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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: Q4QIS2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.507 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.408 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 582 | 584 | PF00675 | 0.393 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 582 | 584 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 245 | 249 | PF00082 | 0.459 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 594 | 598 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 622 | 626 | PF00082 | 0.665 |
CLV_Separin_Metazoa | 402 | 406 | PF03568 | 0.461 |
DEG_APCC_DBOX_1 | 20 | 28 | PF00400 | 0.533 |
DEG_SCF_FBW7_1 | 81 | 86 | PF00400 | 0.508 |
DEG_SPOP_SBC_1 | 199 | 203 | PF00917 | 0.557 |
DEG_SPOP_SBC_1 | 624 | 628 | PF00917 | 0.581 |
DOC_CDC14_PxL_1 | 422 | 430 | PF14671 | 0.370 |
DOC_CYCLIN_RxL_1 | 433 | 441 | PF00134 | 0.387 |
DOC_CYCLIN_RxL_1 | 505 | 513 | PF00134 | 0.454 |
DOC_MAPK_gen_1 | 228 | 236 | PF00069 | 0.602 |
DOC_MAPK_gen_1 | 525 | 533 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 9 | 19 | PF00069 | 0.598 |
DOC_MAPK_MEF2A_6 | 11 | 19 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 228 | 236 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 495 | 503 | PF00069 | 0.455 |
DOC_PP1_SILK_1 | 301 | 306 | PF00149 | 0.263 |
DOC_PP2B_LxvP_1 | 375 | 378 | PF13499 | 0.482 |
DOC_PP2B_LxvP_1 | 496 | 499 | PF13499 | 0.465 |
DOC_PP4_FxxP_1 | 453 | 456 | PF00568 | 0.488 |
DOC_USP7_MATH_1 | 414 | 418 | PF00917 | 0.393 |
DOC_USP7_MATH_1 | 468 | 472 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.629 |
DOC_USP7_UBL2_3 | 124 | 128 | PF12436 | 0.517 |
DOC_USP7_UBL2_3 | 71 | 75 | PF12436 | 0.705 |
DOC_WW_Pin1_4 | 142 | 147 | PF00397 | 0.420 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.616 |
DOC_WW_Pin1_4 | 404 | 409 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.665 |
DOC_WW_Pin1_4 | 79 | 84 | PF00397 | 0.707 |
LIG_14-3-3_CanoR_1 | 139 | 149 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 552 | 559 | PF00244 | 0.407 |
LIG_14-3-3_CanoR_1 | 594 | 600 | PF00244 | 0.478 |
LIG_14-3-3_CterR_2 | 631 | 635 | PF00244 | 0.623 |
LIG_APCC_ABBA_1 | 385 | 390 | PF00400 | 0.406 |
LIG_BIR_III_4 | 84 | 88 | PF00653 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 568 | 575 | PF00928 | 0.378 |
LIG_eIF4E_1 | 388 | 394 | PF01652 | 0.407 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.491 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.351 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.453 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.405 |
LIG_FHA_1 | 507 | 513 | PF00498 | 0.587 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.380 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.444 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.434 |
LIG_FHA_2 | 84 | 90 | PF00498 | 0.770 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.417 |
LIG_GBD_Chelix_1 | 536 | 544 | PF00786 | 0.381 |
LIG_LIR_Gen_1 | 290 | 299 | PF02991 | 0.493 |
LIG_LIR_Gen_1 | 318 | 329 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 366 | 375 | PF02991 | 0.567 |
LIG_LIR_Gen_1 | 398 | 409 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 290 | 294 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 318 | 324 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 366 | 371 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 398 | 404 | PF02991 | 0.437 |
LIG_LYPXL_yS_3 | 425 | 428 | PF13949 | 0.424 |
LIG_NRBOX | 427 | 433 | PF00104 | 0.402 |
LIG_PCNA_yPIPBox_3 | 582 | 591 | PF02747 | 0.453 |
LIG_Pex14_1 | 160 | 164 | PF04695 | 0.506 |
LIG_PTB_Apo_2 | 421 | 428 | PF02174 | 0.275 |
LIG_PTB_Phospho_1 | 421 | 427 | PF10480 | 0.279 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.482 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.399 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.428 |
LIG_SH2_GRB2like | 291 | 294 | PF00017 | 0.301 |
LIG_SH2_SRC | 291 | 294 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 388 | 392 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.463 |
LIG_SH2_STAT5 | 427 | 430 | PF00017 | 0.396 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.357 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 13 | 19 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 508 | 513 | PF11976 | 0.431 |
LIG_TRAF2_1 | 445 | 448 | PF00917 | 0.451 |
LIG_TYR_ITIM | 319 | 324 | PF00017 | 0.434 |
LIG_TYR_ITIM | 423 | 428 | PF00017 | 0.425 |
