Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005829 | cytosol | 2 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
Related structures:
AlphaFold database: A4H951
Term | Name | Level | Count |
---|---|---|---|
GO:0006950 | response to stress | 2 | 1 |
GO:0006979 | response to oxidative stress | 3 | 1 |
GO:0009266 | response to temperature stimulus | 3 | 1 |
GO:0009408 | response to heat | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034599 | cellular response to oxidative stress | 4 | 1 |
GO:0034605 | cellular response to heat | 4 | 1 |
GO:0042221 | response to chemical | 2 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0062197 | cellular response to chemical stress | 4 | 1 |
GO:0070887 | cellular response to chemical stimulus | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 398 | 402 | PF00656 | 0.456 |
CLV_PCSK_SKI1_1 | 328 | 332 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 353 | 357 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 95 | 99 | PF00082 | 0.304 |
DOC_ANK_TNKS_1 | 136 | 143 | PF00023 | 0.427 |
DOC_CYCLIN_RxL_1 | 92 | 101 | PF00134 | 0.329 |
DOC_MAPK_MEF2A_6 | 243 | 250 | PF00069 | 0.498 |
DOC_MAPK_MEF2A_6 | 412 | 419 | PF00069 | 0.450 |
DOC_USP7_MATH_1 | 178 | 182 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.454 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.504 |
LIG_14-3-3_CanoR_1 | 219 | 226 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 388 | 392 | PF00244 | 0.437 |
LIG_Actin_WH2_2 | 83 | 101 | PF00022 | 0.450 |
LIG_AP2alpha_1 | 83 | 87 | PF02296 | 0.450 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.392 |
LIG_BIR_III_2 | 440 | 444 | PF00653 | 0.515 |
LIG_BRCT_BRCA1_1 | 103 | 107 | PF00533 | 0.463 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.452 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.329 |
LIG_BRCT_BRCA1_1 | 79 | 83 | PF00533 | 0.507 |
LIG_BRCT_BRCA1_2 | 189 | 195 | PF00533 | 0.309 |
LIG_Clathr_ClatBox_1 | 182 | 186 | PF01394 | 0.475 |
LIG_deltaCOP1_diTrp_1 | 371 | 376 | PF00928 | 0.335 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.449 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.386 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.427 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.414 |
LIG_FHA_1 | 269 | 275 | PF00498 | 0.337 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.253 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.367 |
LIG_FHA_2 | 1 | 7 | PF00498 | 0.560 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.464 |
LIG_FHA_2 | 222 | 228 | PF00498 | 0.525 |
LIG_FHA_2 | 291 | 297 | PF00498 | 0.510 |
LIG_GBD_Chelix_1 | 89 | 97 | PF00786 | 0.350 |
LIG_LIR_Gen_1 | 103 | 113 | PF02991 | 0.511 |
LIG_LIR_Gen_1 | 326 | 337 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 85 | 93 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 85 | 90 | PF02991 | 0.450 |
LIG_NRBOX | 92 | 98 | PF00104 | 0.253 |
LIG_PCNA_yPIPBox_3 | 219 | 230 | PF02747 | 0.314 |
LIG_PCNA_yPIPBox_3 | 353 | 367 | PF02747 | 0.253 |
LIG_PDZ_Class_3 | 439 | 444 | PF00595 | 0.442 |
LIG_Pex14_2 | 193 | 197 | PF04695 | 0.467 |
LIG_Pex14_2 | 303 | 307 | PF04695 | 0.348 |
LIG_Pex14_2 | 83 | 87 | PF04695 | 0.399 |
LIG_SH2_GRB2like | 406 | 409 | PF00017 | 0.253 |
LIG_SH2_GRB2like | 52 | 55 | PF00017 | 0.410 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.450 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.541 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.253 |
LIG_SUMO_SIM_par_1 | 413 | 418 | PF11976 | 0.441 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.625 |
LIG_TRAF2_1 | 280 | 283 | PF00917 | 0.410 |
LIG_TRAF2_1 | 293 | 296 | PF00917 | 0.277 |
