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: 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: A4HLP1
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 | 84 | 88 | PF00656 | 0.379 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.391 |
CLV_PCSK_KEX2_1 | 115 | 117 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 116 | 120 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.433 |
DEG_APCC_KENBOX_2 | 208 | 212 | PF00400 | 0.497 |
DOC_CKS1_1 | 240 | 245 | PF01111 | 0.334 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 163 | 172 | PF00134 | 0.403 |
DOC_MAPK_FxFP_2 | 122 | 125 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 356 | 362 | PF00069 | 0.412 |
DOC_PP4_FxxP_1 | 122 | 125 | PF00568 | 0.513 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.538 |
DOC_WW_Pin1_4 | 239 | 244 | PF00397 | 0.420 |
LIG_14-3-3_CanoR_1 | 120 | 125 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 234 | 243 | PF00244 | 0.439 |
LIG_APCC_ABBA_1 | 14 | 19 | PF00400 | 0.347 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.435 |
LIG_BRCT_BRCA1_1 | 189 | 193 | PF00533 | 0.237 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 237 | 241 | PF00533 | 0.470 |
LIG_BRCT_BRCA1_1 | 321 | 325 | PF00533 | 0.298 |
LIG_deltaCOP1_diTrp_1 | 186 | 193 | PF00928 | 0.325 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.363 |
LIG_FHA_2 | 32 | 38 | PF00498 | 0.422 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.389 |
LIG_HP1_1 | 233 | 237 | PF01393 | 0.385 |
LIG_KLC1_Yacidic_2 | 83 | 87 | PF13176 | 0.258 |
LIG_LIR_Apic_2 | 119 | 125 | PF02991 | 0.517 |
LIG_LIR_Apic_2 | 210 | 215 | PF02991 | 0.486 |
LIG_LIR_Apic_2 | 238 | 243 | PF02991 | 0.323 |
LIG_LIR_Apic_2 | 355 | 361 | PF02991 | 0.459 |
LIG_LIR_Apic_2 | 73 | 78 | PF02991 | 0.504 |
LIG_LIR_Apic_2 | 87 | 93 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 147 | 157 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 269 | 279 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 130 | 135 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 146 | 152 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 225 | 231 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 269 | 274 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 47 | 51 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 81 | 85 | PF02991 | 0.350 |
LIG_MLH1_MIPbox_1 | 237 | 241 | PF16413 | 0.470 |
LIG_MLH1_MIPbox_1 | 321 | 325 | PF16413 | 0.298 |
LIG_Pex14_1 | 58 | 62 | PF04695 | 0.479 |
LIG_Pex14_2 | 170 | 174 | PF04695 | 0.292 |
LIG_Pex14_2 | 241 | 245 | PF04695 | 0.425 |
LIG_PTB_Apo_2 | 368 | 375 | PF02174 | 0.289 |
LIG_REV1ctd_RIR_1 | 218 | 226 | PF16727 | 0.425 |
LIG_SH2_CRK | 132 | 136 | PF00017 | 0.491 |
LIG_SH2_CRK | 150 | 154 | PF00017 | 0.214 |
LIG_SH2_CRK | 358 | 362 | PF00017 | 0.390 |
LIG_SH2_CRK | 75 | 79 | PF00017 | 0.377 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.277 |
LIG_SH2_GRB2like | 149 | 152 | PF00017 | 0.258 |
LIG_SH2_NCK_1 | 150 | 154 | PF00017 | 0.355 |
LIG_SH2_PTP2 | 212 | 215 | PF00017 | 0.435 |
LIG_SH2_SRC | 212 | 215 | PF00017 | 0.435 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.219 |
LIG_SH2_STAP1 | 82 | 86 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 228 | 231 | PF00017 | 0.263 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 358 | 361 | PF00017 | 0.314 |
LIG_SH2_STAT5 | 373 | 376 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 90 | 93 | PF00017 | 0.438 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.419 |
LIG_SH3_3 | 66 | 72 | PF00018 | 0.607 |
LIG_SUMO_SIM_par_1 | 336 | 342 | PF11976 | 0.339 |
LIG_TRAF2_1 | 244 | 247 | PF00917 | 0.329 |
LIG_WRC_WIRS_1 | 174 | 179 | PF05994 | 0.323 |
MOD_CK1_1 | 179 | 185 | PF00069 | 0.462 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.459 |
MOD_CK1_1 | 333 | 339 | PF00069 | 0.443 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.385 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.344 |
MOD_CK2_1 | 241 | 247 | PF00069 | 0.529 |
MOD_CK2_1 | 97 | 103 | PF00069 | 0.399 |
MOD_GlcNHglycan | 180 | 184 | PF01048 | 0.235 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.388 |
MOD_GlcNHglycan | 216 | 219 | PF01048 | 0.220 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.470 |
MOD_GlcNHglycan | 75 | 78 | PF01048 | 0.493 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.418 |
MOD_GSK3_1 | 235 | 242 | PF00069 | 0.464 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.441 |
MOD_GSK3_1 | 81 | 88 | PF00069 | 0.337 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.358 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.335 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.325 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.447 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.401 |
MOD_NEK2_2 | 85 | 90 | PF00069 | 0.426 |
MOD_PIKK_1 | 311 | 317 | PF00454 | 0.547 |
MOD_PKA_1 | 120 | 126 | PF00069 | 0.474 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.404 |
MOD_PKA_2 | 7 | 13 | PF00069 | 0.483 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.359 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.361 |
MOD_Plk_1 | 333 | 339 | PF00069 | 0.358 |
MOD_Plk_4 | 20 | 26 | PF00069 | 0.406 |
MOD_Plk_4 | 216 | 222 | PF00069 | 0.411 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.230 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.359 |
MOD_Plk_4 | 333 | 339 | PF00069 | 0.341 |
MOD_Plk_4 | 345 | 351 | PF00069 | 0.349 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.251 |
MOD_ProDKin_1 | 239 | 245 | PF00069 | 0.414 |
TRG_DiLeu_BaEn_3 | 186 | 192 | PF01217 | 0.262 |
TRG_ENDOCYTIC_2 | 132 | 135 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 149 | 152 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 320 | 323 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 48 | 51 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 114 | 116 | PF00400 | 0.468 |
TRG_ER_FFAT_2 | 236 | 246 | PF00635 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 3 | 7 | PF00026 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM57 | Leptomonas seymouri | 69% | 95% |
A0A0S4JGX9 | Bodo saltans | 38% | 100% |
A0A1X0P3L5 | Trypanosomatidae | 48% | 100% |
A0A3Q8IME8 | Leishmania donovani | 85% | 100% |
A0A422N3E6 | Trypanosoma rangeli | 48% | 97% |
A4I976 | Leishmania infantum | 86% | 100% |
D0A6D2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9B417 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q407 | Leishmania major | 85% | 100% |
V5BTX0 | Trypanosoma cruzi | 48% | 100% |