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: A0A3S5H795
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 | 343 | 347 | PF00656 | 0.594 |
CLV_C14_Caspase3-7 | 369 | 373 | PF00656 | 0.662 |
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.452 |
CLV_NRD_NRD_1 | 181 | 183 | PF00675 | 0.247 |
CLV_NRD_NRD_1 | 471 | 473 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 626 | 628 | PF00675 | 0.617 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 731 | 733 | PF00675 | 0.517 |
CLV_PCSK_KEX2_1 | 181 | 183 | PF00082 | 0.271 |
CLV_PCSK_KEX2_1 | 471 | 473 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 519 | 521 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 628 | 630 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.247 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 731 | 733 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 628 | 630 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 678 | 680 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.247 |
CLV_PCSK_SKI1_1 | 410 | 414 | PF00082 | 0.350 |
CLV_PCSK_SKI1_1 | 508 | 512 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 731 | 735 | PF00082 | 0.632 |
CLV_Separin_Metazoa | 202 | 206 | PF03568 | 0.447 |
DEG_APCC_DBOX_1 | 148 | 156 | PF00400 | 0.496 |
DEG_SCF_FBW7_1 | 524 | 529 | PF00400 | 0.566 |
DOC_CYCLIN_RxL_1 | 231 | 242 | PF00134 | 0.447 |
DOC_MAPK_gen_1 | 449 | 459 | PF00069 | 0.418 |
DOC_MAPK_gen_1 | 477 | 485 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 728 | 738 | PF00069 | 0.584 |
DOC_MAPK_MEF2A_6 | 452 | 461 | PF00069 | 0.394 |
DOC_MAPK_RevD_3 | 168 | 182 | PF00069 | 0.452 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.343 |
DOC_PP2B_LxvP_1 | 555 | 558 | PF13499 | 0.468 |
DOC_PP4_FxxP_1 | 200 | 203 | PF00568 | 0.447 |
DOC_PP4_FxxP_1 | 296 | 299 | PF00568 | 0.348 |
DOC_USP7_MATH_1 | 160 | 164 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.326 |
DOC_USP7_MATH_1 | 312 | 316 | PF00917 | 0.416 |
DOC_USP7_MATH_1 | 420 | 424 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 548 | 552 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 597 | 601 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 713 | 717 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.597 |
DOC_USP7_UBL2_3 | 535 | 539 | PF12436 | 0.537 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.421 |
DOC_WW_Pin1_4 | 39 | 44 | PF00397 | 0.465 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.628 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.563 |
DOC_WW_Pin1_4 | 622 | 627 | PF00397 | 0.604 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 693 | 698 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 192 | 197 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 290 | 299 | PF00244 | 0.331 |
LIG_14-3-3_CanoR_1 | 442 | 450 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 731 | 737 | PF00244 | 0.606 |
LIG_APCC_ABBAyCdc20_2 | 249 | 255 | PF00400 | 0.447 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.459 |
LIG_BIR_III_4 | 349 | 353 | PF00653 | 0.562 |
LIG_BIR_III_4 | 382 | 386 | PF00653 | 0.381 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.447 |
LIG_BRCT_BRCA1_1 | 292 | 296 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.337 |
LIG_CSL_BTD_1 | 745 | 748 | PF09270 | 0.568 |
LIG_eIF4E_1 | 231 | 237 | PF01652 | 0.447 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.421 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.447 |
LIG_FHA_1 | 282 | 288 | PF00498 | 0.343 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.422 |
LIG_FHA_1 | 720 | 726 | PF00498 | 0.629 |
LIG_FHA_1 | 733 | 739 | PF00498 | 0.543 |
LIG_FHA_2 | 367 | 373 | PF00498 | 0.528 |
LIG_FHA_2 | 400 | 406 | PF00498 | 0.481 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.574 |
LIG_GBD_Chelix_1 | 435 | 443 | PF00786 | 0.322 |
LIG_Integrin_RGD_1 | 366 | 368 | PF01839 | 0.563 |
