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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A0A3Q8IFN9
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006364 | rRNA processing | 8 | 8 |
GO:0006396 | RNA processing | 6 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0016072 | rRNA metabolic process | 7 | 8 |
GO:0034470 | ncRNA processing | 7 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0034660 | ncRNA metabolic process | 6 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0000154 | rRNA modification | 6 | 1 |
GO:0000455 | enzyme-directed rRNA pseudouridine synthesis | 8 | 1 |
GO:0031118 | rRNA pseudouridine synthesis | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003723 | RNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0005488 | binding | 1 | 10 |
GO:0009982 | pseudouridine synthase activity | 4 | 10 |
GO:0016853 | isomerase activity | 2 | 10 |
GO:0016866 | intramolecular transferase activity | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0106029 | tRNA pseudouridine synthase activity | 5 | 1 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 1 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.648 |
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.570 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.215 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.489 |
CLV_PCSK_FUR_1 | 436 | 440 | PF00082 | 0.551 |
CLV_PCSK_FUR_1 | 9 | 13 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 467 | 471 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.494 |
CLV_Separin_Metazoa | 113 | 117 | PF03568 | 0.415 |
CLV_Separin_Metazoa | 279 | 283 | PF03568 | 0.485 |
DEG_SCF_FBW7_2 | 417 | 422 | PF00400 | 0.440 |
DOC_CYCLIN_RxL_1 | 462 | 473 | PF00134 | 0.471 |
DOC_MAPK_gen_1 | 223 | 233 | PF00069 | 0.369 |
DOC_MAPK_gen_1 | 264 | 272 | PF00069 | 0.634 |
DOC_MAPK_MEF2A_6 | 438 | 447 | PF00069 | 0.552 |
DOC_PP1_RVXF_1 | 339 | 346 | PF00149 | 0.375 |
DOC_PP1_RVXF_1 | 472 | 478 | PF00149 | 0.435 |
DOC_PP4_FxxP_1 | 477 | 480 | PF00568 | 0.379 |
DOC_PP4_FxxP_1 | 65 | 68 | PF00568 | 0.409 |
DOC_PP4_FxxP_1 | 71 | 74 | PF00568 | 0.405 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.486 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 528 | 532 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.462 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.738 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.796 |
DOC_WW_Pin1_4 | 211 | 216 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 415 | 420 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.474 |
LIG_14-3-3_CanoR_1 | 129 | 133 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 474 | 478 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 486 | 491 | PF00244 | 0.441 |
LIG_AP2alpha_2 | 442 | 444 | PF02296 | 0.459 |
LIG_BIR_III_4 | 166 | 170 | PF00653 | 0.639 |
LIG_BRCT_BRCA1_1 | 22 | 26 | PF00533 | 0.499 |
LIG_BRCT_BRCA1_1 | 273 | 277 | PF00533 | 0.570 |
LIG_BRCT_BRCA1_1 | 509 | 513 | PF00533 | 0.432 |
LIG_eIF4E_1 | 106 | 112 | PF01652 | 0.396 |
LIG_eIF4E_1 | 84 | 90 | PF01652 | 0.472 |
LIG_EVH1_1 | 352 | 356 | PF00568 | 0.435 |
LIG_EVH1_2 | 67 | 71 | PF00568 | 0.384 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.693 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.574 |
LIG_FHA_1 | 226 | 232 | PF00498 | 0.357 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.455 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.538 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.403 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.413 |
LIG_FHA_1 | 516 | 522 | PF00498 | 0.452 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.515 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.406 |
LIG_FHA_2 | 132 | 138 | PF00498 | 0.643 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.630 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.484 |
LIG_FHA_2 | 47 | 53 | PF00498 | 0.424 |
LIG_KLC1_Yacidic_2 | 430 | 435 | PF13176 | 0.514 |
LIG_LIR_Apic_2 | 4 | 10 | PF02991 | 0.455 |
LIG_LIR_Apic_2 | 476 | 480 | PF02991 | 0.322 |
LIG_LIR_Apic_2 | 70 | 74 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 23 | 30 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 274 | 285 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 291 | 300 | PF02991 | 0.481 |
LIG_LIR_Gen_1 | 303 | 312 | PF02991 | 0.355 |
LIG_LIR_Gen_1 | 411 | 419 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 274 | 280 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 291 | 295 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 303 | 309 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.530 |
LIG_LYPXL_yS_3 | 406 | 409 | PF13949 | 0.348 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.499 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.337 |
LIG_SH2_CRK | 7 | 11 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 414 | 418 | PF00017 | 0.337 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.432 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 292 | 295 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 433 | 436 | PF00017 | 0.467 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.475 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.525 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.507 |
