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:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 3 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 3 |
GO:1990904 | ribonucleoprotein complex | 2 | 3 |
GO:0071011 | precatalytic spliceosome | 4 | 2 |
Related structures:
AlphaFold database: E9AXK8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006397 | mRNA processing | 7 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0008380 | RNA splicing | 7 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0016071 | mRNA metabolic process | 6 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 2 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 2 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 425 | 429 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.639 |
CLV_C14_Caspase3-7 | 618 | 622 | PF00656 | 0.555 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.464 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.592 |
CLV_NRD_NRD_1 | 631 | 633 | PF00675 | 0.631 |
CLV_NRD_NRD_1 | 647 | 649 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.348 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.435 |
CLV_PCSK_FUR_1 | 537 | 541 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.464 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.384 |
CLV_PCSK_KEX2_1 | 537 | 539 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 612 | 614 | PF00082 | 0.593 |
CLV_PCSK_KEX2_1 | 631 | 633 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 612 | 614 | PF00082 | 0.632 |
CLV_PCSK_PC7_1 | 111 | 117 | PF00082 | 0.313 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 263 | 267 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 418 | 422 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.803 |
CLV_PCSK_SKI1_1 | 648 | 652 | PF00082 | 0.549 |
CLV_Separin_Metazoa | 264 | 268 | PF03568 | 0.454 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.538 |
DEG_SPOP_SBC_1 | 180 | 184 | PF00917 | 0.681 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.620 |
DEG_SPOP_SBC_1 | 200 | 204 | PF00917 | 0.533 |
DOC_ANK_TNKS_1 | 495 | 502 | PF00023 | 0.605 |
DOC_CKS1_1 | 390 | 395 | PF01111 | 0.394 |
DOC_CYCLIN_RxL_1 | 124 | 136 | PF00134 | 0.335 |
DOC_CYCLIN_RxL_1 | 260 | 268 | PF00134 | 0.442 |
DOC_CYCLIN_RxL_1 | 414 | 425 | PF00134 | 0.468 |
DOC_CYCLIN_yClb1_LxF_4 | 603 | 608 | PF00134 | 0.549 |
DOC_MAPK_gen_1 | 367 | 377 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 631 | 642 | PF00069 | 0.593 |
DOC_MAPK_MEF2A_6 | 368 | 377 | PF00069 | 0.306 |
DOC_MAPK_MEF2A_6 | 635 | 644 | PF00069 | 0.604 |
DOC_MAPK_NFAT4_5 | 635 | 643 | PF00069 | 0.602 |
DOC_MAPK_RevD_3 | 524 | 540 | PF00069 | 0.598 |
DOC_PP1_RVXF_1 | 603 | 609 | PF00149 | 0.619 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.335 |
DOC_PP4_FxxP_1 | 390 | 393 | PF00568 | 0.317 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.408 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.265 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.676 |
DOC_USP7_MATH_1 | 607 | 611 | PF00917 | 0.569 |
DOC_USP7_MATH_2 | 165 | 171 | PF00917 | 0.416 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.642 |
DOC_WW_Pin1_4 | 336 | 341 | PF00397 | 0.378 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.395 |
LIG_14-3-3_CanoR_1 | 283 | 289 | PF00244 | 0.568 |
LIG_14-3-3_CanoR_1 | 350 | 356 | PF00244 | 0.401 |
LIG_14-3-3_CanoR_1 | 379 | 383 | PF00244 | 0.314 |
LIG_14-3-3_CanoR_1 | 647 | 651 | PF00244 | 0.554 |
LIG_Actin_WH2_2 | 216 | 231 | PF00022 | 0.406 |
LIG_APCC_ABBA_1 | 574 | 579 | PF00400 | 0.678 |
LIG_BRCT_BRCA1_1 | 201 | 205 | PF00533 | 0.425 |
LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.616 |
LIG_Clathr_ClatBox_1 | 575 | 579 | PF01394 | 0.641 |
LIG_CSL_BTD_1 | 429 | 432 | PF09270 | 0.362 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.540 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.416 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.491 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.315 |
LIG_FHA_1 | 639 | 645 | PF00498 | 0.560 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.421 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.548 |
LIG_FHA_2 | 352 | 358 | PF00498 | 0.329 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.471 |
LIG_FHA_2 | 46 | 52 | PF00498 | 0.763 |
LIG_GBD_Chelix_1 | 343 | 351 | PF00786 | 0.426 |
LIG_GBD_Chelix_1 | 369 | 377 | PF00786 | 0.329 |
LIG_LIR_Gen_1 | 151 | 162 | PF02991 | 0.514 |
LIG_LIR_Gen_1 | 208 | 214 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 275 | 284 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 385 | 395 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 655 | 661 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 151 | 157 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 208 | 212 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 275 | 280 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 655 | 661 | PF02991 | 0.630 |
LIG_PCNA_PIPBox_1 | 355 | 364 | PF02747 | 0.452 |
LIG_PCNA_yPIPBox_3 | 418 | 431 | PF02747 | 0.449 |
LIG_PDZ_Class_2 | 656 | 661 | PF00595 | 0.516 |
LIG_PTAP_UEV_1 | 197 | 202 | PF05743 | 0.581 |
LIG_PTB_Apo_2 | 83 | 90 | PF02174 | 0.431 |
LIG_PTB_Phospho_1 | 83 | 89 | PF10480 | 0.425 |
