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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0016604 | nuclear body | 2 | 2 |
GO:0016605 | PML body | 3 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q6T444
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006302 | double-strand break repair | 6 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003697 | single-stranded DNA binding | 5 | 2 |
GO:0003824 | catalytic activity | 1 | 6 |
GO:0005488 | binding | 1 | 2 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 2 |
GO:0070259 | tyrosyl-DNA phosphodiesterase activity | 4 | 2 |
GO:0070260 | 5'-tyrosyl-DNA phosphodiesterase activity | 5 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 321 | 325 | PF00656 | 0.514 |
CLV_C14_Caspase3-7 | 488 | 492 | PF00656 | 0.722 |
CLV_NRD_NRD_1 | 107 | 109 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 111 | 113 | PF00675 | 0.425 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.217 |
CLV_NRD_NRD_1 | 137 | 139 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 552 | 554 | PF00675 | 0.557 |
CLV_PCSK_KEX2_1 | 107 | 109 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 131 | 133 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 137 | 139 | PF00082 | 0.498 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.561 |
CLV_PCSK_SKI1_1 | 238 | 242 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.568 |
DEG_APCC_DBOX_1 | 111 | 119 | PF00400 | 0.484 |
DEG_APCC_DBOX_1 | 292 | 300 | PF00400 | 0.495 |
DEG_APCC_DBOX_1 | 368 | 376 | PF00400 | 0.498 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.674 |
DOC_ANK_TNKS_1 | 607 | 614 | PF00023 | 0.554 |
DOC_CKS1_1 | 166 | 171 | PF01111 | 0.535 |
DOC_CKS1_1 | 178 | 183 | PF01111 | 0.392 |
DOC_CKS1_1 | 315 | 320 | PF01111 | 0.512 |
DOC_CYCLIN_RxL_1 | 107 | 120 | PF00134 | 0.415 |
DOC_MAPK_gen_1 | 454 | 464 | PF00069 | 0.561 |
DOC_MAPK_MEF2A_6 | 293 | 301 | PF00069 | 0.342 |
DOC_PP1_RVXF_1 | 111 | 118 | PF00149 | 0.436 |
DOC_PP1_RVXF_1 | 347 | 354 | PF00149 | 0.584 |
DOC_PP2B_LxvP_1 | 200 | 203 | PF13499 | 0.627 |
DOC_USP7_MATH_1 | 111 | 115 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.689 |
DOC_USP7_MATH_1 | 571 | 575 | PF00917 | 0.687 |
DOC_USP7_MATH_2 | 535 | 541 | PF00917 | 0.486 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.386 |
DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.398 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.397 |
DOC_WW_Pin1_4 | 314 | 319 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 397 | 402 | PF00397 | 0.613 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.534 |
LIG_14-3-3_CanoR_1 | 112 | 116 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 142 | 152 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 238 | 244 | PF00244 | 0.540 |
LIG_14-3-3_CanoR_1 | 347 | 352 | PF00244 | 0.601 |
LIG_14-3-3_CanoR_1 | 371 | 376 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 43 | 47 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 457 | 464 | PF00244 | 0.525 |
LIG_14-3-3_CanoR_1 | 530 | 535 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 553 | 559 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.488 |
LIG_Actin_WH2_2 | 255 | 271 | PF00022 | 0.604 |
LIG_APCC_ABBAyCdc20_2 | 349 | 355 | PF00400 | 0.564 |
LIG_BRCT_BRCA1_1 | 113 | 117 | PF00533 | 0.427 |
LIG_BRCT_BRCA1_1 | 349 | 353 | PF00533 | 0.517 |
LIG_BRCT_BRCA1_1 | 597 | 601 | PF00533 | 0.469 |
LIG_Clathr_ClatBox_1 | 296 | 300 | PF01394 | 0.271 |
LIG_CSL_BTD_1 | 426 | 429 | PF09270 | 0.608 |
LIG_DLG_GKlike_1 | 371 | 378 | PF00625 | 0.438 |
LIG_eIF4E_1 | 79 | 85 | PF01652 | 0.561 |
LIG_FHA_1 | 101 | 107 | PF00498 | 0.495 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.511 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.364 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.440 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.337 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.722 |
LIG_FHA_1 | 306 | 312 | PF00498 | 0.404 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.491 |
LIG_FHA_1 | 441 | 447 | PF00498 | 0.687 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.484 |
LIG_FHA_1 | 508 | 514 | PF00498 | 0.452 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.499 |
