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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005657 | replication fork | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0035861 | site of double-strand break | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0090734 | site of DNA damage | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AV29
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0006950 | response to stress | 2 | 8 |
GO:0006974 | DNA damage response | 4 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0050896 | response to stimulus | 1 | 8 |
GO:0051716 | cellular response to stimulus | 2 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 1 |
GO:0006301 | postreplication repair | 6 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019985 | translesion synthesis | 7 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0042276 | error-prone translesion synthesis | 8 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 8 |
GO:0003677 | DNA binding | 4 | 8 |
GO:0003684 | damaged DNA binding | 5 | 8 |
GO:0005488 | binding | 1 | 8 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
GO:1901363 | heterocyclic compound binding | 2 | 8 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0034061 | DNA polymerase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 344 | 348 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 488 | 492 | PF00656 | 0.352 |
CLV_C14_Caspase3-7 | 539 | 543 | PF00656 | 0.683 |
CLV_MEL_PAP_1 | 439 | 445 | PF00089 | 0.383 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.419 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.715 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.493 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.833 |
CLV_NRD_NRD_1 | 635 | 637 | PF00675 | 0.721 |
CLV_NRD_NRD_1 | 755 | 757 | PF00675 | 0.564 |
CLV_PCSK_FUR_1 | 632 | 636 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.419 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.306 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.834 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.720 |
CLV_PCSK_KEX2_1 | 635 | 637 | PF00082 | 0.718 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 755 | 757 | PF00082 | 0.564 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.348 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 736 | 740 | PF00082 | 0.765 |
CLV_Separin_Metazoa | 203 | 207 | PF03568 | 0.548 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.621 |
DEG_SCF_FBW7_1 | 524 | 529 | PF00400 | 0.601 |
DEG_SPOP_SBC_1 | 384 | 388 | PF00917 | 0.391 |
DOC_ANK_TNKS_1 | 621 | 628 | PF00023 | 0.611 |
DOC_CYCLIN_RxL_1 | 232 | 243 | PF00134 | 0.548 |
DOC_MAPK_gen_1 | 449 | 459 | PF00069 | 0.572 |
DOC_MAPK_gen_1 | 477 | 485 | PF00069 | 0.532 |
DOC_MAPK_gen_1 | 490 | 500 | PF00069 | 0.354 |
DOC_MAPK_gen_1 | 733 | 743 | PF00069 | 0.663 |
DOC_MAPK_MEF2A_6 | 452 | 461 | PF00069 | 0.551 |
DOC_MAPK_RevD_3 | 169 | 183 | PF00069 | 0.546 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 555 | 558 | PF13499 | 0.554 |
DOC_PP2B_PxIxI_1 | 128 | 134 | PF00149 | 0.413 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.548 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.489 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.557 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.767 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.745 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.743 |
DOC_USP7_MATH_1 | 718 | 722 | PF00917 | 0.697 |
DOC_USP7_UBL2_3 | 505 | 509 | PF12436 | 0.352 |
DOC_WW_Pin1_4 | 125 | 130 | PF00397 | 0.427 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.548 |
DOC_WW_Pin1_4 | 463 | 468 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 522 | 527 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 699 | 704 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 193 | 198 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 291 | 300 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 442 | 450 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 519 | 525 | PF00244 | 0.533 |
LIG_APCC_ABBAyCdc20_2 | 250 | 256 | PF00400 | 0.548 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.546 |
LIG_BIR_III_2 | 542 | 546 | PF00653 | 0.539 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.548 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.465 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.489 |
LIG_CSL_BTD_1 | 750 | 753 | PF09270 | 0.619 |
LIG_deltaCOP1_diTrp_1 | 438 | 443 | PF00928 | 0.390 |
LIG_eIF4E_1 | 232 | 238 | PF01652 | 0.548 |
LIG_FHA_1 | 126 | 132 | PF00498 | 0.448 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.524 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.481 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.430 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.749 |
LIG_FHA_1 | 738 | 744 | PF00498 | 0.569 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.632 |
LIG_FHA_2 | 706 | 712 | PF00498 | 0.678 |
LIG_LIR_Apic_2 | 294 | 300 | PF02991 | 0.476 |
LIG_LIR_Apic_2 | 327 | 332 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.548 |
LIG_LIR_Gen_1 | 438 | 446 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 603 | 613 | PF02991 | 0.657 |
LIG_LIR_LC3C_4 | 43 | 47 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 376 | 382 | PF02991 | 0.756 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.654 |
LIG_PCNA_PIPBox_1 | 706 | 715 | PF02747 | 0.676 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.548 |
LIG_SH2_PTP2 | 142 | 145 | PF00017 | 0.548 |
LIG_SH2_SRC | 142 | 145 | PF00017 | 0.518 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.548 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.592 |
