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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HJF6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.315 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.438 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 130 | 134 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.538 |
DEG_APCC_DBOX_1 | 18 | 26 | PF00400 | 0.585 |
DEG_MDM2_SWIB_1 | 290 | 297 | PF02201 | 0.488 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.792 |
DEG_SCF_FBW7_1 | 1 | 8 | PF00400 | 0.510 |
DEG_SPOP_SBC_1 | 193 | 197 | PF00917 | 0.532 |
DEG_SPOP_SBC_1 | 280 | 284 | PF00917 | 0.651 |
DOC_CKS1_1 | 72 | 77 | PF01111 | 0.606 |
DOC_MAPK_DCC_7 | 19 | 27 | PF00069 | 0.454 |
DOC_MAPK_gen_1 | 109 | 119 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 201 | 211 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 110 | 119 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 19 | 27 | PF00069 | 0.665 |
DOC_MAPK_MEF2A_6 | 50 | 57 | PF00069 | 0.369 |
DOC_PP2B_LxvP_1 | 121 | 124 | PF13499 | 0.472 |
DOC_PP4_FxxP_1 | 20 | 23 | PF00568 | 0.458 |
DOC_PP4_FxxP_1 | 346 | 349 | PF00568 | 0.439 |
DOC_USP7_MATH_1 | 193 | 197 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 220 | 224 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 286 | 290 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 386 | 390 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 42 | 46 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.423 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 100 | 105 | PF00397 | 0.550 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.460 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.669 |
LIG_14-3-3_CanoR_1 | 109 | 119 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 269 | 277 | PF00244 | 0.628 |
LIG_14-3-3_CanoR_1 | 387 | 393 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 50 | 56 | PF00244 | 0.589 |
LIG_Actin_RPEL_3 | 102 | 121 | PF02755 | 0.444 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.322 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.600 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.451 |
LIG_CaM_NSCaTE_8 | 129 | 136 | PF13499 | 0.357 |
LIG_deltaCOP1_diTrp_1 | 292 | 299 | PF00928 | 0.425 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.543 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.624 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.645 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.628 |
LIG_FHA_1 | 402 | 408 | PF00498 | 0.486 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.551 |
LIG_FHA_2 | 83 | 89 | PF00498 | 0.546 |
LIG_LIR_Apic_2 | 343 | 349 | PF02991 | 0.441 |
LIG_LIR_Gen_1 | 113 | 124 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 289 | 298 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 304 | 313 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 113 | 119 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 289 | 293 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 304 | 308 | PF02991 | 0.466 |
LIG_MYND_1 | 100 | 104 | PF01753 | 0.514 |
LIG_NRBOX | 258 | 264 | PF00104 | 0.357 |
LIG_Pex14_2 | 290 | 294 | PF04695 | 0.499 |
LIG_PTB_Apo_2 | 14 | 21 | PF02174 | 0.462 |
LIG_Rb_LxCxE_1 | 207 | 225 | PF01857 | 0.312 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.508 |
LIG_SH2_CRK | 352 | 356 | PF00017 | 0.631 |
LIG_SH2_NCK_1 | 159 | 163 | PF00017 | 0.495 |
LIG_SH2_NCK_1 | 352 | 356 | PF00017 | 0.631 |
LIG_SH2_STAT3 | 98 | 101 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.422 |
LIG_SH3_3 | 69 | 75 | PF00018 | 0.669 |
LIG_SUMO_SIM_anti_2 | 54 | 59 | PF11976 | 0.394 |
LIG_TRAF2_1 | 238 | 241 | PF00917 | 0.759 |
LIG_TRAF2_1 | 85 | 88 | PF00917 | 0.498 |
LIG_TYR_ITIM | 350 | 355 | PF00017 | 0.559 |
LIG_WRC_WIRS_1 | 287 | 292 | PF05994 | 0.454 |
LIG_WRC_WIRS_1 | 293 | 298 | PF05994 | 0.339 |
MOD_CDC14_SPxK_1 | 348 | 351 | PF00782 | 0.424 |
MOD_CDK_SPK_2 | 1 | 6 | PF00069 | 0.508 |
MOD_CDK_SPxK_1 | 345 | 351 | PF00069 | 0.433 |
MOD_CDK_SPxxK_3 | 194 | 201 | PF00069 | 0.395 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.554 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.472 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.616 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.706 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.607 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.647 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.500 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.579 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.601 |
MOD_GlcNHglycan | 178 | 181 | PF01048 | 0.343 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.630 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.600 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.324 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.440 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.596 |
MOD_GlcNHglycan | 336 | 339 | PF01048 | 0.580 |
MOD_GlcNHglycan | 342 | 345 | PF01048 | 0.665 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.505 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.584 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.462 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.561 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.572 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.453 |
MOD_N-GLC_1 | 280 | 285 | PF02516 | 0.467 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.391 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.545 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.500 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.451 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.563 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.490 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.594 |
MOD_PIKK_1 | 322 | 328 | PF00454 | 0.606 |
MOD_PIKK_1 | 45 | 51 | PF00454 | 0.532 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.342 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.677 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.701 |
MOD_PKA_2 | 372 | 378 | PF00069 | 0.485 |
MOD_PKA_2 | 386 | 392 | PF00069 | 0.515 |
MOD_PKA_2 | 393 | 399 | PF00069 | 0.591 |
MOD_PKA_2 | 5 | 11 | PF00069 | 0.791 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.361 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.562 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.393 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.509 |
MOD_ProDKin_1 | 100 | 106 | PF00069 | 0.541 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.459 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.628 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.561 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.659 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.667 |
MOD_SUMO_for_1 | 93 | 96 | PF00179 | 0.482 |
MOD_SUMO_rev_2 | 103 | 111 | PF00179 | 0.432 |
MOD_SUMO_rev_2 | 126 | 132 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 87 | 95 | PF00179 | 0.763 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 352 | 355 | PF00928 | 0.632 |
TRG_ER_diArg_1 | 357 | 359 | PF00400 | 0.483 |
TRG_Pf-PMV_PEXEL_1 | 369 | 374 | PF00026 | 0.510 |
TRG_Pf-PMV_PEXEL_1 | 60 | 65 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I3T2 | Leptomonas seymouri | 49% | 98% |
A0A0S4IUI6 | Bodo saltans | 26% | 100% |
A0A1X0NVH2 | Trypanosomatidae | 31% | 100% |
A0A3R7MTX4 | Trypanosoma rangeli | 29% | 100% |
A0A3S7X4N0 | Leishmania donovani | 71% | 99% |
A4I6V1 | Leishmania infantum | 71% | 99% |
D0A7B7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9B1X4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 98% |
Q4Q688 | Leishmania major | 72% | 100% |
V5C1D3 | Trypanosoma cruzi | 29% | 100% |