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:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: E9AE62
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 10 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009451 | RNA modification | 5 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016070 | RNA metabolic process | 5 | 10 |
GO:0032259 | methylation | 2 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0043414 | macromolecule methylation | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0008168 | methyltransferase activity | 4 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 10 |
GO:0003676 | nucleic acid binding | 3 | 5 |
GO:0003723 | RNA binding | 4 | 5 |
GO:0005488 | binding | 1 | 5 |
GO:0097159 | organic cyclic compound binding | 2 | 5 |
GO:1901363 | heterocyclic compound binding | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.679 |
CLV_C14_Caspase3-7 | 505 | 509 | PF00656 | 0.638 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.492 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 584 | 586 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.611 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 626 | 628 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 340 | 342 | PF00082 | 0.635 |
CLV_PCSK_PC1ET2_1 | 690 | 692 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.682 |
CLV_Separin_Metazoa | 581 | 585 | PF03568 | 0.559 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.537 |
DEG_SPOP_SBC_1 | 332 | 336 | PF00917 | 0.617 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.739 |
DOC_CYCLIN_yCln2_LP_2 | 590 | 596 | PF00134 | 0.484 |
DOC_MAPK_DCC_7 | 687 | 697 | PF00069 | 0.473 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.509 |
DOC_MAPK_gen_1 | 47 | 53 | PF00069 | 0.596 |
DOC_MAPK_gen_1 | 584 | 591 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 676 | 685 | PF00069 | 0.589 |
DOC_MAPK_gen_1 | 687 | 697 | PF00069 | 0.523 |
DOC_MAPK_MEF2A_6 | 133 | 141 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 466 | 474 | PF00069 | 0.619 |
DOC_MAPK_MEF2A_6 | 690 | 699 | PF00069 | 0.605 |
DOC_PP2B_LxvP_1 | 427 | 430 | PF13499 | 0.648 |
DOC_PP4_FxxP_1 | 163 | 166 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.588 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 487 | 491 | PF00917 | 0.806 |
DOC_USP7_MATH_1 | 493 | 497 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 541 | 545 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.702 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 393 | 398 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 260 | 264 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 480 | 487 | PF00244 | 0.762 |
LIG_14-3-3_CanoR_1 | 666 | 670 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 676 | 685 | PF00244 | 0.450 |
LIG_14-3-3_CanoR_1 | 80 | 89 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.553 |
LIG_Actin_WH2_2 | 134 | 152 | PF00022 | 0.510 |
LIG_Actin_WH2_2 | 517 | 535 | PF00022 | 0.496 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.676 |
LIG_Clathr_ClatBox_1 | 182 | 186 | PF01394 | 0.463 |
LIG_CSL_BTD_1 | 156 | 159 | PF09270 | 0.521 |
LIG_EVH1_2 | 31 | 35 | PF00568 | 0.564 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.768 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.527 |
LIG_FHA_1 | 694 | 700 | PF00498 | 0.599 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.695 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.610 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.542 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.509 |
LIG_FHA_2 | 576 | 582 | PF00498 | 0.777 |
LIG_LIR_Gen_1 | 542 | 553 | PF02991 | 0.575 |
LIG_LIR_Gen_1 | 648 | 656 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 680 | 688 | PF02991 | 0.401 |
LIG_LIR_LC3C_4 | 242 | 247 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 542 | 548 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 639 | 643 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 648 | 653 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 671 | 677 | PF02991 | 0.508 |
LIG_LIR_Nem_3 | 680 | 685 | PF02991 | 0.404 |
LIG_MAD2 | 203 | 211 | PF02301 | 0.490 |
LIG_Pex14_1 | 674 | 678 | PF04695 | 0.476 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.532 |
LIG_Pex14_2 | 678 | 682 | PF04695 | 0.455 |
LIG_PTB_Apo_2 | 171 | 178 | PF02174 | 0.569 |
LIG_SH2_CRK | 529 | 533 | PF00017 | 0.476 |
LIG_SH2_CRK | 545 | 549 | PF00017 | 0.476 |
LIG_SH2_CRK | 640 | 644 | PF00017 | 0.566 |
LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.453 |
LIG_SH2_SRC | 367 | 370 | PF00017 | 0.552 |
LIG_SH2_SRC | 650 | 653 | PF00017 | 0.651 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 547 | 550 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 552 | 555 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 652 | 655 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 684 | 687 | PF00017 | 0.488 |
LIG_SH3_3 | 233 | 239 | PF00018 | 0.724 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.597 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.781 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.687 |
