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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3S5H4X8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.605 |
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.619 |
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.627 |
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.497 |
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.458 |
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.593 |
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.546 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.638 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.337 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.322 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.337 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.359 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.435 |
CLV_Separin_Metazoa | 277 | 281 | PF03568 | 0.436 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.651 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.657 |
DEG_SPOP_SBC_1 | 97 | 101 | PF00917 | 0.706 |
DOC_MAPK_gen_1 | 293 | 300 | PF00069 | 0.337 |
DOC_MAPK_RevD_3 | 257 | 272 | PF00069 | 0.323 |
DOC_PP1_RVXF_1 | 295 | 301 | PF00149 | 0.474 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.396 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.652 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.621 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.686 |
LIG_14-3-3_CanoR_1 | 127 | 136 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.694 |
LIG_Actin_WH2_2 | 303 | 319 | PF00022 | 0.533 |
LIG_BIR_III_2 | 218 | 222 | PF00653 | 0.648 |
LIG_BIR_III_4 | 333 | 337 | PF00653 | 0.511 |
LIG_Clathr_ClatBox_1 | 172 | 176 | PF01394 | 0.351 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.435 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.472 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.476 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.681 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.647 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.583 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.650 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.627 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.660 |
LIG_GBD_Chelix_1 | 147 | 155 | PF00786 | 0.340 |
LIG_LIR_Apic_2 | 388 | 393 | PF02991 | 0.662 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.620 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.520 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.549 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.410 |
LIG_NRBOX | 203 | 209 | PF00104 | 0.537 |
LIG_Pex14_1 | 136 | 140 | PF04695 | 0.507 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.431 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.398 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.322 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.407 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.284 |
LIG_SH2_GRB2like | 57 | 60 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.506 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.612 |
LIG_SUMO_SIM_anti_2 | 152 | 158 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 171 | 176 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 287 | 292 | PF11976 | 0.353 |
LIG_TYR_ITIM | 236 | 241 | PF00017 | 0.393 |
LIG_TYR_ITIM | 268 | 273 | PF00017 | 0.402 |
LIG_UBA3_1 | 288 | 293 | PF00899 | 0.415 |
LIG_UBA3_1 | 77 | 84 | PF00899 | 0.581 |
MOD_CDK_SPxxK_3 | 198 | 205 | PF00069 | 0.504 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.713 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.662 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.629 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.404 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.612 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.679 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.670 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.563 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.449 |
MOD_GlcNHglycan | 333 | 337 | PF01048 | 0.603 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.631 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.642 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.553 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.480 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.533 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.534 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.622 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.616 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.494 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.336 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.568 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.651 |
MOD_NEK2_2 | 43 | 48 | PF00069 | 0.492 |
MOD_PK_1 | 287 | 293 | PF00069 | 0.358 |
MOD_PKA_1 | 363 | 369 | PF00069 | 0.560 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.528 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.699 |
MOD_PKB_1 | 127 | 135 | PF00069 | 0.578 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.623 |
MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.440 |
MOD_Plk_2-3 | 34 | 40 | PF00069 | 0.573 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.502 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.357 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.648 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.733 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.475 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.454 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.467 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.689 |
MOD_SUMO_rev_2 | 367 | 377 | PF00179 | 0.628 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.557 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.419 |
TRG_NES_CRM1_1 | 231 | 243 | PF08389 | 0.452 |
TRG_NES_CRM1_1 | 50 | 62 | PF08389 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.572 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.561 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAV1 | Leptomonas seymouri | 61% | 95% |
A0A0S4JHJ5 | Bodo saltans | 29% | 100% |
A0A1X0NJT7 | Trypanosomatidae | 34% | 100% |
A0A3S5IQM7 | Trypanosoma rangeli | 35% | 98% |
A4H3A3 | Leishmania braziliensis | 83% | 100% |
A4HRK9 | Leishmania infantum | 100% | 100% |
E9AC81 | Leishmania major | 95% | 100% |
E9AJH3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BAQ0 | Trypanosoma cruzi | 36% | 100% |