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:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9B2L0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.568 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.647 |
CLV_NRD_NRD_1 | 221 | 223 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 523 | 525 | PF00675 | 0.656 |
CLV_NRD_NRD_1 | 560 | 562 | PF00675 | 0.641 |
CLV_NRD_NRD_1 | 564 | 566 | PF00675 | 0.647 |
CLV_PCSK_FUR_1 | 112 | 116 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.403 |
CLV_PCSK_KEX2_1 | 290 | 292 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 436 | 438 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.629 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 133 | 135 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 290 | 292 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 436 | 438 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 521 | 523 | PF00082 | 0.629 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.577 |
CLV_PCSK_PC7_1 | 286 | 292 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.539 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.734 |
DEG_APCC_DBOX_1 | 72 | 80 | PF00400 | 0.428 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.508 |
DEG_SPOP_SBC_1 | 305 | 309 | PF00917 | 0.706 |
DOC_CYCLIN_RxL_1 | 142 | 149 | PF00134 | 0.388 |
DOC_CYCLIN_yCln2_LP_2 | 281 | 284 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 251 | 261 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 273 | 281 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 254 | 261 | PF00069 | 0.462 |
DOC_MAPK_MEF2A_6 | 407 | 416 | PF00069 | 0.553 |
DOC_MAPK_NFAT4_5 | 254 | 262 | PF00069 | 0.467 |
DOC_PP1_RVXF_1 | 69 | 75 | PF00149 | 0.498 |
DOC_PP2B_LxvP_1 | 281 | 284 | PF13499 | 0.528 |
DOC_PP4_MxPP_1 | 439 | 442 | PF00568 | 0.573 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.746 |
DOC_USP7_MATH_1 | 329 | 333 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 505 | 509 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.594 |
LIG_14-3-3_CanoR_1 | 145 | 155 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 22 | 30 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 32 | 41 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 393 | 399 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 415 | 422 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 445 | 451 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 511 | 519 | PF00244 | 0.605 |
LIG_14-3-3_CanoR_1 | 537 | 542 | PF00244 | 0.553 |
LIG_Actin_WH2_2 | 432 | 447 | PF00022 | 0.587 |
LIG_AP_GAE_1 | 548 | 554 | PF02883 | 0.540 |
LIG_AP2alpha_2 | 349 | 351 | PF02296 | 0.374 |
LIG_BIR_III_4 | 102 | 106 | PF00653 | 0.544 |
LIG_BRCT_BRCA1_1 | 233 | 237 | PF00533 | 0.423 |
LIG_BRCT_BRCA1_1 | 363 | 367 | PF00533 | 0.407 |
LIG_deltaCOP1_diTrp_1 | 479 | 488 | PF00928 | 0.649 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.468 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.397 |
LIG_FHA_1 | 445 | 451 | PF00498 | 0.617 |
LIG_FHA_1 | 557 | 563 | PF00498 | 0.599 |
LIG_FHA_2 | 382 | 388 | PF00498 | 0.424 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.331 |
LIG_LIR_Apic_2 | 361 | 366 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 364 | 374 | PF02991 | 0.415 |
LIG_LIR_Gen_1 | 548 | 557 | PF02991 | 0.522 |
LIG_LIR_LC3C_4 | 40 | 44 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 364 | 370 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 399 | 405 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 548 | 554 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.297 |
LIG_MAD2 | 433 | 441 | PF02301 | 0.367 |
LIG_MLH1_MIPbox_1 | 233 | 237 | PF16413 | 0.423 |
LIG_PCNA_yPIPBox_3 | 265 | 275 | PF02747 | 0.416 |
LIG_PTAP_UEV_1 | 12 | 17 | PF05743 | 0.462 |
LIG_SH2_CRK | 363 | 367 | PF00017 | 0.391 |
LIG_SH2_GRB2like | 129 | 132 | PF00017 | 0.354 |
LIG_SH2_NCK_1 | 140 | 144 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 363 | 367 | PF00017 | 0.476 |
LIG_SH2_NCK_1 | 459 | 463 | PF00017 | 0.565 |
LIG_SH2_SRC | 140 | 143 | PF00017 | 0.421 |
LIG_SH2_SRC | 160 | 163 | PF00017 | 0.445 |
LIG_SH2_STAP1 | 547 | 551 | PF00017 | 0.573 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.354 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 236 | 239 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.367 |
LIG_SH3_3 | 10 | 16 | PF00018 | 0.507 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.612 |
LIG_SUMO_SIM_anti_2 | 277 | 283 | PF11976 | 0.553 |
LIG_SUMO_SIM_anti_2 | 40 | 46 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 39 | 46 | PF11976 | 0.402 |
LIG_TRAF2_1 | 468 | 471 | PF00917 | 0.613 |
