Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 2 |
Pissara et al. | yes | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 4 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 12 |
NetGPI | no | yes: 0, no: 12 |
Related structures:
AlphaFold database: A4H9H6
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 | 351 | 355 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 670 | 674 | PF00656 | 0.527 |
CLV_C14_Caspase3-7 | 9 | 13 | PF00656 | 0.574 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.312 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.451 |
CLV_PCSK_KEX2_1 | 450 | 452 | PF00082 | 0.496 |
CLV_PCSK_PC1ET2_1 | 406 | 408 | PF00082 | 0.451 |
CLV_PCSK_PC1ET2_1 | 450 | 452 | PF00082 | 0.474 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.423 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 516 | 520 | PF00082 | 0.401 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.340 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.303 |
CLV_Separin_Metazoa | 265 | 269 | PF03568 | 0.272 |
CLV_Separin_Metazoa | 310 | 314 | PF03568 | 0.479 |
DEG_APCC_DBOX_1 | 424 | 432 | PF00400 | 0.333 |
DEG_SCF_TRCP1_1 | 645 | 650 | PF00400 | 0.636 |
DEG_SPOP_SBC_1 | 484 | 488 | PF00917 | 0.353 |
DEG_SPOP_SBC_1 | 692 | 696 | PF00917 | 0.534 |
DOC_CKS1_1 | 419 | 424 | PF01111 | 0.482 |
DOC_CKS1_1 | 682 | 687 | PF01111 | 0.534 |
DOC_CYCLIN_RxL_1 | 412 | 421 | PF00134 | 0.469 |
DOC_MAPK_gen_1 | 450 | 457 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 231 | 240 | PF00069 | 0.380 |
DOC_MAPK_MEF2A_6 | 450 | 459 | PF00069 | 0.339 |
DOC_MAPK_NFAT4_5 | 231 | 239 | PF00069 | 0.474 |
DOC_PP1_RVXF_1 | 266 | 272 | PF00149 | 0.479 |
DOC_PP1_RVXF_1 | 359 | 366 | PF00149 | 0.339 |
DOC_PP4_FxxP_1 | 271 | 274 | PF00568 | 0.467 |
DOC_USP7_MATH_1 | 291 | 295 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 436 | 440 | PF00917 | 0.402 |
DOC_USP7_MATH_1 | 471 | 475 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.622 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 324 | 329 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 418 | 423 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 457 | 462 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.787 |
DOC_WW_Pin1_4 | 671 | 676 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 681 | 686 | PF00397 | 0.515 |
LIG_14-3-3_CanoR_1 | 210 | 214 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 231 | 237 | PF00244 | 0.469 |
LIG_14-3-3_CanoR_1 | 297 | 303 | PF00244 | 0.393 |
LIG_14-3-3_CanoR_1 | 313 | 320 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 368 | 372 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 385 | 393 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 485 | 490 | PF00244 | 0.348 |
LIG_Actin_WH2_2 | 564 | 580 | PF00022 | 0.292 |
LIG_APCC_ABBA_1 | 312 | 317 | PF00400 | 0.339 |
LIG_BIR_III_2 | 79 | 83 | PF00653 | 0.440 |
LIG_BRCT_BRCA1_1 | 462 | 466 | PF00533 | 0.475 |
LIG_EH1_1 | 375 | 383 | PF00400 | 0.376 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.708 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.415 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.381 |
LIG_FHA_1 | 562 | 568 | PF00498 | 0.485 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.649 |
LIG_FHA_1 | 682 | 688 | PF00498 | 0.533 |
LIG_FHA_1 | 693 | 699 | PF00498 | 0.565 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.473 |
LIG_FHA_2 | 223 | 229 | PF00498 | 0.445 |
LIG_GBD_Chelix_1 | 173 | 181 | PF00786 | 0.303 |
LIG_LIR_Gen_1 | 105 | 116 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 118 | 128 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 235 | 245 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 347 | 357 | PF02991 | 0.374 |
LIG_LIR_Gen_1 | 414 | 423 | PF02991 | 0.433 |