LIG_SH3_3 | 440 | 446 | PF00018 | 0.548 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 110 | 116 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 227 | 235 | PF11976 | 0.351 |
LIG_SUMO_SIM_anti_2 | 85 | 93 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 214 | 220 | PF11976 | 0.398 |
LIG_SUMO_SIM_par_1 | 85 | 93 | PF11976 | 0.407 |
LIG_TYR_ITIM | 404 | 409 | PF00017 | 0.349 |
LIG_UBA3_1 | 18 | 25 | PF00899 | 0.486 |
LIG_WRC_WIRS_1 | 487 | 492 | PF05994 | 0.420 |
LIG_WW_3 | 66 | 70 | PF00397 | 0.471 |
MOD_CDC14_SPxK_1 | 178 | 181 | PF00782 | 0.635 |
MOD_CDC14_SPxK_1 | 483 | 486 | PF00782 | 0.493 |
MOD_CDK_SPxK_1 | 175 | 181 | PF00069 | 0.634 |
MOD_CDK_SPxK_1 | 415 | 421 | PF00069 | 0.513 |
MOD_CDK_SPxK_1 | 480 | 486 | PF00069 | 0.468 |
MOD_CDK_SPxxK_3 | 175 | 182 | PF00069 | 0.700 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.571 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.696 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.755 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.432 |
MOD_CK1_1 | 273 | 279 | PF00069 | 0.422 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.343 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.428 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.625 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.469 |
MOD_CK2_1 | 273 | 279 | PF00069 | 0.341 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.760 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.784 |
MOD_GlcNHglycan | 227 | 231 | PF01048 | 0.376 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.279 |
MOD_GlcNHglycan | 448 | 454 | PF01048 | 0.568 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.576 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.690 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.719 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.751 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.715 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.705 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.495 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.406 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.391 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.485 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.441 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.474 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.425 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.445 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.324 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.413 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.468 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.423 |
MOD_NEK2_2 | 153 | 158 | PF00069 | 0.545 |
MOD_PIKK_1 | 29 | 35 | PF00454 | 0.358 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.433 |
MOD_PIKK_1 | 511 | 517 | PF00454 | 0.358 |
MOD_PK_1 | 284 | 290 | PF00069 | 0.337 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.632 |
MOD_PKA_2 | 473 | 479 | PF00069 | 0.326 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.431 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.481 |
MOD_Plk_1 | 153 | 159 | PF00069 | 0.701 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.366 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.398 |
MOD_Plk_1 | 507 | 513 | PF00069 | 0.489 |
MOD_Plk_1 | 84 | 90 | PF00069 | 0.494 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.395 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.445 |
MOD_Plk_4 | 302 | 308 | PF00069 | 0.402 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.496 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.397 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.496 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.465 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.740 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.793 |
MOD_ProDKin_1 | 211 | 217 | PF00069 | 0.551 |
MOD_ProDKin_1 | 415 | 421 | PF00069 | 0.452 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.524 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.479 |
MOD_SUMO_rev_2 | 70 | 80 | PF00179 | 0.385 |
TRG_DiLeu_BaEn_1 | 85 | 90 | PF01217 | 0.470 |
TRG_DiLeu_BaEn_2 | 301 | 307 | PF01217 | 0.357 |
TRG_DiLeu_BaEn_2 | 439 | 445 | PF01217 | 0.484 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.433 |
TRG_ER_diArg_1 | 181 | 183 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.321 |
TRG_ER_diArg_1 | 436 | 439 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.498 |
TRG_Pf-PMV_PEXEL_1 | 182 | 186 | PF00026 | 0.689 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IME7 | Leptomonas seymouri | 48% | 100% |
A0A0S4JCR9 | Bodo saltans | 29% | 89% |
A0A3R7MB50 | Trypanosoma rangeli | 35% | 100% |
A4HIC8 | Leishmania braziliensis | 75% | 100% |
A4I5M1 | Leishmania infantum | 99% | 100% |
E9B0W6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q7A0 | Leishmania major | 90% | 100% |
V5DQK8 | Trypanosoma cruzi | 35% | 100% |