LIG_SH2_STAT3 | 479 | 482 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.417 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.548 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.568 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.556 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.548 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.773 |
LIG_SH3_3 | 725 | 731 | PF00018 | 0.528 |
LIG_SH3_3 | 747 | 753 | PF00018 | 0.705 |
LIG_SH3_4 | 280 | 287 | PF00018 | 0.482 |
LIG_SUMO_SIM_anti_2 | 456 | 461 | PF11976 | 0.542 |
LIG_SUMO_SIM_anti_2 | 564 | 569 | PF11976 | 0.560 |
LIG_SUMO_SIM_par_1 | 284 | 290 | PF11976 | 0.489 |
LIG_SUMO_SIM_par_1 | 561 | 566 | PF11976 | 0.482 |
LIG_SUMO_SIM_par_1 | 651 | 658 | PF11976 | 0.723 |
LIG_SUMO_SIM_par_1 | 726 | 732 | PF11976 | 0.527 |
LIG_SUMO_SIM_par_1 | 81 | 86 | PF11976 | 0.427 |
LIG_TRAF2_1 | 764 | 767 | PF00917 | 0.552 |
MOD_CDK_SPxxK_3 | 83 | 90 | PF00069 | 0.243 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.552 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.627 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.697 |
MOD_CK1_1 | 729 | 735 | PF00069 | 0.696 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.533 |
MOD_CK2_1 | 134 | 140 | PF00069 | 0.243 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.601 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.784 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.665 |
MOD_Cter_Amidation | 363 | 366 | PF01082 | 0.568 |
MOD_DYRK1A_RPxSP_1 | 369 | 373 | PF00069 | 0.554 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.597 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.414 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.489 |
MOD_GlcNHglycan | 290 | 294 | PF01048 | 0.500 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.499 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.370 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.454 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.774 |
MOD_GlcNHglycan | 592 | 596 | PF01048 | 0.730 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.635 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.607 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.693 |
MOD_GlcNHglycan | 636 | 639 | PF01048 | 0.626 |
MOD_GlcNHglycan | 692 | 696 | PF01048 | 0.630 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.705 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.414 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.608 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.600 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.685 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.624 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.689 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.568 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.758 |
MOD_N-GLC_1 | 663 | 668 | PF02516 | 0.692 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.516 |
MOD_NEK2_1 | 412 | 417 | PF00069 | 0.431 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.349 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.536 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.243 |
MOD_PIKK_1 | 385 | 391 | PF00454 | 0.355 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.243 |
MOD_PK_1 | 756 | 762 | PF00069 | 0.485 |
MOD_PKA_1 | 508 | 514 | PF00069 | 0.409 |
MOD_PKA_1 | 634 | 640 | PF00069 | 0.536 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.414 |
MOD_PKA_2 | 412 | 418 | PF00069 | 0.439 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.568 |
MOD_PKA_2 | 634 | 640 | PF00069 | 0.536 |
MOD_PKA_2 | 714 | 720 | PF00069 | 0.681 |
MOD_PKB_1 | 632 | 640 | PF00069 | 0.714 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.444 |
MOD_Plk_1 | 736 | 742 | PF00069 | 0.520 |
MOD_Plk_2-3 | 134 | 140 | PF00069 | 0.243 |
MOD_Plk_2-3 | 663 | 669 | PF00069 | 0.749 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.479 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.392 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.483 |
MOD_ProDKin_1 | 125 | 131 | PF00069 | 0.243 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.557 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.414 |
MOD_ProDKin_1 | 463 | 469 | PF00069 | 0.507 |
MOD_ProDKin_1 | 522 | 528 | PF00069 | 0.710 |
MOD_ProDKin_1 | 699 | 705 | PF00069 | 0.734 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.515 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.452 |
MOD_SUMO_rev_2 | 488 | 495 | PF00179 | 0.343 |
MOD_SUMO_rev_2 | 678 | 685 | PF00179 | 0.693 |
TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_1 | 453 | 458 | PF01217 | 0.551 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_3 | 744 | 750 | PF01217 | 0.544 |
TRG_DiLeu_BaEn_3 | 766 | 772 | PF01217 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.414 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.414 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.414 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.487 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 631 | 634 | PF00400 | 0.720 |
TRG_NLS_MonoExtC_3 | 364 | 369 | PF00514 | 0.799 |
TRG_NLS_MonoExtN_4 | 365 | 370 | PF00514 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.438 |
TRG_Pf-PMV_PEXEL_1 | 177 | 181 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.543 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 646 | 651 | PF00026 | 0.603 |
TRG_Pf-PMV_PEXEL_1 | 707 | 711 | PF00026 | 0.616 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEU7 | Leptomonas seymouri | 50% | 97% |
A0A3S5H795 | Leishmania donovani | 85% | 100% |
A4HBQ9 | Leishmania braziliensis | 72% | 100% |
A4HZ61 | Leishmania infantum | 80% | 98% |
E8NHQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QCF3 | Leishmania major | 78% | 100% |