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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4Q5L9
Term | Name | Level | Count |
---|---|---|---|
GO:0006470 | protein dephosphorylation | 5 | 10 |
GO:0006793 | phosphorus metabolic process | 3 | 10 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0016311 | dephosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
GO:0022607 | cellular component assembly | 4 | 2 |
GO:0030030 | cell projection organization | 4 | 2 |
GO:0030031 | cell projection assembly | 5 | 2 |
GO:0036211 | protein modification process | 4 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0043412 | macromolecule modification | 4 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044782 | cilium organization | 5 | 2 |
GO:0060271 | cilium assembly | 6 | 2 |
GO:0070925 | organelle assembly | 5 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 2 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004721 | phosphoprotein phosphatase activity | 3 | 10 |
GO:0004725 | protein tyrosine phosphatase activity | 4 | 10 |
GO:0008138 | protein tyrosine/serine/threonine phosphatase activity | 4 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0016791 | phosphatase activity | 5 | 10 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 263 | 267 | PF00656 | 0.561 |
CLV_C14_Caspase3-7 | 42 | 46 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.781 |
CLV_NRD_NRD_1 | 229 | 231 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.780 |
CLV_NRD_NRD_1 | 343 | 345 | PF00675 | 0.417 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.759 |
CLV_NRD_NRD_1 | 399 | 401 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 509 | 511 | PF00675 | 0.783 |
CLV_NRD_NRD_1 | 579 | 581 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.751 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.781 |
CLV_PCSK_KEX2_1 | 342 | 344 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 37 | 39 | PF00082 | 0.758 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.578 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 509 | 511 | PF00082 | 0.777 |
CLV_PCSK_KEX2_1 | 579 | 581 | PF00082 | 0.715 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.751 |
CLV_PCSK_PC1ET2_1 | 31 | 33 | PF00082 | 0.781 |
CLV_PCSK_PC1ET2_1 | 489 | 491 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 279 | 283 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.532 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 462 | 466 | PF00082 | 0.528 |
CLV_PCSK_SKI1_1 | 486 | 490 | PF00082 | 0.474 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.520 |
DEG_APCC_DBOX_1 | 406 | 414 | PF00400 | 0.418 |
DEG_MDM2_SWIB_1 | 463 | 471 | PF02201 | 0.391 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.693 |
DEG_SCF_FBW7_1 | 521 | 528 | PF00400 | 0.613 |
DEG_SPOP_SBC_1 | 520 | 524 | PF00917 | 0.788 |
DOC_CYCLIN_RxL_1 | 298 | 310 | PF00134 | 0.478 |
DOC_CYCLIN_yCln2_LP_2 | 108 | 114 | PF00134 | 0.566 |
DOC_CYCLIN_yCln2_LP_2 | 402 | 408 | PF00134 | 0.493 |
DOC_MAPK_gen_1 | 190 | 197 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 404 | 414 | PF00069 | 0.395 |
DOC_MAPK_MEF2A_6 | 390 | 398 | PF00069 | 0.534 |
DOC_PP2B_LxvP_1 | 518 | 521 | PF13499 | 0.735 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.432 |
DOC_PP4_FxxP_1 | 554 | 557 | PF00568 | 0.586 |
DOC_SPAK_OSR1_1 | 344 | 348 | PF12202 | 0.467 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 318 | 322 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.705 |
DOC_USP7_UBL2_3 | 190 | 194 | PF12436 | 0.369 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.726 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.662 |
DOC_WW_Pin1_4 | 366 | 371 | PF00397 | 0.437 |
DOC_WW_Pin1_4 | 450 | 455 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.580 |
