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: A4HK44
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 | 0.508 |
CLV_C14_Caspase3-7 | 41 | 45 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 595 | 599 | PF00656 | 0.762 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 239 | 241 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 342 | 344 | PF00675 | 0.433 |
CLV_NRD_NRD_1 | 398 | 400 | PF00675 | 0.542 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.748 |
CLV_NRD_NRD_1 | 545 | 547 | PF00675 | 0.527 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.744 |
CLV_PCSK_KEX2_1 | 239 | 241 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.772 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 398 | 400 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 488 | 490 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.527 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.744 |
CLV_PCSK_PC1ET2_1 | 30 | 32 | PF00082 | 0.772 |
CLV_PCSK_PC1ET2_1 | 383 | 385 | PF00082 | 0.394 |
CLV_PCSK_PC1ET2_1 | 488 | 490 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 398 | 402 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 461 | 465 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 485 | 489 | PF00082 | 0.482 |
DEG_APCC_DBOX_1 | 31 | 39 | PF00400 | 0.531 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.517 |
DEG_APCC_DBOX_1 | 405 | 413 | PF00400 | 0.421 |
DEG_APCC_DBOX_1 | 507 | 515 | PF00400 | 0.500 |
DEG_MDM2_SWIB_1 | 462 | 470 | PF02201 | 0.387 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.693 |
DOC_CDC14_PxL_1 | 514 | 522 | PF14671 | 0.505 |
DOC_CKS1_1 | 169 | 174 | PF01111 | 0.342 |
DOC_CYCLIN_RxL_1 | 297 | 307 | PF00134 | 0.463 |
DOC_CYCLIN_yCln2_LP_2 | 107 | 113 | PF00134 | 0.567 |
DOC_CYCLIN_yCln2_LP_2 | 401 | 407 | PF00134 | 0.502 |
DOC_MAPK_FxFP_2 | 594 | 597 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 189 | 196 | PF00069 | 0.401 |
DOC_MAPK_gen_1 | 403 | 413 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 389 | 397 | PF00069 | 0.542 |
DOC_PP4_FxxP_1 | 164 | 167 | PF00568 | 0.434 |
DOC_PP4_FxxP_1 | 524 | 527 | PF00568 | 0.517 |
DOC_PP4_FxxP_1 | 594 | 597 | PF00568 | 0.543 |
DOC_SPAK_OSR1_1 | 343 | 347 | PF12202 | 0.460 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 50 | 54 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.758 |
DOC_USP7_MATH_2 | 558 | 564 | PF00917 | 0.519 |
DOC_USP7_UBL2_3 | 189 | 193 | PF12436 | 0.369 |
DOC_USP7_UBL2_3 | 21 | 25 | PF12436 | 0.733 |
DOC_USP7_UBL2_3 | 30 | 34 | PF12436 | 0.655 |
DOC_WW_Pin1_4 | 168 | 173 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 365 | 370 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 100 | 106 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 254 | 261 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 345 | 350 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 364 | 369 | PF00244 | 0.236 |
LIG_14-3-3_CanoR_1 | 384 | 388 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 406 | 410 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 49 | 55 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 508 | 512 | PF00244 | 0.669 |
LIG_14-3-3_CanoR_1 | 545 | 553 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 592 | 597 | PF00244 | 0.776 |
LIG_APCC_ABBA_1 | 279 | 284 | PF00400 | 0.428 |
LIG_BIR_III_2 | 478 | 482 | PF00653 | 0.330 |
LIG_BRCT_BRCA1_1 | 255 | 259 | PF00533 | 0.426 |
LIG_BRCT_BRCA1_1 | 520 | 524 | PF00533 | 0.517 |
LIG_eIF4E_1 | 289 | 295 | PF01652 | 0.474 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.461 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.701 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.722 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.520 |
