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: E9B6W9
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_C14_Caspase3-7 | 392 | 396 | PF00656 | 0.736 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.478 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 313 | 315 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 313 | 315 | PF00082 | 0.564 |
CLV_PCSK_PC7_1 | 309 | 315 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 143 | 147 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.499 |
CLV_PCSK_SKI1_1 | 344 | 348 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.406 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.554 |
DOC_CYCLIN_yCln2_LP_2 | 132 | 138 | PF00134 | 0.324 |
DOC_MAPK_gen_1 | 123 | 132 | PF00069 | 0.495 |
DOC_MAPK_gen_1 | 80 | 89 | PF00069 | 0.263 |
DOC_MAPK_HePTP_8 | 162 | 174 | PF00069 | 0.507 |
DOC_MAPK_MEF2A_6 | 112 | 120 | PF00069 | 0.482 |
DOC_MAPK_MEF2A_6 | 165 | 174 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 324 | 333 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 82 | 91 | PF00069 | 0.340 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.486 |
DOC_PP4_FxxP_1 | 356 | 359 | PF00568 | 0.543 |
DOC_USP7_MATH_1 | 187 | 191 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 230 | 234 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 51 | 55 | PF00917 | 0.247 |
DOC_USP7_UBL2_3 | 143 | 147 | PF12436 | 0.514 |
DOC_USP7_UBL2_3 | 22 | 26 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 12 | 17 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 273 | 278 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 201 | 205 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 213 | 222 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 271 | 277 | PF00244 | 0.444 |
LIG_14-3-3_CanoR_1 | 314 | 323 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 350 | 359 | PF00244 | 0.449 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.699 |
LIG_BRCT_BRCA1_1 | 352 | 356 | PF00533 | 0.447 |
LIG_deltaCOP1_diTrp_1 | 368 | 374 | PF00928 | 0.384 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.321 |
LIG_FHA_2 | 237 | 243 | PF00498 | 0.222 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.489 |
LIG_FHA_2 | 379 | 385 | PF00498 | 0.670 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.668 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.584 |
LIG_LIR_Apic_2 | 122 | 127 | PF02991 | 0.488 |
LIG_LIR_Apic_2 | 353 | 359 | PF02991 | 0.545 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 217 | 227 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 203 | 208 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 246 | 252 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 48 | 52 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 53 | 59 | PF02991 | 0.351 |
LIG_Pex14_1 | 370 | 374 | PF04695 | 0.383 |
LIG_SH2_CRK | 241 | 245 | PF00017 | 0.330 |
LIG_SH2_GRB2like | 378 | 381 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 161 | 164 | PF00017 | 0.490 |
LIG_SH2_STAP1 | 249 | 253 | PF00017 | 0.520 |
LIG_SH2_STAP1 | 378 | 382 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 136 | 139 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 161 | 164 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 221 | 224 | PF00017 | 0.331 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.445 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.569 |
LIG_SUMO_SIM_anti_2 | 57 | 65 | PF11976 | 0.514 |
LIG_SUMO_SIM_anti_2 | 85 | 92 | PF11976 | 0.248 |
LIG_TRAF2_1 | 277 | 280 | PF00917 | 0.624 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.484 |
LIG_TYR_ITIM | 247 | 252 | PF00017 | 0.423 |
LIG_TYR_ITSM | 237 | 244 | PF00017 | 0.217 |
LIG_WRC_WIRS_1 | 216 | 221 | PF05994 | 0.339 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.766 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.467 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.589 |
MOD_CK2_1 | 187 | 193 | PF00069 | 0.490 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.467 |
MOD_CK2_1 | 378 | 384 | PF00069 | 0.619 |
MOD_Cter_Amidation | 23 | 26 | PF01082 | 0.469 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.501 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.483 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.763 |
MOD_GSK3_1 | 14 | 21 | PF00069 | 0.685 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.340 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.621 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.444 |
MOD_GSK3_1 | 374 | 381 | PF00069 | 0.497 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.594 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.554 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.745 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.335 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.488 |
MOD_PIKK_1 | 350 | 356 | PF00454 | 0.424 |
MOD_PIKK_1 | 37 | 43 | PF00454 | 0.568 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.408 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.444 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.560 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.511 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.447 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.586 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.555 |
MOD_Plk_1 | 389 | 395 | PF00069 | 0.678 |
MOD_Plk_1 | 45 | 51 | PF00069 | 0.434 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.325 |
MOD_Plk_4 | 236 | 242 | PF00069 | 0.271 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.494 |
MOD_ProDKin_1 | 12 | 18 | PF00069 | 0.598 |
MOD_ProDKin_1 | 273 | 279 | PF00069 | 0.530 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.662 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.547 |
TRG_DiLeu_BaEn_1 | 58 | 63 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_1 | 97 | 102 | PF01217 | 0.424 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.339 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.490 |
TRG_ENDOCYTIC_2 | 205 | 208 | PF00928 | 0.347 |
TRG_ENDOCYTIC_2 | 221 | 224 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 249 | 252 | PF00928 | 0.356 |
TRG_ER_diArg_1 | 118 | 121 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.521 |
TRG_NLS_MonoExtN_4 | 22 | 29 | PF00514 | 0.458 |
TRG_Pf-PMV_PEXEL_1 | 99 | 104 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P968 | Leptomonas seymouri | 74% | 100% |
A0A0S4JSR6 | Bodo saltans | 45% | 71% |
A0A1X0P6F9 | Trypanosomatidae | 58% | 100% |
A0A3R7KSW5 | Trypanosoma rangeli | 53% | 100% |
A0A3S7X9V3 | Leishmania donovani | 91% | 100% |
A4HNA8 | Leishmania braziliensis | 80% | 100% |
A4IBX9 | Leishmania infantum | 91% | 100% |
C9ZYM8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9AFR6 | Leishmania major | 89% | 100% |
V5BXU3 | Trypanosoma cruzi | 54% | 100% |