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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0071011 | precatalytic spliceosome | 4 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: E9AYV9
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 10 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 10 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006396 | RNA processing | 6 | 10 |
GO:0006397 | mRNA processing | 7 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0008380 | RNA splicing | 7 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0016071 | mRNA metabolic process | 6 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.418 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.441 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 381 | 383 | PF00675 | 0.358 |
CLV_NRD_NRD_1 | 386 | 388 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 486 | 488 | PF00675 | 0.447 |
CLV_PCSK_KEX2_1 | 190 | 192 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 263 | 265 | PF00082 | 0.698 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 386 | 388 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 486 | 488 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 263 | 265 | PF00082 | 0.698 |
CLV_PCSK_PC1ET2_1 | 72 | 74 | PF00082 | 0.560 |
CLV_PCSK_PC7_1 | 382 | 388 | PF00082 | 0.324 |
CLV_PCSK_PC7_1 | 482 | 488 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.291 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 662 | 666 | PF00082 | 0.500 |
CLV_Separin_Metazoa | 498 | 502 | PF03568 | 0.430 |
DEG_SPOP_SBC_1 | 235 | 239 | PF00917 | 0.632 |
DEG_SPOP_SBC_1 | 252 | 256 | PF00917 | 0.589 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.264 |
DOC_CYCLIN_RxL_1 | 289 | 300 | PF00134 | 0.301 |
DOC_CYCLIN_yCln2_LP_2 | 281 | 287 | PF00134 | 0.521 |
DOC_MAPK_gen_1 | 386 | 396 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 486 | 493 | PF00069 | 0.359 |
DOC_MAPK_gen_1 | 558 | 567 | PF00069 | 0.443 |
DOC_MAPK_MEF2A_6 | 561 | 569 | PF00069 | 0.386 |
DOC_PP2B_LxvP_1 | 107 | 110 | PF13499 | 0.335 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.475 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.463 |
DOC_PP4_FxxP_1 | 401 | 404 | PF00568 | 0.397 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.462 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.415 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 650 | 654 | PF00917 | 0.366 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.566 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.604 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.381 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.532 |
LIG_14-3-3_CanoR_1 | 168 | 175 | PF00244 | 0.626 |
LIG_14-3-3_CanoR_1 | 190 | 195 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 203 | 210 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 249 | 257 | PF00244 | 0.684 |
LIG_14-3-3_CanoR_1 | 342 | 350 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 405 | 411 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 566 | 576 | PF00244 | 0.439 |
LIG_Actin_WH2_2 | 580 | 596 | PF00022 | 0.433 |
LIG_APCC_ABBA_1 | 100 | 105 | PF00400 | 0.456 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.703 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.522 |
LIG_BIR_III_2 | 517 | 521 | PF00653 | 0.424 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.522 |
LIG_Clathr_ClatBox_1 | 147 | 151 | PF01394 | 0.321 |
LIG_Clathr_ClatBox_1 | 452 | 456 | PF01394 | 0.415 |
LIG_Clathr_ClatBox_1 | 655 | 659 | PF01394 | 0.347 |
LIG_CSL_BTD_1 | 672 | 675 | PF09270 | 0.388 |
LIG_deltaCOP1_diTrp_1 | 273 | 280 | PF00928 | 0.582 |
LIG_deltaCOP1_diTrp_1 | 628 | 637 | PF00928 | 0.472 |
LIG_eIF4E_1 | 103 | 109 | PF01652 | 0.338 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.610 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.526 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.606 |
LIG_FHA_1 | 391 | 397 | PF00498 | 0.368 |
LIG_FHA_1 | 475 | 481 | PF00498 | 0.425 |
LIG_FHA_1 | 619 | 625 | PF00498 | 0.392 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.426 |
LIG_FHA_2 | 167 | 173 | PF00498 | 0.597 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.560 |
LIG_FHA_2 | 566 | 572 | PF00498 | 0.303 |
LIG_FHA_2 | 614 | 620 | PF00498 | 0.232 |
LIG_LIR_Apic_2 | 521 | 527 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 116 | 126 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 327 | 335 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 363 | 369 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 371 | 379 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 634 | 644 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 93 | 104 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 116 | 121 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 363 | 367 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 464 | 470 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 595 | 600 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 634 | 640 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 93 | 99 | PF02991 | 0.365 |
LIG_PCNA_yPIPBox_3 | 136 | 148 | PF02747 | 0.455 |
LIG_Pex14_1 | 276 | 280 | PF04695 | 0.581 |
LIG_Pex14_1 | 373 | 377 | PF04695 | 0.346 |
LIG_SH2_CRK | 467 | 471 | PF00017 | 0.400 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.461 |
LIG_SH2_CRK | 524 | 528 | PF00017 | 0.488 |
LIG_SH2_PTP2 | 156 | 159 | PF00017 | 0.469 |
LIG_SH2_SRC | 103 | 106 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 118 | 122 | PF00017 | 0.304 |
LIG_SH2_STAP1 | 686 | 690 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 156 | 159 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 576 | 579 | PF00017 | 0.451 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.322 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.648 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.611 |
