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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WZ73
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.567 |
CLV_C14_Caspase3-7 | 386 | 390 | PF00656 | 0.788 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.728 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.690 |
CLV_PCSK_FUR_1 | 308 | 312 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.747 |
CLV_PCSK_PC1ET2_1 | 304 | 306 | PF00082 | 0.533 |
CLV_PCSK_PC7_1 | 310 | 316 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 336 | 340 | PF00082 | 0.612 |
DOC_ANK_TNKS_1 | 155 | 162 | PF00023 | 0.551 |
DOC_CYCLIN_RxL_1 | 287 | 294 | PF00134 | 0.426 |
DOC_CYCLIN_RxL_1 | 330 | 344 | PF00134 | 0.657 |
DOC_MAPK_gen_1 | 186 | 195 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 416 | 422 | PF00069 | 0.713 |
DOC_MAPK_MEF2A_6 | 396 | 404 | PF00069 | 0.641 |
DOC_PP1_RVXF_1 | 225 | 232 | PF00149 | 0.445 |
DOC_PP1_RVXF_1 | 334 | 341 | PF00149 | 0.648 |
DOC_PP1_RVXF_1 | 560 | 567 | PF00149 | 0.570 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.698 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 265 | 269 | PF00917 | 0.556 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.744 |
DOC_USP7_MATH_1 | 366 | 370 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 514 | 518 | PF00917 | 0.726 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.794 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.638 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.688 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.763 |
LIG_14-3-3_CanoR_1 | 188 | 196 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 290 | 300 | PF00244 | 0.512 |
LIG_14-3-3_CanoR_1 | 308 | 316 | PF00244 | 0.625 |
LIG_14-3-3_CanoR_1 | 326 | 334 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 455 | 463 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 569 | 573 | PF00244 | 0.650 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.704 |
LIG_BIR_III_2 | 389 | 393 | PF00653 | 0.637 |
LIG_Clathr_ClatBox_1 | 339 | 343 | PF01394 | 0.607 |
LIG_eIF4E_1 | 333 | 339 | PF01652 | 0.652 |
LIG_FHA_1 | 326 | 332 | PF00498 | 0.611 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.645 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.531 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.714 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.688 |
LIG_FHA_2 | 115 | 121 | PF00498 | 0.652 |
LIG_FHA_2 | 381 | 387 | PF00498 | 0.777 |
LIG_FHA_2 | 584 | 590 | PF00498 | 0.699 |
LIG_GBD_Chelix_1 | 471 | 479 | PF00786 | 0.709 |
LIG_LIR_Apic_2 | 133 | 138 | PF02991 | 0.615 |
LIG_LIR_Gen_1 | 13 | 23 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 357 | 368 | PF02991 | 0.718 |
LIG_LIR_Gen_1 | 44 | 55 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 565 | 574 | PF02991 | 0.634 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 357 | 363 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 66 | 72 | PF02991 | 0.469 |
LIG_NRBOX | 287 | 293 | PF00104 | 0.460 |
LIG_PDZ_Class_1 | 591 | 596 | PF00595 | 0.623 |
LIG_Pex14_2 | 404 | 408 | PF04695 | 0.550 |
LIG_Rb_pABgroove_1 | 12 | 20 | PF01858 | 0.646 |
LIG_Rb_pABgroove_1 | 295 | 303 | PF01858 | 0.502 |
LIG_REV1ctd_RIR_1 | 564 | 573 | PF16727 | 0.634 |
LIG_SH2_CRK | 47 | 51 | PF00017 | 0.471 |
LIG_SH2_CRK | 476 | 480 | PF00017 | 0.734 |
LIG_SH2_PTP2 | 360 | 363 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 47 | 51 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.356 |
LIG_SH2_STAT5 | 360 | 363 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 462 | 465 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.685 |
LIG_SH3_1 | 156 | 162 | PF00018 | 0.596 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.647 |
LIG_SH3_3 | 235 | 241 | PF00018 | 0.595 |
LIG_SH3_3 | 360 | 366 | PF00018 | 0.566 |
LIG_SH3_3 | 389 | 395 | PF00018 | 0.651 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.779 |
LIG_SH3_3 | 503 | 509 | PF00018 | 0.703 |
LIG_SUMO_SIM_anti_2 | 359 | 365 | PF11976 | 0.713 |
LIG_SUMO_SIM_par_1 | 165 | 171 | PF11976 | 0.584 |
LIG_TRAF2_1 | 221 | 224 | PF00917 | 0.499 |
LIG_TYR_ITIM | 45 | 50 | PF00017 | 0.582 |
LIG_TYR_ITIM | 474 | 479 | PF00017 | 0.722 |
LIG_UBA3_1 | 331 | 336 | PF00899 | 0.698 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.670 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.508 |
MOD_CK1_1 | 341 | 347 | PF00069 | 0.700 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.697 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.626 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.668 |
MOD_CK1_1 | 521 | 527 | PF00069 | 0.769 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.595 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.684 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.732 |
MOD_CK2_1 | 380 | 386 | PF00069 | 0.776 |
MOD_CK2_1 | 514 | 520 | PF00069 | 0.716 |
MOD_CK2_1 | 526 | 532 | PF00069 | 0.750 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.561 |
MOD_CK2_1 | 583 | 589 | PF00069 | 0.655 |
MOD_GlcNHglycan | 24 | 28 | PF01048 | 0.711 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.644 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.659 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.647 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.767 |
MOD_GlcNHglycan | 522 | 526 | PF01048 | 0.747 |
MOD_GlcNHglycan | 528 | 532 | PF01048 | 0.788 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.625 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.582 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.721 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.723 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.557 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.703 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.650 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.637 |
MOD_N-GLC_1 | 322 | 327 | PF02516 | 0.724 |
MOD_N-GLC_1 | 366 | 371 | PF02516 | 0.714 |
MOD_N-GLC_1 | 591 | 596 | PF02516 | 0.673 |
MOD_NEK2_1 | 196 | 201 | PF00069 | 0.622 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.473 |
MOD_NEK2_1 | 286 | 291 | PF00069 | 0.506 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.717 |
MOD_NEK2_1 | 454 | 459 | PF00069 | 0.711 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.554 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.686 |
MOD_PIKK_1 | 430 | 436 | PF00454 | 0.736 |
MOD_PIKK_1 | 88 | 94 | PF00454 | 0.635 |
MOD_PKA_1 | 304 | 310 | PF00069 | 0.452 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.631 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.715 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.738 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.626 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.642 |
MOD_PKA_2 | 583 | 589 | PF00069 | 0.595 |
MOD_PKB_1 | 186 | 194 | PF00069 | 0.585 |
MOD_Plk_1 | 356 | 362 | PF00069 | 0.693 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.669 |
MOD_Plk_2-3 | 114 | 120 | PF00069 | 0.659 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.588 |
MOD_Plk_2-3 | 538 | 544 | PF00069 | 0.737 |
MOD_Plk_2-3 | 560 | 566 | PF00069 | 0.683 |
MOD_Plk_4 | 356 | 362 | PF00069 | 0.513 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.670 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.564 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.631 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.635 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.687 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.760 |
MOD_SUMO_rev_2 | 412 | 419 | PF00179 | 0.648 |
MOD_SUMO_rev_2 | 588 | 593 | PF00179 | 0.720 |
MOD_SUMO_rev_2 | 82 | 91 | PF00179 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 287 | 292 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 334 | 339 | PF01217 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 344 | 349 | PF01217 | 0.641 |
TRG_DiLeu_BaLyEn_6 | 475 | 480 | PF01217 | 0.687 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.700 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.735 |
TRG_ENDOCYTIC_2 | 72 | 75 | PF00928 | 0.530 |
TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 308 | 311 | PF00400 | 0.709 |
TRG_ER_diArg_1 | 314 | 316 | PF00400 | 0.661 |
TRG_Pf-PMV_PEXEL_1 | 194 | 198 | PF00026 | 0.562 |
TRG_Pf-PMV_PEXEL_1 | 347 | 351 | PF00026 | 0.593 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZM0 | Leptomonas seymouri | 46% | 100% |
A0A1X0NY83 | Trypanosomatidae | 27% | 100% |
A0A422NL47 | Trypanosoma rangeli | 29% | 100% |
A4HEJ9 | Leishmania braziliensis | 77% | 100% |
A4I1J9 | Leishmania infantum | 100% | 100% |
C9ZK33 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AXN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q9T8 | Leishmania major | 91% | 99% |