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: 14 |
NetGPI | no | yes: 0, no: 14 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0016604 | nuclear body | 2 | 1 |
GO:0016605 | PML body | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AJU5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006281 | DNA repair | 5 | 1 |
GO:0006302 | double-strand break repair | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006950 | response to stress | 2 | 1 |
GO:0006974 | DNA damage response | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003677 | DNA binding | 4 | 1 |
GO:0003697 | single-stranded DNA binding | 5 | 1 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0005488 | binding | 1 | 1 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 1 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0070259 | tyrosyl-DNA phosphodiesterase activity | 4 | 1 |
GO:0070260 | 5'-tyrosyl-DNA phosphodiesterase activity | 5 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 302 | 306 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.474 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 88 | 90 | PF00675 | 0.444 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.441 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 88 | 90 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.510 |
CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.390 |
DEG_APCC_DBOX_1 | 273 | 281 | PF00400 | 0.486 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.531 |
DOC_CKS1_1 | 159 | 164 | PF01111 | 0.406 |
DOC_CKS1_1 | 296 | 301 | PF01111 | 0.514 |
DOC_CYCLIN_RxL_1 | 88 | 101 | PF00134 | 0.403 |
DOC_MAPK_gen_1 | 434 | 444 | PF00069 | 0.556 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 343 | 351 | PF00069 | 0.562 |
DOC_PP1_RVXF_1 | 328 | 335 | PF00149 | 0.553 |
DOC_PP1_RVXF_1 | 92 | 99 | PF00149 | 0.432 |
DOC_PP2B_LxvP_1 | 181 | 184 | PF13499 | 0.592 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.354 |
DOC_USP7_MATH_1 | 338 | 342 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 551 | 555 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 639 | 643 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.402 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.377 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.486 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 213 | 218 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 295 | 300 | PF00397 | 0.482 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.496 |
DOC_WW_Pin1_4 | 473 | 478 | PF00397 | 0.570 |
LIG_14-3-3_CanoR_1 | 123 | 133 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 17 | 27 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 219 | 225 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 328 | 333 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 352 | 357 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 437 | 444 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 510 | 515 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.493 |
LIG_14-3-3_CanoR_1 | 611 | 615 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 650 | 654 | PF00244 | 0.577 |
LIG_14-3-3_CanoR_1 | 80 | 86 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 93 | 97 | PF00244 | 0.302 |
LIG_Actin_WH2_2 | 236 | 252 | PF00022 | 0.552 |
LIG_Actin_WH2_2 | 607 | 625 | PF00022 | 0.364 |
LIG_APCC_ABBAyCdc20_2 | 330 | 336 | PF00400 | 0.543 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.580 |
LIG_BRCT_BRCA1_1 | 330 | 334 | PF00533 | 0.516 |
LIG_BRCT_BRCA1_1 | 577 | 581 | PF00533 | 0.492 |
LIG_BRCT_BRCA1_1 | 94 | 98 | PF00533 | 0.422 |
LIG_CSL_BTD_1 | 407 | 410 | PF09270 | 0.613 |
LIG_DLG_GKlike_1 | 352 | 359 | PF00625 | 0.443 |
LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.577 |
LIG_FHA_1 | 159 | 165 | PF00498 | 0.520 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.346 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.450 |
LIG_FHA_1 | 273 | 279 | PF00498 | 0.334 |
LIG_FHA_1 | 287 | 293 | PF00498 | 0.392 |
LIG_FHA_1 | 392 | 398 | PF00498 | 0.494 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.663 |
LIG_FHA_1 | 446 | 452 | PF00498 | 0.486 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.337 |
LIG_FHA_1 | 488 | 494 | PF00498 | 0.452 |
LIG_FHA_1 | 523 | 529 | PF00498 | 0.498 |
LIG_FHA_1 | 533 | 539 | PF00498 | 0.486 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.648 |
LIG_FHA_1 | 60 | 66 | PF00498 | 0.483 |
LIG_FHA_1 | 617 | 623 | PF00498 | 0.529 |
LIG_FHA_1 | 82 | 88 | PF00498 | 0.509 |
LIG_FHA_2 | 193 | 199 | PF00498 | 0.525 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.552 |
LIG_FHA_2 | 484 | 490 | PF00498 | 0.385 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.406 |
LIG_FHA_2 | 511 | 517 | PF00498 | 0.478 |
LIG_Integrin_RGD_1 | 633 | 635 | PF01839 | 0.482 |
LIG_LIR_Apic_2 | 472 | 477 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 207 | 218 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 239 | 249 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 185 | 189 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 207 | 213 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 215 | 221 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 31 | 36 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 433 | 438 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 595 | 599 | PF02991 | 0.441 |
LIG_MAD2 | 179 | 187 | PF02301 | 0.565 |
LIG_NRBOX | 244 | 250 | PF00104 | 0.568 |
LIG_NRBOX | 278 | 284 | PF00104 | 0.485 |
LIG_NRBOX | 355 | 361 | PF00104 | 0.494 |
LIG_PCNA_yPIPBox_3 | 533 | 543 | PF02747 | 0.561 |
LIG_SH2_STAP1 | 120 | 124 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 612 | 616 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 134 | 137 | PF00017 | 0.434 |
LIG_SH2_STAT5 | 172 | 175 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 307 | 310 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.497 |
LIG_SH2_STAT5 | 474 | 477 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.511 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.478 |
