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: A4HCS9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 168 | 172 | PF00656 | 0.428 |
CLV_NRD_NRD_1 | 209 | 211 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 337 | 339 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.517 |
CLV_PCSK_FUR_1 | 335 | 339 | PF00082 | 0.388 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 349 | 351 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.643 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.266 |
DEG_APCC_DBOX_1 | 186 | 194 | PF00400 | 0.487 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.577 |
DEG_SCF_FBW7_1 | 263 | 269 | PF00400 | 0.360 |
DOC_CDC14_PxL_1 | 4 | 12 | PF14671 | 0.437 |
DOC_CKS1_1 | 263 | 268 | PF01111 | 0.360 |
DOC_CYCLIN_RxL_1 | 12 | 22 | PF00134 | 0.421 |
DOC_CYCLIN_RxL_1 | 278 | 287 | PF00134 | 0.286 |
DOC_MAPK_gen_1 | 210 | 216 | PF00069 | 0.587 |
DOC_MAPK_gen_1 | 335 | 345 | PF00069 | 0.508 |
DOC_MAPK_gen_1 | 98 | 106 | PF00069 | 0.309 |
DOC_PP1_RVXF_1 | 279 | 285 | PF00149 | 0.266 |
DOC_PP2B_LxvP_1 | 275 | 278 | PF13499 | 0.266 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.410 |
DOC_USP7_MATH_1 | 300 | 304 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.430 |
DOC_USP7_UBL2_3 | 47 | 51 | PF12436 | 0.484 |
DOC_WW_Pin1_4 | 220 | 225 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 262 | 267 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 71 | 76 | PF00397 | 0.366 |
LIG_14-3-3_CanoR_1 | 194 | 198 | PF00244 | 0.268 |
LIG_14-3-3_CanoR_1 | 247 | 252 | PF00244 | 0.318 |
LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 329 | 334 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.390 |
LIG_Actin_WH2_2 | 113 | 128 | PF00022 | 0.462 |
LIG_Actin_WH2_2 | 32 | 49 | PF00022 | 0.433 |
LIG_APCC_ABBAyCdc20_2 | 101 | 107 | PF00400 | 0.440 |
LIG_BIR_III_2 | 171 | 175 | PF00653 | 0.401 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.451 |
LIG_Clathr_ClatBox_1 | 311 | 315 | PF01394 | 0.489 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.555 |
LIG_deltaCOP1_diTrp_1 | 110 | 119 | PF00928 | 0.305 |
LIG_deltaCOP1_diTrp_1 | 166 | 173 | PF00928 | 0.306 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.395 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.322 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.332 |
LIG_FHA_1 | 34 | 40 | PF00498 | 0.363 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.432 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.379 |
LIG_LIR_Gen_1 | 114 | 121 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 43 | 53 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 178 | 183 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 196 | 201 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 248 | 254 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 43 | 48 | PF02991 | 0.512 |
LIG_Pex14_1 | 169 | 173 | PF04695 | 0.307 |
LIG_PTB_Apo_2 | 192 | 199 | PF02174 | 0.486 |
LIG_PTB_Phospho_1 | 192 | 198 | PF10480 | 0.485 |
LIG_SH2_CRK | 291 | 295 | PF00017 | 0.300 |
LIG_SH2_GRB2like | 203 | 206 | PF00017 | 0.305 |
LIG_SH2_GRB2like | 84 | 87 | PF00017 | 0.457 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.457 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.525 |
LIG_SH2_STAP1 | 347 | 351 | PF00017 | 0.512 |
LIG_SH2_STAT3 | 203 | 206 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.481 |
LIG_SH3_1 | 221 | 227 | PF00018 | 0.384 |
LIG_SH3_2 | 8 | 13 | PF14604 | 0.438 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.512 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.411 |
LIG_SH3_3 | 294 | 300 | PF00018 | 0.298 |
LIG_SH3_3 | 319 | 325 | PF00018 | 0.340 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.645 |
LIG_SUMO_SIM_par_1 | 309 | 315 | PF11976 | 0.489 |
LIG_TYR_ITIM | 289 | 294 | PF00017 | 0.300 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.471 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.372 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.489 |
MOD_CK2_1 | 247 | 253 | PF00069 | 0.458 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.389 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.429 |
MOD_GlcNHglycan | 242 | 245 | PF01048 | 0.452 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.399 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.354 |
MOD_GSK3_1 | 242 | 249 | PF00069 | 0.371 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.244 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.385 |
MOD_LATS_1 | 327 | 333 | PF00433 | 0.350 |
MOD_N-GLC_1 | 245 | 250 | PF02516 | 0.507 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.376 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.342 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.260 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.429 |
MOD_NEK2_1 | 24 | 29 | PF00069 | 0.344 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.382 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.369 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.271 |
MOD_NEK2_2 | 67 | 72 | PF00069 | 0.387 |
MOD_PKA_2 | 125 | 131 | PF00069 | 0.386 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.293 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.410 |
MOD_PKA_2 | 246 | 252 | PF00069 | 0.319 |
MOD_PKA_2 | 328 | 334 | PF00069 | 0.350 |
MOD_PKA_2 | 355 | 361 | PF00069 | 0.411 |
MOD_PKA_2 | 58 | 64 | PF00069 | 0.441 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.455 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.377 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.339 |
MOD_Plk_4 | 115 | 121 | PF00069 | 0.458 |
MOD_Plk_4 | 165 | 171 | PF00069 | 0.455 |
MOD_Plk_4 | 193 | 199 | PF00069 | 0.521 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.360 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.331 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.318 |
MOD_Plk_4 | 318 | 324 | PF00069 | 0.290 |
MOD_ProDKin_1 | 220 | 226 | PF00069 | 0.513 |
MOD_ProDKin_1 | 262 | 268 | PF00069 | 0.266 |
MOD_ProDKin_1 | 71 | 77 | PF00069 | 0.358 |
TRG_DiLeu_BaEn_1 | 73 | 78 | PF01217 | 0.483 |
TRG_DiLeu_BaLyEn_6 | 188 | 193 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 278 | 283 | PF01217 | 0.411 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.721 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.336 |
TRG_ENDOCYTIC_2 | 291 | 294 | PF00928 | 0.300 |
TRG_NES_CRM1_1 | 138 | 151 | PF08389 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 344 | 348 | PF00026 | 0.462 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I936 | Leptomonas seymouri | 79% | 95% |
A0A0S4IRF9 | Bodo saltans | 45% | 100% |
A0A1X0NXH8 | Trypanosomatidae | 51% | 100% |
A0A3Q8ICH4 | Leishmania donovani | 87% | 96% |
A0A422MYI7 | Trypanosoma rangeli | 51% | 100% |
A4I0A3 | Leishmania infantum | 87% | 96% |
C9ZV29 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 100% |
E9AW68 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 96% |
Q4QBB0 | Leishmania major | 87% | 100% |
V5BFN3 | Trypanosoma cruzi | 52% | 100% |