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: 14 |
NetGPI | no | yes: 0, no: 14 |
Related structures:
AlphaFold database: A0A3S5H7Q5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 27 | 29 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.483 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.708 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.708 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 94 | 98 | PF00082 | 0.480 |
DEG_APCC_DBOX_1 | 142 | 150 | PF00400 | 0.494 |
DOC_MAPK_gen_1 | 92 | 99 | PF00069 | 0.434 |
DOC_MAPK_MEF2A_6 | 92 | 99 | PF00069 | 0.434 |
DOC_MAPK_NFAT4_5 | 92 | 100 | PF00069 | 0.435 |
DOC_PP2B_PxIxI_1 | 22 | 28 | PF00149 | 0.409 |
DOC_USP7_MATH_1 | 131 | 135 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.605 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.392 |
LIG_14-3-3_CanoR_1 | 35 | 45 | PF00244 | 0.376 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.543 |
LIG_deltaCOP1_diTrp_1 | 218 | 227 | PF00928 | 0.334 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.424 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.415 |
LIG_FHA_2 | 177 | 183 | PF00498 | 0.438 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.492 |
LIG_FHA_2 | 98 | 104 | PF00498 | 0.376 |
LIG_LIR_Gen_1 | 85 | 96 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 62 | 68 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 74 | 79 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 85 | 91 | PF02991 | 0.467 |
LIG_Pex14_1 | 174 | 178 | PF04695 | 0.346 |
LIG_PTB_Apo_2 | 151 | 158 | PF02174 | 0.504 |
LIG_SH2_CRK | 65 | 69 | PF00017 | 0.443 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 184 | 188 | PF00017 | 0.415 |
LIG_SH3_4 | 6 | 13 | PF00018 | 0.566 |
LIG_SUMO_SIM_anti_2 | 185 | 190 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 39 | 46 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 50 | 55 | PF11976 | 0.479 |
LIG_TYR_ITIM | 63 | 68 | PF00017 | 0.534 |
LIG_UBA3_1 | 189 | 195 | PF00899 | 0.458 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.520 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.692 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.679 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.433 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.432 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.433 |
MOD_CK2_1 | 176 | 182 | PF00069 | 0.394 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.364 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.615 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.737 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.619 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.605 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.473 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.585 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.543 |
MOD_GSK3_1 | 176 | 183 | PF00069 | 0.388 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.514 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.391 |
MOD_N-GLC_1 | 17 | 22 | PF02516 | 0.753 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.377 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.646 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.461 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.546 |
MOD_PKA_2 | 36 | 42 | PF00069 | 0.491 |
MOD_PKA_2 | 55 | 61 | PF00069 | 0.435 |
MOD_PKB_1 | 35 | 43 | PF00069 | 0.392 |
MOD_Plk_1 | 102 | 108 | PF00069 | 0.438 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.639 |
MOD_Plk_1 | 167 | 173 | PF00069 | 0.408 |
MOD_Plk_4 | 120 | 126 | PF00069 | 0.486 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.391 |
MOD_SUMO_for_1 | 194 | 197 | PF00179 | 0.366 |
TRG_ENDOCYTIC_2 | 65 | 68 | PF00928 | 0.462 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.391 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.533 |
TRG_NLS_MonoExtC_3 | 55 | 60 | PF00514 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 41 | 46 | PF00026 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 66 | 71 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I730 | Leptomonas seymouri | 25% | 100% |
A0A0N1I8Q6 | Leptomonas seymouri | 40% | 100% |
A0A0N1PCW5 | Leptomonas seymouri | 31% | 100% |
A0A3Q8IF19 | Leishmania donovani | 41% | 100% |
A4HJM7 | Leishmania braziliensis | 55% | 100% |
A4HJM8 | Leishmania braziliensis | 36% | 100% |
A4I749 | Leishmania infantum | 99% | 99% |
A4I750 | Leishmania infantum | 41% | 100% |
E9B243 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 99% |
E9B244 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4Q616 | Leishmania major | 23% | 100% |
Q4Q617 | Leishmania major | 40% | 100% |
Q4Q618 | Leishmania major | 84% | 100% |