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: E9AX92
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.601 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 187 | 189 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 39 | 41 | PF00675 | 0.586 |
CLV_PCSK_FUR_1 | 37 | 41 | PF00082 | 0.598 |
CLV_PCSK_KEX2_1 | 154 | 156 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 39 | 41 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 186 | 188 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 154 | 158 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.480 |
CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.511 |
CLV_Separin_Metazoa | 34 | 38 | PF03568 | 0.587 |
DOC_CYCLIN_RxL_1 | 195 | 202 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 133 | 141 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 51 | 58 | PF00069 | 0.531 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.598 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.267 |
DOC_USP7_MATH_1 | 41 | 45 | PF00917 | 0.649 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.534 |
DOC_WW_Pin1_4 | 108 | 113 | PF00397 | 0.543 |
DOC_WW_Pin1_4 | 205 | 210 | PF00397 | 0.686 |
LIG_14-3-3_CanoR_1 | 166 | 173 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 203 | 209 | PF00244 | 0.589 |
LIG_14-3-3_CanoR_1 | 40 | 46 | PF00244 | 0.590 |
LIG_Actin_WH2_2 | 24 | 41 | PF00022 | 0.558 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.523 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.612 |
LIG_Clathr_ClatBox_1 | 9 | 13 | PF01394 | 0.482 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.536 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.277 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.500 |
LIG_FHA_1 | 65 | 71 | PF00498 | 0.638 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.424 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.578 |
LIG_LIR_Gen_1 | 179 | 189 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 83 | 93 | PF02991 | 0.488 |
LIG_LIR_LC3C_4 | 137 | 141 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.538 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.490 |
LIG_NRBOX | 87 | 93 | PF00104 | 0.423 |
LIG_RPA_C_Fungi | 35 | 47 | PF08784 | 0.541 |
LIG_SH2_SRC | 189 | 192 | PF00017 | 0.517 |
LIG_SH2_STAP1 | 144 | 148 | PF00017 | 0.426 |
LIG_SH2_STAP1 | 189 | 193 | PF00017 | 0.515 |
LIG_SH3_3 | 208 | 214 | PF00018 | 0.689 |
LIG_SUMO_SIM_anti_2 | 27 | 34 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 6 | 13 | PF11976 | 0.542 |
LIG_TRAF2_1 | 60 | 63 | PF00917 | 0.716 |
MOD_CDK_SPK_2 | 108 | 113 | PF00069 | 0.540 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.479 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.457 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.565 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.602 |
MOD_GlcNHglycan | 170 | 173 | PF01048 | 0.417 |
MOD_GlcNHglycan | 62 | 67 | PF01048 | 0.752 |
MOD_GlcNHglycan | 73 | 78 | PF01048 | 0.645 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.411 |
MOD_GSK3_1 | 205 | 212 | PF00069 | 0.494 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.535 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.594 |
MOD_N-GLC_1 | 41 | 46 | PF02516 | 0.560 |
MOD_NEK2_1 | 173 | 178 | PF00069 | 0.425 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.537 |
MOD_PIKK_1 | 192 | 198 | PF00454 | 0.406 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.608 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.598 |
MOD_Plk_1 | 117 | 123 | PF00069 | 0.559 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.651 |
MOD_Plk_4 | 173 | 179 | PF00069 | 0.425 |
MOD_Plk_4 | 4 | 10 | PF00069 | 0.591 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.640 |
MOD_ProDKin_1 | 108 | 114 | PF00069 | 0.545 |
MOD_ProDKin_1 | 205 | 211 | PF00069 | 0.690 |
MOD_SUMO_rev_2 | 175 | 183 | PF00179 | 0.592 |
TRG_DiLeu_BaEn_4 | 130 | 136 | PF01217 | 0.585 |
TRG_ENDOCYTIC_2 | 182 | 185 | PF00928 | 0.587 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.630 |
TRG_ER_diArg_1 | 187 | 189 | PF00400 | 0.617 |
TRG_ER_diArg_1 | 36 | 39 | PF00400 | 0.559 |
TRG_ER_diArg_1 | 98 | 101 | PF00400 | 0.554 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.621 |
TRG_Pf-PMV_PEXEL_1 | 127 | 131 | PF00026 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 133 | 137 | PF00026 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 155 | 159 | PF00026 | 0.579 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM96 | Leptomonas seymouri | 45% | 96% |
A0A1X0P602 | Trypanosomatidae | 35% | 69% |
A0A3Q8ID59 | Leishmania donovani | 88% | 100% |
A0A422NF37 | Trypanosoma rangeli | 32% | 69% |
A4HDW3 | Leishmania braziliensis | 75% | 100% |
A4I158 | Leishmania infantum | 89% | 100% |
D0A5E3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 68% |
Q4QA80 | Leishmania major | 85% | 100% |
V5BXK9 | Trypanosoma cruzi | 32% | 69% |