LIG_FHA_1 | 553 | 559 | PF00498 | 0.480 |
LIG_FHA_1 | 576 | 582 | PF00498 | 0.674 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.554 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.470 |
LIG_FHA_2 | 160 | 166 | PF00498 | 0.552 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.523 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.552 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.382 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.399 |
LIG_FHA_2 | 531 | 537 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 491 | 497 | PF02991 | 0.599 |
LIG_LIR_Gen_1 | 226 | 237 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 258 | 268 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 317 | 327 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 204 | 208 | PF02991 | 0.665 |
LIG_LIR_Nem_3 | 226 | 232 | PF02991 | 0.407 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 258 | 264 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 317 | 322 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 453 | 458 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 5 | 10 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 50 | 55 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 615 | 619 | PF02991 | 0.442 |
LIG_NRBOX | 114 | 120 | PF00104 | 0.493 |
LIG_NRBOX | 263 | 269 | PF00104 | 0.612 |
LIG_NRBOX | 297 | 303 | PF00104 | 0.462 |
LIG_NRBOX | 374 | 380 | PF00104 | 0.490 |
LIG_PCNA_PIPBox_1 | 1 | 10 | PF02747 | 0.687 |
LIG_PCNA_yPIPBox_3 | 553 | 563 | PF02747 | 0.558 |
LIG_PTAP_UEV_1 | 338 | 343 | PF05743 | 0.515 |
LIG_SH2_STAP1 | 139 | 143 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 153 | 156 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.454 |
LIG_SH2_STAT5 | 469 | 472 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 494 | 497 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.712 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.516 |
LIG_SH3_3 | 175 | 181 | PF00018 | 0.467 |
LIG_SH3_3 | 200 | 206 | PF00018 | 0.595 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.487 |
LIG_SH3_3 | 336 | 342 | PF00018 | 0.694 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.636 |
LIG_SUMO_SIM_anti_2 | 294 | 300 | PF11976 | 0.409 |
LIG_SUMO_SIM_par_1 | 191 | 197 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 294 | 300 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 448 | 453 | PF11976 | 0.620 |
LIG_SUMO_SIM_par_1 | 509 | 514 | PF11976 | 0.460 |
LIG_SUMO_SIM_par_1 | 66 | 71 | PF11976 | 0.484 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.481 |
LIG_TRAF2_1 | 566 | 569 | PF00917 | 0.607 |
LIG_UBA3_1 | 105 | 113 | PF00899 | 0.412 |
LIG_Vh1_VBS_1 | 548 | 566 | PF01044 | 0.544 |
MOD_CDC14_SPxK_1 | 496 | 499 | PF00782 | 0.536 |
MOD_CDK_SPxK_1 | 232 | 238 | PF00069 | 0.456 |
MOD_CDK_SPxK_1 | 493 | 499 | PF00069 | 0.581 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.380 |
MOD_CK1_1 | 209 | 215 | PF00069 | 0.470 |
MOD_CK1_1 | 25 | 31 | PF00069 | 0.755 |
MOD_CK1_1 | 438 | 444 | PF00069 | 0.720 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.481 |
MOD_CK1_1 | 647 | 653 | PF00069 | 0.642 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.806 |
MOD_CK2_1 | 159 | 165 | PF00069 | 0.582 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.446 |
MOD_CK2_1 | 402 | 408 | PF00069 | 0.582 |
MOD_CK2_1 | 503 | 509 | PF00069 | 0.403 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.396 |
MOD_Cter_Amidation | 135 | 138 | PF01082 | 0.510 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.722 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.415 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.337 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.768 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.592 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.565 |
MOD_GlcNHglycan | 386 | 389 | PF01048 | 0.553 |
MOD_GlcNHglycan | 437 | 440 | PF01048 | 0.756 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.426 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.438 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.701 |
MOD_GlcNHglycan | 646 | 650 | PF01048 | 0.616 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.654 |
