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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QHS8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.485 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 38 | 42 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.577 |
CLV_MEL_PAP_1 | 417 | 423 | PF00089 | 0.617 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.653 |
CLV_PCSK_SKI1_1 | 464 | 468 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.757 |
CLV_PCSK_SKI1_1 | 607 | 611 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.384 |
DEG_ODPH_VHL_1 | 247 | 260 | PF01847 | 0.501 |
DEG_SPOP_SBC_1 | 52 | 56 | PF00917 | 0.732 |
DEG_SPOP_SBC_1 | 522 | 526 | PF00917 | 0.733 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.517 |
DOC_PP1_RVXF_1 | 437 | 444 | PF00149 | 0.638 |
DOC_PP2B_LxvP_1 | 371 | 374 | PF13499 | 0.580 |
DOC_PP2B_LxvP_1 | 582 | 585 | PF13499 | 0.549 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 490 | 495 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 518 | 523 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.713 |
LIG_14-3-3_CanoR_1 | 175 | 181 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 454 | 458 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 577 | 583 | PF00244 | 0.635 |
LIG_14-3-3_CanoR_1 | 586 | 592 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 67 | 75 | PF00244 | 0.376 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.597 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.428 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.613 |
LIG_BRCT_BRCA1_1 | 492 | 496 | PF00533 | 0.616 |
LIG_Clathr_ClatBox_1 | 103 | 107 | PF01394 | 0.424 |
LIG_CtBP_PxDLS_1 | 619 | 623 | PF00389 | 0.536 |
LIG_deltaCOP1_diTrp_1 | 197 | 205 | PF00928 | 0.629 |
LIG_DLG_GKlike_1 | 420 | 428 | PF00625 | 0.637 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.564 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.554 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.708 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.701 |
LIG_FHA_1 | 554 | 560 | PF00498 | 0.563 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.686 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.471 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.520 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.727 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.651 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.470 |
LIG_LIR_LC3C_4 | 259 | 264 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 440 | 446 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 590 | 594 | PF02991 | 0.620 |
LIG_LYPXL_SIV_4 | 602 | 610 | PF13949 | 0.598 |
LIG_PDZ_Class_1 | 618 | 623 | PF00595 | 0.529 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.359 |
LIG_Pex14_2 | 549 | 553 | PF04695 | 0.471 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.675 |
LIG_SH2_NCK_1 | 366 | 370 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 366 | 370 | PF00017 | 0.481 |
LIG_SH2_STAT3 | 347 | 350 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.700 |
LIG_SH2_STAT5 | 568 | 571 | PF00017 | 0.504 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.654 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.655 |
LIG_SUMO_SIM_anti_2 | 100 | 105 | PF11976 | 0.463 |
LIG_SUMO_SIM_anti_2 | 259 | 264 | PF11976 | 0.348 |
LIG_SUMO_SIM_anti_2 | 41 | 47 | PF11976 | 0.673 |
LIG_SUMO_SIM_anti_2 | 556 | 563 | PF11976 | 0.450 |
LIG_SUMO_SIM_anti_2 | 86 | 97 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 157 | 162 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 261 | 268 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 556 | 563 | PF11976 | 0.455 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.747 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.741 |
LIG_TRAF2_2 | 453 | 458 | PF00917 | 0.665 |
LIG_TRFH_1 | 342 | 346 | PF08558 | 0.502 |
LIG_TYR_ITIM | 412 | 417 | PF00017 | 0.607 |
LIG_WRC_WIRS_1 | 588 | 593 | PF05994 | 0.656 |
MOD_CDK_SPxxK_3 | 60 | 67 | PF00069 | 0.473 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.635 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.697 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.671 |
MOD_CK1_1 | 517 | 523 | PF00069 | 0.743 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.703 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.641 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.715 |
MOD_CK1_1 | 578 | 584 | PF00069 | 0.661 |
MOD_CK1_1 | 590 | 596 | PF00069 | 0.637 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.583 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.422 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.744 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.475 |
MOD_CK2_1 | 310 | 316 | PF00069 | 0.578 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.627 |
MOD_CK2_1 | 560 | 566 | PF00069 | 0.512 |
MOD_CK2_1 | 590 | 596 | PF00069 | 0.649 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.556 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.477 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.538 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.618 |
MOD_GlcNHglycan | 221 | 224 | PF01048 | 0.581 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.454 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.695 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.674 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.751 |
MOD_GlcNHglycan | 318 | 322 | PF01048 | 0.512 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.600 |
MOD_GlcNHglycan | 458 | 462 | PF01048 | 0.722 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.677 |
MOD_GlcNHglycan | 535 | 538 | PF01048 | 0.649 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.505 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.410 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.589 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.441 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.513 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.691 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.722 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.647 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.673 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.530 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.626 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.669 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.657 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.745 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.654 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.681 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.687 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.440 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.405 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.661 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.480 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.360 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.470 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.373 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.605 |
MOD_NEK2_1 | 457 | 462 | PF00069 | 0.596 |
MOD_NEK2_1 | 610 | 615 | PF00069 | 0.592 |
MOD_OFUCOSY | 509 | 514 | PF10250 | 0.518 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.583 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.524 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.632 |
MOD_PKA_2 | 174 | 180 | PF00069 | 0.667 |
MOD_PKA_2 | 219 | 225 | PF00069 | 0.457 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.601 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.446 |
MOD_Plk_1 | 364 | 370 | PF00069 | 0.480 |
MOD_Plk_1 | 457 | 463 | PF00069 | 0.650 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.313 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.509 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.599 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.514 |
MOD_ProDKin_1 | 490 | 496 | PF00069 | 0.718 |
MOD_ProDKin_1 | 518 | 524 | PF00069 | 0.731 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.700 |
TRG_DiLeu_BaLyEn_6 | 281 | 286 | PF01217 | 0.548 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.610 |
TRG_NES_CRM1_1 | 34 | 49 | PF08389 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 245 | 250 | PF00026 | 0.362 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.550 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H8 | Leptomonas seymouri | 48% | 81% |
A0A1X0NMF5 | Trypanosomatidae | 29% | 100% |
A0A3S7WQU1 | Leishmania donovani | 91% | 100% |
A4H5S4 | Leishmania braziliensis | 76% | 85% |
A4HU17 | Leishmania infantum | 91% | 100% |
D0A9I5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AMU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
V5B2B3 | Trypanosoma cruzi | 32% | 100% |