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: 19 |
NetGPI | no | yes: 0, no: 19 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 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: A4HPL6
Term | Name | Level | Count |
---|---|---|---|
GO:0003352 | regulation of cilium movement | 6 | 20 |
GO:0032886 | regulation of microtubule-based process | 4 | 20 |
GO:0050789 | regulation of biological process | 2 | 20 |
GO:0050794 | regulation of cellular process | 3 | 20 |
GO:0060632 | regulation of microtubule-based movement | 5 | 20 |
GO:0065007 | biological regulation | 1 | 20 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.242 |
CLV_NRD_NRD_1 | 261 | 263 | PF00675 | 0.279 |
CLV_NRD_NRD_1 | 328 | 330 | PF00675 | 0.691 |
CLV_NRD_NRD_1 | 86 | 88 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 261 | 263 | PF00082 | 0.258 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 86 | 88 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.405 |
CLV_PCSK_SKI1_1 | 286 | 290 | PF00082 | 0.285 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 68 | 72 | PF00082 | 0.369 |
DEG_SPOP_SBC_1 | 24 | 28 | PF00917 | 0.439 |
DOC_CYCLIN_RxL_1 | 182 | 191 | PF00134 | 0.342 |
DOC_CYCLIN_RxL_1 | 282 | 292 | PF00134 | 0.373 |
DOC_MAPK_gen_1 | 222 | 232 | PF00069 | 0.459 |
DOC_MAPK_gen_1 | 279 | 289 | PF00069 | 0.386 |
DOC_MAPK_gen_1 | 329 | 337 | PF00069 | 0.542 |
DOC_MAPK_gen_1 | 63 | 71 | PF00069 | 0.369 |
DOC_MAPK_MEF2A_6 | 225 | 232 | PF00069 | 0.457 |
DOC_MAPK_MEF2A_6 | 63 | 71 | PF00069 | 0.322 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 293 | 297 | PF00917 | 0.629 |
DOC_USP7_UBL2_3 | 227 | 231 | PF12436 | 0.461 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.454 |
DOC_WW_Pin1_4 | 299 | 304 | PF00397 | 0.717 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.651 |
LIG_14-3-3_CanoR_1 | 140 | 150 | PF00244 | 0.436 |
LIG_EH1_1 | 64 | 72 | PF00400 | 0.480 |
LIG_eIF4E_1 | 182 | 188 | PF01652 | 0.328 |
LIG_FHA_1 | 175 | 181 | PF00498 | 0.441 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.609 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.735 |
LIG_FHA_1 | 318 | 324 | PF00498 | 0.622 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.556 |
LIG_LIR_LC3C_4 | 176 | 181 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 162 | 168 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 263 | 268 | PF02991 | 0.451 |
LIG_LYPXL_S_1 | 146 | 150 | PF13949 | 0.394 |
LIG_LYPXL_yS_3 | 147 | 150 | PF13949 | 0.281 |
LIG_PCNA_yPIPBox_3 | 97 | 106 | PF02747 | 0.373 |
LIG_SH2_CRK | 109 | 113 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 168 | 172 | PF00017 | 0.361 |
LIG_SH2_SRC | 168 | 171 | PF00017 | 0.358 |
LIG_SH2_STAT3 | 248 | 251 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 219 | 222 | PF00017 | 0.543 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.752 |
LIG_TRAF2_1 | 73 | 76 | PF00917 | 0.502 |
LIG_UBA3_1 | 112 | 121 | PF00899 | 0.289 |
LIG_WRC_WIRS_1 | 139 | 144 | PF05994 | 0.247 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.399 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.696 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.644 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.738 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.728 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.390 |
MOD_CK2_1 | 125 | 131 | PF00069 | 0.335 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.450 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.676 |
MOD_CK2_1 | 70 | 76 | PF00069 | 0.338 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.458 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.770 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.362 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.466 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.627 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.693 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.733 |
MOD_GSK3_1 | 36 | 43 | PF00069 | 0.582 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.592 |
MOD_N-GLC_1 | 154 | 159 | PF02516 | 0.620 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.483 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.489 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.524 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.422 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.466 |
MOD_PKA_1 | 261 | 267 | PF00069 | 0.392 |
MOD_PKA_2 | 261 | 267 | PF00069 | 0.467 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.402 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.472 |
MOD_PKA_2 | 49 | 55 | PF00069 | 0.450 |
MOD_Plk_1 | 13 | 19 | PF00069 | 0.416 |
MOD_Plk_1 | 174 | 180 | PF00069 | 0.538 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.491 |
MOD_Plk_2-3 | 13 | 19 | PF00069 | 0.451 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.568 |
MOD_Plk_4 | 76 | 82 | PF00069 | 0.391 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.456 |
MOD_ProDKin_1 | 299 | 305 | PF00069 | 0.718 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.648 |
MOD_SUMO_for_1 | 166 | 169 | PF00179 | 0.319 |
MOD_SUMO_rev_2 | 189 | 194 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_1 | 175 | 180 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.416 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.519 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.472 |
TRG_ENDOCYTIC_2 | 265 | 268 | PF00928 | 0.424 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.282 |
TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.501 |
TRG_ER_diArg_1 | 86 | 88 | PF00400 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 118 | 122 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 185 | 189 | PF00026 | 0.308 |
TRG_Pf-PMV_PEXEL_1 | 19 | 23 | PF00026 | 0.546 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I4K9 | Leptomonas seymouri | 60% | 100% |
A0A0S4JE13 | Bodo saltans | 37% | 100% |
A0A0S4JHQ4 | Bodo saltans | 37% | 100% |
A0A1X0P0N8 | Trypanosomatidae | 25% | 100% |
A0A1X0P4D1 | Trypanosomatidae | 43% | 100% |
A0A3Q8IRH9 | Leishmania donovani | 24% | 100% |
A0A3S7XB90 | Leishmania donovani | 77% | 100% |
A0A422MZF7 | Trypanosoma rangeli | 43% | 100% |
A4HPW7 | Leishmania braziliensis | 25% | 100% |
A4ID48 | Leishmania infantum | 77% | 100% |
A4IDM9 | Leishmania infantum | 24% | 100% |
D0A4B5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0A8J8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9ATC8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
E9ATN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q0W4 | Leishmania major | 25% | 100% |
Q4Q169 | Leishmania major | 77% | 100% |
V5B6Z0 | Trypanosoma cruzi | 43% | 100% |