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. | 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: 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: Q4Q407
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016874 | ligase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 347 | 351 | PF00656 | 0.331 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.465 |
DEG_APCC_KENBOX_2 | 207 | 211 | PF00400 | 0.519 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 162 | 171 | PF00134 | 0.399 |
DOC_MAPK_FxFP_2 | 122 | 125 | PF00069 | 0.453 |
DOC_MAPK_gen_1 | 355 | 361 | PF00069 | 0.431 |
DOC_MAPK_gen_1 | 8 | 16 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 11 | 18 | PF00069 | 0.388 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.534 |
DOC_USP7_MATH_1 | 232 | 236 | PF00917 | 0.435 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.588 |
LIG_14-3-3_CanoR_1 | 120 | 125 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 168 | 172 | PF00244 | 0.391 |
LIG_14-3-3_CanoR_1 | 233 | 237 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 267 | 271 | PF00244 | 0.329 |
LIG_Actin_WH2_2 | 152 | 170 | PF00022 | 0.483 |
LIG_APCC_ABBA_1 | 14 | 19 | PF00400 | 0.393 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.470 |
LIG_BRCT_BRCA1_1 | 215 | 219 | PF00533 | 0.508 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.399 |
LIG_CaM_NSCaTE_8 | 187 | 194 | PF13499 | 0.286 |
LIG_deltaCOP1_diTrp_1 | 186 | 190 | PF00928 | 0.340 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.379 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.389 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.462 |
LIG_HP1_1 | 232 | 236 | PF01393 | 0.394 |
LIG_LIR_Apic_2 | 119 | 125 | PF02991 | 0.539 |
LIG_LIR_Apic_2 | 147 | 153 | PF02991 | 0.397 |
LIG_LIR_Apic_2 | 209 | 214 | PF02991 | 0.505 |
LIG_LIR_Apic_2 | 354 | 360 | PF02991 | 0.482 |
LIG_LIR_Gen_1 | 268 | 278 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 318 | 329 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 170 | 176 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 186 | 190 | PF02991 | 0.486 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 268 | 273 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 316 | 322 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 81 | 85 | PF02991 | 0.379 |
LIG_MLH1_MIPbox_1 | 317 | 321 | PF16413 | 0.399 |
LIG_PDZ_Class_1 | 383 | 388 | PF00595 | 0.518 |
LIG_Pex14_1 | 58 | 62 | PF04695 | 0.487 |
LIG_Pex14_2 | 169 | 173 | PF04695 | 0.312 |
LIG_PTB_Apo_2 | 238 | 245 | PF02174 | 0.370 |
LIG_REV1ctd_RIR_1 | 217 | 225 | PF16727 | 0.431 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.522 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.406 |
LIG_SH2_GRB2like | 239 | 242 | PF00017 | 0.372 |
LIG_SH2_PTP2 | 150 | 153 | PF00017 | 0.350 |
LIG_SH2_PTP2 | 211 | 214 | PF00017 | 0.426 |
LIG_SH2_SRC | 150 | 153 | PF00017 | 0.350 |
LIG_SH2_SRC | 211 | 214 | PF00017 | 0.426 |
LIG_SH2_SRC | 239 | 242 | PF00017 | 0.372 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.413 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.395 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 320 | 323 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 372 | 375 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 62 | 65 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.386 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.444 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.593 |
LIG_SUMO_SIM_par_1 | 335 | 341 | PF11976 | 0.364 |
LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.345 |
MOD_CK1_1 | 235 | 241 | PF00069 | 0.620 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.362 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.543 |
MOD_GlcNHglycan | 199 | 202 | PF01048 | 0.394 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.248 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.625 |
MOD_GlcNHglycan | 263 | 266 | PF01048 | 0.479 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.499 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.406 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.456 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.504 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.474 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.382 |
MOD_NEK2_1 | 158 | 163 | PF00069 | 0.379 |
MOD_NEK2_1 | 167 | 172 | PF00069 | 0.387 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.474 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.420 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.420 |
MOD_PIKK_1 | 310 | 316 | PF00454 | 0.569 |
MOD_PKA_1 | 120 | 126 | PF00069 | 0.491 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.486 |
MOD_PKA_2 | 232 | 238 | PF00069 | 0.411 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.445 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.487 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.432 |
MOD_Plk_1 | 332 | 338 | PF00069 | 0.382 |
MOD_Plk_2-3 | 332 | 338 | PF00069 | 0.358 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.416 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.430 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.434 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.329 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.460 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.373 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.430 |
MOD_SUMO_for_1 | 100 | 103 | PF00179 | 0.489 |
TRG_DiLeu_BaEn_2 | 185 | 191 | PF01217 | 0.312 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.528 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 319 | 322 | PF00928 | 0.348 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.490 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.558 |
TRG_Pf-PMV_PEXEL_1 | 365 | 369 | PF00026 | 0.291 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM57 | Leptomonas seymouri | 67% | 95% |
A0A0S4JGX9 | Bodo saltans | 38% | 100% |
A0A1X0P3L5 | Trypanosomatidae | 48% | 100% |
A0A3Q8IME8 | Leishmania donovani | 95% | 100% |
A0A422N3E6 | Trypanosoma rangeli | 49% | 97% |
A4HLP1 | Leishmania braziliensis | 85% | 100% |
A4I976 | Leishmania infantum | 95% | 100% |
D0A6D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 99% |
E9B417 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BTX0 | Trypanosoma cruzi | 47% | 100% |