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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AYG9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.471 |
DEG_SPOP_SBC_1 | 114 | 118 | PF00917 | 0.437 |
DEG_SPOP_SBC_1 | 81 | 85 | PF00917 | 0.480 |
DOC_CYCLIN_yCln2_LP_2 | 33 | 39 | PF00134 | 0.546 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.371 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.456 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.696 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.384 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 277 | 282 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.392 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.394 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 294 | 304 | PF00244 | 0.517 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.499 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.437 |
LIG_deltaCOP1_diTrp_1 | 270 | 273 | PF00928 | 0.670 |
LIG_EH_1 | 196 | 200 | PF12763 | 0.433 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.568 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.497 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.450 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.392 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.595 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.548 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.389 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.479 |
LIG_LIR_Apic_2 | 25 | 29 | PF02991 | 0.385 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.667 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.476 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.420 |
LIG_PCNA_yPIPBox_3 | 294 | 304 | PF02747 | 0.498 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.517 |
LIG_SH2_NCK_1 | 188 | 192 | PF00017 | 0.346 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 241 | 244 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.415 |
LIG_SH3_1 | 275 | 281 | PF00018 | 0.438 |
LIG_SH3_3 | 275 | 281 | PF00018 | 0.438 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.546 |
LIG_SH3_3 | 76 | 82 | PF00018 | 0.427 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.381 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.449 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.372 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.573 |
LIG_WRC_WIRS_1 | 304 | 309 | PF05994 | 0.519 |
MOD_CAAXbox | 314 | 317 | PF01239 | 0.643 |
MOD_CDK_SPK_2 | 25 | 30 | PF00069 | 0.421 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.571 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.440 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.485 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.594 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.550 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.618 |
MOD_CK2_1 | 216 | 222 | PF00069 | 0.622 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.482 |
MOD_GlcNHglycan | 103 | 107 | PF01048 | 0.777 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.494 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.417 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.385 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.660 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.746 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.660 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.701 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.478 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.408 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.579 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.690 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.538 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.491 |
MOD_N-GLC_1 | 124 | 129 | PF02516 | 0.609 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.415 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.472 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.433 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.616 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.476 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.446 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.734 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.515 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.437 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.522 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.560 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.772 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.657 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.523 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.540 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.777 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.618 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.380 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.516 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.391 |
MOD_ProDKin_1 | 277 | 283 | PF00069 | 0.486 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.388 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.605 |
TRG_DiLeu_LyEn_5 | 17 | 22 | PF01217 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7P7 | Leptomonas seymouri | 57% | 94% |
A0A1X0P7Q6 | Trypanosomatidae | 37% | 100% |
A0A3Q8ICA3 | Leishmania donovani | 91% | 100% |
A4HF34 | Leishmania braziliensis | 76% | 100% |
A4I2B8 | Leishmania infantum | 91% | 100% |
C9ZX95 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
Q4Q903 | Leishmania major | 91% | 100% |
V5AV59 | Trypanosoma cruzi | 36% | 100% |