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:0005635 | nuclear envelope | 4 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S7X1V8
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045292 | mRNA cis splicing, via spliceosome | 9 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 172 | 176 | PF00656 | 0.686 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 656 | 658 | PF00675 | 0.244 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.238 |
CLV_PCSK_KEX2_1 | 618 | 620 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.336 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 618 | 620 | PF00082 | 0.255 |
CLV_PCSK_PC1ET2_1 | 9 | 11 | PF00082 | 0.531 |
CLV_PCSK_PC7_1 | 5 | 11 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 679 | 683 | PF00082 | 0.242 |
DEG_APCC_DBOX_1 | 263 | 271 | PF00400 | 0.605 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.585 |
DEG_SPOP_SBC_1 | 52 | 56 | PF00917 | 0.578 |
DEG_SPOP_SBC_1 | 98 | 102 | PF00917 | 0.481 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 457 | 466 | PF00134 | 0.575 |
DOC_CYCLIN_yCln2_LP_2 | 609 | 615 | PF00134 | 0.442 |
DOC_MAPK_gen_1 | 261 | 270 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 63 | 73 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 664 | 672 | PF00069 | 0.536 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.609 |
DOC_MAPK_MEF2A_6 | 63 | 72 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 664 | 672 | PF00069 | 0.536 |
DOC_PP1_RVXF_1 | 667 | 673 | PF00149 | 0.473 |
DOC_PP1_RVXF_1 | 677 | 683 | PF00149 | 0.411 |
DOC_PP2B_LxvP_1 | 484 | 487 | PF13499 | 0.618 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.617 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.617 |
DOC_USP7_MATH_2 | 296 | 302 | PF00917 | 0.610 |
DOC_USP7_UBL2_3 | 312 | 316 | PF12436 | 0.581 |
DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 384 | 389 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 448 | 453 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 627 | 632 | PF00397 | 0.496 |
LIG_14-3-3_CanoR_1 | 27 | 34 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 408 | 414 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 440 | 445 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 669 | 673 | PF00244 | 0.442 |
LIG_deltaCOP1_diTrp_1 | 234 | 242 | PF00928 | 0.467 |
LIG_deltaCOP1_diTrp_1 | 602 | 610 | PF00928 | 0.536 |
LIG_eIF4E_1 | 262 | 268 | PF01652 | 0.606 |
LIG_eIF4E_1 | 362 | 368 | PF01652 | 0.642 |
LIG_eIF4E_1 | 675 | 681 | PF01652 | 0.496 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.416 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.524 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.500 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.494 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.665 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.576 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.659 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.685 |
LIG_FHA_2 | 389 | 395 | PF00498 | 0.574 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.570 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.498 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.442 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.442 |
LIG_Integrin_RGD_1 | 163 | 165 | PF01839 | 0.573 |
LIG_LIR_Apic_2 | 2 | 6 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 191 | 201 | PF02991 | 0.713 |
LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 502 | 509 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 606 | 615 | PF02991 | 0.442 |
LIG_LIR_Gen_1 | 636 | 645 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 191 | 197 | PF02991 | 0.727 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 502 | 508 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 582 | 586 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 608 | 614 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 636 | 641 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 671 | 675 | PF02991 | 0.546 |
LIG_LYPXL_S_1 | 610 | 614 | PF13949 | 0.242 |
LIG_LYPXL_yS_3 | 611 | 614 | PF13949 | 0.442 |
LIG_NRBOX | 21 | 27 | PF00104 | 0.507 |
LIG_NRBOX | 265 | 271 | PF00104 | 0.474 |
LIG_NRP_CendR_1 | 690 | 691 | PF00754 | 0.242 |
LIG_PTB_Apo_2 | 683 | 690 | PF02174 | 0.442 |
LIG_PTB_Phospho_1 | 683 | 689 | PF10480 | 0.442 |
LIG_REV1ctd_RIR_1 | 679 | 687 | PF16727 | 0.442 |
LIG_RPA_C_Fungi | 426 | 438 | PF08784 | 0.522 |
LIG_SH2_CRK | 425 | 429 | PF00017 | 0.410 |
LIG_SH2_CRK | 638 | 642 | PF00017 | 0.279 |
LIG_SH2_NCK_1 | 171 | 175 | PF00017 | 0.587 |
LIG_SH2_NCK_1 | 649 | 653 | PF00017 | 0.279 |
LIG_SH2_SRC | 171 | 174 | PF00017 | 0.606 |
LIG_SH2_SRC | 182 | 185 | PF00017 | 0.546 |
LIG_SH2_SRC | 649 | 652 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 262 | 266 | PF00017 | 0.473 |
LIG_SH2_STAP1 | 505 | 509 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 605 | 609 | PF00017 | 0.279 |
LIG_SH2_STAP1 | 649 | 653 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.584 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.336 |
LIG_SH3_3 | 103 | 109 | PF00018 | 0.357 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.723 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.652 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.650 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.586 |
LIG_SH3_3 | 628 | 634 | PF00018 | 0.349 |
LIG_SH3_3 | 642 | 648 | PF00018 | 0.209 |
LIG_SUMO_SIM_anti_2 | 265 | 271 | PF11976 | 0.605 |
LIG_SUMO_SIM_anti_2 | 47 | 56 | PF11976 | 0.399 |
LIG_SUMO_SIM_anti_2 | 69 | 74 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 370 | 375 | PF11976 | 0.643 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.587 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.744 |
LIG_TRAF2_1 | 467 | 470 | PF00917 | 0.398 |
LIG_TYR_ITIM | 609 | 614 | PF00017 | 0.279 |
LIG_WRC_WIRS_1 | 441 | 446 | PF05994 | 0.338 |
