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. | yes | 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. | no | 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:0000932 | P-body | 5 | 2 |
GO:0005634 | nucleus | 5 | 8 |
GO:0005737 | cytoplasm | 2 | 8 |
GO:0010494 | cytoplasmic stress granule | 5 | 2 |
GO:0030015 | CCR4-NOT core complex | 3 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0035770 | ribonucleoprotein granule | 3 | 2 |
GO:0036464 | cytoplasmic ribonucleoprotein granule | 4 | 2 |
GO:0043226 | organelle | 2 | 8 |
GO:0043227 | membrane-bounded organelle | 3 | 8 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 8 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 8 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0099080 | supramolecular complex | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
GO:0140535 | intracellular protein-containing complex | 2 | 8 |
Related structures:
AlphaFold database: Q4Q9Q5
Term | Name | Level | Count |
---|---|---|---|
GO:0000289 | nuclear-transcribed mRNA poly(A) tail shortening | 8 | 2 |
GO:0000956 | nuclear-transcribed mRNA catabolic process | 7 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 8 |
GO:0006401 | RNA catabolic process | 5 | 2 |
GO:0006402 | mRNA catabolic process | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009057 | macromolecule catabolic process | 4 | 2 |
GO:0009889 | regulation of biosynthetic process | 4 | 8 |
GO:0009892 | negative regulation of metabolic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0010468 | regulation of gene expression | 5 | 8 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 8 |
GO:0010605 | negative regulation of macromolecule metabolic process | 5 | 2 |
GO:0010629 | negative regulation of gene expression | 6 | 2 |
GO:0016070 | RNA metabolic process | 5 | 2 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 8 |
GO:0019222 | regulation of metabolic process | 3 | 8 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 8 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0048519 | negative regulation of biological process | 3 | 2 |
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:0071704 | organic substance metabolic process | 2 | 2 |
GO:0080090 | regulation of primary metabolic process | 4 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 8 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.580 |
CLV_C14_Caspase3-7 | 20 | 24 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 339 | 343 | PF00656 | 0.641 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.291 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.204 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.749 |
CLV_NRD_NRD_1 | 413 | 415 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.333 |
CLV_PCSK_FUR_1 | 149 | 153 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.333 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.749 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.641 |
CLV_PCSK_KEX2_1 | 49 | 51 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 396 | 398 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 49 | 51 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.864 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.333 |
DEG_SCF_FBW7_1 | 470 | 476 | PF00400 | 0.816 |
DEG_SPOP_SBC_1 | 282 | 286 | PF00917 | 0.687 |
DEG_SPOP_SBC_1 | 456 | 460 | PF00917 | 0.682 |
DEG_SPOP_SBC_1 | 600 | 604 | PF00917 | 0.533 |
DOC_CKS1_1 | 470 | 475 | PF01111 | 0.786 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 508 | 517 | PF00134 | 0.385 |
DOC_CYCLIN_yCln2_LP_2 | 305 | 308 | PF00134 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 461 | 467 | PF00134 | 0.660 |
DOC_MAPK_gen_1 | 154 | 164 | PF00069 | 0.514 |
DOC_MAPK_gen_1 | 226 | 233 | PF00069 | 0.668 |
DOC_MAPK_gen_1 | 72 | 79 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 226 | 233 | PF00069 | 0.630 |
DOC_PP2B_LxvP_1 | 305 | 308 | PF13499 | 0.677 |
DOC_PP4_FxxP_1 | 220 | 223 | PF00568 | 0.537 |
DOC_USP7_MATH_1 | 282 | 286 | PF00917 | 0.791 |
DOC_USP7_MATH_1 | 287 | 291 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 374 | 378 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 449 | 453 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 473 | 477 | PF00917 | 0.808 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.543 |
DOC_USP7_UBL2_3 | 247 | 251 | PF12436 | 0.712 |
DOC_USP7_UBL2_3 | 49 | 53 | PF12436 | 0.533 |
DOC_USP7_UBL2_3 | 496 | 500 | PF12436 | 0.579 |
DOC_USP7_UBL2_3 | 72 | 76 | PF12436 | 0.533 |
DOC_WW_Pin1_4 | 242 | 247 | PF00397 | 0.655 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.764 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 283 | 288 | PF00397 | 0.766 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.812 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.748 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.652 |
LIG_14-3-3_CanoR_1 | 609 | 615 | PF00244 | 0.564 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.591 |
LIG_BIR_III_2 | 532 | 536 | PF00653 | 0.506 |
LIG_BRCT_BRCA1_1 | 345 | 349 | PF00533 | 0.660 |
LIG_BRCT_BRCA1_1 | 610 | 614 | PF00533 | 0.533 |
LIG_EVH1_1 | 485 | 489 | PF00568 | 0.668 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.534 |
LIG_FHA_1 | 254 | 260 | PF00498 | 0.664 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.645 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.722 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.560 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.717 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.741 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.491 |
LIG_FHA_2 | 332 | 338 | PF00498 | 0.672 |
LIG_FHA_2 | 600 | 606 | PF00498 | 0.540 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.515 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.506 |
LIG_Integrin_isoDGR_2 | 147 | 149 | PF01839 | 0.333 |
LIG_LIR_Apic_2 | 218 | 223 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 215 | 225 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 23 | 33 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 549 | 559 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 611 | 617 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 215 | 220 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 23 | 28 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 557 | 563 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 569 | 573 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 611 | 617 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 632 | 636 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.533 |
