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: 10 |
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 | yes | yes: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HFF2
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004518 | nuclease activity | 4 | 9 |
GO:0004519 | endonuclease activity | 5 | 9 |
GO:0004521 | RNA endonuclease activity | 5 | 9 |
GO:0004525 | ribonuclease III activity | 6 | 9 |
GO:0004540 | RNA nuclease activity | 4 | 9 |
GO:0016787 | hydrolase activity | 2 | 9 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 9 |
GO:0016891 | RNA endonuclease activity, producing 5'-phosphomonoesters | 6 | 9 |
GO:0016893 | endonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 9 |
GO:0032296 | double-stranded RNA-specific ribonuclease activity | 5 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.681 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.596 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.404 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.576 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.456 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 92 | 94 | PF00082 | 0.374 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 92 | 94 | PF00082 | 0.374 |
CLV_PCSK_PC7_1 | 213 | 219 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.486 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.429 |
DEG_APCC_DBOX_1 | 168 | 176 | PF00400 | 0.492 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.557 |
DEG_SCF_FBW7_1 | 57 | 63 | PF00400 | 0.515 |
DOC_CKS1_1 | 57 | 62 | PF01111 | 0.479 |
DOC_CYCLIN_RxL_1 | 71 | 80 | PF00134 | 0.569 |
DOC_MAPK_gen_1 | 115 | 126 | PF00069 | 0.441 |
DOC_MAPK_gen_1 | 128 | 134 | PF00069 | 0.407 |
DOC_MAPK_gen_1 | 71 | 79 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 119 | 126 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 61 | 70 | PF00069 | 0.522 |
DOC_MAPK_NFAT4_5 | 119 | 127 | PF00069 | 0.510 |
DOC_MAPK_NFAT4_5 | 61 | 69 | PF00069 | 0.403 |
DOC_MAPK_RevD_3 | 77 | 93 | PF00069 | 0.353 |
DOC_PP2B_LxvP_1 | 257 | 260 | PF13499 | 0.498 |
DOC_PP4_FxxP_1 | 365 | 368 | PF00568 | 0.662 |
DOC_PP4_FxxP_1 | 375 | 378 | PF00568 | 0.657 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.751 |
DOC_USP7_UBL2_3 | 337 | 341 | PF12436 | 0.548 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.691 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 225 | 235 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 313 | 319 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 348 | 354 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 398 | 402 | PF00244 | 0.686 |
LIG_14-3-3_CanoR_1 | 56 | 60 | PF00244 | 0.659 |
LIG_14-3-3_CanoR_1 | 61 | 67 | PF00244 | 0.566 |
LIG_14-3-3_CanoR_1 | 71 | 75 | PF00244 | 0.463 |
LIG_CaM_IQ_9 | 336 | 352 | PF13499 | 0.477 |
LIG_EH1_1 | 203 | 211 | PF00400 | 0.567 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.429 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.519 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.677 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.483 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.457 |
LIG_FHA_2 | 329 | 335 | PF00498 | 0.646 |
LIG_FHA_2 | 37 | 43 | PF00498 | 0.709 |
LIG_FHA_2 | 406 | 412 | PF00498 | 0.650 |
LIG_LIR_Apic_2 | 364 | 368 | PF02991 | 0.664 |
LIG_LIR_Gen_1 | 150 | 159 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 280 | 291 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 150 | 156 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.363 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.554 |
LIG_NRBOX | 133 | 139 | PF00104 | 0.364 |
LIG_NRBOX | 73 | 79 | PF00104 | 0.513 |
LIG_PCNA_yPIPBox_3 | 128 | 138 | PF02747 | 0.383 |
LIG_PCNA_yPIPBox_3 | 355 | 366 | PF02747 | 0.491 |
LIG_SH2_CRK | 130 | 134 | PF00017 | 0.496 |
LIG_SH2_CRK | 380 | 384 | PF00017 | 0.660 |
LIG_SH2_NCK_1 | 283 | 287 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 181 | 185 | PF00017 | 0.563 |
LIG_SH2_STAT3 | 204 | 207 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 184 | 187 | PF00017 | 0.514 |
LIG_SH3_1 | 174 | 180 | PF00018 | 0.509 |
LIG_SH3_3 | 174 | 180 | PF00018 | 0.509 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.364 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.448 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.452 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.626 |
LIG_SH3_3 | 54 | 60 | PF00018 | 0.503 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.480 |
