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 |
Related structures:
AlphaFold database: Q4QAY5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 156 | 160 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.618 |
CLV_C14_Caspase3-7 | 421 | 425 | PF00656 | 0.520 |
CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 319 | 321 | PF00675 | 0.457 |
CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.558 |
CLV_PCSK_KEX2_1 | 319 | 321 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.529 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.658 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 355 | 359 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 496 | 500 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.559 |
DEG_APCC_DBOX_1 | 180 | 188 | PF00400 | 0.498 |
DEG_APCC_DBOX_1 | 307 | 315 | PF00400 | 0.417 |
DEG_APCC_DBOX_1 | 32 | 40 | PF00400 | 0.516 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.637 |
DOC_CDC14_PxL_1 | 613 | 621 | PF14671 | 0.442 |
DOC_CKS1_1 | 499 | 504 | PF01111 | 0.572 |
DOC_CYCLIN_RxL_1 | 573 | 585 | PF00134 | 0.490 |
DOC_CYCLIN_RxL_1 | 628 | 636 | PF00134 | 0.501 |
DOC_CYCLIN_yCln2_LP_2 | 489 | 495 | PF00134 | 0.450 |
DOC_MAPK_DCC_7 | 640 | 649 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 459 | 467 | PF00069 | 0.346 |
DOC_MAPK_MEF2A_6 | 308 | 315 | PF00069 | 0.473 |
DOC_MAPK_MEF2A_6 | 40 | 47 | PF00069 | 0.570 |
DOC_MAPK_MEF2A_6 | 536 | 544 | PF00069 | 0.440 |
DOC_MAPK_NFAT4_5 | 308 | 316 | PF00069 | 0.516 |
DOC_PP2B_LxvP_1 | 302 | 305 | PF13499 | 0.456 |
DOC_PP2B_LxvP_1 | 9 | 12 | PF13499 | 0.659 |
DOC_PP4_FxxP_1 | 286 | 289 | PF00568 | 0.541 |
DOC_PP4_FxxP_1 | 499 | 502 | PF00568 | 0.645 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.521 |
DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.530 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 408 | 413 | PF00397 | 0.528 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.565 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.507 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 262 | 268 | PF00244 | 0.269 |
LIG_14-3-3_CanoR_1 | 308 | 314 | PF00244 | 0.530 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.578 |
LIG_14-3-3_CanoR_1 | 391 | 396 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 51 | 56 | PF00244 | 0.622 |
LIG_14-3-3_CanoR_1 | 567 | 572 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 578 | 583 | PF00244 | 0.455 |
LIG_Actin_WH2_2 | 309 | 327 | PF00022 | 0.426 |
LIG_Actin_WH2_2 | 482 | 498 | PF00022 | 0.535 |
LIG_APCC_ABBA_1 | 43 | 48 | PF00400 | 0.574 |
LIG_APCC_ABBA_1 | 580 | 585 | PF00400 | 0.521 |
LIG_APCC_ABBA_1 | 610 | 615 | PF00400 | 0.500 |
LIG_BIR_III_2 | 538 | 542 | PF00653 | 0.464 |
LIG_eIF4E_1 | 359 | 365 | PF01652 | 0.532 |
LIG_eIF4E_1 | 613 | 619 | PF01652 | 0.470 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.633 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.502 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.489 |
LIG_FHA_1 | 449 | 455 | PF00498 | 0.446 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.506 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.439 |
LIG_FHA_2 | 405 | 411 | PF00498 | 0.580 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.529 |
LIG_GBD_Chelix_1 | 225 | 233 | PF00786 | 0.341 |
LIG_GBD_Chelix_1 | 95 | 103 | PF00786 | 0.569 |
LIG_LIR_Apic_2 | 497 | 502 | PF02991 | 0.512 |
LIG_LIR_Gen_1 | 142 | 148 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 356 | 366 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 531 | 542 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 97 | 104 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 142 | 147 | PF02991 | 0.447 |
LIG_LIR_Nem_3 | 327 | 332 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.525 |
LIG_LIR_Nem_3 | 627 | 633 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.497 |
LIG_NRBOX | 451 | 457 | PF00104 | 0.465 |
LIG_PCNA_PIPBox_1 | 53 | 62 | PF02747 | 0.514 |
LIG_Pex14_1 | 512 | 516 | PF04695 | 0.466 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.620 |
LIG_SH2_CRK | 359 | 363 | PF00017 | 0.582 |
LIG_SH2_GRB2like | 326 | 329 | PF00017 | 0.505 |
LIG_SH2_SRC | 422 | 425 | PF00017 | 0.504 |
LIG_SH2_SRC | 613 | 616 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.536 |
LIG_SH2_STAP1 | 326 | 330 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 419 | 423 | PF00017 | 0.538 |
LIG_SH2_STAP1 | 516 | 520 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.406 |
LIG_SH2_STAT5 | 266 | 269 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 399 | 402 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 607 | 610 | PF00017 | 0.490 |
LIG_SH3_1 | 406 | 412 | PF00018 | 0.602 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.405 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.602 |
LIG_SH3_3 | 640 | 646 | PF00018 | 0.384 |
LIG_Sin3_3 | 300 | 307 | PF02671 | 0.505 |
LIG_Sin3_3 | 434 | 441 | PF02671 | 0.470 |
LIG_SUMO_SIM_anti_2 | 451 | 456 | PF11976 | 0.420 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.537 |
LIG_SUMO_SIM_par_1 | 645 | 651 | PF11976 | 0.438 |
LIG_TRAF2_1 | 11 | 14 | PF00917 | 0.731 |
LIG_TRAF2_1 | 137 | 140 | PF00917 | 0.507 |
