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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9APC3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.638 |
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.610 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 191 | 193 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.536 |
CLV_NRD_NRD_1 | 281 | 283 | PF00675 | 0.792 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.693 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.781 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.573 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 476 | 478 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.538 |
CLV_PCSK_FUR_1 | 290 | 294 | PF00082 | 0.668 |
CLV_PCSK_FUR_1 | 468 | 472 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 16 | 18 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 281 | 283 | PF00082 | 0.646 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.628 |
CLV_PCSK_KEX2_1 | 425 | 427 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 72 | 74 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 16 | 18 | PF00082 | 0.601 |
CLV_PCSK_PC1ET2_1 | 191 | 193 | PF00082 | 0.474 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.549 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.699 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.464 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.557 |
CLV_PCSK_PC1ET2_1 | 348 | 350 | PF00082 | 0.628 |
CLV_PCSK_PC1ET2_1 | 425 | 427 | PF00082 | 0.541 |
CLV_PCSK_PC1ET2_1 | 65 | 67 | PF00082 | 0.481 |
CLV_PCSK_PC7_1 | 68 | 74 | PF00082 | 0.495 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.652 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.625 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.751 |
CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 389 | 393 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 73 | 77 | PF00082 | 0.591 |
DEG_SCF_FBW7_1 | 120 | 126 | PF00400 | 0.611 |
DOC_CKS1_1 | 120 | 125 | PF01111 | 0.821 |
DOC_MAPK_gen_1 | 245 | 252 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 323 | 330 | PF00069 | 0.586 |
DOC_MAPK_gen_1 | 425 | 432 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 245 | 252 | PF00069 | 0.476 |
DOC_MAPK_RevD_3 | 171 | 186 | PF00069 | 0.380 |
DOC_PP1_RVXF_1 | 324 | 331 | PF00149 | 0.580 |
DOC_PP2B_LxvP_1 | 152 | 155 | PF13499 | 0.795 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.711 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 447 | 451 | PF00917 | 0.538 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.635 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.614 |
DOC_USP7_UBL2_3 | 185 | 189 | PF12436 | 0.454 |
DOC_USP7_UBL2_3 | 224 | 228 | PF12436 | 0.595 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.822 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.511 |
LIG_14-3-3_CanoR_1 | 254 | 260 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 461 | 467 | PF00244 | 0.508 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.581 |
LIG_BIR_III_4 | 303 | 307 | PF00653 | 0.562 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.625 |
LIG_FHA_2 | 269 | 275 | PF00498 | 0.477 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.715 |
LIG_LIR_Gen_1 | 136 | 144 | PF02991 | 0.549 |
LIG_LIR_Gen_1 | 357 | 367 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.630 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 452 | 458 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 485 | 489 | PF02991 | 0.634 |
LIG_PDZ_Class_2 | 485 | 490 | PF00595 | 0.524 |
LIG_SH2_NCK_1 | 359 | 363 | PF00017 | 0.604 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.484 |
LIG_SH3_2 | 128 | 133 | PF14604 | 0.605 |
LIG_SH3_3 | 117 | 123 | PF00018 | 0.716 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.720 |
LIG_SH3_3 | 148 | 154 | PF00018 | 0.754 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.506 |
LIG_SUMO_SIM_anti_2 | 360 | 366 | PF11976 | 0.504 |
LIG_TRAF2_1 | 100 | 103 | PF00917 | 0.508 |
LIG_TRAF2_1 | 177 | 180 | PF00917 | 0.575 |
LIG_TRAF2_1 | 207 | 210 | PF00917 | 0.457 |
LIG_TRAF2_1 | 450 | 453 | PF00917 | 0.399 |
LIG_UBA3_1 | 181 | 189 | PF00899 | 0.349 |
