ5 | Escherichia fergusonii (strain ATCC 35469 / DSM 13698 / CCUG 18766 / IAM 14443 / JCM 21226 / LMG 7866 / NBRC 102419 / NCTC 12128 / CDC 0568-73) | 26% | 100% |
B7XJI2 | Enterocytozoon bieneusi (strain H348) | 21% | 100% |
C6DI71 | Pectobacterium carotovorum subsp. carotovorum (strain PC1) | 27% | 100% |
C9XTA5 | Cronobacter turicensis (strain DSM 18703 / CCUG 55852 / LMG 23827 / z3032) | 29% | 100% |
D0A5V3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 99% |
D0A7B6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
D0KC77 | Pectobacterium parmentieri (strain WPP163) | 28% | 100% |
D0Z9R0 | Edwardsiella tarda (strain EIB202) | 28% | 100% |
D2TUZ4 | Citrobacter rodentium (strain ICC168) | 26% | 100% |
D4GGR2 | Pantoea ananatis (strain LMG 20103) | 26% | 100% |
D4ICL5 | Erwinia amylovora (strain ATCC 49946 / CCPPB 0273 / Ea273 / 27-3) | 27% | 100% |
D8MKW4 | Erwinia billingiae (strain Eb661) | 28% | 100% |
E0SLH6 | Dickeya dadantii (strain 3937) | 26% | 100% |
E1SKR8 | Pantoea vagans (strain C9-1) | 26% | 100% |
E3G381 | Enterobacter lignolyticus (strain SCF1) | 26% | 100% |
E6WHK1 | Pantoea sp. (strain At-9b) | 27% | 100% |
E8XYF5 | Rahnella sp. (strain Y9602) | 27% | 100% |
E9AD77 | Leishmania major | 96% | 100% |
E9ANR5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 97% |
E9AZ01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
P27859 | Escherichia coli (strain K12) | 27% | 100% |
P34220 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 91% |
P37545 | Bacillus subtilis (strain 168) | 23% | 100% |
P44718 | Haemophilus influenzae (strain ATCC 51907 / DSM 11121 / KW20 / Rd) | 23% | 100% |
P57436 | Buchnera aphidicola subsp. Acyrthosiphon pisum (strain APS) | 22% | 100% |
Q0SZ31 | Shigella flexneri serotype 5b (strain 8401) | 27% | 100% |
Q148G4 | Bos taurus | 32% | 100% |
Q4QGV4 | Leishmania major | 29% | 100% |
Q640V9 | Xenopus laevis | 33% | 100% |
Q6DAQ1 | Pectobacterium atrosepticum (strain SCRI 1043 / ATCC BAA-672) | 26% | 100% |
Q6GML7 | Danio rerio | 31% | 100% |
Q6P1N9 | Homo sapiens | 33% | 100% |
Q6P8M1 | Mus musculus | 33% | 100% |
Q9L6M2 | Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) | 26% | 100% |
Q9UUF1 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
V5BRW2 | Trypanosoma cruzi | 31% | 100% |