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: E9AE60
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 400 | 404 | PF00656 | 0.564 |
CLV_C14_Caspase3-7 | 418 | 422 | PF00656 | 0.612 |
CLV_NRD_NRD_1 | 370 | 372 | PF00675 | 0.640 |
CLV_NRD_NRD_1 | 42 | 44 | PF00675 | 0.688 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.624 |
CLV_PCSK_FUR_1 | 40 | 44 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 343 | 345 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 370 | 372 | PF00082 | 0.640 |
CLV_PCSK_KEX2_1 | 42 | 44 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 473 | 475 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 343 | 345 | PF00082 | 0.725 |
CLV_PCSK_PC1ET2_1 | 473 | 475 | PF00082 | 0.548 |
DEG_SPOP_SBC_1 | 348 | 352 | PF00917 | 0.726 |
DOC_ANK_TNKS_1 | 451 | 458 | PF00023 | 0.679 |
DOC_CKS1_1 | 273 | 278 | PF01111 | 0.437 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.662 |
DOC_CYCLIN_yCln2_LP_2 | 146 | 152 | PF00134 | 0.770 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.576 |
DOC_PP2B_LxvP_1 | 189 | 192 | PF13499 | 0.631 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.777 |
DOC_PP4_FxxP_1 | 6 | 9 | PF00568 | 0.730 |
DOC_SPAK_OSR1_1 | 238 | 242 | PF12202 | 0.688 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 348 | 352 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.724 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.639 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.715 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.799 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.756 |
LIG_14-3-3_CanoR_1 | 121 | 131 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 238 | 242 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 362 | 367 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 370 | 377 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 64 | 74 | PF00244 | 0.703 |
LIG_APCC_ABBA_1 | 90 | 95 | PF00400 | 0.723 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.772 |
LIG_BIR_III_4 | 421 | 425 | PF00653 | 0.695 |
LIG_BIR_III_4 | 429 | 433 | PF00653 | 0.617 |
LIG_BIR_III_4 | 480 | 484 | PF00653 | 0.702 |
LIG_deltaCOP1_diTrp_1 | 310 | 315 | PF00928 | 0.644 |
LIG_deltaCOP1_diTrp_1 | 373 | 380 | PF00928 | 0.536 |
LIG_eIF4E_1 | 12 | 18 | PF01652 | 0.522 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.712 |
LIG_FHA_1 | 355 | 361 | PF00498 | 0.581 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.673 |
LIG_FHA_1 | 386 | 392 | PF00498 | 0.511 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.691 |
LIG_FHA_1 | 448 | 454 | PF00498 | 0.642 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.436 |
LIG_FHA_2 | 328 | 334 | PF00498 | 0.682 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.769 |
LIG_LIR_Apic_2 | 3 | 9 | PF02991 | 0.566 |
LIG_LIR_Gen_1 | 132 | 142 | PF02991 | 0.643 |
LIG_LIR_Nem_3 | 13 | 18 | PF02991 | 0.746 |
LIG_LIR_Nem_3 | 132 | 137 | PF02991 | 0.723 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 91 | 96 | PF02991 | 0.661 |
LIG_MYND_1 | 517 | 521 | PF01753 | 0.617 |
LIG_PCNA_PIPBox_1 | 498 | 507 | PF02747 | 0.663 |
LIG_SH2_CRK | 134 | 138 | PF00017 | 0.719 |
LIG_SH2_GRB2like | 12 | 15 | PF00017 | 0.571 |
LIG_SH2_PTP2 | 270 | 273 | PF00017 | 0.458 |
LIG_SH2_STAP1 | 134 | 138 | PF00017 | 0.719 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.483 |
LIG_SH2_STAT3 | 282 | 285 | PF00017 | 0.586 |
LIG_SH2_STAT3 | 324 | 327 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 181 | 184 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.709 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.675 |
LIG_SH3_3 | 298 | 304 | PF00018 | 0.603 |
LIG_SH3_3 | 441 | 447 | PF00018 | 0.749 |
LIG_SH3_3 | 514 | 520 | PF00018 | 0.663 |
LIG_SUMO_SIM_anti_2 | 203 | 208 | PF11976 | 0.465 |
LIG_SUMO_SIM_anti_2 | 78 | 84 | PF11976 | 0.627 |
LIG_UBA3_1 | 379 | 387 | PF00899 | 0.607 |
LIG_WW_1 | 520 | 523 | PF00397 | 0.539 |
LIG_WW_1 | 9 | 12 | PF00397 | 0.533 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.715 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.798 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.608 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.536 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.630 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.756 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.786 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.564 |
MOD_CK2_1 | 272 | 278 | PF00069 | 0.430 |
MOD_CK2_1 | 327 | 333 | PF00069 | 0.600 |
MOD_CK2_1 | 334 | 340 | PF00069 | 0.705 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.772 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.545 |
MOD_GlcNHglycan | 218 | 222 | PF01048 | 0.527 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.587 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.784 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.805 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.765 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.531 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.489 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.826 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.651 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.654 |
MOD_GSK3_1 | 327 | 334 | PF00069 | 0.648 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.711 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.619 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.751 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.628 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.748 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.721 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.679 |
MOD_N-GLC_1 | 295 | 300 | PF02516 | 0.577 |
MOD_N-GLC_1 | 405 | 410 | PF02516 | 0.737 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.721 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.742 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.603 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.719 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.656 |
MOD_NEK2_1 | 326 | 331 | PF00069 | 0.628 |
MOD_NEK2_1 | 380 | 385 | PF00069 | 0.698 |
MOD_NEK2_1 | 397 | 402 | PF00069 | 0.509 |
MOD_PIKK_1 | 114 | 120 | PF00454 | 0.704 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.784 |
MOD_PK_1 | 280 | 286 | PF00069 | 0.690 |
MOD_PKA_1 | 343 | 349 | PF00069 | 0.724 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.621 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.604 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.624 |
MOD_PKA_2 | 369 | 375 | PF00069 | 0.695 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.763 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.690 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.806 |
MOD_Plk_1 | 85 | 91 | PF00069 | 0.706 |
MOD_Plk_2-3 | 295 | 301 | PF00069 | 0.542 |
MOD_Plk_2-3 | 369 | 375 | PF00069 | 0.625 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.675 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.562 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.694 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.716 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.667 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.628 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.451 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.718 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.799 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.754 |
MOD_SUMO_for_1 | 416 | 419 | PF00179 | 0.588 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.704 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.558 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.701 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.598 |
TRG_ER_diArg_1 | 41 | 43 | PF00400 | 0.683 |
TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.616 |
TRG_NES_CRM1_1 | 456 | 469 | PF08389 | 0.546 |
TRG_Pf-PMV_PEXEL_1 | 242 | 246 | PF00026 | 0.515 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXW3 | Leptomonas seymouri | 26% | 92% |
A0A3Q8IDU7 | Leishmania donovani | 88% | 100% |
A4HHJ8 | Leishmania braziliensis | 68% | 100% |
A4I4Q7 | Leishmania infantum | 88% | 100% |
E9ALM5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |