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 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QCF4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006364 | rRNA processing | 8 | 2 |
GO:0006396 | RNA processing | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016072 | rRNA metabolic process | 7 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
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 | 260 | 264 | PF00656 | 0.753 |
CLV_C14_Caspase3-7 | 267 | 271 | PF00656 | 0.744 |
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.544 |
CLV_C14_Caspase3-7 | 7 | 11 | PF00656 | 0.627 |
CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 315 | 317 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.404 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.582 |
CLV_PCSK_FUR_1 | 14 | 18 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.694 |
CLV_PCSK_KEX2_1 | 238 | 240 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 315 | 317 | PF00082 | 0.408 |
CLV_PCSK_PC1ET2_1 | 238 | 240 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.240 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.648 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 484 | 488 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 535 | 539 | PF00082 | 0.362 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 656 | 660 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 71 | 75 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 90 | 94 | PF00082 | 0.330 |
DEG_SPOP_SBC_1 | 442 | 446 | PF00917 | 0.765 |
DEG_SPOP_SBC_1 | 469 | 473 | PF00917 | 0.628 |
DOC_CYCLIN_RxL_1 | 127 | 135 | PF00134 | 0.537 |
DOC_CYCLIN_RxL_1 | 515 | 526 | PF00134 | 0.476 |
DOC_CYCLIN_RxL_1 | 653 | 661 | PF00134 | 0.603 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 646 | 655 | PF00134 | 0.496 |
DOC_CYCLIN_yCln2_LP_2 | 651 | 657 | PF00134 | 0.506 |
DOC_MAPK_gen_1 | 16 | 27 | PF00069 | 0.558 |
DOC_MAPK_gen_1 | 315 | 323 | PF00069 | 0.443 |
DOC_MAPK_gen_1 | 552 | 562 | PF00069 | 0.595 |
DOC_MAPK_gen_1 | 632 | 640 | PF00069 | 0.641 |
DOC_MAPK_MEF2A_6 | 174 | 182 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 632 | 640 | PF00069 | 0.675 |
DOC_PP1_RVXF_1 | 409 | 416 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 46 | 52 | PF00149 | 0.606 |
DOC_PP1_RVXF_1 | 516 | 523 | PF00149 | 0.476 |
DOC_PP2B_LxvP_1 | 531 | 534 | PF13499 | 0.476 |
DOC_PP4_FxxP_1 | 675 | 678 | PF00568 | 0.400 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.781 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.763 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 537 | 541 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 593 | 597 | PF00917 | 0.655 |
DOC_USP7_MATH_1 | 613 | 617 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.511 |
DOC_USP7_UBL2_3 | 170 | 174 | PF12436 | 0.425 |
DOC_USP7_UBL2_3 | 318 | 322 | PF12436 | 0.451 |
DOC_USP7_UBL2_3 | 452 | 456 | PF12436 | 0.824 |
DOC_USP7_UBL2_3 | 635 | 639 | PF12436 | 0.643 |
DOC_USP7_UBL2_3 | 81 | 85 | PF12436 | 0.437 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 443 | 448 | PF00397 | 0.792 |
LIG_14-3-3_CanoR_1 | 239 | 246 | PF00244 | 0.776 |
LIG_14-3-3_CanoR_1 | 315 | 321 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 394 | 402 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 484 | 493 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 546 | 556 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 66 | 71 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 676 | 685 | PF00244 | 0.589 |
LIG_Actin_WH2_2 | 164 | 181 | PF00022 | 0.539 |
LIG_Actin_WH2_2 | 306 | 324 | PF00022 | 0.470 |
LIG_APCC_ABBA_1 | 378 | 383 | PF00400 | 0.500 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.689 |
LIG_BRCT_BRCA1_1 | 539 | 543 | PF00533 | 0.562 |
LIG_EH_1 | 628 | 632 | PF12763 | 0.495 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.476 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.476 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.552 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.442 |
LIG_FHA_1 | 548 | 554 | PF00498 | 0.537 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.569 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.463 |
LIG_FHA_2 | 219 | 225 | PF00498 | 0.654 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.564 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.528 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.562 |
LIG_FHA_2 | 691 | 697 | PF00498 | 0.618 |
LIG_Integrin_isoDGR_2 | 105 | 107 | PF01839 | 0.362 |
LIG_Integrin_isoDGR_2 | 409 | 411 | PF01839 | 0.564 |
LIG_LIR_Apic_2 | 120 | 126 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 34 | 45 | PF02991 | 0.443 |
LIG_LIR_Gen_1 | 383 | 392 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 521 | 530 | PF02991 | 0.500 |
LIG_LIR_LC3C_4 | 622 | 627 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 521 | 525 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 86 | 92 | PF02991 | 0.495 |
LIG_Pex14_2 | 150 | 154 | PF04695 | 0.476 |
LIG_RPA_C_Fungi | 48 | 60 | PF08784 | 0.564 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.328 |
LIG_SH2_CRK | 123 | 127 | PF00017 | 0.328 |