LIG_14-3-3_CanoR_1 | 101 | 107 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 255 | 262 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 346 | 351 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 365 | 370 | PF00244 | 0.429 |
LIG_14-3-3_CanoR_1 | 407 | 411 | PF00244 | 0.400 |
LIG_14-3-3_CanoR_1 | 509 | 513 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 516 | 521 | PF00244 | 0.724 |
LIG_14-3-3_CanoR_1 | 549 | 557 | PF00244 | 0.722 |
LIG_14-3-3_CanoR_1 | 593 | 603 | PF00244 | 0.784 |
LIG_APCC_ABBA_1 | 280 | 285 | PF00400 | 0.432 |
LIG_APCC_ABBAyCdc20_2 | 279 | 285 | PF00400 | 0.387 |
LIG_BRCT_BRCA1_1 | 256 | 260 | PF00533 | 0.433 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.495 |
LIG_BRCT_BRCA1_1 | 550 | 554 | PF00533 | 0.534 |
LIG_eIF4E_1 | 290 | 296 | PF01652 | 0.477 |
LIG_FHA_1 | 120 | 126 | PF00498 | 0.457 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.783 |
LIG_FHA_2 | 560 | 566 | PF00498 | 0.687 |
LIG_LIR_Apic_2 | 161 | 166 | PF02991 | 0.425 |
LIG_LIR_Apic_2 | 551 | 557 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 69 | 78 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 104 | 110 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 288 | 293 | PF02991 | 0.383 |
LIG_LIR_Nem_3 | 415 | 420 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 473 | 478 | PF02991 | 0.471 |
LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.666 |
LIG_LYPXL_yS_3 | 110 | 113 | PF13949 | 0.501 |
LIG_MLH1_MIPbox_1 | 414 | 418 | PF16413 | 0.306 |
LIG_NRBOX | 300 | 306 | PF00104 | 0.420 |
LIG_NRP_CendR_1 | 602 | 605 | PF00754 | 0.812 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.344 |
LIG_Pex14_2 | 441 | 445 | PF04695 | 0.559 |
LIG_Pex14_2 | 463 | 467 | PF04695 | 0.382 |
LIG_PTB_Apo_2 | 428 | 435 | PF02174 | 0.496 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.376 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.572 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.792 |
LIG_SH2_GRB2like | 475 | 478 | PF00017 | 0.452 |
LIG_SH2_NCK_1 | 478 | 482 | PF00017 | 0.530 |
LIG_SH2_SRC | 214 | 217 | PF00017 | 0.444 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.420 |
LIG_Sin3_3 | 225 | 232 | PF02671 | 0.408 |
LIG_SUMO_SIM_anti_2 | 222 | 230 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 352 | 357 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 516 | 524 | PF11976 | 0.734 |
LIG_SUMO_SIM_par_1 | 555 | 566 | PF11976 | 0.657 |
LIG_TRAF2_1 | 389 | 392 | PF00917 | 0.642 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.481 |
LIG_UBA3_1 | 300 | 309 | PF00899 | 0.430 |
LIG_WRC_WIRS_1 | 355 | 360 | PF05994 | 0.406 |
LIG_WRC_WIRS_1 | 438 | 443 | PF05994 | 0.539 |
LIG_WW_3 | 506 | 510 | PF00397 | 0.743 |
MOD_CDK_SPxxK_3 | 450 | 457 | PF00069 | 0.515 |
MOD_CDK_SPxxK_3 | 509 | 516 | PF00069 | 0.615 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.716 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.501 |
MOD_CK1_1 | 354 | 360 | PF00069 | 0.391 |
MOD_CK1_1 | 366 | 372 | PF00069 | 0.376 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.754 |
MOD_CK1_1 | 519 | 525 | PF00069 | 0.760 |
MOD_CK1_1 | 545 | 551 | PF00069 | 0.722 |
MOD_CK2_1 | 158 | 164 | PF00069 | 0.442 |
MOD_CK2_1 | 386 | 392 | PF00069 | 0.661 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.485 |
MOD_CK2_1 | 520 | 526 | PF00069 | 0.752 |
MOD_CK2_1 | 559 | 565 | PF00069 | 0.694 |
MOD_Cter_Amidation | 583 | 586 | PF01082 | 0.550 |
MOD_GlcNHglycan | 143 | 147 | PF01048 | 0.517 |
MOD_GlcNHglycan | 15 | 19 | PF01048 | 0.628 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.490 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.426 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.355 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.721 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.590 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.443 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.444 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.445 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.487 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.774 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.729 |