LIG_TRAF2_1 | 57 | 60 | PF00917 | 0.472 |
LIG_TYR_ITIM | 138 | 143 | PF00017 | 0.340 |
LIG_TYR_ITIM | 62 | 67 | PF00017 | 0.498 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.656 |
MOD_CK1_1 | 361 | 367 | PF00069 | 0.384 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.703 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.666 |
MOD_CK2_1 | 307 | 313 | PF00069 | 0.631 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.398 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.565 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.346 |
MOD_Cter_Amidation | 563 | 566 | PF01082 | 0.563 |
MOD_GlcNHglycan | 12 | 16 | PF01048 | 0.536 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.526 |
MOD_GlcNHglycan | 185 | 188 | PF01048 | 0.676 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.617 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.660 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.682 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.542 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.631 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.547 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.626 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.542 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.627 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.554 |
MOD_LATS_1 | 413 | 419 | PF00433 | 0.603 |
MOD_N-GLC_1 | 320 | 325 | PF02516 | 0.671 |
MOD_N-GLC_1 | 445 | 450 | PF02516 | 0.520 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.413 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.597 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.483 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.399 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.310 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.322 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.383 |
MOD_NEK2_1 | 444 | 449 | PF00069 | 0.582 |
MOD_NEK2_1 | 453 | 458 | PF00069 | 0.598 |
MOD_NEK2_1 | 488 | 493 | PF00069 | 0.609 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.527 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.623 |
MOD_NEK2_2 | 358 | 363 | PF00069 | 0.367 |
MOD_OFUCOSY | 230 | 235 | PF10250 | 0.482 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.745 |
MOD_PIKK_1 | 415 | 421 | PF00454 | 0.606 |
MOD_PIKK_1 | 466 | 472 | PF00454 | 0.752 |
MOD_PKA_1 | 523 | 529 | PF00069 | 0.568 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.426 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.445 |
MOD_PKA_2 | 394 | 400 | PF00069 | 0.587 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.612 |
MOD_PKA_2 | 488 | 494 | PF00069 | 0.607 |
MOD_PKA_2 | 510 | 516 | PF00069 | 0.720 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.488 |
MOD_PKB_1 | 522 | 530 | PF00069 | 0.686 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.598 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.300 |
MOD_Plk_1 | 445 | 451 | PF00069 | 0.697 |
MOD_Plk_1 | 505 | 511 | PF00069 | 0.724 |
MOD_Plk_2-3 | 381 | 387 | PF00069 | 0.535 |
MOD_Plk_2-3 | 54 | 60 | PF00069 | 0.389 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.563 |
MOD_Plk_4 | 358 | 364 | PF00069 | 0.492 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.339 |
MOD_Plk_4 | 372 | 378 | PF00069 | 0.442 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.590 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.585 |
TRG_DiLeu_BaEn_1 | 274 | 279 | PF01217 | 0.543 |
TRG_DiLeu_BaEn_1 | 482 | 487 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 142 | 147 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 140 | 143 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.444 |
TRG_ENDOCYTIC_2 | 30 | 33 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.367 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.403 |
TRG_ER_diArg_1 | 392 | 395 | PF00400 | 0.596 |
TRG_ER_diArg_1 | 522 | 524 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 560 | 563 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 71 | 74 | PF00400 | 0.494 |
TRG_NLS_MonoCore_2 | 520 | 525 | PF00514 | 0.596 |
TRG_NLS_MonoExtN_4 | 518 | 525 | PF00514 | 0.672 |
TRG_Pf-PMV_PEXEL_1 | 88 | 93 | PF00026 | 0.536 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I873 | Leptomonas seymouri | 55% | 98% |
A0A1X0NWB4 | Trypanosomatidae | 33% | 100% |
A0A3S7X5C7 | Leishmania donovani | 88% | 100% |
A0A422N8X2 | Trypanosoma rangeli | 31% | 100% |
A4HK67 | Leishmania braziliensis | 77% | 100% |
A4I7Q2 | Leishmania infantum | 88% | 100% |
D0A9V7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
Q4Q5J6 | Leishmania major | 89% | 100% |
V5BQN4 | Trypanosoma cruzi | 34% | 100% |