| 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: 20 |
| 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. | yes | yes: 8 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 0, no: 7 |
| NetGPI | no | yes: 0, no: 7 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 8 |
| GO:0005737 | cytoplasm | 2 | 8 |
| GO:0030015 | CCR4-NOT core complex | 3 | 8 |
| GO:0032991 | protein-containing complex | 1 | 8 |
| GO:0043226 | organelle | 2 | 8 |
| GO:0043227 | membrane-bounded organelle | 3 | 8 |
| GO:0043229 | intracellular organelle | 3 | 8 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
| GO:0110165 | cellular anatomical entity | 1 | 8 |
| GO:0140535 | intracellular protein-containing complex | 2 | 8 |
| GO:0000932 | P-body | 5 | 1 |
| GO:0010494 | cytoplasmic stress granule | 5 | 1 |
| GO:0035770 | ribonucleoprotein granule | 3 | 1 |
| GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 1 |
| GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
| GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
| GO:0099080 | supramolecular complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H7F0
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006355 | regulation of DNA-templated transcription | 6 | 8 |
| GO:0009889 | regulation of biosynthetic process | 4 | 8 |
| GO:0010468 | regulation of gene expression | 5 | 8 |
| GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 8 |
| GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 8 |
| GO:0019222 | regulation of metabolic process | 3 | 8 |
| GO:0031323 | regulation of cellular metabolic process | 4 | 8 |
| GO:0031326 | regulation of cellular biosynthetic process | 5 | 8 |
| GO:0050789 | regulation of biological process | 2 | 8 |
| GO:0050794 | regulation of cellular process | 3 | 8 |
| GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 8 |
| GO:0051252 | regulation of RNA metabolic process | 5 | 8 |
| GO:0060255 | regulation of macromolecule metabolic process | 4 | 8 |
| GO:0065007 | biological regulation | 1 | 8 |
| GO:0080090 | regulation of primary metabolic process | 4 | 8 |
| GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 8 |
| GO:2001141 | regulation of RNA biosynthetic process | 6 | 8 |
| GO:0000289 | nuclear-transcribed mRNA poly(A) tail shortening | 8 | 1 |
| GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 1 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
| GO:0006401 | RNA catabolic process | 5 | 1 |
| GO:0006402 | mRNA catabolic process | 6 | 1 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009056 | catabolic process | 2 | 1 |
| GO:0009057 | macromolecule catabolic process | 4 | 1 |
| GO:0009892 | negative regulation of metabolic process | 4 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 1 |
| GO:0010629 | negative regulation of gene expression | 6 | 1 |
| GO:0016070 | RNA metabolic process | 5 | 1 |
| GO:0016071 | mRNA metabolic process | 6 | 1 |
| GO:0019439 | aromatic compound catabolic process | 4 | 1 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
| GO:0034655 | nucleobase-containing compound catabolic process | 4 | 1 |
| GO:0043170 | macromolecule metabolic process | 3 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044248 | cellular catabolic process | 3 | 1 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
| GO:0044270 | cellular nitrogen compound catabolic process | 4 | 1 |
| GO:0046483 | heterocycle metabolic process | 3 | 1 |
| GO:0046700 | heterocycle catabolic process | 4 | 1 |
| GO:0048519 | negative regulation of biological process | 3 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0090304 | nucleic acid metabolic process | 4 | 1 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
