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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9B0U5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 35 | 39 | PF00656 | 0.576 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 60 | 62 | PF00675 | 0.596 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.778 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 60 | 62 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.558 |
DEG_APCC_KENBOX_2 | 134 | 138 | PF00400 | 0.536 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.603 |
DOC_CYCLIN_RxL_1 | 123 | 136 | PF00134 | 0.452 |
DOC_CYCLIN_RxL_1 | 220 | 234 | PF00134 | 0.631 |
DOC_MAPK_gen_1 | 365 | 371 | PF00069 | 0.362 |
DOC_MAPK_MEF2A_6 | 380 | 389 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 127 | 134 | PF00149 | 0.544 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.707 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.670 |
LIG_14-3-3_CanoR_1 | 116 | 124 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 127 | 132 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 169 | 175 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 177 | 183 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 232 | 239 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 300 | 304 | PF00244 | 0.618 |
LIG_14-3-3_CanoR_1 | 307 | 316 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 358 | 363 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 43 | 49 | PF00244 | 0.582 |
LIG_AP2alpha_2 | 9 | 11 | PF02296 | 0.511 |
LIG_BIR_III_2 | 41 | 45 | PF00653 | 0.645 |
LIG_BRCT_BRCA1_1 | 129 | 133 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_2 | 129 | 135 | PF00533 | 0.524 |
LIG_CtBP_PxDLS_1 | 221 | 225 | PF00389 | 0.596 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.694 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.685 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.522 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.501 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.576 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.597 |
LIG_FHA_2 | 178 | 184 | PF00498 | 0.602 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.542 |
LIG_FHA_2 | 359 | 365 | PF00498 | 0.481 |
LIG_LIR_Gen_1 | 17 | 24 | PF02991 | 0.561 |
LIG_LIR_Gen_1 | 244 | 253 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 391 | 396 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 17 | 23 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 391 | 395 | PF02991 | 0.373 |
LIG_PCNA_yPIPBox_3 | 202 | 216 | PF02747 | 0.624 |
LIG_Rb_LxCxE_1 | 97 | 118 | PF01857 | 0.364 |
LIG_SH2_CRK | 392 | 396 | PF00017 | 0.379 |
LIG_SH2_NCK_1 | 7 | 11 | PF00017 | 0.484 |
LIG_SH2_SRC | 20 | 23 | PF00017 | 0.630 |
LIG_SH2_SRC | 7 | 10 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 20 | 24 | PF00017 | 0.702 |
LIG_SH2_STAP1 | 392 | 396 | PF00017 | 0.379 |
LIG_SH2_STAP1 | 96 | 100 | PF00017 | 0.420 |
LIG_SH2_STAT3 | 268 | 271 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 188 | 191 | PF00017 | 0.465 |
LIG_SH3_3 | 190 | 196 | PF00018 | 0.650 |
LIG_SUMO_SIM_anti_2 | 160 | 168 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 218 | 225 | PF11976 | 0.586 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.504 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.520 |
LIG_TYR_ITIM | 18 | 23 | PF00017 | 0.530 |
LIG_Vh1_VBS_1 | 152 | 170 | PF01044 | 0.527 |
MOD_CK1_1 | 181 | 187 | PF00069 | 0.695 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.667 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.669 |
MOD_CK2_1 | 119 | 125 | PF00069 | 0.416 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.544 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.701 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.623 |
MOD_CK2_1 | 207 | 213 | PF00069 | 0.769 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.499 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.399 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.443 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.634 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.670 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.647 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.478 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.468 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.529 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.562 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.662 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.566 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.550 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.646 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.652 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.601 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.423 |
MOD_NEK2_1 | 182 | 187 | PF00069 | 0.727 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.724 |
MOD_NEK2_1 | 228 | 233 | PF00069 | 0.532 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.499 |
MOD_NEK2_2 | 243 | 248 | PF00069 | 0.459 |
MOD_NEK2_2 | 77 | 82 | PF00069 | 0.676 |
MOD_PIKK_1 | 200 | 206 | PF00454 | 0.718 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.691 |
MOD_PIKK_1 | 315 | 321 | PF00454 | 0.427 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.506 |
MOD_PKA_1 | 60 | 66 | PF00069 | 0.590 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.467 |
MOD_PKA_2 | 168 | 174 | PF00069 | 0.444 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.739 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.656 |
MOD_PKA_2 | 59 | 65 | PF00069 | 0.638 |
MOD_PKB_1 | 127 | 135 | PF00069 | 0.469 |
MOD_PKB_1 | 356 | 364 | PF00069 | 0.559 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.679 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.575 |
MOD_Plk_2-3 | 22 | 28 | PF00069 | 0.535 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.457 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.579 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.671 |
MOD_SUMO_rev_2 | 101 | 110 | PF00179 | 0.447 |
MOD_SUMO_rev_2 | 372 | 382 | PF00179 | 0.500 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.563 |
TRG_DiLeu_BaEn_3 | 161 | 167 | PF01217 | 0.515 |
TRG_ENDOCYTIC_2 | 20 | 23 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.374 |
TRG_ER_diArg_1 | 148 | 151 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.387 |
TRG_ER_diArg_1 | 357 | 360 | PF00400 | 0.548 |
TRG_ER_diArg_1 | 59 | 61 | PF00400 | 0.604 |
TRG_Pf-PMV_PEXEL_1 | 140 | 144 | PF00026 | 0.544 |
TRG_Pf-PMV_PEXEL_1 | 331 | 336 | PF00026 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 373 | 377 | PF00026 | 0.499 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I207 | Leptomonas seymouri | 42% | 100% |
A0A3Q8IBZ6 | Leishmania donovani | 85% | 100% |
A0A422P3J4 | Trypanosoma rangeli | 30% | 100% |
A4HIB6 | Leishmania braziliensis | 68% | 98% |
A4I5K0 | Leishmania infantum | 85% | 100% |
Q4Q7C1 | Leishmania major | 85% | 98% |
V5B8Y5 | Trypanosoma cruzi | 28% | 100% |