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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005829 | cytosol | 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: A0A3S7WZ42
Term | Name | Level | Count |
---|---|---|---|
GO:0009966 | regulation of signal transduction | 4 | 10 |
GO:0010646 | regulation of cell communication | 4 | 10 |
GO:0023051 | regulation of signaling | 3 | 10 |
GO:0048583 | regulation of response to stimulus | 3 | 10 |
GO:0050789 | regulation of biological process | 2 | 10 |
GO:0050794 | regulation of cellular process | 3 | 10 |
GO:0065007 | biological regulation | 1 | 10 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0035303 | regulation of dephosphorylation | 7 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0019899 | enzyme binding | 3 | 1 |
GO:0019902 | phosphatase binding | 4 | 1 |
GO:0019903 | protein phosphatase binding | 5 | 1 |
GO:0051721 | protein phosphatase 2A binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 138 | 142 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 314 | 318 | PF00656 | 0.502 |
CLV_NRD_NRD_1 | 244 | 246 | PF00675 | 0.330 |
CLV_NRD_NRD_1 | 320 | 322 | PF00675 | 0.320 |
CLV_PCSK_FUR_1 | 240 | 244 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 100 | 102 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 320 | 322 | PF00082 | 0.312 |
CLV_PCSK_PC1ET2_1 | 100 | 102 | PF00082 | 0.327 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.293 |
CLV_PCSK_PC7_1 | 240 | 246 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.302 |
DEG_MDM2_SWIB_1 | 52 | 59 | PF02201 | 0.530 |
DEG_SPOP_SBC_1 | 370 | 374 | PF00917 | 0.480 |
DOC_ANK_TNKS_1 | 436 | 443 | PF00023 | 0.394 |
DOC_CKS1_1 | 82 | 87 | PF01111 | 0.447 |
DOC_CYCLIN_yCln2_LP_2 | 82 | 88 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 320 | 326 | PF00069 | 0.466 |
DOC_MAPK_MEF2A_6 | 178 | 187 | PF00069 | 0.551 |
DOC_PP1_RVXF_1 | 182 | 188 | PF00149 | 0.530 |
DOC_PP1_RVXF_1 | 273 | 279 | PF00149 | 0.448 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 370 | 374 | PF00917 | 0.517 |
DOC_USP7_MATH_2 | 137 | 143 | PF00917 | 0.524 |
DOC_WW_Pin1_4 | 63 | 68 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 81 | 86 | PF00397 | 0.451 |
LIG_14-3-3_CanoR_1 | 220 | 226 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 328 | 332 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 348 | 356 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 57 | 65 | PF00244 | 0.530 |
LIG_APCC_ABBA_1 | 183 | 188 | PF00400 | 0.530 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.535 |
LIG_CSL_BTD_1 | 82 | 85 | PF09270 | 0.465 |
LIG_deltaCOP1_diTrp_1 | 451 | 457 | PF00928 | 0.490 |
LIG_DLG_GKlike_1 | 292 | 300 | PF00625 | 0.502 |
LIG_eIF4E_1 | 86 | 92 | PF01652 | 0.502 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.530 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.450 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.513 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.447 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.447 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.447 |
LIG_FHA_2 | 258 | 264 | PF00498 | 0.490 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.489 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.490 |
LIG_HOMEOBOX | 187 | 190 | PF00046 | 0.530 |
LIG_LIR_Gen_1 | 10 | 18 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 330 | 339 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 408 | 417 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 51 | 59 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 10 | 14 | PF02991 | 0.582 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 330 | 334 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 408 | 412 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 51 | 55 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 80 | 86 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.511 |
LIG_Pex14_1 | 182 | 186 | PF04695 | 0.465 |
LIG_Pex14_2 | 52 | 56 | PF04695 | 0.490 |
LIG_RPA_C_Fungi | 215 | 227 | PF08784 | 0.360 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.284 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.373 |
LIG_SH2_STAT3 | 387 | 390 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.308 |
LIG_SH3_3 | 131 | 137 | PF00018 | 0.532 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.372 |
LIG_SH3_3 | 358 | 364 | PF00018 | 0.253 |
LIG_SH3_3 | 92 | 98 | PF00018 | 0.365 |
LIG_SUMO_SIM_anti_2 | 191 | 197 | PF11976 | 0.312 |
LIG_TRAF2_1 | 171 | 174 | PF00917 | 0.324 |
LIG_TRAF2_1 | 231 | 234 | PF00917 | 0.167 |
LIG_TRAF2_1 | 256 | 259 | PF00917 | 0.400 |
LIG_TRAF2_1 | 405 | 408 | PF00917 | 0.286 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.732 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.577 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.353 |
MOD_CK2_1 | 121 | 127 | PF00069 | 0.666 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.533 |
MOD_CK2_1 | 168 | 174 | PF00069 | 0.327 |
MOD_CK2_1 | 257 | 263 | PF00069 | 0.399 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.236 |
MOD_CK2_1 | 287 | 293 | PF00069 | 0.289 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.307 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.344 |
MOD_CMANNOS | 454 | 457 | PF00535 | 0.344 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.741 |
MOD_GlcNHglycan | 141 | 144 | PF01048 | 0.551 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.583 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.431 |
MOD_GlcNHglycan | 451 | 454 | PF01048 | 0.356 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.379 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.660 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.662 |
MOD_GSK3_1 | 146 | 153 | PF00069 | 0.540 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.363 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.360 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.244 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.405 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.300 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.645 |
MOD_N-GLC_1 | 155 | 160 | PF02516 | 0.516 |
MOD_N-GLC_1 | 2 | 7 | PF02516 | 0.610 |
MOD_N-GLC_1 | 30 | 35 | PF02516 | 0.404 |
MOD_NEK2_1 | 176 | 181 | PF00069 | 0.304 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.434 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.400 |
MOD_NEK2_1 | 276 | 281 | PF00069 | 0.325 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.315 |
MOD_PIKK_1 | 210 | 216 | PF00454 | 0.308 |
MOD_PKA_2 | 135 | 141 | PF00069 | 0.723 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.293 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.354 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.251 |
MOD_Plk_1 | 264 | 270 | PF00069 | 0.360 |
MOD_Plk_1 | 292 | 298 | PF00069 | 0.408 |
MOD_Plk_1 | 30 | 36 | PF00069 | 0.420 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.308 |
MOD_Plk_1 | 37 | 43 | PF00069 | 0.351 |
MOD_Plk_2-3 | 197 | 203 | PF00069 | 0.333 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.340 |
MOD_Plk_4 | 292 | 298 | PF00069 | 0.429 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.284 |
MOD_ProDKin_1 | 63 | 69 | PF00069 | 0.313 |
MOD_ProDKin_1 | 81 | 87 | PF00069 | 0.289 |
MOD_SUMO_for_1 | 229 | 232 | PF00179 | 0.360 |
MOD_SUMO_rev_2 | 191 | 201 | PF00179 | 0.312 |
MOD_SUMO_rev_2 | 232 | 236 | PF00179 | 0.400 |
TRG_DiLeu_BaEn_1 | 191 | 196 | PF01217 | 0.312 |
TRG_DiLeu_BaEn_4 | 165 | 171 | PF01217 | 0.360 |
TRG_DiLeu_BaEn_4 | 263 | 269 | PF01217 | 0.332 |
TRG_DiLeu_BaEn_4 | 433 | 439 | PF01217 | 0.308 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.284 |
TRG_ER_diArg_1 | 243 | 245 | PF00400 | 0.293 |
TRG_ER_diArg_1 | 268 | 271 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 319 | 321 | PF00400 | 0.354 |
TRG_NLS_MonoCore_2 | 241 | 246 | PF00514 | 0.308 |
TRG_NLS_MonoExtN_4 | 240 | 246 | PF00514 | 0.317 |
TRG_Pf-PMV_PEXEL_1 | 160 | 164 | PF00026 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 168 | 173 | PF00026 | 0.384 |
TRG_Pf-PMV_PEXEL_1 | 247 | 252 | PF00026 | 0.344 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.320 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCB4 | Leptomonas seymouri | 71% | 100% |
A0A0S4JC44 | Bodo saltans | 37% | 100% |
A0A1X0NM51 | Trypanosomatidae | 46% | 100% |
A4HE53 | Leishmania braziliensis | 84% | 100% |
A4I1I1 | Leishmania infantum | 100% | 100% |
C9ZJY7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9AXL6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4Q9V6 | Leishmania major | 94% | 100% |