| GO:1901361 | organic cyclic compound catabolic process | 4 | 1 |
| GO:1901575 | organic substance catabolic process | 3 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.546 |
| CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.504 |
| CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.257 |
| CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.171 |
| CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.555 |
| CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.300 |
| CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.300 |
| CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.300 |
| CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.574 |
| CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.259 |
| CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.301 |
| CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.300 |
| CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.836 |
| CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.300 |
| CLV_PCSK_SKI1_1 | 570 | 574 | PF00082 | 0.300 |
| CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.326 |
| DEG_SCF_FBW7_1 | 463 | 469 | PF00400 | 0.783 |
| DEG_SPOP_SBC_1 | 275 | 279 | PF00917 | 0.566 |
| DEG_SPOP_SBC_1 | 281 | 285 | PF00917 | 0.678 |
| DEG_SPOP_SBC_1 | 449 | 453 | PF00917 | 0.656 |
| DEG_SPOP_SBC_1 | 593 | 597 | PF00917 | 0.500 |
| DOC_CKS1_1 | 463 | 468 | PF01111 | 0.755 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 501 | 510 | PF00134 | 0.351 |
| DOC_CYCLIN_yCln2_LP_2 | 297 | 300 | PF00134 | 0.768 |
| DOC_CYCLIN_yCln2_LP_2 | 454 | 460 | PF00134 | 0.626 |
| DOC_MAPK_gen_1 | 227 | 234 | PF00069 | 0.630 |
| DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.504 |
| DOC_MAPK_MEF2A_6 | 227 | 234 | PF00069 | 0.592 |
| DOC_PP2B_LxvP_1 | 297 | 300 | PF13499 | 0.626 |
| DOC_PP2B_LxvP_1 | 454 | 457 | PF13499 | 0.616 |
| DOC_PP4_FxxP_1 | 221 | 224 | PF00568 | 0.504 |
| DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.723 |
| DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.698 |
| DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.660 |
| DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.500 |
| DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.687 |
| DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.775 |
| DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.510 |
| DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.439 |
| DOC_USP7_UBL2_3 | 248 | 252 | PF12436 | 0.683 |
| DOC_USP7_UBL2_3 | 489 | 493 | PF12436 | 0.541 |
| DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.500 |
| DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.500 |
| DOC_WW_Pin1_4 | 243 | 248 | PF00397 | 0.611 |
| DOC_WW_Pin1_4 | 252 | 257 | PF00397 | 0.622 |
| DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.616 |
| DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.725 |
| DOC_WW_Pin1_4 | 290 | 295 | PF00397 | 0.665 |
| DOC_WW_Pin1_4 | 301 | 306 | PF00397 | 0.694 |
| DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.657 |
| DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.686 |
| DOC_WW_Pin1_4 | 396 | 401 | PF00397 | 0.714 |
| DOC_WW_Pin1_4 | 427 | 432 | PF00397 | 0.629 |
| DOC_WW_Pin1_4 | 459 | 464 | PF00397 | 0.713 |
| DOC_WW_Pin1_4 | 488 | 493 | PF00397 | 0.614 |
| LIG_14-3-3_CanoR_1 | 602 | 608 | PF00244 | 0.512 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.597 |
| LIG_BIR_III_2 | 525 | 529 | PF00653 | 0.505 |
| LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.640 |
| LIG_BRCT_BRCA1_1 | 474 | 478 | PF00533 | 0.537 |
| LIG_BRCT_BRCA1_1 | 603 | 607 | PF00533 | 0.500 |
| LIG_EVH1_1 | 478 | 482 | PF00568 | 0.650 |
| LIG_FHA_1 | 187 | 193 | PF00498 | 0.492 |
