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: A4H3P5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 243 | 245 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 72 | 74 | PF00675 | 0.413 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.574 |
CLV_PCSK_PC1ET2_1 | 235 | 237 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 107 | 111 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 193 | 197 | PF00082 | 0.328 |
CLV_PCSK_SKI1_1 | 25 | 29 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 332 | 336 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.386 |
DEG_APCC_DBOX_1 | 24 | 32 | PF00400 | 0.430 |
DEG_APCC_DBOX_1 | 72 | 80 | PF00400 | 0.532 |
DEG_Kelch_Keap1_1 | 166 | 171 | PF01344 | 0.472 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.286 |
DOC_CYCLIN_RxL_1 | 103 | 113 | PF00134 | 0.401 |
DOC_CYCLIN_RxL_1 | 183 | 194 | PF00134 | 0.474 |
DOC_CYCLIN_RxL_1 | 38 | 46 | PF00134 | 0.365 |
DOC_MAPK_gen_1 | 73 | 81 | PF00069 | 0.546 |
DOC_MAPK_MEF2A_6 | 148 | 156 | PF00069 | 0.348 |
DOC_MAPK_MEF2A_6 | 172 | 181 | PF00069 | 0.409 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.445 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 272 | 276 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.479 |
DOC_USP7_UBL2_3 | 155 | 159 | PF12436 | 0.294 |
DOC_USP7_UBL2_3 | 245 | 249 | PF12436 | 0.340 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.443 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 2 | 11 | PF00244 | 0.433 |
LIG_14-3-3_CanoR_1 | 73 | 77 | PF00244 | 0.335 |
LIG_Actin_WH2_2 | 102 | 117 | PF00022 | 0.288 |
LIG_APCC_ABBA_1 | 289 | 294 | PF00400 | 0.474 |
LIG_BIR_III_4 | 194 | 198 | PF00653 | 0.350 |
LIG_Clathr_ClatBox_1 | 188 | 192 | PF01394 | 0.451 |
LIG_FAT_LD_1 | 181 | 189 | PF03623 | 0.401 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.338 |
LIG_FHA_2 | 326 | 332 | PF00498 | 0.491 |
LIG_GBD_Chelix_1 | 180 | 188 | PF00786 | 0.407 |
LIG_IBAR_NPY_1 | 130 | 132 | PF08397 | 0.267 |
LIG_Integrin_RGD_1 | 204 | 206 | PF01839 | 0.495 |
LIG_LIR_Gen_1 | 119 | 127 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 225 | 234 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 46 | 56 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 96 | 106 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 119 | 124 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 96 | 101 | PF02991 | 0.494 |
LIG_PCNA_PIPBox_1 | 58 | 67 | PF02747 | 0.389 |
LIG_Pex14_1 | 330 | 334 | PF04695 | 0.470 |
LIG_SH2_CRK | 121 | 125 | PF00017 | 0.375 |
LIG_SH2_GRB2like | 237 | 240 | PF00017 | 0.272 |
LIG_SH2_SRC | 293 | 296 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 112 | 116 | PF00017 | 0.280 |
LIG_SH2_STAP1 | 121 | 125 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 226 | 230 | PF00017 | 0.262 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.384 |
LIG_SH3_3 | 266 | 272 | PF00018 | 0.550 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 187 | 192 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 177 | 183 | PF11976 | 0.457 |
LIG_SUMO_SIM_par_1 | 187 | 192 | PF11976 | 0.392 |
LIG_TRAF2_1 | 305 | 308 | PF00917 | 0.477 |
LIG_UBA3_1 | 152 | 159 | PF00899 | 0.281 |
LIG_UBA3_1 | 229 | 235 | PF00899 | 0.383 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.501 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.466 |
MOD_Cter_Amidation | 84 | 87 | PF01082 | 0.417 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.477 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.523 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.458 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.571 |
MOD_N-GLC_1 | 325 | 330 | PF02516 | 0.584 |
MOD_N-GLC_2 | 239 | 241 | PF02516 | 0.469 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.431 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.502 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.297 |
MOD_Plk_1 | 325 | 331 | PF00069 | 0.526 |
MOD_Plk_4 | 116 | 122 | PF00069 | 0.318 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.283 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.459 |
MOD_Plk_4 | 7 | 13 | PF00069 | 0.421 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.297 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 105 | 110 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 19 | 24 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.329 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 108 | 113 | PF00026 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 41 | 46 | PF00026 | 0.366 |
TRG_Pf-PMV_PEXEL_1 | 50 | 55 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 59 | 63 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P542 | Leptomonas seymouri | 64% | 87% |
A0A0S4IVU1 | Bodo saltans | 38% | 99% |
A0A1X0P922 | Trypanosomatidae | 50% | 87% |
A0A451EJT2 | Leishmania donovani | 86% | 85% |
C9ZKH7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E8NHC8 | Leishmania infantum | 86% | 85% |
E9ACM8 | Leishmania major | 84% | 100% |
E9AJW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 99% |
V5DTZ7 | Trypanosoma cruzi | 50% | 84% |