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 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ALM3
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 | 240 | 244 | PF00656 | 0.346 |
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 198 | 200 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 448 | 450 | PF00675 | 0.727 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.287 |
CLV_NRD_NRD_1 | 619 | 621 | PF00675 | 0.610 |
CLV_PCSK_KEX2_1 | 124 | 126 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 318 | 320 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.547 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.607 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 619 | 621 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 683 | 685 | PF00082 | 0.437 |
CLV_PCSK_PC1ET2_1 | 124 | 126 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 335 | 337 | PF00082 | 0.623 |
CLV_PCSK_PC1ET2_1 | 683 | 685 | PF00082 | 0.437 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 548 | 552 | PF00082 | 0.287 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.396 |
CLV_Separin_Metazoa | 574 | 578 | PF03568 | 0.533 |
DEG_APCC_DBOX_1 | 137 | 145 | PF00400 | 0.531 |
DEG_SPOP_SBC_1 | 438 | 442 | PF00917 | 0.500 |
DOC_CKS1_1 | 388 | 393 | PF01111 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 583 | 589 | PF00134 | 0.502 |
DOC_MAPK_gen_1 | 199 | 207 | PF00069 | 0.506 |
DOC_MAPK_gen_1 | 47 | 53 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 133 | 141 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 459 | 467 | PF00069 | 0.624 |
DOC_PP4_FxxP_1 | 163 | 166 | PF00568 | 0.486 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.341 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.673 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.479 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.825 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 512 | 516 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 688 | 692 | PF00917 | 0.489 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 487 | 492 | PF00397 | 0.783 |
DOC_WW_Pin1_4 | 499 | 504 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 103 | 112 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 133 | 137 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 260 | 264 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 432 | 436 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 567 | 576 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 577 | 585 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 669 | 678 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 80 | 89 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 93 | 99 | PF00244 | 0.523 |
LIG_Actin_WH2_2 | 510 | 528 | PF00022 | 0.496 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.684 |
LIG_Clathr_ClatBox_1 | 182 | 186 | PF01394 | 0.464 |
LIG_CSL_BTD_1 | 156 | 159 | PF09270 | 0.505 |
LIG_EVH1_2 | 31 | 35 | PF00568 | 0.526 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.521 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.693 |
LIG_FHA_2 | 312 | 318 | PF00498 | 0.434 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.747 |
LIG_LIR_Gen_1 | 535 | 546 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 641 | 649 | PF02991 | 0.658 |
LIG_LIR_Gen_1 | 673 | 681 | PF02991 | 0.389 |
LIG_LIR_LC3C_4 | 243 | 247 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 632 | 636 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 641 | 646 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 664 | 670 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 673 | 678 | PF02991 | 0.384 |
LIG_MAD2 | 203 | 211 | PF02301 | 0.489 |
LIG_Pex14_1 | 667 | 671 | PF04695 | 0.482 |
LIG_Pex14_2 | 163 | 167 | PF04695 | 0.528 |
LIG_Pex14_2 | 671 | 675 | PF04695 | 0.427 |
LIG_PTB_Apo_2 | 171 | 178 | PF02174 | 0.575 |
LIG_SH2_CRK | 522 | 526 | PF00017 | 0.476 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.476 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.568 |
LIG_SH2_PTP2 | 50 | 53 | PF00017 | 0.432 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.522 |
LIG_SH2_SRC | 643 | 646 | PF00017 | 0.648 |
LIG_SH2_STAP1 | 589 | 593 | PF00017 | 0.602 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 540 | 543 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 545 | 548 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 645 | 648 | PF00017 | 0.727 |
LIG_SH2_STAT5 | 677 | 680 | PF00017 | 0.488 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.526 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.651 |
LIG_SH3_3 | 579 | 585 | PF00018 | 0.539 |
LIG_Sin3_3 | 579 | 586 | PF02671 | 0.382 |
LIG_TRAF2_1 | 88 | 91 | PF00917 | 0.598 |
LIG_UBA3_1 | 510 | 516 | PF00899 | 0.550 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.704 |
