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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HGB5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 292 | 296 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.549 |
CLV_NRD_NRD_1 | 231 | 233 | PF00675 | 0.676 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 388 | 390 | PF00675 | 0.693 |
CLV_PCSK_KEX2_1 | 138 | 140 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 388 | 390 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 138 | 140 | PF00082 | 0.472 |
CLV_PCSK_PC7_1 | 200 | 206 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 270 | 274 | PF00082 | 0.548 |
CLV_PCSK_SKI1_1 | 305 | 309 | PF00082 | 0.645 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.505 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.546 |
DOC_CYCLIN_RxL_1 | 101 | 111 | PF00134 | 0.647 |
DOC_MAPK_gen_1 | 101 | 108 | PF00069 | 0.627 |
DOC_MAPK_gen_1 | 215 | 224 | PF00069 | 0.567 |
DOC_MAPK_JIP1_4 | 102 | 108 | PF00069 | 0.695 |
DOC_PP2B_LxvP_1 | 377 | 380 | PF13499 | 0.654 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.552 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.497 |
DOC_USP7_UBL2_3 | 326 | 330 | PF12436 | 0.558 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.565 |
LIG_14-3-3_CanoR_1 | 104 | 109 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 159 | 168 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.594 |
LIG_14-3-3_CanoR_1 | 225 | 229 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 270 | 275 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 277 | 283 | PF00244 | 0.682 |
LIG_14-3-3_CanoR_1 | 317 | 323 | PF00244 | 0.524 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.546 |
LIG_FHA_1 | 271 | 277 | PF00498 | 0.560 |
LIG_FHA_1 | 372 | 378 | PF00498 | 0.707 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.643 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.530 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.670 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.535 |
LIG_FHA_2 | 290 | 296 | PF00498 | 0.613 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.617 |
LIG_LIR_Apic_2 | 345 | 349 | PF02991 | 0.641 |
LIG_LIR_Apic_2 | 370 | 376 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 162 | 173 | PF02991 | 0.544 |
LIG_LIR_Gen_1 | 193 | 203 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 53 | 64 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.614 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.543 |
LIG_Pex14_1 | 306 | 310 | PF04695 | 0.524 |
LIG_PTB_Apo_2 | 275 | 282 | PF02174 | 0.649 |
LIG_PTB_Apo_2 | 340 | 347 | PF02174 | 0.565 |
LIG_PTB_Phospho_1 | 275 | 281 | PF10480 | 0.648 |
LIG_PTB_Phospho_1 | 340 | 346 | PF10480 | 0.563 |
LIG_SH2_CRK | 56 | 60 | PF00017 | 0.582 |
LIG_SH2_GRB2like | 56 | 59 | PF00017 | 0.591 |
LIG_SH2_NCK_1 | 195 | 199 | PF00017 | 0.567 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.594 |
LIG_SH2_NCK_1 | 310 | 314 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 359 | 363 | PF00017 | 0.634 |
LIG_SH2_NCK_1 | 56 | 60 | PF00017 | 0.538 |
LIG_SH2_SRC | 259 | 262 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 310 | 314 | PF00017 | 0.433 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.644 |
LIG_SH2_STAT3 | 30 | 33 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 369 | 372 | PF00017 | 0.536 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.546 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.585 |
LIG_SH3_3 | 38 | 44 | PF00018 | 0.545 |
LIG_TYR_ITIM | 54 | 59 | PF00017 | 0.540 |
LIG_WW_3 | 16 | 20 | PF00397 | 0.585 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.672 |
MOD_CK2_1 | 223 | 229 | PF00069 | 0.635 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.467 |
MOD_CK2_1 | 249 | 255 | PF00069 | 0.586 |
MOD_CK2_1 | 357 | 363 | PF00069 | 0.623 |
MOD_GlcNHglycan | 172 | 176 | PF01048 | 0.546 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.523 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.579 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.546 |
MOD_GlcNHglycan | 85 | 89 | PF01048 | 0.512 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.485 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.559 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.572 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.466 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.592 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.763 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.684 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.571 |
MOD_N-GLC_1 | 270 | 275 | PF02516 | 0.543 |
MOD_N-GLC_1 | 75 | 80 | PF02516 | 0.607 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.568 |
MOD_NEK2_1 | 223 | 228 | PF00069 | 0.498 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.627 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.718 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.560 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.566 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.616 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.560 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.555 |
MOD_PIKK_1 | 289 | 295 | PF00454 | 0.486 |
MOD_PIKK_1 | 75 | 81 | PF00454 | 0.589 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.522 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.600 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.680 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.528 |
MOD_PKB_1 | 204 | 212 | PF00069 | 0.672 |
MOD_Plk_1 | 206 | 212 | PF00069 | 0.668 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.603 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.636 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.559 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.612 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.544 |
MOD_Plk_4 | 368 | 374 | PF00069 | 0.691 |
MOD_Plk_4 | 379 | 385 | PF00069 | 0.700 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.648 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.562 |
MOD_SUMO_for_1 | 137 | 140 | PF00179 | 0.518 |
MOD_SUMO_rev_2 | 174 | 184 | PF00179 | 0.436 |
TRG_AP2beta_CARGO_1 | 207 | 217 | PF09066 | 0.574 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.563 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 369 | 372 | PF00928 | 0.582 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 203 | 206 | PF00400 | 0.551 |
TRG_NLS_MonoCore_2 | 100 | 105 | PF00514 | 0.686 |
TRG_Pf-PMV_PEXEL_1 | 104 | 109 | PF00026 | 0.691 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDT5 | Leptomonas seymouri | 65% | 91% |
A0A0S4JAK0 | Bodo saltans | 29% | 100% |
A0A1X0NYG9 | Trypanosomatidae | 50% | 92% |
A0A3Q8IEQ6 | Leishmania donovani | 84% | 99% |
A0A3R7KQJ1 | Trypanosoma rangeli | 49% | 91% |
A4I3E9 | Leishmania infantum | 85% | 99% |
D0A7Z8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 94% |
E9AZN6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 99% |
Q4Q8J5 | Leishmania major | 85% | 100% |
V5BQC0 | Trypanosoma cruzi | 48% | 90% |