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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AGU4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 163 | 165 | PF00675 | 0.573 |
CLV_PCSK_KEX2_1 | 163 | 165 | PF00082 | 0.573 |
CLV_Separin_Metazoa | 212 | 216 | PF03568 | 0.490 |
DEG_APCC_DBOX_1 | 113 | 121 | PF00400 | 0.540 |
DOC_MAPK_gen_1 | 236 | 245 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 101 | 109 | PF00069 | 0.489 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.699 |
DOC_WW_Pin1_4 | 164 | 169 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 194 | 199 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 244 | 250 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 43 | 48 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 5 | 11 | PF00244 | 0.688 |
LIG_APCC_ABBA_1 | 45 | 50 | PF00400 | 0.533 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.449 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.484 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.515 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.476 |
LIG_FHA_2 | 129 | 135 | PF00498 | 0.523 |
LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.479 |
LIG_LIR_Gen_1 | 42 | 52 | PF02991 | 0.514 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.412 |
LIG_MYND_3 | 250 | 254 | PF01753 | 0.620 |
LIG_NRBOX | 154 | 160 | PF00104 | 0.434 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.460 |
LIG_SH3_3 | 162 | 168 | PF00018 | 0.541 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 61 | 66 | PF11976 | 0.388 |
MOD_CK1_1 | 188 | 194 | PF00069 | 0.498 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.571 |
MOD_DYRK1A_RPxSP_1 | 164 | 168 | PF00069 | 0.482 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.508 |
MOD_GlcNHglycan | 187 | 190 | PF01048 | 0.385 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.593 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.432 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.497 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.454 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.432 |
MOD_N-GLC_1 | 150 | 155 | PF02516 | 0.565 |
MOD_N-GLC_1 | 52 | 57 | PF02516 | 0.525 |
MOD_N-GLC_2 | 98 | 100 | PF02516 | 0.561 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.452 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.503 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.637 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.430 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.598 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.681 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.538 |
MOD_OFUCOSY | 12 | 18 | PF10250 | 0.631 |
MOD_PIKK_1 | 138 | 144 | PF00454 | 0.537 |
MOD_PKA_2 | 243 | 249 | PF00069 | 0.535 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.700 |
MOD_Plk_1 | 150 | 156 | PF00069 | 0.572 |
MOD_Plk_4 | 128 | 134 | PF00069 | 0.525 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.562 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.503 |
MOD_ProDKin_1 | 164 | 170 | PF00069 | 0.619 |
MOD_ProDKin_1 | 194 | 200 | PF00069 | 0.504 |
MOD_SUMO_for_1 | 202 | 205 | PF00179 | 0.580 |
MOD_SUMO_rev_2 | 225 | 231 | PF00179 | 0.539 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.573 |
TRG_NES_CRM1_1 | 208 | 221 | PF08389 | 0.409 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IYT2 | Bodo saltans | 26% | 79% |
A0A1X0NXA5 | Trypanosomatidae | 31% | 93% |
A0A3Q8IB00 | Leishmania donovani | 99% | 100% |
A0A3R7N8W3 | Trypanosoma rangeli | 35% | 97% |
A4HBJ8 | Leishmania braziliensis | 63% | 100% |
D0A1J5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 85% |
E9AUW7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4QCL5 | Leishmania major | 91% | 100% |