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: A4HIC9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 241 | 243 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.632 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.546 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.402 |
CLV_PCSK_PC1ET2_1 | 288 | 290 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 365 | 369 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.459 |
DEG_APCC_DBOX_1 | 313 | 321 | PF00400 | 0.357 |
DEG_APCC_DBOX_1 | 340 | 348 | PF00400 | 0.594 |
DEG_COP1_1 | 2 | 10 | PF00400 | 0.538 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.512 |
DEG_SCF_FBW7_2 | 367 | 372 | PF00400 | 0.446 |
DOC_CDC14_PxL_1 | 30 | 38 | PF14671 | 0.511 |
DOC_CYCLIN_RxL_1 | 420 | 429 | PF00134 | 0.659 |
DOC_MAPK_gen_1 | 288 | 296 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 407 | 417 | PF00069 | 0.641 |
DOC_MAPK_MEF2A_6 | 21 | 30 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 376 | 384 | PF00069 | 0.621 |
DOC_MAPK_MEF2A_6 | 410 | 419 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 423 | 432 | PF00069 | 0.629 |
DOC_MAPK_RevD_3 | 352 | 366 | PF00069 | 0.482 |
DOC_PP1_RVXF_1 | 19 | 25 | PF00149 | 0.533 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.397 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.543 |
DOC_WW_Pin1_4 | 119 | 124 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.634 |
LIG_14-3-3_CanoR_1 | 145 | 154 | PF00244 | 0.697 |
LIG_14-3-3_CanoR_1 | 199 | 204 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 242 | 252 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 401 | 409 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 410 | 417 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 70 | 76 | PF00244 | 0.576 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.516 |
LIG_CaM_IQ_9 | 82 | 97 | PF13499 | 0.400 |
LIG_Clathr_ClatBox_1 | 23 | 27 | PF01394 | 0.432 |
LIG_deltaCOP1_diTrp_1 | 209 | 214 | PF00928 | 0.596 |
LIG_EH1_1 | 23 | 31 | PF00400 | 0.486 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.701 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.494 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.607 |
LIG_FHA_1 | 296 | 302 | PF00498 | 0.501 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.673 |
LIG_FHA_2 | 104 | 110 | PF00498 | 0.657 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.452 |
LIG_FHA_2 | 252 | 258 | PF00498 | 0.330 |
LIG_FHA_2 | 422 | 428 | PF00498 | 0.604 |
LIG_FHA_2 | 52 | 58 | PF00498 | 0.615 |
LIG_LIR_Gen_1 | 42 | 50 | PF02991 | 0.517 |
LIG_LIR_Gen_1 | 71 | 78 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 263 | 267 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 357 | 362 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.510 |
LIG_Pex14_2 | 146 | 150 | PF04695 | 0.470 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.549 |
LIG_SH2_PTP2 | 25 | 28 | PF00017 | 0.374 |
LIG_SH2_SRC | 25 | 28 | PF00017 | 0.627 |
LIG_SH2_SRC | 299 | 302 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 260 | 264 | PF00017 | 0.326 |
LIG_SH2_STAP1 | 292 | 296 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 92 | 96 | PF00017 | 0.602 |
LIG_SH2_STAT3 | 303 | 306 | PF00017 | 0.484 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.481 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.499 |
LIG_SUMO_SIM_anti_2 | 152 | 161 | PF11976 | 0.574 |
LIG_SUMO_SIM_anti_2 | 326 | 331 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 152 | 161 | PF11976 | 0.581 |
LIG_SUMO_SIM_par_1 | 33 | 39 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 350 | 355 | PF11976 | 0.647 |
LIG_TRAF2_1 | 106 | 109 | PF00917 | 0.427 |
LIG_TRAF2_1 | 224 | 227 | PF00917 | 0.341 |
LIG_TRAF2_1 | 276 | 279 | PF00917 | 0.613 |
LIG_TRAF2_1 | 369 | 372 | PF00917 | 0.448 |
LIG_TYR_ITIM | 23 | 28 | PF00017 | 0.379 |
LIG_UBA3_1 | 36 | 44 | PF00899 | 0.551 |
LIG_WRC_WIRS_1 | 47 | 52 | PF05994 | 0.585 |
MOD_CDK_SPxK_1 | 352 | 358 | PF00069 | 0.676 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.563 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.718 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.557 |
