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: A4HRK9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.649 |
CLV_C14_Caspase3-7 | 215 | 219 | PF00656 | 0.676 |
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 330 | 334 | PF00656 | 0.584 |
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 383 | 387 | PF00656 | 0.681 |
CLV_C14_Caspase3-7 | 67 | 71 | PF00656 | 0.643 |
CLV_NRD_NRD_1 | 270 | 272 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.675 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 293 | 295 | PF00082 | 0.378 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.636 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.388 |
CLV_PCSK_PC1ET2_1 | 293 | 295 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.609 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 24 | 28 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 297 | 301 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.450 |
CLV_Separin_Metazoa | 277 | 281 | PF03568 | 0.566 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.691 |
DEG_SPOP_SBC_1 | 225 | 229 | PF00917 | 0.696 |
DEG_SPOP_SBC_1 | 97 | 101 | PF00917 | 0.738 |
DOC_MAPK_gen_1 | 293 | 300 | PF00069 | 0.394 |
DOC_MAPK_RevD_3 | 257 | 272 | PF00069 | 0.380 |
DOC_PP1_RVXF_1 | 295 | 301 | PF00149 | 0.508 |
DOC_PP2B_LxvP_1 | 155 | 158 | PF13499 | 0.461 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 251 | 255 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.698 |
DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.634 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.535 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 249 | 254 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.724 |
LIG_14-3-3_CanoR_1 | 127 | 136 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 363 | 369 | PF00244 | 0.723 |
LIG_Actin_WH2_2 | 303 | 319 | PF00022 | 0.523 |
LIG_BIR_III_2 | 218 | 222 | PF00653 | 0.705 |
LIG_BIR_III_4 | 333 | 337 | PF00653 | 0.595 |
LIG_Clathr_ClatBox_1 | 172 | 176 | PF01394 | 0.411 |
LIG_FHA_1 | 13 | 19 | PF00498 | 0.484 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.523 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.444 |
LIG_FHA_1 | 91 | 97 | PF00498 | 0.684 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.681 |
LIG_FHA_2 | 208 | 214 | PF00498 | 0.628 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.672 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.721 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.683 |
LIG_GBD_Chelix_1 | 147 | 155 | PF00786 | 0.406 |
LIG_LIR_Apic_2 | 388 | 393 | PF02991 | 0.786 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 252 | 262 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 275 | 283 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 135 | 139 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.673 |
LIG_LIR_Nem_3 | 252 | 258 | PF02991 | 0.446 |
LIG_NRBOX | 203 | 209 | PF00104 | 0.579 |
LIG_Pex14_1 | 136 | 140 | PF04695 | 0.530 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.473 |
LIG_SH2_CRK | 144 | 148 | PF00017 | 0.468 |
LIG_SH2_CRK | 169 | 173 | PF00017 | 0.372 |
LIG_SH2_CRK | 255 | 259 | PF00017 | 0.442 |
LIG_SH2_CRK | 270 | 274 | PF00017 | 0.331 |
LIG_SH2_GRB2like | 57 | 60 | PF00017 | 0.545 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.468 |
LIG_SH2_STAP1 | 255 | 259 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 140 | 143 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.468 |
LIG_SH3_3 | 218 | 224 | PF00018 | 0.752 |
LIG_SUMO_SIM_anti_2 | 152 | 158 | PF11976 | 0.501 |
LIG_SUMO_SIM_par_1 | 171 | 176 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 287 | 292 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 83 | 91 | PF11976 | 0.439 |
LIG_TYR_ITIM | 236 | 241 | PF00017 | 0.462 |
LIG_TYR_ITIM | 268 | 273 | PF00017 | 0.457 |
LIG_UBA3_1 | 288 | 293 | PF00899 | 0.540 |
LIG_UBA3_1 | 77 | 84 | PF00899 | 0.708 |
MOD_CDK_SPxxK_3 | 198 | 205 | PF00069 | 0.552 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.738 |
MOD_CK1_1 | 367 | 373 | PF00069 | 0.713 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.682 |
MOD_CK2_1 | 147 | 153 | PF00069 | 0.478 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.652 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.727 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.711 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.555 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.478 |
MOD_GlcNHglycan | 333 | 337 | PF01048 | 0.653 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.690 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.679 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.586 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.539 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.606 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.511 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.671 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.672 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.564 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.400 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.607 |
MOD_NEK2_1 | 96 | 101 | PF00069 | 0.701 |
MOD_NEK2_2 | 43 | 48 | PF00069 | 0.477 |
MOD_PK_1 | 287 | 293 | PF00069 | 0.417 |
MOD_PKA_1 | 363 | 369 | PF00069 | 0.636 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.643 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.726 |
MOD_PKB_1 | 127 | 135 | PF00069 | 0.528 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.651 |
MOD_Plk_2-3 | 213 | 219 | PF00069 | 0.501 |
MOD_Plk_2-3 | 34 | 40 | PF00069 | 0.549 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.554 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.416 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.603 |
MOD_Plk_4 | 385 | 391 | PF00069 | 0.759 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.529 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.502 |
MOD_ProDKin_1 | 249 | 255 | PF00069 | 0.509 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.728 |
MOD_SUMO_rev_2 | 367 | 377 | PF00179 | 0.722 |
TRG_ENDOCYTIC_2 | 144 | 147 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 169 | 172 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.318 |
TRG_ENDOCYTIC_2 | 270 | 273 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.506 |
TRG_ER_diArg_1 | 126 | 129 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 285 | 287 | PF00400 | 0.475 |
TRG_NES_CRM1_1 | 231 | 243 | PF08389 | 0.548 |
TRG_NES_CRM1_1 | 50 | 62 | PF08389 | 0.578 |
TRG_Pf-PMV_PEXEL_1 | 191 | 195 | PF00026 | 0.585 |
TRG_Pf-PMV_PEXEL_1 | 271 | 275 | PF00026 | 0.446 |
TRG_Pf-PMV_PEXEL_1 | 287 | 292 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 314 | 318 | PF00026 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAV1 | Leptomonas seymouri | 61% | 95% |
A0A0S4JHJ5 | Bodo saltans | 30% | 100% |
A0A1X0NJT7 | Trypanosomatidae | 34% | 100% |
A0A3S5H4X8 | Leishmania donovani | 100% | 100% |
A0A3S5IQM7 | Trypanosoma rangeli | 36% | 98% |
A4H3A3 | Leishmania braziliensis | 83% | 100% |
E9AC81 | Leishmania major | 94% | 100% |
E9AJH3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BAQ0 | Trypanosoma cruzi | 36% | 100% |