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: 1 |
NetGPI | no | yes: 0, no: 1 |
Related structures:
AlphaFold database: A0A3Q8IE04
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 34 | 36 | PF00675 | 0.408 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 155 | 159 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.363 |
CLV_Separin_Metazoa | 57 | 61 | PF03568 | 0.419 |
DOC_MAPK_gen_1 | 35 | 43 | PF00069 | 0.393 |
DOC_MAPK_gen_1 | 60 | 67 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 96 | 103 | PF00069 | 0.338 |
DOC_MAPK_NFAT4_5 | 96 | 104 | PF00069 | 0.343 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.419 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.465 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 161 | 167 | PF00244 | 0.449 |
LIG_APCC_ABBA_1 | 219 | 224 | PF00400 | 0.463 |
LIG_BIR_III_4 | 21 | 25 | PF00653 | 0.422 |
LIG_BRCT_BRCA1_1 | 188 | 192 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 199 | 203 | PF00533 | 0.406 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.441 |
LIG_FHA_1 | 38 | 44 | PF00498 | 0.394 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.437 |
LIG_LIR_Nem_3 | 84 | 90 | PF02991 | 0.336 |
LIG_PTB_Apo_2 | 66 | 73 | PF02174 | 0.353 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.420 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.372 |
LIG_SH2_STAP1 | 170 | 174 | PF00017 | 0.420 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 79 | 82 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 87 | 90 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 98 | 101 | PF00017 | 0.329 |
LIG_SUMO_SIM_par_1 | 179 | 185 | PF11976 | 0.440 |
LIG_SUMO_SIM_par_1 | 39 | 46 | PF11976 | 0.401 |
LIG_TRAF2_1 | 204 | 207 | PF00917 | 0.414 |
LIG_TYR_ITIM | 88 | 93 | PF00017 | 0.354 |
MOD_CDK_SPxxK_3 | 224 | 231 | PF00069 | 0.478 |
MOD_CK1_1 | 116 | 122 | PF00069 | 0.482 |
MOD_CK2_1 | 145 | 151 | PF00069 | 0.454 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.406 |
MOD_Cter_Amidation | 33 | 36 | PF01082 | 0.417 |
MOD_GlcNHglycan | 118 | 121 | PF01048 | 0.492 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.435 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.467 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.430 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.406 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.397 |
MOD_N-GLC_1 | 6 | 11 | PF02516 | 0.468 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.411 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.454 |
MOD_NEK2_2 | 23 | 28 | PF00069 | 0.400 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.417 |
MOD_PK_1 | 81 | 87 | PF00069 | 0.353 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.456 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.470 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.440 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.437 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.455 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.474 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.421 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 98 | 101 | PF00928 | 0.329 |
TRG_Pf-PMV_PEXEL_1 | 28 | 32 | PF00026 | 0.399 |