LIG_LIR_LC3C_4 | 564 | 568 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 105 | 111 | PF02991 | 0.320 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 16 | 22 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 330 | 335 | PF02991 | 0.367 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 463 | 469 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 504 | 510 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.331 |
LIG_NRBOX | 294 | 300 | PF00104 | 0.458 |
LIG_PCNA_PIPBox_1 | 109 | 118 | PF02747 | 0.402 |
LIG_PCNA_PIPBox_1 | 230 | 239 | PF02747 | 0.365 |
LIG_PCNA_PIPBox_1 | 86 | 95 | PF02747 | 0.456 |
LIG_PCNA_yPIPBox_3 | 85 | 93 | PF02747 | 0.456 |
LIG_Pex14_2 | 185 | 189 | PF04695 | 0.479 |
LIG_SH2_CRK | 108 | 112 | PF00017 | 0.396 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.348 |
LIG_SH2_CRK | 335 | 339 | PF00017 | 0.459 |
LIG_SH2_GRB2like | 507 | 510 | PF00017 | 0.490 |
LIG_SH2_NCK_1 | 489 | 493 | PF00017 | 0.457 |
LIG_SH2_PTP2 | 237 | 240 | PF00017 | 0.356 |
LIG_SH2_SRC | 489 | 492 | PF00017 | 0.459 |
LIG_SH2_SRC | 62 | 65 | PF00017 | 0.481 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.334 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 237 | 240 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.426 |
LIG_SH2_STAT5 | 510 | 513 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.310 |
LIG_SH3_3 | 322 | 328 | PF00018 | 0.539 |
LIG_SH3_3 | 458 | 464 | PF00018 | 0.430 |
LIG_Sin3_3 | 416 | 423 | PF02671 | 0.479 |
LIG_SUMO_SIM_anti_2 | 197 | 202 | PF11976 | 0.337 |
LIG_SUMO_SIM_anti_2 | 468 | 474 | PF11976 | 0.379 |
LIG_SUMO_SIM_anti_2 | 490 | 496 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 590 | 596 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 131 | 136 | PF11976 | 0.470 |
LIG_SUMO_SIM_par_1 | 190 | 197 | PF11976 | 0.472 |
LIG_SUMO_SIM_par_1 | 46 | 52 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 468 | 474 | PF11976 | 0.473 |
LIG_TRAF2_1 | 13 | 16 | PF00917 | 0.625 |
LIG_TRAF2_1 | 225 | 228 | PF00917 | 0.519 |
LIG_TRAF2_1 | 600 | 603 | PF00917 | 0.580 |
LIG_UBA3_1 | 398 | 406 | PF00899 | 0.470 |
LIG_UBA3_1 | 549 | 555 | PF00899 | 0.436 |
LIG_WRC_WIRS_1 | 73 | 78 | PF05994 | 0.487 |
MOD_CDK_SPxxK_3 | 418 | 425 | PF00069 | 0.517 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.483 |
MOD_CK1_1 | 202 | 208 | PF00069 | 0.322 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.484 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.346 |
MOD_CK1_1 | 460 | 466 | PF00069 | 0.421 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.497 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.767 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.719 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.479 |
MOD_CK2_1 | 222 | 228 | PF00069 | 0.459 |
MOD_CK2_1 | 371 | 377 | PF00069 | 0.310 |
MOD_CK2_1 | 477 | 483 | PF00069 | 0.366 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.331 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.516 |
MOD_GlcNHglycan | 546 | 549 | PF01048 | 0.519 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.429 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.637 |
MOD_GlcNHglycan | 687 | 690 | PF01048 | 0.808 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.481 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.374 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.391 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.390 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.326 |
MOD_GSK3_1 | 643 | 650 | PF00069 | 0.634 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.757 |
MOD_N-GLC_1 | 202 | 207 | PF02516 | 0.359 |
MOD_N-GLC_1 | 622 | 627 | PF02516 | 0.467 |
MOD_N-GLC_1 | 671 | 676 | PF02516 | 0.525 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.446 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.374 |
MOD_NEK2_1 | 298 | 303 | PF00069 | 0.369 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.316 |
