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: 5 |
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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005930 | axoneme | 2 | 1 |
GO:0030992 | intraciliary transport particle B | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WWV8
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007018 | microtubule-based movement | 3 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010970 | transport along microtubule | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0030705 | cytoskeleton-dependent intracellular transport | 4 | 1 |
GO:0031503 | protein-containing complex localization | 2 | 1 |
GO:0032886 | regulation of microtubule-based process | 4 | 1 |
GO:0033043 | regulation of organelle organization | 5 | 1 |
GO:0042073 | intraciliary transport | 3 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051128 | regulation of cellular component organization | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051493 | regulation of cytoskeleton organization | 6 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0070507 | regulation of microtubule cytoskeleton organization | 5 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0099111 | microtubule-based transport | 4 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 6 |
GO:0005515 | protein binding | 2 | 6 |
GO:0008017 | microtubule binding | 5 | 6 |
GO:0008092 | cytoskeletal protein binding | 3 | 6 |
GO:0015631 | tubulin binding | 4 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.636 |
CLV_C14_Caspase3-7 | 55 | 59 | PF00656 | 0.636 |
CLV_NRD_NRD_1 | 125 | 127 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 174 | 176 | PF00675 | 0.568 |
CLV_NRD_NRD_1 | 223 | 225 | PF00675 | 0.786 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.850 |
CLV_NRD_NRD_1 | 333 | 335 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 428 | 430 | PF00675 | 0.435 |
CLV_PCSK_FUR_1 | 164 | 168 | PF00082 | 0.741 |
CLV_PCSK_FUR_1 | 172 | 176 | PF00082 | 0.654 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.631 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 180 | 182 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.725 |
CLV_PCSK_KEX2_1 | 273 | 275 | PF00082 | 0.863 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 333 | 335 | PF00082 | 0.321 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.767 |
CLV_PCSK_PC1ET2_1 | 180 | 182 | PF00082 | 0.514 |
CLV_PCSK_PC1ET2_1 | 225 | 227 | PF00082 | 0.729 |
CLV_PCSK_PC1ET2_1 | 273 | 275 | PF00082 | 0.863 |
CLV_PCSK_PC1ET2_1 | 325 | 327 | PF00082 | 0.435 |
CLV_PCSK_PC7_1 | 168 | 174 | PF00082 | 0.759 |
CLV_PCSK_PC7_1 | 221 | 227 | PF00082 | 0.869 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.435 |
DEG_APCC_DBOX_1 | 378 | 386 | PF00400 | 0.636 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.691 |
DOC_MAPK_gen_1 | 65 | 71 | PF00069 | 0.636 |
DOC_MAPK_RevD_3 | 311 | 326 | PF00069 | 0.636 |
DOC_PP1_RVXF_1 | 66 | 72 | PF00149 | 0.636 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.865 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.699 |
DOC_USP7_MATH_1 | 89 | 93 | PF00917 | 0.538 |
DOC_USP7_UBL2_3 | 61 | 65 | PF12436 | 0.636 |
DOC_WW_Pin1_4 | 260 | 265 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.592 |
LIG_14-3-3_CanoR_1 | 20 | 26 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 428 | 435 | PF00244 | 0.636 |
LIG_Actin_WH2_2 | 446 | 462 | PF00022 | 0.636 |
LIG_BIR_III_2 | 261 | 265 | PF00653 | 0.839 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.608 |
LIG_FHA_1 | 20 | 26 | PF00498 | 0.636 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.693 |
