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: Q4Q9Z3
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016491 | oxidoreductase activity | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043169 | cation binding | 3 | 12 |
GO:0046872 | metal ion binding | 4 | 12 |
GO:0051213 | dioxygenase activity | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 185 | 189 | PF00656 | 0.562 |
CLV_C14_Caspase3-7 | 305 | 309 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 417 | 421 | PF00656 | 0.637 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 159 | 161 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.592 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.620 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.411 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 291 | 295 | PF00082 | 0.620 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 381 | 385 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 60 | 64 | PF00082 | 0.286 |
DEG_APCC_DBOX_1 | 8 | 16 | PF00400 | 0.442 |
DEG_MDM2_SWIB_1 | 364 | 372 | PF02201 | 0.281 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.653 |
DOC_CDC14_PxL_1 | 347 | 355 | PF14671 | 0.266 |
DOC_MAPK_gen_1 | 159 | 167 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 266 | 273 | PF00069 | 0.592 |
DOC_MAPK_MEF2A_6 | 344 | 352 | PF00069 | 0.393 |
DOC_PP1_RVXF_1 | 58 | 64 | PF00149 | 0.332 |
DOC_PP4_FxxP_1 | 395 | 398 | PF00568 | 0.302 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.687 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 75 | 79 | PF00917 | 0.624 |
DOC_USP7_MATH_2 | 94 | 100 | PF00917 | 0.394 |
DOC_WW_Pin1_4 | 373 | 378 | PF00397 | 0.281 |
DOC_WW_Pin1_4 | 90 | 95 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 99 | 104 | PF00397 | 0.376 |
LIG_14-3-3_CanoR_1 | 214 | 222 | PF00244 | 0.341 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.266 |
LIG_FHA_1 | 293 | 299 | PF00498 | 0.637 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.305 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.224 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.328 |
LIG_FHA_2 | 317 | 323 | PF00498 | 0.305 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.401 |
LIG_HCF-1_HBM_1 | 36 | 39 | PF13415 | 0.474 |
LIG_LIR_Gen_1 | 150 | 157 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 346 | 353 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 36 | 47 | PF02991 | 0.487 |
LIG_LIR_Nem_3 | 104 | 109 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 346 | 350 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.266 |
LIG_LYPXL_yS_3 | 258 | 261 | PF13949 | 0.386 |
LIG_MYND_3 | 350 | 354 | PF01753 | 0.360 |
LIG_Pex14_2 | 190 | 194 | PF04695 | 0.470 |
LIG_Pex14_2 | 364 | 368 | PF04695 | 0.266 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.360 |
LIG_SH2_CRK | 347 | 351 | PF00017 | 0.403 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 202 | 206 | PF00017 | 0.354 |
LIG_SH2_STAT3 | 142 | 145 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 257 | 260 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 112 | 115 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 206 | 209 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.332 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.386 |
LIG_SH3_3 | 221 | 227 | PF00018 | 0.468 |
LIG_SUMO_SIM_anti_2 | 324 | 330 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 324 | 330 | PF11976 | 0.411 |
LIG_WRC_WIRS_1 | 242 | 247 | PF05994 | 0.390 |
MOD_CDK_SPxK_1 | 373 | 379 | PF00069 | 0.266 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.434 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.555 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.290 |
MOD_CK1_1 | 388 | 394 | PF00069 | 0.287 |
MOD_CK1_1 | 99 | 105 | PF00069 | 0.373 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.399 |
MOD_GlcNHglycan | 103 | 106 | PF01048 | 0.411 |
MOD_GlcNHglycan | 115 | 118 | PF01048 | 0.420 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.589 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.524 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.606 |
MOD_GSK3_1 | 148 | 155 | PF00069 | 0.519 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.566 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.419 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.348 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.400 |
MOD_N-GLC_1 | 87 | 92 | PF02516 | 0.503 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.483 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.468 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.641 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.371 |
MOD_NEK2_2 | 241 | 246 | PF00069 | 0.384 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.628 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.633 |
MOD_PIKK_1 | 327 | 333 | PF00454 | 0.411 |
MOD_PIKK_1 | 87 | 93 | PF00454 | 0.423 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.475 |
MOD_PKA_2 | 222 | 228 | PF00069 | 0.441 |
MOD_PKA_2 | 388 | 394 | PF00069 | 0.271 |
MOD_Plk_1 | 311 | 317 | PF00069 | 0.340 |
MOD_Plk_1 | 321 | 327 | PF00069 | 0.293 |
MOD_Plk_1 | 87 | 93 | PF00069 | 0.423 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.533 |
MOD_Plk_4 | 2 | 8 | PF00069 | 0.489 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.287 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.266 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.577 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.427 |
MOD_ProDKin_1 | 373 | 379 | PF00069 | 0.281 |
MOD_ProDKin_1 | 90 | 96 | PF00069 | 0.382 |
MOD_ProDKin_1 | 99 | 105 | PF00069 | 0.378 |
MOD_SUMO_rev_2 | 188 | 197 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 338 | 346 | PF00179 | 0.281 |
TRG_AP2beta_CARGO_1 | 240 | 249 | PF09066 | 0.476 |
TRG_DiLeu_BaEn_1 | 354 | 359 | PF01217 | 0.360 |
TRG_DiLeu_BaEn_4 | 149 | 155 | PF01217 | 0.522 |
TRG_DiLeu_BaLyEn_6 | 403 | 408 | PF01217 | 0.426 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 153 | 156 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 347 | 350 | PF00928 | 0.300 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.283 |
TRG_ER_diArg_1 | 138 | 140 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.580 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3U5 | Leptomonas seymouri | 83% | 99% |
A0A0S4JVQ8 | Bodo saltans | 46% | 100% |
A0A1X0NLX7 | Trypanosomatidae | 58% | 100% |
A0A3Q8IBQ1 | Leishmania donovani | 97% | 100% |
A0A422NXL7 | Trypanosoma rangeli | 62% | 100% |
A4HE36 | Leishmania braziliensis | 92% | 100% |
A4I1E2 | Leishmania infantum | 97% | 100% |
C9ZJV9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 61% | 100% |
E9AXH9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
V5BGC6 | Trypanosoma cruzi | 65% | 100% |