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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HKZ1
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.757 |
CLV_C14_Caspase3-7 | 323 | 327 | PF00656 | 0.563 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 392 | 394 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.476 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 391 | 393 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 7 | 9 | PF00082 | 0.695 |
CLV_PCSK_PC1ET2_1 | 12 | 14 | PF00082 | 0.714 |
CLV_PCSK_PC1ET2_1 | 391 | 393 | PF00082 | 0.448 |
CLV_PCSK_PC1ET2_1 | 7 | 9 | PF00082 | 0.725 |
CLV_PCSK_PC7_1 | 20 | 26 | PF00082 | 0.498 |
CLV_PCSK_PC7_1 | 8 | 14 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.745 |
CLV_PCSK_SKI1_1 | 225 | 229 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.424 |
CLV_Separin_Metazoa | 17 | 21 | PF03568 | 0.605 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.746 |
DEG_APCC_DBOX_1 | 444 | 452 | PF00400 | 0.481 |
DEG_SPOP_SBC_1 | 498 | 502 | PF00917 | 0.456 |
DOC_CYCLIN_RxL_1 | 222 | 232 | PF00134 | 0.438 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 471 | 480 | PF00134 | 0.477 |
DOC_CYCLIN_yCln2_LP_2 | 522 | 525 | PF00134 | 0.336 |
DOC_MAPK_DCC_7 | 12 | 21 | PF00069 | 0.638 |
DOC_MAPK_MEF2A_6 | 243 | 251 | PF00069 | 0.452 |
DOC_MAPK_MEF2A_6 | 270 | 277 | PF00069 | 0.363 |
DOC_MAPK_MEF2A_6 | 492 | 499 | PF00069 | 0.458 |
DOC_MAPK_NFAT4_5 | 270 | 278 | PF00069 | 0.407 |
DOC_PP2B_LxvP_1 | 19 | 22 | PF13499 | 0.725 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.420 |
DOC_PP2B_LxvP_1 | 522 | 525 | PF13499 | 0.336 |
DOC_PP4_FxxP_1 | 15 | 18 | PF00568 | 0.720 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.562 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.665 |
DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 38 | 42 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 383 | 387 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 498 | 502 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 530 | 534 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 619 | 623 | PF00917 | 0.510 |
DOC_USP7_UBL2_3 | 266 | 270 | PF12436 | 0.419 |
DOC_USP7_UBL2_3 | 363 | 367 | PF12436 | 0.561 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.700 |
DOC_WW_Pin1_4 | 511 | 516 | PF00397 | 0.582 |
LIG_14-3-3_CanoR_1 | 165 | 173 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 184 | 194 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 198 | 206 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 209 | 217 | PF00244 | 0.320 |
LIG_14-3-3_CanoR_1 | 407 | 416 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 433 | 437 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 445 | 449 | PF00244 | 0.400 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.626 |
LIG_BIR_III_2 | 300 | 304 | PF00653 | 0.300 |
LIG_BRCT_BRCA1_1 | 610 | 614 | PF00533 | 0.422 |
LIG_deltaCOP1_diTrp_1 | 49 | 53 | PF00928 | 0.315 |
LIG_eIF4E_1 | 272 | 278 | PF01652 | 0.445 |
LIG_EVH1_2 | 524 | 528 | PF00568 | 0.316 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.468 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.444 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.512 |
LIG_FHA_1 | 502 | 508 | PF00498 | 0.728 |
LIG_FHA_1 | 517 | 523 | PF00498 | 0.470 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.435 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.330 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.468 |
LIG_FHA_2 | 209 | 215 | PF00498 | 0.519 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.576 |
LIG_FHA_2 | 410 | 416 | PF00498 | 0.488 |
LIG_LIR_Apic_2 | 14 | 18 | PF02991 | 0.718 |
LIG_LIR_Apic_2 | 181 | 186 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.458 |
LIG_LIR_Gen_1 | 435 | 444 | PF02991 | 0.362 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 629 | 637 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 133 | 137 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 49 | 53 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 609 | 615 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 629 | 635 | PF02991 | 0.202 |
LIG_NRBOX | 276 | 282 | PF00104 | 0.311 |
LIG_SH2_CRK | 183 | 187 | PF00017 | 0.477 |
LIG_SH2_CRK | 272 | 276 | PF00017 | 0.443 |
LIG_SH2_NCK_1 | 288 | 292 | PF00017 | 0.445 |
LIG_SH2_NCK_1 | 615 | 619 | PF00017 | 0.487 |
LIG_SH2_STAP1 | 615 | 619 | PF00017 | 0.472 |
LIG_SH2_STAT3 | 635 | 638 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 615 | 618 | PF00017 | 0.219 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.237 |
LIG_SH3_1 | 492 | 498 | PF00018 | 0.456 |
LIG_SH3_2 | 35 | 40 | PF14604 | 0.523 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.605 |
LIG_SH3_3 | 492 | 498 | PF00018 | 0.456 |
LIG_SH3_3 | 560 | 566 | PF00018 | 0.421 |
LIG_SH3_3 | 620 | 626 | PF00018 | 0.385 |
LIG_Sin3_3 | 216 | 223 | PF02671 | 0.265 |
LIG_SUMO_SIM_anti_2 | 214 | 221 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 218 | 224 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 274 | 279 | PF11976 | 0.361 |
LIG_TRAF2_1 | 109 | 112 | PF00917 | 0.558 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.625 |
LIG_TRAF2_1 | 28 | 31 | PF00917 | 0.533 |
LIG_TRAF2_1 | 355 | 358 | PF00917 | 0.482 |
