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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0032838 | plasma membrane bounded cell projection cytoplasm | 4 | 1 |
GO:0097014 | ciliary plasm | 5 | 1 |
GO:0099568 | cytoplasmic region | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HNA8
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004427 | inorganic diphosphate phosphatase activity | 6 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 259 | 261 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 144 | 146 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 259 | 261 | PF00082 | 0.446 |
CLV_PCSK_KEX2_1 | 310 | 312 | PF00082 | 0.556 |
CLV_PCSK_PC1ET2_1 | 144 | 146 | PF00082 | 0.513 |
CLV_PCSK_PC1ET2_1 | 22 | 24 | PF00082 | 0.765 |
CLV_PCSK_PC1ET2_1 | 310 | 312 | PF00082 | 0.556 |
CLV_PCSK_PC7_1 | 306 | 312 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 96 | 100 | PF00082 | 0.399 |
DOC_CKS1_1 | 60 | 65 | PF01111 | 0.562 |
DOC_MAPK_gen_1 | 120 | 129 | PF00069 | 0.493 |
DOC_MAPK_HePTP_8 | 159 | 171 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 109 | 117 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 162 | 171 | PF00069 | 0.469 |
DOC_MAPK_MEF2A_6 | 321 | 330 | PF00069 | 0.339 |
DOC_PP4_FxxP_1 | 353 | 356 | PF00568 | 0.539 |
DOC_USP7_MATH_1 | 184 | 188 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.403 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.776 |
DOC_USP7_UBL2_3 | 18 | 22 | PF12436 | 0.549 |
DOC_WW_Pin1_4 | 315 | 320 | PF00397 | 0.366 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 138 | 146 | PF00244 | 0.484 |
LIG_14-3-3_CanoR_1 | 210 | 219 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.625 |
LIG_Actin_WH2_2 | 148 | 164 | PF00022 | 0.266 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.656 |
LIG_BRCT_BRCA1_1 | 349 | 353 | PF00533 | 0.435 |
LIG_deltaCOP1_diTrp_1 | 365 | 371 | PF00928 | 0.380 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.273 |
LIG_FHA_1 | 162 | 168 | PF00498 | 0.454 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.337 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.401 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.367 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.482 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.587 |
LIG_LIR_Apic_2 | 350 | 356 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 2 | 7 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 214 | 224 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 50 | 60 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 214 | 219 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 243 | 249 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.350 |
LIG_Pex14_1 | 367 | 371 | PF04695 | 0.379 |
LIG_SH2_CRK | 238 | 242 | PF00017 | 0.329 |
LIG_SH2_CRK | 3 | 7 | PF00017 | 0.492 |
LIG_SH2_PTP2 | 158 | 161 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 246 | 250 | PF00017 | 0.519 |
LIG_SH2_STAP1 | 269 | 273 | PF00017 | 0.393 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.592 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 158 | 161 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 269 | 272 | PF00017 | 0.436 |
LIG_SH3_3 | 353 | 359 | PF00018 | 0.568 |
LIG_SUMO_SIM_anti_2 | 54 | 62 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 54 | 62 | PF11976 | 0.512 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.616 |
LIG_TYR_ITIM | 200 | 205 | PF00017 | 0.263 |
LIG_TYR_ITIM | 244 | 249 | PF00017 | 0.422 |
LIG_WRC_WIRS_1 | 213 | 218 | PF05994 | 0.342 |
MOD_CDC14_SPxK_1 | 318 | 321 | PF00782 | 0.379 |
MOD_CDK_SPxK_1 | 315 | 321 | PF00069 | 0.410 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.644 |
MOD_CK2_1 | 184 | 190 | PF00069 | 0.488 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.463 |
MOD_CK2_1 | 366 | 372 | PF00069 | 0.403 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.514 |
MOD_GlcNHglycan | 81 | 84 | PF01048 | 0.479 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.722 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.622 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.470 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.476 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.408 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.727 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.278 |
MOD_N-GLC_1 | 42 | 47 | PF02516 | 0.546 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.702 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.326 |
MOD_NEK2_1 | 7 | 12 | PF00069 | 0.668 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.351 |
MOD_PIKK_1 | 137 | 143 | PF00454 | 0.276 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.569 |
MOD_PIKK_1 | 347 | 353 | PF00454 | 0.413 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.471 |
MOD_PKB_1 | 77 | 85 | PF00069 | 0.507 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.441 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.587 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.428 |
MOD_ProDKin_1 | 315 | 321 | PF00069 | 0.361 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.554 |
MOD_SUMO_for_1 | 383 | 386 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_1 | 55 | 60 | PF01217 | 0.383 |
TRG_DiLeu_BaEn_1 | 94 | 99 | PF01217 | 0.415 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 158 | 161 | PF00928 | 0.488 |
TRG_ENDOCYTIC_2 | 202 | 205 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 218 | 221 | PF00928 | 0.330 |
TRG_ENDOCYTIC_2 | 238 | 241 | PF00928 | 0.227 |
TRG_ENDOCYTIC_2 | 246 | 249 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.575 |
TRG_ER_diArg_1 | 115 | 118 | PF00400 | 0.460 |
TRG_ER_diArg_1 | 77 | 80 | PF00400 | 0.518 |
TRG_Pf-PMV_PEXEL_1 | 96 | 101 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P968 | Leptomonas seymouri | 75% | 100% |
A0A0S4JSR6 | Bodo saltans | 44% | 70% |
A0A1X0P6F9 | Trypanosomatidae | 54% | 100% |
A0A3R7KSW5 | Trypanosoma rangeli | 53% | 100% |
A0A3S7X9V3 | Leishmania donovani | 81% | 99% |
A4IBX9 | Leishmania infantum | 82% | 99% |
C9ZYM8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9AFR6 | Leishmania major | 80% | 100% |
E9B6W9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
V5BXU3 | Trypanosoma cruzi | 53% | 100% |