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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005929 | cilium | 4 | 11 |
GO:0042995 | cell projection | 2 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043227 | membrane-bounded organelle | 3 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 11 |
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 |
Related structures:
AlphaFold database: A0A3S5H558
Term | Name | Level | Count |
---|---|---|---|
GO:0006457 | protein folding | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0000226 | microtubule cytoskeleton organization | 3 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007010 | cytoskeleton organization | 5 | 1 |
GO:0007017 | microtubule-based process | 2 | 1 |
GO:0007021 | tubulin complex assembly | 6 | 1 |
GO:0007023 | post-chaperonin tubulin folding pathway | 3 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0065003 | protein-containing complex assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 12 |
GO:0005515 | protein binding | 2 | 12 |
GO:0008092 | cytoskeletal protein binding | 3 | 12 |
GO:0015631 | tubulin binding | 4 | 12 |
GO:0043014 | alpha-tubulin binding | 5 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 17 | 21 | PF00656 | 0.403 |
CLV_C14_Caspase3-7 | 320 | 324 | PF00656 | 0.384 |
CLV_C14_Caspase3-7 | 374 | 378 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 395 | 399 | PF00656 | 0.621 |
CLV_PCSK_SKI1_1 | 128 | 132 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.356 |
CLV_PCSK_SKI1_1 | 303 | 307 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 331 | 335 | PF00082 | 0.455 |
CLV_PCSK_SKI1_1 | 385 | 389 | PF00082 | 0.521 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.501 |
DEG_SCF_FBW7_1 | 9 | 15 | PF00400 | 0.417 |
DEG_SPOP_SBC_1 | 150 | 154 | PF00917 | 0.569 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.662 |
DOC_CDC14_PxL_1 | 123 | 131 | PF14671 | 0.485 |
DOC_CDC14_PxL_1 | 134 | 142 | PF14671 | 0.514 |
DOC_CDC14_PxL_1 | 175 | 183 | PF14671 | 0.437 |
DOC_CKS1_1 | 521 | 526 | PF01111 | 0.531 |
DOC_CKS1_1 | 6 | 11 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 179 | 188 | PF00134 | 0.528 |
DOC_MAPK_gen_1 | 300 | 310 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 424 | 432 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 45 | 52 | PF00069 | 0.621 |
DOC_MAPK_gen_1 | 58 | 67 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 414 | 422 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 426 | 434 | PF00069 | 0.491 |
DOC_MAPK_MEF2A_6 | 61 | 69 | PF00069 | 0.516 |
DOC_MAPK_MEF2A_6 | 71 | 79 | PF00069 | 0.371 |
DOC_PP2B_LxvP_1 | 270 | 273 | PF13499 | 0.500 |
DOC_PP4_MxPP_1 | 143 | 146 | PF00568 | 0.548 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.732 |
DOC_USP7_MATH_1 | 4 | 8 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 424 | 428 | PF12436 | 0.471 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.707 |
DOC_WW_Pin1_4 | 471 | 476 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.514 |
DOC_WW_Pin1_4 | 8 | 13 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 128 | 133 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 303 | 308 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 336 | 346 | PF00244 | 0.372 |
LIG_14-3-3_CanoR_1 | 508 | 512 | PF00244 | 0.487 |
LIG_14-3-3_CanoR_1 | 64 | 68 | PF00244 | 0.506 |
LIG_deltaCOP1_diTrp_1 | 44 | 49 | PF00928 | 0.662 |
LIG_eIF4E_1 | 382 | 388 | PF01652 | 0.506 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.425 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.535 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.359 |
LIG_FHA_1 | 285 | 291 | PF00498 | 0.550 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.442 |
LIG_FHA_1 | 332 | 338 | PF00498 | 0.236 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.472 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.392 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.514 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.427 |
LIG_FHA_2 | 190 | 196 | PF00498 | 0.522 |
LIG_FHA_2 | 343 | 349 | PF00498 | 0.517 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.465 |
LIG_Integrin_isoDGR_2 | 350 | 352 | PF01839 | 0.289 |
LIG_LIR_Gen_1 | 338 | 344 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 44 | 52 | PF02991 | 0.591 |
LIG_LIR_Gen_1 | 447 | 456 | PF02991 | 0.486 |
LIG_LIR_LC3C_4 | 66 | 69 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 224 | 230 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 241 | 246 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 338 | 342 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 44 | 50 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 447 | 451 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 531 | 537 | PF02991 | 0.465 |
LIG_LYPXL_yS_3 | 417 | 420 | PF13949 | 0.403 |
LIG_MYND_1 | 138 | 142 | PF01753 | 0.510 |
LIG_PTB_Apo_2 | 160 | 167 | PF02174 | 0.451 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.409 |
LIG_SH2_CRK | 339 | 343 | PF00017 | 0.425 |
LIG_SH2_NCK_1 | 461 | 465 | PF00017 | 0.597 |
LIG_SH2_PTP2 | 448 | 451 | PF00017 | 0.530 |
LIG_SH2_STAP1 | 339 | 343 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 461 | 465 | PF00017 | 0.626 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 261 | 264 | PF00017 | 0.471 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 354 | 357 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 448 | 451 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 456 | 459 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 544 | 547 | PF00017 | 0.526 |
