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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3Q8IAS3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 239 | 243 | PF00656 | 0.598 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.702 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.681 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.686 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.764 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 81 | 83 | PF00675 | 0.477 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 81 | 83 | PF00082 | 0.507 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.786 |
CLV_PCSK_PC1ET2_1 | 257 | 259 | PF00082 | 0.771 |
CLV_PCSK_PC7_1 | 104 | 110 | PF00082 | 0.776 |
CLV_PCSK_PC7_1 | 164 | 170 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.761 |
CLV_PCSK_SKI1_1 | 411 | 415 | PF00082 | 0.616 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.413 |
DEG_SCF_FBW7_1 | 284 | 291 | PF00400 | 0.769 |
DOC_CKS1_1 | 285 | 290 | PF01111 | 0.775 |
DOC_CYCLIN_RxL_1 | 133 | 143 | PF00134 | 0.578 |
DOC_MAPK_gen_1 | 55 | 63 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 81 | 88 | PF00069 | 0.484 |
DOC_MAPK_MEF2A_6 | 19 | 26 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 56 | 65 | PF00069 | 0.422 |
DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.445 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.437 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.518 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.464 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.780 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 340 | 344 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.488 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 264 | 269 | PF00397 | 0.794 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.615 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.557 |
LIG_14-3-3_CanoR_1 | 19 | 23 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.777 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.685 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.758 |
LIG_14-3-3_CanoR_1 | 316 | 325 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.485 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.496 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.750 |
LIG_CtBP_PxDLS_1 | 237 | 241 | PF00389 | 0.678 |
LIG_EH_1 | 176 | 180 | PF12763 | 0.671 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.537 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.529 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.415 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.354 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.623 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.576 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.643 |
LIG_FHA_2 | 294 | 300 | PF00498 | 0.754 |
LIG_FHA_2 | 401 | 407 | PF00498 | 0.662 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.558 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.494 |
LIG_LIR_Apic_2 | 83 | 87 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 328 | 338 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.622 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.466 |
LIG_MAD2 | 280 | 288 | PF02301 | 0.613 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.489 |
LIG_PTB_Apo_2 | 74 | 81 | PF02174 | 0.525 |
LIG_PTB_Phospho_1 | 74 | 80 | PF10480 | 0.521 |
LIG_REV1ctd_RIR_1 | 411 | 415 | PF16727 | 0.670 |
LIG_SH2_CRK | 175 | 179 | PF00017 | 0.672 |
LIG_SH2_CRK | 330 | 334 | PF00017 | 0.431 |
LIG_SH2_GRB2like | 175 | 178 | PF00017 | 0.668 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.579 |
LIG_SH2_NCK_1 | 175 | 179 | PF00017 | 0.740 |
LIG_SH2_NCK_1 | 330 | 334 | PF00017 | 0.431 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 330 | 334 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 223 | 226 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 352 | 355 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.475 |
LIG_SH3_3 | 231 | 237 | PF00018 | 0.648 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.723 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.483 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.520 |
LIG_SUMO_SIM_anti_2 | 379 | 385 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 152 | 157 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 2 | 10 | PF11976 | 0.571 |
LIG_SUMO_SIM_par_1 | 331 | 337 | PF11976 | 0.479 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.632 |
LIG_TRAF2_1 | 403 | 406 | PF00917 | 0.629 |
LIG_TYR_ITSM | 115 | 122 | PF00017 | 0.539 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.426 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.725 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.759 |
MOD_CK1_1 | 293 | 299 | PF00069 | 0.721 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.546 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.428 |
MOD_CK2_1 | 340 | 346 | PF00069 | 0.538 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.622 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.544 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.717 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.522 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.734 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.807 |
MOD_GlcNHglycan | 292 | 295 | PF01048 | 0.693 |
MOD_GlcNHglycan | 341 | 345 | PF01048 | 0.589 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.567 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.453 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.685 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.742 |
MOD_GSK3_1 | 340 | 347 | PF00069 | 0.600 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.636 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.524 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.561 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.570 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.388 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.409 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.822 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.696 |
MOD_PKA_1 | 257 | 263 | PF00069 | 0.739 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.333 |
MOD_PKA_2 | 197 | 203 | PF00069 | 0.762 |
MOD_PKA_2 | 257 | 263 | PF00069 | 0.754 |
MOD_PKA_2 | 315 | 321 | PF00069 | 0.540 |
MOD_PKB_1 | 196 | 204 | PF00069 | 0.689 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.581 |
MOD_Plk_1 | 250 | 256 | PF00069 | 0.567 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.448 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.288 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.391 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.418 |
MOD_Plk_4 | 328 | 334 | PF00069 | 0.448 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.463 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.482 |
MOD_ProDKin_1 | 264 | 270 | PF00069 | 0.796 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.751 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.619 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.554 |
MOD_SUMO_for_1 | 353 | 356 | PF00179 | 0.544 |
MOD_SUMO_rev_2 | 405 | 413 | PF00179 | 0.735 |
TRG_DiLeu_BaEn_1 | 328 | 333 | PF01217 | 0.451 |
TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.537 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.529 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.513 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.621 |
TRG_ENDOCYTIC_2 | 330 | 333 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 188 | 190 | PF00400 | 0.668 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.744 |
TRG_ER_diArg_1 | 278 | 281 | PF00400 | 0.776 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 80 | 82 | PF00400 | 0.537 |
TRG_NLS_MonoExtN_4 | 104 | 111 | PF00514 | 0.733 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.429 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.710 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB46 | Leptomonas seymouri | 62% | 100% |
A0A1X0NNC7 | Trypanosomatidae | 32% | 100% |
A4H5M8 | Leishmania braziliensis | 78% | 96% |
A4HTW5 | Leishmania infantum | 97% | 97% |
E9AMQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 94% |
Q4QHX3 | Leishmania major | 93% | 100% |