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: A0A3Q8IF34
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 | 123 | 127 | PF00656 | 0.461 |
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.523 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.461 |
CLV_NRD_NRD_1 | 458 | 460 | PF00675 | 0.581 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 534 | 536 | PF00675 | 0.556 |
CLV_NRD_NRD_1 | 56 | 58 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 324 | 328 | PF00082 | 0.401 |
CLV_PCSK_FUR_1 | 498 | 502 | PF00082 | 0.365 |
CLV_PCSK_FUR_1 | 531 | 535 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.401 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 458 | 460 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 361 | 363 | PF00082 | 0.350 |
CLV_PCSK_PC1ET2_1 | 377 | 379 | PF00082 | 0.630 |
CLV_PCSK_PC1ET2_1 | 500 | 502 | PF00082 | 0.373 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 207 | 211 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.183 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 396 | 400 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 76 | 80 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.311 |
DEG_APCC_DBOX_1 | 162 | 170 | PF00400 | 0.518 |
DEG_APCC_DBOX_1 | 229 | 237 | PF00400 | 0.542 |
DEG_APCC_DBOX_1 | 532 | 540 | PF00400 | 0.283 |
DOC_CDC14_PxL_1 | 150 | 158 | PF14671 | 0.511 |
DOC_CDC14_PxL_1 | 176 | 184 | PF14671 | 0.511 |
DOC_CYCLIN_RxL_1 | 201 | 213 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 419 | 427 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 55 | 65 | PF00069 | 0.569 |
DOC_MAPK_MEF2A_6 | 421 | 429 | PF00069 | 0.401 |
DOC_PP1_RVXF_1 | 199 | 206 | PF00149 | 0.437 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.438 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.519 |
LIG_14-3-3_CanoR_1 | 304 | 313 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 314 | 323 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 343 | 350 | PF00244 | 0.485 |
LIG_APCC_ABBA_1 | 269 | 274 | PF00400 | 0.506 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.650 |
LIG_Clathr_ClatBox_1 | 109 | 113 | PF01394 | 0.508 |
LIG_Clathr_ClatBox_1 | 233 | 237 | PF01394 | 0.422 |
LIG_Clathr_ClatBox_1 | 275 | 279 | PF01394 | 0.362 |
LIG_Clathr_ClatBox_1 | 436 | 440 | PF01394 | 0.458 |
LIG_FHA_1 | 156 | 162 | PF00498 | 0.523 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.508 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.435 |
LIG_FHA_1 | 68 | 74 | PF00498 | 0.385 |
LIG_FHA_2 | 143 | 149 | PF00498 | 0.474 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.523 |
LIG_FHA_2 | 233 | 239 | PF00498 | 0.476 |
LIG_FHA_2 | 33 | 39 | PF00498 | 0.524 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.445 |
LIG_FHA_2 | 488 | 494 | PF00498 | 0.467 |
LIG_LIR_Gen_1 | 113 | 122 | PF02991 | 0.436 |
LIG_LIR_Gen_1 | 431 | 439 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 113 | 117 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 118 | 122 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.562 |
LIG_LIR_Nem_3 | 258 | 263 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 465 | 471 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 493 | 497 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 74 | 78 | PF02991 | 0.358 |
LIG_LRP6_Inhibitor_1 | 95 | 101 | PF00058 | 0.457 |
LIG_PCNA_yPIPBox_3 | 484 | 495 | PF02747 | 0.351 |
LIG_Pex14_2 | 451 | 455 | PF04695 | 0.361 |
LIG_Rb_LxCxE_1 | 96 | 118 | PF01857 | 0.318 |
LIG_RPA_C_Fungi | 515 | 527 | PF08784 | 0.438 |
LIG_SH2_CRK | 263 | 267 | PF00017 | 0.477 |
LIG_SH2_GRB2like | 140 | 143 | PF00017 | 0.384 |
LIG_SH2_NCK_1 | 119 | 123 | PF00017 | 0.405 |
LIG_SH2_NCK_1 | 263 | 267 | PF00017 | 0.445 |
LIG_SH2_SRC | 175 | 178 | PF00017 | 0.384 |
LIG_SH2_STAP1 | 140 | 144 | PF00017 | 0.384 |
LIG_SH2_STAT3 | 470 | 473 | PF00017 | 0.620 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.496 |
