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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AYM3
Term | Name | Level | Count |
---|---|---|---|
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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 240 | 242 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 539 | 541 | PF00675 | 0.504 |
CLV_PCSK_KEX2_1 | 240 | 242 | PF00082 | 0.693 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 539 | 541 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 570 | 572 | PF00082 | 0.467 |
CLV_PCSK_PC1ET2_1 | 570 | 572 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.754 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.366 |
CLV_PCSK_SKI1_1 | 636 | 640 | PF00082 | 0.525 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.402 |
DEG_SCF_FBW7_1 | 164 | 169 | PF00400 | 0.726 |
DOC_CKS1_1 | 387 | 392 | PF01111 | 0.479 |
DOC_CYCLIN_RxL_1 | 382 | 391 | PF00134 | 0.377 |
DOC_CYCLIN_RxL_1 | 435 | 446 | PF00134 | 0.372 |
DOC_CYCLIN_yCln2_LP_2 | 279 | 285 | PF00134 | 0.385 |
DOC_MAPK_DCC_7 | 187 | 196 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 16 | 25 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 438 | 444 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 16 | 25 | PF00069 | 0.465 |
DOC_PP1_RVXF_1 | 133 | 140 | PF00149 | 0.489 |
DOC_PP1_RVXF_1 | 462 | 469 | PF00149 | 0.355 |
DOC_PP1_RVXF_1 | 497 | 504 | PF00149 | 0.342 |
DOC_SPAK_OSR1_1 | 48 | 52 | PF12202 | 0.427 |
DOC_USP7_MATH_1 | 156 | 160 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.380 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.722 |
DOC_WW_Pin1_4 | 209 | 214 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 67 | 72 | PF00397 | 0.427 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 215 | 224 | PF00244 | 0.662 |
LIG_14-3-3_CanoR_1 | 230 | 239 | PF00244 | 0.570 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 276 | 282 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 343 | 351 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 35 | 42 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 438 | 443 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 600 | 605 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 607 | 612 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 636 | 644 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 92 | 97 | PF00244 | 0.340 |
LIG_Actin_WH2_2 | 330 | 345 | PF00022 | 0.367 |
LIG_APCC_ABBA_1 | 7 | 12 | PF00400 | 0.521 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.302 |
LIG_BRCT_BRCA1_1 | 74 | 78 | PF00533 | 0.474 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.189 |
LIG_Clathr_ClatBox_1 | 221 | 225 | PF01394 | 0.738 |
LIG_Clathr_ClatBox_1 | 252 | 256 | PF01394 | 0.543 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.499 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.730 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.664 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.401 |
LIG_FHA_1 | 578 | 584 | PF00498 | 0.499 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.454 |
LIG_FHA_2 | 126 | 132 | PF00498 | 0.510 |
LIG_FHA_2 | 517 | 523 | PF00498 | 0.364 |
LIG_FHA_2 | 542 | 548 | PF00498 | 0.570 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.419 |
LIG_Integrin_isoDGR_2 | 151 | 153 | PF01839 | 0.722 |
LIG_LIR_Gen_1 | 138 | 145 | PF02991 | 0.535 |
LIG_LIR_Gen_1 | 280 | 289 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 336 | 346 | PF02991 | 0.329 |
LIG_LIR_Gen_1 | 409 | 420 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 426 | 437 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 476 | 484 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 529 | 538 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 617 | 627 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 138 | 142 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 280 | 286 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 336 | 341 | PF02991 | 0.332 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 426 | 432 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 472 | 478 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 529 | 533 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 617 | 623 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 633 | 638 | PF02991 | 0.355 |
LIG_MYND_1 | 386 | 390 | PF01753 | 0.480 |
LIG_NRBOX | 412 | 418 | PF00104 | 0.335 |
LIG_PCNA_PIPBox_1 | 628 | 637 | PF02747 | 0.382 |
LIG_PCNA_yPIPBox_3 | 528 | 538 | PF02747 | 0.465 |
LIG_PCNA_yPIPBox_3 | 628 | 636 | PF02747 | 0.384 |
LIG_Pex14_1 | 45 | 49 | PF04695 | 0.427 |
LIG_Pex14_2 | 96 | 100 | PF04695 | 0.302 |
LIG_SH2_CRK | 19 | 23 | PF00017 | 0.322 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.381 |
LIG_SH2_NCK_1 | 244 | 248 | PF00017 | 0.706 |
LIG_SH2_NCK_1 | 401 | 405 | PF00017 | 0.512 |
LIG_SH2_PTP2 | 383 | 386 | PF00017 | 0.431 |
LIG_SH2_SRC | 412 | 415 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.361 |
LIG_SH2_STAP1 | 36 | 40 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 374 | 378 | PF00017 | 0.389 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.369 |
LIG_SH2_STAP1 | 478 | 482 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.532 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 604 | 607 | PF00017 | 0.333 |
LIG_SH3_1 | 311 | 317 | PF00018 | 0.368 |
LIG_SH3_2 | 454 | 459 | PF14604 | 0.405 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.727 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.589 |
LIG_SH3_3 | 311 | 317 | PF00018 | 0.369 |
LIG_SH3_3 | 352 | 358 | PF00018 | 0.431 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.410 |
LIG_SH3_3 | 478 | 484 | PF00018 | 0.397 |
