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: 4 |
Pissara et al. | no | yes: 12 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HC80
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.289 |
CLV_C14_Caspase3-7 | 459 | 463 | PF00656 | 0.334 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.440 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.659 |
CLV_PCSK_KEX2_1 | 413 | 415 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 504 | 506 | PF00082 | 0.611 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.684 |
CLV_PCSK_KEX2_1 | 540 | 542 | PF00082 | 0.738 |
CLV_PCSK_KEX2_1 | 556 | 558 | PF00082 | 0.622 |
CLV_PCSK_PC1ET2_1 | 413 | 415 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.483 |
CLV_PCSK_PC1ET2_1 | 504 | 506 | PF00082 | 0.611 |
CLV_PCSK_PC1ET2_1 | 529 | 531 | PF00082 | 0.647 |
CLV_PCSK_PC1ET2_1 | 540 | 542 | PF00082 | 0.727 |
CLV_PCSK_PC7_1 | 525 | 531 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.344 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.432 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 363 | 367 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.514 |
DEG_APCC_DBOX_1 | 204 | 212 | PF00400 | 0.451 |
DEG_APCC_DBOX_1 | 482 | 490 | PF00400 | 0.557 |
DEG_SPOP_SBC_1 | 57 | 61 | PF00917 | 0.494 |
DOC_CDC14_PxL_1 | 328 | 336 | PF14671 | 0.398 |
DOC_CYCLIN_RxL_1 | 479 | 488 | PF00134 | 0.542 |
DOC_MAPK_RevD_3 | 400 | 414 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 100 | 106 | PF00149 | 0.337 |
DOC_PP1_RVXF_1 | 208 | 215 | PF00149 | 0.340 |
DOC_PP1_RVXF_1 | 441 | 448 | PF00149 | 0.458 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.565 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.710 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.776 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 123 | 133 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 248 | 258 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.281 |
LIG_14-3-3_CanoR_1 | 280 | 287 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 305 | 312 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 320 | 330 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 412 | 419 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 530 | 537 | PF00244 | 0.742 |
LIG_Actin_WH2_2 | 109 | 125 | PF00022 | 0.475 |
LIG_BIR_III_2 | 182 | 186 | PF00653 | 0.450 |
LIG_BRCT_BRCA1_1 | 200 | 204 | PF00533 | 0.449 |
LIG_CaM_IQ_9 | 517 | 532 | PF13499 | 0.513 |
LIG_Clathr_ClatBox_1 | 397 | 401 | PF01394 | 0.445 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.355 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.367 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.435 |
LIG_FHA_1 | 26 | 32 | PF00498 | 0.653 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.527 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.420 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.437 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.598 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.466 |
LIG_FHA_2 | 338 | 344 | PF00498 | 0.480 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.464 |
LIG_LIR_Apic_2 | 255 | 261 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 274 | 283 | PF02991 | 0.335 |
LIG_LIR_Gen_1 | 61 | 71 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 201 | 207 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 274 | 278 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 440 | 445 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 61 | 67 | PF02991 | 0.384 |
LIG_LRP6_Inhibitor_1 | 467 | 473 | PF00058 | 0.421 |
LIG_LYPXL_S_1 | 330 | 334 | PF13949 | 0.333 |
LIG_LYPXL_S_1 | 373 | 377 | PF13949 | 0.458 |
LIG_LYPXL_yS_3 | 331 | 334 | PF13949 | 0.339 |
LIG_LYPXL_yS_3 | 374 | 377 | PF13949 | 0.464 |
LIG_NRBOX | 207 | 213 | PF00104 | 0.451 |
LIG_NRP_CendR_1 | 560 | 561 | PF00754 | 0.706 |
LIG_PCNA_yPIPBox_3 | 291 | 300 | PF02747 | 0.478 |
LIG_RPA_C_Fungi | 407 | 419 | PF08784 | 0.417 |
LIG_SH2_CRK | 378 | 382 | PF00017 | 0.372 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.437 |
LIG_SH2_CRK | 64 | 68 | PF00017 | 0.397 |
LIG_SH2_SRC | 258 | 261 | PF00017 | 0.494 |
LIG_SH2_SRC | 376 | 379 | PF00017 | 0.235 |
LIG_SH2_STAT3 | 81 | 84 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 81 | 84 | PF00017 | 0.487 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.385 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.660 |
