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:0005929 | cilium | 4 | 10 |
GO:0042995 | cell projection | 2 | 10 |
GO:0043226 | organelle | 2 | 10 |
GO:0043227 | membrane-bounded organelle | 3 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 10 |
GO:0005813 | centrosome | 3 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0030990 | intraciliary transport particle | 2 | 1 |
GO:0030992 | intraciliary transport particle B | 2 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0031514 | motile cilium | 5 | 1 |
Related structures:
AlphaFold database: A4HEE7
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 10 |
GO:0030030 | cell projection organization | 4 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
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:0010970 | transport along microtubule | 4 | 1 |
GO:0022607 | cellular component assembly | 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:0035720 | intraciliary anterograde transport | 4 | 1 |
GO:0035735 | intraciliary transport involved in cilium assembly | 4 | 1 |
GO:0042073 | intraciliary transport | 3 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 399 | 403 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 448 | 452 | PF00656 | 0.690 |
CLV_NRD_NRD_1 | 179 | 181 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.772 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.669 |
CLV_PCSK_KEX2_1 | 179 | 181 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.725 |
CLV_PCSK_PC7_1 | 310 | 316 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 106 | 110 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 419 | 423 | PF00082 | 0.677 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.276 |
DEG_SCF_FBW7_1 | 322 | 327 | PF00400 | 0.653 |
DEG_SCF_FBW7_1 | 455 | 461 | PF00400 | 0.518 |
DOC_CDC14_PxL_1 | 15 | 23 | PF14671 | 0.276 |
DOC_CKS1_1 | 455 | 460 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 179 | 186 | PF00134 | 0.342 |
DOC_CYCLIN_RxL_1 | 257 | 266 | PF00134 | 0.393 |
DOC_MAPK_gen_1 | 76 | 83 | PF00069 | 0.300 |
DOC_MAPK_MEF2A_6 | 76 | 83 | PF00069 | 0.300 |
DOC_MAPK_NFAT4_5 | 76 | 84 | PF00069 | 0.335 |
DOC_PP1_RVXF_1 | 258 | 265 | PF00149 | 0.393 |
DOC_PP1_RVXF_1 | 60 | 66 | PF00149 | 0.301 |
DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.278 |
DOC_USP7_MATH_1 | 458 | 462 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 105 | 109 | PF12436 | 0.300 |
DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.276 |
DOC_USP7_UBL2_3 | 271 | 275 | PF12436 | 0.341 |
DOC_USP7_UBL2_3 | 296 | 300 | PF12436 | 0.541 |
DOC_USP7_UBL2_3 | 76 | 80 | PF12436 | 0.276 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.522 |
LIG_14-3-3_CanoR_1 | 170 | 177 | PF00244 | 0.276 |
LIG_14-3-3_CanoR_1 | 20 | 25 | PF00244 | 0.270 |
LIG_14-3-3_CanoR_1 | 379 | 385 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 62 | 66 | PF00244 | 0.335 |
LIG_14-3-3_CanoR_1 | 7 | 16 | PF00244 | 0.489 |
LIG_Actin_WH2_2 | 287 | 302 | PF00022 | 0.590 |
LIG_Actin_WH2_2 | 90 | 107 | PF00022 | 0.276 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.406 |
LIG_BRCT_BRCA1_1 | 147 | 151 | PF00533 | 0.276 |
LIG_BRCT_BRCA1_1 | 460 | 464 | PF00533 | 0.721 |
LIG_Clathr_ClatBox_1 | 21 | 25 | PF01394 | 0.276 |
LIG_EH1_1 | 91 | 99 | PF00400 | 0.393 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.337 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.513 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.393 |
LIG_FHA_2 | 109 | 115 | PF00498 | 0.300 |
LIG_FHA_2 | 205 | 211 | PF00498 | 0.211 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.599 |
LIG_FHA_2 | 397 | 403 | PF00498 | 0.525 |
LIG_GBD_Chelix_1 | 100 | 108 | PF00786 | 0.276 |
LIG_Integrin_RGD_1 | 161 | 163 | PF01839 | 0.341 |
LIG_LIR_Apic_2 | 25 | 30 | PF02991 | 0.276 |
LIG_LIR_Gen_1 | 115 | 126 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 115 | 121 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 2 | 6 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 257 | 262 | PF02991 | 0.288 |
LIG_LIR_Nem_3 | 64 | 69 | PF02991 | 0.418 |
LIG_LYPXL_yS_3 | 18 | 21 | PF13949 | 0.276 |
LIG_MLH1_MIPbox_1 | 148 | 152 | PF16413 | 0.335 |
LIG_NRBOX | 180 | 186 | PF00104 | 0.335 |
LIG_PDZ_Class_1 | 475 | 480 | PF00595 | 0.608 |
LIG_PTB_Apo_2 | 231 | 238 | PF02174 | 0.393 |
LIG_PTB_Apo_2 | 258 | 265 | PF02174 | 0.276 |
LIG_REV1ctd_RIR_1 | 63 | 71 | PF16727 | 0.278 |
LIG_SH2_GRB2like | 241 | 244 | PF00017 | 0.393 |
LIG_SH2_SRC | 241 | 244 | PF00017 | 0.393 |
LIG_SH2_SRC | 46 | 49 | PF00017 | 0.276 |
LIG_SH2_STAT3 | 255 | 258 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 336 | 339 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.534 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.637 |
LIG_TRAF2_1 | 355 | 358 | PF00917 | 0.630 |
LIG_TRAF2_1 | 93 | 96 | PF00917 | 0.276 |
LIG_TYR_ITIM | 16 | 21 | PF00017 | 0.276 |
