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: E9AV18
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 332 | 336 | PF00656 | 0.637 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.516 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.639 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 463 | 465 | PF00082 | 0.639 |
CLV_PCSK_KEX2_1 | 84 | 86 | PF00082 | 0.737 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.592 |
CLV_PCSK_PC1ET2_1 | 463 | 465 | PF00082 | 0.750 |
CLV_PCSK_PC1ET2_1 | 84 | 86 | PF00082 | 0.737 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 37 | 41 | PF00082 | 0.546 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.418 |
DEG_SCF_FBW7_1 | 148 | 154 | PF00400 | 0.527 |
DEG_SCF_FBW7_2 | 520 | 527 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 320 | 324 | PF00917 | 0.740 |
DOC_CDC14_PxL_1 | 131 | 139 | PF14671 | 0.538 |
DOC_CDC14_PxL_1 | 192 | 200 | PF14671 | 0.538 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.521 |
DOC_CKS1_1 | 484 | 489 | PF01111 | 0.703 |
DOC_CYCLIN_yCln2_LP_2 | 198 | 204 | PF00134 | 0.557 |
DOC_CYCLIN_yCln2_LP_2 | 443 | 449 | PF00134 | 0.605 |
DOC_MAPK_gen_1 | 142 | 148 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 413 | 420 | PF00069 | 0.669 |
DOC_MAPK_MEF2A_6 | 413 | 422 | PF00069 | 0.774 |
DOC_MAPK_MEF2A_6 | 521 | 528 | PF00069 | 0.513 |
DOC_PP2B_LxvP_1 | 193 | 196 | PF13499 | 0.473 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.718 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 214 | 218 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 405 | 409 | PF00917 | 0.773 |
DOC_USP7_MATH_1 | 478 | 482 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.703 |
DOC_USP7_MATH_1 | 515 | 519 | PF00917 | 0.729 |
DOC_USP7_MATH_1 | 70 | 74 | PF00917 | 0.480 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.430 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.819 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.709 |
LIG_14-3-3_CanoR_1 | 343 | 347 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 37 | 45 | PF00244 | 0.610 |
LIG_14-3-3_CanoR_1 | 464 | 468 | PF00244 | 0.645 |
LIG_14-3-3_CanoR_1 | 483 | 487 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 516 | 520 | PF00244 | 0.665 |
LIG_14-3-3_CanoR_1 | 8 | 13 | PF00244 | 0.751 |
LIG_Actin_WH2_2 | 127 | 144 | PF00022 | 0.569 |
LIG_APCC_ABBA_1 | 248 | 253 | PF00400 | 0.471 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.739 |
LIG_BRCT_BRCA1_1 | 304 | 308 | PF00533 | 0.658 |
LIG_BRCT_BRCA1_1 | 322 | 326 | PF00533 | 0.449 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.633 |
LIG_FHA_1 | 148 | 154 | PF00498 | 0.495 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.439 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.649 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.547 |
LIG_FHA_1 | 376 | 382 | PF00498 | 0.560 |
LIG_FHA_1 | 413 | 419 | PF00498 | 0.750 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.563 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.592 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.539 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.480 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.582 |
LIG_FHA_2 | 330 | 336 | PF00498 | 0.713 |
LIG_FHA_2 | 38 | 44 | PF00498 | 0.523 |
LIG_FHA_2 | 395 | 401 | PF00498 | 0.707 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.655 |
LIG_LIR_Gen_1 | 109 | 119 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 305 | 315 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 305 | 311 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.483 |
LIG_MYND_1 | 196 | 200 | PF01753 | 0.543 |
LIG_MYND_1 | 450 | 454 | PF01753 | 0.638 |
LIG_MYND_3 | 134 | 138 | PF01753 | 0.533 |
LIG_NRBOX | 176 | 182 | PF00104 | 0.491 |
LIG_NRBOX | 223 | 229 | PF00104 | 0.650 |
LIG_SH2_CRK | 119 | 123 | PF00017 | 0.514 |
LIG_SH2_NCK_1 | 304 | 308 | PF00017 | 0.576 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 304 | 308 | PF00017 | 0.674 |
LIG_SH2_STAT3 | 129 | 132 | PF00017 | 0.441 |
LIG_SH2_STAT3 | 62 | 65 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 298 | 301 | PF00017 | 0.588 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.555 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.422 |
LIG_SH3_3 | 364 | 370 | PF00018 | 0.541 |
LIG_SH3_3 | 415 | 421 | PF00018 | 0.729 |
LIG_SH3_3 | 444 | 450 | PF00018 | 0.635 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.675 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.687 |