LIG_TYR_ITSM | 296 | 303 | PF00017 | 0.408 |
LIG_UBA3_1 | 517 | 525 | PF00899 | 0.491 |
LIG_WRC_WIRS_1 | 368 | 373 | PF05994 | 0.600 |
MOD_CDK_SPK_2 | 240 | 245 | PF00069 | 0.533 |
MOD_CDK_SPK_2 | 617 | 622 | PF00069 | 0.585 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.504 |
MOD_CK1_1 | 203 | 209 | PF00069 | 0.724 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.714 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.608 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.709 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.712 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.534 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.583 |
MOD_CK2_1 | 442 | 448 | PF00069 | 0.419 |
MOD_CK2_1 | 624 | 630 | PF00069 | 0.610 |
MOD_CK2_1 | 83 | 89 | PF00069 | 0.727 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.424 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.488 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.563 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.603 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.500 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.325 |
MOD_GlcNHglycan | 40 | 44 | PF01048 | 0.710 |
MOD_GlcNHglycan | 465 | 468 | PF01048 | 0.583 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.648 |
MOD_GlcNHglycan | 578 | 581 | PF01048 | 0.392 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.555 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.690 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.400 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.757 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.675 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.539 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.440 |
MOD_GSK3_1 | 438 | 445 | PF00069 | 0.404 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.554 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.513 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.716 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.387 |
MOD_N-GLC_1 | 442 | 447 | PF02516 | 0.413 |
MOD_N-GLC_1 | 607 | 612 | PF02516 | 0.612 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.677 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.521 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.404 |
MOD_NEK2_1 | 313 | 318 | PF00069 | 0.362 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.563 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.470 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.405 |
MOD_NEK2_1 | 438 | 443 | PF00069 | 0.392 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.745 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.402 |
MOD_NEK2_1 | 616 | 621 | PF00069 | 0.548 |
MOD_NEK2_2 | 315 | 320 | PF00069 | 0.391 |
MOD_PIKK_1 | 456 | 462 | PF00454 | 0.461 |
MOD_PK_1 | 516 | 522 | PF00069 | 0.324 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.734 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.386 |
MOD_PKB_1 | 198 | 206 | PF00069 | 0.530 |
MOD_Plk_1 | 88 | 94 | PF00069 | 0.562 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.531 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.424 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.396 |
MOD_Plk_4 | 595 | 601 | PF00069 | 0.576 |
MOD_ProDKin_1 | 142 | 148 | PF00069 | 0.421 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.607 |
MOD_ProDKin_1 | 404 | 410 | PF00069 | 0.429 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.670 |
MOD_ProDKin_1 | 79 | 85 | PF00069 | 0.704 |
MOD_SUMO_rev_2 | 254 | 264 | PF00179 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 453 | 458 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.498 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.442 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.456 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 21 | 24 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 581 | 583 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.605 |
TRG_NES_CRM1_1 | 26 | 38 | PF08389 | 0.566 |
TRG_NES_CRM1_1 | 366 | 381 | PF08389 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 391 | 395 | PF00026 | 0.391 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I7J6 | Leptomonas seymouri | 61% | 99% |
A0A3S5H5W7 | Leishmania donovani | 94% | 100% |
A4H4W6 | Leishmania braziliensis | 73% | 100% |
A4HT40 | Leishmania infantum | 94% | 100% |
C9ZUU8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AL32 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B8V4 | Trypanosoma cruzi | 33% | 100% |