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: A0A3Q8IAT9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 191 | 195 | PF00656 | 0.728 |
CLV_C14_Caspase3-7 | 222 | 226 | PF00656 | 0.735 |
CLV_C14_Caspase3-7 | 252 | 256 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 121 | 123 | PF00675 | 0.519 |
CLV_NRD_NRD_1 | 145 | 147 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.782 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.690 |
CLV_NRD_NRD_1 | 74 | 76 | PF00675 | 0.643 |
CLV_PCSK_FUR_1 | 143 | 147 | PF00082 | 0.604 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 187 | 189 | PF00082 | 0.769 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.719 |
CLV_PCSK_KEX2_1 | 74 | 76 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 177 | 179 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.719 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.612 |
CLV_Separin_Metazoa | 285 | 289 | PF03568 | 0.585 |
DEG_COP1_1 | 261 | 270 | PF00400 | 0.547 |
DEG_Nend_UBRbox_4 | 1 | 3 | PF02207 | 0.576 |
DEG_SPOP_SBC_1 | 53 | 57 | PF00917 | 0.673 |
DEG_SPOP_SBC_1 | 66 | 70 | PF00917 | 0.493 |
DOC_CYCLIN_RxL_1 | 139 | 152 | PF00134 | 0.585 |
DOC_CYCLIN_RxL_1 | 22 | 36 | PF00134 | 0.721 |
DOC_MAPK_gen_1 | 122 | 129 | PF00069 | 0.619 |
DOC_PP2B_LxvP_1 | 265 | 268 | PF13499 | 0.629 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.747 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 256 | 260 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 53 | 57 | PF00917 | 0.754 |
DOC_USP7_MATH_1 | 66 | 70 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.656 |
DOC_USP7_UBL2_3 | 59 | 63 | PF12436 | 0.730 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.749 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 18 | 25 | PF00244 | 0.652 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.761 |
LIG_14-3-3_CanoR_1 | 280 | 287 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 325 | 332 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 42 | 49 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 97 | 105 | PF00244 | 0.499 |
LIG_BRCT_BRCA1_1 | 45 | 49 | PF00533 | 0.690 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.564 |
LIG_FHA_2 | 250 | 256 | PF00498 | 0.674 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.702 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.566 |
LIG_IBAR_NPY_1 | 179 | 181 | PF08397 | 0.582 |
LIG_LIR_Gen_1 | 113 | 121 | PF02991 | 0.513 |
LIG_LIR_Gen_1 | 229 | 237 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 229 | 235 | PF02991 | 0.553 |
LIG_PDZ_Class_2 | 358 | 363 | PF00595 | 0.672 |
LIG_SH2_NCK_1 | 348 | 352 | PF00017 | 0.608 |
LIG_SH2_STAP1 | 232 | 236 | PF00017 | 0.580 |
LIG_SH2_STAP1 | 293 | 297 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 348 | 352 | PF00017 | 0.653 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.642 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.608 |
LIG_SUMO_SIM_par_1 | 263 | 269 | PF11976 | 0.549 |
LIG_TRAF2_1 | 135 | 138 | PF00917 | 0.593 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.555 |
LIG_UBA3_1 | 169 | 177 | PF00899 | 0.595 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.585 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.584 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.742 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.699 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.650 |
MOD_CK1_1 | 52 | 58 | PF00069 | 0.687 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.581 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.668 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.661 |
MOD_CK2_1 | 244 | 250 | PF00069 | 0.441 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.707 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.668 |
MOD_GlcNHglycan | 238 | 241 | PF01048 | 0.573 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.588 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.656 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.614 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.546 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.703 |
MOD_GSK3_1 | 236 | 243 | PF00069 | 0.641 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.640 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.721 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.453 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.661 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.666 |
MOD_LATS_1 | 26 | 32 | PF00433 | 0.618 |
MOD_NEK2_1 | 110 | 115 | PF00069 | 0.563 |
MOD_NEK2_1 | 206 | 211 | PF00069 | 0.564 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.601 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.694 |
MOD_NEK2_1 | 49 | 54 | PF00069 | 0.717 |
MOD_NEK2_2 | 268 | 273 | PF00069 | 0.636 |
MOD_NEK2_2 | 34 | 39 | PF00069 | 0.625 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.603 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.576 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.767 |
MOD_PKA_2 | 17 | 23 | PF00069 | 0.656 |
MOD_PKA_2 | 187 | 193 | PF00069 | 0.705 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.613 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.709 |
MOD_PKA_2 | 73 | 79 | PF00069 | 0.721 |
MOD_PKA_2 | 96 | 102 | PF00069 | 0.506 |
MOD_Plk_1 | 151 | 157 | PF00069 | 0.580 |
MOD_Plk_1 | 268 | 274 | PF00069 | 0.507 |
MOD_Plk_1 | 346 | 352 | PF00069 | 0.698 |
MOD_Plk_2-3 | 225 | 231 | PF00069 | 0.600 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.588 |
MOD_Plk_4 | 268 | 274 | PF00069 | 0.602 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.745 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.733 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.665 |
TRG_DiLeu_BaEn_2 | 230 | 236 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 143 | 148 | PF01217 | 0.635 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.542 |
TRG_DiLeu_BaLyEn_6 | 168 | 173 | PF01217 | 0.629 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 143 | 146 | PF00400 | 0.494 |
TRG_NLS_MonoExtC_3 | 58 | 63 | PF00514 | 0.749 |
TRG_NLS_MonoExtN_4 | 59 | 64 | PF00514 | 0.762 |
TRG_Pf-PMV_PEXEL_1 | 145 | 149 | PF00026 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 156 | 161 | PF00026 | 0.559 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4X3 | Leptomonas seymouri | 39% | 97% |
A0A1X0NTI1 | Trypanosomatidae | 32% | 100% |
A0A422N4X5 | Trypanosoma rangeli | 31% | 100% |
A4HCJ6 | Leishmania braziliensis | 74% | 100% |
A4I016 | Leishmania infantum | 100% | 100% |
C9ZQ77 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AVY9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QBJ0 | Leishmania major | 91% | 100% |
V5ARZ4 | Trypanosoma cruzi | 30% | 100% |