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: 3 |
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: 16 |
NetGPI | no | yes: 0, no: 16 |
Related structures:
AlphaFold database: A4HJM8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 146 | 150 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 160 | 164 | PF00656 | 0.632 |
CLV_C14_Caspase3-7 | 210 | 214 | PF00656 | 0.529 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.573 |
CLV_PCSK_PC1ET2_1 | 181 | 183 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 183 | 187 | PF00082 | 0.656 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.613 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.469 |
DOC_CYCLIN_RxL_1 | 178 | 188 | PF00134 | 0.539 |
DOC_MAPK_gen_1 | 74 | 81 | PF00069 | 0.633 |
DOC_MAPK_MEF2A_6 | 74 | 81 | PF00069 | 0.633 |
DOC_MAPK_NFAT4_5 | 74 | 82 | PF00069 | 0.633 |
DOC_PP1_RVXF_1 | 1 | 8 | PF00149 | 0.528 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 143 | 147 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.568 |
LIG_14-3-3_CanoR_1 | 158 | 165 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 38 | 47 | PF00244 | 0.629 |
LIG_APCC_ABBAyCdc20_2 | 182 | 188 | PF00400 | 0.540 |
LIG_deltaCOP1_diTrp_1 | 153 | 159 | PF00928 | 0.533 |
LIG_eIF4E_1 | 165 | 171 | PF01652 | 0.439 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.593 |
LIG_FHA_1 | 203 | 209 | PF00498 | 0.447 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.564 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.523 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.408 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.635 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.555 |
LIG_GBD_Chelix_1 | 167 | 175 | PF00786 | 0.474 |
LIG_NRBOX | 166 | 172 | PF00104 | 0.389 |
LIG_PDZ_Class_3 | 216 | 221 | PF00595 | 0.665 |
LIG_Pex14_1 | 155 | 159 | PF04695 | 0.571 |
LIG_SH2_STAP1 | 165 | 169 | PF00017 | 0.570 |
LIG_SH3_3 | 105 | 111 | PF00018 | 0.752 |
LIG_SH3_3 | 83 | 89 | PF00018 | 0.514 |
LIG_Sin3_3 | 168 | 175 | PF02671 | 0.397 |
LIG_SUMO_SIM_anti_2 | 166 | 171 | PF11976 | 0.582 |
LIG_SUMO_SIM_anti_2 | 49 | 54 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 168 | 173 | PF11976 | 0.394 |
LIG_SUMO_SIM_par_1 | 23 | 33 | PF11976 | 0.603 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.458 |
LIG_TYR_ITIM | 45 | 50 | PF00017 | 0.619 |
LIG_UBA3_1 | 171 | 178 | PF00899 | 0.619 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.668 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.585 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.485 |
MOD_CK2_1 | 189 | 195 | PF00069 | 0.470 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.530 |
MOD_Cter_Amidation | 179 | 182 | PF01082 | 0.550 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.616 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.466 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.634 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.544 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.560 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.570 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.625 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.650 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.516 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.541 |
MOD_PIKK_1 | 18 | 24 | PF00454 | 0.608 |
MOD_PK_1 | 106 | 112 | PF00069 | 0.528 |
MOD_PK_1 | 158 | 164 | PF00069 | 0.571 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.542 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.563 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.675 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.685 |
MOD_SUMO_rev_2 | 203 | 208 | PF00179 | 0.473 |
TRG_DiLeu_BaEn_1 | 166 | 171 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_4 | 203 | 209 | PF01217 | 0.422 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.567 |
TRG_ER_diArg_1 | 182 | 185 | PF00400 | 0.548 |
TRG_NLS_MonoCore_2 | 180 | 185 | PF00514 | 0.550 |
TRG_NLS_MonoExtN_4 | 178 | 185 | PF00514 | 0.542 |
TRG_Pf-PMV_PEXEL_1 | 23 | 28 | PF00026 | 0.592 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I730 | Leptomonas seymouri | 26% | 100% |
A0A0N1I8Q6 | Leptomonas seymouri | 45% | 97% |
A0A0N1PCW5 | Leptomonas seymouri | 36% | 100% |
A0A3Q8IF19 | Leishmania donovani | 78% | 100% |
A0A3Q8IKA6 | Leishmania donovani | 22% | 100% |
A0A3S5H7Q5 | Leishmania donovani | 36% | 94% |
A4HJM7 | Leishmania braziliensis | 37% | 100% |
A4HJM9 | Leishmania braziliensis | 23% | 100% |
A4I749 | Leishmania infantum | 36% | 94% |
A4I750 | Leishmania infantum | 78% | 100% |
A4I751 | Leishmania infantum | 22% | 100% |
E9B243 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 94% |
E9B244 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9B245 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
Q4Q617 | Leishmania major | 76% | 100% |