LIG_SH2_STAT5 | 470 | 473 | PF00017 | 0.533 |
LIG_SH2_STAT5 | 542 | 545 | PF00017 | 0.454 |
LIG_SUMO_SIM_anti_2 | 407 | 413 | PF11976 | 0.459 |
LIG_SUMO_SIM_anti_2 | 424 | 429 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 183 | 189 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 231 | 241 | PF11976 | 0.553 |
LIG_SUMO_SIM_par_1 | 69 | 74 | PF11976 | 0.474 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.499 |
LIG_TYR_ITIM | 117 | 122 | PF00017 | 0.405 |
LIG_UBA3_1 | 477 | 484 | PF00899 | 0.513 |
LIG_WRC_WIRS_1 | 72 | 77 | PF05994 | 0.496 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.581 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.622 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.502 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.319 |
MOD_CK2_1 | 10 | 16 | PF00069 | 0.538 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.398 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.554 |
MOD_CK2_1 | 330 | 336 | PF00069 | 0.524 |
MOD_CK2_1 | 428 | 434 | PF00069 | 0.358 |
MOD_CK2_1 | 487 | 493 | PF00069 | 0.487 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.513 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.548 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.535 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.413 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.560 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.480 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.398 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.385 |
MOD_N-GLC_1 | 413 | 418 | PF02516 | 0.476 |
MOD_N-GLC_1 | 82 | 87 | PF02516 | 0.399 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.625 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.281 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.313 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.457 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.564 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.407 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.374 |
MOD_PK_1 | 421 | 427 | PF00069 | 0.448 |
MOD_PK_1 | 520 | 526 | PF00069 | 0.468 |
MOD_PKA_2 | 342 | 348 | PF00069 | 0.521 |
MOD_Plk_1 | 115 | 121 | PF00069 | 0.300 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.384 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.383 |
MOD_Plk_1 | 413 | 419 | PF00069 | 0.531 |
MOD_Plk_1 | 512 | 518 | PF00069 | 0.441 |
MOD_Plk_1 | 82 | 88 | PF00069 | 0.473 |
MOD_Plk_2-3 | 330 | 336 | PF00069 | 0.441 |
MOD_Plk_4 | 105 | 111 | PF00069 | 0.405 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.269 |
MOD_Plk_4 | 512 | 518 | PF00069 | 0.459 |
MOD_Plk_4 | 520 | 526 | PF00069 | 0.481 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.359 |
MOD_SUMO_for_1 | 510 | 513 | PF00179 | 0.431 |
MOD_SUMO_rev_2 | 48 | 56 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_3 | 544 | 550 | PF01217 | 0.317 |
TRG_ENDOCYTIC_2 | 119 | 122 | PF00928 | 0.405 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 198 | 201 | PF00400 | 0.305 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.531 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.367 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 396 | 400 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 448 | 452 | PF00026 | 0.403 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.610 |
TRG_Pf-PMV_PEXEL_1 | 534 | 538 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB70 | Leptomonas seymouri | 71% | 99% |
A0A0S4JNZ9 | Bodo saltans | 38% | 99% |
A0A1X0P2D5 | Trypanosomatidae | 44% | 100% |
A0A422NMM2 | Trypanosoma rangeli | 42% | 100% |
A4HIV0 | Leishmania braziliensis | 82% | 100% |
A4I655 | Leishmania infantum | 100% | 100% |
C9ZRH5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9B1D8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q6S4 | Leishmania major | 95% | 100% |
Q9H069 | Homo sapiens | 27% | 100% |
V5DNR7 | Trypanosoma cruzi | 43% | 100% |