MOD_CK1_1 | 232 | 238 | PF00069 | 0.681 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.542 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.760 |
MOD_CK1_1 | 504 | 510 | PF00069 | 0.616 |
MOD_CK1_1 | 568 | 574 | PF00069 | 0.703 |
MOD_CK1_1 | 603 | 609 | PF00069 | 0.507 |
MOD_CK2_1 | 311 | 317 | PF00069 | 0.432 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.744 |
MOD_CK2_1 | 652 | 658 | PF00069 | 0.708 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.629 |
MOD_GlcNHglycan | 17 | 20 | PF01048 | 0.597 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.613 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.534 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.449 |
MOD_GlcNHglycan | 337 | 341 | PF01048 | 0.738 |
MOD_GlcNHglycan | 442 | 445 | PF01048 | 0.722 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.632 |
MOD_GlcNHglycan | 506 | 509 | PF01048 | 0.679 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.699 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.696 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.666 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.641 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.740 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.467 |
MOD_GSK3_1 | 427 | 434 | PF00069 | 0.467 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.754 |
MOD_GSK3_1 | 476 | 483 | PF00069 | 0.774 |
MOD_GSK3_1 | 487 | 494 | PF00069 | 0.798 |
MOD_GSK3_1 | 495 | 502 | PF00069 | 0.708 |
MOD_GSK3_1 | 532 | 539 | PF00069 | 0.479 |
MOD_GSK3_1 | 596 | 603 | PF00069 | 0.497 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.635 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.508 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.582 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.581 |
MOD_N-GLC_1 | 603 | 608 | PF02516 | 0.597 |
MOD_NEK2_1 | 178 | 183 | PF00069 | 0.398 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.533 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.561 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.804 |
MOD_NEK2_1 | 670 | 675 | PF00069 | 0.444 |
MOD_NEK2_1 | 81 | 86 | PF00069 | 0.713 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.570 |
MOD_NEK2_2 | 444 | 449 | PF00069 | 0.692 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.670 |
MOD_PIKK_1 | 379 | 385 | PF00454 | 0.626 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.823 |
MOD_PKA_2 | 132 | 138 | PF00069 | 0.578 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.549 |
MOD_PKA_2 | 431 | 437 | PF00069 | 0.714 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.663 |
MOD_PKB_1 | 336 | 344 | PF00069 | 0.710 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.444 |
MOD_Plk_1 | 603 | 609 | PF00069 | 0.548 |
MOD_Plk_4 | 132 | 138 | PF00069 | 0.461 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.461 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.537 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.401 |
MOD_Plk_4 | 527 | 533 | PF00069 | 0.476 |
MOD_Plk_4 | 536 | 542 | PF00069 | 0.476 |
MOD_Plk_4 | 671 | 677 | PF00069 | 0.527 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.711 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.703 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.673 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.579 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.683 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.673 |
MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.616 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.529 |
MOD_ProDKin_1 | 487 | 493 | PF00069 | 0.784 |
MOD_ProDKin_1 | 499 | 505 | PF00069 | 0.705 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.593 |
MOD_SUMO_rev_2 | 588 | 598 | PF00179 | 0.638 |
TRG_DiLeu_BaLyEn_6 | 394 | 399 | PF01217 | 0.646 |
TRG_DiLeu_BaLyEn_6 | 621 | 626 | PF01217 | 0.635 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.424 |
TRG_ENDOCYTIC_2 | 522 | 525 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.476 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.532 |
TRG_ENDOCYTIC_2 | 643 | 646 | PF00928 | 0.602 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.508 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.514 |
TRG_ER_diArg_1 | 547 | 549 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 567 | 570 | PF00400 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 319 | 324 | PF00026 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 39 | 43 | PF00026 | 0.677 |
TRG_Pf-PMV_PEXEL_1 | 402 | 406 | PF00026 | 0.402 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B6 | Leptomonas seymouri | 45% | 100% |
A0A1X0P1I1 | Trypanosomatidae | 33% | 100% |
A0A3S7X2L4 | Leishmania donovani | 88% | 100% |
A0A422NNK7 | Trypanosoma rangeli | 31% | 100% |
A4HHJ9 | Leishmania braziliensis | 68% | 100% |
C9ZLE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AE62 | Leishmania major | 86% | 100% |
V5DCM2 | Trypanosoma cruzi | 30% | 100% |