LIG_SH3_3 | 506 | 512 | PF00018 | 0.479 |
LIG_SUMO_SIM_anti_2 | 551 | 557 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 251 | 256 | PF11976 | 0.519 |
LIG_SUMO_SIM_par_1 | 333 | 340 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 394 | 399 | PF11976 | 0.435 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.526 |
LIG_WRC_WIRS_1 | 338 | 343 | PF05994 | 0.426 |
LIG_WRC_WIRS_1 | 515 | 520 | PF05994 | 0.504 |
MOD_CDC14_SPxK_1 | 184 | 187 | PF00782 | 0.644 |
MOD_CDC14_SPxK_1 | 212 | 215 | PF00782 | 0.727 |
MOD_CDK_SPxK_1 | 162 | 168 | PF00069 | 0.734 |
MOD_CDK_SPxK_1 | 181 | 187 | PF00069 | 0.737 |
MOD_CDK_SPxK_1 | 209 | 215 | PF00069 | 0.733 |
MOD_CDK_SPxxK_3 | 198 | 205 | PF00069 | 0.672 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.412 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.640 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.324 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.488 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.406 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.343 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.501 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.439 |
MOD_CK2_1 | 516 | 522 | PF00069 | 0.377 |
MOD_CK2_1 | 634 | 640 | PF00069 | 0.410 |
MOD_DYRK1A_RPxSP_1 | 162 | 166 | PF00069 | 0.671 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.307 |
MOD_GlcNHglycan | 12 | 16 | PF01048 | 0.431 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.708 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.668 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.757 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.743 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.645 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.599 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.506 |
MOD_GlcNHglycan | 36 | 39 | PF01048 | 0.427 |
MOD_GlcNHglycan | 375 | 379 | PF01048 | 0.355 |
MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.375 |
MOD_GlcNHglycan | 53 | 57 | PF01048 | 0.286 |
MOD_GlcNHglycan | 547 | 551 | PF01048 | 0.383 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.470 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.671 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.745 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.472 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.391 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.440 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.309 |
MOD_LATS_1 | 598 | 604 | PF00433 | 0.376 |
MOD_N-GLC_1 | 146 | 151 | PF02516 | 0.648 |
MOD_N-GLC_1 | 256 | 261 | PF02516 | 0.667 |
MOD_N-GLC_1 | 607 | 612 | PF02516 | 0.447 |
MOD_N-GLC_1 | 614 | 619 | PF02516 | 0.471 |
MOD_N-GLC_1 | 96 | 101 | PF02516 | 0.388 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.493 |
MOD_NEK2_1 | 458 | 463 | PF00069 | 0.510 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.365 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.528 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.420 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.372 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.204 |
MOD_NEK2_2 | 630 | 635 | PF00069 | 0.447 |
MOD_NEK2_2 | 72 | 77 | PF00069 | 0.439 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.378 |
MOD_PIKK_1 | 614 | 620 | PF00454 | 0.487 |
MOD_PK_1 | 187 | 193 | PF00069 | 0.764 |
MOD_PK_1 | 607 | 613 | PF00069 | 0.246 |
MOD_PKA_1 | 438 | 444 | PF00069 | 0.365 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.718 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.396 |
MOD_PKA_2 | 438 | 444 | PF00069 | 0.365 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.601 |
MOD_Plk_1 | 290 | 296 | PF00069 | 0.335 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.433 |
MOD_Plk_1 | 523 | 529 | PF00069 | 0.474 |
MOD_Plk_1 | 607 | 613 | PF00069 | 0.445 |
MOD_Plk_1 | 96 | 102 | PF00069 | 0.427 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.467 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.628 |
MOD_Plk_4 | 337 | 343 | PF00069 | 0.422 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.247 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.448 |
MOD_Plk_4 | 438 | 444 | PF00069 | 0.384 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.439 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.667 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.511 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.721 |
MOD_ProDKin_1 | 209 | 215 | PF00069 | 0.623 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.485 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.549 |
MOD_ProDKin_1 | 67 | 73 | PF00069 | 0.427 |
MOD_SUMO_for_1 | 569 | 572 | PF00179 | 0.417 |
TRG_DiLeu_BaEn_2 | 56 | 62 | PF01217 | 0.420 |
TRG_DiLeu_BaLyEn_6 | 311 | 316 | PF01217 | 0.383 |
TRG_DiLeu_BaLyEn_6 | 383 | 388 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 581 | 586 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.392 |
TRG_ER_diArg_1 | 239 | 241 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.383 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.487 |
TRG_NES_CRM1_1 | 406 | 421 | PF08389 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 27 | 32 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7K5 | Leptomonas seymouri | 77% | 97% |
A0A1X0P796 | Trypanosomatidae | 57% | 100% |
A0A3Q8IPI1 | Leishmania donovani | 97% | 100% |
A0A3R7KRV6 | Trypanosoma rangeli | 56% | 100% |
A4HF87 | Leishmania braziliensis | 87% | 100% |
A4I2H0 | Leishmania infantum | 97% | 100% |
C9ZX25 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
Q4Q8U9 | Leishmania major | 95% | 100% |
V5B8Y7 | Trypanosoma cruzi | 57% | 100% |