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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9AVX6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 439 | 443 | PF00656 | 0.552 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 310 | 312 | PF00675 | 0.702 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 50 | 52 | PF00082 | 0.542 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 333 | 335 | PF00082 | 0.677 |
CLV_PCSK_PC1ET2_1 | 458 | 460 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 50 | 52 | PF00082 | 0.584 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.613 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 341 | 345 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.566 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.464 |
DOC_CKS1_1 | 388 | 393 | PF01111 | 0.454 |
DOC_PP1_RVXF_1 | 339 | 345 | PF00149 | 0.360 |
DOC_PP2B_LxvP_1 | 157 | 160 | PF13499 | 0.521 |
DOC_SPAK_OSR1_1 | 493 | 497 | PF12202 | 0.370 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.305 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 404 | 408 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 435 | 439 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.743 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 447 | 452 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 152 | 160 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 203 | 207 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 8 | 14 | PF00244 | 0.669 |
LIG_Actin_RPEL_3 | 486 | 505 | PF02755 | 0.486 |
LIG_BRCT_BRCA1_1 | 135 | 139 | PF00533 | 0.618 |
LIG_BRCT_BRCA1_1 | 391 | 395 | PF00533 | 0.553 |
LIG_BRCT_BRCA1_1 | 432 | 436 | PF00533 | 0.396 |
LIG_BRCT_BRCA1_1 | 87 | 91 | PF00533 | 0.603 |
LIG_Clathr_ClatBox_1 | 304 | 308 | PF01394 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 171 | 180 | PF00928 | 0.480 |
LIG_EVH1_2 | 453 | 457 | PF00568 | 0.453 |
LIG_FHA_1 | 281 | 287 | PF00498 | 0.444 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.264 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.388 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.478 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.485 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.770 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.385 |
LIG_FHA_2 | 466 | 472 | PF00498 | 0.618 |
LIG_IBAR_NPY_1 | 500 | 502 | PF08397 | 0.551 |
LIG_LIR_Apic_2 | 242 | 247 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 351 | 357 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 171 | 182 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 193 | 202 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 490 | 499 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 470 | 475 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 490 | 494 | PF02991 | 0.376 |
LIG_PCNA_yPIPBox_3 | 329 | 341 | PF02747 | 0.263 |
LIG_PDZ_Class_2 | 501 | 506 | PF00595 | 0.418 |
LIG_Pex14_1 | 174 | 178 | PF04695 | 0.465 |
LIG_PTB_Apo_2 | 291 | 298 | PF02174 | 0.362 |
LIG_SH2_CRK | 484 | 488 | PF00017 | 0.582 |
LIG_SH2_CRK | 502 | 506 | PF00017 | 0.364 |
LIG_SH2_GRB2like | 28 | 31 | PF00017 | 0.601 |
LIG_SH2_NCK_1 | 108 | 112 | PF00017 | 0.596 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.600 |
LIG_SH2_NCK_1 | 432 | 436 | PF00017 | 0.548 |
LIG_SH2_NCK_1 | 475 | 479 | PF00017 | 0.500 |
LIG_SH2_NCK_1 | 484 | 488 | PF00017 | 0.463 |
LIG_SH2_STAP1 | 432 | 436 | PF00017 | 0.396 |
LIG_SH2_STAP1 | 502 | 506 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.503 |
LIG_SH3_3 | 385 | 391 | PF00018 | 0.385 |
LIG_SH3_3 | 394 | 400 | PF00018 | 0.495 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.526 |
LIG_SUMO_SIM_anti_2 | 56 | 61 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 303 | 308 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 384 | 390 | PF11976 | 0.384 |
LIG_TRAF2_1 | 415 | 418 | PF00917 | 0.543 |
LIG_TRFH_1 | 497 | 501 | PF08558 | 0.550 |
LIG_WRC_WIRS_1 | 177 | 182 | PF05994 | 0.414 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.590 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.560 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.398 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.579 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.803 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.459 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.608 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.536 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.534 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.775 |
MOD_CK2_1 | 465 | 471 | PF00069 | 0.503 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.770 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.775 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.654 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.587 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.750 |
MOD_GlcNHglycan | 406 | 409 | PF01048 | 0.696 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.787 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.772 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.462 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.534 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.485 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.717 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.555 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.532 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.557 |
MOD_N-GLC_1 | 297 | 302 | PF02516 | 0.643 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.811 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.400 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.403 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.408 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.292 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.384 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.392 |
MOD_NEK2_1 | 430 | 435 | PF00069 | 0.584 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.513 |
MOD_NEK2_2 | 2 | 7 | PF00069 | 0.755 |
MOD_NEK2_2 | 247 | 252 | PF00069 | 0.281 |
MOD_PIKK_1 | 152 | 158 | PF00454 | 0.561 |
MOD_PIKK_1 | 312 | 318 | PF00454 | 0.514 |
MOD_PKA_1 | 310 | 316 | PF00069 | 0.516 |
MOD_PKA_1 | 7 | 13 | PF00069 | 0.621 |
MOD_PKA_2 | 202 | 208 | PF00069 | 0.423 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.446 |
MOD_PKA_2 | 310 | 316 | PF00069 | 0.460 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.440 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.740 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.620 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.610 |
MOD_PKB_1 | 423 | 431 | PF00069 | 0.485 |
MOD_Plk_1 | 366 | 372 | PF00069 | 0.502 |
MOD_Plk_1 | 441 | 447 | PF00069 | 0.556 |
MOD_Plk_1 | 55 | 61 | PF00069 | 0.607 |
MOD_Plk_1 | 98 | 104 | PF00069 | 0.394 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.605 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.336 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.376 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.552 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.567 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.528 |
MOD_Plk_4 | 9 | 15 | PF00069 | 0.819 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.510 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.419 |
MOD_ProDKin_1 | 447 | 453 | PF00069 | 0.533 |
MOD_SUMO_for_1 | 457 | 460 | PF00179 | 0.421 |
MOD_SUMO_for_1 | 97 | 100 | PF00179 | 0.605 |
TRG_DiLeu_BaEn_1 | 351 | 356 | PF01217 | 0.397 |
TRG_DiLeu_BaEn_1 | 56 | 61 | PF01217 | 0.430 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.573 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 91 | 94 | PF00400 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 51 | 55 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NV61 | Trypanosomatidae | 39% | 100% |
A0A3Q8ICC1 | Leishmania donovani | 91% | 100% |
A4HCI4 | Leishmania braziliensis | 82% | 100% |
A4I003 | Leishmania infantum | 91% | 100% |
Q4QBK3 | Leishmania major | 89% | 100% |
V5ANV0 | Trypanosoma cruzi | 36% | 100% |