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: Q4Q8T7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 123 | 127 | PF00656 | 0.387 |
CLV_C14_Caspase3-7 | 458 | 462 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 682 | 684 | PF00675 | 0.547 |
CLV_PCSK_KEX2_1 | 102 | 104 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.549 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.567 |
CLV_PCSK_PC7_1 | 678 | 684 | PF00082 | 0.635 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 519 | 523 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 540 | 544 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.677 |
DEG_APCC_DBOX_1 | 478 | 486 | PF00400 | 0.405 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.592 |
DOC_CYCLIN_RxL_1 | 574 | 585 | PF00134 | 0.305 |
DOC_MAPK_gen_1 | 575 | 584 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 618 | 627 | PF00069 | 0.577 |
DOC_MAPK_MEF2A_6 | 205 | 213 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 395 | 404 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 528 | 536 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 575 | 582 | PF00149 | 0.428 |
DOC_PP2B_LxvP_1 | 317 | 320 | PF13499 | 0.445 |
DOC_PP2B_LxvP_1 | 532 | 535 | PF13499 | 0.391 |
DOC_PP4_FxxP_1 | 243 | 246 | PF00568 | 0.591 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.536 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 311 | 315 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.448 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 462 | 466 | PF00917 | 0.563 |
DOC_USP7_UBL2_3 | 413 | 417 | PF12436 | 0.470 |
DOC_WW_Pin1_4 | 248 | 253 | PF00397 | 0.567 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.626 |
LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.567 |
LIG_14-3-3_CanoR_1 | 281 | 287 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 4 | 9 | PF00244 | 0.671 |
LIG_14-3-3_CanoR_1 | 419 | 425 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 519 | 526 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 528 | 536 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 575 | 580 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 682 | 690 | PF00244 | 0.582 |
LIG_Actin_WH2_2 | 535 | 551 | PF00022 | 0.343 |
LIG_BIR_III_4 | 75 | 79 | PF00653 | 0.456 |
LIG_BRCT_BRCA1_1 | 323 | 327 | PF00533 | 0.370 |
LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.329 |
LIG_deltaCOP1_diTrp_1 | 234 | 243 | PF00928 | 0.382 |
LIG_FHA_1 | 185 | 191 | PF00498 | 0.344 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.461 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.318 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.463 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.483 |
LIG_FHA_1 | 640 | 646 | PF00498 | 0.506 |
LIG_FHA_2 | 176 | 182 | PF00498 | 0.538 |
LIG_FHA_2 | 251 | 257 | PF00498 | 0.460 |
LIG_FHA_2 | 45 | 51 | PF00498 | 0.531 |
LIG_FHA_2 | 553 | 559 | PF00498 | 0.606 |
LIG_FHA_2 | 586 | 592 | PF00498 | 0.458 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.446 |
LIG_GBD_Chelix_1 | 474 | 482 | PF00786 | 0.343 |
LIG_LIR_Apic_2 | 219 | 225 | PF02991 | 0.523 |
LIG_LIR_Apic_2 | 241 | 246 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 150 | 158 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 256 | 265 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 346 | 354 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 578 | 589 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 82 | 93 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 150 | 154 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 30 | 35 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 346 | 351 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 499 | 505 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 578 | 584 | PF02991 | 0.561 |
LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.476 |
LIG_PCNA_PIPBox_1 | 12 | 21 | PF02747 | 0.540 |
LIG_PCNA_yPIPBox_3 | 6 | 19 | PF02747 | 0.581 |
LIG_Rb_pABgroove_1 | 422 | 430 | PF01858 | 0.402 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.508 |
LIG_SH2_CRK | 502 | 506 | PF00017 | 0.463 |
LIG_SH2_SRC | 69 | 72 | PF00017 | 0.316 |
LIG_SH2_STAP1 | 173 | 177 | PF00017 | 0.492 |
LIG_SH2_STAP1 | 214 | 218 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 69 | 73 | PF00017 | 0.526 |
LIG_SH2_STAT3 | 517 | 520 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 18 | 21 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.495 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.461 |
LIG_SH3_3 | 431 | 437 | PF00018 | 0.437 |
LIG_Sin3_3 | 606 | 613 | PF02671 | 0.416 |
LIG_SUMO_SIM_par_1 | 128 | 134 | PF11976 | 0.433 |
LIG_TRAF2_1 | 113 | 116 | PF00917 | 0.493 |
LIG_TRAF2_1 | 38 | 41 | PF00917 | 0.428 |
LIG_TRAF2_1 | 555 | 558 | PF00917 | 0.463 |
LIG_TRAF2_1 | 68 | 71 | PF00917 | 0.323 |
LIG_UBA3_1 | 190 | 198 | PF00899 | 0.404 |
LIG_WRC_WIRS_1 | 345 | 350 | PF05994 | 0.432 |
MOD_CDK_SPK_2 | 639 | 644 | PF00069 | 0.530 |
MOD_CDK_SPxxK_3 | 248 | 255 | PF00069 | 0.477 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.419 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.426 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.370 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.543 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.478 |
MOD_CK1_1 | 639 | 645 | PF00069 | 0.411 |
MOD_CK2_1 | 110 | 116 | PF00069 | 0.576 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.569 |
MOD_CK2_1 | 217 | 223 | PF00069 | 0.466 |
MOD_CK2_1 | 35 | 41 | PF00069 | 0.439 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.466 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.441 |
MOD_CK2_1 | 585 | 591 | PF00069 | 0.490 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.451 |
MOD_CK2_1 | 651 | 657 | PF00069 | 0.391 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.552 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.385 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.373 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.470 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.410 |
MOD_GlcNHglycan | 375 | 378 | PF01048 | 0.267 |
MOD_GlcNHglycan | 457 | 460 | PF01048 | 0.426 |
MOD_GlcNHglycan | 464 | 467 | PF01048 | 0.591 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.411 |
MOD_GlcNHglycan | 666 | 670 | PF01048 | 0.531 |
MOD_GlcNHglycan | 686 | 689 | PF01048 | 0.464 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.402 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.428 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.484 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.498 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.490 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.380 |
MOD_GSK3_1 | 496 | 503 | PF00069 | 0.433 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.551 |
MOD_LATS_1 | 681 | 687 | PF00433 | 0.531 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.368 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.494 |
MOD_NEK2_1 | 306 | 311 | PF00069 | 0.483 |
MOD_NEK2_1 | 344 | 349 | PF00069 | 0.359 |
MOD_NEK2_1 | 404 | 409 | PF00069 | 0.357 |
MOD_NEK2_1 | 427 | 432 | PF00069 | 0.556 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.435 |
MOD_NEK2_1 | 51 | 56 | PF00069 | 0.390 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.410 |
MOD_NEK2_1 | 582 | 587 | PF00069 | 0.296 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.404 |
MOD_NEK2_2 | 365 | 370 | PF00069 | 0.467 |
MOD_NEK2_2 | 481 | 486 | PF00069 | 0.416 |
MOD_NEK2_2 | 512 | 517 | PF00069 | 0.366 |
MOD_PIKK_1 | 404 | 410 | PF00454 | 0.479 |
MOD_PIKK_1 | 504 | 510 | PF00454 | 0.394 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.323 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.561 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.515 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.392 |
MOD_PKA_2 | 487 | 493 | PF00069 | 0.461 |
MOD_PKA_2 | 527 | 533 | PF00069 | 0.568 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.495 |
MOD_PKA_2 | 684 | 690 | PF00069 | 0.703 |
MOD_PKB_1 | 2 | 10 | PF00069 | 0.544 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.346 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.395 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.494 |
MOD_Plk_4 | 239 | 245 | PF00069 | 0.494 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.357 |
MOD_Plk_4 | 420 | 426 | PF00069 | 0.367 |
MOD_Plk_4 | 443 | 449 | PF00069 | 0.331 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.418 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.479 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.217 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.373 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.365 |
MOD_Plk_4 | 659 | 665 | PF00069 | 0.579 |
MOD_ProDKin_1 | 248 | 254 | PF00069 | 0.563 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.501 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.521 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.617 |
MOD_SUMO_rev_2 | 384 | 393 | PF00179 | 0.404 |
MOD_SUMO_rev_2 | 457 | 465 | PF00179 | 0.556 |
TRG_AP2beta_CARGO_1 | 346 | 355 | PF09066 | 0.431 |
TRG_DiLeu_BaEn_1 | 30 | 35 | PF01217 | 0.456 |
TRG_DiLeu_BaEn_1 | 500 | 505 | PF01217 | 0.467 |
TRG_DiLeu_BaLyEn_6 | 313 | 318 | PF01217 | 0.573 |
TRG_DiLeu_BaLyEn_6 | 641 | 646 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.463 |
TRG_ER_diArg_1 | 102 | 104 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 13 | 15 | PF00400 | 0.597 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 617 | 620 | PF00400 | 0.620 |
TRG_ER_diArg_1 | 682 | 685 | PF00400 | 0.592 |
TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 563 | 567 | PF00026 | 0.439 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7K6 | Leptomonas seymouri | 66% | 89% |
A0A0S4JKX7 | Bodo saltans | 28% | 84% |
A0A1X0P8M4 | Trypanosomatidae | 38% | 92% |
A0A3Q8IG37 | Leishmania donovani | 94% | 100% |
A0A3S5ISN2 | Trypanosoma rangeli | 43% | 89% |
A4HF99 | Leishmania braziliensis | 83% | 88% |
A4I2H6 | Leishmania infantum | 94% | 100% |
C9ZX12 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 95% |
E9AYN5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5AS65 | Trypanosoma cruzi | 43% | 89% |