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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: Q4QBH6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.686 |
CLV_C14_Caspase3-7 | 444 | 448 | PF00656 | 0.602 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.564 |
CLV_NRD_NRD_1 | 297 | 299 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.588 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 297 | 299 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.588 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.701 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.457 |
CLV_Separin_Metazoa | 352 | 356 | PF03568 | 0.495 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.616 |
DOC_AGCK_PIF_1 | 495 | 500 | PF00069 | 0.583 |
DOC_CYCLIN_RxL_1 | 52 | 61 | PF00134 | 0.546 |
DOC_CYCLIN_yCln2_LP_2 | 149 | 155 | PF00134 | 0.653 |
DOC_CYCLIN_yCln2_LP_2 | 363 | 369 | PF00134 | 0.554 |
DOC_MAPK_gen_1 | 114 | 123 | PF00069 | 0.464 |
DOC_MAPK_gen_1 | 212 | 222 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 303 | 313 | PF00069 | 0.716 |
DOC_MAPK_MEF2A_6 | 117 | 125 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 50 | 56 | PF00149 | 0.720 |
DOC_PP1_RVXF_1 | 597 | 603 | PF00149 | 0.458 |
DOC_PP2B_LxvP_1 | 149 | 152 | PF13499 | 0.640 |
DOC_PP2B_LxvP_1 | 465 | 468 | PF13499 | 0.678 |
DOC_PP4_FxxP_1 | 423 | 426 | PF00568 | 0.593 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 445 | 449 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 501 | 505 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.606 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.586 |
LIG_14-3-3_CanoR_1 | 150 | 156 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 217 | 223 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 427 | 432 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 441 | 450 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 471 | 476 | PF00244 | 0.408 |
LIG_BIR_III_2 | 554 | 558 | PF00653 | 0.643 |
LIG_BRCT_BRCA1_1 | 163 | 167 | PF00533 | 0.663 |
LIG_BRCT_BRCA1_1 | 472 | 476 | PF00533 | 0.617 |
LIG_BRCT_BRCA1_1 | 498 | 502 | PF00533 | 0.570 |
LIG_BRCT_BRCA1_1 | 58 | 62 | PF00533 | 0.566 |
LIG_BRCT_BRCA1_1 | 588 | 592 | PF00533 | 0.562 |
LIG_BRCT_BRCA1_1 | 76 | 80 | PF00533 | 0.368 |
LIG_Clathr_ClatBox_1 | 579 | 583 | PF01394 | 0.530 |
LIG_FHA_1 | 131 | 137 | PF00498 | 0.499 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.575 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.540 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.674 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.552 |
LIG_FHA_1 | 477 | 483 | PF00498 | 0.580 |
LIG_FHA_1 | 503 | 509 | PF00498 | 0.592 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.412 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.484 |
LIG_FHA_1 | 551 | 557 | PF00498 | 0.706 |
LIG_FHA_1 | 566 | 572 | PF00498 | 0.411 |
LIG_FHA_1 | 574 | 580 | PF00498 | 0.430 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.681 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.556 |
LIG_GBD_Chelix_1 | 87 | 95 | PF00786 | 0.340 |
LIG_LIR_Apic_2 | 404 | 410 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 164 | 169 | PF02991 | 0.642 |
LIG_LIR_Gen_1 | 216 | 223 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 349 | 359 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 470 | 480 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 589 | 600 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 164 | 168 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 216 | 222 | PF02991 | 0.617 |
LIG_LIR_Nem_3 | 26 | 30 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 349 | 354 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 540 | 544 | PF02991 | 0.652 |
LIG_LIR_Nem_3 | 589 | 595 | PF02991 | 0.586 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 99 | 105 | PF02991 | 0.651 |
LIG_Pex14_2 | 219 | 223 | PF04695 | 0.408 |
LIG_Pex14_2 | 472 | 476 | PF04695 | 0.501 |
LIG_Pex14_2 | 481 | 485 | PF04695 | 0.550 |
LIG_Pex14_2 | 498 | 502 | PF04695 | 0.292 |
LIG_PTB_Apo_2 | 545 | 552 | PF02174 | 0.441 |
LIG_PTB_Phospho_1 | 545 | 551 | PF10480 | 0.444 |
LIG_REV1ctd_RIR_1 | 533 | 543 | PF16727 | 0.609 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.651 |
LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.641 |
LIG_SH2_STAP1 | 67 | 71 | PF00017 | 0.625 |
LIG_SH2_STAT3 | 7 | 10 | PF00017 | 0.768 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.542 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.643 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 478 | 481 | PF00017 | 0.571 |
LIG_SH2_STAT5 | 551 | 554 | PF00017 | 0.647 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.610 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.570 |
LIG_SUMO_SIM_par_1 | 156 | 161 | PF11976 | 0.617 |
LIG_SUMO_SIM_par_1 | 364 | 370 | PF11976 | 0.606 |
LIG_SUMO_SIM_par_1 | 593 | 598 | PF11976 | 0.580 |