LIG_SUMO_SIM_anti_2 | 261 | 267 | PF11976 | 0.531 |
LIG_SUMO_SIM_par_1 | 14 | 19 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 326 | 332 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 62 | 67 | PF11976 | 0.656 |
LIG_TYR_ITIM | 281 | 286 | PF00017 | 0.381 |
LIG_WRC_WIRS_1 | 362 | 367 | PF05994 | 0.678 |
MOD_CDK_SPK_2 | 308 | 313 | PF00069 | 0.691 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.493 |
MOD_CDK_SPxxK_3 | 218 | 225 | PF00069 | 0.668 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.546 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.556 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.610 |
MOD_CK1_1 | 316 | 322 | PF00069 | 0.601 |
MOD_CK1_1 | 36 | 42 | PF00069 | 0.687 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.466 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.611 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.625 |
MOD_DYRK1A_RPxSP_1 | 218 | 222 | PF00069 | 0.698 |
MOD_DYRK1A_RPxSP_1 | 56 | 60 | PF00069 | 0.495 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.704 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.632 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.687 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.568 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.485 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.449 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.484 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.623 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.613 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.671 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.591 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.487 |
MOD_N-GLC_1 | 147 | 152 | PF02516 | 0.439 |
MOD_N-GLC_1 | 99 | 104 | PF02516 | 0.551 |
MOD_N-GLC_2 | 359 | 361 | PF02516 | 0.672 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.485 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.415 |
MOD_NEK2_1 | 16 | 21 | PF00069 | 0.640 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.543 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.571 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.538 |
MOD_PIKK_1 | 303 | 309 | PF00454 | 0.610 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.615 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.622 |
MOD_PKA_1 | 115 | 121 | PF00069 | 0.520 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.460 |
MOD_PKA_2 | 216 | 222 | PF00069 | 0.603 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.583 |
MOD_PKA_2 | 397 | 403 | PF00069 | 0.670 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.660 |
MOD_PKA_2 | 70 | 76 | PF00069 | 0.461 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.725 |
MOD_Plk_1 | 396 | 402 | PF00069 | 0.685 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.548 |
MOD_Plk_4 | 159 | 165 | PF00069 | 0.415 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.661 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.639 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.687 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.484 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.471 |
MOD_SUMO_rev_2 | 287 | 296 | PF00179 | 0.527 |
TRG_DiLeu_BaEn_1 | 334 | 339 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 12 | 17 | PF01217 | 0.481 |
TRG_DiLeu_BaLyEn_6 | 168 | 173 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 130 | 133 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 283 | 286 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 372 | 375 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 380 | 383 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.427 |
TRG_ER_diArg_1 | 101 | 104 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 115 | 117 | PF00400 | 0.328 |
TRG_ER_diArg_1 | 119 | 122 | PF00400 | 0.284 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 168 | 171 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.615 |
TRG_NES_CRM1_1 | 287 | 300 | PF08389 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 75 | 80 | PF00026 | 0.570 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6V9 | Leptomonas seymouri | 57% | 99% |
A0A1X0P3V7 | Trypanosomatidae | 51% | 100% |
A0A3Q8ID52 | Leishmania donovani | 89% | 100% |
A0A3R7MNH0 | Trypanosoma rangeli | 51% | 100% |
A4I2M1 | Leishmania infantum | 89% | 100% |
D0A5N3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9AD11 | Leishmania major | 89% | 100% |
E9AYT6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |