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: 3 |
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: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 7 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A4HFP7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 196 | 200 | PF00656 | 0.462 |
CLV_C14_Caspase3-7 | 310 | 314 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 52 | 56 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.494 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 374 | 376 | PF00675 | 0.420 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.423 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.529 |
CLV_PCSK_KEX2_1 | 374 | 376 | PF00082 | 0.476 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.565 |
CLV_PCSK_PC7_1 | 230 | 236 | PF00082 | 0.547 |
CLV_PCSK_PC7_1 | 370 | 376 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 11 | 15 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 111 | 115 | PF00082 | 0.487 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.479 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.481 |
CLV_Separin_Metazoa | 106 | 110 | PF03568 | 0.561 |
CLV_Separin_Metazoa | 186 | 190 | PF03568 | 0.541 |
DEG_APCC_DBOX_1 | 259 | 267 | PF00400 | 0.479 |
DEG_APCC_DBOX_1 | 373 | 381 | PF00400 | 0.527 |
DEG_APCC_KENBOX_2 | 273 | 277 | PF00400 | 0.314 |
DOC_CYCLIN_RxL_1 | 182 | 192 | PF00134 | 0.365 |
DOC_CYCLIN_RxL_1 | 8 | 18 | PF00134 | 0.339 |
DOC_MAPK_gen_1 | 171 | 180 | PF00069 | 0.546 |
DOC_MAPK_gen_1 | 31 | 39 | PF00069 | 0.503 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.315 |
DOC_MAPK_NFAT4_5 | 289 | 297 | PF00069 | 0.317 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.521 |
DOC_USP7_UBL2_3 | 237 | 241 | PF12436 | 0.489 |
DOC_USP7_UBL2_3 | 408 | 412 | PF12436 | 0.509 |
LIG_14-3-3_CanoR_1 | 230 | 238 | PF00244 | 0.350 |
LIG_14-3-3_CanoR_1 | 243 | 252 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 407 | 415 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 71 | 80 | PF00244 | 0.508 |
LIG_APCC_ABBA_1 | 290 | 295 | PF00400 | 0.315 |
LIG_APCC_ABBAyCdc20_2 | 289 | 295 | PF00400 | 0.314 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.480 |
LIG_BIR_III_4 | 199 | 203 | PF00653 | 0.341 |
LIG_Clathr_ClatBox_1 | 13 | 17 | PF01394 | 0.530 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.415 |
LIG_FHA_1 | 164 | 170 | PF00498 | 0.492 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.462 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.476 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.624 |
LIG_FHA_2 | 245 | 251 | PF00498 | 0.579 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.516 |
LIG_LIR_Gen_1 | 360 | 369 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 360 | 364 | PF02991 | 0.315 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.354 |
LIG_PCNA_PIPBox_1 | 399 | 408 | PF02747 | 0.330 |
LIG_PCNA_yPIPBox_3 | 393 | 406 | PF02747 | 0.317 |
LIG_Rb_pABgroove_1 | 322 | 330 | PF01858 | 0.514 |
LIG_SH2_GRB2like | 376 | 379 | PF00017 | 0.358 |
LIG_SH2_NCK_1 | 361 | 365 | PF00017 | 0.527 |
LIG_SH2_STAP1 | 328 | 332 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 132 | 135 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.464 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.295 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.424 |
LIG_SUMO_SIM_par_1 | 5 | 10 | PF11976 | 0.544 |
LIG_TRAF2_1 | 128 | 131 | PF00917 | 0.490 |
LIG_UBA3_1 | 13 | 21 | PF00899 | 0.411 |
LIG_UBA3_1 | 6 | 11 | PF00899 | 0.438 |
MOD_CK1_1 | 100 | 106 | PF00069 | 0.637 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.502 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.450 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.559 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.679 |
MOD_CK1_1 | 62 | 68 | PF00069 | 0.594 |
MOD_CK1_1 | 72 | 78 | PF00069 | 0.555 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.453 |
MOD_CK2_1 | 131 | 137 | PF00069 | 0.475 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.595 |
MOD_CK2_1 | 2 | 8 | PF00069 | 0.575 |
MOD_CK2_1 | 22 | 28 | PF00069 | 0.431 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.485 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.667 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.414 |
MOD_GlcNHglycan | 352 | 355 | PF01048 | 0.598 |
MOD_GlcNHglycan | 387 | 391 | PF01048 | 0.308 |
MOD_GlcNHglycan | 408 | 411 | PF01048 | 0.597 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.655 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.548 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.505 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.624 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.616 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.361 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.428 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.446 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.429 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.567 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.395 |
MOD_PIKK_1 | 40 | 46 | PF00454 | 0.450 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.669 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.550 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.396 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.481 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.571 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.413 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.587 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.667 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.714 |
MOD_PKB_1 | 64 | 72 | PF00069 | 0.613 |
MOD_Plk_1 | 239 | 245 | PF00069 | 0.523 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.481 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.530 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.388 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.602 |
MOD_Plk_4 | 327 | 333 | PF00069 | 0.497 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.603 |
MOD_SUMO_for_1 | 119 | 122 | PF00179 | 0.605 |
MOD_SUMO_rev_2 | 209 | 216 | PF00179 | 0.464 |
MOD_SUMO_rev_2 | 72 | 81 | PF00179 | 0.584 |
TRG_ENDOCYTIC_2 | 282 | 285 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.527 |
TRG_ER_diArg_1 | 170 | 173 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 259 | 261 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 374 | 376 | PF00400 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 375 | 379 | PF00026 | 0.528 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHJ5 | Leptomonas seymouri | 59% | 100% |
A0A1X0P450 | Trypanosomatidae | 29% | 100% |
A0A3R7M124 | Trypanosoma rangeli | 26% | 100% |
A0A3S7X0N0 | Leishmania donovani | 72% | 100% |
A4I2S2 | Leishmania infantum | 72% | 100% |
D0A5Y0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9ADA0 | Leishmania major | 70% | 100% |
E9AZ25 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
V5AT73 | Trypanosoma cruzi | 26% | 100% |