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: A4I7L5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.487 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.655 |
CLV_PCSK_KEX2_1 | 235 | 237 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 181 | 185 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.644 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.527 |
DEG_SPOP_SBC_1 | 258 | 262 | PF00917 | 0.575 |
DOC_MAPK_DCC_7 | 217 | 226 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 217 | 226 | PF00069 | 0.586 |
DOC_PP2B_LxvP_1 | 77 | 80 | PF13499 | 0.514 |
DOC_PP4_FxxP_1 | 28 | 31 | PF00568 | 0.411 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.494 |
DOC_PP4_MxPP_1 | 120 | 123 | PF00568 | 0.545 |
DOC_USP7_MATH_1 | 123 | 127 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.696 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 129 | 134 | PF00397 | 0.675 |
LIG_14-3-3_CanoR_1 | 175 | 185 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 217 | 222 | PF00244 | 0.718 |
LIG_14-3-3_CanoR_1 | 235 | 242 | PF00244 | 0.386 |
LIG_14-3-3_CanoR_1 | 71 | 80 | PF00244 | 0.424 |
LIG_Actin_WH2_2 | 221 | 237 | PF00022 | 0.521 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.395 |
LIG_BRCT_BRCA1_1 | 6 | 10 | PF00533 | 0.380 |
LIG_Clathr_ClatBox_1 | 184 | 188 | PF01394 | 0.471 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.365 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.472 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.358 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.393 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.459 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.554 |
LIG_IRF3_LxIS_1 | 267 | 272 | PF10401 | 0.474 |
LIG_LIR_Apic_2 | 26 | 31 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 261 | 267 | PF02991 | 0.567 |
LIG_LIR_Apic_2 | 292 | 296 | PF02991 | 0.497 |
LIG_LIR_Gen_1 | 266 | 276 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 40 | 49 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 186 | 192 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 266 | 271 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 284 | 290 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 292 | 297 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 37 | 41 | PF02991 | 0.442 |
LIG_MLH1_MIPbox_1 | 6 | 10 | PF16413 | 0.380 |
LIG_Pex14_2 | 28 | 32 | PF04695 | 0.389 |
LIG_Pex14_2 | 91 | 95 | PF04695 | 0.493 |
LIG_SH2_CRK | 189 | 193 | PF00017 | 0.402 |
LIG_SH2_CRK | 294 | 298 | PF00017 | 0.435 |
LIG_SH2_SRC | 264 | 267 | PF00017 | 0.527 |
LIG_SH2_SRC | 268 | 271 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 39 | 43 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 268 | 271 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 9 | 12 | PF00017 | 0.423 |
LIG_SH3_3 | 133 | 139 | PF00018 | 0.581 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.688 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.533 |
LIG_SH3_3 | 46 | 52 | PF00018 | 0.397 |
LIG_SUMO_SIM_par_1 | 183 | 188 | PF11976 | 0.456 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.395 |
LIG_TRAF2_1 | 157 | 160 | PF00917 | 0.508 |
LIG_TRAF2_1 | 200 | 203 | PF00917 | 0.664 |
LIG_TYR_ITIM | 187 | 192 | PF00017 | 0.451 |
LIG_WRC_WIRS_1 | 35 | 40 | PF05994 | 0.531 |
LIG_WW_2 | 222 | 225 | PF00397 | 0.565 |
LIG_WW_3 | 253 | 257 | PF00397 | 0.556 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.704 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.505 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.554 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.714 |
MOD_GlcNHglycan | 206 | 209 | PF01048 | 0.782 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.778 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.495 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.362 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.183 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.593 |
MOD_GSK3_1 | 125 | 132 | PF00069 | 0.705 |
MOD_GSK3_1 | 204 | 211 | PF00069 | 0.756 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.729 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.276 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.492 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.434 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.369 |
MOD_PIKK_1 | 10 | 16 | PF00454 | 0.470 |
MOD_PIKK_1 | 154 | 160 | PF00454 | 0.391 |
MOD_PKA_1 | 235 | 241 | PF00069 | 0.488 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.791 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.370 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.460 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.498 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.369 |
MOD_Plk_4 | 259 | 265 | PF00069 | 0.616 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.277 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.387 |
MOD_ProDKin_1 | 129 | 135 | PF00069 | 0.667 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.470 |
TRG_DiLeu_BaLyEn_6 | 172 | 177 | PF01217 | 0.448 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.472 |
TRG_ENDOCYTIC_2 | 189 | 192 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.508 |
TRG_ENDOCYTIC_2 | 294 | 297 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 41 | 44 | PF00928 | 0.376 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.504 |
TRG_ER_diArg_1 | 297 | 299 | PF00400 | 0.460 |
TRG_Pf-PMV_PEXEL_1 | 56 | 61 | PF00026 | 0.593 |
TRG_Pf-PMV_PEXEL_1 | 76 | 81 | PF00026 | 0.441 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I005 | Leptomonas seymouri | 71% | 100% |
A0A0S4KR83 | Bodo saltans | 40% | 100% |
A0A1X0NUS9 | Trypanosomatidae | 55% | 100% |
A0A3Q8IGT0 | Leishmania donovani | 100% | 100% |
A4HK47 | Leishmania braziliensis | 86% | 100% |
D0A9T4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B2J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q5L6 | Leishmania major | 96% | 100% |
V5AQU0 | Trypanosoma cruzi | 56% | 100% |