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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4IAI6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.492 |
CLV_C14_Caspase3-7 | 228 | 232 | PF00656 | 0.427 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 573 | 575 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 209 | 211 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.515 |
CLV_PCSK_KEX2_1 | 614 | 616 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 342 | 344 | PF00082 | 0.531 |
CLV_PCSK_PC1ET2_1 | 614 | 616 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.433 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.560 |
CLV_Separin_Metazoa | 488 | 492 | PF03568 | 0.340 |
DEG_APCC_DBOX_1 | 403 | 411 | PF00400 | 0.475 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.491 |
DOC_CDC14_PxL_1 | 585 | 593 | PF14671 | 0.366 |
DOC_CYCLIN_RxL_1 | 218 | 228 | PF00134 | 0.480 |
DOC_MAPK_gen_1 | 345 | 353 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 461 | 471 | PF00069 | 0.646 |
DOC_MAPK_MEF2A_6 | 27 | 36 | PF00069 | 0.407 |
DOC_MAPK_MEF2A_6 | 365 | 373 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 464 | 473 | PF00069 | 0.547 |
DOC_MAPK_MEF2A_6 | 584 | 592 | PF00069 | 0.380 |
DOC_MAPK_NFAT4_5 | 464 | 472 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 183 | 189 | PF00149 | 0.323 |
DOC_PP2B_LxvP_1 | 68 | 71 | PF13499 | 0.338 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 446 | 450 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 453 | 457 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 555 | 559 | PF00917 | 0.434 |
DOC_USP7_UBL2_3 | 461 | 465 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 456 | 461 | PF00397 | 0.603 |
DOC_WW_Pin1_4 | 474 | 479 | PF00397 | 0.463 |
DOC_WW_Pin1_4 | 560 | 565 | PF00397 | 0.492 |
LIG_14-3-3_CanoR_1 | 209 | 213 | PF00244 | 0.621 |
LIG_14-3-3_CanoR_1 | 345 | 351 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 404 | 414 | PF00244 | 0.385 |
LIG_14-3-3_CanoR_1 | 430 | 437 | PF00244 | 0.661 |
LIG_14-3-3_CanoR_1 | 503 | 509 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 573 | 581 | PF00244 | 0.427 |
LIG_APCC_ABBA_1 | 490 | 495 | PF00400 | 0.402 |
LIG_BIR_III_2 | 445 | 449 | PF00653 | 0.669 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 366 | 370 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 4 | 8 | PF00533 | 0.410 |
LIG_deltaCOP1_diTrp_1 | 23 | 29 | PF00928 | 0.463 |
LIG_deltaCOP1_diTrp_1 | 389 | 393 | PF00928 | 0.350 |
LIG_eIF4E_1 | 238 | 244 | PF01652 | 0.380 |
LIG_FAT_LD_1 | 578 | 586 | PF03623 | 0.308 |
LIG_FHA_1 | 117 | 123 | PF00498 | 0.557 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.463 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.414 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.495 |
LIG_FHA_1 | 327 | 333 | PF00498 | 0.396 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.511 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.412 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.468 |
LIG_FHA_2 | 72 | 78 | PF00498 | 0.468 |
LIG_LIR_Gen_1 | 367 | 375 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 630 | 639 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 64 | 75 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 374 | 379 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.308 |
LIG_LYPXL_yS_3 | 42 | 45 | PF13949 | 0.562 |
LIG_PDZ_Class_3 | 653 | 658 | PF00595 | 0.556 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.348 |
LIG_SH2_GRB2like | 115 | 118 | PF00017 | 0.508 |
LIG_SH2_PTP2 | 323 | 326 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 618 | 621 | PF00017 | 0.537 |
LIG_SH3_3 | 104 | 110 | PF00018 | 0.373 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.463 |
LIG_SH3_3 | 40 | 46 | PF00018 | 0.551 |
LIG_SH3_3 | 454 | 460 | PF00018 | 0.696 |
LIG_SH3_3 | 475 | 481 | PF00018 | 0.467 |
LIG_SH3_3 | 486 | 492 | PF00018 | 0.323 |
LIG_SH3_3 | 583 | 589 | PF00018 | 0.394 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.385 |
LIG_SUMO_SIM_anti_2 | 329 | 334 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 310 | 317 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 349 | 355 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 469 | 475 | PF11976 | 0.445 |
LIG_TRAF2_1 | 279 | 282 | PF00917 | 0.479 |
LIG_WRC_WIRS_1 | 629 | 634 | PF05994 | 0.590 |
MOD_CDK_SPK_2 | 213 | 218 | PF00069 | 0.624 |
MOD_CDK_SPK_2 | 456 | 461 | PF00069 | 0.495 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.510 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.276 |
MOD_CK1_1 | 197 | 203 | PF00069 | 0.684 |
MOD_CK1_1 | 286 | 292 | PF00069 | 0.582 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.464 |