LIG_SUMO_SIM_par_1 | 232 | 238 | PF11976 | 0.506 |
LIG_SUMO_SIM_par_1 | 694 | 700 | PF11976 | 0.599 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.630 |
LIG_UBA3_1 | 517 | 523 | PF00899 | 0.550 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.649 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.567 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.710 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.783 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.792 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.420 |
MOD_CK2_1 | 316 | 322 | PF00069 | 0.545 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.760 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.774 |
MOD_CK2_1 | 659 | 665 | PF00069 | 0.694 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.643 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.675 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.540 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.592 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.760 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.729 |
MOD_GlcNHglycan | 446 | 449 | PF01048 | 0.725 |
MOD_GlcNHglycan | 487 | 490 | PF01048 | 0.787 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.714 |
MOD_GlcNHglycan | 661 | 664 | PF01048 | 0.670 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.681 |
MOD_GSK3_1 | 357 | 364 | PF00069 | 0.651 |
MOD_GSK3_1 | 391 | 398 | PF00069 | 0.758 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.476 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.708 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.707 |
MOD_GSK3_1 | 539 | 546 | PF00069 | 0.479 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.673 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.570 |
MOD_N-GLC_1 | 251 | 256 | PF02516 | 0.455 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.656 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.404 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.550 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.651 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.771 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.464 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.733 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.434 |
MOD_NEK2_2 | 451 | 456 | PF00069 | 0.683 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.668 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.644 |
MOD_PIKK_1 | 384 | 390 | PF00454 | 0.634 |
MOD_PIKK_1 | 395 | 401 | PF00454 | 0.565 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.768 |
MOD_PIKK_1 | 488 | 494 | PF00454 | 0.803 |
MOD_PKA_1 | 584 | 590 | PF00069 | 0.476 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.561 |
MOD_PKA_2 | 575 | 581 | PF00069 | 0.735 |
MOD_PKA_2 | 584 | 590 | PF00069 | 0.539 |
MOD_PKA_2 | 665 | 671 | PF00069 | 0.526 |
MOD_PKA_2 | 678 | 684 | PF00069 | 0.445 |
MOD_PKB_1 | 341 | 349 | PF00069 | 0.718 |
MOD_Plk_1 | 251 | 257 | PF00069 | 0.517 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.574 |
MOD_Plk_2-3 | 37 | 43 | PF00069 | 0.511 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.484 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.573 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.401 |
MOD_Plk_4 | 534 | 540 | PF00069 | 0.476 |
MOD_Plk_4 | 543 | 549 | PF00069 | 0.476 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.548 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.716 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.630 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.664 |
MOD_ProDKin_1 | 393 | 399 | PF00069 | 0.748 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.668 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 401 | 406 | PF01217 | 0.665 |
TRG_DiLeu_BaLyEn_6 | 628 | 633 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.453 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 545 | 548 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 640 | 643 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 650 | 653 | PF00928 | 0.605 |
TRG_ER_diArg_1 | 122 | 125 | PF00400 | 0.636 |
TRG_ER_diArg_1 | 323 | 325 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 341 | 344 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 573 | 576 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 583 | 585 | PF00400 | 0.494 |
TRG_NLS_Bipartite_1 | 323 | 344 | PF00514 | 0.681 |
TRG_Pf-PMV_PEXEL_1 | 324 | 329 | PF00026 | 0.676 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.710 |
TRG_Pf-PMV_PEXEL_1 | 409 | 413 | PF00026 | 0.399 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B6 | Leptomonas seymouri | 44% | 100% |
A0A1X0P1I1 | Trypanosomatidae | 30% | 100% |
A0A3S7X2L4 | Leishmania donovani | 90% | 100% |
A0A422NNK7 | Trypanosoma rangeli | 29% | 100% |
A4HHJ9 | Leishmania braziliensis | 68% | 95% |
C9ZLE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9ALM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
V5DCM2 | Trypanosoma cruzi | 29% | 100% |