LIG_WW_1 | 259 | 262 | PF00397 | 0.630 |
LIG_WW_3 | 258 | 262 | PF00397 | 0.621 |
LIG_WW_3 | 597 | 601 | PF00397 | 0.279 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.697 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.432 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.735 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.805 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.644 |
MOD_CK1_1 | 448 | 454 | PF00069 | 0.539 |
MOD_CK1_1 | 48 | 54 | PF00069 | 0.673 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.697 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.560 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.502 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.724 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.648 |
MOD_CK2_1 | 338 | 344 | PF00069 | 0.722 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.547 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.497 |
MOD_CK2_1 | 98 | 104 | PF00069 | 0.487 |
MOD_Cter_Amidation | 7 | 10 | PF01082 | 0.620 |
MOD_DYRK1A_RPxSP_1 | 212 | 216 | PF00069 | 0.664 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.693 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.797 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.500 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.613 |
MOD_GlcNHglycan | 350 | 354 | PF01048 | 0.681 |
MOD_GlcNHglycan | 364 | 367 | PF01048 | 0.601 |
MOD_GlcNHglycan | 402 | 405 | PF01048 | 0.775 |
MOD_GlcNHglycan | 409 | 412 | PF01048 | 0.460 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.472 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.690 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.644 |
MOD_GlcNHglycan | 558 | 561 | PF01048 | 0.688 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.598 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.491 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.669 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.755 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.617 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.682 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.729 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.357 |
MOD_N-GLC_1 | 546 | 551 | PF02516 | 0.679 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.279 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.388 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.414 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.361 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.379 |
MOD_NEK2_1 | 302 | 307 | PF00069 | 0.617 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.613 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.649 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.410 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.279 |
MOD_NEK2_1 | 641 | 646 | PF00069 | 0.279 |
MOD_NEK2_1 | 682 | 687 | PF00069 | 0.338 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.418 |
MOD_NEK2_2 | 315 | 320 | PF00069 | 0.604 |
MOD_NEK2_2 | 605 | 610 | PF00069 | 0.279 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.582 |
MOD_PIKK_1 | 581 | 587 | PF00454 | 0.279 |
MOD_PKA_1 | 10 | 16 | PF00069 | 0.611 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.635 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.375 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.699 |
MOD_PKA_2 | 407 | 413 | PF00069 | 0.631 |
MOD_PKA_2 | 445 | 451 | PF00069 | 0.498 |
MOD_PKA_2 | 668 | 674 | PF00069 | 0.279 |
MOD_PKA_2 | 682 | 688 | PF00069 | 0.279 |
MOD_PKB_1 | 438 | 446 | PF00069 | 0.349 |
MOD_Plk_1 | 453 | 459 | PF00069 | 0.558 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.279 |
MOD_Plk_1 | 605 | 611 | PF00069 | 0.279 |
MOD_Plk_2-3 | 338 | 344 | PF00069 | 0.639 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.400 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.366 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.501 |
MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.607 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.737 |
MOD_ProDKin_1 | 384 | 390 | PF00069 | 0.668 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.771 |
MOD_ProDKin_1 | 448 | 454 | PF00069 | 0.474 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.654 |
MOD_ProDKin_1 | 627 | 633 | PF00069 | 0.355 |
MOD_SUMO_for_1 | 311 | 314 | PF00179 | 0.617 |
MOD_SUMO_for_1 | 319 | 322 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_1 | 263 | 268 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_2 | 140 | 146 | PF01217 | 0.486 |
TRG_ENDOCYTIC_2 | 194 | 197 | PF00928 | 0.739 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.391 |
TRG_ENDOCYTIC_2 | 505 | 508 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 611 | 614 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 638 | 641 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 649 | 652 | PF00928 | 0.279 |
TRG_ENDOCYTIC_2 | 678 | 681 | PF00928 | 0.279 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 654 | 657 | PF00400 | 0.410 |
TRG_ER_diArg_1 | 689 | 691 | PF00400 | 0.279 |
TRG_NLS_MonoCore_2 | 8 | 13 | PF00514 | 0.651 |
TRG_NLS_MonoExtC_3 | 656 | 662 | PF00514 | 0.410 |
TRG_NLS_MonoExtC_3 | 8 | 14 | PF00514 | 0.558 |
TRG_NLS_MonoExtN_4 | 6 | 13 | PF00514 | 0.601 |
TRG_NLS_MonoExtN_4 | 655 | 661 | PF00514 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 105 | 110 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 460 | 464 | PF00026 | 0.578 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1P4 | Leptomonas seymouri | 62% | 100% |
A0A1X0NRC2 | Trypanosomatidae | 37% | 100% |
A0A422N9D9 | Trypanosoma rangeli | 39% | 100% |
A4HGT7 | Leishmania braziliensis | 86% | 100% |
A4I3W4 | Leishmania infantum | 100% | 100% |
D0A932 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9B054 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q831 | Leishmania major | 95% | 100% |
V5APW4 | Trypanosoma cruzi | 38% | 100% |