LIG_UBA3_1 | 97 | 105 | PF00899 | 0.276 |
LIG_WRC_WIRS_1 | 24 | 29 | PF05994 | 0.317 |
LIG_WRC_WIRS_1 | 6 | 11 | PF05994 | 0.337 |
MOD_CDK_SPK_2 | 334 | 339 | PF00069 | 0.500 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.282 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.276 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.296 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.505 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.542 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.539 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.676 |
MOD_CK1_1 | 447 | 453 | PF00069 | 0.645 |
MOD_CK1_1 | 456 | 462 | PF00069 | 0.659 |
MOD_CK1_1 | 466 | 472 | PF00069 | 0.580 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.300 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.307 |
MOD_CK2_1 | 23 | 29 | PF00069 | 0.425 |
MOD_CK2_1 | 324 | 330 | PF00069 | 0.710 |
MOD_CK2_1 | 351 | 357 | PF00069 | 0.648 |
MOD_CK2_1 | 443 | 449 | PF00069 | 0.729 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.677 |
MOD_CK2_1 | 5 | 11 | PF00069 | 0.339 |
MOD_Cter_Amidation | 312 | 315 | PF01082 | 0.747 |
MOD_GlcNHglycan | 202 | 205 | PF01048 | 0.393 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.393 |
MOD_GlcNHglycan | 311 | 314 | PF01048 | 0.789 |
MOD_GlcNHglycan | 316 | 319 | PF01048 | 0.618 |
MOD_GlcNHglycan | 351 | 357 | PF01048 | 0.696 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.604 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.673 |
MOD_GlcNHglycan | 47 | 51 | PF01048 | 0.300 |
MOD_GlcNHglycan | 471 | 475 | PF01048 | 0.612 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.273 |
MOD_GSK3_1 | 200 | 207 | PF00069 | 0.357 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.382 |
MOD_GSK3_1 | 314 | 321 | PF00069 | 0.701 |
MOD_GSK3_1 | 352 | 359 | PF00069 | 0.627 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.639 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.650 |
MOD_GSK3_1 | 449 | 456 | PF00069 | 0.631 |
MOD_GSK3_1 | 458 | 465 | PF00069 | 0.518 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.393 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.655 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.359 |
MOD_N-GLC_1 | 128 | 133 | PF02516 | 0.393 |
MOD_N-GLC_1 | 200 | 205 | PF02516 | 0.306 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.343 |
MOD_PKA_1 | 314 | 320 | PF00069 | 0.726 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.276 |
MOD_PKA_2 | 309 | 315 | PF00069 | 0.699 |
MOD_PKA_2 | 387 | 393 | PF00069 | 0.745 |
MOD_PKA_2 | 61 | 67 | PF00069 | 0.335 |
MOD_PKB_1 | 164 | 172 | PF00069 | 0.276 |
MOD_PKB_1 | 417 | 425 | PF00069 | 0.809 |
MOD_Plk_1 | 116 | 122 | PF00069 | 0.300 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.723 |
MOD_Plk_1 | 50 | 56 | PF00069 | 0.393 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.155 |
MOD_Plk_2-3 | 364 | 370 | PF00069 | 0.787 |
MOD_Plk_2-3 | 445 | 451 | PF00069 | 0.638 |
MOD_Plk_2-3 | 463 | 469 | PF00069 | 0.677 |
MOD_Plk_2-3 | 5 | 11 | PF00069 | 0.339 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.335 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.393 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.723 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.348 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.657 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.483 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.521 |
MOD_SUMO_rev_2 | 131 | 136 | PF00179 | 0.393 |
MOD_SUMO_rev_2 | 205 | 213 | PF00179 | 0.276 |
MOD_SUMO_rev_2 | 240 | 248 | PF00179 | 0.383 |
MOD_SUMO_rev_2 | 281 | 287 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 292 | 302 | PF00179 | 0.541 |
TRG_DiLeu_BaEn_1 | 11 | 16 | PF01217 | 0.339 |
TRG_DiLeu_BaEn_1 | 407 | 412 | PF01217 | 0.723 |
TRG_DiLeu_BaLyEn_6 | 17 | 22 | PF01217 | 0.225 |
TRG_DiLeu_LyEn_5 | 11 | 16 | PF01217 | 0.339 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.276 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.276 |
TRG_ER_diArg_1 | 164 | 167 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 179 | 182 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 344 | 347 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 378 | 380 | PF00400 | 0.688 |
TRG_ER_diArg_1 | 415 | 417 | PF00400 | 0.732 |
TRG_ER_diArg_1 | 433 | 436 | PF00400 | 0.723 |
TRG_Pf-PMV_PEXEL_1 | 179 | 183 | PF00026 | 0.300 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKV6 | Leptomonas seymouri | 76% | 100% |
A0A0S4IPW0 | Bodo saltans | 66% | 100% |
A0A3S7WZA7 | Leishmania donovani | 88% | 99% |
A0A422N0X8 | Trypanosoma rangeli | 66% | 96% |
A4I1I7 | Leishmania infantum | 88% | 99% |
C9ZJX9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9AXM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4Q9V0 | Leishmania major | 85% | 100% |