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: 2 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4I364
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 | 10 |
GO:0008270 | zinc ion binding | 6 | 10 |
GO:0043167 | ion binding | 2 | 10 |
GO:0043169 | cation binding | 3 | 10 |
GO:0046872 | metal ion binding | 4 | 10 |
GO:0046914 | transition metal ion binding | 5 | 10 |
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 | 0.614 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.274 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.274 |
CLV_PCSK_SKI1_1 | 189 | 193 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.384 |
CLV_PCSK_SKI1_1 | 321 | 325 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.484 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.611 |
CLV_PCSK_SKI1_1 | 580 | 584 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.634 |
DEG_APCC_DBOX_1 | 265 | 273 | PF00400 | 0.408 |
DEG_SCF_FBW7_1 | 139 | 144 | PF00400 | 0.366 |
DEG_SPOP_SBC_1 | 141 | 145 | PF00917 | 0.399 |
DOC_CYCLIN_RxL_1 | 474 | 486 | PF00134 | 0.518 |
DOC_CYCLIN_yCln2_LP_2 | 95 | 101 | PF00134 | 0.371 |
DOC_MAPK_MEF2A_6 | 266 | 274 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 30 | 37 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 376 | 385 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 4 | 13 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 66 | 75 | PF00069 | 0.420 |
DOC_PP1_RVXF_1 | 352 | 358 | PF00149 | 0.627 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.497 |
DOC_PP2B_LxvP_1 | 95 | 98 | PF13499 | 0.364 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.399 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.425 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.559 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.398 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 24 | 29 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 444 | 449 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.587 |
LIG_14-3-3_CanoR_1 | 189 | 194 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 400 | 404 | PF00244 | 0.522 |
LIG_14-3-3_CanoR_1 | 580 | 585 | PF00244 | 0.353 |
LIG_Actin_WH2_2 | 484 | 500 | PF00022 | 0.384 |
LIG_APCC_ABBA_1 | 383 | 388 | PF00400 | 0.597 |
LIG_BRCT_BRCA1_1 | 205 | 209 | PF00533 | 0.403 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.518 |
LIG_BRCT_BRCA1_1 | 557 | 561 | PF00533 | 0.486 |
LIG_BRCT_BRCA1_1 | 574 | 578 | PF00533 | 0.293 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.433 |
LIG_Clathr_ClatBox_1 | 559 | 563 | PF01394 | 0.398 |
LIG_deltaCOP1_diTrp_1 | 512 | 515 | PF00928 | 0.424 |
LIG_eIF4E_1 | 205 | 211 | PF01652 | 0.416 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.264 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.307 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.353 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.466 |
LIG_FHA_1 | 530 | 536 | PF00498 | 0.388 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.407 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.323 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.437 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.354 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.578 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.352 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 277 | 287 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 447 | 457 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 558 | 569 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 571 | 581 | PF02991 | 0.350 |
LIG_LIR_Gen_1 | 602 | 611 | PF02991 | 0.622 |
LIG_LIR_Gen_1 | 89 | 99 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 194 | 200 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 277 | 283 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 447 | 452 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 512 | 516 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 571 | 576 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 602 | 607 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 89 | 95 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 96 | 102 | PF02991 | 0.327 |
LIG_LYPXL_SIV_4 | 525 | 533 | PF13949 | 0.384 |
LIG_NRBOX | 552 | 558 | PF00104 | 0.332 |
LIG_Pex14_1 | 584 | 588 | PF04695 | 0.336 |
LIG_Pex14_2 | 578 | 582 | PF04695 | 0.449 |
LIG_Rb_pABgroove_1 | 501 | 509 | PF01858 | 0.347 |
LIG_SH2_CRK | 449 | 453 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.378 |
LIG_SH2_STAP1 | 193 | 197 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 205 | 209 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 307 | 311 | PF00017 | 0.595 |
LIG_SH2_STAP1 | 568 | 572 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.371 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.665 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 482 | 485 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 495 | 498 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 526 | 529 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.320 |
LIG_SH3_2 | 363 | 368 | PF14604 | 0.668 |
LIG_SH3_3 | 158 | 164 | PF00018 | 0.379 |
LIG_SH3_3 | 297 | 303 | PF00018 | 0.737 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.703 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 236 | 243 | PF11976 | 0.300 |
