Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 6 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AKX0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 284 | 288 | PF00656 | 0.748 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 204 | 206 | PF00675 | 0.388 |
CLV_PCSK_SKI1_1 | 149 | 153 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 4 | 8 | PF00082 | 0.425 |
DEG_APCC_DBOX_1 | 37 | 45 | PF00400 | 0.406 |
DEG_APCC_DBOX_1 | 389 | 397 | PF00400 | 0.660 |
DOC_CYCLIN_RxL_1 | 1 | 9 | PF00134 | 0.487 |
DOC_MAPK_gen_1 | 104 | 111 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 205 | 213 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 226 | 234 | PF00069 | 0.380 |
DOC_PP2B_LxvP_1 | 170 | 173 | PF13499 | 0.568 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.643 |
DOC_PP2B_PxIxI_1 | 403 | 409 | PF00149 | 0.671 |
DOC_USP7_MATH_1 | 281 | 285 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.654 |
DOC_USP7_MATH_1 | 97 | 101 | PF00917 | 0.281 |
DOC_USP7_UBL2_3 | 145 | 149 | PF12436 | 0.502 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.476 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.773 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.342 |
LIG_14-3-3_CanoR_1 | 104 | 112 | PF00244 | 0.559 |
LIG_14-3-3_CanoR_1 | 30 | 37 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.414 |
LIG_AP2alpha_2 | 348 | 350 | PF02296 | 0.705 |
LIG_BIR_III_2 | 401 | 405 | PF00653 | 0.639 |
LIG_CaM_IQ_9 | 213 | 228 | PF13499 | 0.515 |
LIG_Clathr_ClatBox_1 | 110 | 114 | PF01394 | 0.433 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.508 |
LIG_FHA_1 | 127 | 133 | PF00498 | 0.504 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.466 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.486 |
LIG_FHA_1 | 213 | 219 | PF00498 | 0.410 |
LIG_FHA_2 | 123 | 129 | PF00498 | 0.455 |
LIG_LIR_Apic_2 | 277 | 281 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 347 | 358 | PF02991 | 0.709 |
LIG_LIR_Gen_1 | 47 | 56 | PF02991 | 0.456 |
LIG_LIR_LC3C_4 | 176 | 181 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 219 | 225 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 347 | 353 | PF02991 | 0.699 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.706 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.420 |
LIG_MYND_1 | 255 | 259 | PF01753 | 0.779 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.533 |
LIG_PDZ_Class_2 | 430 | 435 | PF00595 | 0.698 |
LIG_Pex14_2 | 429 | 433 | PF04695 | 0.565 |
LIG_SH2_CRK | 222 | 226 | PF00017 | 0.573 |
LIG_SH2_CRK | 278 | 282 | PF00017 | 0.502 |
LIG_SH2_CRK | 317 | 321 | PF00017 | 0.715 |
LIG_SH2_CRK | 48 | 52 | PF00017 | 0.414 |
LIG_SH2_NCK_1 | 124 | 128 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.491 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.610 |
LIG_SH2_NCK_1 | 317 | 321 | PF00017 | 0.715 |
LIG_SH2_NCK_1 | 48 | 52 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 168 | 172 | PF00017 | 0.511 |
LIG_SH2_STAP1 | 48 | 52 | PF00017 | 0.475 |
LIG_SH2_STAP1 | 80 | 84 | PF00017 | 0.540 |
LIG_SH2_STAT5 | 124 | 127 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.525 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 168 | 171 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 64 | 67 | PF00017 | 0.405 |
LIG_SH3_2 | 325 | 330 | PF14604 | 0.602 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.473 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.675 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.656 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.701 |
LIG_SH3_3 | 373 | 379 | PF00018 | 0.655 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.686 |
LIG_SUMO_SIM_anti_2 | 114 | 120 | PF11976 | 0.546 |
LIG_SUMO_SIM_anti_2 | 176 | 181 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 9 | 15 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 209 | 215 | PF11976 | 0.399 |
LIG_TYR_ITIM | 220 | 225 | PF00017 | 0.562 |
MOD_CDK_SPK_2 | 71 | 76 | PF00069 | 0.342 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.278 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.703 |
MOD_CK1_1 | 274 | 280 | PF00069 | 0.746 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.605 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.684 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.502 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.509 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.615 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.717 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.617 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.517 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.695 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.720 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.814 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.722 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.679 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.754 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.724 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.487 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.424 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.519 |
MOD_GSK3_1 | 257 | 264 | PF00069 | 0.720 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.537 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.766 |
MOD_GSK3_1 | 412 | 419 | PF00069 | 0.689 |
MOD_GSK3_1 | 78 | 85 | PF00069 | 0.478 |
MOD_N-GLC_1 | 100 | 105 | PF02516 | 0.538 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.783 |
MOD_N-GLC_1 | 332 | 337 | PF02516 | 0.671 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.536 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.509 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.616 |
MOD_NEK2_2 | 126 | 131 | PF00069 | 0.559 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.452 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.615 |
MOD_PKA_2 | 220 | 226 | PF00069 | 0.443 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.575 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.435 |
MOD_PKA_2 | 97 | 103 | PF00069 | 0.567 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.463 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.544 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.431 |
MOD_Plk_4 | 126 | 132 | PF00069 | 0.514 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.390 |
MOD_Plk_4 | 369 | 375 | PF00069 | 0.742 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.636 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.432 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.476 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.773 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.625 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.339 |
MOD_SUMO_rev_2 | 190 | 199 | PF00179 | 0.555 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.462 |
TRG_DiLeu_BaEn_1 | 9 | 14 | PF01217 | 0.413 |
TRG_DiLeu_BaEn_2 | 415 | 421 | PF01217 | 0.708 |
TRG_DiLeu_LyEn_5 | 40 | 45 | PF01217 | 0.530 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 222 | 225 | PF00928 | 0.572 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 390 | 393 | PF00400 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 82 | 86 | PF00026 | 0.497 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKD5 | Leptomonas seymouri | 65% | 97% |
A0A1X0NKR8 | Trypanosomatidae | 38% | 100% |
A0A3R7KW02 | Trypanosoma rangeli | 38% | 100% |
A0A3S5H5T3 | Leishmania donovani | 88% | 97% |
A4H4Q5 | Leishmania braziliensis | 76% | 100% |
A4HSY4 | Leishmania infantum | 88% | 97% |
C9ZTL3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
Q4QIY5 | Leishmania major | 86% | 100% |
V5BXU6 | Trypanosoma cruzi | 35% | 100% |