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: A0A3S7WW52
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 359 | 363 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.474 |
CLV_NRD_NRD_1 | 141 | 143 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 151 | 153 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 191 | 193 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.506 |
CLV_PCSK_PC1ET2_1 | 375 | 377 | PF00082 | 0.521 |
CLV_PCSK_PC1ET2_1 | 99 | 101 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.505 |
DEG_SPOP_SBC_1 | 315 | 319 | PF00917 | 0.601 |
DOC_ANK_TNKS_1 | 141 | 148 | PF00023 | 0.418 |
DOC_CKS1_1 | 18 | 23 | PF01111 | 0.479 |
DOC_CYCLIN_RxL_1 | 363 | 373 | PF00134 | 0.518 |
DOC_CYCLIN_RxL_1 | 43 | 54 | PF00134 | 0.407 |
DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.330 |
DOC_MAPK_gen_1 | 76 | 86 | PF00069 | 0.371 |
DOC_MAPK_gen_1 | 99 | 106 | PF00069 | 0.463 |
DOC_MAPK_MEF2A_6 | 273 | 280 | PF00069 | 0.587 |
DOC_MAPK_MEF2A_6 | 57 | 66 | PF00069 | 0.330 |
DOC_MAPK_MEF2A_6 | 87 | 94 | PF00069 | 0.382 |
DOC_MAPK_MEF2A_6 | 99 | 106 | PF00069 | 0.347 |
DOC_PP1_RVXF_1 | 159 | 165 | PF00149 | 0.344 |
DOC_USP7_MATH_1 | 200 | 204 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.420 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.779 |
DOC_WW_Pin1_4 | 244 | 249 | PF00397 | 0.630 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.581 |
LIG_14-3-3_CanoR_1 | 151 | 160 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 179 | 186 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 191 | 197 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 255 | 261 | PF00244 | 0.499 |
LIG_APCC_ABBAyCdc20_2 | 69 | 75 | PF00400 | 0.509 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.657 |
LIG_BIR_III_4 | 266 | 270 | PF00653 | 0.573 |
LIG_BIR_III_4 | 29 | 33 | PF00653 | 0.443 |
LIG_CaM_IQ_9 | 335 | 351 | PF13499 | 0.454 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.526 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.380 |
LIG_FHA_1 | 18 | 24 | PF00498 | 0.382 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.461 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.493 |
LIG_FHA_2 | 122 | 128 | PF00498 | 0.327 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.592 |
LIG_FHA_2 | 35 | 41 | PF00498 | 0.473 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.604 |
LIG_LIR_Apic_2 | 224 | 230 | PF02991 | 0.646 |
LIG_LIR_Apic_2 | 282 | 287 | PF02991 | 0.608 |
LIG_LIR_Gen_1 | 89 | 98 | PF02991 | 0.337 |
LIG_LIR_Nem_3 | 174 | 180 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.338 |
LIG_NRBOX | 93 | 99 | PF00104 | 0.404 |
LIG_PCNA_PIPBox_1 | 49 | 58 | PF02747 | 0.453 |
LIG_PCNA_yPIPBox_3 | 46 | 56 | PF02747 | 0.457 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.687 |
LIG_SH2_CRK | 301 | 305 | PF00017 | 0.613 |
LIG_SH2_NCK_1 | 264 | 268 | PF00017 | 0.652 |
LIG_SH2_NCK_1 | 284 | 288 | PF00017 | 0.606 |
LIG_SH2_PTP2 | 91 | 94 | PF00017 | 0.348 |
LIG_SH2_STAP1 | 264 | 268 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 264 | 267 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 284 | 287 | PF00017 | 0.737 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 55 | 58 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 91 | 94 | PF00017 | 0.348 |
LIG_SH3_2 | 21 | 26 | PF14604 | 0.411 |
LIG_SH3_3 | 18 | 24 | PF00018 | 0.509 |
LIG_SH3_3 | 303 | 309 | PF00018 | 0.647 |
LIG_SH3_4 | 59 | 66 | PF00018 | 0.446 |
LIG_Sin3_3 | 377 | 384 | PF02671 | 0.449 |
LIG_SUMO_SIM_par_1 | 317 | 325 | PF11976 | 0.505 |
LIG_SUMO_SIM_par_1 | 366 | 373 | PF11976 | 0.513 |
LIG_TYR_ITIM | 175 | 180 | PF00017 | 0.352 |
LIG_UBA3_1 | 367 | 375 | PF00899 | 0.457 |
MOD_CDK_SPxxK_3 | 201 | 208 | PF00069 | 0.548 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.712 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.704 |
MOD_CK1_1 | 247 | 253 | PF00069 | 0.578 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.745 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.342 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.634 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.619 |
MOD_CK2_1 | 3 | 9 | PF00069 | 0.700 |
MOD_CK2_1 | 314 | 320 | PF00069 | 0.609 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.659 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.651 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.571 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.663 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.703 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.656 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.594 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.626 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.633 |
MOD_LATS_1 | 190 | 196 | PF00433 | 0.547 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.771 |
MOD_N-GLC_2 | 81 | 83 | PF02516 | 0.354 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.714 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.515 |
MOD_NEK2_2 | 74 | 79 | PF00069 | 0.390 |
MOD_PIKK_1 | 282 | 288 | PF00454 | 0.618 |
MOD_PKA_1 | 151 | 157 | PF00069 | 0.516 |
MOD_PKA_1 | 192 | 198 | PF00069 | 0.701 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.516 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.390 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.657 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.559 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.526 |
MOD_PKA_2 | 356 | 362 | PF00069 | 0.446 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.636 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.534 |
MOD_Plk_1 | 74 | 80 | PF00069 | 0.371 |
MOD_Plk_2-3 | 121 | 127 | PF00069 | 0.448 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.326 |
MOD_Plk_4 | 287 | 293 | PF00069 | 0.573 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.523 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.469 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.698 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.780 |
MOD_ProDKin_1 | 244 | 250 | PF00069 | 0.631 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.582 |
MOD_SUMO_for_1 | 58 | 61 | PF00179 | 0.444 |
MOD_SUMO_rev_2 | 121 | 131 | PF00179 | 0.452 |
TRG_DiLeu_BaEn_1 | 158 | 163 | PF01217 | 0.463 |
TRG_DiLeu_BaEn_1 | 61 | 66 | PF01217 | 0.452 |
TRG_DiLeu_LyEn_5 | 158 | 163 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 55 | 58 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 91 | 94 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 151 | 153 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 159 | 162 | PF00400 | 0.295 |
TRG_ER_diArg_1 | 191 | 193 | PF00400 | 0.511 |
TRG_NES_CRM1_1 | 158 | 171 | PF08389 | 0.472 |
TRG_NES_CRM1_1 | 40 | 54 | PF08389 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 130 | 134 | PF00026 | 0.467 |
TRG_Pf-PMV_PEXEL_1 | 329 | 334 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 336 | 340 | PF00026 | 0.541 |
TRG_Pf-PMV_PEXEL_1 | 366 | 371 | PF00026 | 0.517 |
TRG_Pf-PMV_PEXEL_1 | 76 | 80 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HYV9 | Leptomonas seymouri | 54% | 96% |
A0A1X0NWT1 | Trypanosomatidae | 37% | 100% |
A0A422N975 | Trypanosoma rangeli | 37% | 100% |
A4HYY8 | Leishmania infantum | 99% | 100% |
C9ZIJ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 97% |
E9AIK2 | Leishmania braziliensis | 79% | 96% |
E9AUT4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QCP9 | Leishmania major | 94% | 100% |