LIG_LIR_Apic_2 | 160 | 165 | PF02991 | 0.426 |
LIG_LIR_Apic_2 | 521 | 527 | PF02991 | 0.511 |
LIG_LIR_Apic_2 | 567 | 573 | PF02991 | 0.540 |
LIG_LIR_Apic_2 | 591 | 597 | PF02991 | 0.543 |
LIG_LIR_Apic_2 | 6 | 12 | PF02991 | 0.708 |
LIG_LIR_Gen_1 | 431 | 440 | PF02991 | 0.524 |
LIG_LIR_Gen_1 | 68 | 77 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 160 | 164 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 287 | 292 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 431 | 436 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 472 | 477 | PF02991 | 0.448 |
LIG_LYPXL_yS_3 | 109 | 112 | PF13949 | 0.501 |
LIG_NRBOX | 299 | 305 | PF00104 | 0.418 |
LIG_NRP_CendR_1 | 603 | 604 | PF00754 | 0.764 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.344 |
LIG_Pex14_2 | 440 | 444 | PF04695 | 0.565 |
LIG_Pex14_2 | 462 | 466 | PF04695 | 0.378 |
LIG_PTB_Apo_2 | 427 | 434 | PF02174 | 0.507 |
LIG_SH2_CRK | 289 | 293 | PF00017 | 0.372 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.575 |
LIG_SH2_CRK | 9 | 13 | PF00017 | 0.764 |
LIG_SH2_GRB2like | 474 | 477 | PF00017 | 0.455 |
LIG_SH2_NCK_1 | 477 | 481 | PF00017 | 0.533 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.444 |
LIG_SH2_SRC | 417 | 420 | PF00017 | 0.315 |
LIG_SH2_STAP1 | 215 | 219 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.531 |
LIG_SH3_2 | 540 | 545 | PF14604 | 0.542 |
LIG_SH3_3 | 524 | 530 | PF00018 | 0.697 |
LIG_SH3_3 | 534 | 540 | PF00018 | 0.709 |
LIG_SUMO_SIM_anti_2 | 223 | 229 | PF11976 | 0.400 |
LIG_SUMO_SIM_anti_2 | 351 | 356 | PF11976 | 0.429 |
LIG_TRAF2_1 | 388 | 391 | PF00917 | 0.618 |
LIG_TRFH_1 | 539 | 543 | PF08558 | 0.532 |
LIG_TYR_ITIM | 107 | 112 | PF00017 | 0.481 |
LIG_UBA3_1 | 299 | 308 | PF00899 | 0.429 |
LIG_WRC_WIRS_1 | 354 | 359 | PF05994 | 0.404 |
LIG_WW_3 | 505 | 509 | PF00397 | 0.704 |
MOD_CDC14_SPxK_1 | 542 | 545 | PF00782 | 0.531 |
MOD_CDK_SPxK_1 | 539 | 545 | PF00069 | 0.533 |
MOD_CDK_SPxxK_3 | 449 | 456 | PF00069 | 0.513 |
MOD_CDK_SPxxK_3 | 539 | 546 | PF00069 | 0.533 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.504 |
MOD_CK1_1 | 353 | 359 | PF00069 | 0.408 |
MOD_CK1_1 | 365 | 371 | PF00069 | 0.422 |
MOD_CK1_1 | 510 | 516 | PF00069 | 0.710 |
MOD_CK1_1 | 544 | 550 | PF00069 | 0.729 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.371 |
MOD_CK2_1 | 157 | 163 | PF00069 | 0.438 |
MOD_CK2_1 | 385 | 391 | PF00069 | 0.637 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.483 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.436 |
MOD_GlcNHglycan | 142 | 146 | PF01048 | 0.516 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.463 |
MOD_GlcNHglycan | 332 | 335 | PF01048 | 0.421 |
MOD_GlcNHglycan | 413 | 416 | PF01048 | 0.362 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.404 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.570 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.408 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.442 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.531 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.436 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.462 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.477 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.370 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.723 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.389 |
MOD_LATS_1 | 116 | 122 | PF00433 | 0.558 |
MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.426 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.314 |
MOD_N-GLC_1 | 531 | 536 | PF02516 | 0.524 |