| LIG_FHA_1 | 255 | 261 | PF00498 | 0.635 |
| LIG_FHA_1 | 351 | 357 | PF00498 | 0.618 |
| LIG_FHA_1 | 372 | 378 | PF00498 | 0.700 |
| LIG_FHA_1 | 449 | 455 | PF00498 | 0.679 |
| LIG_FHA_1 | 507 | 513 | PF00498 | 0.491 |
| LIG_FHA_2 | 324 | 330 | PF00498 | 0.653 |
| LIG_FHA_2 | 593 | 599 | PF00498 | 0.537 |
| LIG_FHA_2 | 604 | 610 | PF00498 | 0.514 |
| LIG_FHA_2 | 7 | 13 | PF00498 | 0.472 |
| LIG_Integrin_isoDGR_2 | 147 | 149 | PF01839 | 0.300 |
| LIG_LIR_Apic_2 | 219 | 224 | PF02991 | 0.504 |
| LIG_LIR_Gen_1 | 216 | 226 | PF02991 | 0.459 |
| LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.459 |
| LIG_LIR_Gen_1 | 542 | 552 | PF02991 | 0.534 |
| LIG_LIR_Gen_1 | 604 | 610 | PF02991 | 0.514 |
| LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.459 |
| LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.459 |
| LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.569 |
| LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.494 |
| LIG_LIR_Nem_3 | 562 | 566 | PF02991 | 0.500 |
| LIG_LIR_Nem_3 | 604 | 610 | PF02991 | 0.464 |
| LIG_LIR_Nem_3 | 625 | 629 | PF02991 | 0.503 |
| LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.500 |
| LIG_PCNA_PIPBox_1 | 546 | 555 | PF02747 | 0.483 |
| LIG_PCNA_yPIPBox_3 | 541 | 553 | PF02747 | 0.483 |
| LIG_Pex14_2 | 610 | 614 | PF04695 | 0.457 |
| LIG_PTB_Apo_2 | 65 | 72 | PF02174 | 0.500 |
| LIG_PTB_Phospho_1 | 65 | 71 | PF10480 | 0.500 |
| LIG_REV1ctd_RIR_1 | 170 | 178 | PF16727 | 0.504 |
| LIG_SH2_NCK_1 | 518 | 522 | PF00017 | 0.500 |
| LIG_SH2_SRC | 518 | 521 | PF00017 | 0.500 |
| LIG_SH2_STAT3 | 140 | 143 | PF00017 | 0.500 |
| LIG_SH2_STAT3 | 529 | 532 | PF00017 | 0.500 |
| LIG_SH2_STAT3 | 557 | 560 | PF00017 | 0.457 |
| LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.510 |
| LIG_SH2_STAT5 | 566 | 569 | PF00017 | 0.457 |
| LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.500 |
| LIG_SH2_STAT5 | 628 | 631 | PF00017 | 0.519 |
| LIG_SH3_1 | 227 | 233 | PF00018 | 0.590 |
| LIG_SH3_1 | 388 | 394 | PF00018 | 0.651 |
| LIG_SH3_1 | 514 | 520 | PF00018 | 0.500 |
| LIG_SH3_3 | 227 | 233 | PF00018 | 0.603 |
| LIG_SH3_3 | 241 | 247 | PF00018 | 0.567 |
| LIG_SH3_3 | 388 | 394 | PF00018 | 0.734 |
| LIG_SH3_3 | 428 | 434 | PF00018 | 0.686 |
| LIG_SH3_3 | 460 | 466 | PF00018 | 0.815 |
| LIG_SH3_3 | 471 | 477 | PF00018 | 0.585 |
| LIG_SH3_3 | 514 | 520 | PF00018 | 0.491 |
| LIG_SH3_3 | 525 | 531 | PF00018 | 0.433 |
| LIG_SUMO_SIM_anti_2 | 208 | 214 | PF11976 | 0.504 |
| LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.573 |
| LIG_TRAF2_1 | 384 | 387 | PF00917 | 0.657 |
| LIG_WRC_WIRS_1 | 218 | 223 | PF05994 | 0.500 |
| LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.504 |
| LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.457 |
| MOD_CDK_SPK_2 | 243 | 248 | PF00069 | 0.670 |
| MOD_CDK_SPK_2 | 267 | 272 | PF00069 | 0.649 |
| MOD_CDK_SPK_2 | 488 | 493 | PF00069 | 0.545 |
| MOD_CDK_SPxK_1 | 488 | 494 | PF00069 | 0.537 |
| MOD_CDK_SPxxK_3 | 366 | 373 | PF00069 | 0.634 |
| MOD_CK1_1 | 246 | 252 | PF00069 | 0.655 |
| MOD_CK1_1 | 351 | 357 | PF00069 | 0.568 |
| MOD_CK1_1 | 462 | 468 | PF00069 | 0.685 |
| MOD_CK1_1 | 469 | 475 | PF00069 | 0.581 |
| MOD_CK1_1 | 488 | 494 | PF00069 | 0.399 |
| MOD_CK2_1 | 115 | 121 | PF00069 | 0.500 |
| MOD_CK2_1 | 234 | 240 | PF00069 | 0.641 |
| MOD_CK2_1 | 267 | 273 | PF00069 | 0.709 |
| MOD_CK2_1 | 342 | 348 | PF00069 | 0.648 |
| MOD_CK2_1 | 36 | 42 | PF00069 | 0.500 |
| MOD_CK2_1 | 442 | 448 | PF00069 | 0.704 |
| MOD_CK2_1 | 592 | 598 | PF00069 | 0.526 |
| MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.300 |
| MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.271 |
| MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.278 |
| MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.639 |
| MOD_GlcNHglycan | 350 | 353 | PF01048 | 0.479 |
| MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.606 |
| MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.304 |
| MOD_GlcNHglycan | 443 | 447 | PF01048 | 0.676 |
| MOD_GSK3_1 | 213 | 220 | PF00069 | 0.500 |
| MOD_GSK3_1 | 243 | 250 | PF00069 | 0.752 |
| MOD_GSK3_1 | 252 | 259 | PF00069 | 0.687 |
| MOD_GSK3_1 | 262 | 269 | PF00069 | 0.563 |
| MOD_GSK3_1 | 271 | 278 | PF00069 | 0.553 |
| MOD_GSK3_1 | 335 | 342 | PF00069 | 0.817 |
| MOD_GSK3_1 | 350 | 357 | PF00069 | 0.493 |
| MOD_GSK3_1 | 371 | 378 | PF00069 | 0.631 |
| MOD_GSK3_1 | 438 | 445 | PF00069 | 0.566 |
| MOD_GSK3_1 | 462 | 469 | PF00069 | 0.731 |
| MOD_GSK3_1 | 592 | 599 | PF00069 | 0.483 |
| MOD_GSK3_1 | 97 | 104 | PF00069 | 0.474 |
| MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.264 |
| MOD_NEK2_1 | 499 | 504 | PF00069 | 0.578 |
| MOD_NEK2_1 | 77 | 82 | PF00069 | 0.503 |
| MOD_NEK2_2 | 603 | 608 | PF00069 | 0.500 |
| MOD_PIKK_1 | 282 | 288 | PF00454 | 0.577 |
| MOD_PIKK_1 | 354 | 360 | PF00454 | 0.617 |
| MOD_PIKK_1 | 472 | 478 | PF00454 | 0.701 |
| MOD_PKA_2 | 601 | 607 | PF00069 | 0.513 |
| MOD_Plk_1 | 213 | 219 | PF00069 | 0.500 |
| MOD_Plk_1 | 328 | 334 | PF00069 | 0.622 |
| MOD_Plk_1 | 499 | 505 | PF00069 | 0.292 |
| MOD_Plk_2-3 | 186 | 192 | PF00069 | 0.492 |
| MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.500 |
| MOD_Plk_4 | 174 | 180 | PF00069 | 0.504 |
| MOD_Plk_4 | 213 | 219 | PF00069 | 0.500 |
| MOD_Plk_4 | 450 | 456 | PF00069 | 0.695 |
| MOD_Plk_4 | 548 | 554 | PF00069 | 0.472 |
| MOD_Plk_4 | 603 | 609 | PF00069 | 0.500 |
| MOD_Plk_4 | 61 | 67 | PF00069 | 0.504 |
| MOD_ProDKin_1 | 243 | 249 | PF00069 | 0.612 |
| MOD_ProDKin_1 | 252 | 258 | PF00069 | 0.621 |
| MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.616 |
| MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.723 |
| MOD_ProDKin_1 | 290 | 296 | PF00069 | 0.665 |
| MOD_ProDKin_1 | 301 | 307 | PF00069 | 0.694 |
| MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.657 |
| MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.687 |
| MOD_ProDKin_1 | 396 | 402 | PF00069 | 0.713 |
| MOD_ProDKin_1 | 427 | 433 | PF00069 | 0.628 |
| MOD_ProDKin_1 | 459 | 465 | PF00069 | 0.714 |
| MOD_ProDKin_1 | 488 | 494 | PF00069 | 0.605 |
| MOD_SUMO_for_1 | 173 | 176 | PF00179 | 0.504 |
| MOD_SUMO_for_1 | 48 | 51 | PF00179 | 0.500 |
| MOD_SUMO_rev_2 | 219 | 228 | PF00179 | 0.647 |
| MOD_SUMO_rev_2 | 235 | 244 | PF00179 | 0.644 |
| MOD_SUMO_rev_2 | 369 | 375 | PF00179 | 0.723 |
| MOD_SUMO_rev_2 | 380 | 389 | PF00179 | 0.611 |
| MOD_SUMO_rev_2 | 45 | 55 | PF00179 | 0.500 |
| MOD_SUMO_rev_2 | 620 | 629 | PF00179 | 0.457 |
| MOD_SUMO_rev_2 | 95 | 100 | PF00179 | 0.500 |
| TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.457 |
| TRG_DiLeu_LyEn_5 | 10 | 15 | PF01217 | 0.457 |
| TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.457 |
| TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.457 |
| TRG_ENDOCYTIC_2 | 544 | 547 | PF00928 | 0.492 |
| TRG_ENDOCYTIC_2 | 587 | 590 | PF00928 | 0.534 |
| TRG_ENDOCYTIC_2 | 605 | 608 | PF00928 | 0.534 |
| TRG_ENDOCYTIC_2 | 626 | 629 | PF00928 | 0.457 |
| TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.500 |
| TRG_ER_diArg_1 | 514 | 517 | PF00400 | 0.501 |
| TRG_NES_CRM1_1 | 197 | 213 | PF08389 | 0.573 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IMJ8 | Leptomonas seymouri | 68% | 94% |
| A4HE86 | Leishmania braziliensis | 87% | 100% |
| A4I1N2 | Leishmania infantum | 100% | 100% |
| C9ZK81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
| E9AXR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
| Q4Q9Q5 | Leishmania major | 94% | 100% |