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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HBQ8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 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:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 261 | 265 | PF00656 | 0.747 |
CLV_C14_Caspase3-7 | 331 | 335 | PF00656 | 0.557 |
CLV_MEL_PAP_1 | 307 | 313 | PF00089 | 0.432 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.717 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 316 | 318 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.431 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.408 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.431 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.502 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.654 |
CLV_PCSK_PC7_1 | 16 | 22 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.258 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 534 | 538 | PF00082 | 0.360 |
CLV_PCSK_SKI1_1 | 557 | 561 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.604 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.541 |
DEG_APCC_KENBOX_2 | 403 | 407 | PF00400 | 0.353 |
DEG_SPOP_SBC_1 | 468 | 472 | PF00917 | 0.633 |
DEG_SPOP_SBC_1 | 473 | 477 | PF00917 | 0.550 |
DOC_CYCLIN_RxL_1 | 127 | 135 | PF00134 | 0.537 |
DOC_CYCLIN_RxL_1 | 514 | 525 | PF00134 | 0.466 |
DOC_CYCLIN_RxL_1 | 652 | 660 | PF00134 | 0.607 |
DOC_CYCLIN_yClb1_LxF_4 | 319 | 325 | PF00134 | 0.421 |
DOC_MAPK_gen_1 | 18 | 27 | PF00069 | 0.570 |
DOC_MAPK_gen_1 | 316 | 324 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 401 | 409 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 551 | 561 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 631 | 639 | PF00069 | 0.642 |
DOC_MAPK_gen_1 | 81 | 89 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 174 | 182 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 631 | 639 | PF00069 | 0.675 |
DOC_PP1_RVXF_1 | 410 | 417 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.622 |
DOC_PP1_RVXF_1 | 515 | 522 | PF00149 | 0.476 |
DOC_PP2B_LxvP_1 | 530 | 533 | PF13499 | 0.476 |
DOC_PP4_FxxP_1 | 674 | 677 | PF00568 | 0.400 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.769 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 592 | 596 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.505 |
DOC_USP7_UBL2_3 | 319 | 323 | PF12436 | 0.462 |
DOC_USP7_UBL2_3 | 451 | 455 | PF12436 | 0.811 |
DOC_USP7_UBL2_3 | 456 | 460 | PF12436 | 0.708 |
DOC_USP7_UBL2_3 | 634 | 638 | PF12436 | 0.656 |
DOC_USP7_UBL2_3 | 655 | 659 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 188 | 193 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.585 |
DOC_WW_Pin1_4 | 469 | 474 | PF00397 | 0.649 |
LIG_14-3-3_CanoR_1 | 174 | 179 | PF00244 | 0.532 |
LIG_14-3-3_CanoR_1 | 239 | 246 | PF00244 | 0.768 |
LIG_14-3-3_CanoR_1 | 310 | 318 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 395 | 403 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 483 | 492 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 545 | 555 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 627 | 631 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 675 | 684 | PF00244 | 0.577 |
LIG_Actin_WH2_2 | 164 | 181 | PF00022 | 0.543 |
LIG_Actin_WH2_2 | 307 | 325 | PF00022 | 0.481 |
LIG_Actin_WH2_2 | 643 | 661 | PF00022 | 0.471 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.701 |
LIG_BRCT_BRCA1_1 | 538 | 542 | PF00533 | 0.562 |
LIG_DLG_GKlike_1 | 174 | 182 | PF00625 | 0.404 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.468 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.577 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.586 |
LIG_FHA_1 | 387 | 393 | PF00498 | 0.477 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.535 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.537 |
LIG_FHA_1 | 575 | 581 | PF00498 | 0.580 |
LIG_FHA_1 | 589 | 595 | PF00498 | 0.614 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.464 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.609 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.525 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.525 |
LIG_FHA_2 | 520 | 526 | PF00498 | 0.562 |
LIG_FHA_2 | 690 | 696 | PF00498 | 0.623 |
LIG_Integrin_isoDGR_2 | 105 | 107 | PF01839 | 0.362 |
LIG_Integrin_isoDGR_2 | 410 | 412 | PF01839 | 0.564 |
LIG_LIR_Apic_2 | 120 | 126 | PF02991 | 0.466 |
LIG_LIR_Apic_2 | 629 | 635 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 184 | 192 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 520 | 529 | PF02991 | 0.500 |
LIG_LIR_LC3C_4 | 477 | 482 | PF02991 | 0.516 |
LIG_LIR_LC3C_4 | 621 | 626 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 184 | 188 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 520 | 524 | PF02991 | 0.476 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.476 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.476 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.467 |
LIG_SH2_CRK | 369 | 373 | PF00017 | 0.405 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.603 |
LIG_SH2_NCK_1 | 632 | 636 | PF00017 | 0.603 |
LIG_SH2_STAT3 | 172 | 175 | PF00017 | 0.551 |
LIG_SH2_STAT3 | 367 | 370 | PF00017 | 0.466 |
LIG_SH2_STAT3 | 691 | 694 | PF00017 | 0.574 |