LIG_LIR_Apic_2 | 293 | 299 | PF02991 | 0.332 |
LIG_LIR_Apic_2 | 326 | 331 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 138 | 148 | PF02991 | 0.447 |
LIG_LIR_Gen_1 | 24 | 35 | PF02991 | 0.453 |
LIG_LIR_Gen_1 | 438 | 446 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 502 | 510 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 603 | 613 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 24 | 30 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 438 | 443 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 47 | 52 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 502 | 506 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 603 | 608 | PF02991 | 0.563 |
LIG_PCNA_PIPBox_1 | 701 | 710 | PF02747 | 0.583 |
LIG_SH2_NCK_1 | 27 | 31 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 141 | 144 | PF00017 | 0.447 |
LIG_SH2_SRC | 141 | 144 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 258 | 262 | PF00017 | 0.447 |
LIG_SH2_STAP1 | 446 | 450 | PF00017 | 0.456 |
LIG_SH2_STAT3 | 479 | 482 | PF00017 | 0.461 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.465 |
LIG_SH2_STAT5 | 464 | 467 | PF00017 | 0.432 |
LIG_SH3_2 | 530 | 535 | PF14604 | 0.540 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.447 |
LIG_SH3_3 | 400 | 406 | PF00018 | 0.435 |
LIG_SH3_3 | 480 | 486 | PF00018 | 0.430 |
LIG_SH3_3 | 518 | 524 | PF00018 | 0.599 |
LIG_SH3_3 | 52 | 58 | PF00018 | 0.447 |
LIG_SH3_3 | 527 | 533 | PF00018 | 0.569 |
LIG_SH3_3 | 538 | 544 | PF00018 | 0.798 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.611 |
LIG_SH3_4 | 279 | 286 | PF00018 | 0.349 |
LIG_SH3_4 | 535 | 542 | PF00018 | 0.536 |
LIG_SUMO_SIM_anti_2 | 456 | 462 | PF11976 | 0.387 |
LIG_SUMO_SIM_anti_2 | 564 | 569 | PF11976 | 0.488 |
LIG_SUMO_SIM_par_1 | 283 | 289 | PF11976 | 0.347 |
LIG_SUMO_SIM_par_1 | 42 | 47 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 561 | 566 | PF11976 | 0.406 |
LIG_SUMO_SIM_par_1 | 646 | 653 | PF11976 | 0.622 |
LIG_SUMO_SIM_par_1 | 80 | 85 | PF11976 | 0.383 |
LIG_TRAF2_1 | 148 | 151 | PF00917 | 0.391 |
MOD_CDC14_SPxK_1 | 596 | 599 | PF00782 | 0.520 |
MOD_CDC14_SPxK_1 | 625 | 628 | PF00782 | 0.606 |
MOD_CDK_SPK_2 | 622 | 627 | PF00069 | 0.604 |
MOD_CDK_SPxK_1 | 593 | 599 | PF00069 | 0.561 |
MOD_CDK_SPxK_1 | 622 | 628 | PF00069 | 0.605 |
MOD_CDK_SPxxK_3 | 622 | 629 | PF00069 | 0.606 |
MOD_CDK_SPxxK_3 | 679 | 686 | PF00069 | 0.612 |
MOD_CDK_SPxxK_3 | 82 | 89 | PF00069 | 0.192 |
MOD_CK1_1 | 423 | 429 | PF00069 | 0.380 |
MOD_CK1_1 | 606 | 612 | PF00069 | 0.519 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.597 |
MOD_CK1_1 | 68 | 74 | PF00069 | 0.225 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.480 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.590 |
MOD_CK1_1 | 751 | 757 | PF00069 | 0.545 |
MOD_CK2_1 | 133 | 139 | PF00069 | 0.192 |
MOD_CK2_1 | 441 | 447 | PF00069 | 0.444 |
MOD_CK2_1 | 715 | 721 | PF00069 | 0.697 |
MOD_CK2_1 | 751 | 757 | PF00069 | 0.580 |
MOD_Cter_Amidation | 676 | 679 | PF01082 | 0.716 |
MOD_DYRK1A_RPxSP_1 | 520 | 524 | PF00069 | 0.600 |
MOD_DYRK1A_RPxSP_1 | 679 | 683 | PF00069 | 0.601 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.328 |
MOD_GlcNHglycan | 259 | 263 | PF01048 | 0.282 |
MOD_GlcNHglycan | 274 | 277 | PF01048 | 0.356 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.344 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.365 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.262 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.551 |
MOD_GlcNHglycan | 551 | 554 | PF01048 | 0.744 |
MOD_GlcNHglycan | 592 | 596 | PF01048 | 0.714 |
MOD_GlcNHglycan | 605 | 608 | PF01048 | 0.523 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.595 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.592 |
MOD_GlcNHglycan | 688 | 691 | PF01048 | 0.599 |
