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: 8 |
NetGPI | no | yes: 0, no: 8 |
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: A4HHJ9
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 9 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009451 | RNA modification | 5 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0032259 | methylation | 2 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0043414 | macromolecule methylation | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 9 |
GO:0008168 | methyltransferase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 9 |
GO:0003676 | nucleic acid binding | 3 | 4 |
GO:0003723 | RNA binding | 4 | 4 |
GO:0005488 | binding | 1 | 4 |
GO:0097159 | organic cyclic compound binding | 2 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 4 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.520 |
CLV_C14_Caspase3-7 | 608 | 612 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 737 | 741 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.459 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.229 |
CLV_NRD_NRD_1 | 623 | 625 | PF00675 | 0.450 |
CLV_NRD_NRD_1 | 90 | 92 | PF00675 | 0.421 |
CLV_PCSK_KEX2_1 | 365 | 367 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.346 |
CLV_PCSK_KEX2_1 | 623 | 625 | PF00082 | 0.450 |
CLV_PCSK_KEX2_1 | 89 | 91 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 365 | 367 | PF00082 | 0.620 |
CLV_PCSK_PC7_1 | 380 | 386 | PF00082 | 0.445 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.769 |
CLV_PCSK_SKI1_1 | 415 | 419 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.509 |
DEG_APCC_DBOX_1 | 179 | 187 | PF00400 | 0.384 |
DEG_SIAH_1 | 189 | 197 | PF03145 | 0.274 |
DEG_SPOP_SBC_1 | 146 | 150 | PF00917 | 0.436 |
DEG_SPOP_SBC_1 | 549 | 553 | PF00917 | 0.503 |
DOC_CYCLIN_RxL_1 | 412 | 420 | PF00134 | 0.272 |
DOC_CYCLIN_yCln2_LP_2 | 629 | 635 | PF00134 | 0.429 |
DOC_MAPK_gen_1 | 241 | 249 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 623 | 630 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 715 | 724 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 726 | 736 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 89 | 95 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 175 | 183 | PF00069 | 0.450 |
DOC_MAPK_MEF2A_6 | 505 | 513 | PF00069 | 0.528 |
DOC_MAPK_MEF2A_6 | 623 | 630 | PF00069 | 0.298 |
DOC_MAPK_MEF2A_6 | 729 | 738 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 482 | 489 | PF00149 | 0.491 |
DOC_PP4_FxxP_1 | 205 | 208 | PF00568 | 0.424 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.461 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 190 | 194 | PF00917 | 0.395 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.789 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.755 |
DOC_USP7_MATH_1 | 550 | 554 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 707 | 711 | PF00917 | 0.388 |
DOC_USP7_MATH_2 | 396 | 402 | PF00917 | 0.488 |
DOC_USP7_UBL2_3 | 726 | 730 | PF12436 | 0.300 |
DOC_WW_Pin1_4 | 11 | 16 | PF00397 | 0.611 |
DOC_WW_Pin1_4 | 148 | 153 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.340 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.546 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 302 | 306 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 337 | 341 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 383 | 389 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 57 | 64 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 688 | 693 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 697 | 706 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 715 | 724 | PF00244 | 0.358 |
LIG_Actin_WH2_2 | 556 | 574 | PF00022 | 0.441 |
LIG_BIR_III_2 | 49 | 53 | PF00653 | 0.435 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.342 |
LIG_Clathr_ClatBox_1 | 224 | 228 | PF01394 | 0.376 |
LIG_CSL_BTD_1 | 198 | 201 | PF09270 | 0.421 |
LIG_DLG_GKlike_1 | 688 | 695 | PF00625 | 0.381 |
LIG_EH1_1 | 665 | 673 | PF00400 | 0.369 |
LIG_EVH1_2 | 73 | 77 | PF00568 | 0.382 |
LIG_FHA_1 | 348 | 354 | PF00498 | 0.526 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.441 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.482 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.519 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.393 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.711 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.740 |
LIG_LIR_Apic_2 | 125 | 131 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 581 | 592 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 719 | 727 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 565 | 571 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 581 | 587 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 678 | 682 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 710 | 716 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 719 | 724 | PF02991 | 0.326 |
LIG_MAD2 | 245 | 253 | PF02301 | 0.423 |
LIG_PCNA_PIPBox_1 | 20 | 29 | PF02747 | 0.453 |
LIG_PCNA_yPIPBox_3 | 20 | 28 | PF02747 | 0.455 |
LIG_Pex14_1 | 713 | 717 | PF04695 | 0.379 |
LIG_Pex14_2 | 205 | 209 | PF04695 | 0.381 |
LIG_Pex14_2 | 717 | 721 | PF04695 | 0.363 |
LIG_SH2_CRK | 568 | 572 | PF00017 | 0.435 |
LIG_SH2_CRK | 584 | 588 | PF00017 | 0.480 |
LIG_SH2_CRK | 679 | 683 | PF00017 | 0.453 |
LIG_SH2_PTP2 | 689 | 692 | PF00017 | 0.377 |
LIG_SH2_PTP2 | 92 | 95 | PF00017 | 0.358 |
LIG_SH2_SRC | 409 | 412 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 413 | 417 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 406 | 409 | PF00017 | 0.279 |
LIG_SH2_STAT5 | 586 | 589 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 689 | 692 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 723 | 726 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.372 |
LIG_SH3_3 | 108 | 114 | PF00018 | 0.433 |
LIG_SH3_3 | 276 | 282 | PF00018 | 0.700 |
LIG_SH3_3 | 321 | 327 | PF00018 | 0.446 |
LIG_SH3_3 | 405 | 411 | PF00018 | 0.533 |
LIG_SH3_3 | 625 | 631 | PF00018 | 0.498 |
LIG_TRAF2_1 | 361 | 364 | PF00917 | 0.349 |