MOD_GlcNHglycan | 670 | 673 | PF01048 | 0.757 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.525 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.752 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.533 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.436 |
MOD_GSK3_1 | 38 | 45 | PF00069 | 0.326 |
MOD_GSK3_1 | 421 | 428 | PF00069 | 0.555 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.525 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.486 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.558 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.441 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.639 |
MOD_GSK3_1 | 634 | 641 | PF00069 | 0.521 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.606 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.402 |
MOD_N-GLC_1 | 446 | 451 | PF02516 | 0.677 |
MOD_N-GLC_1 | 634 | 639 | PF02516 | 0.601 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.527 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.582 |
MOD_NEK2_1 | 407 | 412 | PF00069 | 0.402 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.640 |
MOD_NEK2_1 | 503 | 508 | PF00069 | 0.432 |
MOD_NEK2_1 | 511 | 516 | PF00069 | 0.355 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.566 |
MOD_NEK2_1 | 644 | 649 | PF00069 | 0.670 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.488 |
MOD_NEK2_2 | 196 | 201 | PF00069 | 0.338 |
MOD_NEK2_2 | 489 | 494 | PF00069 | 0.633 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.595 |
MOD_PIKK_1 | 513 | 519 | PF00454 | 0.547 |
MOD_PIKK_1 | 540 | 546 | PF00454 | 0.596 |
MOD_PIKK_1 | 552 | 558 | PF00454 | 0.513 |
MOD_PIKK_1 | 564 | 570 | PF00454 | 0.618 |
MOD_PK_1 | 347 | 353 | PF00069 | 0.608 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.469 |
MOD_PKA_2 | 159 | 165 | PF00069 | 0.544 |
MOD_PKA_2 | 42 | 48 | PF00069 | 0.447 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.556 |
MOD_PKA_2 | 552 | 558 | PF00069 | 0.573 |
MOD_PKB_1 | 369 | 377 | PF00069 | 0.404 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.524 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.400 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.497 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.420 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.455 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.517 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.629 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.446 |
MOD_Plk_4 | 489 | 495 | PF00069 | 0.623 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.396 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.472 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.386 |
MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.492 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.394 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.409 |
MOD_ProDKin_1 | 314 | 320 | PF00069 | 0.475 |
MOD_ProDKin_1 | 397 | 403 | PF00069 | 0.601 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.512 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.537 |
MOD_SUMO_for_1 | 623 | 626 | PF00179 | 0.553 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.454 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.455 |
TRG_ER_diArg_1 | 106 | 108 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 131 | 133 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 137 | 139 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 287 | 289 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 368 | 371 | PF00400 | 0.505 |
TRG_Pf-PMV_PEXEL_1 | 546 | 550 | PF00026 | 0.591 |
TRG_Pf-PMV_PEXEL_1 | 561 | 565 | PF00026 | 0.558 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HUJ3 | Leptomonas seymouri | 56% | 100% |
A0A0S4J9X6 | Bodo saltans | 33% | 83% |
A0A1X0P940 | Trypanosomatidae | 43% | 75% |
A0A3R7NI16 | Trypanosoma rangeli | 26% | 73% |
A0A3S5H550 | Leishmania donovani | 96% | 100% |
A0A422NMS5 | Trypanosoma rangeli | 42% | 74% |
A4H3M3 | Leishmania braziliensis | 77% | 99% |
C9ZRZ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 76% |
D0A265 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 73% |
E9AG51 | Leishmania infantum | 96% | 100% |
E9AJU5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BPW5 | Trypanosoma cruzi | 26% | 73% |