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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A4HEP8
Term | Name | Level | Count |
---|---|---|---|
GO:0001522 | pseudouridine synthesis | 6 | 6 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006396 | RNA processing | 6 | 6 |
GO:0006399 | tRNA metabolic process | 7 | 6 |
GO:0006400 | tRNA modification | 6 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008033 | tRNA processing | 8 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009451 | RNA modification | 5 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016070 | RNA metabolic process | 5 | 6 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0031119 | tRNA pseudouridine synthesis | 7 | 4 |
GO:0034470 | ncRNA processing | 7 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034660 | ncRNA metabolic process | 6 | 6 |
GO:0043170 | macromolecule metabolic process | 3 | 6 |
GO:0043412 | macromolecule modification | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0090304 | nucleic acid metabolic process | 4 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1990481 | mRNA pseudouridine synthesis | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0004730 | pseudouridylate synthase activity | 5 | 8 |
GO:0005488 | binding | 1 | 11 |
GO:0009982 | pseudouridine synthase activity | 4 | 11 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 8 |
GO:0016836 | hydro-lyase activity | 4 | 8 |
GO:0016853 | isomerase activity | 2 | 11 |
GO:0016866 | intramolecular transferase activity | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
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 | 585 | 589 | PF00656 | 0.526 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.309 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.327 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 407 | 409 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.309 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 407 | 409 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 653 | 655 | PF00082 | 0.568 |
CLV_PCSK_PC7_1 | 4 | 10 | PF00082 | 0.702 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 153 | 157 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 407 | 411 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 515 | 519 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 666 | 670 | PF00082 | 0.467 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.746 |
DEG_SPOP_SBC_1 | 357 | 361 | PF00917 | 0.369 |
DOC_CKS1_1 | 409 | 414 | PF01111 | 0.476 |
DOC_CYCLIN_yCln2_LP_2 | 161 | 164 | PF00134 | 0.411 |
DOC_MAPK_DCC_7 | 194 | 204 | PF00069 | 0.486 |
DOC_MAPK_FxFP_2 | 288 | 291 | PF00069 | 0.381 |
DOC_MAPK_gen_1 | 123 | 131 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 149 | 158 | PF00069 | 0.372 |
DOC_MAPK_gen_1 | 19 | 29 | PF00069 | 0.363 |
DOC_MAPK_gen_1 | 311 | 318 | PF00069 | 0.396 |
DOC_MAPK_gen_1 | 672 | 682 | PF00069 | 0.507 |
DOC_MAPK_HePTP_8 | 277 | 289 | PF00069 | 0.328 |
DOC_MAPK_MEF2A_6 | 22 | 31 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.318 |
DOC_PP1_RVXF_1 | 284 | 290 | PF00149 | 0.436 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.358 |
DOC_PP2B_LxvP_1 | 161 | 164 | PF13499 | 0.362 |
DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.321 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.548 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.440 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.640 |
DOC_WD40_RPTOR_TOS_1 | 251 | 256 | PF00400 | 0.516 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 348 | 353 | PF00397 | 0.606 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.371 |
DOC_WW_Pin1_4 | 519 | 524 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 573 | 578 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 633 | 638 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 124 | 130 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 407 | 412 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 492 | 499 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 84 | 92 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 96 | 102 | PF00244 | 0.300 |
LIG_Actin_WH2_2 | 49 | 64 | PF00022 | 0.354 |
LIG_APCC_ABBA_1 | 304 | 309 | PF00400 | 0.543 |
LIG_BIR_III_4 | 450 | 454 | PF00653 | 0.431 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.402 |
LIG_CaM_IQ_9 | 179 | 195 | PF13499 | 0.281 |
LIG_EH1_1 | 50 | 58 | PF00400 | 0.265 |
LIG_EH1_1 | 92 | 100 | PF00400 | 0.299 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.383 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.560 |
LIG_FHA_1 | 351 | 357 | PF00498 | 0.610 |
LIG_FHA_1 | 358 | 364 | PF00498 | 0.457 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.456 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.341 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.291 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.564 |
LIG_FHA_2 | 634 | 640 | PF00498 | 0.593 |
LIG_LIR_Gen_1 | 166 | 175 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 245 | 255 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 531 | 539 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 627 | 637 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 245 | 251 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 36 | 41 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 513 | 517 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 531 | 536 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.550 |
LIG_PCNA_yPIPBox_3 | 144 | 155 | PF02747 | 0.334 |
LIG_Pex14_2 | 648 | 652 | PF04695 | 0.633 |
LIG_RPA_C_Fungi | 254 | 266 | PF08784 | 0.599 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.304 |
LIG_SH2_CRK | 159 | 163 | PF00017 | 0.322 |
LIG_SH2_CRK | 514 | 518 | PF00017 | 0.545 |
LIG_SH2_GRB2like | 248 | 251 | PF00017 | 0.456 |
LIG_SH2_PTP2 | 201 | 204 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 429 | 433 | PF00017 | 0.396 |
LIG_SH2_STAT3 | 420 | 423 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 647 | 650 | PF00017 | 0.456 |
LIG_SH3_3 | 263 | 269 | PF00018 | 0.450 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.370 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.393 |
