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: 6 |
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:0000159 | protein phosphatase type 2A complex | 5 | 1 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005929 | cilium | 4 | 1 |
GO:0008287 | protein serine/threonine phosphatase complex | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0036064 | ciliary basal body | 3 | 1 |
GO:0042995 | cell projection | 2 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0051286 | cell tip | 3 | 1 |
GO:0060187 | cell pole | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:0120025 | plasma membrane bounded cell projection | 3 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
GO:1903293 | phosphatase complex | 3 | 1 |
Related structures:
AlphaFold database: E9AIC2
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 1 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016311 | dephosphorylation | 5 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0019208 | phosphatase regulator activity | 3 | 1 |
GO:0019888 | protein phosphatase regulator activity | 4 | 1 |
GO:0030234 | enzyme regulator activity | 2 | 1 |
GO:0098772 | molecular function regulator activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 126 | 130 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 229 | 233 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 581 | 585 | PF00656 | 0.441 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.524 |
CLV_NRD_NRD_1 | 148 | 150 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 196 | 198 | PF00675 | 0.350 |
CLV_PCSK_KEX2_1 | 148 | 150 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 196 | 198 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 333 | 337 | PF00082 | 0.272 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.345 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.319 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 583 | 587 | PF00082 | 0.435 |
CLV_Separin_Metazoa | 58 | 62 | PF03568 | 0.369 |
DEG_APCC_DBOX_1 | 176 | 184 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 504 | 512 | PF00400 | 0.441 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.616 |
DEG_ODPH_VHL_1 | 409 | 420 | PF01847 | 0.417 |
DEG_SPOP_SBC_1 | 116 | 120 | PF00917 | 0.673 |
DOC_ANK_TNKS_1 | 147 | 154 | PF00023 | 0.524 |
DOC_CYCLIN_yCln2_LP_2 | 83 | 89 | PF00134 | 0.433 |
DOC_MAPK_DCC_7 | 539 | 547 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 40 | 49 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 425 | 433 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 40 | 49 | PF00069 | 0.502 |
DOC_MAPK_MEF2A_6 | 539 | 547 | PF00069 | 0.422 |
DOC_MAPK_NFAT4_5 | 42 | 50 | PF00069 | 0.503 |
DOC_PP2B_LxvP_1 | 287 | 290 | PF13499 | 0.384 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.465 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.325 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.421 |
DOC_USP7_MATH_1 | 276 | 280 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.387 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 469 | 473 | PF00917 | 0.355 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.361 |
DOC_USP7_MATH_1 | 588 | 592 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.685 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 400 | 405 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 158 | 165 | PF00244 | 0.333 |
LIG_14-3-3_CanoR_1 | 22 | 27 | PF00244 | 0.379 |
LIG_14-3-3_CanoR_1 | 262 | 272 | PF00244 | 0.420 |
LIG_14-3-3_CanoR_1 | 341 | 350 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 351 | 355 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 457 | 465 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 572 | 580 | PF00244 | 0.544 |
LIG_Actin_WH2_2 | 347 | 362 | PF00022 | 0.334 |
LIG_APCC_ABBA_1 | 535 | 540 | PF00400 | 0.521 |
LIG_BIR_III_4 | 328 | 332 | PF00653 | 0.420 |
LIG_Clathr_ClatBox_1 | 84 | 88 | PF01394 | 0.239 |
LIG_eIF4E_1 | 79 | 85 | PF01652 | 0.256 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.420 |
LIG_FHA_1 | 370 | 376 | PF00498 | 0.377 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.350 |
LIG_FHA_1 | 457 | 463 | PF00498 | 0.474 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.396 |
LIG_FHA_1 | 565 | 571 | PF00498 | 0.407 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.483 |
LIG_FHA_2 | 174 | 180 | PF00498 | 0.491 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.384 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.259 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.580 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.384 |
LIG_LIR_Gen_1 | 142 | 150 | PF02991 | 0.348 |
LIG_LIR_Gen_1 | 2 | 11 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 528 | 534 | PF02991 | 0.454 |
LIG_MYND_1 | 411 | 415 | PF01753 | 0.396 |
LIG_Pex14_1 | 270 | 274 | PF04695 | 0.299 |
LIG_PTB_Apo_2 | 108 | 115 | PF02174 | 0.274 |
LIG_SH2_CRK | 295 | 299 | PF00017 | 0.420 |
LIG_SH2_CRK | 512 | 516 | PF00017 | 0.407 |
LIG_SH2_STAP1 | 79 | 83 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 48 | 51 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 52 | 55 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.490 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.427 |
LIG_SH3_3 | 494 | 500 | PF00018 | 0.431 |
LIG_SUMO_SIM_par_1 | 257 | 263 | PF11976 | 0.479 |