MOD_GlcNHglycan | 715 | 718 | PF01048 | 0.584 |
MOD_GlcNHglycan | 759 | 762 | PF01048 | 0.495 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.282 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.301 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.541 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.170 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.447 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.721 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.606 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.596 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.683 |
MOD_GSK3_1 | 677 | 684 | PF00069 | 0.697 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.623 |
MOD_GSK3_1 | 753 | 760 | PF00069 | 0.611 |
MOD_N-GLC_1 | 658 | 663 | PF02516 | 0.549 |
MOD_N-GLC_1 | 68 | 73 | PF02516 | 0.170 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.350 |
MOD_NEK2_1 | 44 | 49 | PF00069 | 0.170 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.195 |
MOD_OFUCOSY | 336 | 342 | PF10250 | 0.334 |
MOD_PIKK_1 | 44 | 50 | PF00454 | 0.170 |
MOD_PIKK_1 | 681 | 687 | PF00454 | 0.550 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.192 |
MOD_PKA_1 | 65 | 71 | PF00069 | 0.170 |
MOD_PKA_1 | 731 | 737 | PF00069 | 0.505 |
MOD_PKA_2 | 191 | 197 | PF00069 | 0.282 |
MOD_PKA_2 | 441 | 447 | PF00069 | 0.425 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.181 |
MOD_PKA_2 | 709 | 715 | PF00069 | 0.618 |
MOD_PKA_2 | 731 | 737 | PF00069 | 0.505 |
MOD_PKB_1 | 627 | 635 | PF00069 | 0.616 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.411 |
MOD_Plk_2-3 | 133 | 139 | PF00069 | 0.192 |
MOD_Plk_2-3 | 658 | 664 | PF00069 | 0.601 |
MOD_Plk_4 | 281 | 287 | PF00069 | 0.344 |
MOD_Plk_4 | 48 | 54 | PF00069 | 0.262 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.336 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.246 |
MOD_ProDKin_1 | 39 | 45 | PF00069 | 0.307 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.651 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.561 |
MOD_ProDKin_1 | 622 | 628 | PF00069 | 0.605 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.645 |
MOD_ProDKin_1 | 693 | 699 | PF00069 | 0.625 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.328 |
MOD_SUMO_rev_2 | 362 | 371 | PF00179 | 0.562 |
MOD_SUMO_rev_2 | 673 | 680 | PF00179 | 0.617 |
TRG_DiLeu_BaEn_1 | 233 | 238 | PF01217 | 0.350 |
TRG_DiLeu_BaEn_1 | 453 | 458 | PF01217 | 0.399 |
TRG_DiLeu_BaEn_1 | 502 | 507 | PF01217 | 0.364 |
TRG_DiLeu_BaEn_3 | 739 | 745 | PF01217 | 0.510 |
TRG_DiLeu_BaLyEn_6 | 173 | 178 | PF01217 | 0.282 |
TRG_DiLeu_BaLyEn_6 | 570 | 575 | PF01217 | 0.370 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 27 | 30 | PF00928 | 0.282 |
TRG_ER_diArg_1 | 248 | 251 | PF00400 | 0.291 |
TRG_ER_diArg_1 | 393 | 396 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 519 | 521 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 570 | 573 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 626 | 629 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.294 |
TRG_ER_diArg_1 | 730 | 732 | PF00400 | 0.515 |
TRG_NES_CRM1_1 | 564 | 576 | PF08389 | 0.330 |
TRG_NLS_MonoExtC_3 | 626 | 631 | PF00514 | 0.609 |
TRG_NLS_MonoExtN_4 | 626 | 632 | PF00514 | 0.611 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.282 |
TRG_Pf-PMV_PEXEL_1 | 396 | 401 | PF00026 | 0.380 |
TRG_Pf-PMV_PEXEL_1 | 599 | 603 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 702 | 706 | PF00026 | 0.589 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEU7 | Leptomonas seymouri | 49% | 97% |
A4HBQ9 | Leishmania braziliensis | 74% | 100% |
A4HZ61 | Leishmania infantum | 93% | 100% |
E8NHQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
E9AV29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
Q4QCF3 | Leishmania major | 86% | 100% |
Q8H2D5 | Arabidopsis thaliana | 27% | 100% |