LIG_SUMO_SIM_par_1 | 471 | 476 | PF11976 | 0.362 |
LIG_SxIP_EBH_1 | 135 | 149 | PF03271 | 0.399 |
LIG_TRAF2_1 | 597 | 600 | PF00917 | 0.786 |
LIG_TRFH_1 | 159 | 163 | PF08558 | 0.431 |
LIG_TYR_ITIM | 199 | 204 | PF00017 | 0.472 |
LIG_UBA3_1 | 376 | 382 | PF00899 | 0.304 |
LIG_UBA3_1 | 57 | 62 | PF00899 | 0.381 |
MOD_CDC14_SPxK_1 | 404 | 407 | PF00782 | 0.403 |
MOD_CDK_SPxK_1 | 401 | 407 | PF00069 | 0.390 |
MOD_CDK_SPxxK_3 | 401 | 408 | PF00069 | 0.434 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.518 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.474 |
MOD_CK1_1 | 257 | 263 | PF00069 | 0.476 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.634 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.577 |
MOD_CK1_1 | 528 | 534 | PF00069 | 0.335 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.356 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.555 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.529 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.475 |
MOD_CK2_1 | 498 | 504 | PF00069 | 0.531 |
MOD_CK2_1 | 618 | 624 | PF00069 | 0.631 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.592 |
MOD_DYRK1A_RPxSP_1 | 408 | 412 | PF00069 | 0.478 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.399 |
MOD_GlcNHglycan | 137 | 140 | PF01048 | 0.566 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.391 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.394 |
MOD_GlcNHglycan | 211 | 215 | PF01048 | 0.537 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.600 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.757 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.447 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.678 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.579 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.491 |
MOD_GlcNHglycan | 494 | 497 | PF01048 | 0.494 |
MOD_GlcNHglycan | 639 | 643 | PF01048 | 0.490 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.581 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.541 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.597 |
MOD_GSK3_1 | 513 | 520 | PF00069 | 0.564 |
MOD_GSK3_1 | 524 | 531 | PF00069 | 0.510 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.607 |
MOD_GSK3_1 | 607 | 614 | PF00069 | 0.748 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.346 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.496 |
MOD_N-GLC_1 | 436 | 441 | PF02516 | 0.500 |
MOD_N-GLC_1 | 540 | 545 | PF02516 | 0.325 |
MOD_N-GLC_1 | 589 | 594 | PF02516 | 0.734 |
MOD_N-GLC_2 | 232 | 234 | PF02516 | 0.266 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.480 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.364 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.358 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.321 |
MOD_NEK2_1 | 421 | 426 | PF00069 | 0.316 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.604 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.276 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.374 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.554 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.634 |
MOD_PK_1 | 130 | 136 | PF00069 | 0.251 |
MOD_PKA_1 | 407 | 413 | PF00069 | 0.376 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.345 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.375 |
MOD_PKA_2 | 443 | 449 | PF00069 | 0.395 |
MOD_PKB_1 | 490 | 498 | PF00069 | 0.486 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.377 |
MOD_Plk_1 | 429 | 435 | PF00069 | 0.489 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.335 |
MOD_Plk_1 | 540 | 546 | PF00069 | 0.366 |
MOD_Plk_1 | 683 | 689 | PF00069 | 0.514 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.449 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.472 |
MOD_Plk_4 | 219 | 225 | PF00069 | 0.532 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.438 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.358 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.361 |
MOD_Plk_4 | 394 | 400 | PF00069 | 0.348 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.626 |
MOD_Plk_4 | 528 | 534 | PF00069 | 0.380 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.432 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.573 |
MOD_ProDKin_1 | 348 | 354 | PF00069 | 0.596 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.418 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.367 |
MOD_ProDKin_1 | 519 | 525 | PF00069 | 0.396 |
MOD_ProDKin_1 | 573 | 579 | PF00069 | 0.598 |
MOD_ProDKin_1 | 633 | 639 | PF00069 | 0.622 |
MOD_SUMO_rev_2 | 550 | 556 | PF00179 | 0.326 |
MOD_SUMO_rev_2 | 585 | 594 | PF00179 | 0.617 |
TRG_DiLeu_BaEn_1 | 301 | 306 | PF01217 | 0.460 |
TRG_DiLeu_BaEn_1 | 504 | 509 | PF01217 | 0.395 |
TRG_DiLeu_BaEn_2 | 370 | 376 | PF01217 | 0.308 |
TRG_DiLeu_BaEn_2 | 528 | 534 | PF01217 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 532 | 537 | PF01217 | 0.421 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.282 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.392 |
TRG_ENDOCYTIC_2 | 248 | 251 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 418 | 421 | PF00928 | 0.351 |
TRG_ENDOCYTIC_2 | 514 | 517 | PF00928 | 0.542 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.309 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 559 | 562 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 654 | 657 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 7 | 9 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.429 |
TRG_NLS_MonoExtC_3 | 652 | 657 | PF00514 | 0.607 |
TRG_NLS_MonoExtN_4 | 650 | 657 | PF00514 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.357 |
TRG_Pf-PMV_PEXEL_1 | 554 | 558 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5J6 | Leptomonas seymouri | 59% | 100% |
A0A0S4KL20 | Bodo saltans | 34% | 93% |
A0A1X0NSY0 | Trypanosomatidae | 40% | 100% |
A0A3Q8ICM8 | Leishmania donovani | 79% | 99% |
A0A3R7KTM1 | Trypanosoma rangeli | 40% | 100% |
A4I1X8 | Leishmania infantum | 79% | 99% |
C9ZS41 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
E9AY24 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 99% |
Q4Q9E9 | Leishmania major | 80% | 100% |