LIG_SUMO_SIM_anti_2 | 313 | 319 | PF11976 | 0.325 |
LIG_SUMO_SIM_par_1 | 154 | 160 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 356 | 362 | PF11976 | 0.500 |
LIG_SUMO_SIM_par_1 | 396 | 401 | PF11976 | 0.414 |
LIG_SUMO_SIM_par_1 | 69 | 74 | PF11976 | 0.367 |
LIG_TRFH_1 | 328 | 332 | PF08558 | 0.352 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.435 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.529 |
MOD_CK1_1 | 383 | 389 | PF00069 | 0.449 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.766 |
MOD_CK1_1 | 548 | 554 | PF00069 | 0.749 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.750 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.530 |
MOD_CK2_1 | 321 | 327 | PF00069 | 0.403 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.452 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.482 |
MOD_Cter_Amidation | 558 | 561 | PF01082 | 0.657 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.488 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.510 |
MOD_GlcNHglycan | 429 | 432 | PF01048 | 0.462 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.301 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.358 |
MOD_GSK3_1 | 300 | 307 | PF00069 | 0.388 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.553 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.404 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.491 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.766 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.510 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.400 |
MOD_N-GLC_1 | 422 | 427 | PF02516 | 0.528 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.425 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.307 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.348 |
MOD_NEK2_1 | 359 | 364 | PF00069 | 0.482 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.498 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.515 |
MOD_NEK2_1 | 494 | 499 | PF00069 | 0.493 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.425 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.766 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.513 |
MOD_PKA_1 | 412 | 418 | PF00069 | 0.507 |
MOD_PKA_1 | 528 | 534 | PF00069 | 0.757 |
MOD_PKA_2 | 236 | 242 | PF00069 | 0.495 |
MOD_PKA_2 | 279 | 285 | PF00069 | 0.509 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.557 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.400 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.623 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.775 |
MOD_PKB_1 | 505 | 513 | PF00069 | 0.610 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.448 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.365 |
MOD_Plk_1 | 422 | 428 | PF00069 | 0.517 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.355 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.455 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.452 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.436 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.403 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.774 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.468 |
MOD_SUMO_rev_2 | 533 | 542 | PF00179 | 0.675 |
MOD_SUMO_rev_2 | 544 | 548 | PF00179 | 0.559 |
TRG_DiLeu_BaEn_1 | 96 | 101 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.354 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.402 |
TRG_ENDOCYTIC_2 | 374 | 377 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.437 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.392 |
TRG_NES_CRM1_1 | 277 | 290 | PF08389 | 0.312 |
TRG_NES_CRM1_1 | 62 | 74 | PF08389 | 0.379 |
TRG_NLS_MonoExtC_3 | 411 | 417 | PF00514 | 0.502 |
TRG_NLS_MonoExtN_4 | 525 | 532 | PF00514 | 0.591 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4V0 | Leptomonas seymouri | 68% | 95% |
A0A0S4JSH7 | Bodo saltans | 30% | 100% |
A0A1X0NTF0 | Trypanosomatidae | 44% | 99% |
A0A3Q8IC40 | Leishmania donovani | 84% | 100% |
A0A3R7NVM0 | Trypanosoma rangeli | 41% | 100% |
A4HZQ8 | Leishmania infantum | 84% | 100% |
C9ZSF1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AVL4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4QBW5 | Leishmania major | 84% | 100% |
V5BFQ6 | Trypanosoma cruzi | 41% | 100% |