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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3Q8IGM4
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009451 | RNA modification | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0032259 | methylation | 2 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0043414 | macromolecule methylation | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003723 | RNA binding | 4 | 8 |
GO:0003824 | catalytic activity | 1 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0008168 | methyltransferase activity | 4 | 8 |
GO:0016740 | transferase activity | 2 | 8 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 394 | 398 | PF00656 | 0.474 |
CLV_C14_Caspase3-7 | 517 | 521 | PF00656 | 0.342 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 375 | 377 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 557 | 559 | PF00675 | 0.271 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 501 | 503 | PF00082 | 0.495 |
CLV_PCSK_PC1ET2_1 | 501 | 503 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 115 | 119 | PF00082 | 0.607 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.295 |
DEG_APCC_DBOX_1 | 307 | 315 | PF00400 | 0.529 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.588 |
DEG_SPOP_SBC_1 | 326 | 330 | PF00917 | 0.718 |
DOC_CKS1_1 | 98 | 103 | PF01111 | 0.630 |
DOC_CYCLIN_RxL_1 | 160 | 172 | PF00134 | 0.557 |
DOC_CYCLIN_RxL_1 | 552 | 563 | PF00134 | 0.499 |
DOC_CYCLIN_yClb1_LxF_4 | 592 | 598 | PF00134 | 0.529 |
DOC_MAPK_DCC_7 | 676 | 684 | PF00069 | 0.529 |
DOC_MAPK_gen_1 | 112 | 121 | PF00069 | 0.580 |
DOC_MAPK_gen_1 | 447 | 456 | PF00069 | 0.521 |
DOC_MAPK_JIP1_4 | 165 | 171 | PF00069 | 0.496 |
DOC_MAPK_MEF2A_6 | 115 | 123 | PF00069 | 0.564 |
DOC_MAPK_MEF2A_6 | 161 | 170 | PF00069 | 0.562 |
DOC_MAPK_MEF2A_6 | 405 | 412 | PF00069 | 0.404 |
DOC_MAPK_NFAT4_5 | 405 | 413 | PF00069 | 0.405 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.529 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.641 |
DOC_PP4_FxxP_1 | 110 | 113 | PF00568 | 0.690 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.559 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.497 |
DOC_WW_Pin1_4 | 327 | 332 | PF00397 | 0.777 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.790 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 568 | 573 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.660 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 141 | 150 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 24 | 28 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 267 | 271 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 308 | 312 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 327 | 331 | PF00244 | 0.793 |
LIG_14-3-3_CanoR_1 | 459 | 468 | PF00244 | 0.596 |
LIG_14-3-3_CanoR_1 | 608 | 617 | PF00244 | 0.495 |
LIG_Actin_WH2_2 | 359 | 377 | PF00022 | 0.539 |
LIG_APCC_ABBA_1 | 682 | 687 | PF00400 | 0.575 |
LIG_BRCT_BRCA1_1 | 193 | 197 | PF00533 | 0.512 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.577 |
LIG_EVH1_1 | 332 | 336 | PF00568 | 0.700 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.564 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.559 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.614 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.557 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.393 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.483 |
LIG_FHA_1 | 582 | 588 | PF00498 | 0.485 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.490 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.657 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.595 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.654 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.566 |
LIG_FHA_2 | 392 | 398 | PF00498 | 0.390 |
LIG_FHA_2 | 583 | 589 | PF00498 | 0.473 |
LIG_LIR_Apic_2 | 108 | 113 | PF02991 | 0.646 |
LIG_LIR_Apic_2 | 59 | 65 | PF02991 | 0.546 |
LIG_LIR_Gen_1 | 519 | 530 | PF02991 | 0.496 |
LIG_LIR_Gen_1 | 683 | 693 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 135 | 140 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 282 | 286 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.627 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 600 | 604 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.582 |
LIG_LYPXL_yS_3 | 601 | 604 | PF13949 | 0.495 |
LIG_MYND_1 | 538 | 542 | PF01753 | 0.471 |
LIG_NRBOX | 310 | 316 | PF00104 | 0.545 |
LIG_NRBOX | 408 | 414 | PF00104 | 0.459 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.438 |
LIG_NRBOX | 81 | 87 | PF00104 | 0.556 |
LIG_PCNA_PIPBox_1 | 454 | 463 | PF02747 | 0.538 |
LIG_PCNA_yPIPBox_3 | 445 | 457 | PF02747 | 0.470 |
LIG_PDZ_Class_1 | 703 | 708 | PF00595 | 0.607 |
LIG_Pex14_2 | 696 | 700 | PF04695 | 0.343 |
LIG_RPA_C_Fungi | 605 | 617 | PF08784 | 0.372 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.622 |
LIG_SH2_CRK | 62 | 66 | PF00017 | 0.559 |
LIG_SH2_NCK_1 | 14 | 18 | PF00017 | 0.622 |
LIG_SH2_NCK_1 | 62 | 66 | PF00017 | 0.607 |
LIG_SH2_NCK_1 | 685 | 689 | PF00017 | 0.590 |
LIG_SH2_SRC | 12 | 15 | PF00017 | 0.638 |
LIG_SH2_SRC | 186 | 189 | PF00017 | 0.408 |
LIG_SH2_SRC | 685 | 688 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 7 | 11 | PF00017 | 0.610 |
LIG_SH2_STAT3 | 10 | 13 | PF00017 | 0.691 |
LIG_SH2_STAT3 | 626 | 629 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 10 | 13 | PF00017 | 0.655 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 705 | 708 | PF00017 | 0.622 |
LIG_SH3_1 | 160 | 166 | PF00018 | 0.631 |
LIG_SH3_1 | 569 | 575 | PF00018 | 0.408 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.683 |
LIG_SH3_3 | 24 | 30 | PF00018 | 0.583 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.771 |
LIG_SH3_3 | 569 | 575 | PF00018 | 0.408 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.565 |
LIG_SUMO_SIM_anti_2 | 670 | 676 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 166 | 172 | PF11976 | 0.360 |
LIG_TRAF2_1 | 417 | 420 | PF00917 | 0.575 |
LIG_TRAF2_1 | 448 | 451 | PF00917 | 0.514 |
LIG_TRAF2_1 | 586 | 589 | PF00917 | 0.360 |