LIG_PCNA_PIPBox_1 | 553 | 562 | PF02747 | 0.516 |
LIG_PCNA_yPIPBox_3 | 548 | 560 | PF02747 | 0.516 |
LIG_Pex14_2 | 617 | 621 | PF04695 | 0.491 |
LIG_PTB_Apo_2 | 65 | 72 | PF02174 | 0.533 |
LIG_PTB_Phospho_1 | 65 | 71 | PF10480 | 0.533 |
LIG_REV1ctd_RIR_1 | 169 | 177 | PF16727 | 0.537 |
LIG_SH2_NCK_1 | 525 | 529 | PF00017 | 0.533 |
LIG_SH2_SRC | 525 | 528 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 140 | 143 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 536 | 539 | PF00017 | 0.533 |
LIG_SH2_STAT3 | 564 | 567 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 536 | 539 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 573 | 576 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 635 | 638 | PF00017 | 0.564 |
LIG_SH3_1 | 226 | 232 | PF00018 | 0.726 |
LIG_SH3_1 | 396 | 402 | PF00018 | 0.687 |
LIG_SH3_1 | 521 | 527 | PF00018 | 0.533 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.737 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.592 |
LIG_SH3_3 | 382 | 388 | PF00018 | 0.669 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.676 |
LIG_SH3_3 | 435 | 441 | PF00018 | 0.704 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.850 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.617 |
LIG_SH3_3 | 521 | 527 | PF00018 | 0.510 |
LIG_SH3_3 | 532 | 538 | PF00018 | 0.466 |
LIG_SUMO_SIM_anti_2 | 207 | 213 | PF11976 | 0.537 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.607 |
LIG_TRAF2_1 | 392 | 395 | PF00917 | 0.687 |
LIG_WRC_WIRS_1 | 217 | 222 | PF05994 | 0.533 |
LIG_WRC_WIRS_1 | 62 | 67 | PF05994 | 0.537 |
LIG_WRC_WIRS_1 | 88 | 93 | PF05994 | 0.491 |
MOD_CDK_SPK_2 | 242 | 247 | PF00069 | 0.702 |
MOD_CDK_SPK_2 | 266 | 271 | PF00069 | 0.685 |
MOD_CDK_SPK_2 | 495 | 500 | PF00069 | 0.584 |
MOD_CDK_SPxK_1 | 495 | 501 | PF00069 | 0.575 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.703 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.712 |
MOD_CK1_1 | 476 | 482 | PF00069 | 0.617 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.389 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.533 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.677 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.739 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.666 |
MOD_CK2_1 | 36 | 42 | PF00069 | 0.533 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.698 |
MOD_CK2_1 | 599 | 605 | PF00069 | 0.533 |
MOD_Cter_Amidation | 130 | 133 | PF01082 | 0.333 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.302 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.311 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.657 |
MOD_GlcNHglycan | 358 | 361 | PF01048 | 0.511 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.333 |
MOD_GlcNHglycan | 450 | 454 | PF01048 | 0.701 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.767 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.543 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.814 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.755 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.687 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.792 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.834 |
MOD_GSK3_1 | 358 | 365 | PF00069 | 0.558 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.691 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.709 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.545 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.508 |
MOD_N-GLC_1 | 36 | 41 | PF02516 | 0.297 |
MOD_NEK2_1 | 506 | 511 | PF00069 | 0.600 |
MOD_NEK2_1 | 77 | 82 | PF00069 | 0.533 |
MOD_NEK2_2 | 610 | 615 | PF00069 | 0.533 |
MOD_PIKK_1 | 362 | 368 | PF00454 | 0.645 |
MOD_PKA_2 | 608 | 614 | PF00069 | 0.533 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.540 |
MOD_Plk_1 | 336 | 342 | PF00069 | 0.640 |
MOD_Plk_1 | 506 | 512 | PF00069 | 0.325 |
MOD_Plk_2-3 | 185 | 191 | PF00069 | 0.525 |
MOD_Plk_2-3 | 212 | 218 | PF00069 | 0.533 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.599 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.546 |
MOD_Plk_4 | 457 | 463 | PF00069 | 0.724 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.506 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.537 |
MOD_Plk_4 | 610 | 616 | PF00069 | 0.533 |
MOD_ProDKin_1 | 242 | 248 | PF00069 | 0.656 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.684 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.764 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.649 |
MOD_ProDKin_1 | 283 | 289 | PF00069 | 0.763 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.688 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.715 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.810 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.660 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.749 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.643 |
MOD_SUMO_for_1 | 172 | 175 | PF00179 | 0.537 |
MOD_SUMO_for_1 | 48 | 51 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 218 | 227 | PF00179 | 0.674 |
MOD_SUMO_rev_2 | 234 | 243 | PF00179 | 0.684 |
MOD_SUMO_rev_2 | 377 | 383 | PF00179 | 0.752 |
MOD_SUMO_rev_2 | 45 | 55 | PF00179 | 0.533 |
MOD_SUMO_rev_2 | 627 | 636 | PF00179 | 0.491 |
MOD_SUMO_rev_2 | 95 | 100 | PF00179 | 0.533 |
TRG_DiLeu_BaEn_1 | 10 | 15 | PF01217 | 0.491 |
TRG_DiLeu_LyEn_5 | 10 | 15 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 217 | 220 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 551 | 554 | PF00928 | 0.491 |
TRG_ENDOCYTIC_2 | 594 | 597 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 633 | 636 | PF00928 | 0.491 |
TRG_ER_diArg_1 | 149 | 152 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 521 | 524 | PF00400 | 0.533 |
TRG_NES_CRM1_1 | 196 | 212 | PF08389 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IMJ8 | Leptomonas seymouri | 66% | 95% |
A0A3S5H7F0 | Leishmania donovani | 94% | 100% |
A4HE86 | Leishmania braziliensis | 87% | 100% |
A4I1N2 | Leishmania infantum | 94% | 100% |
C9ZK81 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AXR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 99% |