LIG_UBA3_1 | 58 | 65 | PF00899 | 0.529 |
MOD_CDK_SPK_2 | 124 | 129 | PF00069 | 0.499 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.498 |
MOD_CDK_SPxxK_3 | 21 | 28 | PF00069 | 0.501 |
MOD_CK1_1 | 147 | 153 | PF00069 | 0.578 |
MOD_CK1_1 | 268 | 274 | PF00069 | 0.471 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.639 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.806 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.633 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.637 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.471 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.771 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.426 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.571 |
MOD_Cter_Amidation | 222 | 225 | PF01082 | 0.567 |
MOD_GlcNHglycan | 142 | 147 | PF01048 | 0.584 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.800 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.748 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.659 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.708 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.666 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.645 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.718 |
MOD_NEK2_1 | 144 | 149 | PF00069 | 0.588 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.513 |
MOD_PIKK_1 | 434 | 440 | PF00454 | 0.404 |
MOD_PIKK_1 | 51 | 57 | PF00454 | 0.509 |
MOD_PKA_1 | 281 | 287 | PF00069 | 0.548 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.606 |
MOD_PKA_1 | 326 | 332 | PF00069 | 0.553 |
MOD_PKA_2 | 160 | 166 | PF00069 | 0.739 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.581 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.574 |
MOD_PKA_2 | 326 | 332 | PF00069 | 0.632 |
MOD_PKA_2 | 447 | 453 | PF00069 | 0.550 |
MOD_PKB_1 | 292 | 300 | PF00069 | 0.704 |
MOD_Plk_2-3 | 136 | 142 | PF00069 | 0.555 |
MOD_Plk_2-3 | 169 | 175 | PF00069 | 0.568 |
MOD_Plk_2-3 | 347 | 353 | PF00069 | 0.457 |
MOD_Plk_4 | 147 | 153 | PF00069 | 0.757 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.822 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.506 |
MOD_SUMO_for_1 | 184 | 187 | PF00179 | 0.347 |
MOD_SUMO_for_1 | 482 | 485 | PF00179 | 0.522 |
MOD_SUMO_rev_2 | 24 | 33 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 258 | 268 | PF00179 | 0.467 |
MOD_SUMO_rev_2 | 347 | 355 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 450 | 458 | PF00179 | 0.471 |
MOD_SUMO_rev_2 | 473 | 480 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_1 | 410 | 415 | PF01217 | 0.536 |
TRG_DiLeu_BaEn_4 | 179 | 185 | PF01217 | 0.349 |
TRG_DiLeu_BaEn_4 | 453 | 459 | PF01217 | 0.378 |
TRG_DiLeu_LyEn_5 | 410 | 415 | PF01217 | 0.571 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.599 |
TRG_ER_diArg_1 | 197 | 200 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 280 | 282 | PF00400 | 0.611 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.626 |
TRG_ER_diArg_1 | 325 | 328 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 411 | 414 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 468 | 471 | PF00400 | 0.539 |
TRG_NLS_Bipartite_1 | 281 | 295 | PF00514 | 0.534 |
TRG_NLS_Bipartite_1 | 3 | 20 | PF00514 | 0.604 |
TRG_NLS_MonoCore_2 | 128 | 133 | PF00514 | 0.605 |
TRG_NLS_MonoCore_2 | 289 | 294 | PF00514 | 0.666 |
TRG_NLS_MonoExtC_3 | 128 | 133 | PF00514 | 0.688 |
TRG_NLS_MonoExtC_3 | 223 | 228 | PF00514 | 0.554 |
TRG_NLS_MonoExtC_3 | 289 | 294 | PF00514 | 0.710 |
TRG_NLS_MonoExtN_4 | 128 | 133 | PF00514 | 0.680 |
TRG_NLS_MonoExtN_4 | 224 | 231 | PF00514 | 0.575 |
TRG_NLS_MonoExtN_4 | 28 | 35 | PF00514 | 0.545 |
TRG_NLS_MonoExtN_4 | 290 | 295 | PF00514 | 0.623 |
TRG_NLS_MonoExtN_4 | 323 | 329 | PF00514 | 0.561 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.549 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE43 | Leptomonas seymouri | 57% | 97% |
A0A3S7WSJ6 | Leishmania donovani | 86% | 100% |
A0A422NGB0 | Trypanosoma rangeli | 37% | 100% |
A4H787 | Leishmania braziliensis | 72% | 99% |
A4HVM7 | Leishmania infantum | 86% | 100% |
D0A6M7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
Q4QG55 | Leishmania major | 85% | 100% |
V5AVQ1 | Trypanosoma cruzi | 35% | 100% |