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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 14 |
GO:0042995 | cell projection | 2 | 14 |
GO:0043226 | organelle | 2 | 14 |
GO:0043227 | membrane-bounded organelle | 3 | 14 |
GO:0110165 | cellular anatomical entity | 1 | 14 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 14 |
GO:0016020 | membrane | 2 | 1 |
Related structures:
AlphaFold database: E9AGK6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.532 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 78 | 82 | PF00082 | 0.526 |
CLV_Separin_Metazoa | 406 | 410 | PF03568 | 0.453 |
DEG_APCC_DBOX_1 | 51 | 59 | PF00400 | 0.582 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.577 |
DOC_CDC14_PxL_1 | 199 | 207 | PF14671 | 0.460 |
DOC_CDC14_PxL_1 | 332 | 340 | PF14671 | 0.480 |
DOC_CDC14_PxL_1 | 377 | 385 | PF14671 | 0.411 |
DOC_CDC14_PxL_1 | 422 | 430 | PF14671 | 0.516 |
DOC_CYCLIN_RxL_1 | 277 | 286 | PF00134 | 0.506 |
DOC_CYCLIN_RxL_1 | 72 | 85 | PF00134 | 0.468 |
DOC_MAPK_gen_1 | 45 | 55 | PF00069 | 0.397 |
DOC_MAPK_HePTP_8 | 69 | 81 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 112 | 119 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 139 | 147 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 72 | 81 | PF00069 | 0.524 |
DOC_PP1_RVXF_1 | 315 | 321 | PF00149 | 0.441 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.581 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 190 | 199 | PF00244 | 0.475 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 252 | 261 | PF00244 | 0.442 |
LIG_14-3-3_CanoR_1 | 280 | 285 | PF00244 | 0.511 |
LIG_14-3-3_CanoR_1 | 317 | 321 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 369 | 377 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 52 | 56 | PF00244 | 0.556 |
LIG_14-3-3_CanoR_1 | 72 | 78 | PF00244 | 0.272 |
LIG_14-3-3_CanoR_1 | 9 | 15 | PF00244 | 0.484 |
LIG_Actin_WH2_2 | 325 | 341 | PF00022 | 0.508 |
LIG_BIR_III_4 | 93 | 97 | PF00653 | 0.440 |
LIG_Clathr_ClatBox_1 | 157 | 161 | PF01394 | 0.411 |
LIG_DLG_GKlike_1 | 139 | 146 | PF00625 | 0.483 |
LIG_DLG_GKlike_1 | 280 | 287 | PF00625 | 0.501 |
LIG_FHA_1 | 205 | 211 | PF00498 | 0.462 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.437 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.489 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.449 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.423 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.530 |
LIG_GBD_Chelix_1 | 65 | 73 | PF00786 | 0.469 |
LIG_Integrin_RGD_1 | 120 | 122 | PF01839 | 0.515 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 387 | 396 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.487 |
LIG_NRBOX | 64 | 70 | PF00104 | 0.463 |
LIG_NRBOX | 76 | 82 | PF00104 | 0.379 |
LIG_PCNA_PIPBox_1 | 180 | 189 | PF02747 | 0.228 |
LIG_RPA_C_Fungi | 185 | 197 | PF08784 | 0.414 |
LIG_RPA_C_Fungi | 5 | 17 | PF08784 | 0.409 |
LIG_SH2_CRK | 200 | 204 | PF00017 | 0.492 |
LIG_SH2_PTP2 | 430 | 433 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 359 | 362 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.522 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.503 |
LIG_SUMO_SIM_anti_2 | 124 | 132 | PF11976 | 0.560 |
LIG_SUMO_SIM_anti_2 | 142 | 147 | PF11976 | 0.543 |
LIG_SUMO_SIM_anti_2 | 272 | 277 | PF11976 | 0.378 |
LIG_SUMO_SIM_anti_2 | 404 | 409 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 206 | 212 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 279 | 286 | PF11976 | 0.518 |
LIG_TYR_ITIM | 428 | 433 | PF00017 | 0.533 |
MOD_CDK_SPK_2 | 445 | 450 | PF00069 | 0.432 |
MOD_CDK_SPK_2 | 56 | 61 | PF00069 | 0.523 |
MOD_CDK_SPxxK_3 | 56 | 63 | PF00069 | 0.481 |
MOD_CK1_1 | 189 | 195 | PF00069 | 0.417 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.476 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.481 |
MOD_CK1_1 | 256 | 262 | PF00069 | 0.417 |
MOD_CK1_1 | 269 | 275 | PF00069 | 0.380 |
MOD_CK1_1 | 283 | 289 | PF00069 | 0.439 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.490 |
MOD_CK1_1 | 445 | 451 | PF00069 | 0.437 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.452 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.539 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.627 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.482 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.351 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.369 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.402 |
MOD_GlcNHglycan | 345 | 348 | PF01048 | 0.433 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.414 |
MOD_GSK3_1 | 124 | 131 | PF00069 | 0.529 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.583 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.427 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.411 |
MOD_GSK3_1 | 252 | 259 | PF00069 | 0.437 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.463 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.473 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.467 |
MOD_LATS_1 | 250 | 256 | PF00433 | 0.396 |
MOD_LATS_1 | 292 | 298 | PF00433 | 0.373 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.545 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.489 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.487 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.460 |
MOD_NEK2_1 | 282 | 287 | PF00069 | 0.511 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.379 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.586 |
MOD_PIKK_1 | 175 | 181 | PF00454 | 0.502 |
MOD_PK_1 | 294 | 300 | PF00069 | 0.478 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.535 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.598 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.458 |
MOD_PKA_2 | 316 | 322 | PF00069 | 0.500 |
MOD_PKA_2 | 51 | 57 | PF00069 | 0.593 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.517 |
MOD_Plk_1 | 17 | 23 | PF00069 | 0.538 |
MOD_Plk_1 | 386 | 392 | PF00069 | 0.522 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.498 |
MOD_Plk_2-3 | 316 | 322 | PF00069 | 0.461 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.535 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.437 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.445 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.540 |
MOD_Plk_4 | 271 | 277 | PF00069 | 0.255 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.503 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.580 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.491 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.427 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.462 |
MOD_SUMO_rev_2 | 209 | 214 | PF00179 | 0.463 |
TRG_DiLeu_BaLyEn_6 | 27 | 32 | PF01217 | 0.547 |
TRG_DiLeu_BaLyEn_6 | 277 | 282 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 60 | 65 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 75 | 80 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 336 | 339 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 381 | 384 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.440 |
TRG_NES_CRM1_1 | 201 | 211 | PF08389 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 63 | 67 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 78 | 82 | PF00026 | 0.480 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P3F9 | Leptomonas seymouri | 33% | 87% |
A0A0N0P8N9 | Leptomonas seymouri | 31% | 69% |
A0A0N1HZK9 | Leptomonas seymouri | 31% | 86% |
A0A0N1I0W0 | Leptomonas seymouri | 28% | 89% |
A0A0N1I1E8 | Leptomonas seymouri | 27% | 100% |
A0A1X0NEN5 | Trypanosomatidae | 26% | 78% |
A0A1X0NG16 | Trypanosomatidae | 25% | 79% |
A0A3Q8I8N4 | Leishmania donovani | 99% | 100% |
A4H3R1 | Leishmania braziliensis | 29% | 66% |
A4H7G0 | Leishmania braziliensis | 77% | 100% |
E9APJ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QFY4 | Leishmania major | 94% | 100% |