LIG_FHA_1 | 247 | 253 | PF00498 | 0.852 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.577 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.833 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.636 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.636 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.734 |
LIG_FHA_2 | 196 | 202 | PF00498 | 0.799 |
LIG_FHA_2 | 277 | 283 | PF00498 | 0.765 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.636 |
LIG_LIR_Gen_1 | 105 | 115 | PF02991 | 0.636 |
LIG_LIR_Gen_1 | 287 | 296 | PF02991 | 0.797 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.636 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.796 |
LIG_PCNA_yPIPBox_3 | 7 | 16 | PF02747 | 0.636 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.528 |
LIG_SH3_1 | 240 | 246 | PF00018 | 0.841 |
LIG_SH3_3 | 240 | 246 | PF00018 | 0.724 |
LIG_TRAF2_1 | 156 | 159 | PF00917 | 0.745 |
LIG_TRAF2_1 | 160 | 163 | PF00917 | 0.685 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.870 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.636 |
LIG_TRAF2_1 | 96 | 99 | PF00917 | 0.636 |
LIG_WRC_WIRS_1 | 38 | 43 | PF05994 | 0.580 |
LIG_WW_3 | 242 | 246 | PF00397 | 0.839 |
MOD_CK1_1 | 150 | 156 | PF00069 | 0.752 |
MOD_CK1_1 | 212 | 218 | PF00069 | 0.749 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.549 |
MOD_CK2_1 | 143 | 149 | PF00069 | 0.869 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.593 |
MOD_CK2_1 | 195 | 201 | PF00069 | 0.835 |
MOD_CK2_1 | 276 | 282 | PF00069 | 0.773 |
MOD_CK2_1 | 431 | 437 | PF00069 | 0.636 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.636 |
MOD_Cter_Amidation | 271 | 274 | PF01082 | 0.857 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.687 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.760 |
MOD_GlcNHglycan | 149 | 152 | PF01048 | 0.761 |
MOD_GlcNHglycan | 211 | 214 | PF01048 | 0.796 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.733 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.380 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.703 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.836 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.756 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.615 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.592 |
MOD_NEK2_1 | 42 | 47 | PF00069 | 0.634 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.619 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.453 |
MOD_PIKK_1 | 5 | 11 | PF00454 | 0.582 |
MOD_PKA_1 | 126 | 132 | PF00069 | 0.661 |
MOD_PKA_1 | 147 | 153 | PF00069 | 0.758 |
MOD_PKA_1 | 225 | 231 | PF00069 | 0.827 |
MOD_PKA_1 | 428 | 434 | PF00069 | 0.636 |
MOD_PKA_2 | 19 | 25 | PF00069 | 0.483 |
MOD_PKA_2 | 225 | 231 | PF00069 | 0.772 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.636 |
MOD_PKA_2 | 459 | 465 | PF00069 | 0.636 |
MOD_PKA_2 | 89 | 95 | PF00069 | 0.538 |
MOD_PKB_1 | 224 | 232 | PF00069 | 0.750 |
MOD_Plk_1 | 431 | 437 | PF00069 | 0.636 |
MOD_Plk_2-3 | 278 | 284 | PF00069 | 0.840 |
MOD_Plk_4 | 37 | 43 | PF00069 | 0.552 |
MOD_Plk_4 | 459 | 465 | PF00069 | 0.636 |
MOD_Plk_4 | 473 | 479 | PF00069 | 0.470 |
MOD_ProDKin_1 | 260 | 266 | PF00069 | 0.628 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.592 |
MOD_SUMO_rev_2 | 146 | 156 | PF00179 | 0.753 |
MOD_SUMO_rev_2 | 294 | 301 | PF00179 | 0.755 |
MOD_SUMO_rev_2 | 309 | 316 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 58 | 67 | PF00179 | 0.636 |
TRG_DiLeu_BaEn_1 | 380 | 385 | PF01217 | 0.608 |
TRG_ER_diArg_1 | 172 | 175 | PF00400 | 0.601 |
TRG_NES_CRM1_1 | 401 | 416 | PF08389 | 0.636 |
TRG_NLS_MonoExtC_3 | 272 | 278 | PF00514 | 0.861 |
TRG_NLS_MonoExtN_4 | 270 | 277 | PF00514 | 0.858 |
TRG_Pf-PMV_PEXEL_1 | 32 | 36 | PF00026 | 0.435 |