LIG_Rb_LxCxE_1 | 397 | 417 | PF01857 | 0.417 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.446 |
LIG_SH2_NCK_1 | 380 | 384 | PF00017 | 0.309 |
LIG_SH2_PTP2 | 232 | 235 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 321 | 324 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 387 | 390 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 658 | 661 | PF00017 | 0.548 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.469 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.579 |
LIG_SH3_3 | 439 | 445 | PF00018 | 0.473 |
LIG_SH3_3 | 523 | 529 | PF00018 | 0.525 |
LIG_SH3_3 | 623 | 629 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 557 | 568 | PF11976 | 0.630 |
LIG_SUMO_SIM_anti_2 | 641 | 646 | PF11976 | 0.550 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.508 |
LIG_TRFH_1 | 380 | 384 | PF08558 | 0.425 |
LIG_TYR_ITIM | 326 | 331 | PF00017 | 0.356 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.612 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.558 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.591 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.495 |
MOD_CK1_1 | 531 | 537 | PF00069 | 0.552 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.611 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.602 |
MOD_CK2_1 | 275 | 281 | PF00069 | 0.314 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.506 |
MOD_CK2_1 | 45 | 51 | PF00069 | 0.749 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.677 |
MOD_Cter_Amidation | 645 | 648 | PF01082 | 0.615 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.665 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.565 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.571 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.487 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.611 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.520 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.627 |
MOD_GlcNHglycan | 42 | 46 | PF01048 | 0.646 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.460 |
MOD_GlcNHglycan | 590 | 594 | PF01048 | 0.694 |
MOD_GlcNHglycan | 621 | 625 | PF01048 | 0.657 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.637 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.516 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.624 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.495 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.592 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.710 |
MOD_GSK3_1 | 201 | 208 | PF00069 | 0.551 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.387 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.735 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.621 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.626 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.668 |
MOD_N-GLC_1 | 56 | 61 | PF02516 | 0.722 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.463 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.291 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.426 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.484 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.426 |
MOD_NEK2_1 | 638 | 643 | PF00069 | 0.545 |
MOD_NEK2_2 | 646 | 651 | PF00069 | 0.506 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.497 |
MOD_PIKK_1 | 469 | 475 | PF00454 | 0.611 |
MOD_PIKK_1 | 477 | 483 | PF00454 | 0.553 |
MOD_PKA_2 | 282 | 288 | PF00069 | 0.411 |
MOD_PKA_2 | 292 | 298 | PF00069 | 0.414 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.369 |
MOD_PKA_2 | 646 | 652 | PF00069 | 0.612 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.411 |
MOD_Plk_2-3 | 275 | 281 | PF00069 | 0.253 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.540 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.497 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.545 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.549 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.640 |
MOD_ProDKin_1 | 336 | 342 | PF00069 | 0.372 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.393 |
TRG_DiLeu_BaEn_3 | 336 | 342 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 237 | 242 | PF01217 | 0.459 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.504 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.436 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 658 | 661 | PF00928 | 0.671 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.473 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 536 | 539 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.624 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.435 |
TRG_NLS_MonoExtN_4 | 609 | 616 | PF00514 | 0.645 |
TRG_Pf-PMV_PEXEL_1 | 511 | 515 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 525 | 530 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 540 | 544 | PF00026 | 0.547 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBP9 | Leptomonas seymouri | 60% | 100% |
A0A1X0NM33 | Trypanosomatidae | 33% | 100% |
A0A3Q8IDC3 | Leishmania donovani | 92% | 100% |
A0A422P1Y9 | Trypanosoma rangeli | 33% | 100% |
A4HE72 | Leishmania braziliensis | 82% | 100% |
A4I1H4 | Leishmania infantum | 91% | 100% |
C9ZJZ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4Q9W3 | Leishmania major | 91% | 100% |