MOD_N-GLC_1 | 598 | 603 | PF02516 | 0.542 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.344 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.481 |
MOD_NEK2_1 | 295 | 300 | PF00069 | 0.403 |
MOD_NEK2_1 | 304 | 309 | PF00069 | 0.344 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.488 |
MOD_NEK2_1 | 385 | 390 | PF00069 | 0.642 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.392 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.400 |
MOD_NEK2_1 | 492 | 497 | PF00069 | 0.478 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.480 |
MOD_NEK2_2 | 101 | 106 | PF00069 | 0.406 |
MOD_NEK2_2 | 483 | 488 | PF00069 | 0.520 |
MOD_NEK2_2 | 50 | 55 | PF00069 | 0.381 |
MOD_PIKK_1 | 213 | 219 | PF00454 | 0.444 |
MOD_PIKK_1 | 253 | 259 | PF00454 | 0.441 |
MOD_PIKK_1 | 547 | 553 | PF00454 | 0.647 |
MOD_PIKK_1 | 95 | 101 | PF00454 | 0.389 |
MOD_PK_1 | 345 | 351 | PF00069 | 0.526 |
MOD_PKA_1 | 30 | 36 | PF00069 | 0.800 |
MOD_PKA_1 | 383 | 389 | PF00069 | 0.389 |
MOD_PKA_1 | 578 | 584 | PF00069 | 0.769 |
MOD_PKA_2 | 228 | 234 | PF00069 | 0.307 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.410 |
MOD_PKA_2 | 30 | 36 | PF00069 | 0.767 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.494 |
MOD_PKA_2 | 383 | 389 | PF00069 | 0.311 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.400 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.292 |
MOD_PKA_2 | 507 | 513 | PF00069 | 0.714 |
MOD_PKA_2 | 544 | 550 | PF00069 | 0.706 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.769 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.400 |
MOD_PKB_1 | 343 | 351 | PF00069 | 0.552 |
MOD_Plk_1 | 328 | 334 | PF00069 | 0.525 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.402 |
MOD_Plk_1 | 531 | 537 | PF00069 | 0.619 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.435 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.458 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.411 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.490 |
MOD_Plk_4 | 54 | 60 | PF00069 | 0.552 |
MOD_ProDKin_1 | 168 | 174 | PF00069 | 0.342 |
MOD_ProDKin_1 | 365 | 371 | PF00069 | 0.430 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.515 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.539 |
MOD_SUMO_rev_2 | 560 | 567 | PF00179 | 0.769 |
TRG_DiLeu_BaEn_1 | 223 | 228 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 299 | 304 | PF01217 | 0.413 |
TRG_DiLeu_BaLyEn_6 | 570 | 575 | PF01217 | 0.528 |
TRG_ENDOCYTIC_2 | 109 | 112 | PF00928 | 0.426 |
TRG_ENDOCYTIC_2 | 161 | 164 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 289 | 292 | PF00928 | 0.378 |
TRG_ENDOCYTIC_2 | 477 | 480 | PF00928 | 0.516 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.531 |
TRG_ER_diArg_1 | 341 | 343 | PF00400 | 0.444 |
TRG_ER_diArg_1 | 397 | 399 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 545 | 548 | PF00400 | 0.527 |
TRG_ER_diArg_1 | 577 | 579 | PF00400 | 0.744 |
TRG_NES_CRM1_1 | 262 | 275 | PF08389 | 0.457 |
TRG_NLS_MonoCore_2 | 26 | 31 | PF00514 | 0.764 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.444 |
TRG_NLS_MonoExtC_3 | 26 | 31 | PF00514 | 0.781 |
TRG_NLS_MonoExtN_4 | 25 | 32 | PF00514 | 0.742 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILW9 | Leptomonas seymouri | 74% | 99% |
A0A0S4KLI7 | Bodo saltans | 45% | 100% |
A0A1X0NUR4 | Trypanosomatidae | 63% | 100% |
A0A3Q8IG01 | Leishmania donovani | 84% | 100% |
A4I7L8 | Leishmania infantum | 83% | 100% |
D0A9T0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B2I7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
Q4Q5L9 | Leishmania major | 84% | 100% |