LIG_TRAF2_1 | 70 | 73 | PF00917 | 0.410 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.450 |
LIG_WRC_WIRS_1 | 247 | 252 | PF05994 | 0.450 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.500 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.311 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.541 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.481 |
MOD_CK2_1 | 221 | 227 | PF00069 | 0.401 |
MOD_CK2_1 | 277 | 283 | PF00069 | 0.411 |
MOD_CK2_1 | 290 | 296 | PF00069 | 0.295 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.338 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.371 |
MOD_GlcNHglycan | 203 | 206 | PF01048 | 0.516 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.262 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.334 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.394 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.404 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.424 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.397 |
MOD_GSK3_1 | 290 | 297 | PF00069 | 0.383 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.440 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.440 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.392 |
MOD_GSK3_1 | 7 | 14 | PF00069 | 0.329 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.436 |
MOD_N-GLC_1 | 101 | 106 | PF02516 | 0.498 |
MOD_N-GLC_1 | 201 | 206 | PF02516 | 0.542 |
MOD_N-GLC_1 | 377 | 382 | PF02516 | 0.334 |
MOD_N-GLC_1 | 65 | 70 | PF02516 | 0.359 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.539 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.366 |
MOD_NEK2_1 | 171 | 176 | PF00069 | 0.550 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.390 |
MOD_NEK2_1 | 285 | 290 | PF00069 | 0.391 |
MOD_NEK2_1 | 46 | 51 | PF00069 | 0.424 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.277 |
MOD_NEK2_1 | 98 | 103 | PF00069 | 0.409 |
MOD_NEK2_2 | 246 | 251 | PF00069 | 0.253 |
MOD_NEK2_2 | 25 | 30 | PF00069 | 0.450 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.544 |
MOD_PIKK_1 | 219 | 225 | PF00454 | 0.434 |
MOD_PIKK_1 | 377 | 383 | PF00454 | 0.253 |
MOD_PKA_2 | 156 | 162 | PF00069 | 0.317 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.447 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.400 |
MOD_PKA_2 | 46 | 52 | PF00069 | 0.416 |
MOD_Plk_1 | 101 | 107 | PF00069 | 0.450 |
MOD_Plk_1 | 178 | 184 | PF00069 | 0.525 |
MOD_Plk_1 | 258 | 264 | PF00069 | 0.447 |
MOD_Plk_1 | 318 | 324 | PF00069 | 0.345 |
MOD_Plk_1 | 415 | 421 | PF00069 | 0.381 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.406 |
MOD_Plk_4 | 178 | 184 | PF00069 | 0.586 |
MOD_Plk_4 | 38 | 44 | PF00069 | 0.441 |
MOD_SUMO_for_1 | 355 | 358 | PF00179 | 0.450 |
MOD_SUMO_rev_2 | 14 | 21 | PF00179 | 0.350 |
MOD_SUMO_rev_2 | 294 | 299 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 369 | 375 | PF00179 | 0.396 |
TRG_DiLeu_BaEn_1 | 203 | 208 | PF01217 | 0.514 |
TRG_DiLeu_BaEn_1 | 358 | 363 | PF01217 | 0.450 |
TRG_DiLeu_BaEn_1 | 92 | 97 | PF01217 | 0.278 |
TRG_DiLeu_BaEn_4 | 294 | 300 | PF01217 | 0.410 |
TRG_DiLeu_LyEn_5 | 92 | 97 | PF01217 | 0.253 |
TRG_NES_CRM1_1 | 77 | 92 | PF08389 | 0.450 |
TRG_Pf-PMV_PEXEL_1 | 137 | 141 | PF00026 | 0.350 |
TRG_Pf-PMV_PEXEL_1 | 219 | 223 | PF00026 | 0.395 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5L4 | Leptomonas seymouri | 61% | 100% |
A0A1X0NSU0 | Trypanosomatidae | 36% | 100% |
A0A3Q8IAQ3 | Leishmania donovani | 80% | 100% |
A0A422NH16 | Trypanosoma rangeli | 33% | 100% |
A4HXG5 | Leishmania infantum | 81% | 100% |
C9ZP52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AR60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
Q4QEA3 | Leishmania major | 82% | 100% |