LIG_SUMO_SIM_anti_2 | 313 | 320 | PF11976 | 0.390 |
LIG_SUMO_SIM_anti_2 | 653 | 659 | PF11976 | 0.379 |
LIG_SUMO_SIM_par_1 | 653 | 659 | PF11976 | 0.355 |
LIG_TRAF2_1 | 312 | 315 | PF00917 | 0.518 |
LIG_TYR_ITIM | 46 | 51 | PF00017 | 0.406 |
LIG_TYR_ITIM | 465 | 470 | PF00017 | 0.351 |
LIG_TYR_ITSM | 114 | 121 | PF00017 | 0.423 |
LIG_UBA3_1 | 144 | 149 | PF00899 | 0.233 |
LIG_UBA3_1 | 194 | 199 | PF00899 | 0.428 |
MOD_CDK_SPxK_1 | 149 | 155 | PF00069 | 0.450 |
MOD_CK1_1 | 171 | 177 | PF00069 | 0.584 |
MOD_CK1_1 | 251 | 257 | PF00069 | 0.537 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.704 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.379 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.638 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.429 |
MOD_CK2_1 | 166 | 172 | PF00069 | 0.574 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.505 |
MOD_CK2_1 | 613 | 619 | PF00069 | 0.230 |
MOD_CK2_1 | 92 | 98 | PF00069 | 0.423 |
MOD_Cter_Amidation | 70 | 73 | PF01082 | 0.545 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.393 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.797 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.588 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.418 |
MOD_GlcNHglycan | 445 | 448 | PF01048 | 0.496 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.335 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.437 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.459 |
MOD_GlcNHglycan | 651 | 655 | PF01048 | 0.404 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.424 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.586 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.444 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.659 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.805 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.704 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.337 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.398 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.214 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.563 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.717 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.204 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.405 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.443 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.419 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.391 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.348 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.451 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.443 |
MOD_NEK2_1 | 667 | 672 | PF00069 | 0.395 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.428 |
MOD_NEK2_2 | 609 | 614 | PF00069 | 0.301 |
MOD_NEK2_2 | 620 | 625 | PF00069 | 0.313 |
MOD_PIKK_1 | 518 | 524 | PF00454 | 0.411 |
MOD_PIKK_1 | 547 | 553 | PF00454 | 0.463 |
MOD_PIKK_1 | 673 | 679 | PF00454 | 0.511 |
MOD_PKA_1 | 190 | 196 | PF00069 | 0.330 |
MOD_PKA_1 | 72 | 78 | PF00069 | 0.572 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.447 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.344 |
MOD_PKA_2 | 218 | 224 | PF00069 | 0.380 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.618 |
MOD_PKA_2 | 341 | 347 | PF00069 | 0.478 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.526 |
MOD_PKA_2 | 457 | 463 | PF00069 | 0.404 |
MOD_PKA_2 | 565 | 571 | PF00069 | 0.391 |
MOD_PKA_2 | 644 | 650 | PF00069 | 0.540 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.666 |
MOD_Plk_1 | 540 | 546 | PF00069 | 0.556 |
MOD_Plk_1 | 650 | 656 | PF00069 | 0.366 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.393 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.339 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.599 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.483 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.439 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.241 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.565 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.255 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.470 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.250 |
MOD_Plk_4 | 679 | 685 | PF00069 | 0.413 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.377 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.519 |
MOD_SUMO_rev_2 | 111 | 116 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 229 | 235 | PF00179 | 0.592 |
TRG_DiLeu_BaEn_4 | 123 | 129 | PF01217 | 0.356 |
TRG_DiLeu_BaLyEn_6 | 291 | 296 | PF01217 | 0.286 |
TRG_DiLeu_BaLyEn_6 | 305 | 310 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 606 | 611 | PF01217 | 0.359 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 291 | 294 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 385 | 387 | PF00400 | 0.355 |
TRG_NES_CRM1_1 | 98 | 112 | PF08389 | 0.416 |
TRG_Pf-PMV_PEXEL_1 | 38 | 43 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 85 | 89 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYM3 | Leptomonas seymouri | 63% | 100% |
A0A3R7KHV4 | Trypanosoma rangeli | 35% | 100% |
A0A3S5H7H4 | Leishmania donovani | 91% | 100% |
A4HFI4 | Leishmania braziliensis | 79% | 100% |
D0A5R0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 100% |
E9AD35 | Leishmania major | 92% | 100% |
E9AHC8 | Leishmania infantum | 92% | 100% |
G5EEG7 | Caenorhabditis elegans | 24% | 100% |
Q2TAY7 | Homo sapiens | 25% | 100% |
Q2TBS9 | Bos taurus | 25% | 100% |
Q3UKJ7 | Mus musculus | 25% | 100% |
Q5ZME8 | Gallus gallus | 25% | 100% |
Q6NRT3 | Xenopus laevis | 25% | 100% |
Q6P4J8 | Xenopus tropicalis | 25% | 100% |
Q76B40 | Cricetulus griseus | 25% | 100% |
Q7ZVA0 | Danio rerio | 24% | 100% |
Q99M63 | Rattus norvegicus | 25% | 100% |
V5B9I2 | Trypanosoma cruzi | 34% | 100% |