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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8ICP9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 346 | 352 | PF00089 | 0.463 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 309 | 311 | PF00675 | 0.612 |
CLV_NRD_NRD_1 | 45 | 47 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 75 | 77 | PF00675 | 0.649 |
CLV_PCSK_KEX2_1 | 149 | 151 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 309 | 311 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 45 | 47 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.733 |
CLV_PCSK_PC1ET2_1 | 149 | 151 | PF00082 | 0.518 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.743 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 173 | 177 | PF00082 | 0.341 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.476 |
CLV_PCSK_SKI1_1 | 379 | 383 | PF00082 | 0.389 |
DEG_APCC_DBOX_1 | 17 | 25 | PF00400 | 0.473 |
DEG_APCC_DBOX_1 | 487 | 495 | PF00400 | 0.423 |
DEG_COP1_1 | 78 | 89 | PF00400 | 0.495 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.516 |
DEG_SCF_SKP2-CKS1_1 | 401 | 408 | PF00560 | 0.472 |
DOC_AGCK_PIF_1 | 347 | 352 | PF00069 | 0.466 |
DOC_CKS1_1 | 435 | 440 | PF01111 | 0.525 |
DOC_CYCLIN_yCln2_LP_2 | 435 | 441 | PF00134 | 0.550 |
DOC_CYCLIN_yCln2_LP_2 | 447 | 453 | PF00134 | 0.527 |
DOC_MAPK_gen_1 | 138 | 146 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 256 | 263 | PF00069 | 0.467 |
DOC_MAPK_MEF2A_6 | 329 | 337 | PF00069 | 0.483 |
DOC_MIT_MIM_1 | 198 | 207 | PF04212 | 0.459 |
DOC_PP1_RVXF_1 | 341 | 348 | PF00149 | 0.438 |
DOC_PP1_RVXF_1 | 377 | 383 | PF00149 | 0.328 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.494 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.759 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.695 |
DOC_USP7_MATH_1 | 362 | 366 | PF00917 | 0.464 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.684 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 96 | 100 | PF00917 | 0.625 |
DOC_USP7_UBL2_3 | 141 | 145 | PF12436 | 0.478 |
DOC_USP7_UBL2_3 | 290 | 294 | PF12436 | 0.476 |
DOC_USP7_UBL2_3 | 55 | 59 | PF12436 | 0.692 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.590 |
DOC_WW_Pin1_4 | 434 | 439 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 154 | 159 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 349 | 353 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 482 | 489 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 62 | 67 | PF00244 | 0.814 |
LIG_Actin_WH2_2 | 436 | 454 | PF00022 | 0.541 |
LIG_BRCT_BRCA1_1 | 464 | 468 | PF00533 | 0.444 |
LIG_BRCT_BRCA1_1 | 495 | 499 | PF00533 | 0.296 |
LIG_CtBP_PxDLS_1 | 409 | 413 | PF00389 | 0.473 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.705 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.526 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.431 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.510 |
LIG_FHA_1 | 384 | 390 | PF00498 | 0.411 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.543 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.513 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.423 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.450 |
LIG_FHA_2 | 420 | 426 | PF00498 | 0.515 |
LIG_FHA_2 | 481 | 487 | PF00498 | 0.454 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.369 |
LIG_LIR_Apic_2 | 507 | 512 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 140 | 148 | PF02991 | 0.516 |
LIG_LIR_Gen_1 | 348 | 357 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.389 |
LIG_PDZ_Class_2 | 508 | 513 | PF00595 | 0.409 |
LIG_Pex14_2 | 142 | 146 | PF04695 | 0.379 |
LIG_RPA_C_Fungi | 477 | 489 | PF08784 | 0.431 |
LIG_SH2_CRK | 11 | 15 | PF00017 | 0.508 |
LIG_SH2_STAP1 | 355 | 359 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 164 | 167 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.398 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.488 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.286 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.541 |
LIG_SH3_3 | 418 | 424 | PF00018 | 0.289 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.745 |
LIG_SUMO_SIM_anti_2 | 120 | 127 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 120 | 127 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 248 | 255 | PF11976 | 0.496 |
LIG_SUMO_SIM_par_1 | 277 | 285 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 417 | 422 | PF11976 | 0.508 |
MOD_CDK_SPxK_1 | 402 | 408 | PF00069 | 0.473 |
MOD_CDK_SPxK_1 | 434 | 440 | PF00069 | 0.520 |
MOD_CK1_1 | 214 | 220 | PF00069 | 0.402 |