MOD_NEK2_1 | 381 | 386 | PF00069 | 0.400 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.365 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.380 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.418 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.547 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.297 |
MOD_PIKK_1 | 598 | 604 | PF00454 | 0.577 |
MOD_PIKK_1 | 616 | 622 | PF00454 | 0.633 |
MOD_PIKK_1 | 678 | 684 | PF00454 | 0.527 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.578 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.494 |
MOD_PKA_2 | 209 | 215 | PF00069 | 0.377 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.353 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.383 |
MOD_PKA_2 | 484 | 490 | PF00069 | 0.349 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.347 |
MOD_Plk_1 | 202 | 208 | PF00069 | 0.352 |
MOD_Plk_1 | 24 | 30 | PF00069 | 0.369 |
MOD_Plk_1 | 281 | 287 | PF00069 | 0.398 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.451 |
MOD_Plk_1 | 477 | 483 | PF00069 | 0.376 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.404 |
MOD_Plk_4 | 232 | 238 | PF00069 | 0.415 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.327 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.357 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.381 |
MOD_Plk_4 | 510 | 516 | PF00069 | 0.404 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.373 |
MOD_ProDKin_1 | 324 | 330 | PF00069 | 0.512 |
MOD_ProDKin_1 | 418 | 424 | PF00069 | 0.534 |
MOD_ProDKin_1 | 457 | 463 | PF00069 | 0.428 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.787 |
MOD_ProDKin_1 | 671 | 677 | PF00069 | 0.527 |
MOD_ProDKin_1 | 681 | 687 | PF00069 | 0.515 |
TRG_DiLeu_BaEn_1 | 377 | 382 | PF01217 | 0.471 |
TRG_DiLeu_BaLyEn_6 | 294 | 299 | PF01217 | 0.449 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 427 | 432 | PF01217 | 0.342 |
TRG_DiLeu_BaLyEn_6 | 472 | 477 | PF01217 | 0.333 |
TRG_DiLeu_BaLyEn_6 | 68 | 73 | PF01217 | 0.353 |
TRG_ENDOCYTIC_2 | 108 | 111 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 237 | 240 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.350 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.459 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 287 | 290 | PF00400 | 0.502 |
TRG_ER_diArg_1 | 442 | 445 | PF00400 | 0.424 |
TRG_ER_diArg_1 | 523 | 526 | PF00400 | 0.428 |
TRG_NES_CRM1_1 | 26 | 39 | PF08389 | 0.492 |
TRG_NES_CRM1_1 | 426 | 440 | PF08389 | 0.366 |
TRG_NES_CRM1_1 | 90 | 102 | PF08389 | 0.412 |
TRG_Pf-PMV_PEXEL_1 | 400 | 404 | PF00026 | 0.388 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.348 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHR7 | Leptomonas seymouri | 87% | 97% |
A0A0S4J1S0 | Bodo saltans | 54% | 100% |
A0A1X0P6U3 | Trypanosomatidae | 58% | 100% |
A0A3Q8IBL0 | Leishmania donovani | 23% | 100% |
A0A3R7KDP1 | Trypanosoma rangeli | 55% | 100% |
A0A3S7WUV3 | Leishmania donovani | 93% | 100% |
A4HXU2 | Leishmania infantum | 93% | 100% |
A4HYP6 | Leishmania infantum | 23% | 100% |
C9ZZW6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
E9AIC2 | Leishmania braziliensis | 25% | 100% |
E9ARK4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
P30153 | Homo sapiens | 21% | 100% |
P30154 | Homo sapiens | 21% | 100% |
P36179 | Drosophila melanogaster | 22% | 100% |
P54612 | Sus scrofa | 21% | 100% |
P54613 | Sus scrofa | 21% | 100% |
Q32PI5 | Bos taurus | 21% | 100% |
Q38950 | Arabidopsis thaliana | 22% | 100% |
Q38951 | Arabidopsis thaliana | 22% | 100% |
Q4QCX5 | Leishmania major | 23% | 100% |
Q4QDX5 | Leishmania major | 93% | 100% |
Q4QQT4 | Rattus norvegicus | 20% | 100% |
Q54QR9 | Dictyostelium discoideum | 23% | 100% |
Q76MZ3 | Mus musculus | 21% | 100% |
V5DN32 | Trypanosoma cruzi | 54% | 100% |