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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4H5M8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_MEL_PAP_1 | 144 | 150 | PF00089 | 0.360 |
CLV_NRD_NRD_1 | 106 | 108 | PF00675 | 0.605 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.537 |
CLV_NRD_NRD_1 | 188 | 190 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.351 |
CLV_PCSK_KEX2_1 | 108 | 110 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 253 | 255 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 108 | 110 | PF00082 | 0.700 |
CLV_PCSK_PC7_1 | 104 | 110 | PF00082 | 0.646 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 395 | 399 | PF00082 | 0.597 |
DEG_ODPH_VHL_1 | 111 | 122 | PF01847 | 0.440 |
DEG_SCF_FBW7_1 | 274 | 280 | PF00400 | 0.717 |
DEG_SPOP_SBC_1 | 277 | 281 | PF00917 | 0.520 |
DOC_CKS1_1 | 274 | 279 | PF01111 | 0.718 |
DOC_CYCLIN_RxL_1 | 133 | 143 | PF00134 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 88 | PF00134 | 0.274 |
DOC_MAPK_gen_1 | 55 | 63 | PF00069 | 0.358 |
DOC_MAPK_MEF2A_6 | 19 | 26 | PF00069 | 0.329 |
DOC_MAPK_MEF2A_6 | 56 | 65 | PF00069 | 0.375 |
DOC_PP1_RVXF_1 | 134 | 140 | PF00149 | 0.364 |
DOC_PP1_RVXF_1 | 79 | 85 | PF00149 | 0.282 |
DOC_PP2B_LxvP_1 | 63 | 66 | PF13499 | 0.359 |
DOC_PP4_FxxP_1 | 32 | 35 | PF00568 | 0.479 |
DOC_PP4_FxxP_1 | 84 | 87 | PF00568 | 0.458 |
DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.478 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 277 | 281 | PF00917 | 0.725 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.449 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.516 |
LIG_14-3-3_CanoR_1 | 205 | 213 | PF00244 | 0.703 |
LIG_14-3-3_CanoR_1 | 222 | 228 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 253 | 260 | PF00244 | 0.642 |
LIG_14-3-3_CanoR_1 | 262 | 270 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 272 | 277 | PF00244 | 0.488 |
LIG_14-3-3_CanoR_1 | 44 | 50 | PF00244 | 0.406 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.498 |
LIG_BRCT_BRCA1_1 | 175 | 179 | PF00533 | 0.629 |
LIG_EH_1 | 176 | 180 | PF12763 | 0.642 |
LIG_FHA_1 | 115 | 121 | PF00498 | 0.490 |
LIG_FHA_1 | 132 | 138 | PF00498 | 0.486 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.375 |
LIG_FHA_1 | 222 | 228 | PF00498 | 0.595 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.515 |
LIG_FHA_1 | 337 | 343 | PF00498 | 0.528 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.516 |
LIG_FHA_2 | 385 | 391 | PF00498 | 0.553 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.509 |
LIG_LIR_Apic_2 | 29 | 35 | PF02991 | 0.451 |
LIG_LIR_Apic_2 | 83 | 87 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.491 |
LIG_LIR_Gen_1 | 312 | 322 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 77 | 87 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.633 |
LIG_LIR_Nem_3 | 251 | 255 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 77 | 82 | PF02991 | 0.476 |
LIG_Pex14_2 | 84 | 88 | PF04695 | 0.466 |
LIG_REV1ctd_RIR_1 | 395 | 399 | PF16727 | 0.622 |
LIG_SH2_CRK | 314 | 318 | PF00017 | 0.353 |
LIG_SH2_GRB2like | 90 | 93 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 314 | 318 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 116 | 120 | PF00017 | 0.478 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.353 |
LIG_SH2_STAP1 | 46 | 50 | PF00017 | 0.351 |
LIG_SH2_STAT5 | 116 | 119 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.440 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.470 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.385 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.435 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.516 |
LIG_SUMO_SIM_anti_2 | 2 | 9 | PF11976 | 0.443 |
LIG_SUMO_SIM_anti_2 | 363 | 369 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 152 | 157 | PF11976 | 0.376 |
LIG_SUMO_SIM_par_1 | 315 | 321 | PF11976 | 0.439 |
LIG_TRAF2_1 | 229 | 232 | PF00917 | 0.629 |
LIG_TYR_ITSM | 115 | 122 | PF00017 | 0.494 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.459 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.621 |
MOD_CK1_1 | 279 | 285 | PF00069 | 0.674 |
MOD_CK1_1 | 329 | 335 | PF00069 | 0.523 |
MOD_CK2_1 | 294 | 300 | PF00069 | 0.614 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.530 |
MOD_CK2_1 | 384 | 390 | PF00069 | 0.558 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.499 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.676 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.479 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.718 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.546 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.527 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.418 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.611 |
MOD_GSK3_1 | 268 | 275 | PF00069 | 0.656 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.562 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.554 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.428 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.518 |
MOD_N-GLC_1 | 127 | 132 | PF02516 | 0.531 |
MOD_N-GLC_1 | 294 | 299 | PF02516 | 0.629 |
MOD_N-GLC_2 | 265 | 267 | PF02516 | 0.512 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.328 |
MOD_NEK2_1 | 50 | 55 | PF00069 | 0.328 |
MOD_PIKK_1 | 216 | 222 | PF00454 | 0.489 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.550 |
MOD_PKA_1 | 253 | 259 | PF00069 | 0.638 |
MOD_PKA_1 | 272 | 278 | PF00069 | 0.513 |
MOD_PKA_2 | 184 | 190 | PF00069 | 0.489 |
MOD_PKA_2 | 195 | 201 | PF00069 | 0.553 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.575 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.651 |
MOD_PKA_2 | 379 | 385 | PF00069 | 0.506 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.461 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.374 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.414 |
MOD_Plk_2-3 | 294 | 300 | PF00069 | 0.544 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.385 |
MOD_Plk_4 | 312 | 318 | PF00069 | 0.386 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.445 |
MOD_Plk_4 | 45 | 51 | PF00069 | 0.417 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.380 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.435 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.623 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.802 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.513 |
MOD_SUMO_for_1 | 337 | 340 | PF00179 | 0.500 |
MOD_SUMO_rev_2 | 390 | 397 | PF00179 | 0.609 |
TRG_DiLeu_BaEn_1 | 312 | 317 | PF01217 | 0.402 |
TRG_DiLeu_BaLyEn_6 | 16 | 21 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 338 | 343 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.557 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.355 |
TRG_ER_diArg_1 | 202 | 205 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.350 |
TRG_NLS_MonoExtN_4 | 104 | 111 | PF00514 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.349 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.584 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB46 | Leptomonas seymouri | 63% | 100% |
A0A1X0NNC7 | Trypanosomatidae | 33% | 100% |
A0A3Q8IAS3 | Leishmania donovani | 78% | 96% |
A4HTW5 | Leishmania infantum | 77% | 99% |
D0A9C9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AMQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 79% | 100% |
Q4QHX3 | Leishmania major | 78% | 100% |