LIG_SH3_1 | 121 | 127 | PF00018 | 0.500 |
LIG_SH3_3 | 121 | 127 | PF00018 | 0.500 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.375 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.427 |
LIG_SH3_3 | 195 | 201 | PF00018 | 0.626 |
LIG_SH3_3 | 222 | 228 | PF00018 | 0.584 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.529 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.479 |
LIG_SH3_3 | 412 | 418 | PF00018 | 0.499 |
LIG_SH3_4 | 503 | 510 | PF00018 | 0.536 |
LIG_SUMO_SIM_anti_2 | 192 | 198 | PF11976 | 0.564 |
LIG_SUMO_SIM_anti_2 | 361 | 366 | PF11976 | 0.473 |
LIG_SUMO_SIM_anti_2 | 63 | 69 | PF11976 | 0.518 |
LIG_SUMO_SIM_par_1 | 449 | 454 | PF11976 | 0.493 |
LIG_SUMO_SIM_par_1 | 515 | 523 | PF11976 | 0.503 |
LIG_TYR_ITIM | 337 | 342 | PF00017 | 0.418 |
LIG_TYR_ITIM | 415 | 420 | PF00017 | 0.439 |
LIG_TYR_ITIM | 532 | 537 | PF00017 | 0.391 |
LIG_UBA3_1 | 307 | 311 | PF00899 | 0.480 |
LIG_WRC_WIRS_1 | 332 | 337 | PF05994 | 0.330 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.538 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.449 |
MOD_CK1_1 | 204 | 210 | PF00069 | 0.710 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.406 |
MOD_CK1_1 | 485 | 491 | PF00069 | 0.238 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.746 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.306 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.375 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.649 |
MOD_CK2_1 | 112 | 118 | PF00069 | 0.444 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.511 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.720 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.607 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.649 |
MOD_GlcNHglycan | 512 | 515 | PF01048 | 0.308 |
MOD_GlcNHglycan | 81 | 85 | PF01048 | 0.684 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.555 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.392 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.489 |
MOD_GSK3_1 | 197 | 204 | PF00069 | 0.646 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.459 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.182 |
MOD_GSK3_1 | 342 | 349 | PF00069 | 0.391 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.768 |
MOD_GSK3_1 | 437 | 444 | PF00069 | 0.623 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.614 |
MOD_GSK3_1 | 474 | 481 | PF00069 | 0.299 |
MOD_N-GLC_1 | 161 | 166 | PF02516 | 0.445 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.552 |
MOD_N-GLC_1 | 213 | 218 | PF02516 | 0.632 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.419 |
MOD_N-GLC_1 | 346 | 351 | PF02516 | 0.368 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.440 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.399 |
MOD_NEK2_1 | 316 | 321 | PF00069 | 0.514 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.184 |
MOD_PIKK_1 | 255 | 261 | PF00454 | 0.472 |
MOD_PIKK_1 | 475 | 481 | PF00454 | 0.425 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.353 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.532 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.355 |
MOD_PKA_2 | 63 | 69 | PF00069 | 0.506 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.432 |
MOD_Plk_1 | 189 | 195 | PF00069 | 0.336 |
MOD_Plk_1 | 312 | 318 | PF00069 | 0.432 |
MOD_Plk_2-3 | 30 | 36 | PF00069 | 0.627 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.455 |
MOD_Plk_4 | 272 | 278 | PF00069 | 0.477 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.411 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.456 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.603 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.471 |
MOD_Plk_4 | 538 | 544 | PF00069 | 0.388 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.506 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.646 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.704 |
MOD_ProDKin_1 | 471 | 477 | PF00069 | 0.415 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.391 |
TRG_DiLeu_BaEn_1 | 118 | 123 | PF01217 | 0.491 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 339 | 342 | PF00928 | 0.373 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 448 | 451 | PF00928 | 0.530 |
TRG_ENDOCYTIC_2 | 534 | 537 | PF00928 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 167 | 171 | PF00026 | 0.427 |
TRG_Pf-PMV_PEXEL_1 | 173 | 177 | PF00026 | 0.463 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HTC4 | Leptomonas seymouri | 63% | 100% |
A0A0S4JLX2 | Bodo saltans | 38% | 100% |
A0A1X0P967 | Trypanosomatidae | 42% | 100% |
A0A422NHN6 | Trypanosoma rangeli | 44% | 100% |
A4H3N8 | Leishmania braziliensis | 81% | 100% |
A4HRW5 | Leishmania infantum | 100% | 100% |
C9ZKH0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9ACM2 | Leishmania major | 93% | 100% |
E9AJW0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q15813 | Homo sapiens | 23% | 100% |
Q32KS0 | Bos taurus | 23% | 100% |
Q5RBD9 | Pongo abelii | 23% | 100% |
Q5U508 | Xenopus laevis | 22% | 100% |
Q8CIV8 | Mus musculus | 22% | 100% |
Q8GRL7 | Arabidopsis thaliana | 25% | 100% |
V5C274 | Trypanosoma cruzi | 42% | 100% |