LIG_TRFH_1 | 171 | 175 | PF08558 | 0.571 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.519 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.567 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.627 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.477 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.468 |
MOD_CK1_1 | 221 | 227 | PF00069 | 0.423 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.407 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.502 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.498 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.488 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.455 |
MOD_CK2_1 | 203 | 209 | PF00069 | 0.519 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.293 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.606 |
MOD_CK2_1 | 404 | 410 | PF00069 | 0.554 |
MOD_CK2_1 | 482 | 488 | PF00069 | 0.571 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.505 |
MOD_CK2_1 | 589 | 595 | PF00069 | 0.534 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.739 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.633 |
MOD_GlcNHglycan | 13 | 17 | PF01048 | 0.601 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.554 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.464 |
MOD_GlcNHglycan | 220 | 223 | PF01048 | 0.467 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.269 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.660 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.469 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.505 |
MOD_GlcNHglycan | 531 | 534 | PF01048 | 0.470 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.460 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.510 |
MOD_GlcNHglycan | 595 | 599 | PF01048 | 0.497 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.754 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.558 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.605 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.611 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.454 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.435 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.319 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.417 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.381 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.607 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.500 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.302 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.530 |
MOD_N-GLC_1 | 309 | 314 | PF02516 | 0.424 |
MOD_N-GLC_2 | 577 | 579 | PF02516 | 0.404 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.474 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.489 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.475 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.449 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.545 |
MOD_NEK2_1 | 572 | 577 | PF00069 | 0.507 |
MOD_NEK2_1 | 589 | 594 | PF00069 | 0.292 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.580 |
MOD_NEK2_2 | 232 | 237 | PF00069 | 0.439 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.561 |
MOD_PK_1 | 51 | 57 | PF00069 | 0.626 |
MOD_PKA_2 | 142 | 148 | PF00069 | 0.461 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.784 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.270 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.495 |
MOD_Plk_1 | 309 | 315 | PF00069 | 0.415 |
MOD_Plk_1 | 404 | 410 | PF00069 | 0.598 |
MOD_Plk_1 | 624 | 630 | PF00069 | 0.497 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.481 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.428 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.511 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.578 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.491 |
MOD_Plk_4 | 578 | 584 | PF00069 | 0.472 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.543 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.399 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.601 |
MOD_ProDKin_1 | 408 | 414 | PF00069 | 0.521 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.564 |
TRG_DiLeu_BaEn_1 | 615 | 620 | PF01217 | 0.495 |
TRG_DiLeu_BaLyEn_6 | 286 | 291 | PF01217 | 0.509 |
TRG_DiLeu_BaLyEn_6 | 614 | 619 | PF01217 | 0.548 |
TRG_DiLeu_BaLyEn_6 | 643 | 648 | PF01217 | 0.490 |
TRG_DiLeu_BaLyEn_6 | 99 | 104 | PF01217 | 0.622 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.583 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.548 |
TRG_ENDOCYTIC_2 | 607 | 610 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 193 | 195 | PF00400 | 0.558 |
TRG_ER_diArg_1 | 318 | 320 | PF00400 | 0.462 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.547 |
TRG_NES_CRM1_1 | 35 | 48 | PF08389 | 0.573 |
TRG_Pf-PMV_PEXEL_1 | 102 | 106 | PF00026 | 0.581 |
TRG_Pf-PMV_PEXEL_1 | 194 | 199 | PF00026 | 0.553 |
TRG_Pf-PMV_PEXEL_1 | 237 | 242 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 631 | 636 | PF00026 | 0.492 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKS3 | Leptomonas seymouri | 54% | 78% |
A0A1X0NXC2 | Trypanosomatidae | 26% | 83% |
A0A3Q8IBR0 | Leishmania donovani | 94% | 100% |
A0A3R7RJS0 | Trypanosoma rangeli | 28% | 82% |
A4HD37 | Leishmania braziliensis | 85% | 77% |
C9ZNR6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 80% |
E9AH15 | Leishmania infantum | 94% | 100% |
E9AWI5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5BFS5 | Trypanosoma cruzi | 26% | 82% |