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 | 12 |
GO:0042995 | cell projection | 2 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 12 |
GO:0000164 | protein phosphatase type 1 complex | 5 | 1 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1903293 | phosphatase complex | 3 | 1 |
Related structures:
AlphaFold database: A4HIV0
Term | Name | Level | Count |
---|---|---|---|
GO:0001539 | cilium or flagellum-dependent cell motility | 3 | 1 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010562 | positive regulation of phosphorus metabolic process | 6 | 1 |
GO:0010604 | positive regulation of macromolecule metabolic process | 5 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0031399 | regulation of protein modification process | 6 | 1 |
GO:0031401 | positive regulation of protein modification process | 7 | 1 |
GO:0035303 | regulation of dephosphorylation | 7 | 1 |
GO:0035304 | regulation of protein dephosphorylation | 7 | 1 |
GO:0035306 | positive regulation of dephosphorylation | 8 | 1 |
GO:0035307 | positive regulation of protein dephosphorylation | 8 | 1 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0048870 | cell motility | 2 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051173 | positive regulation of nitrogen compound metabolic process | 5 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051247 | positive regulation of protein metabolic process | 6 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0060285 | cilium-dependent cell motility | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0004857 | enzyme inhibitor activity | 3 | 1 |
GO:0004864 | protein phosphatase inhibitor activity | 5 | 1 |
GO:0004865 | protein serine/threonine phosphatase inhibitor activity | 6 | 1 |
GO:0019208 | phosphatase regulator activity | 3 | 1 |
GO:0019212 | phosphatase inhibitor activity | 4 | 1 |
GO:0019888 | protein phosphatase regulator activity | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
GO:0140678 | molecular function inhibitor activity | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.552 |
CLV_C14_Caspase3-7 | 548 | 552 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.505 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.422 |
CLV_PCSK_FUR_1 | 498 | 502 | PF00082 | 0.388 |
CLV_PCSK_FUR_1 | 531 | 535 | PF00082 | 0.494 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.662 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.390 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.506 |
CLV_PCSK_KEX2_1 | 544 | 546 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.404 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.662 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.397 |
CLV_PCSK_PC1ET2_1 | 544 | 546 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.340 |
CLV_Separin_Metazoa | 274 | 278 | PF03568 | 0.477 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.532 |
DEG_APCC_DBOX_1 | 229 | 237 | PF00400 | 0.557 |
DOC_ANK_TNKS_1 | 276 | 283 | PF00023 | 0.469 |
DOC_CYCLIN_RxL_1 | 201 | 213 | PF00134 | 0.462 |
DOC_MAPK_gen_1 | 419 | 427 | PF00069 | 0.420 |
DOC_MAPK_gen_1 | 531 | 541 | PF00069 | 0.285 |
DOC_MAPK_gen_1 | 54 | 65 | PF00069 | 0.550 |
DOC_MAPK_MEF2A_6 | 421 | 429 | PF00069 | 0.412 |
DOC_MAPK_MEF2A_6 | 534 | 543 | PF00069 | 0.278 |
DOC_PP1_RVXF_1 | 199 | 206 | PF00149 | 0.461 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.430 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.625 |
LIG_Actin_WH2_2 | 352 | 368 | PF00022 | 0.355 |
LIG_APCC_ABBA_1 | 269 | 274 | PF00400 | 0.568 |
LIG_APCC_ABBA_1 | 276 | 281 | PF00400 | 0.457 |
LIG_Clathr_ClatBox_1 | 109 | 113 | PF01394 | 0.507 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.439 |
LIG_Clathr_ClatBox_1 | 436 | 440 | PF01394 | 0.477 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.520 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.608 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.472 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.411 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.495 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.536 |
LIG_FHA_2 | 268 | 274 | PF00498 | 0.531 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.536 |
LIG_FHA_2 | 339 | 345 | PF00498 | 0.428 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.334 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.490 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.474 |
LIG_GBD_Chelix_1 | 383 | 391 | PF00786 | 0.450 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 270 | 280 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 431 | 439 | PF02991 | 0.368 |
LIG_LIR_Gen_1 | 493 | 502 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.373 |
LIG_PCNA_yPIPBox_3 | 405 | 419 | PF02747 | 0.433 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.398 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.461 |
LIG_SH2_GRB2like | 140 | 143 | PF00017 | 0.554 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.536 |
LIG_SH2_NCK_1 | 263 | 267 | PF00017 | 0.454 |
LIG_SH2_SRC | 175 | 178 | PF00017 | 0.554 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.554 |
LIG_SH2_STAT3 | 470 | 473 | PF00017 | 0.670 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.547 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.482 |
LIG_SUMO_SIM_anti_2 | 407 | 414 | PF11976 | 0.483 |
LIG_SUMO_SIM_anti_2 | 423 | 429 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.536 |
LIG_SUMO_SIM_par_1 | 69 | 74 | PF11976 | 0.487 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.566 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.435 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.536 |
LIG_UBA3_1 | 477 | 484 | PF00899 | 0.544 |
LIG_WRC_WIRS_1 | 72 | 77 | PF05994 | 0.507 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.455 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.624 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.514 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.452 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.532 |
MOD_CK2_1 | 32 | 38 | PF00069 | 0.442 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.384 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.293 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.507 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.517 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.507 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.421 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.601 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.380 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.402 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.396 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.424 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.459 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.481 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.471 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.690 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.438 |
MOD_NEK2_1 | 516 | 521 | PF00069 | 0.391 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.400 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.427 |
MOD_PIKK_1 | 378 | 384 | PF00454 | 0.592 |
MOD_PK_1 | 520 | 526 | PF00069 | 0.531 |
MOD_PKA_1 | 544 | 550 | PF00069 | 0.289 |
MOD_PKA_2 | 519 | 525 | PF00069 | 0.436 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.421 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.472 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.560 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.314 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.479 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.493 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.450 |
MOD_Plk_4 | 267 | 273 | PF00069 | 0.314 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.286 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.514 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.372 |
MOD_SUMO_for_1 | 510 | 513 | PF00179 | 0.448 |
MOD_SUMO_rev_2 | 48 | 56 | PF00179 | 0.597 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.390 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.472 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.390 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.426 |
TRG_ER_diArg_1 | 56 | 58 | PF00400 | 0.484 |
TRG_Pf-PMV_PEXEL_1 | 448 | 452 | PF00026 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.585 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB70 | Leptomonas seymouri | 70% | 99% |
A0A0S4JNZ9 | Bodo saltans | 39% | 99% |
A0A1X0P2D5 | Trypanosomatidae | 44% | 100% |
A0A3Q8IF34 | Leishmania donovani | 82% | 100% |
A0A422NMM2 | Trypanosoma rangeli | 43% | 100% |
A4I655 | Leishmania infantum | 82% | 100% |
A8IVX2 | Chlamydomonas reinhardtii | 26% | 100% |
C9ZRH5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9B1D8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4Q6S4 | Leishmania major | 83% | 100% |
V5DNR7 | Trypanosoma cruzi | 43% | 100% |