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 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3Q8IG01
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:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0016311 | dephosphorylation | 5 | 10 |
GO:0019538 | protein metabolic process | 3 | 10 |
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:0071704 | organic substance metabolic process | 2 | 10 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 10 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022607 | cellular component assembly | 4 | 1 |
GO:0030030 | cell projection organization | 4 | 1 |
GO:0030031 | cell projection assembly | 5 | 1 |
GO:0044782 | cilium organization | 5 | 1 |
GO:0060271 | cilium assembly | 6 | 1 |
GO:0070925 | organelle assembly | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0120031 | plasma membrane bounded cell projection assembly | 6 | 1 |
GO:0120036 | plasma membrane bounded cell projection organization | 5 | 1 |
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 | 262 | 266 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.657 |
CLV_C14_Caspase3-7 | 596 | 600 | PF00656 | 0.775 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.770 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 508 | 510 | PF00675 | 0.799 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.698 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.771 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.757 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 508 | 510 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.698 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.771 |
CLV_PCSK_PC1ET2_1 | 36 | 38 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.517 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.378 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.498 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.519 |
DEG_APCC_DBOX_1 | 405 | 413 | PF00400 | 0.419 |
DEG_MDM2_SWIB_1 | 462 | 470 | PF02201 | 0.390 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.705 |
DEG_SPOP_SBC_1 | 519 | 523 | PF00917 | 0.789 |
DOC_CYCLIN_RxL_1 | 297 | 307 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 107 | 113 | PF00134 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 401 | 407 | PF00134 | 0.495 |
DOC_MAPK_gen_1 | 189 | 196 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 403 | 413 | PF00069 | 0.397 |
DOC_MAPK_MEF2A_6 | 389 | 397 | PF00069 | 0.555 |
DOC_PP2B_LxvP_1 | 517 | 520 | PF13499 | 0.739 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.435 |
DOC_SPAK_OSR1_1 | 343 | 347 | PF12202 | 0.464 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 594 | 598 | PF00917 | 0.701 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.369 |
DOC_USP7_UBL2_3 | 25 | 29 | PF12436 | 0.718 |
DOC_USP7_UBL2_3 | 30 | 34 | PF12436 | 0.654 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.730 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 254 | 261 | PF00244 | 0.388 |
LIG_14-3-3_CanoR_1 | 345 | 350 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 508 | 512 | PF00244 | 0.725 |
LIG_14-3-3_CanoR_1 | 548 | 556 | PF00244 | 0.743 |
LIG_14-3-3_CanoR_1 | 592 | 602 | PF00244 | 0.781 |
LIG_APCC_ABBA_1 | 279 | 284 | PF00400 | 0.433 |
LIG_APCC_ABBAyCdc20_2 | 278 | 284 | PF00400 | 0.388 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.431 |
LIG_eIF4E_1 | 289 | 295 | PF01652 | 0.477 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.432 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.787 |
LIG_FHA_2 | 559 | 565 | PF00498 | 0.689 |
LIG_Integrin_RGD_1 | 19 | 21 | PF01839 | 0.615 |
LIG_LIR_Apic_2 | 160 | 165 | PF02991 | 0.426 |
LIG_LIR_Apic_2 | 6 | 12 | PF02991 | 0.744 |
LIG_LIR_Gen_1 | 414 | 423 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 68 | 77 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 414 | 419 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.447 |
LIG_LYPXL_yS_3 | 109 | 112 | PF13949 | 0.502 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.417 |
LIG_NRP_CendR_1 | 601 | 604 | PF00754 | 0.812 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.344 |
LIG_Pex14_2 | 440 | 444 | PF04695 | 0.567 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.384 |
LIG_PTB_Apo_2 | 427 | 434 | PF02174 | 0.492 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.376 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.543 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.806 |
LIG_SH2_GRB2like | 474 | 477 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 477 | 481 | PF00017 | 0.535 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.401 |
LIG_SH3_2 | 527 | 532 | PF14604 | 0.607 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.742 |
LIG_SH3_3 | 550 | 556 | PF00018 | 0.795 |
LIG_Sin3_3 | 224 | 231 | PF02671 | 0.408 |
LIG_SUMO_SIM_anti_2 | 221 | 229 | PF11976 | 0.402 |
LIG_SUMO_SIM_anti_2 | 351 | 356 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 515 | 523 | PF11976 | 0.736 |
LIG_SUMO_SIM_par_1 | 554 | 565 | PF11976 | 0.667 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.639 |
LIG_TRAF2_1 | 522 | 525 | PF00917 | 0.704 |
LIG_TYR_ITIM | 107 | 112 | PF00017 | 0.482 |
