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: E9AQ60
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 348 | 350 | PF00675 | 0.529 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.473 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 348 | 350 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 395 | 397 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.505 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.554 |
CLV_PCSK_PC1ET2_1 | 330 | 332 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 444 | 448 | PF00082 | 0.513 |
DEG_APCC_DBOX_1 | 116 | 124 | PF00400 | 0.477 |
DEG_APCC_DBOX_1 | 398 | 406 | PF00400 | 0.430 |
DEG_SCF_FBW7_1 | 87 | 94 | PF00400 | 0.506 |
DOC_ANK_TNKS_1 | 162 | 169 | PF00023 | 0.580 |
DOC_CKS1_1 | 152 | 157 | PF01111 | 0.370 |
DOC_CKS1_1 | 24 | 29 | PF01111 | 0.473 |
DOC_CKS1_1 | 351 | 356 | PF01111 | 0.466 |
DOC_CYCLIN_RxL_1 | 236 | 245 | PF00134 | 0.498 |
DOC_CYCLIN_yCln2_LP_2 | 18 | 24 | PF00134 | 0.680 |
DOC_MAPK_gen_1 | 219 | 228 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 329 | 337 | PF00069 | 0.630 |
DOC_PP4_FxxP_1 | 150 | 153 | PF00568 | 0.338 |
DOC_PP4_FxxP_1 | 24 | 27 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 419 | 422 | PF00568 | 0.491 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 442 | 446 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.795 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 151 | 156 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 23 | 28 | PF00397 | 0.680 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 350 | 355 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.694 |
LIG_14-3-3_CanoR_1 | 221 | 226 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.388 |
LIG_14-3-3_CterR_2 | 444 | 448 | PF00244 | 0.525 |
LIG_Actin_WH2_2 | 219 | 234 | PF00022 | 0.366 |
LIG_APCC_ABBA_1 | 210 | 215 | PF00400 | 0.548 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.769 |
LIG_BRCT_BRCA1_1 | 244 | 248 | PF00533 | 0.513 |
LIG_BRCT_BRCA1_1 | 357 | 361 | PF00533 | 0.445 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.442 |
LIG_FHA_2 | 24 | 30 | PF00498 | 0.616 |
LIG_FHA_2 | 280 | 286 | PF00498 | 0.612 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.674 |
LIG_LIR_Apic_2 | 148 | 153 | PF02991 | 0.360 |
LIG_LIR_Apic_2 | 23 | 27 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 198 | 205 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 224 | 233 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 234 | 242 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.501 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.598 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 224 | 228 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 51 | 56 | PF02991 | 0.453 |
LIG_Pex14_2 | 126 | 130 | PF04695 | 0.357 |
LIG_Pex14_2 | 146 | 150 | PF04695 | 0.489 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.631 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.550 |
LIG_SH2_NCK_1 | 63 | 67 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 401 | 404 | PF00017 | 0.411 |
LIG_SH3_1 | 348 | 354 | PF00018 | 0.552 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.380 |
LIG_SH3_3 | 348 | 354 | PF00018 | 0.457 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.401 |
LIG_SH3_3 | 402 | 408 | PF00018 | 0.382 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.713 |
LIG_SUMO_SIM_par_1 | 439 | 445 | PF11976 | 0.470 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.702 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.493 |
LIG_TRAF2_1 | 362 | 365 | PF00917 | 0.440 |
LIG_TRFH_1 | 201 | 205 | PF08558 | 0.610 |
LIG_UBA3_1 | 360 | 366 | PF00899 | 0.467 |
LIG_UBA3_1 | 440 | 447 | PF00899 | 0.551 |
LIG_WRC_WIRS_1 | 147 | 152 | PF05994 | 0.359 |
MOD_CDK_SPK_2 | 151 | 156 | PF00069 | 0.365 |
MOD_CDK_SPxxK_3 | 350 | 357 | PF00069 | 0.462 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.720 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.441 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.616 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.496 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.554 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.471 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.676 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.406 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.664 |
MOD_GlcNHglycan | 285 | 289 | PF01048 | 0.731 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.643 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.710 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.498 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.496 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.583 |
MOD_GlcNHglycan | 53 | 56 | PF01048 | 0.367 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.748 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.664 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.685 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.672 |
MOD_GSK3_1 | 279 | 286 | PF00069 | 0.594 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.410 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.650 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.621 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.655 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.640 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.701 |
MOD_N-GLC_1 | 385 | 390 | PF02516 | 0.464 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.406 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.474 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.544 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.567 |
MOD_NEK2_2 | 442 | 447 | PF00069 | 0.557 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.421 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.548 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.614 |
MOD_Plk_1 | 436 | 442 | PF00069 | 0.521 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.521 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.528 |
MOD_ProDKin_1 | 151 | 157 | PF00069 | 0.370 |
MOD_ProDKin_1 | 23 | 29 | PF00069 | 0.684 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.545 |
MOD_ProDKin_1 | 350 | 356 | PF00069 | 0.475 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.692 |
MOD_SUMO_rev_2 | 103 | 111 | PF00179 | 0.371 |
MOD_SUMO_rev_2 | 240 | 248 | PF00179 | 0.406 |
MOD_SUMO_rev_2 | 358 | 367 | PF00179 | 0.459 |
MOD_SUMO_rev_2 | 77 | 85 | PF00179 | 0.571 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 405 | 410 | PF01217 | 0.417 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 200 | 203 | PF00928 | 0.595 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.546 |
TRG_ER_diArg_1 | 348 | 350 | PF00400 | 0.544 |
TRG_NES_CRM1_1 | 218 | 229 | PF08389 | 0.406 |
TRG_Pf-PMV_PEXEL_1 | 171 | 175 | PF00026 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.527 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I615 | Leptomonas seymouri | 71% | 100% |
A0A1X0NTS1 | Trypanosomatidae | 36% | 100% |
A0A3S5H6U7 | Leishmania donovani | 88% | 100% |
A0A422NLQ5 | Trypanosoma rangeli | 40% | 100% |
A4H835 | Leishmania braziliensis | 77% | 100% |
A4HWG0 | Leishmania infantum | 88% | 100% |
C9ZP02 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
Q4QFC3 | Leishmania major | 90% | 100% |