LIG_SH3_3 | 493 | 499 | PF00018 | 0.482 |
LIG_SH3_3 | 504 | 510 | PF00018 | 0.704 |
LIG_SH3_3 | 519 | 525 | PF00018 | 0.769 |
LIG_SH3_3 | 531 | 537 | PF00018 | 0.684 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.625 |
LIG_Sin3_3 | 455 | 462 | PF02671 | 0.732 |
LIG_SUMO_SIM_par_1 | 189 | 194 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 226 | 233 | PF11976 | 0.601 |
LIG_TRAF2_1 | 136 | 139 | PF00917 | 0.473 |
LIG_TRAF2_1 | 300 | 303 | PF00917 | 0.624 |
LIG_TRAF2_1 | 40 | 43 | PF00917 | 0.599 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.520 |
LIG_UBA3_1 | 133 | 142 | PF00899 | 0.520 |
MOD_CDK_SPxxK_3 | 77 | 84 | PF00069 | 0.713 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.697 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.670 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.676 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.660 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.581 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.443 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.601 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.557 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.523 |
MOD_Cter_Amidation | 411 | 414 | PF01082 | 0.577 |
MOD_DYRK1A_RPxSP_1 | 483 | 487 | PF00069 | 0.524 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.534 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.743 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.647 |
MOD_GlcNHglycan | 238 | 242 | PF01048 | 0.735 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.735 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.616 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.490 |
MOD_GSK3_1 | 10 | 17 | PF00069 | 0.736 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.483 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.618 |
MOD_GSK3_1 | 310 | 317 | PF00069 | 0.653 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.663 |
MOD_GSK3_1 | 33 | 40 | PF00069 | 0.578 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.760 |
MOD_GSK3_1 | 463 | 470 | PF00069 | 0.575 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.681 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.680 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.658 |
MOD_N-GLC_1 | 401 | 406 | PF02516 | 0.719 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.699 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.414 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.483 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.653 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.462 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.280 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.532 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.723 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.726 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.704 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.556 |
MOD_PK_1 | 414 | 420 | PF00069 | 0.583 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.751 |
MOD_PKA_1 | 463 | 469 | PF00069 | 0.679 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.572 |
MOD_PKA_2 | 463 | 469 | PF00069 | 0.683 |
MOD_PKA_2 | 482 | 488 | PF00069 | 0.621 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.616 |
MOD_PKA_2 | 95 | 101 | PF00069 | 0.515 |
MOD_Plk_1 | 8 | 14 | PF00069 | 0.607 |
MOD_Plk_4 | 180 | 186 | PF00069 | 0.489 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.577 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.428 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.706 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.818 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.714 |
TRG_DiLeu_BaEn_1 | 187 | 192 | PF01217 | 0.511 |
TRG_DiLeu_BaLyEn_6 | 390 | 395 | PF01217 | 0.600 |
TRG_DiLeu_BaLyEn_6 | 418 | 423 | PF01217 | 0.736 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.516 |
TRG_ER_diArg_1 | 27 | 30 | PF00400 | 0.530 |
TRG_NLS_MonoExtN_4 | 254 | 261 | PF00514 | 0.519 |
TRG_NLS_MonoExtN_4 | 461 | 467 | PF00514 | 0.749 |
TRG_Pf-PMV_PEXEL_1 | 260 | 264 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IAT9 | Leptomonas seymouri | 57% | 95% |
A0A3Q8IAT2 | Leishmania donovani | 90% | 100% |
A0A422NBI2 | Trypanosoma rangeli | 28% | 100% |
A4HBP8 | Leishmania braziliensis | 75% | 97% |
A4HZ50 | Leishmania infantum | 83% | 94% |
D0A1Q2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
Q4QCG4 | Leishmania major | 84% | 97% |
V5BKP0 | Trypanosoma cruzi | 29% | 100% |