LIG_SH3_3 | 181 | 187 | PF00018 | 0.580 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.491 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.700 |
LIG_SH3_3 | 341 | 347 | PF00018 | 0.654 |
LIG_SH3_3 | 369 | 375 | PF00018 | 0.630 |
LIG_SH3_3 | 411 | 417 | PF00018 | 0.438 |
LIG_SUMO_SIM_anti_2 | 275 | 281 | PF11976 | 0.426 |
LIG_SUMO_SIM_par_1 | 172 | 178 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 428 | 433 | PF11976 | 0.597 |
LIG_SUMO_SIM_par_1 | 47 | 52 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 489 | 494 | PF11976 | 0.461 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.465 |
LIG_TRAF2_1 | 546 | 549 | PF00917 | 0.604 |
LIG_UBA3_1 | 86 | 94 | PF00899 | 0.416 |
MOD_CDC14_SPxK_1 | 476 | 479 | PF00782 | 0.534 |
MOD_CDK_SPxK_1 | 213 | 219 | PF00069 | 0.443 |
MOD_CDK_SPxK_1 | 473 | 479 | PF00069 | 0.583 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.397 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.405 |
MOD_CK1_1 | 418 | 424 | PF00069 | 0.698 |
MOD_CK1_1 | 648 | 654 | PF00069 | 0.787 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.450 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.588 |
MOD_CK2_1 | 483 | 489 | PF00069 | 0.408 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.402 |
MOD_Cter_Amidation | 116 | 119 | PF01082 | 0.517 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.782 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.426 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.339 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.581 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.606 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.555 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.739 |
MOD_GlcNHglycan | 438 | 441 | PF01048 | 0.443 |
MOD_GlcNHglycan | 461 | 464 | PF01048 | 0.667 |
MOD_GlcNHglycan | 468 | 472 | PF01048 | 0.468 |
MOD_GlcNHglycan | 493 | 496 | PF01048 | 0.448 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.692 |
MOD_GlcNHglycan | 566 | 569 | PF01048 | 0.666 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.515 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.363 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.552 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.751 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.456 |
MOD_GSK3_1 | 402 | 409 | PF00069 | 0.537 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.620 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.486 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.621 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.454 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.633 |
MOD_GSK3_1 | 571 | 578 | PF00069 | 0.468 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.456 |
MOD_GSK3_1 | 645 | 652 | PF00069 | 0.642 |
MOD_N-GLC_1 | 219 | 224 | PF02516 | 0.401 |
MOD_N-GLC_1 | 426 | 431 | PF02516 | 0.652 |
MOD_N-GLC_1 | 614 | 619 | PF02516 | 0.554 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.419 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.621 |
MOD_NEK2_1 | 483 | 488 | PF00069 | 0.440 |
MOD_NEK2_1 | 491 | 496 | PF00069 | 0.359 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.373 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.496 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.555 |
MOD_NEK2_2 | 469 | 474 | PF00069 | 0.635 |
MOD_PIKK_1 | 402 | 408 | PF00454 | 0.606 |
MOD_PIKK_1 | 493 | 499 | PF00454 | 0.562 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.590 |
MOD_PIKK_1 | 532 | 538 | PF00454 | 0.518 |
MOD_PIKK_1 | 544 | 550 | PF00454 | 0.614 |
MOD_PK_1 | 328 | 334 | PF00069 | 0.575 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.442 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.552 |
MOD_PKA_2 | 532 | 538 | PF00069 | 0.574 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.509 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.749 |
MOD_PKA_2 | 69 | 75 | PF00069 | 0.417 |
MOD_PKA_2 | 92 | 98 | PF00069 | 0.496 |
MOD_Plk_1 | 219 | 225 | PF00069 | 0.400 |
MOD_Plk_1 | 388 | 394 | PF00069 | 0.513 |
MOD_Plk_1 | 49 | 55 | PF00069 | 0.415 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.545 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.606 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.442 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.625 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.400 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.481 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.375 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.479 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.407 |
MOD_ProDKin_1 | 213 | 219 | PF00069 | 0.391 |
MOD_ProDKin_1 | 295 | 301 | PF00069 | 0.480 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.555 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.504 |
MOD_ProDKin_1 | 473 | 479 | PF00069 | 0.574 |
MOD_SUMO_for_1 | 603 | 606 | PF00179 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 620 | 625 | PF01217 | 0.447 |
TRG_ENDOCYTIC_2 | 307 | 310 | PF00928 | 0.456 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 112 | 114 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 118 | 120 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 268 | 270 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 327 | 330 | PF00400 | 0.599 |
TRG_ER_diArg_1 | 87 | 89 | PF00400 | 0.470 |
TRG_Pf-PMV_PEXEL_1 | 541 | 545 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 63 | 68 | PF00026 | 0.406 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUJ3 | Leptomonas seymouri | 56% | 98% |
A0A0S4J9X6 | Bodo saltans | 33% | 81% |
A0A1X0NSS8 | Trypanosomatidae | 26% | 67% |
A0A1X0P940 | Trypanosomatidae | 43% | 73% |
A0A3R7NI16 | Trypanosoma rangeli | 27% | 71% |
A0A3S5H550 | Leishmania donovani | 91% | 97% |
A0A422NMS5 | Trypanosoma rangeli | 41% | 72% |
A4H3M3 | Leishmania braziliensis | 78% | 100% |
C9ZRZ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 73% |
D0A265 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 71% |
E9AG51 | Leishmania infantum | 91% | 97% |
Q6T444 | Leishmania major | 91% | 100% |
V5BPW5 | Trypanosoma cruzi | 26% | 71% |