LIG_UBA3_1 | 299 | 308 | PF00899 | 0.427 |
LIG_WRC_WIRS_1 | 354 | 359 | PF05994 | 0.406 |
LIG_WRC_WIRS_1 | 437 | 442 | PF05994 | 0.419 |
LIG_WW_3 | 505 | 509 | PF00397 | 0.735 |
MOD_CDK_SPxxK_3 | 449 | 456 | PF00069 | 0.516 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.502 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.410 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.425 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.758 |
MOD_CK1_1 | 518 | 524 | PF00069 | 0.764 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.742 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.442 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.646 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.487 |
MOD_CK2_1 | 519 | 525 | PF00069 | 0.758 |
MOD_CK2_1 | 558 | 564 | PF00069 | 0.698 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.495 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.480 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.425 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.355 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.428 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.440 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.464 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.484 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.777 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.633 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.733 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.390 |
MOD_LATS_1 | 116 | 122 | PF00433 | 0.556 |
MOD_N-GLC_1 | 118 | 123 | PF02516 | 0.467 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.423 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.340 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.486 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.403 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.342 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.487 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.297 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.392 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.460 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.489 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.544 |
MOD_NEK2_1 | 541 | 546 | PF00069 | 0.722 |
MOD_NEK2_2 | 101 | 106 | PF00069 | 0.407 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.541 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.444 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.446 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.599 |
MOD_PIKK_1 | 542 | 548 | PF00454 | 0.757 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.390 |
MOD_PK_1 | 345 | 351 | PF00069 | 0.482 |
MOD_PKA_1 | 30 | 36 | PF00069 | 0.802 |
MOD_PKA_1 | 578 | 584 | PF00069 | 0.722 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.398 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.768 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.497 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.302 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.355 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.765 |
MOD_PKA_2 | 547 | 553 | PF00069 | 0.735 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.722 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.395 |
MOD_PKB_1 | 343 | 351 | PF00069 | 0.554 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.551 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.414 |
MOD_Plk_1 | 537 | 543 | PF00069 | 0.658 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.436 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.444 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.408 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.512 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.603 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.553 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.432 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.519 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.732 |
MOD_SUMO_rev_2 | 560 | 567 | PF00179 | 0.750 |
MOD_SUMO_rev_2 | 596 | 602 | PF00179 | 0.739 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.413 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.427 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.416 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.363 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 276 | 279 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 507 | 509 | PF00400 | 0.720 |
TRG_ER_diArg_1 | 577 | 579 | PF00400 | 0.696 |
TRG_NES_CRM1_1 | 262 | 275 | PF08389 | 0.473 |
TRG_NLS_MonoCore_2 | 27 | 32 | PF00514 | 0.760 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.444 |
TRG_NLS_MonoExtC_3 | 27 | 32 | PF00514 | 0.776 |
TRG_NLS_MonoExtN_4 | 25 | 32 | PF00514 | 0.741 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW9 | Leptomonas seymouri | 75% | 99% |
A0A0S4KLI7 | Bodo saltans | 47% | 100% |
A0A1X0NUR4 | Trypanosomatidae | 66% | 100% |
A4HK44 | Leishmania braziliensis | 84% | 100% |
A4I7L8 | Leishmania infantum | 100% | 100% |
D0A9T0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9B2I7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q5L9 | Leishmania major | 96% | 100% |