LIG_TRAF2_1 | 636 | 639 | PF00917 | 0.342 |
LIG_TYR_ITAM | 565 | 587 | PF00017 | 0.380 |
LIG_WRC_WIRS_1 | 533 | 538 | PF05994 | 0.506 |
LIG_WW_1 | 403 | 406 | PF00397 | 0.357 |
MOD_CDK_SPxK_1 | 148 | 154 | PF00069 | 0.449 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.673 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.562 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.596 |
MOD_CK1_1 | 541 | 547 | PF00069 | 0.749 |
MOD_CK1_1 | 552 | 558 | PF00069 | 0.387 |
MOD_CK1_1 | 614 | 620 | PF00069 | 0.681 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.479 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.437 |
MOD_CK2_1 | 358 | 364 | PF00069 | 0.385 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.461 |
MOD_CK2_1 | 517 | 523 | PF00069 | 0.720 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.594 |
MOD_CK2_1 | 698 | 704 | PF00069 | 0.533 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.392 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.668 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.430 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.526 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.681 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.694 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.646 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.641 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.287 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.548 |
MOD_GlcNHglycan | 700 | 703 | PF01048 | 0.608 |
MOD_GlcNHglycan | 740 | 744 | PF01048 | 0.470 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.545 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.601 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.377 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.765 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.518 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.417 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.559 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.530 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.404 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.704 |
MOD_GSK3_1 | 527 | 534 | PF00069 | 0.723 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.731 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.577 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.460 |
MOD_LATS_1 | 686 | 692 | PF00433 | 0.385 |
MOD_N-GLC_1 | 293 | 298 | PF02516 | 0.351 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.336 |
MOD_N-GLC_1 | 477 | 482 | PF02516 | 0.530 |
MOD_NEK2_1 | 122 | 127 | PF00069 | 0.539 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.436 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.486 |
MOD_NEK2_1 | 347 | 352 | PF00069 | 0.548 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.270 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.770 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.485 |
MOD_NEK2_1 | 695 | 700 | PF00069 | 0.418 |
MOD_NEK2_1 | 717 | 722 | PF00069 | 0.352 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.294 |
MOD_NEK2_2 | 532 | 537 | PF00069 | 0.504 |
MOD_OFUCOSY | 33 | 39 | PF10250 | 0.434 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.654 |
MOD_PIKK_1 | 319 | 325 | PF00454 | 0.608 |
MOD_PIKK_1 | 527 | 533 | PF00454 | 0.750 |
MOD_PKA_1 | 383 | 389 | PF00069 | 0.453 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.491 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.337 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.461 |
MOD_PKA_2 | 717 | 723 | PF00069 | 0.335 |
MOD_Plk_1 | 123 | 129 | PF00069 | 0.412 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.472 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.392 |
MOD_Plk_1 | 640 | 646 | PF00069 | 0.483 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.530 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.549 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.406 |
MOD_Plk_4 | 349 | 355 | PF00069 | 0.478 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.295 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.338 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.459 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.449 |
MOD_Plk_4 | 717 | 723 | PF00069 | 0.463 |
MOD_ProDKin_1 | 11 | 17 | PF00069 | 0.611 |
MOD_ProDKin_1 | 148 | 154 | PF00069 | 0.637 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.337 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.564 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.647 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.543 |
MOD_SUMO_rev_2 | 132 | 137 | PF00179 | 0.365 |
MOD_SUMO_rev_2 | 634 | 644 | PF00179 | 0.450 |
TRG_DiLeu_BaEn_4 | 363 | 369 | PF01217 | 0.347 |
TRG_DiLeu_BaLyEn_6 | 279 | 284 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 440 | 445 | PF01217 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 667 | 672 | PF01217 | 0.502 |
TRG_ENDOCYTIC_2 | 568 | 571 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 584 | 587 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 679 | 682 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 689 | 692 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 92 | 95 | PF00928 | 0.358 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 383 | 385 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 593 | 595 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 622 | 624 | PF00400 | 0.423 |
TRG_ER_diArg_1 | 89 | 91 | PF00400 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.459 |
TRG_Pf-PMV_PEXEL_1 | 366 | 371 | PF00026 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 448 | 452 | PF00026 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 81 | 85 | PF00026 | 0.509 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5B6 | Leptomonas seymouri | 43% | 100% |
A0A1X0P1I1 | Trypanosomatidae | 32% | 100% |
A0A3S7X2L4 | Leishmania donovani | 69% | 100% |
A0A422NNK7 | Trypanosoma rangeli | 33% | 100% |
E9AE62 | Leishmania major | 68% | 100% |
E9ALM3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |
V5DCM2 | Trypanosoma cruzi | 31% | 100% |