LIG_TYR_ITIM | 189 | 194 | PF00017 | 0.694 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.754 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.581 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.588 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.710 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.707 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.594 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.565 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.663 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.762 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.573 |
MOD_GlcNHglycan | 102 | 105 | PF01048 | 0.516 |
MOD_GlcNHglycan | 20 | 23 | PF01048 | 0.544 |
MOD_GlcNHglycan | 209 | 212 | PF01048 | 0.681 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.477 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.737 |
MOD_GlcNHglycan | 443 | 446 | PF01048 | 0.622 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.561 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.604 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.441 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.599 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.632 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.548 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.667 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.444 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.488 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.423 |
MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.636 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.670 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.620 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.590 |
MOD_NEK2_1 | 502 | 507 | PF00069 | 0.552 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.466 |
MOD_NEK2_1 | 586 | 591 | PF00069 | 0.611 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.507 |
MOD_NEK2_2 | 218 | 223 | PF00069 | 0.412 |
MOD_NEK2_2 | 261 | 266 | PF00069 | 0.454 |
MOD_NEK2_2 | 530 | 535 | PF00069 | 0.379 |
MOD_NEK2_2 | 542 | 547 | PF00069 | 0.399 |
MOD_NEK2_2 | 573 | 578 | PF00069 | 0.514 |
MOD_PK_1 | 427 | 433 | PF00069 | 0.378 |
MOD_PK_1 | 97 | 103 | PF00069 | 0.598 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.661 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.664 |
MOD_PKA_2 | 296 | 302 | PF00069 | 0.533 |
MOD_PKA_2 | 470 | 476 | PF00069 | 0.384 |
MOD_PKA_2 | 74 | 80 | PF00069 | 0.429 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.684 |
MOD_Plk_1 | 246 | 252 | PF00069 | 0.421 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.694 |
MOD_Plk_1 | 439 | 445 | PF00069 | 0.628 |
MOD_Plk_1 | 565 | 571 | PF00069 | 0.517 |
MOD_Plk_1 | 587 | 593 | PF00069 | 0.618 |
MOD_Plk_2-3 | 74 | 80 | PF00069 | 0.429 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.541 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.638 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.622 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.436 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.477 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.756 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.489 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.573 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.579 |
MOD_Plk_4 | 566 | 572 | PF00069 | 0.621 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.441 |
MOD_Plk_4 | 588 | 594 | PF00069 | 0.504 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.598 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.416 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.650 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.583 |
MOD_SUMO_for_1 | 169 | 172 | PF00179 | 0.562 |
MOD_SUMO_for_1 | 37 | 40 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_1 | 566 | 571 | PF01217 | 0.555 |
TRG_DiLeu_BaEn_2 | 587 | 593 | PF01217 | 0.618 |
TRG_DiLeu_BaLyEn_6 | 504 | 509 | PF01217 | 0.595 |
TRG_DiLeu_BaLyEn_6 | 559 | 564 | PF01217 | 0.469 |
TRG_DiLeu_BaLyEn_6 | 575 | 580 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 102 | 105 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.568 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.596 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.649 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.583 |
TRG_ER_diArg_1 | 145 | 148 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 297 | 300 | PF00400 | 0.608 |
TRG_ER_diArg_1 | 537 | 539 | PF00400 | 0.554 |
TRG_NLS_MonoExtC_3 | 145 | 150 | PF00514 | 0.519 |
TRG_NLS_MonoExtN_4 | 146 | 151 | PF00514 | 0.523 |
TRG_Pf-PMV_PEXEL_1 | 251 | 255 | PF00026 | 0.682 |
TRG_Pf-PMV_PEXEL_1 | 562 | 566 | PF00026 | 0.475 |
TRG_Pf-PMV_PEXEL_1 | 578 | 583 | PF00026 | 0.432 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICD4 | Leishmania donovani | 84% | 100% |
A4HCL3 | Leishmania braziliensis | 59% | 100% |
A4I037 | Leishmania infantum | 84% | 100% |
E9AW00 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |