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: E9ADJ6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.674 |
CLV_NRD_NRD_1 | 23 | 25 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 346 | 348 | PF00675 | 0.490 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.674 |
CLV_PCSK_KEX2_1 | 346 | 348 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.367 |
DEG_COP1_1 | 238 | 246 | PF00400 | 0.374 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.657 |
DOC_CKS1_1 | 150 | 155 | PF01111 | 0.438 |
DOC_CYCLIN_yCln2_LP_2 | 317 | 323 | PF00134 | 0.537 |
DOC_MAPK_gen_1 | 235 | 243 | PF00069 | 0.432 |
DOC_PP2B_LxvP_1 | 283 | 286 | PF13499 | 0.474 |
DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.279 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 84 | 89 | PF00397 | 0.394 |
LIG_14-3-3_CanoR_1 | 142 | 147 | PF00244 | 0.346 |
LIG_14-3-3_CanoR_1 | 2 | 6 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 27 | 36 | PF00244 | 0.623 |
LIG_Actin_RPEL_3 | 66 | 85 | PF02755 | 0.353 |
LIG_Actin_WH2_2 | 59 | 75 | PF00022 | 0.373 |
LIG_APCC_ABBA_1 | 16 | 21 | PF00400 | 0.571 |
LIG_BIR_III_2 | 251 | 255 | PF00653 | 0.342 |
LIG_BRCT_BRCA1_1 | 106 | 110 | PF00533 | 0.442 |
LIG_BRCT_BRCA1_1 | 89 | 93 | PF00533 | 0.443 |
LIG_DLG_GKlike_1 | 142 | 150 | PF00625 | 0.387 |
LIG_FHA_1 | 150 | 156 | PF00498 | 0.346 |
LIG_FHA_1 | 61 | 67 | PF00498 | 0.490 |
LIG_FHA_1 | 84 | 90 | PF00498 | 0.449 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.470 |
LIG_LIR_Apic_2 | 101 | 106 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 266 | 270 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.314 |
LIG_MYND_1 | 244 | 248 | PF01753 | 0.322 |
LIG_MYND_3 | 253 | 257 | PF01753 | 0.389 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.462 |
LIG_Pex14_2 | 348 | 352 | PF04695 | 0.454 |
LIG_REV1ctd_RIR_1 | 203 | 211 | PF16727 | 0.448 |
LIG_REV1ctd_RIR_1 | 231 | 241 | PF16727 | 0.403 |
LIG_REV1ctd_RIR_1 | 285 | 294 | PF16727 | 0.532 |
LIG_REV1ctd_RIR_1 | 326 | 335 | PF16727 | 0.372 |
LIG_SH2_CRK | 103 | 107 | PF00017 | 0.516 |
LIG_SH2_CRK | 57 | 61 | PF00017 | 0.482 |
LIG_SH2_NCK_1 | 103 | 107 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 186 | 189 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 242 | 245 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.368 |
LIG_SH3_3 | 147 | 153 | PF00018 | 0.466 |
LIG_SUMO_SIM_par_1 | 335 | 341 | PF11976 | 0.392 |
LIG_TRAF2_1 | 145 | 148 | PF00917 | 0.398 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.326 |
MOD_CK1_1 | 260 | 266 | PF00069 | 0.410 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.396 |
MOD_CK2_1 | 142 | 148 | PF00069 | 0.384 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.445 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.441 |
MOD_GlcNHglycan | 177 | 182 | PF01048 | 0.502 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.445 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.382 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.432 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.434 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.612 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.332 |
MOD_N-GLC_1 | 257 | 262 | PF02516 | 0.409 |
MOD_N-GLC_1 | 43 | 48 | PF02516 | 0.387 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.634 |
MOD_NEK2_1 | 125 | 130 | PF00069 | 0.403 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.384 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.320 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.548 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.430 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.457 |
MOD_PKA_1 | 38 | 44 | PF00069 | 0.433 |
MOD_PKA_2 | 1 | 7 | PF00069 | 0.647 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.416 |
MOD_PKA_2 | 72 | 78 | PF00069 | 0.448 |
MOD_Plk_1 | 146 | 152 | PF00069 | 0.375 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.468 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.346 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.350 |
MOD_Plk_4 | 31 | 37 | PF00069 | 0.421 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.283 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.329 |
MOD_ProDKin_1 | 84 | 90 | PF00069 | 0.398 |
TRG_DiLeu_BaEn_1 | 366 | 371 | PF01217 | 0.486 |
TRG_DiLeu_BaEn_2 | 120 | 126 | PF01217 | 0.393 |
TRG_DiLeu_BaEn_4 | 178 | 184 | PF01217 | 0.580 |
TRG_DiLeu_LyEn_5 | 366 | 371 | PF01217 | 0.572 |
TRG_ENDOCYTIC_2 | 267 | 270 | PF00928 | 0.478 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.472 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.682 |
TRG_ER_diArg_1 | 345 | 347 | PF00400 | 0.471 |
TRG_NLS_MonoCore_2 | 23 | 28 | PF00514 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 369 | 374 | PF00026 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2W1 | Leptomonas seymouri | 74% | 100% |
A0A0S4ISK5 | Bodo saltans | 46% | 100% |
A0A1X0NRI0 | Trypanosomatidae | 53% | 100% |
A0A3Q8ICV5 | Leishmania donovani | 97% | 100% |
A4HFZ3 | Leishmania braziliensis | 88% | 100% |
A4I312 | Leishmania infantum | 97% | 100% |
C9ZJH9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
E9AZC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BNB6 | Trypanosoma cruzi | 59% | 100% |