LIG_SUMO_SIM_par_1 | 268 | 273 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 33 | 39 | PF11976 | 0.418 |
LIG_TRAF2_1 | 387 | 390 | PF00917 | 0.718 |
LIG_TYR_ITIM | 97 | 102 | PF00017 | 0.359 |
LIG_TYR_ITSM | 445 | 452 | PF00017 | 0.511 |
LIG_UBA3_1 | 210 | 215 | PF00899 | 0.409 |
LIG_WRC_WIRS_1 | 275 | 280 | PF05994 | 0.324 |
LIG_WRC_WIRS_1 | 601 | 606 | PF05994 | 0.601 |
LIG_WRC_WIRS_1 | 611 | 616 | PF05994 | 0.612 |
MOD_CDC14_SPxK_1 | 27 | 30 | PF00782 | 0.375 |
MOD_CDK_SPxK_1 | 24 | 30 | PF00069 | 0.473 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.390 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.611 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.386 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.416 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.408 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.633 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.719 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.384 |
MOD_CK2_1 | 610 | 616 | PF00069 | 0.595 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.608 |
MOD_GlcNHglycan | 173 | 177 | PF01048 | 0.609 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.600 |
MOD_GlcNHglycan | 388 | 394 | PF01048 | 0.406 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.595 |
MOD_GlcNHglycan | 593 | 596 | PF01048 | 0.330 |
MOD_GSK3_1 | 137 | 144 | PF00069 | 0.377 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.581 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.409 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.395 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.431 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.666 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.358 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.415 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.395 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.303 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.474 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.423 |
MOD_GSK3_1 | 580 | 587 | PF00069 | 0.299 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.331 |
MOD_N-GLC_1 | 156 | 161 | PF02516 | 0.540 |
MOD_N-GLC_1 | 381 | 386 | PF02516 | 0.444 |
MOD_N-GLC_1 | 40 | 45 | PF02516 | 0.579 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.387 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.384 |
MOD_N-GLC_2 | 348 | 350 | PF02516 | 0.390 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.534 |
MOD_NEK2_1 | 142 | 147 | PF00069 | 0.397 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.556 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.405 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.719 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.406 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.492 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.299 |
MOD_NEK2_1 | 533 | 538 | PF00069 | 0.423 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.544 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.391 |
MOD_NEK2_2 | 58 | 63 | PF00069 | 0.442 |
MOD_NEK2_2 | 76 | 81 | PF00069 | 0.379 |
MOD_PIKK_1 | 626 | 632 | PF00454 | 0.636 |
MOD_PKA_2 | 399 | 405 | PF00069 | 0.522 |
MOD_PKA_2 | 542 | 548 | PF00069 | 0.558 |
MOD_PKB_1 | 224 | 232 | PF00069 | 0.339 |
MOD_Plk_1 | 376 | 382 | PF00069 | 0.682 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.378 |
MOD_Plk_1 | 533 | 539 | PF00069 | 0.459 |
MOD_Plk_1 | 584 | 590 | PF00069 | 0.271 |
MOD_Plk_2-3 | 234 | 240 | PF00069 | 0.368 |
MOD_Plk_2-3 | 612 | 618 | PF00069 | 0.631 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.380 |
MOD_Plk_4 | 270 | 276 | PF00069 | 0.377 |
MOD_Plk_4 | 301 | 307 | PF00069 | 0.617 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.643 |
MOD_Plk_4 | 447 | 453 | PF00069 | 0.559 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.658 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.314 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.481 |
MOD_Plk_4 | 533 | 539 | PF00069 | 0.377 |
MOD_Plk_4 | 542 | 548 | PF00069 | 0.613 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.323 |
MOD_Plk_4 | 572 | 578 | PF00069 | 0.258 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.377 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.357 |
MOD_ProDKin_1 | 24 | 30 | PF00069 | 0.556 |
MOD_ProDKin_1 | 444 | 450 | PF00069 | 0.511 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.585 |
TRG_DiLeu_BaEn_1 | 286 | 291 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 197 | 200 | PF00928 | 0.420 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.293 |
TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 123 | 126 | PF00400 | 0.402 |
TRG_ER_diArg_1 | 223 | 226 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 354 | 357 | PF00400 | 0.606 |
TRG_ER_diArg_1 | 439 | 441 | PF00400 | 0.455 |
TRG_NES_CRM1_1 | 551 | 563 | PF08389 | 0.360 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAS2 | Leptomonas seymouri | 56% | 100% |
A0A3Q8IHD5 | Leishmania donovani | 99% | 100% |
A0A3R7MRQ1 | Trypanosoma rangeli | 33% | 97% |
A4HFD1 | Leishmania braziliensis | 75% | 98% |
C9ZKV0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 87% |
E9ACY9 | Leishmania major | 93% | 100% |
E9AYR4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BGA4 | Trypanosoma cruzi | 33% | 93% |