MOD_CK1_1 | 246 | 252 | PF00069 | 0.430 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.520 |
MOD_CK1_1 | 30 | 36 | PF00069 | 0.703 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.747 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.464 |
MOD_CK1_1 | 469 | 475 | PF00069 | 0.420 |
MOD_CK1_1 | 79 | 85 | PF00069 | 0.706 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.617 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.416 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.482 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.661 |
MOD_CK2_1 | 381 | 387 | PF00069 | 0.536 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.485 |
MOD_CK2_1 | 480 | 486 | PF00069 | 0.337 |
MOD_CK2_1 | 501 | 507 | PF00069 | 0.501 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.724 |
MOD_CK2_1 | 72 | 78 | PF00069 | 0.622 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.714 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.319 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.360 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.647 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.687 |
MOD_GlcNHglycan | 471 | 475 | PF01048 | 0.425 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.369 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.717 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.780 |
MOD_GSK3_1 | 101 | 108 | PF00069 | 0.545 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.445 |
MOD_GSK3_1 | 243 | 250 | PF00069 | 0.377 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.731 |
MOD_GSK3_1 | 267 | 274 | PF00069 | 0.491 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.678 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.284 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.646 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.447 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.401 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.713 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.676 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.585 |
MOD_N-GLC_1 | 410 | 415 | PF02516 | 0.551 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.566 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.473 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.368 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.330 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.595 |
MOD_NEK2_2 | 362 | 367 | PF00069 | 0.474 |
MOD_PIKK_1 | 222 | 228 | PF00454 | 0.387 |
MOD_PK_1 | 154 | 160 | PF00069 | 0.469 |
MOD_PK_1 | 243 | 249 | PF00069 | 0.399 |
MOD_PK_1 | 62 | 68 | PF00069 | 0.708 |
MOD_PKA_1 | 76 | 82 | PF00069 | 0.682 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.604 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.663 |
MOD_PKA_2 | 320 | 326 | PF00069 | 0.674 |
MOD_PKA_2 | 348 | 354 | PF00069 | 0.466 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.466 |
MOD_PKA_2 | 501 | 507 | PF00069 | 0.356 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.712 |
MOD_PKB_1 | 241 | 249 | PF00069 | 0.378 |
MOD_PKB_1 | 60 | 68 | PF00069 | 0.760 |
MOD_Plk_1 | 214 | 220 | PF00069 | 0.481 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.386 |
MOD_Plk_1 | 355 | 361 | PF00069 | 0.376 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.399 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.611 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.508 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.392 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.775 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.372 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.594 |
MOD_ProDKin_1 | 434 | 440 | PF00069 | 0.457 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.658 |
TRG_DiLeu_BaEn_1 | 215 | 220 | PF01217 | 0.412 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 240 | 243 | PF00400 | 0.354 |
TRG_NLS_Bipartite_1 | 45 | 63 | PF00514 | 0.810 |
TRG_NLS_MonoExtC_3 | 189 | 194 | PF00514 | 0.645 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5P1 | Leptomonas seymouri | 64% | 100% |
A0A0S4JK75 | Bodo saltans | 32% | 100% |
A0A1X0NFD4 | Trypanosomatidae | 36% | 99% |
A0A3R7KS12 | Trypanosoma rangeli | 46% | 100% |
A4HJM1 | Leishmania braziliensis | 79% | 100% |
A4I743 | Leishmania infantum | 99% | 100% |
C9ZME4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 90% |
C9ZWN9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 90% |
E9B237 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q624 | Leishmania major | 90% | 100% |
V5B2M4 | Trypanosoma cruzi | 44% | 100% |