LIG_SH2_STAT5 | 345 | 348 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 691 | 694 | PF00017 | 0.599 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.537 |
LIG_SH3_3 | 634 | 640 | PF00018 | 0.549 |
LIG_SH3_3 | 647 | 653 | PF00018 | 0.561 |
LIG_SH3_4 | 634 | 641 | PF00018 | 0.652 |
LIG_SUMO_SIM_anti_2 | 615 | 621 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 370 | 376 | PF11976 | 0.439 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.645 |
LIG_TRAF2_1 | 692 | 695 | PF00917 | 0.532 |
MOD_CDC14_SPxK_1 | 291 | 294 | PF00782 | 0.519 |
MOD_CDK_SPxK_1 | 288 | 294 | PF00069 | 0.527 |
MOD_CDK_SPxxK_3 | 188 | 195 | PF00069 | 0.227 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.318 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.680 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.555 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.749 |
MOD_CK1_1 | 472 | 478 | PF00069 | 0.630 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.582 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.351 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.352 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.621 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.529 |
MOD_CK2_1 | 664 | 670 | PF00069 | 0.540 |
MOD_CK2_1 | 689 | 695 | PF00069 | 0.588 |
MOD_Cter_Amidation | 235 | 238 | PF01082 | 0.752 |
MOD_Cter_Amidation | 314 | 317 | PF01082 | 0.426 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.328 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.227 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.738 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.762 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.603 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.621 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.705 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.655 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.328 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.617 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.476 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.677 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.444 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.423 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.549 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.500 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.532 |
MOD_LATS_1 | 112 | 118 | PF00433 | 0.328 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.457 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.371 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.363 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.557 |
MOD_NEK2_1 | 425 | 430 | PF00069 | 0.436 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.598 |
MOD_NEK2_1 | 588 | 593 | PF00069 | 0.438 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.589 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.488 |
MOD_NEK2_2 | 618 | 623 | PF00069 | 0.552 |
MOD_OFUCOSY | 385 | 390 | PF10250 | 0.462 |
MOD_PKA_2 | 173 | 179 | PF00069 | 0.227 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.679 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.444 |
MOD_PKA_2 | 626 | 632 | PF00069 | 0.577 |
MOD_PKB_1 | 237 | 245 | PF00069 | 0.692 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.440 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.384 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.606 |
MOD_Plk_1 | 425 | 431 | PF00069 | 0.240 |
MOD_Plk_2-3 | 328 | 334 | PF00069 | 0.353 |
MOD_Plk_2-3 | 388 | 394 | PF00069 | 0.320 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.474 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.351 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.575 |
MOD_Plk_4 | 476 | 482 | PF00069 | 0.640 |
MOD_Plk_4 | 523 | 529 | PF00069 | 0.379 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.203 |
MOD_ProDKin_1 | 188 | 194 | PF00069 | 0.371 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.584 |
MOD_ProDKin_1 | 469 | 475 | PF00069 | 0.645 |
MOD_SUMO_rev_2 | 187 | 197 | PF00179 | 0.420 |
MOD_SUMO_rev_2 | 454 | 462 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 47 | 56 | PF00179 | 0.435 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.425 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.428 |
TRG_ER_diArg_1 | 237 | 240 | PF00400 | 0.678 |
TRG_ER_diArg_1 | 316 | 318 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 325 | 327 | PF00400 | 0.409 |
TRG_NLS_MonoCore_2 | 237 | 242 | PF00514 | 0.735 |
TRG_NLS_MonoExtC_3 | 236 | 241 | PF00514 | 0.735 |
TRG_NLS_MonoExtN_4 | 237 | 242 | PF00514 | 0.707 |
TRG_Pf-PMV_PEXEL_1 | 130 | 135 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 205 | 209 | PF00026 | 0.413 |
TRG_Pf-PMV_PEXEL_1 | 401 | 405 | PF00026 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 483 | 488 | PF00026 | 0.449 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P856 | Leptomonas seymouri | 64% | 100% |
A0A0S4J214 | Bodo saltans | 46% | 100% |
A0A1X0NXJ9 | Trypanosomatidae | 47% | 100% |
A0A3R7MLR3 | Trypanosoma rangeli | 48% | 100% |
A0A3S7WWF8 | Leishmania donovani | 82% | 100% |
A4HZ60 | Leishmania infantum | 82% | 100% |
D0A1I1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AV28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QCF4 | Leishmania major | 83% | 100% |
V5BDT6 | Trypanosoma cruzi | 47% | 100% |