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: A4HU17
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 129 | 133 | PF00656 | 0.484 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.735 |
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.470 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.581 |
CLV_MEL_PAP_1 | 417 | 423 | PF00089 | 0.677 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.608 |
CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.666 |
CLV_PCSK_SKI1_1 | 600 | 604 | PF00082 | 0.507 |
DEG_ODPH_VHL_1 | 247 | 260 | PF01847 | 0.526 |
DEG_SPOP_SBC_1 | 515 | 519 | PF00917 | 0.732 |
DEG_SPOP_SBC_1 | 52 | 56 | PF00917 | 0.749 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.540 |
DOC_MAPK_MEF2A_6 | 609 | 616 | PF00069 | 0.554 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.552 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.713 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.788 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 580 | 584 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 605 | 609 | PF00917 | 0.501 |
DOC_WW_Pin1_4 | 342 | 347 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.699 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.780 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.717 |
LIG_14-3-3_CanoR_1 | 327 | 336 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 453 | 457 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 570 | 576 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 579 | 585 | PF00244 | 0.376 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.636 |
LIG_BIR_III_2 | 187 | 191 | PF00653 | 0.567 |
LIG_BRCT_BRCA1_1 | 230 | 234 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 35 | 39 | PF00533 | 0.651 |
LIG_BRCT_BRCA1_1 | 485 | 489 | PF00533 | 0.607 |
LIG_Clathr_ClatBox_1 | 103 | 107 | PF01394 | 0.470 |
LIG_deltaCOP1_diTrp_1 | 197 | 205 | PF00928 | 0.734 |
LIG_DLG_GKlike_1 | 420 | 428 | PF00625 | 0.694 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.555 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.599 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.572 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.491 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.639 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.625 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.525 |
LIG_FHA_1 | 572 | 578 | PF00498 | 0.627 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.536 |
LIG_FHA_2 | 127 | 133 | PF00498 | 0.550 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.722 |
LIG_FHA_2 | 182 | 188 | PF00498 | 0.691 |
LIG_FHA_2 | 306 | 312 | PF00498 | 0.538 |
LIG_LIR_Gen_1 | 288 | 299 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 583 | 587 | PF02991 | 0.506 |
LIG_LYPXL_SIV_4 | 595 | 603 | PF13949 | 0.560 |
LIG_MYND_1 | 576 | 580 | PF01753 | 0.524 |
LIG_PDZ_Class_2 | 611 | 616 | PF00595 | 0.375 |
LIG_Pex14_2 | 234 | 238 | PF04695 | 0.407 |
LIG_Pex14_2 | 542 | 546 | PF04695 | 0.443 |
LIG_SH2_CRK | 414 | 418 | PF00017 | 0.740 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.605 |
LIG_SH2_STAT3 | 347 | 350 | PF00017 | 0.589 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.761 |
LIG_SH2_STAT5 | 561 | 564 | PF00017 | 0.493 |
LIG_SH3_3 | 574 | 580 | PF00018 | 0.645 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.684 |
LIG_SUMO_SIM_anti_2 | 100 | 105 | PF11976 | 0.492 |
LIG_SUMO_SIM_anti_2 | 259 | 264 | PF11976 | 0.385 |
LIG_SUMO_SIM_anti_2 | 41 | 49 | PF11976 | 0.745 |
LIG_SUMO_SIM_anti_2 | 549 | 556 | PF11976 | 0.432 |
LIG_SUMO_SIM_anti_2 | 86 | 97 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 102 | 107 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 157 | 162 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 261 | 268 | PF11976 | 0.374 |
LIG_SUMO_SIM_par_1 | 549 | 556 | PF11976 | 0.434 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.764 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.812 |
LIG_TRAF2_1 | 556 | 559 | PF00917 | 0.404 |
LIG_TRAF2_2 | 452 | 457 | PF00917 | 0.682 |
LIG_TRFH_1 | 342 | 346 | PF08558 | 0.531 |
LIG_TYR_ITIM | 412 | 417 | PF00017 | 0.659 |
LIG_WRC_WIRS_1 | 581 | 586 | PF05994 | 0.558 |
MOD_CDC14_SPxK_1 | 478 | 481 | PF00782 | 0.582 |
MOD_CDK_SPxK_1 | 475 | 481 | PF00069 | 0.585 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.454 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.812 |
MOD_CK1_1 | 302 | 308 | PF00069 | 0.716 |
MOD_CK1_1 | 374 | 380 | PF00069 | 0.540 |
MOD_CK1_1 | 416 | 422 | PF00069 | 0.683 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.744 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.694 |
MOD_CK1_1 | 529 | 535 | PF00069 | 0.636 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.699 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.628 |
MOD_CK1_1 | 583 | 589 | PF00069 | 0.549 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.608 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.454 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.736 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.508 |
MOD_CK2_1 | 305 | 311 | PF00069 | 0.604 |
MOD_CK2_1 | 372 | 378 | PF00069 | 0.669 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.635 |
MOD_CK2_1 | 553 | 559 | PF00069 | 0.494 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.600 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.578 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.484 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.701 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.658 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.492 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.713 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.622 |
MOD_GlcNHglycan | 311 | 315 | PF01048 | 0.758 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.649 |
MOD_GlcNHglycan | 457 | 461 | PF01048 | 0.679 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.667 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.646 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.439 |
MOD_GlcNHglycan | 555 | 558 | PF01048 | 0.477 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.509 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.473 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.558 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.701 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.744 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.593 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.661 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.698 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.650 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.685 |
MOD_GSK3_1 | 452 | 459 | PF00069 | 0.651 |
MOD_GSK3_1 | 475 | 482 | PF00069 | 0.713 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.599 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.735 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.692 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.667 |
MOD_GSK3_1 | 79 | 86 | PF00069 | 0.485 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.361 |
MOD_N-GLC_1 | 171 | 176 | PF02516 | 0.698 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.542 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.344 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.621 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.606 |
MOD_NEK2_1 | 401 | 406 | PF00069 | 0.556 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.633 |
MOD_NEK2_1 | 603 | 608 | PF00069 | 0.524 |
MOD_PIKK_1 | 305 | 311 | PF00454 | 0.629 |
MOD_PIKK_1 | 401 | 407 | PF00454 | 0.496 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.663 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.477 |
MOD_PKA_2 | 452 | 458 | PF00069 | 0.600 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.490 |
MOD_Plk_1 | 456 | 462 | PF00069 | 0.669 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.541 |
MOD_Plk_4 | 583 | 589 | PF00069 | 0.516 |
MOD_ProDKin_1 | 342 | 348 | PF00069 | 0.539 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.624 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.691 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.782 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.706 |
TRG_DiLeu_BaEn_1 | 41 | 46 | PF01217 | 0.568 |
TRG_DiLeu_BaLyEn_6 | 281 | 286 | PF01217 | 0.581 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.663 |
TRG_NES_CRM1_1 | 34 | 49 | PF08389 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.378 |
TRG_Pf-PMV_PEXEL_1 | 245 | 250 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 284 | 288 | PF00026 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 327 | 331 | PF00026 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2H8 | Leptomonas seymouri | 47% | 81% |
A0A1X0NMF5 | Trypanosomatidae | 30% | 100% |
A0A3S7WQU1 | Leishmania donovani | 100% | 100% |
A4H5S4 | Leishmania braziliensis | 76% | 100% |
D0A9I5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
E9AMU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QHS8 | Leishmania major | 91% | 100% |
V5B2B3 | Trypanosoma cruzi | 32% | 100% |