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: A0A3S7WV76
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.449 |
CLV_NRD_NRD_1 | 385 | 387 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.526 |
CLV_NRD_NRD_1 | 499 | 501 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.691 |
CLV_PCSK_FUR_1 | 559 | 563 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 176 | 178 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.452 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 385 | 387 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 474 | 476 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 499 | 501 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.452 |
CLV_PCSK_PC7_1 | 470 | 476 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 317 | 321 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 386 | 390 | PF00082 | 0.579 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 506 | 510 | PF00082 | 0.535 |
DEG_APCC_DBOX_1 | 444 | 452 | PF00400 | 0.355 |
DEG_MDM2_SWIB_1 | 526 | 533 | PF02201 | 0.286 |
DOC_ANK_TNKS_1 | 31 | 38 | PF00023 | 0.471 |
DOC_CYCLIN_RxL_1 | 460 | 472 | PF00134 | 0.338 |
DOC_CYCLIN_RxL_1 | 85 | 96 | PF00134 | 0.445 |
DOC_CYCLIN_yCln2_LP_2 | 12 | 18 | PF00134 | 0.469 |
DOC_CYCLIN_yCln2_LP_2 | 452 | 458 | PF00134 | 0.473 |
DOC_MAPK_DCC_7 | 298 | 306 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 120 | 129 | PF00069 | 0.487 |
DOC_MAPK_gen_1 | 298 | 306 | PF00069 | 0.475 |
DOC_MAPK_gen_1 | 439 | 448 | PF00069 | 0.347 |
DOC_MAPK_HePTP_8 | 438 | 450 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 123 | 131 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 298 | 306 | PF00069 | 0.505 |
DOC_MAPK_MEF2A_6 | 362 | 370 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 441 | 450 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 81 | 89 | PF00069 | 0.366 |
DOC_MAPK_NFAT4_5 | 445 | 453 | PF00069 | 0.446 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 410 | 414 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.445 |
DOC_USP7_UBL2_3 | 412 | 416 | PF12436 | 0.346 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.402 |
DOC_WW_Pin1_4 | 439 | 444 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.465 |
LIG_14-3-3_CanoR_1 | 114 | 119 | PF00244 | 0.580 |
LIG_14-3-3_CanoR_1 | 150 | 154 | PF00244 | 0.522 |
LIG_14-3-3_CterR_2 | 559 | 563 | PF00244 | 0.574 |
LIG_APCC_ABBA_1 | 159 | 164 | PF00400 | 0.525 |
LIG_deltaCOP1_diTrp_1 | 189 | 196 | PF00928 | 0.384 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.501 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.411 |
LIG_FHA_1 | 198 | 204 | PF00498 | 0.417 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.461 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.357 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.361 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.340 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.331 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.397 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.324 |
LIG_FHA_2 | 442 | 448 | PF00498 | 0.413 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.514 |
LIG_FHA_2 | 77 | 83 | PF00498 | 0.431 |
LIG_LIR_Gen_1 | 189 | 197 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 434 | 443 | PF02991 | 0.305 |
LIG_LIR_Gen_1 | 44 | 53 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 520 | 531 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 336 | 342 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 434 | 440 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 44 | 48 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 520 | 526 | PF02991 | 0.335 |
LIG_LYPXL_yS_3 | 255 | 258 | PF13949 | 0.393 |
LIG_NBox_RRM_1 | 543 | 553 | PF00076 | 0.355 |
LIG_NRBOX | 239 | 245 | PF00104 | 0.369 |
LIG_PCNA_yPIPBox_3 | 377 | 389 | PF02747 | 0.396 |
LIG_Pex14_2 | 526 | 530 | PF04695 | 0.284 |
LIG_Rb_pABgroove_1 | 462 | 470 | PF01858 | 0.356 |
LIG_SH2_CRK | 22 | 26 | PF00017 | 0.336 |
LIG_SH2_CRK | 27 | 31 | PF00017 | 0.363 |
LIG_SH2_CRK | 398 | 402 | PF00017 | 0.464 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 512 | 516 | PF00017 | 0.360 |
LIG_SH2_STAP1 | 523 | 527 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 232 | 235 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.290 |
LIG_SH3_2 | 455 | 460 | PF14604 | 0.409 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.451 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.389 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.405 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 279 | 284 | PF11976 | 0.297 |
LIG_SUMO_SIM_anti_2 | 444 | 450 | PF11976 | 0.445 |
LIG_SUMO_SIM_par_1 | 126 | 133 | PF11976 | 0.391 |
LIG_SUMO_SIM_par_1 | 163 | 171 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 264 | 273 | PF11976 | 0.503 |
LIG_SUMO_SIM_par_1 | 277 | 284 | PF11976 | 0.258 |
LIG_SUMO_SIM_par_1 | 428 | 434 | PF11976 | 0.434 |
LIG_SUMO_SIM_par_1 | 447 | 454 | PF11976 | 0.238 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.483 |
LIG_TRAF2_1 | 216 | 219 | PF00917 | 0.543 |
LIG_TRAF2_1 | 91 | 94 | PF00917 | 0.454 |
LIG_TYR_ITIM | 25 | 30 | PF00017 | 0.448 |
LIG_UBA3_1 | 16 | 23 | PF00899 | 0.364 |
LIG_WRC_WIRS_1 | 411 | 416 | PF05994 | 0.329 |
LIG_WRC_WIRS_1 | 42 | 47 | PF05994 | 0.419 |
MOD_CDC14_SPxK_1 | 442 | 445 | PF00782 | 0.337 |
MOD_CDK_SPK_2 | 312 | 317 | PF00069 | 0.455 |
MOD_CDK_SPxK_1 | 439 | 445 | PF00069 | 0.355 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.467 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.418 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.390 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.579 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.512 |
MOD_CK2_1 | 192 | 198 | PF00069 | 0.385 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.339 |
MOD_CK2_1 | 281 | 287 | PF00069 | 0.473 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.433 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.322 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.563 |
MOD_GlcNHglycan | 398 | 401 | PF01048 | 0.461 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.538 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.299 |
MOD_GlcNHglycan | 9 | 12 | PF01048 | 0.522 |
MOD_GlcNHglycan | 93 | 99 | PF01048 | 0.538 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.479 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.480 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.530 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.356 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.443 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.396 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.411 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.391 |
MOD_N-GLC_2 | 199 | 201 | PF02516 | 0.396 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.393 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.400 |
MOD_PK_1 | 114 | 120 | PF00069 | 0.510 |
MOD_PK_1 | 123 | 129 | PF00069 | 0.319 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.588 |
MOD_PKA_2 | 149 | 155 | PF00069 | 0.522 |
MOD_PKA_2 | 345 | 351 | PF00069 | 0.533 |
MOD_PKB_1 | 112 | 120 | PF00069 | 0.587 |
MOD_Plk_1 | 263 | 269 | PF00069 | 0.413 |
MOD_Plk_2-3 | 192 | 198 | PF00069 | 0.407 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.466 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.377 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.487 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.502 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.445 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.344 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.437 |
MOD_Plk_4 | 410 | 416 | PF00069 | 0.355 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.427 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.430 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.401 |
MOD_ProDKin_1 | 439 | 445 | PF00069 | 0.509 |
MOD_ProDKin_1 | 451 | 457 | PF00069 | 0.465 |
TRG_DiLeu_BaEn_1 | 207 | 212 | PF01217 | 0.419 |
TRG_DiLeu_BaEn_1 | 254 | 259 | PF01217 | 0.447 |
TRG_DiLeu_BaEn_1 | 82 | 87 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_2 | 191 | 197 | PF01217 | 0.421 |
TRG_DiLeu_BaEn_4 | 333 | 339 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.357 |
TRG_ENDOCYTIC_2 | 22 | 25 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.341 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 398 | 401 | PF00928 | 0.401 |
TRG_ENDOCYTIC_2 | 523 | 526 | PF00928 | 0.335 |
TRG_ER_diArg_1 | 149 | 151 | PF00400 | 0.474 |
TRG_ER_diArg_1 | 176 | 178 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.585 |
TRG_ER_diArg_1 | 30 | 32 | PF00400 | 0.405 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.355 |
TRG_ER_diArg_1 | 474 | 476 | PF00400 | 0.595 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 559 | 562 | PF00400 | 0.665 |
TRG_NES_CRM1_1 | 425 | 436 | PF08389 | 0.377 |
TRG_Pf-PMV_PEXEL_1 | 298 | 303 | PF00026 | 0.448 |
TRG_Pf-PMV_PEXEL_1 | 465 | 469 | PF00026 | 0.323 |
TRG_Pf-PMV_PEXEL_1 | 88 | 93 | PF00026 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRD6 | Leptomonas seymouri | 57% | 100% |
A0A1X0P7Z6 | Trypanosomatidae | 30% | 100% |
A0A3R7M1T0 | Trypanosoma rangeli | 30% | 100% |
D0A560 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9AGQ6 | Leishmania infantum | 100% | 100% |
E9AI61 | Leishmania braziliensis | 79% | 100% |
E9ARU0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QDN3 | Leishmania major | 94% | 100% |
V5BDF3 | Trypanosoma cruzi | 31% | 100% |