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: 12 |
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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: A0A3Q8ICM9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 181 | 185 | PF00656 | 0.394 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.354 |
CLV_NRD_NRD_1 | 54 | 56 | PF00675 | 0.403 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.429 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 43 | 45 | PF00082 | 0.343 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 43 | 45 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 277 | 281 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.349 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.325 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.620 |
DOC_MAPK_DCC_7 | 8 | 16 | PF00069 | 0.526 |
DOC_MAPK_gen_1 | 187 | 193 | PF00069 | 0.387 |
DOC_MAPK_gen_1 | 42 | 50 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 77 | 85 | PF00069 | 0.249 |
DOC_MAPK_MEF2A_6 | 378 | 385 | PF00069 | 0.342 |
DOC_MAPK_MEF2A_6 | 8 | 16 | PF00069 | 0.476 |
DOC_PP2B_LxvP_1 | 326 | 329 | PF13499 | 0.362 |
DOC_PP2B_LxvP_1 | 369 | 372 | PF13499 | 0.328 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 389 | 393 | PF00917 | 0.445 |
DOC_USP7_UBL2_3 | 38 | 42 | PF12436 | 0.401 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.518 |
DOC_WW_Pin1_4 | 97 | 102 | PF00397 | 0.444 |
LIG_14-3-3_CanoR_1 | 102 | 107 | PF00244 | 0.224 |
LIG_14-3-3_CanoR_1 | 152 | 156 | PF00244 | 0.413 |
LIG_14-3-3_CanoR_1 | 17 | 24 | PF00244 | 0.362 |
LIG_14-3-3_CanoR_1 | 240 | 248 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 344 | 353 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 60 | 66 | PF00244 | 0.382 |
LIG_APCC_ABBA_1 | 206 | 211 | PF00400 | 0.362 |
LIG_BRCT_BRCA1_1 | 172 | 176 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 223 | 227 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.325 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.535 |
LIG_EH1_1 | 134 | 142 | PF00400 | 0.300 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.348 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.413 |
LIG_FHA_1 | 331 | 337 | PF00498 | 0.471 |
LIG_FHA_1 | 345 | 351 | PF00498 | 0.387 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.603 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.369 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.312 |
LIG_LIR_Gen_1 | 100 | 109 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 125 | 135 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 264 | 274 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 278 | 288 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 100 | 106 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 120 | 126 | PF02991 | 0.371 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 278 | 283 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 333 | 338 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.337 |
LIG_MLH1_MIPbox_1 | 172 | 176 | PF16413 | 0.413 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.402 |
LIG_SH2_CRK | 166 | 170 | PF00017 | 0.281 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.481 |
LIG_SH2_GRB2like | 134 | 137 | PF00017 | 0.325 |
LIG_SH2_STAP1 | 89 | 93 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.438 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.259 |
LIG_SH3_1 | 9 | 15 | PF00018 | 0.472 |
LIG_SH3_2 | 12 | 17 | PF14604 | 0.413 |
LIG_SH3_3 | 193 | 199 | PF00018 | 0.429 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.410 |
LIG_SH3_3 | 9 | 15 | PF00018 | 0.454 |
LIG_SUMO_SIM_anti_2 | 270 | 276 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 395 | 400 | PF11976 | 0.549 |
LIG_SUMO_SIM_anti_2 | 81 | 87 | PF11976 | 0.249 |
LIG_SUMO_SIM_par_1 | 197 | 203 | PF11976 | 0.468 |
LIG_SUMO_SIM_par_1 | 394 | 400 | PF11976 | 0.547 |
LIG_SUMO_SIM_par_1 | 81 | 87 | PF11976 | 0.249 |
LIG_TYR_ITIM | 247 | 252 | PF00017 | 0.362 |
MOD_CDK_SPK_2 | 97 | 102 | PF00069 | 0.299 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.423 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.415 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.588 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.325 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.345 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.321 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.315 |
MOD_GlcNHglycan | 172 | 175 | PF01048 | 0.394 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.413 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.654 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.452 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.322 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.350 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.172 |
MOD_N-GLC_1 | 262 | 267 | PF02516 | 0.344 |
MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.312 |
MOD_N-GLC_1 | 344 | 349 | PF02516 | 0.372 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.375 |
MOD_NEK2_1 | 248 | 253 | PF00069 | 0.271 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.362 |
MOD_NEK2_1 | 330 | 335 | PF00069 | 0.234 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.231 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.411 |
MOD_NEK2_2 | 339 | 344 | PF00069 | 0.287 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.414 |
MOD_PIKK_1 | 302 | 308 | PF00454 | 0.330 |
MOD_PIKK_1 | 318 | 324 | PF00454 | 0.268 |
MOD_PK_1 | 61 | 67 | PF00069 | 0.413 |
MOD_PKA_2 | 151 | 157 | PF00069 | 0.413 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.360 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.348 |
MOD_Plk_1 | 262 | 268 | PF00069 | 0.327 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.409 |
MOD_Plk_4 | 156 | 162 | PF00069 | 0.374 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.302 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.281 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.531 |
MOD_ProDKin_1 | 97 | 103 | PF00069 | 0.444 |
MOD_SUMO_rev_2 | 224 | 234 | PF00179 | 0.347 |
MOD_SUMO_rev_2 | 31 | 40 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 64 | 70 | PF00179 | 0.356 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 134 | 137 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 166 | 169 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 175 | 178 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.488 |
TRG_NES_CRM1_1 | 205 | 219 | PF08389 | 0.404 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBN4 | Leptomonas seymouri | 69% | 100% |
A0A0S4JPD3 | Bodo saltans | 26% | 93% |
A0A1X0NY42 | Trypanosomatidae | 37% | 100% |
A0A422P4K0 | Trypanosoma rangeli | 38% | 97% |
A4HEB8 | Leishmania braziliensis | 84% | 100% |
A4I1R3 | Leishmania infantum | 100% | 100% |
C9ZKB9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AXU8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q9M3 | Leishmania major | 92% | 100% |