LIG_SUMO_SIM_par_1 | 492 | 499 | PF11976 | 0.257 |
LIG_UBA3_1 | 553 | 561 | PF00899 | 0.420 |
MOD_CDK_SPxxK_3 | 400 | 407 | PF00069 | 0.489 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.713 |
MOD_CK1_1 | 163 | 169 | PF00069 | 0.367 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.250 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.346 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.420 |
MOD_CK1_1 | 495 | 501 | PF00069 | 0.361 |
MOD_CK1_1 | 6 | 12 | PF00069 | 0.456 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.355 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.391 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.434 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.409 |
MOD_CK2_1 | 89 | 95 | PF00069 | 0.419 |
MOD_Cter_Amidation | 330 | 333 | PF01082 | 0.420 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.732 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.692 |
MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.470 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.440 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.324 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.400 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.501 |
MOD_GSK3_1 | 115 | 122 | PF00069 | 0.592 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.425 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.470 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.389 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.391 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.404 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.340 |
MOD_GSK3_1 | 588 | 595 | PF00069 | 0.579 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.377 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.492 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.417 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.370 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.295 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.442 |
MOD_NEK2_1 | 592 | 597 | PF00069 | 0.616 |
MOD_PIKK_1 | 431 | 437 | PF00454 | 0.231 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.336 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.416 |
MOD_PKA_2 | 350 | 356 | PF00069 | 0.420 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.455 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.469 |
MOD_Plk_1 | 266 | 272 | PF00069 | 0.299 |
MOD_Plk_1 | 345 | 351 | PF00069 | 0.381 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.375 |
MOD_Plk_2-3 | 94 | 100 | PF00069 | 0.383 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.323 |
MOD_Plk_4 | 241 | 247 | PF00069 | 0.410 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.389 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.508 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.409 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.435 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.357 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.339 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.356 |
MOD_ProDKin_1 | 400 | 406 | PF00069 | 0.487 |
MOD_SUMO_for_1 | 227 | 230 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 399 | 409 | PF00179 | 0.575 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.339 |
TRG_ER_diArg_1 | 147 | 149 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 195 | 197 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 270 | 273 | PF00400 | 0.299 |
TRG_ER_diArg_1 | 426 | 429 | PF00400 | 0.365 |
TRG_NES_CRM1_1 | 88 | 101 | PF08389 | 0.453 |
TRG_Pf-PMV_PEXEL_1 | 148 | 152 | PF00026 | 0.465 |
TRG_Pf-PMV_PEXEL_1 | 262 | 267 | PF00026 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 301 | 305 | PF00026 | 0.327 |
TRG_Pf-PMV_PEXEL_1 | 572 | 576 | PF00026 | 0.554 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHR7 | Leptomonas seymouri | 25% | 82% |
A0A0N1IM26 | Leptomonas seymouri | 83% | 100% |
A0A0S4IUU5 | Bodo saltans | 26% | 95% |
A0A0S4J1S0 | Bodo saltans | 23% | 97% |
A0A0S4J2C5 | Bodo saltans | 52% | 100% |
A0A1X0NWU2 | Trypanosomatidae | 59% | 100% |
A0A3Q8IBL0 | Leishmania donovani | 91% | 100% |
A0A3R7MGY7 | Trypanosoma rangeli | 58% | 100% |
A0A3S7WUV3 | Leishmania donovani | 25% | 84% |
A4H9H6 | Leishmania braziliensis | 25% | 84% |
A4HXU2 | Leishmania infantum | 25% | 84% |
A4HYP6 | Leishmania infantum | 91% | 100% |
C9ZI85 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AUK9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
P30153 | Homo sapiens | 36% | 100% |
P30154 | Homo sapiens | 34% | 100% |
P31383 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 94% |
P36179 | Drosophila melanogaster | 33% | 100% |
P54612 | Sus scrofa | 36% | 100% |
P54613 | Sus scrofa | 34% | 100% |
Q09543 | Caenorhabditis elegans | 33% | 100% |
Q32PI5 | Bos taurus | 36% | 100% |
Q38845 | Arabidopsis thaliana | 34% | 100% |
Q38950 | Arabidopsis thaliana | 34% | 100% |
Q38951 | Arabidopsis thaliana | 33% | 100% |
Q4QCX5 | Leishmania major | 90% | 100% |
Q4QDX5 | Leishmania major | 24% | 84% |
Q4QQT4 | Rattus norvegicus | 34% | 100% |
Q54QR9 | Dictyostelium discoideum | 33% | 100% |
Q76MZ3 | Mus musculus | 36% | 100% |
Q7TNP2 | Mus musculus | 34% | 100% |
Q9UT08 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 100% |
V5C089 | Trypanosoma cruzi | 57% | 100% |