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: A4HF34
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.590 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.540 |
DEG_SPOP_SBC_1 | 102 | 106 | PF00917 | 0.522 |
DEG_SPOP_SBC_1 | 80 | 84 | PF00917 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 33 | 39 | PF00134 | 0.602 |
DOC_PP1_RVXF_1 | 213 | 219 | PF00149 | 0.420 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.450 |
DOC_PP4_FxxP_1 | 203 | 206 | PF00568 | 0.526 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.714 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.713 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.632 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 202 | 207 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.429 |
LIG_14-3-3_CanoR_1 | 156 | 161 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.473 |
LIG_14-3-3_CanoR_1 | 298 | 308 | PF00244 | 0.576 |
LIG_14-3-3_CanoR_1 | 89 | 97 | PF00244 | 0.625 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.569 |
LIG_BIR_III_4 | 15 | 19 | PF00653 | 0.350 |
LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.405 |
LIG_BRCT_BRCA1_1 | 296 | 300 | PF00533 | 0.510 |
LIG_deltaCOP1_diTrp_1 | 274 | 277 | PF00928 | 0.680 |
LIG_EH_1 | 200 | 204 | PF12763 | 0.498 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.487 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.577 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.463 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.482 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.618 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.467 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.518 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.631 |
LIG_FHA_2 | 102 | 108 | PF00498 | 0.723 |
LIG_FHA_2 | 300 | 306 | PF00498 | 0.524 |
LIG_LIR_Apic_2 | 25 | 29 | PF02991 | 0.449 |
LIG_LIR_Apic_2 | 274 | 280 | PF02991 | 0.719 |
LIG_LIR_Gen_1 | 263 | 273 | PF02991 | 0.684 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.495 |
LIG_NRBOX | 147 | 153 | PF00104 | 0.497 |
LIG_PCNA_yPIPBox_3 | 298 | 308 | PF02747 | 0.576 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.580 |
LIG_SH2_NCK_1 | 192 | 196 | PF00017 | 0.422 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.568 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.493 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.602 |
LIG_SUMO_SIM_par_1 | 169 | 174 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.451 |
LIG_SUMO_SIM_par_1 | 291 | 297 | PF11976 | 0.645 |
LIG_WRC_WIRS_1 | 308 | 313 | PF05994 | 0.598 |
MOD_CAAXbox | 318 | 321 | PF01239 | 0.679 |
MOD_CDK_SPK_2 | 25 | 30 | PF00069 | 0.503 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.689 |
MOD_CK1_1 | 126 | 132 | PF00069 | 0.590 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.503 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.534 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.744 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.617 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.543 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.697 |
MOD_CK2_1 | 101 | 107 | PF00069 | 0.754 |
MOD_CK2_1 | 299 | 305 | PF00069 | 0.526 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.545 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.440 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.688 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.685 |
MOD_GlcNHglycan | 99 | 102 | PF01048 | 0.702 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.604 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.532 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.491 |
MOD_GSK3_1 | 163 | 170 | PF00069 | 0.429 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.761 |
MOD_GSK3_1 | 286 | 293 | PF00069 | 0.590 |
MOD_GSK3_1 | 307 | 314 | PF00069 | 0.575 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.651 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.695 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.634 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.480 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.510 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.481 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.761 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.530 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.485 |
MOD_NEK2_2 | 48 | 53 | PF00069 | 0.428 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.782 |
MOD_PIKK_1 | 299 | 305 | PF00454 | 0.593 |
MOD_PKA_2 | 88 | 94 | PF00069 | 0.705 |
MOD_Plk_1 | 248 | 254 | PF00069 | 0.588 |
MOD_Plk_1 | 273 | 279 | PF00069 | 0.730 |
MOD_Plk_1 | 48 | 54 | PF00069 | 0.420 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.762 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.571 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.545 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.744 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.622 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.469 |
MOD_ProDKin_1 | 202 | 208 | PF00069 | 0.531 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.465 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.427 |
TRG_DiLeu_BaLyEn_6 | 134 | 139 | PF01217 | 0.678 |
TRG_DiLeu_BaLyEn_6 | 212 | 217 | PF01217 | 0.397 |
TRG_DiLeu_LyEn_5 | 17 | 22 | PF01217 | 0.559 |
TRG_Pf-PMV_PEXEL_1 | 189 | 193 | PF00026 | 0.522 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7P7 | Leptomonas seymouri | 57% | 95% |
A0A1X0P7Q6 | Trypanosomatidae | 35% | 100% |
A0A3Q8ICA3 | Leishmania donovani | 77% | 100% |
A4I2B8 | Leishmania infantum | 77% | 100% |
C9ZX95 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 100% |
E9AYG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4Q903 | Leishmania major | 75% | 98% |
V5AV59 | Trypanosoma cruzi | 37% | 100% |