LIG_UBA3_1 | 314 | 319 | PF00899 | 0.677 |
MOD_CDK_SPK_2 | 37 | 42 | PF00069 | 0.632 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.713 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.632 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.669 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.630 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.539 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.680 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.705 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.685 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.408 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.377 |
MOD_CK1_1 | 581 | 587 | PF00069 | 0.269 |
MOD_CK1_1 | 635 | 641 | PF00069 | 0.651 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.665 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.597 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.745 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.644 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.568 |
MOD_CK2_1 | 582 | 588 | PF00069 | 0.329 |
MOD_CK2_1 | 73 | 79 | PF00069 | 0.510 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.667 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.520 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.675 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.278 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.526 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.659 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.623 |
MOD_GlcNHglycan | 477 | 480 | PF01048 | 0.589 |
MOD_GlcNHglycan | 512 | 516 | PF01048 | 0.715 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.318 |
MOD_GlcNHglycan | 619 | 623 | PF01048 | 0.345 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.510 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.534 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.445 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.646 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.620 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.610 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.623 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.769 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.611 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.543 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.685 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.423 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.646 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.567 |
MOD_GSK3_1 | 546 | 553 | PF00069 | 0.389 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.360 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.356 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.664 |
MOD_N-GLC_1 | 220 | 225 | PF02516 | 0.695 |
MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.411 |
MOD_N-GLC_1 | 474 | 479 | PF02516 | 0.620 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.641 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.622 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.595 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.421 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.636 |
MOD_NEK2_1 | 560 | 565 | PF00069 | 0.356 |
MOD_NEK2_1 | 597 | 602 | PF00069 | 0.400 |
MOD_NEK2_1 | 700 | 705 | PF00069 | 0.426 |
MOD_PK_1 | 52 | 58 | PF00069 | 0.721 |
MOD_PKA_1 | 502 | 508 | PF00069 | 0.568 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.652 |
MOD_PKA_2 | 140 | 146 | PF00069 | 0.650 |
MOD_PKA_2 | 180 | 186 | PF00069 | 0.360 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.611 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.624 |
MOD_PKA_2 | 288 | 294 | PF00069 | 0.442 |
MOD_PKA_2 | 307 | 313 | PF00069 | 0.630 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.716 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.410 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.560 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.721 |
MOD_Plk_1 | 618 | 624 | PF00069 | 0.351 |
MOD_Plk_2-3 | 686 | 692 | PF00069 | 0.595 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.636 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.558 |
MOD_Plk_4 | 266 | 272 | PF00069 | 0.572 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.530 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.403 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.510 |
MOD_Plk_4 | 404 | 410 | PF00069 | 0.306 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.617 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.740 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.498 |
MOD_ProDKin_1 | 327 | 333 | PF00069 | 0.777 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.789 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.629 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.674 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.647 |
MOD_ProDKin_1 | 568 | 574 | PF00069 | 0.408 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.657 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.596 |
MOD_SUMO_rev_2 | 276 | 286 | PF00179 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 135 | 140 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 452 | 457 | PF01217 | 0.371 |
TRG_DiLeu_BaLyEn_6 | 668 | 673 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 685 | 688 | PF00928 | 0.580 |
TRG_ER_diArg_1 | 227 | 229 | PF00400 | 0.537 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 445 | 448 | PF00400 | 0.506 |
TRG_NLS_MonoExtC_3 | 500 | 506 | PF00514 | 0.588 |
TRG_NLS_MonoExtN_4 | 498 | 505 | PF00514 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 502 | 506 | PF00026 | 0.560 |
TRG_Pf-PMV_PEXEL_1 | 558 | 562 | PF00026 | 0.326 |
TRG_Pf-PMV_PEXEL_1 | 615 | 619 | PF00026 | 0.351 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PA86 | Leptomonas seymouri | 49% | 99% |
A0A0S4JUU1 | Bodo saltans | 31% | 100% |
A0A1X0NZU0 | Trypanosomatidae | 36% | 100% |
A4HEK2 | Leishmania braziliensis | 78% | 100% |
A4I1J6 | Leishmania infantum | 99% | 100% |
Q4Q9U1 | Leishmania major | 92% | 100% |
Q84MA1 | Arabidopsis thaliana | 25% | 100% |