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: E9AZ61
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.488 |
CLV_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.604 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.625 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.518 |
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 202 | 204 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.630 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 433 | 435 | PF00675 | 0.592 |
CLV_PCSK_FUR_1 | 105 | 109 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.518 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 202 | 204 | PF00082 | 0.510 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 433 | 435 | PF00082 | 0.592 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.408 |
DEG_APCC_DBOX_1 | 95 | 103 | PF00400 | 0.492 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.721 |
DEG_SPOP_SBC_1 | 21 | 25 | PF00917 | 0.443 |
DOC_CDC14_PxL_1 | 267 | 275 | PF14671 | 0.575 |
DOC_CYCLIN_RxL_1 | 197 | 211 | PF00134 | 0.502 |
DOC_MAPK_gen_1 | 202 | 209 | PF00069 | 0.492 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.727 |
DOC_MAPK_MEF2A_6 | 202 | 209 | PF00069 | 0.409 |
DOC_MAPK_NFAT4_5 | 202 | 210 | PF00069 | 0.413 |
DOC_PP1_RVXF_1 | 119 | 125 | PF00149 | 0.555 |
DOC_PP4_FxxP_1 | 274 | 277 | PF00568 | 0.672 |
DOC_USP7_MATH_1 | 336 | 340 | PF00917 | 0.488 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.549 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 424 | 429 | PF00397 | 0.575 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 257 | 266 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 355 | 361 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 380 | 398 | PF00022 | 0.438 |
LIG_AP2alpha_1 | 149 | 153 | PF02296 | 0.395 |
LIG_APCC_ABBA_1 | 63 | 68 | PF00400 | 0.460 |
LIG_BIR_III_2 | 268 | 272 | PF00653 | 0.669 |
LIG_BIR_III_2 | 291 | 295 | PF00653 | 0.772 |
LIG_BIR_III_2 | 319 | 323 | PF00653 | 0.551 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.536 |
LIG_CaM_IQ_9 | 150 | 166 | PF13499 | 0.561 |
LIG_CSL_BTD_1 | 18 | 21 | PF09270 | 0.571 |
LIG_CtBP_PxDLS_1 | 423 | 427 | PF00389 | 0.671 |
LIG_FHA_1 | 130 | 136 | PF00498 | 0.491 |
LIG_FHA_1 | 258 | 264 | PF00498 | 0.580 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.573 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.484 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.638 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.594 |
LIG_FHA_2 | 371 | 377 | PF00498 | 0.469 |
LIG_FHA_2 | 398 | 404 | PF00498 | 0.464 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.606 |
LIG_HCF-1_HBM_1 | 175 | 178 | PF13415 | 0.519 |
LIG_LIR_Gen_1 | 151 | 161 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 367 | 377 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 151 | 156 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 367 | 372 | PF02991 | 0.543 |
LIG_LIR_Nem_3 | 389 | 395 | PF02991 | 0.440 |
LIG_MYND_1 | 271 | 275 | PF01753 | 0.667 |
LIG_Pex14_2 | 149 | 153 | PF04695 | 0.395 |
LIG_REV1ctd_RIR_1 | 154 | 164 | PF16727 | 0.488 |
LIG_REV1ctd_RIR_1 | 390 | 400 | PF16727 | 0.434 |
LIG_SH2_NCK_1 | 87 | 91 | PF00017 | 0.486 |
LIG_SH2_STAP1 | 55 | 59 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.445 |
LIG_SH3_2 | 428 | 433 | PF14604 | 0.562 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.658 |
LIG_SH3_3 | 425 | 431 | PF00018 | 0.525 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.492 |
LIG_TRAF2_1 | 234 | 237 | PF00917 | 0.544 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.485 |
LIG_TYR_ITIM | 85 | 90 | PF00017 | 0.459 |
LIG_WRC_WIRS_1 | 153 | 158 | PF05994 | 0.465 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.435 |
MOD_CK1_1 | 414 | 420 | PF00069 | 0.641 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.530 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.572 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.419 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.398 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.541 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.505 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.496 |
MOD_CK2_1 | 397 | 403 | PF00069 | 0.441 |
MOD_CK2_1 | 426 | 432 | PF00069 | 0.660 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.460 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.585 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.477 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.615 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.614 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.568 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.496 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.544 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.538 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.456 |
MOD_GSK3_1 | 69 | 76 | PF00069 | 0.533 |
MOD_N-GLC_1 | 21 | 26 | PF02516 | 0.661 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.630 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.533 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.546 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.525 |
MOD_PKB_1 | 354 | 362 | PF00069 | 0.490 |
MOD_PKB_1 | 75 | 83 | PF00069 | 0.583 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.481 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.525 |
MOD_Plk_2-3 | 208 | 214 | PF00069 | 0.444 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.463 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.549 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.494 |
MOD_ProDKin_1 | 424 | 430 | PF00069 | 0.572 |
MOD_SUMO_rev_2 | 129 | 138 | PF00179 | 0.564 |
TRG_AP2beta_CARGO_1 | 151 | 160 | PF09066 | 0.481 |
TRG_DiLeu_BaEn_1 | 403 | 408 | PF01217 | 0.500 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.413 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.435 |
TRG_ENDOCYTIC_2 | 44 | 47 | PF00928 | 0.480 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.464 |
TRG_ER_diArg_1 | 146 | 149 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 162 | 164 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.642 |
TRG_ER_diArg_1 | 201 | 203 | PF00400 | 0.493 |
TRG_ER_diArg_1 | 219 | 222 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 354 | 356 | PF00400 | 0.451 |
TRG_ER_diArg_1 | 433 | 435 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 75 | 78 | PF00400 | 0.573 |
TRG_NES_CRM1_1 | 386 | 399 | PF08389 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 139 | 144 | PF00026 | 0.440 |
TRG_Pf-PMV_PEXEL_1 | 203 | 208 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.426 |
TRG_Pf-PMV_PEXEL_1 | 402 | 406 | PF00026 | 0.486 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE13 | Leptomonas seymouri | 63% | 90% |
A0A1X0P4A4 | Trypanosomatidae | 48% | 92% |
A0A381ML35 | Leishmania infantum | 96% | 100% |
A0A3Q8IGD4 | Leishmania donovani | 96% | 100% |
A0A3Q8IQ02 | Leishmania donovani | 96% | 100% |
A0A3R7LRX2 | Trypanosoma rangeli | 52% | 97% |
A4HFT4 | Leishmania braziliensis | 83% | 99% |
D0A626 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 98% |
E9ADD6 | Leishmania major | 96% | 100% |