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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B293
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 139 | 143 | PF00656 | 0.282 |
CLV_C14_Caspase3-7 | 183 | 187 | PF00656 | 0.600 |
CLV_PCSK_SKI1_1 | 108 | 112 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.553 |
CLV_Separin_Metazoa | 78 | 82 | PF03568 | 0.424 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.553 |
DEG_SCF_FBW7_2 | 97 | 104 | PF00400 | 0.299 |
DOC_CDC14_PxL_1 | 196 | 204 | PF14671 | 0.676 |
DOC_CYCLIN_yCln2_LP_2 | 90 | 96 | PF00134 | 0.481 |
DOC_MAPK_DCC_7 | 145 | 155 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 7 | 15 | PF00069 | 0.476 |
DOC_MAPK_MEF2A_6 | 7 | 15 | PF00069 | 0.476 |
DOC_PP1_RVXF_1 | 234 | 241 | PF00149 | 0.495 |
DOC_PP2B_LxvP_1 | 42 | 45 | PF13499 | 0.460 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.546 |
DOC_USP7_MATH_1 | 3 | 7 | PF00917 | 0.368 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.612 |
DOC_WW_Pin1_4 | 167 | 172 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 89 | 94 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.470 |
LIG_14-3-3_CanoR_1 | 108 | 113 | PF00244 | 0.558 |
LIG_14-3-3_CanoR_1 | 208 | 218 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 65 | 70 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 7 | 12 | PF00244 | 0.482 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.508 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.521 |
LIG_FHA_1 | 89 | 95 | PF00498 | 0.431 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.452 |
LIG_FHA_2 | 137 | 143 | PF00498 | 0.537 |
LIG_FHA_2 | 66 | 72 | PF00498 | 0.536 |
LIG_FHA_2 | 93 | 99 | PF00498 | 0.454 |
LIG_LIR_Apic_2 | 163 | 169 | PF02991 | 0.560 |
LIG_LIR_Apic_2 | 17 | 23 | PF02991 | 0.568 |
LIG_LIR_Gen_1 | 132 | 143 | PF02991 | 0.539 |
LIG_LIR_Gen_1 | 172 | 181 | PF02991 | 0.589 |
LIG_LIR_Nem_3 | 132 | 138 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 172 | 177 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 197 | 202 | PF02991 | 0.597 |
LIG_LIR_Nem_3 | 63 | 67 | PF02991 | 0.509 |
LIG_LYPXL_yS_3 | 199 | 202 | PF13949 | 0.619 |
LIG_NRBOX | 230 | 236 | PF00104 | 0.513 |
LIG_PDZ_Class_2 | 245 | 250 | PF00595 | 0.585 |
LIG_SH2_CRK | 135 | 139 | PF00017 | 0.519 |
LIG_SH2_CRK | 20 | 24 | PF00017 | 0.575 |
LIG_SH2_CRK | 64 | 68 | PF00017 | 0.590 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.493 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.639 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.575 |
LIG_SH3_1 | 145 | 151 | PF00018 | 0.583 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.567 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.545 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.587 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.420 |
LIG_SUMO_SIM_anti_2 | 10 | 17 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 136 | 142 | PF11976 | 0.451 |
LIG_SUMO_SIM_anti_2 | 91 | 98 | PF11976 | 0.478 |
LIG_SUMO_SIM_par_1 | 10 | 17 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 136 | 142 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 151 | 157 | PF11976 | 0.631 |
LIG_SUMO_SIM_par_1 | 65 | 71 | PF11976 | 0.602 |
LIG_SUMO_SIM_par_1 | 91 | 98 | PF11976 | 0.483 |
LIG_TRAF2_1 | 102 | 105 | PF00917 | 0.353 |
LIG_TYR_ITIM | 133 | 138 | PF00017 | 0.333 |
LIG_TYR_ITIM | 62 | 67 | PF00017 | 0.580 |
LIG_UBA3_1 | 234 | 241 | PF00899 | 0.495 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.713 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.632 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.628 |
MOD_CK1_1 | 92 | 98 | PF00069 | 0.448 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.729 |
MOD_CK2_1 | 65 | 71 | PF00069 | 0.524 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.674 |
MOD_GSK3_1 | 122 | 129 | PF00069 | 0.588 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.510 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.622 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.546 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.531 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.475 |
MOD_N-GLC_1 | 60 | 65 | PF02516 | 0.512 |
MOD_N-GLC_2 | 227 | 229 | PF02516 | 0.611 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.523 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.648 |
MOD_PK_1 | 7 | 13 | PF00069 | 0.479 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.637 |
MOD_Plk_1 | 60 | 66 | PF00069 | 0.511 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.458 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.494 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.591 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.445 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.613 |
MOD_ProDKin_1 | 167 | 173 | PF00069 | 0.636 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.650 |
MOD_ProDKin_1 | 89 | 95 | PF00069 | 0.523 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.477 |
TRG_DiLeu_BaLyEn_6 | 20 | 25 | PF01217 | 0.554 |
TRG_ENDOCYTIC_2 | 135 | 138 | PF00928 | 0.524 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.676 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.566 |
TRG_ENDOCYTIC_2 | 64 | 67 | PF00928 | 0.541 |
TRG_ER_diArg_1 | 207 | 210 | PF00400 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJH1 | Leptomonas seymouri | 47% | 97% |
A0A3Q8IF52 | Leishmania donovani | 88% | 100% |
A0A3R7LVK8 | Trypanosoma rangeli | 25% | 100% |
A4HJT2 | Leishmania braziliensis | 70% | 100% |
A4I798 | Leishmania infantum | 88% | 100% |
Q4Q5W5 | Leishmania major | 87% | 100% |