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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XCH5
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0032446 | protein modification by small protein conjugation | 6 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 12 |
GO:0071569 | protein ufmylation | 7 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0006950 | response to stress | 2 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0030162 | regulation of proteolysis | 6 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0032434 | regulation of proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0042176 | regulation of protein catabolic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903050 | regulation of proteolysis involved in protein catabolic process | 7 | 1 |
GO:1990564 | protein polyufmylation | 8 | 1 |
GO:1990592 | protein K69-linked ufmylation | 9 | 1 |
GO:2000058 | regulation of ubiquitin-dependent protein catabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 12 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 12 |
GO:0061666 | UFM1 ligase activity | 5 | 12 |
GO:0071568 | UFM1 transferase activity | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 520 | 524 | PF00656 | 0.337 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 308 | 310 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.437 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 308 | 310 | PF00082 | 0.538 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.241 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 61 | 63 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 494 | 498 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 576 | 580 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 730 | 734 | PF00082 | 0.469 |
CLV_Separin_Metazoa | 195 | 199 | PF03568 | 0.350 |
CLV_Separin_Metazoa | 458 | 462 | PF03568 | 0.519 |
DEG_APCC_DBOX_1 | 585 | 593 | PF00400 | 0.369 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.609 |
DOC_CDC14_PxL_1 | 352 | 360 | PF14671 | 0.466 |
DOC_CYCLIN_RxL_1 | 573 | 583 | PF00134 | 0.446 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 37 | 46 | PF00134 | 0.302 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.310 |
DOC_MAPK_gen_1 | 431 | 437 | PF00069 | 0.625 |
DOC_MAPK_gen_1 | 585 | 592 | PF00069 | 0.517 |
DOC_MAPK_gen_1 | 627 | 637 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 321 | 329 | PF00069 | 0.653 |
DOC_MAPK_MEF2A_6 | 364 | 371 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 39 | 47 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 628 | 637 | PF00069 | 0.419 |
DOC_MAPK_NFAT4_5 | 40 | 48 | PF00069 | 0.394 |
DOC_MIT_MIM_1 | 8 | 16 | PF04212 | 0.417 |
DOC_PP1_RVXF_1 | 511 | 518 | PF00149 | 0.353 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.289 |
DOC_PP2B_LxvP_1 | 449 | 452 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 552 | 555 | PF13499 | 0.465 |
DOC_PP4_FxxP_1 | 622 | 625 | PF00568 | 0.424 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 292 | 296 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.581 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.423 |
DOC_USP7_MATH_1 | 648 | 652 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 94 | 98 | PF00917 | 0.299 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.674 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.436 |
LIG_14-3-3_CanoR_1 | 326 | 330 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 504 | 510 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 532 | 542 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 585 | 590 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 691 | 699 | PF00244 | 0.491 |
LIG_14-3-3_CanoR_1 | 730 | 735 | PF00244 | 0.466 |
LIG_APCC_ABBA_1 | 375 | 380 | PF00400 | 0.524 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.375 |
LIG_BRCT_BRCA1_2 | 146 | 152 | PF00533 | 0.350 |
LIG_eIF4E_1 | 203 | 209 | PF01652 | 0.417 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.279 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.431 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.534 |
LIG_FHA_1 | 665 | 671 | PF00498 | 0.456 |
LIG_FHA_1 | 729 | 735 | PF00498 | 0.564 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.425 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.435 |
LIG_FHA_2 | 578 | 584 | PF00498 | 0.441 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.510 |
LIG_FHA_2 | 723 | 729 | PF00498 | 0.532 |
LIG_GBD_Chelix_1 | 470 | 478 | PF00786 | 0.477 |
LIG_LIR_Apic_2 | 276 | 281 | PF02991 | 0.524 |
LIG_LIR_Apic_2 | 621 | 625 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 175 | 186 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 503 | 512 | PF02991 | 0.435 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.303 |
LIG_LIR_Gen_1 | 632 | 642 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 231 | 237 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 258 | 262 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 503 | 508 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 632 | 637 | PF02991 | 0.539 |
LIG_LYPXL_S_1 | 395 | 399 | PF13949 | 0.551 |
LIG_LYPXL_yS_3 | 396 | 399 | PF13949 | 0.552 |
LIG_NRBOX | 41 | 47 | PF00104 | 0.261 |
LIG_NRBOX | 664 | 670 | PF00104 | 0.405 |
LIG_PCNA_PIPBox_1 | 143 | 152 | PF02747 | 0.302 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.274 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.596 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 634 | 637 | PF00017 | 0.410 |
LIG_SH2_SRC | 117 | 120 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 174 | 177 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.274 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 634 | 637 | PF00017 | 0.508 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.524 |
LIG_SH3_3 | 675 | 681 | PF00018 | 0.356 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.289 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.400 |
LIG_SUMO_SIM_par_1 | 407 | 412 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 614 | 621 | PF11976 | 0.540 |
