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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9ATJ2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.802 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 237 | 239 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 334 | 336 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 390 | 392 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 396 | 398 | PF00675 | 0.571 |
CLV_PCSK_FUR_1 | 278 | 282 | PF00082 | 0.762 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.633 |
CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 280 | 282 | PF00082 | 0.837 |
CLV_PCSK_KEX2_1 | 334 | 336 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 396 | 398 | PF00082 | 0.697 |
CLV_PCSK_PC1ET2_1 | 28 | 30 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 280 | 282 | PF00082 | 0.837 |
CLV_PCSK_SKI1_1 | 255 | 259 | PF00082 | 0.753 |
CLV_PCSK_SKI1_1 | 29 | 33 | PF00082 | 0.747 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.629 |
DEG_MDM2_SWIB_1 | 158 | 165 | PF02201 | 0.596 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.787 |
DEG_SPOP_SBC_1 | 51 | 55 | PF00917 | 0.727 |
DOC_CYCLIN_yCln2_LP_2 | 135 | 141 | PF00134 | 0.648 |
DOC_CYCLIN_yCln2_LP_2 | 31 | 34 | PF00134 | 0.750 |
DOC_MAPK_DCC_7 | 293 | 303 | PF00069 | 0.718 |
DOC_PP2B_LxvP_1 | 135 | 138 | PF13499 | 0.650 |
DOC_PP2B_LxvP_1 | 265 | 268 | PF13499 | 0.821 |
DOC_PP2B_LxvP_1 | 31 | 34 | PF13499 | 0.750 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.690 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.778 |
DOC_USP7_MATH_1 | 351 | 355 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 359 | 363 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.805 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.364 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.726 |
LIG_14-3-3_CanoR_1 | 199 | 209 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 2 | 9 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.516 |
LIG_BRCT_BRCA1_1 | 154 | 158 | PF00533 | 0.595 |
LIG_EVH1_2 | 68 | 72 | PF00568 | 0.744 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.632 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.585 |
LIG_FHA_1 | 298 | 304 | PF00498 | 0.698 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.690 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.803 |
LIG_LIR_Gen_1 | 155 | 166 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.544 |
LIG_NRBOX | 40 | 46 | PF00104 | 0.701 |
LIG_PCNA_yPIPBox_3 | 408 | 422 | PF02747 | 0.696 |
LIG_Pex14_2 | 127 | 131 | PF04695 | 0.622 |
LIG_Pex14_2 | 154 | 158 | PF04695 | 0.595 |
LIG_SH2_NCK_1 | 9 | 13 | PF00017 | 0.481 |
LIG_SH2_STAT3 | 149 | 152 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 410 | 413 | PF00017 | 0.695 |
LIG_SH3_3 | 116 | 122 | PF00018 | 0.646 |
LIG_SH3_3 | 211 | 217 | PF00018 | 0.706 |
LIG_SH3_3 | 253 | 259 | PF00018 | 0.619 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.733 |
LIG_SH3_3 | 314 | 320 | PF00018 | 0.657 |
LIG_SUMO_SIM_anti_2 | 300 | 305 | PF11976 | 0.695 |
LIG_SUMO_SIM_par_1 | 216 | 223 | PF11976 | 0.549 |
LIG_SUMO_SIM_par_1 | 373 | 378 | PF11976 | 0.751 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.819 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.616 |
MOD_CK1_1 | 223 | 229 | PF00069 | 0.554 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.559 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.459 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.681 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.614 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.776 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.620 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.703 |
MOD_CK2_1 | 417 | 423 | PF00069 | 0.608 |
MOD_Cter_Amidation | 278 | 281 | PF01082 | 0.839 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.518 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.313 |
MOD_GlcNHglycan | 204 | 207 | PF01048 | 0.855 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.533 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.742 |
MOD_GlcNHglycan | 246 | 249 | PF01048 | 0.649 |
MOD_GlcNHglycan | 250 | 253 | PF01048 | 0.621 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.750 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.790 |
MOD_GlcNHglycan | 342 | 346 | PF01048 | 0.686 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.631 |
MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.576 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.760 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.715 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.600 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.595 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.512 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.678 |
MOD_GSK3_1 | 219 | 226 | PF00069 | 0.560 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.697 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.663 |
MOD_GSK3_1 | 364 | 371 | PF00069 | 0.711 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.648 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.546 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.368 |
MOD_N-GLC_1 | 248 | 253 | PF02516 | 0.681 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.415 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.485 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.748 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.630 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.745 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.516 |
MOD_NEK2_2 | 139 | 144 | PF00069 | 0.642 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.681 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.616 |
MOD_Plk_1 | 186 | 192 | PF00069 | 0.527 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.618 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.538 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.767 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.643 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.717 |
MOD_SUMO_rev_2 | 174 | 182 | PF00179 | 0.711 |
MOD_SUMO_rev_2 | 357 | 365 | PF00179 | 0.740 |
TRG_DiLeu_BaEn_1 | 178 | 183 | PF01217 | 0.620 |
TRG_DiLeu_BaEn_1 | 40 | 45 | PF01217 | 0.618 |
TRG_DiLeu_BaLyEn_6 | 167 | 172 | PF01217 | 0.716 |
TRG_DiLeu_BaLyEn_6 | 214 | 219 | PF01217 | 0.526 |
TRG_DiLeu_BaLyEn_6 | 253 | 258 | PF01217 | 0.756 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.633 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 395 | 397 | PF00400 | 0.700 |
TRG_NES_CRM1_1 | 373 | 384 | PF08389 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.717 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ILA1 | Leishmania donovani | 85% | 100% |
A4HPS7 | Leishmania braziliensis | 67% | 100% |
A4IE65 | Leishmania infantum | 85% | 100% |
Q4Q106 | Leishmania major | 84% | 100% |