LIG_SH2_CRK | 368 | 372 | PF00017 | 0.407 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.598 |
LIG_SH2_NCK_1 | 633 | 637 | PF00017 | 0.598 |
LIG_SH2_STAT3 | 172 | 175 | PF00017 | 0.433 |
LIG_SH2_STAT3 | 366 | 369 | PF00017 | 0.465 |
LIG_SH2_STAT3 | 692 | 695 | PF00017 | 0.569 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 692 | 695 | PF00017 | 0.594 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.413 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.441 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.550 |
LIG_SH3_4 | 635 | 642 | PF00018 | 0.650 |
LIG_SUMO_SIM_par_1 | 369 | 375 | PF11976 | 0.447 |
LIG_TRAF2_1 | 222 | 225 | PF00917 | 0.706 |
LIG_TRAF2_1 | 253 | 256 | PF00917 | 0.746 |
LIG_TRAF2_1 | 693 | 696 | PF00917 | 0.526 |
LIG_UBA3_1 | 320 | 326 | PF00899 | 0.412 |
MOD_CDC14_SPxK_1 | 290 | 293 | PF00782 | 0.523 |
MOD_CDK_SPxK_1 | 287 | 293 | PF00069 | 0.530 |
MOD_CDK_SPxxK_3 | 445 | 452 | PF00069 | 0.682 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.325 |
MOD_CK1_1 | 471 | 477 | PF00069 | 0.631 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.563 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.351 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.359 |
MOD_CK2_1 | 218 | 224 | PF00069 | 0.647 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.529 |
MOD_CK2_1 | 49 | 55 | PF00069 | 0.539 |
MOD_CK2_1 | 665 | 671 | PF00069 | 0.574 |
MOD_CK2_1 | 690 | 696 | PF00069 | 0.582 |
MOD_Cter_Amidation | 235 | 238 | PF01082 | 0.770 |
MOD_Cter_Amidation | 313 | 316 | PF01082 | 0.424 |
MOD_Cter_Amidation | 454 | 457 | PF01082 | 0.766 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.328 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.769 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.613 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.639 |
MOD_GlcNHglycan | 449 | 452 | PF01048 | 0.815 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.677 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.725 |
MOD_GlcNHglycan | 607 | 610 | PF01048 | 0.603 |
MOD_GlcNHglycan | 641 | 644 | PF01048 | 0.445 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.327 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.748 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.430 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.559 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.721 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.673 |
MOD_GSK3_1 | 520 | 527 | PF00069 | 0.403 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.552 |
MOD_LATS_1 | 112 | 118 | PF00433 | 0.328 |
MOD_LATS_1 | 64 | 70 | PF00433 | 0.538 |
MOD_N-GLC_1 | 327 | 332 | PF02516 | 0.446 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.745 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.363 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.597 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.617 |
MOD_NEK2_1 | 631 | 636 | PF00069 | 0.596 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.487 |
MOD_NEK2_1 | 83 | 88 | PF00069 | 0.452 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.569 |
MOD_PIKK_1 | 485 | 491 | PF00454 | 0.351 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.504 |
MOD_PKA_2 | 631 | 637 | PF00069 | 0.619 |
MOD_PKB_1 | 394 | 402 | PF00069 | 0.339 |
MOD_Plk_1 | 302 | 308 | PF00069 | 0.427 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.423 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.609 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.351 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.540 |
MOD_Plk_4 | 316 | 322 | PF00069 | 0.522 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.474 |
MOD_Plk_4 | 524 | 530 | PF00069 | 0.392 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.240 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.571 |
MOD_ProDKin_1 | 443 | 449 | PF00069 | 0.790 |
TRG_DiLeu_BaEn_1 | 129 | 134 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 123 | 128 | PF01217 | 0.474 |
TRG_DiLeu_BaLyEn_6 | 397 | 402 | PF01217 | 0.433 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.314 |
TRG_ENDOCYTIC_2 | 368 | 371 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 15 | 17 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 315 | 317 | PF00400 | 0.408 |
TRG_NLS_MonoCore_2 | 237 | 242 | PF00514 | 0.746 |
TRG_NLS_MonoExtC_3 | 16 | 21 | PF00514 | 0.660 |
TRG_NLS_MonoExtC_3 | 236 | 241 | PF00514 | 0.748 |
TRG_NLS_MonoExtN_4 | 14 | 21 | PF00514 | 0.713 |
TRG_NLS_MonoExtN_4 | 235 | 242 | PF00514 | 0.710 |
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 | 400 | 404 | PF00026 | 0.488 |
TRG_Pf-PMV_PEXEL_1 | 484 | 489 | PF00026 | 0.449 |
TRG_Pf-PMV_PEXEL_1 | 656 | 660 | PF00026 | 0.448 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P856 | Leptomonas seymouri | 64% | 100% |
A0A0S4J214 | Bodo saltans | 46% | 100% |
A0A1X0NXJ9 | Trypanosomatidae | 47% | 100% |
A0A3R7MLR3 | Trypanosoma rangeli | 49% | 100% |
A0A3S7WWF8 | Leishmania donovani | 94% | 100% |
A4HBQ8 | Leishmania braziliensis | 83% | 100% |
A4HZ60 | Leishmania infantum | 94% | 100% |
D0A1I1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AV28 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
V5BDT6 | Trypanosoma cruzi | 47% | 100% |