MOD_CK1_1 | 409 | 415 | PF00069 | 0.434 |
MOD_CK1_1 | 449 | 455 | PF00069 | 0.756 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.433 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.460 |
MOD_CK1_1 | 507 | 513 | PF00069 | 0.565 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.468 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.533 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.418 |
MOD_CK2_1 | 555 | 561 | PF00069 | 0.449 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.441 |
MOD_CK2_1 | 631 | 637 | PF00069 | 0.568 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.298 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.499 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.596 |
MOD_GlcNHglycan | 285 | 288 | PF01048 | 0.467 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.439 |
MOD_GlcNHglycan | 358 | 362 | PF01048 | 0.587 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.498 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.708 |
MOD_GlcNHglycan | 525 | 528 | PF01048 | 0.580 |
MOD_GlcNHglycan | 574 | 577 | PF01048 | 0.376 |
MOD_GlcNHglycan | 619 | 622 | PF01048 | 0.612 |
MOD_GlcNHglycan | 626 | 629 | PF01048 | 0.531 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.575 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.567 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.621 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.520 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.477 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.364 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.369 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.718 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.542 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.304 |
MOD_GSK3_1 | 617 | 624 | PF00069 | 0.581 |
MOD_GSK3_1 | 647 | 654 | PF00069 | 0.563 |
MOD_N-GLC_1 | 116 | 121 | PF02516 | 0.599 |
MOD_N-GLC_2 | 179 | 181 | PF02516 | 0.498 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.501 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.486 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.462 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.431 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.672 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.443 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.492 |
MOD_PIKK_1 | 286 | 292 | PF00454 | 0.427 |
MOD_PIKK_1 | 334 | 340 | PF00454 | 0.537 |
MOD_PIKK_1 | 501 | 507 | PF00454 | 0.495 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.641 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.602 |
MOD_PKA_2 | 403 | 409 | PF00069 | 0.389 |
MOD_PKA_2 | 429 | 435 | PF00069 | 0.641 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.558 |
MOD_PKA_2 | 572 | 578 | PF00069 | 0.419 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.503 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.447 |
MOD_Plk_1 | 371 | 377 | PF00069 | 0.350 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.490 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.496 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.418 |
MOD_Plk_4 | 371 | 377 | PF00069 | 0.389 |
MOD_Plk_4 | 504 | 510 | PF00069 | 0.607 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.377 |
MOD_Plk_4 | 621 | 627 | PF00069 | 0.557 |
MOD_Plk_4 | 89 | 95 | PF00069 | 0.331 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.684 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.606 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.796 |
MOD_ProDKin_1 | 456 | 462 | PF00069 | 0.603 |
MOD_ProDKin_1 | 474 | 480 | PF00069 | 0.464 |
MOD_ProDKin_1 | 560 | 566 | PF00069 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.511 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 208 | 210 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 246 | 249 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 343 | 346 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 534 | 537 | PF00400 | 0.360 |
TRG_NES_CRM1_1 | 529 | 542 | PF08389 | 0.479 |
TRG_Pf-PMV_PEXEL_1 | 121 | 125 | PF00026 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 222 | 227 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7E9 | Leptomonas seymouri | 53% | 100% |
A0A0S4KIT9 | Bodo saltans | 28% | 96% |
A0A1X0PA76 | Trypanosomatidae | 33% | 100% |
A0A3Q8IHL1 | Leishmania donovani | 100% | 100% |
A0A422NVA9 | Trypanosoma rangeli | 34% | 100% |
A4HBD8 | Leishmania braziliensis | 76% | 100% |
C9ZLQ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9B5L0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
Q4Q2C6 | Leishmania major | 91% | 100% |
V5DMS9 | Trypanosoma cruzi | 34% | 100% |