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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A0A3Q8ICH4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 363 | 365 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.495 |
CLV_PCSK_FUR_1 | 349 | 353 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.444 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.582 |
DEG_APCC_DBOX_1 | 186 | 194 | PF00400 | 0.524 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.658 |
DEG_SCF_FBW7_1 | 277 | 283 | PF00400 | 0.389 |
DOC_CKS1_1 | 277 | 282 | PF01111 | 0.389 |
DOC_CYCLIN_RxL_1 | 292 | 301 | PF00134 | 0.319 |
DOC_CYCLIN_yCln2_LP_2 | 4 | 10 | PF00134 | 0.554 |
DOC_MAPK_DCC_7 | 62 | 70 | PF00069 | 0.373 |
DOC_MAPK_gen_1 | 62 | 70 | PF00069 | 0.577 |
DOC_MAPK_gen_1 | 98 | 106 | PF00069 | 0.341 |
DOC_PP1_RVXF_1 | 293 | 299 | PF00149 | 0.297 |
DOC_PP2B_LxvP_1 | 289 | 292 | PF13499 | 0.297 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 314 | 318 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.514 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.527 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.681 |
DOC_WW_Pin1_4 | 276 | 281 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.387 |
LIG_14-3-3_CanoR_1 | 235 | 240 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 249 | 255 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 343 | 348 | PF00244 | 0.401 |
LIG_Actin_WH2_2 | 113 | 128 | PF00022 | 0.484 |
LIG_Actin_WH2_2 | 32 | 49 | PF00022 | 0.529 |
LIG_Actin_WH2_2 | 4 | 21 | PF00022 | 0.474 |
LIG_APCC_ABBAyCdc20_2 | 101 | 107 | PF00400 | 0.462 |
LIG_BRCT_BRCA1_1 | 261 | 265 | PF00533 | 0.490 |
LIG_Clathr_ClatBox_1 | 325 | 329 | PF01394 | 0.433 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.624 |
LIG_deltaCOP1_diTrp_1 | 110 | 119 | PF00928 | 0.335 |
LIG_deltaCOP1_diTrp_1 | 166 | 173 | PF00928 | 0.339 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.480 |
LIG_FHA_1 | 19 | 25 | PF00498 | 0.576 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.355 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.297 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.406 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.453 |
LIG_LIR_Gen_1 | 114 | 121 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 166 | 176 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.560 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 166 | 172 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 262 | 268 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.548 |
LIG_PCNA_PIPBox_1 | 194 | 203 | PF02747 | 0.452 |
LIG_PCNA_yPIPBox_3 | 349 | 361 | PF02747 | 0.460 |
LIG_Pex14_1 | 169 | 173 | PF04695 | 0.341 |
LIG_PTB_Apo_2 | 192 | 199 | PF02174 | 0.518 |
LIG_PTB_Phospho_1 | 192 | 198 | PF10480 | 0.519 |
LIG_SH2_CRK | 305 | 309 | PF00017 | 0.333 |
LIG_SH2_GRB2like | 84 | 87 | PF00017 | 0.479 |
LIG_SH2_NCK_1 | 305 | 309 | PF00017 | 0.292 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.479 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.551 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.554 |
LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 276 | 279 | PF00017 | 0.313 |
LIG_SH3_2 | 240 | 245 | PF14604 | 0.585 |
LIG_SH3_3 | 237 | 243 | PF00018 | 0.716 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.434 |
LIG_SH3_3 | 308 | 314 | PF00018 | 0.297 |
LIG_SH3_3 | 333 | 339 | PF00018 | 0.297 |
LIG_SH3_CIN85_PxpxPR_1 | 240 | 245 | PF14604 | 0.585 |
LIG_SUMO_SIM_par_1 | 323 | 329 | PF11976 | 0.433 |
LIG_TYR_ITIM | 303 | 308 | PF00017 | 0.333 |
LIG_WW_3 | 242 | 246 | PF00397 | 0.577 |
MOD_CDK_SPK_2 | 236 | 241 | PF00069 | 0.620 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.495 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.417 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.433 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.471 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.531 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.433 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.486 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.421 |
MOD_GSK3_1 | 276 | 283 | PF00069 | 0.161 |
MOD_LATS_1 | 341 | 347 | PF00433 | 0.389 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.533 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.412 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.372 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.291 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.472 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.404 |
MOD_NEK2_1 | 321 | 326 | PF00069 | 0.297 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.437 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.431 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.542 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.604 |
MOD_PKA_2 | 248 | 254 | PF00069 | 0.342 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.352 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.398 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.533 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.477 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.413 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.297 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.481 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.477 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.545 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.398 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.378 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.433 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.297 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.677 |
MOD_ProDKin_1 | 276 | 282 | PF00069 | 0.302 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.379 |
TRG_DiLeu_BaEn_1 | 73 | 78 | PF01217 | 0.494 |
TRG_DiLeu_BaLyEn_6 | 292 | 297 | PF01217 | 0.433 |
TRG_DiLeu_BaLyEn_6 | 4 | 9 | PF01217 | 0.718 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 305 | 308 | PF00928 | 0.333 |
TRG_ER_diArg_1 | 210 | 213 | PF00400 | 0.564 |
TRG_NES_CRM1_1 | 138 | 151 | PF08389 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 212 | 216 | PF00026 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 358 | 362 | PF00026 | 0.500 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I936 | Leptomonas seymouri | 79% | 98% |
A0A0S4IRF9 | Bodo saltans | 43% | 100% |
A0A1X0NXH8 | Trypanosomatidae | 49% | 100% |
A0A422MYI7 | Trypanosoma rangeli | 50% | 100% |
A4HCS9 | Leishmania braziliensis | 87% | 99% |
A4I0A3 | Leishmania infantum | 100% | 100% |
C9ZV29 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E9AW68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4QBB0 | Leishmania major | 98% | 100% |
V5BFN3 | Trypanosoma cruzi | 51% | 100% |