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: Q4QA10
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.457 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.545 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.598 |
CLV_NRD_NRD_1 | 283 | 285 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.750 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.553 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.665 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.652 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.550 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 291 | 293 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 8 | 10 | PF00082 | 0.569 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.456 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 291 | 293 | PF00082 | 0.596 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.715 |
CLV_PCSK_PC7_1 | 179 | 185 | PF00082 | 0.637 |
CLV_PCSK_PC7_1 | 206 | 212 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.446 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.597 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.475 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.591 |
DOC_CYCLIN_RxL_1 | 123 | 133 | PF00134 | 0.517 |
DOC_CYCLIN_RxL_1 | 206 | 218 | PF00134 | 0.580 |
DOC_MAPK_gen_1 | 124 | 131 | PF00069 | 0.435 |
DOC_MAPK_gen_1 | 206 | 214 | PF00069 | 0.411 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.666 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.575 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.700 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.582 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.754 |
LIG_14-3-3_CanoR_1 | 178 | 187 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 222 | 232 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 292 | 302 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 332 | 342 | PF00244 | 0.769 |
LIG_APCC_ABBA_1 | 192 | 197 | PF00400 | 0.484 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.554 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.683 |
LIG_CtBP_PxDLS_1 | 326 | 332 | PF00389 | 0.532 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.567 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.687 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.628 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.602 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.694 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.469 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.519 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.544 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.728 |
LIG_GBD_Chelix_1 | 261 | 269 | PF00786 | 0.560 |
LIG_HCF-1_HBM_1 | 174 | 177 | PF13415 | 0.497 |
LIG_LIR_Apic_2 | 193 | 198 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 263 | 274 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.608 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.662 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.562 |
LIG_Pex14_1 | 7 | 11 | PF04695 | 0.511 |
LIG_Pex14_2 | 116 | 120 | PF04695 | 0.470 |
LIG_SH2_CRK | 177 | 181 | PF00017 | 0.659 |
LIG_SH2_NCK_1 | 11 | 15 | PF00017 | 0.383 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.553 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.443 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.379 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.546 |
LIG_SH3_2 | 74 | 79 | PF14604 | 0.673 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.635 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.597 |
LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.419 |
LIG_SUMO_SIM_par_1 | 127 | 133 | PF11976 | 0.491 |
LIG_SxIP_EBH_1 | 39 | 53 | PF03271 | 0.541 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.482 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.564 |
LIG_WRC_WIRS_1 | 131 | 136 | PF05994 | 0.362 |
LIG_WW_3 | 280 | 284 | PF00397 | 0.557 |
MOD_CK1_1 | 190 | 196 | PF00069 | 0.633 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.689 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.611 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.700 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.644 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.489 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.520 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.617 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.688 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.683 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.641 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.608 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.820 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.725 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.665 |
MOD_GlcNHglycan | 66 | 71 | PF01048 | 0.667 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.724 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.646 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.569 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.809 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.643 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.555 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.592 |
MOD_N-GLC_2 | 109 | 111 | PF02516 | 0.543 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.492 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.587 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.513 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.672 |
MOD_PKA_1 | 284 | 290 | PF00069 | 0.548 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.672 |
MOD_PKA_2 | 304 | 310 | PF00069 | 0.671 |
MOD_PKB_1 | 221 | 229 | PF00069 | 0.566 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.722 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.574 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.535 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.691 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.578 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.696 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.638 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.537 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.583 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.760 |
MOD_SUMO_for_1 | 274 | 277 | PF00179 | 0.806 |
MOD_SUMO_for_1 | 363 | 366 | PF00179 | 0.606 |
MOD_SUMO_rev_2 | 103 | 112 | PF00179 | 0.449 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.452 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.553 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.659 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 177 | 179 | PF00400 | 0.663 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.623 |
TRG_ER_diArg_1 | 282 | 284 | PF00400 | 0.562 |
TRG_ER_diArg_1 | 7 | 10 | PF00400 | 0.610 |
TRG_NLS_MonoExtC_3 | 50 | 56 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 48 | 55 | PF00514 | 0.588 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.639 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.596 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILI8 | Leptomonas seymouri | 52% | 92% |
A0A1X0P4C2 | Trypanosomatidae | 29% | 100% |
A0A3S7WYY8 | Leishmania donovani | 84% | 100% |
A0A422MPP3 | Trypanosoma rangeli | 31% | 100% |
A4HE19 | Leishmania braziliensis | 64% | 90% |
A4I1C6 | Leishmania infantum | 84% | 100% |
E9AXG2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
V5BXG5 | Trypanosoma cruzi | 31% | 100% |