MOD_GSK3_1 | 96 | 103 | PF00069 | 0.389 |
MOD_LATS_1 | 117 | 123 | PF00433 | 0.557 |
MOD_N-GLC_1 | 119 | 124 | PF02516 | 0.467 |
MOD_N-GLC_1 | 305 | 310 | PF02516 | 0.427 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.344 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.473 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.403 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.495 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.298 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.368 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.390 |
MOD_NEK2_1 | 493 | 498 | PF00069 | 0.478 |
MOD_NEK2_1 | 499 | 504 | PF00069 | 0.497 |
MOD_NEK2_1 | 542 | 547 | PF00069 | 0.708 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.545 |
MOD_NEK2_2 | 102 | 107 | PF00069 | 0.406 |
MOD_NEK2_2 | 484 | 489 | PF00069 | 0.523 |
MOD_PIKK_1 | 214 | 220 | PF00454 | 0.444 |
MOD_PIKK_1 | 254 | 260 | PF00454 | 0.448 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.764 |
MOD_PIKK_1 | 96 | 102 | PF00454 | 0.389 |
MOD_PK_1 | 346 | 352 | PF00069 | 0.530 |
MOD_PK_1 | 516 | 522 | PF00069 | 0.618 |
MOD_PKA_1 | 31 | 37 | PF00069 | 0.808 |
MOD_PKA_1 | 579 | 585 | PF00069 | 0.744 |
MOD_PKA_2 | 100 | 106 | PF00069 | 0.400 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.416 |
MOD_PKA_2 | 31 | 37 | PF00069 | 0.775 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.465 |
MOD_PKA_2 | 384 | 390 | PF00069 | 0.306 |
MOD_PKA_2 | 406 | 412 | PF00069 | 0.399 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.764 |
MOD_PKA_2 | 548 | 554 | PF00069 | 0.718 |
MOD_PKA_2 | 579 | 585 | PF00069 | 0.712 |
MOD_PKB_1 | 344 | 352 | PF00069 | 0.556 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.555 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.415 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.435 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.458 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.411 |
MOD_Plk_4 | 493 | 499 | PF00069 | 0.511 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.553 |
MOD_ProDKin_1 | 366 | 372 | PF00069 | 0.434 |
MOD_ProDKin_1 | 450 | 456 | PF00069 | 0.517 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.729 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.582 |
MOD_SUMO_rev_2 | 561 | 568 | PF00179 | 0.756 |
MOD_SUMO_rev_2 | 597 | 603 | PF00179 | 0.743 |
TRG_DiLeu_BaEn_1 | 224 | 229 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 300 | 305 | PF01217 | 0.414 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 162 | 165 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.679 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 342 | 344 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 36 | 38 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 398 | 400 | PF00400 | 0.578 |
TRG_ER_diArg_1 | 508 | 510 | PF00400 | 0.789 |
TRG_ER_diArg_1 | 578 | 580 | PF00400 | 0.710 |
TRG_ER_diArg_1 | 585 | 588 | PF00400 | 0.758 |
TRG_ER_diArg_1 | 591 | 594 | PF00400 | 0.782 |
TRG_NES_CRM1_1 | 263 | 276 | PF08389 | 0.483 |
TRG_NLS_MonoCore_2 | 27 | 32 | PF00514 | 0.772 |
TRG_NLS_MonoExtC_3 | 229 | 234 | PF00514 | 0.444 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.789 |
TRG_NLS_MonoExtN_4 | 25 | 32 | PF00514 | 0.751 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW9 | Leptomonas seymouri | 75% | 99% |
A0A0S4KLI7 | Bodo saltans | 46% | 100% |
A0A1X0NUR4 | Trypanosomatidae | 66% | 100% |
A0A3Q8IG01 | Leishmania donovani | 96% | 100% |
A4HK44 | Leishmania braziliensis | 84% | 100% |
A4I7L8 | Leishmania infantum | 96% | 100% |
D0A9T0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B2I7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |