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: 17 |
NetGPI | no | yes: 0, no: 17 |
Related structures:
AlphaFold database: E9ATC8
Term | Name | Level | Count |
---|---|---|---|
GO:0003352 | regulation of cilium movement | 6 | 18 |
GO:0032886 | regulation of microtubule-based process | 4 | 18 |
GO:0050789 | regulation of biological process | 2 | 18 |
GO:0050794 | regulation of cellular process | 3 | 18 |
GO:0060632 | regulation of microtubule-based movement | 5 | 18 |
GO:0065007 | biological regulation | 1 | 18 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 153 | 157 | PF00656 | 0.507 |
CLV_NRD_NRD_1 | 235 | 237 | PF00675 | 0.237 |
CLV_NRD_NRD_1 | 262 | 264 | PF00675 | 0.250 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.487 |
CLV_PCSK_PC1ET2_1 | 303 | 305 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 64 | 66 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.229 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 304 | 308 | PF00082 | 0.740 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 69 | 73 | PF00082 | 0.381 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.574 |
DEG_SPOP_SBC_1 | 294 | 298 | PF00917 | 0.511 |
DOC_CYCLIN_RxL_1 | 183 | 192 | PF00134 | 0.349 |
DOC_MAPK_gen_1 | 223 | 233 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 64 | 72 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 226 | 233 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 64 | 72 | PF00069 | 0.337 |
DOC_USP7_MATH_1 | 239 | 243 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.681 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.615 |
DOC_USP7_MATH_1 | 44 | 48 | PF00917 | 0.617 |
DOC_USP7_UBL2_3 | 228 | 232 | PF12436 | 0.451 |
DOC_WW_Pin1_4 | 28 | 33 | PF00397 | 0.667 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 141 | 148 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 304 | 310 | PF00244 | 0.531 |
LIG_EH1_1 | 65 | 73 | PF00400 | 0.491 |
LIG_eIF4E_1 | 183 | 189 | PF01652 | 0.335 |
LIG_FHA_1 | 142 | 148 | PF00498 | 0.260 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.451 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.703 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.417 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.601 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.553 |
LIG_FHA_2 | 151 | 157 | PF00498 | 0.433 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.524 |
LIG_LIR_Gen_1 | 115 | 124 | PF02991 | 0.448 |
LIG_LIR_Gen_1 | 146 | 155 | PF02991 | 0.524 |
LIG_LIR_LC3C_4 | 177 | 182 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 264 | 269 | PF02991 | 0.449 |
LIG_PCNA_PIPBox_1 | 111 | 120 | PF02747 | 0.326 |
LIG_PCNA_yPIPBox_3 | 109 | 118 | PF02747 | 0.535 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.418 |
LIG_SH2_CRK | 118 | 122 | PF00017 | 0.454 |
LIG_SH2_CRK | 148 | 152 | PF00017 | 0.341 |
LIG_SH2_STAT3 | 249 | 252 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 166 | 169 | PF00017 | 0.612 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.516 |
LIG_SH3_2 | 326 | 331 | PF14604 | 0.539 |
LIG_SH3_3 | 323 | 329 | PF00018 | 0.534 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.759 |
LIG_TRAF2_1 | 27 | 30 | PF00917 | 0.555 |
LIG_TRAF2_1 | 74 | 77 | PF00917 | 0.510 |
LIG_UBA3_1 | 113 | 122 | PF00899 | 0.273 |
MOD_CDK_SPK_2 | 28 | 33 | PF00069 | 0.517 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.400 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.730 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.576 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.655 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.733 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.726 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.431 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.536 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.580 |
MOD_CK2_1 | 295 | 301 | PF00069 | 0.555 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.336 |
MOD_Cter_Amidation | 301 | 304 | PF01082 | 0.466 |
MOD_GlcNHglycan | 310 | 313 | PF01048 | 0.766 |
MOD_GlcNHglycan | 73 | 76 | PF01048 | 0.375 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.501 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.602 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.646 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.736 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.649 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.432 |
MOD_NEK2_1 | 213 | 218 | PF00069 | 0.471 |
MOD_NEK2_1 | 305 | 310 | PF00069 | 0.733 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.430 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.499 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.511 |
MOD_Plk_1 | 213 | 219 | PF00069 | 0.490 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.533 |
MOD_Plk_4 | 143 | 149 | PF00069 | 0.484 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.605 |
MOD_Plk_4 | 77 | 83 | PF00069 | 0.383 |
MOD_ProDKin_1 | 28 | 34 | PF00069 | 0.667 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.512 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.666 |
MOD_SUMO_rev_2 | 190 | 195 | PF00179 | 0.503 |
MOD_SUMO_rev_2 | 296 | 305 | PF00179 | 0.447 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 284 | 289 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 118 | 121 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 148 | 151 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.422 |
TRG_ER_diArg_1 | 245 | 248 | PF00400 | 0.500 |
TRG_Pf-PMV_PEXEL_1 | 186 | 190 | PF00026 | 0.319 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.663 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K9 | Leptomonas seymouri | 60% | 100% |
A0A0S4JE13 | Bodo saltans | 41% | 100% |
A0A0S4JHQ4 | Bodo saltans | 41% | 100% |
A0A0S4JRV9 | Bodo saltans | 23% | 100% |
A0A1X0P4D1 | Trypanosomatidae | 42% | 100% |
A0A3Q8IRH9 | Leishmania donovani | 22% | 100% |
A0A3R7NWF2 | Trypanosoma rangeli | 26% | 100% |
A0A3S7XB90 | Leishmania donovani | 91% | 100% |
A0A422MZF7 | Trypanosoma rangeli | 44% | 100% |
A4HPL6 | Leishmania braziliensis | 78% | 100% |
A4ID48 | Leishmania infantum | 91% | 100% |
A4IDM9 | Leishmania infantum | 22% | 100% |
D0A8J8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 100% |
Q4Q169 | Leishmania major | 90% | 100% |
V5B520 | Trypanosoma cruzi | 24% | 100% |
V5B6Z0 | Trypanosoma cruzi | 42% | 100% |