LIG_SUMO_SIM_par_1 | 731 | 737 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.348 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.350 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.473 |
LIG_TRAF2_1 | 496 | 499 | PF00917 | 0.401 |
LIG_TRAF2_1 | 725 | 728 | PF00917 | 0.467 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.274 |
LIG_UBA3_1 | 377 | 383 | PF00899 | 0.578 |
LIG_UBA3_1 | 589 | 597 | PF00899 | 0.430 |
LIG_WRC_WIRS_1 | 578 | 583 | PF05994 | 0.316 |
LIG_WRC_WIRS_1 | 619 | 624 | PF05994 | 0.451 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.410 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.391 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.735 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.433 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.388 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.435 |
MOD_CK2_1 | 577 | 583 | PF00069 | 0.433 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.477 |
MOD_CK2_1 | 697 | 703 | PF00069 | 0.575 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.501 |
MOD_CK2_1 | 722 | 728 | PF00069 | 0.435 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.332 |
MOD_Cter_Amidation | 306 | 309 | PF01082 | 0.617 |
MOD_GlcNHglycan | 298 | 301 | PF01048 | 0.749 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.607 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.609 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.477 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.562 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.483 |
MOD_GlcNHglycan | 610 | 614 | PF01048 | 0.435 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.402 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.341 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.251 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.594 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.571 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.441 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.596 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.464 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.489 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.446 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.549 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.392 |
MOD_N-GLC_2 | 254 | 256 | PF02516 | 0.278 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.356 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.252 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.255 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.346 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.395 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.374 |
MOD_NEK2_1 | 293 | 298 | PF00069 | 0.635 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.523 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.442 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.512 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.392 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.372 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.373 |
MOD_NEK2_2 | 618 | 623 | PF00069 | 0.422 |
MOD_NEK2_2 | 82 | 87 | PF00069 | 0.346 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.400 |
MOD_PIKK_1 | 173 | 179 | PF00454 | 0.254 |
MOD_PIKK_1 | 566 | 572 | PF00454 | 0.540 |
MOD_PK_1 | 431 | 437 | PF00069 | 0.395 |
MOD_PK_1 | 597 | 603 | PF00069 | 0.459 |
MOD_PK_1 | 646 | 652 | PF00069 | 0.465 |
MOD_PKA_1 | 431 | 437 | PF00069 | 0.497 |
MOD_PKA_1 | 585 | 591 | PF00069 | 0.460 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.632 |
MOD_PKA_2 | 503 | 509 | PF00069 | 0.457 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.476 |
MOD_PKA_2 | 714 | 720 | PF00069 | 0.559 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.403 |
MOD_Plk_1 | 548 | 554 | PF00069 | 0.400 |
MOD_Plk_1 | 597 | 603 | PF00069 | 0.523 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.274 |
MOD_Plk_2-3 | 722 | 728 | PF00069 | 0.468 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.312 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.437 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.326 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.351 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.461 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.482 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.479 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.553 |
MOD_Plk_4 | 664 | 670 | PF00069 | 0.345 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.385 |
MOD_SUMO_for_1 | 60 | 63 | PF00179 | 0.417 |
MOD_SUMO_for_1 | 692 | 695 | PF00179 | 0.480 |
MOD_SUMO_rev_2 | 412 | 422 | PF00179 | 0.427 |
MOD_SUMO_rev_2 | 639 | 648 | PF00179 | 0.523 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.289 |
TRG_DiLeu_BaEn_1 | 400 | 405 | PF01217 | 0.556 |
TRG_DiLeu_BaEn_1 | 5 | 10 | PF01217 | 0.279 |
TRG_DiLeu_BaEn_4 | 100 | 106 | PF01217 | 0.302 |
TRG_DiLeu_BaEn_4 | 194 | 200 | PF01217 | 0.350 |
TRG_DiLeu_BaLyEn_6 | 383 | 388 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 588 | 593 | PF01217 | 0.503 |
TRG_DiLeu_LyEn_5 | 258 | 263 | PF01217 | 0.217 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.552 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.525 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.350 |
TRG_NES_CRM1_1 | 365 | 380 | PF08389 | 0.477 |
TRG_NLS_MonoExtC_3 | 304 | 309 | PF00514 | 0.625 |
TRG_Pf-PMV_PEXEL_1 | 461 | 465 | PF00026 | 0.492 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM39 | Leptomonas seymouri | 67% | 100% |
A0A0S4JTJ6 | Bodo saltans | 35% | 95% |
A0A1X0NLV8 | Trypanosomatidae | 41% | 98% |
A0A422NVV8 | Trypanosoma rangeli | 41% | 99% |
A4HQK2 | Leishmania braziliensis | 82% | 100% |
A4ICC0 | Leishmania infantum | 99% | 100% |
D0A3Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AUB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 99% |
Q4Q075 | Leishmania major | 91% | 100% |
V5AXN4 | Trypanosoma cruzi | 40% | 99% |