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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4HHJ8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.698 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.599 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.686 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.599 |
CLV_PCSK_PC1ET2_1 | 120 | 122 | PF00082 | 0.547 |
DEG_SPOP_SBC_1 | 409 | 413 | PF00917 | 0.611 |
DOC_ANK_TNKS_1 | 451 | 458 | PF00023 | 0.607 |
DOC_CDC14_PxL_1 | 165 | 173 | PF14671 | 0.600 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.681 |
DOC_CYCLIN_yCln2_LP_2 | 146 | 152 | PF00134 | 0.663 |
DOC_CYCLIN_yCln2_LP_2 | 155 | 158 | PF00134 | 0.576 |
DOC_PP1_RVXF_1 | 210 | 217 | PF00149 | 0.422 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.511 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.671 |
DOC_PP4_FxxP_1 | 273 | 276 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.711 |
DOC_SPAK_OSR1_1 | 238 | 242 | PF12202 | 0.615 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 409 | 413 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.728 |
DOC_USP7_MATH_2 | 125 | 131 | PF00917 | 0.522 |
DOC_USP7_MATH_2 | 5 | 11 | PF00917 | 0.525 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.553 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.757 |
DOC_WW_Pin1_4 | 517 | 522 | PF00397 | 0.494 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.489 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 314 | 320 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 370 | 377 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 97 | 106 | PF00244 | 0.606 |
LIG_Actin_WH2_2 | 176 | 192 | PF00022 | 0.431 |
LIG_APCC_ABBA_1 | 90 | 95 | PF00400 | 0.635 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.678 |
LIG_CtBP_PxDLS_1 | 157 | 161 | PF00389 | 0.516 |
LIG_deltaCOP1_diTrp_1 | 310 | 315 | PF00928 | 0.605 |
LIG_EVH1_1 | 445 | 449 | PF00568 | 0.506 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.452 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.495 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.534 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.661 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.478 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.573 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.630 |
LIG_FHA_2 | 414 | 420 | PF00498 | 0.662 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.491 |
LIG_FHA_2 | 60 | 66 | PF00498 | 0.542 |
LIG_FHA_2 | 78 | 84 | PF00498 | 0.471 |
LIG_LIR_Gen_1 | 180 | 189 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 520 | 530 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 126 | 131 | PF02991 | 0.621 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.656 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.584 |
LIG_LIR_Nem_3 | 180 | 185 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.596 |
LIG_LYPXL_yS_3 | 128 | 131 | PF13949 | 0.514 |
LIG_MYND_1 | 129 | 133 | PF01753 | 0.506 |
LIG_MYND_1 | 153 | 157 | PF01753 | 0.515 |
LIG_MYND_1 | 517 | 521 | PF01753 | 0.565 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.429 |
LIG_SH2_STAT3 | 324 | 327 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.493 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.517 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.684 |
LIG_SH3_3 | 295 | 301 | PF00018 | 0.652 |
LIG_SH3_3 | 432 | 438 | PF00018 | 0.608 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.631 |
LIG_SUMO_SIM_par_1 | 172 | 180 | PF11976 | 0.460 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.450 |
LIG_TRAF2_1 | 496 | 499 | PF00917 | 0.489 |
LIG_UBA3_1 | 464 | 470 | PF00899 | 0.462 |
LIG_WW_3 | 43 | 47 | PF00397 | 0.546 |
MOD_CK1_1 | 10 | 16 | PF00069 | 0.508 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.642 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.490 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.635 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.676 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.692 |
MOD_CK2_1 | 349 | 355 | PF00069 | 0.585 |
MOD_CK2_1 | 413 | 419 | PF00069 | 0.757 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.579 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.490 |
MOD_CK2_1 | 59 | 65 | PF00069 | 0.542 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.560 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.640 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.521 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.525 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.589 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.720 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.770 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.761 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.781 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.635 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.473 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.808 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.626 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.660 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.583 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.760 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.619 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.677 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.689 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.721 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.510 |
MOD_N-GLC_1 | 217 | 222 | PF02516 | 0.454 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.578 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.541 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.459 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.614 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.521 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.601 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.706 |
MOD_PIKK_1 | 101 | 107 | PF00454 | 0.609 |
MOD_PIKK_1 | 33 | 39 | PF00454 | 0.622 |
MOD_PIKK_1 | 356 | 362 | PF00454 | 0.528 |
MOD_PIKK_1 | 413 | 419 | PF00454 | 0.652 |
MOD_PK_1 | 280 | 286 | PF00069 | 0.622 |
MOD_PK_1 | 50 | 56 | PF00069 | 0.544 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.472 |
MOD_PKA_2 | 333 | 339 | PF00069 | 0.666 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.609 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.663 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.622 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.680 |
MOD_Plk_1 | 354 | 360 | PF00069 | 0.482 |
MOD_Plk_1 | 427 | 433 | PF00069 | 0.537 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.622 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.605 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.534 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.580 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.601 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.548 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.556 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.679 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.755 |
MOD_ProDKin_1 | 517 | 523 | PF00069 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.705 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.533 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.605 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.493 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.554 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.643 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.591 |
TRG_NES_CRM1_1 | 456 | 469 | PF08389 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.565 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXW3 | Leptomonas seymouri | 26% | 92% |
A0A3Q8IDU7 | Leishmania donovani | 68% | 100% |
A4I4Q7 | Leishmania infantum | 68% | 100% |
E9AE60 | Leishmania major | 68% | 100% |
E9ALM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 100% |