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 | yes | yes: 7, no: 1 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
GO:0005737 | cytoplasm | 2 | 1 |
Related structures:
AlphaFold database: A0A3Q8IHD5
Term | Name | Level | Count |
---|---|---|---|
GO:0000209 | protein polyubiquitination | 8 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 9 |
GO:0008270 | zinc ion binding | 6 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043169 | cation binding | 3 | 9 |
GO:0046872 | metal ion binding | 4 | 9 |
GO:0046914 | transition metal ion binding | 5 | 9 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.698 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.328 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.325 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.676 |
DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.438 |
DEG_SCF_FBW7_1 | 139 | 144 | PF00400 | 0.432 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.427 |
DOC_CYCLIN_RxL_1 | 474 | 486 | PF00134 | 0.598 |
DOC_CYCLIN_yCln2_LP_2 | 95 | 101 | PF00134 | 0.385 |
DOC_MAPK_MEF2A_6 | 266 | 274 | PF00069 | 0.438 |
DOC_MAPK_MEF2A_6 | 30 | 37 | PF00069 | 0.377 |
DOC_MAPK_MEF2A_6 | 376 | 385 | PF00069 | 0.636 |
DOC_MAPK_MEF2A_6 | 66 | 75 | PF00069 | 0.445 |
DOC_PP1_RVXF_1 | 352 | 358 | PF00149 | 0.704 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.525 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.382 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 6 | 10 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.452 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.602 |
LIG_14-3-3_CanoR_1 | 189 | 194 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 580 | 585 | PF00244 | 0.397 |
LIG_Actin_WH2_2 | 484 | 500 | PF00022 | 0.492 |
LIG_APCC_ABBA_1 | 383 | 388 | PF00400 | 0.633 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.424 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.598 |
LIG_BRCT_BRCA1_1 | 557 | 561 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 574 | 578 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.390 |
LIG_Clathr_ClatBox_1 | 559 | 563 | PF01394 | 0.438 |
LIG_deltaCOP1_diTrp_1 | 512 | 515 | PF00928 | 0.451 |
LIG_eIF4E_1 | 205 | 211 | PF01652 | 0.431 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.294 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.517 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.357 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.514 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.421 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.473 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.356 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.467 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.400 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.633 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.398 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 277 | 287 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 447 | 457 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 558 | 569 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 571 | 581 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 602 | 611 | PF02991 | 0.692 |
LIG_LIR_Gen_1 | 89 | 99 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 512 | 516 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 571 | 576 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 602 | 607 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.346 |
LIG_LYPXL_SIV_4 | 525 | 533 | PF13949 | 0.492 |
LIG_NRBOX | 552 | 558 | PF00104 | 0.422 |
LIG_Pex14_1 | 584 | 588 | PF04695 | 0.342 |
LIG_Pex14_2 | 578 | 582 | PF04695 | 0.517 |
LIG_Rb_pABgroove_1 | 501 | 509 | PF01858 | 0.405 |
LIG_SH2_CRK | 449 | 453 | PF00017 | 0.592 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.314 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.705 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.659 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.500 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.338 |
LIG_SH3_2 | 363 | 368 | PF14604 | 0.739 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.384 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.771 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.745 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.614 |
LIG_SUMO_SIM_anti_2 | 236 | 243 | PF11976 | 0.346 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 268 | 273 | PF11976 | 0.492 |
LIG_SUMO_SIM_par_1 | 33 | 39 | PF11976 | 0.431 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.743 |
LIG_TYR_ITIM | 97 | 102 | PF00017 | 0.428 |
LIG_TYR_ITSM | 445 | 452 | PF00017 | 0.559 |
LIG_UBA3_1 | 210 | 215 | PF00899 | 0.427 |
LIG_WRC_WIRS_1 | 275 | 280 | PF05994 | 0.395 |
LIG_WRC_WIRS_1 | 601 | 606 | PF05994 | 0.706 |
LIG_WRC_WIRS_1 | 611 | 616 | PF05994 | 0.661 |
MOD_CDC14_SPxK_1 | 27 | 30 | PF00782 | 0.401 |
MOD_CDK_SPxK_1 | 24 | 30 | PF00069 | 0.516 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.460 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.637 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.445 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.499 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.418 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.711 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.748 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.492 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.664 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.648 |
MOD_GlcNHglycan | 173 | 177 | PF01048 | 0.615 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.625 |
MOD_GlcNHglycan | 388 | 394 | PF01048 | 0.470 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.633 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.429 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.427 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.688 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.465 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.404 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.482 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.739 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.404 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.375 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.478 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.376 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.546 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.383 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.429 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.384 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.586 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.505 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.623 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.398 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.492 |
MOD_N-GLC_2 | 348 | 350 | PF02516 | 0.482 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.567 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.412 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.555 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.457 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.751 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.457 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.492 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.427 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.420 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.562 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.387 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.509 |
MOD_NEK2_2 | 76 | 81 | PF00069 | 0.462 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.689 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.542 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.652 |
MOD_PKB_1 | 224 | 232 | PF00069 | 0.403 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.750 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.423 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.478 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.325 |
MOD_Plk_2-3 | 234 | 240 | PF00069 | 0.448 |
MOD_Plk_2-3 | 612 | 618 | PF00069 | 0.728 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.405 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.427 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.713 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.706 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.623 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.698 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.398 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.470 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.412 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.669 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.384 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.356 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.585 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.460 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.389 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.673 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.558 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.601 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.654 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.335 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.440 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.559 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.431 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.717 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 439 | 441 | PF00400 | 0.510 |
TRG_NES_CRM1_1 | 551 | 563 | PF08389 | 0.444 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAS2 | Leptomonas seymouri | 56% | 100% |
A0A3R7MRQ1 | Trypanosoma rangeli | 33% | 97% |
A4HFD1 | Leishmania braziliensis | 75% | 98% |
A4I364 | Leishmania infantum | 99% | 100% |
E9ACY9 | Leishmania major | 93% | 100% |
E9AYR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BGA4 | Trypanosoma cruzi | 33% | 93% |