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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4HI57
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 49 | 53 | PF00656 | 0.711 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.609 |
CLV_NRD_NRD_1 | 207 | 209 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.624 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 437 | 439 | PF00675 | 0.514 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.625 |
CLV_PCSK_FUR_1 | 21 | 25 | PF00082 | 0.673 |
CLV_PCSK_FUR_1 | 39 | 43 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.661 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.489 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.681 |
CLV_PCSK_PC1ET2_1 | 41 | 43 | PF00082 | 0.645 |
CLV_PCSK_PC7_1 | 19 | 25 | PF00082 | 0.668 |
CLV_PCSK_PC7_1 | 37 | 43 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.595 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.620 |
CLV_Separin_Metazoa | 414 | 418 | PF03568 | 0.595 |
DEG_APCC_DBOX_1 | 436 | 444 | PF00400 | 0.547 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.608 |
DEG_SPOP_SBC_1 | 279 | 283 | PF00917 | 0.706 |
DEG_SPOP_SBC_1 | 362 | 366 | PF00917 | 0.527 |
DOC_CYCLIN_RxL_1 | 472 | 483 | PF00134 | 0.549 |
DOC_MAPK_DCC_7 | 437 | 445 | PF00069 | 0.527 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 333 | 341 | PF00069 | 0.491 |
DOC_MAPK_gen_1 | 389 | 398 | PF00069 | 0.744 |
DOC_MAPK_gen_1 | 437 | 445 | PF00069 | 0.479 |
DOC_MAPK_gen_1 | 86 | 96 | PF00069 | 0.429 |
DOC_MAPK_MEF2A_6 | 247 | 256 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 437 | 446 | PF00069 | 0.474 |
DOC_PP2B_LxvP_1 | 148 | 151 | PF13499 | 0.588 |
DOC_PP2B_LxvP_1 | 256 | 259 | PF13499 | 0.686 |
DOC_PP2B_LxvP_1 | 76 | 79 | PF13499 | 0.555 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.792 |
DOC_USP7_MATH_1 | 408 | 412 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 463 | 467 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.518 |
DOC_USP7_UBL2_3 | 390 | 394 | PF12436 | 0.664 |
DOC_WW_Pin1_4 | 192 | 197 | PF00397 | 0.588 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.610 |
LIG_14-3-3_CanoR_1 | 11 | 18 | PF00244 | 0.656 |
LIG_14-3-3_CanoR_1 | 138 | 142 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 223 | 231 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 3 | 7 | PF00244 | 0.674 |
LIG_14-3-3_CanoR_1 | 406 | 416 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 42 | 50 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 467 | 473 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 475 | 480 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 520 | 530 | PF00244 | 0.756 |
LIG_Actin_WH2_2 | 112 | 130 | PF00022 | 0.609 |
LIG_BIR_III_2 | 431 | 435 | PF00653 | 0.693 |
LIG_BRCT_BRCA1_1 | 13 | 17 | PF00533 | 0.672 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.717 |
LIG_BRCT_BRCA1_1 | 482 | 486 | PF00533 | 0.505 |
LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.469 |
LIG_Clathr_ClatBox_1 | 443 | 447 | PF01394 | 0.481 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.484 |
LIG_deltaCOP1_diTrp_1 | 502 | 510 | PF00928 | 0.501 |
LIG_eIF4E_1 | 225 | 231 | PF01652 | 0.538 |
LIG_EVH1_2 | 267 | 271 | PF00568 | 0.784 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.571 |
LIG_FHA_1 | 225 | 231 | PF00498 | 0.557 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.707 |
LIG_FHA_1 | 314 | 320 | PF00498 | 0.529 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.347 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.696 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.763 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.605 |
LIG_FHA_2 | 3 | 9 | PF00498 | 0.726 |
LIG_GBD_Chelix_1 | 125 | 133 | PF00786 | 0.398 |
LIG_GBD_Chelix_1 | 157 | 165 | PF00786 | 0.562 |
LIG_GBD_Chelix_1 | 497 | 505 | PF00786 | 0.362 |
LIG_IBAR_NPY_1 | 104 | 106 | PF08397 | 0.576 |
LIG_LIR_Apic_2 | 95 | 100 | PF02991 | 0.584 |
LIG_LIR_Gen_1 | 447 | 455 | PF02991 | 0.626 |
LIG_LIR_Nem_3 | 152 | 157 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 483 | 489 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 5 | 9 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 507 | 513 | PF02991 | 0.372 |
LIG_SH2_CRK | 40 | 44 | PF00017 | 0.630 |
LIG_SH2_CRK | 448 | 452 | PF00017 | 0.592 |
LIG_SH2_NCK_1 | 448 | 452 | PF00017 | 0.592 |
LIG_SH2_STAT3 | 420 | 423 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 420 | 423 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 513 | 516 | PF00017 | 0.652 |
LIG_SH3_3 | 128 | 134 | PF00018 | 0.430 |
LIG_SH3_3 | 325 | 331 | PF00018 | 0.513 |
LIG_SH3_3 | 355 | 361 | PF00018 | 0.489 |
LIG_SUMO_SIM_par_1 | 441 | 447 | PF11976 | 0.486 |
LIG_TRAF2_1 | 150 | 153 | PF00917 | 0.565 |
LIG_TYR_ITIM | 4 | 9 | PF00017 | 0.471 |
LIG_TYR_ITIM | 446 | 451 | PF00017 | 0.559 |