MOD_CDC14_SPxK_1 | 37 | 40 | PF00782 | 0.522 |
MOD_CDK_SPxK_1 | 34 | 40 | PF00069 | 0.523 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.555 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.442 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.770 |
MOD_CK1_1 | 501 | 507 | PF00069 | 0.678 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.715 |
MOD_CK1_1 | 61 | 67 | PF00069 | 0.680 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.588 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.718 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.654 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.433 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.299 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.582 |
MOD_CK2_1 | 24 | 30 | PF00069 | 0.596 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.525 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.542 |
MOD_CK2_1 | 409 | 415 | PF00069 | 0.467 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.526 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.460 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.405 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.771 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.763 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.457 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.475 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.309 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.706 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.559 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.585 |
MOD_GlcNHglycan | 45 | 48 | PF01048 | 0.488 |
MOD_GlcNHglycan | 486 | 489 | PF01048 | 0.450 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.707 |
MOD_GlcNHglycan | 516 | 519 | PF01048 | 0.546 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.438 |
MOD_GlcNHglycan | 616 | 619 | PF01048 | 0.356 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.651 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.330 |
MOD_GSK3_1 | 208 | 215 | PF00069 | 0.294 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.234 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.292 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.613 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.495 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.591 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.559 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.391 |
MOD_N-GLC_1 | 88 | 93 | PF02516 | 0.379 |
MOD_NEK2_1 | 187 | 192 | PF00069 | 0.290 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.324 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.480 |
MOD_NEK2_1 | 439 | 444 | PF00069 | 0.402 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.474 |
MOD_NEK2_1 | 552 | 557 | PF00069 | 0.435 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.439 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.514 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.362 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.410 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.301 |
MOD_PIKK_1 | 423 | 429 | PF00454 | 0.581 |
MOD_PIKK_1 | 439 | 445 | PF00454 | 0.425 |
MOD_PIKK_1 | 516 | 522 | PF00454 | 0.424 |
MOD_PIKK_1 | 558 | 564 | PF00454 | 0.447 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.536 |
MOD_PKA_1 | 362 | 368 | PF00069 | 0.563 |
MOD_PKA_2 | 164 | 170 | PF00069 | 0.503 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.297 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.538 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.536 |
MOD_PKA_2 | 432 | 438 | PF00069 | 0.443 |
MOD_PKA_2 | 444 | 450 | PF00069 | 0.365 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.280 |
MOD_Plk_1 | 608 | 614 | PF00069 | 0.403 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.461 |
MOD_Plk_2-3 | 229 | 235 | PF00069 | 0.488 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.527 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.487 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.447 |
MOD_Plk_4 | 276 | 282 | PF00069 | 0.315 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.629 |
MOD_Plk_4 | 531 | 537 | PF00069 | 0.397 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.616 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.700 |
MOD_ProDKin_1 | 511 | 517 | PF00069 | 0.579 |
TRG_DiLeu_BaEn_1 | 229 | 234 | PF01217 | 0.329 |
TRG_DiLeu_BaEn_1 | 547 | 552 | PF01217 | 0.367 |
TRG_DiLeu_BaEn_3 | 236 | 242 | PF01217 | 0.252 |
TRG_DiLeu_BaEn_3 | 76 | 82 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 553 | 558 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 623 | 628 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.704 |
TRG_ER_diArg_1 | 392 | 394 | PF00400 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 225 | 229 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK53 | Leptomonas seymouri | 58% | 99% |
A0A1X0NRY3 | Trypanosomatidae | 28% | 100% |
A0A3Q8IHE5 | Leishmania donovani | 74% | 100% |
A0A422P2Z2 | Trypanosoma rangeli | 27% | 100% |
A4I8H2 | Leishmania infantum | 74% | 100% |
D0AAP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9B3D2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q4S4 | Leishmania major | 72% | 100% |
V5BQY9 | Trypanosoma cruzi | 27% | 100% |