MOD_CK2_1 | 103 | 109 | PF00069 | 0.381 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.442 |
MOD_CK2_1 | 309 | 315 | PF00069 | 0.504 |
MOD_CK2_1 | 387 | 393 | PF00069 | 0.637 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.636 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.564 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.510 |
MOD_Cter_Amidation | 239 | 242 | PF01082 | 0.449 |
MOD_GlcNHglycan | 129 | 132 | PF01048 | 0.668 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.430 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.429 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.672 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.484 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.624 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.715 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.433 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.565 |
MOD_GSK3_1 | 409 | 416 | PF00069 | 0.561 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.590 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.451 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.547 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.736 |
MOD_N-GLC_1 | 78 | 83 | PF02516 | 0.622 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.627 |
MOD_NEK2_1 | 127 | 132 | PF00069 | 0.667 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.606 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.585 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.608 |
MOD_NEK2_1 | 82 | 87 | PF00069 | 0.411 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.668 |
MOD_PIKK_1 | 193 | 199 | PF00454 | 0.476 |
MOD_PIKK_1 | 82 | 88 | PF00454 | 0.439 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.583 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.568 |
MOD_PKA_2 | 395 | 401 | PF00069 | 0.549 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.522 |
MOD_PKB_1 | 199 | 207 | PF00069 | 0.368 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.412 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.520 |
MOD_Plk_1 | 277 | 283 | PF00069 | 0.453 |
MOD_Plk_1 | 78 | 84 | PF00069 | 0.393 |
MOD_Plk_2-3 | 251 | 257 | PF00069 | 0.331 |
MOD_Plk_2-3 | 309 | 315 | PF00069 | 0.504 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.649 |
MOD_Plk_4 | 380 | 386 | PF00069 | 0.522 |
MOD_Plk_4 | 60 | 66 | PF00069 | 0.423 |
MOD_Plk_4 | 78 | 84 | PF00069 | 0.635 |
MOD_ProDKin_1 | 119 | 125 | PF00069 | 0.676 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.741 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.622 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.627 |
MOD_SUMO_for_1 | 255 | 258 | PF00179 | 0.329 |
MOD_SUMO_for_1 | 281 | 284 | PF00179 | 0.604 |
MOD_SUMO_rev_2 | 247 | 255 | PF00179 | 0.424 |
MOD_SUMO_rev_2 | 363 | 368 | PF00179 | 0.477 |
MOD_SUMO_rev_2 | 88 | 97 | PF00179 | 0.554 |
TRG_DiLeu_BaEn_1 | 315 | 320 | PF01217 | 0.610 |
TRG_DiLeu_BaEn_2 | 141 | 147 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_4 | 108 | 114 | PF01217 | 0.538 |
TRG_DiLeu_BaLyEn_6 | 18 | 23 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 31 | 36 | PF01217 | 0.421 |
TRG_DiLeu_BaLyEn_6 | 398 | 403 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 25 | 28 | PF00928 | 0.585 |
TRG_ENDOCYTIC_2 | 359 | 362 | PF00928 | 0.501 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 289 | 292 | PF00400 | 0.585 |
TRG_NLS_MonoExtC_3 | 287 | 293 | PF00514 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 265 | 269 | PF00026 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 345 | 350 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.662 |
TRG_Pf-PMV_PEXEL_1 | 423 | 427 | PF00026 | 0.619 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDD9 | Leptomonas seymouri | 57% | 100% |
A0A1X0P1Q4 | Trypanosomatidae | 38% | 95% |
A0A3S5H7N1 | Leishmania donovani | 76% | 100% |
A0A3S5ISM8 | Trypanosoma rangeli | 35% | 93% |
A4I5M2 | Leishmania infantum | 76% | 100% |
E9B0W7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q799 | Leishmania major | 73% | 100% |
V5B8X3 | Trypanosoma cruzi | 34% | 93% |