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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HJU7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 163 | 167 | PF00656 | 0.475 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.389 |
CLV_PCSK_FUR_1 | 52 | 56 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 54 | 56 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.414 |
CLV_PCSK_PC1ET2_1 | 121 | 123 | PF00082 | 0.687 |
CLV_PCSK_PC1ET2_1 | 78 | 80 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 84 | 88 | PF00082 | 0.372 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.552 |
DEG_SPOP_SBC_1 | 12 | 16 | PF00917 | 0.539 |
DOC_CYCLIN_RxL_1 | 78 | 90 | PF00134 | 0.440 |
DOC_CYCLIN_yCln2_LP_2 | 281 | 287 | PF00134 | 0.448 |
DOC_MAPK_gen_1 | 121 | 131 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 141 | 150 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 144 | 152 | PF00069 | 0.406 |
DOC_MAPK_RevD_3 | 65 | 79 | PF00069 | 0.301 |
DOC_PP1_RVXF_1 | 264 | 270 | PF00149 | 0.415 |
DOC_PP1_RVXF_1 | 288 | 294 | PF00149 | 0.456 |
DOC_PP1_RVXF_1 | 296 | 303 | PF00149 | 0.467 |
DOC_PP2B_LxvP_1 | 248 | 251 | PF13499 | 0.477 |
DOC_SPAK_OSR1_1 | 184 | 188 | PF12202 | 0.541 |
DOC_SPAK_OSR1_1 | 79 | 83 | PF12202 | 0.398 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 322 | 326 | PF00917 | 0.372 |
DOC_USP7_MATH_1 | 328 | 332 | PF00917 | 0.414 |
LIG_14-3-3_CanoR_1 | 184 | 194 | PF00244 | 0.564 |
LIG_14-3-3_CanoR_1 | 195 | 199 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 21 | 31 | PF00244 | 0.676 |
LIG_BRCT_BRCA1_1 | 212 | 216 | PF00533 | 0.435 |
LIG_BRCT_BRCA1_1 | 92 | 96 | PF00533 | 0.348 |
LIG_FHA_1 | 15 | 21 | PF00498 | 0.619 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.359 |
LIG_MLH1_MIPbox_1 | 212 | 216 | PF16413 | 0.435 |
LIG_NRBOX | 148 | 154 | PF00104 | 0.346 |
LIG_PCNA_yPIPBox_3 | 141 | 149 | PF02747 | 0.373 |
LIG_Pex14_1 | 181 | 185 | PF04695 | 0.377 |
LIG_PTB_Apo_2 | 302 | 309 | PF02174 | 0.497 |
LIG_PTB_Phospho_1 | 302 | 308 | PF10480 | 0.495 |
LIG_SH2_GRB2like | 261 | 264 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 270 | 273 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.509 |
LIG_SH2_STAT5 | 74 | 77 | PF00017 | 0.297 |
LIG_SH3_3 | 62 | 68 | PF00018 | 0.375 |
LIG_SUMO_SIM_anti_2 | 331 | 338 | PF11976 | 0.525 |
LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.520 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.478 |
LIG_TRAF2_1 | 3 | 6 | PF00917 | 0.587 |
MOD_CK1_1 | 105 | 111 | PF00069 | 0.555 |
MOD_CK1_1 | 15 | 21 | PF00069 | 0.578 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.320 |
MOD_CK1_1 | 331 | 337 | PF00069 | 0.536 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.429 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.461 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.576 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.550 |
MOD_Cter_Amidation | 76 | 79 | PF01082 | 0.478 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.541 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.445 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.680 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.543 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.660 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.587 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.323 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.567 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.526 |
MOD_N-GLC_1 | 12 | 17 | PF02516 | 0.543 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.432 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.614 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.583 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.377 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.456 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.746 |
MOD_NEK2_1 | 237 | 242 | PF00069 | 0.490 |
MOD_NEK2_1 | 271 | 276 | PF00069 | 0.437 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.580 |
MOD_NEK2_1 | 80 | 85 | PF00069 | 0.466 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.298 |
MOD_NEK2_2 | 164 | 169 | PF00069 | 0.452 |
MOD_NEK2_2 | 265 | 270 | PF00069 | 0.483 |
MOD_PIKK_1 | 225 | 231 | PF00454 | 0.440 |
MOD_PIKK_1 | 328 | 334 | PF00454 | 0.502 |
MOD_PIKK_1 | 97 | 103 | PF00454 | 0.296 |
MOD_PKA_2 | 194 | 200 | PF00069 | 0.399 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.418 |
MOD_PKA_2 | 40 | 46 | PF00069 | 0.569 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.474 |
MOD_Plk_2-3 | 42 | 48 | PF00069 | 0.613 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.699 |
MOD_Plk_4 | 23 | 29 | PF00069 | 0.681 |
MOD_Plk_4 | 265 | 271 | PF00069 | 0.481 |
MOD_Plk_4 | 331 | 337 | PF00069 | 0.516 |
MOD_Plk_4 | 90 | 96 | PF00069 | 0.350 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.562 |
TRG_ER_diArg_1 | 52 | 55 | PF00400 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 84 | 88 | PF00026 | 0.484 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3N2 | Leptomonas seymouri | 59% | 97% |
A0A1X0NIJ4 | Trypanosomatidae | 38% | 100% |
A0A3R7K9T3 | Trypanosoma rangeli | 36% | 100% |
A0A3S7X510 | Leishmania donovani | 81% | 94% |
A4HJV2 | Leishmania braziliensis | 100% | 100% |
A4I7B4 | Leishmania infantum | 80% | 94% |
C9ZWJ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9B2A7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q5U9 | Leishmania major | 79% | 100% |
V5B9A8 | Trypanosoma cruzi | 37% | 100% |