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: A4I2B8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 254 | 258 | PF00656 | 0.539 |
CLV_PCSK_SKI1_1 | 159 | 163 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.473 |
DOC_CYCLIN_yCln2_LP_2 | 33 | 39 | PF00134 | 0.565 |
DOC_PP1_RVXF_1 | 51 | 57 | PF00149 | 0.406 |
DOC_PP4_FxxP_1 | 199 | 202 | PF00568 | 0.482 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.664 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.701 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.600 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.493 |
DOC_WW_Pin1_4 | 25 | 30 | PF00397 | 0.419 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.442 |
LIG_14-3-3_CanoR_1 | 152 | 157 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 260 | 265 | PF00244 | 0.640 |
LIG_14-3-3_CanoR_1 | 294 | 304 | PF00244 | 0.513 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.366 |
LIG_BRCT_BRCA1_1 | 242 | 246 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.442 |
LIG_deltaCOP1_diTrp_1 | 270 | 273 | PF00928 | 0.698 |
LIG_EH_1 | 196 | 200 | PF12763 | 0.456 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.557 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.477 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.456 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.684 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.559 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.419 |
LIG_FHA_2 | 296 | 302 | PF00498 | 0.529 |
LIG_LIR_Apic_2 | 25 | 29 | PF02991 | 0.407 |
LIG_LIR_Apic_2 | 270 | 276 | PF02991 | 0.696 |
LIG_NRBOX | 143 | 149 | PF00104 | 0.458 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.474 |
LIG_PCNA_yPIPBox_3 | 294 | 304 | PF02747 | 0.508 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.542 |
LIG_SH2_NCK_1 | 188 | 192 | PF00017 | 0.377 |
LIG_SH2_PTP2 | 45 | 48 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 241 | 244 | PF00017 | 0.652 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.515 |
LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.271 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.570 |
LIG_SUMO_SIM_par_1 | 12 | 17 | PF11976 | 0.469 |
LIG_SUMO_SIM_par_1 | 165 | 170 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 19 | 25 | PF11976 | 0.413 |
LIG_SUMO_SIM_par_1 | 287 | 293 | PF11976 | 0.565 |
LIG_WRC_WIRS_1 | 304 | 309 | PF05994 | 0.511 |
MOD_CAAXbox | 314 | 317 | PF01239 | 0.580 |
MOD_CDK_SPK_2 | 25 | 30 | PF00069 | 0.445 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.660 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.502 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.751 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.532 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.671 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.698 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.528 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.662 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.398 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.392 |
MOD_GlcNHglycan | 218 | 221 | PF01048 | 0.741 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.665 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.644 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.609 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.404 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.726 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.553 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.473 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.692 |
MOD_N-GLC_1 | 98 | 103 | PF02516 | 0.760 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.460 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.451 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.459 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.715 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.450 |
MOD_NEK2_1 | 303 | 308 | PF00069 | 0.419 |
MOD_PIKK_1 | 228 | 234 | PF00454 | 0.730 |
MOD_PIKK_1 | 240 | 246 | PF00454 | 0.724 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.506 |
MOD_PIKK_1 | 295 | 301 | PF00454 | 0.528 |
MOD_PK_1 | 260 | 266 | PF00069 | 0.608 |
MOD_PKA_2 | 259 | 265 | PF00069 | 0.640 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.600 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.775 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.737 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.493 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.718 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.602 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.559 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.420 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.494 |
MOD_ProDKin_1 | 25 | 31 | PF00069 | 0.427 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.440 |
TRG_DiLeu_BaLyEn_6 | 130 | 135 | PF01217 | 0.631 |
TRG_DiLeu_LyEn_5 | 17 | 22 | PF01217 | 0.504 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7P7 | Leptomonas seymouri | 57% | 94% |
A0A1X0P7Q6 | Trypanosomatidae | 38% | 100% |
A0A3Q8ICA3 | Leishmania donovani | 100% | 100% |
A4HF34 | Leishmania braziliensis | 77% | 99% |
C9ZX95 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AYG9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q903 | Leishmania major | 91% | 100% |
V5AV59 | Trypanosoma cruzi | 36% | 100% |