LIG_WW_1 | 260 | 263 | PF00397 | 0.489 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.570 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.682 |
MOD_CK1_1 | 317 | 323 | PF00069 | 0.671 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.744 |
MOD_CK1_1 | 457 | 463 | PF00069 | 0.599 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.560 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.557 |
MOD_CK2_1 | 408 | 414 | PF00069 | 0.584 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.560 |
MOD_Cter_Amidation | 34 | 37 | PF01082 | 0.639 |
MOD_Cter_Amidation | 52 | 55 | PF01082 | 0.627 |
MOD_GlcNHglycan | 165 | 168 | PF01048 | 0.549 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.680 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.689 |
MOD_GlcNHglycan | 343 | 347 | PF01048 | 0.539 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.677 |
MOD_GlcNHglycan | 455 | 459 | PF01048 | 0.603 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.557 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.504 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.469 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.478 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.587 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.674 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.660 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.534 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.584 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.660 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.664 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.687 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.647 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.565 |
MOD_N-GLC_1 | 121 | 126 | PF02516 | 0.517 |
MOD_N-GLC_1 | 461 | 466 | PF02516 | 0.528 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.517 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.581 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.475 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.462 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.570 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.635 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.708 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.785 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.731 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.655 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.588 |
MOD_NEK2_1 | 489 | 494 | PF00069 | 0.529 |
MOD_PIKK_1 | 293 | 299 | PF00454 | 0.762 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.724 |
MOD_PK_1 | 42 | 48 | PF00069 | 0.759 |
MOD_PKA_1 | 41 | 47 | PF00069 | 0.631 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.595 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.469 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.731 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.646 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.461 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.631 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.664 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.512 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.585 |
MOD_Plk_1 | 217 | 223 | PF00069 | 0.336 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.576 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.512 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.505 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.676 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.706 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.483 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.563 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.512 |
MOD_ProDKin_1 | 192 | 198 | PF00069 | 0.602 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.537 |
MOD_SUMO_for_1 | 235 | 238 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 111 | 119 | PF00179 | 0.584 |
TRG_DiLeu_BaLyEn_6 | 347 | 352 | PF01217 | 0.569 |
TRG_DiLeu_BaLyEn_6 | 484 | 489 | PF01217 | 0.309 |
TRG_ENDOCYTIC_2 | 40 | 43 | PF00928 | 0.637 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.535 |
TRG_ENDOCYTIC_2 | 6 | 9 | PF00928 | 0.605 |
TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.729 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 437 | 439 | PF00400 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 475 | 480 | PF00026 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 487 | 491 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PGI0 | Leptomonas seymouri | 49% | 93% |
A0A1X0P334 | Trypanosomatidae | 35% | 100% |
A0A3Q8IFQ7 | Leishmania donovani | 75% | 100% |
A4I5D3 | Leishmania infantum | 74% | 100% |
C9ZQR5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B0N1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4Q7K1 | Leishmania major | 75% | 100% |