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 | 2 |
GO:0005657 | replication fork | 2 | 2 |
GO:0031974 | membrane-enclosed lumen | 2 | 2 |
GO:0031981 | nuclear lumen | 5 | 2 |
GO:0035861 | site of double-strand break | 3 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043233 | organelle lumen | 3 | 2 |
GO:0070013 | intracellular organelle lumen | 4 | 2 |
GO:0090734 | site of DNA damage | 2 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QCF3
Term | Name | Level | Count |
---|---|---|---|
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006259 | DNA metabolic process | 4 | 8 |
GO:0006281 | DNA repair | 5 | 8 |
GO:0006301 | postreplication repair | 6 | 2 |
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:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0009314 | response to radiation | 3 | 2 |
GO:0009628 | response to abiotic stimulus | 2 | 2 |
GO:0009987 | cellular process | 1 | 8 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019985 | translesion synthesis | 7 | 2 |
GO:0033554 | cellular response to stress | 3 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0042276 | error-prone translesion synthesis | 8 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
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:0071897 | DNA biosynthetic process | 5 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
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:0003824 | catalytic activity | 1 | 2 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 2 |
GO:0005488 | binding | 1 | 8 |
GO:0016740 | transferase activity | 2 | 2 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 2 |
GO:0016779 | nucleotidyltransferase activity | 4 | 2 |
GO:0034061 | DNA polymerase activity | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 8 |
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 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 362 | 366 | PF00656 | 0.624 |
CLV_C14_Caspase3-7 | 388 | 392 | PF00656 | 0.721 |
CLV_C14_Caspase3-7 | 558 | 562 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 354 | 356 | PF00675 | 0.349 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.669 |
CLV_NRD_NRD_1 | 538 | 540 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 83 | 85 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 93 | 95 | PF00675 | 0.307 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 200 | 202 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.669 |
CLV_PCSK_KEX2_1 | 538 | 540 | PF00082 | 0.701 |
CLV_PCSK_KEX2_1 | 647 | 649 | PF00082 | 0.673 |
CLV_PCSK_KEX2_1 | 697 | 699 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 83 | 85 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 93 | 95 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 647 | 649 | PF00082 | 0.661 |
CLV_PCSK_PC1ET2_1 | 697 | 699 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 527 | 531 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 618 | 622 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 750 | 754 | PF00082 | 0.729 |
CLV_Separin_Metazoa | 221 | 225 | PF03568 | 0.483 |
DEG_APCC_DBOX_1 | 167 | 175 | PF00400 | 0.597 |
DEG_APCC_DBOX_1 | 92 | 100 | PF00400 | 0.556 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.537 |
DOC_ANK_TNKS_1 | 635 | 642 | PF00023 | 0.623 |
DOC_CKS1_1 | 483 | 488 | PF01111 | 0.485 |
DOC_CYCLIN_RxL_1 | 250 | 261 | PF00134 | 0.483 |
DOC_MAPK_DCC_7 | 93 | 101 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 471 | 480 | PF00069 | 0.545 |
DOC_MAPK_gen_1 | 496 | 504 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 662 | 670 | PF00069 | 0.654 |
DOC_MAPK_gen_1 | 747 | 757 | PF00069 | 0.650 |
DOC_MAPK_MEF2A_6 | 144 | 151 | PF00069 | 0.471 |
DOC_MAPK_MEF2A_6 | 471 | 480 | PF00069 | 0.526 |
DOC_MAPK_MEF2A_6 | 662 | 670 | PF00069 | 0.602 |
DOC_MAPK_MEF2A_6 | 93 | 101 | PF00069 | 0.471 |
DOC_PP2B_LxvP_1 | 304 | 307 | PF13499 | 0.397 |
DOC_PP2B_LxvP_1 | 574 | 577 | PF13499 | 0.604 |
DOC_PP4_FxxP_1 | 219 | 222 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 315 | 318 | PF00568 | 0.397 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.493 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.474 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.377 |
DOC_USP7_MATH_1 | 331 | 335 | PF00917 | 0.561 |
DOC_USP7_MATH_1 | 439 | 443 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 545 | 549 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 631 | 635 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 712 | 716 | PF00917 | 0.698 |
DOC_USP7_MATH_1 | 732 | 736 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 767 | 771 | PF00917 | 0.596 |
DOC_WW_Pin1_4 | 18 | 23 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 482 | 487 | PF00397 | 0.432 |
DOC_WW_Pin1_4 | 539 | 544 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 57 | 62 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 713 | 718 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.473 |
LIG_14-3-3_CanoR_1 | 100 | 107 | PF00244 | 0.431 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 211 | 216 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 309 | 318 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 461 | 469 | PF00244 | 0.588 |
LIG_14-3-3_CanoR_1 | 618 | 627 | PF00244 | 0.560 |
LIG_14-3-3_CanoR_1 | 750 | 756 | PF00244 | 0.682 |
LIG_APCC_ABBAyCdc20_2 | 268 | 274 | PF00400 | 0.483 |
LIG_BIR_III_4 | 368 | 372 | PF00653 | 0.618 |
LIG_BRCT_BRCA1_1 | 237 | 241 | PF00533 | 0.483 |
LIG_BRCT_BRCA1_1 | 311 | 315 | PF00533 | 0.367 |
LIG_BRCT_BRCA1_1 | 433 | 437 | PF00533 | 0.413 |
LIG_CSL_BTD_1 | 764 | 767 | PF09270 | 0.603 |
LIG_eIF4E_1 | 250 | 256 | PF01652 | 0.483 |
LIG_FHA_1 | 122 | 128 | PF00498 | 0.574 |
LIG_FHA_1 | 192 | 198 | PF00498 | 0.483 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.397 |
LIG_FHA_1 | 739 | 745 | PF00498 | 0.737 |
LIG_FHA_1 | 752 | 758 | PF00498 | 0.567 |
LIG_FHA_2 | 10 | 16 | PF00498 | 0.590 |
LIG_FHA_2 | 386 | 392 | PF00498 | 0.579 |
LIG_FHA_2 | 419 | 425 | PF00498 | 0.588 |
LIG_FHA_2 | 720 | 726 | PF00498 | 0.618 |
LIG_GBD_Chelix_1 | 454 | 462 | PF00786 | 0.400 |
LIG_Integrin_RGD_1 | 385 | 387 | PF01839 | 0.612 |
LIG_LIR_Apic_2 | 111 | 117 | PF02991 | 0.471 |
LIG_LIR_Apic_2 | 312 | 318 | PF02991 | 0.383 |
LIG_LIR_Apic_2 | 345 | 350 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 157 | 167 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 42 | 53 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 457 | 465 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 521 | 529 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 60 | 70 | PF02991 | 0.483 |
LIG_LIR_Gen_1 | 621 | 632 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 773 | 781 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 157 | 163 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.350 |
LIG_LIR_Nem_3 | 42 | 48 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 457 | 462 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 521 | 525 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 60 | 65 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 621 | 627 | PF02991 | 0.588 |
LIG_LIR_Nem_3 | 69 | 73 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 773 | 777 | PF02991 | 0.576 |
LIG_PCNA_PIPBox_1 | 720 | 729 | PF02747 | 0.674 |
LIG_SH2_NCK_1 | 45 | 49 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 160 | 163 | PF00017 | 0.483 |
LIG_SH2_PTP2 | 483 | 486 | PF00017 | 0.418 |
LIG_SH2_SRC | 160 | 163 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 277 | 281 | PF00017 | 0.483 |
LIG_SH2_STAP1 | 465 | 469 | PF00017 | 0.587 |
LIG_SH2_STAT3 | 498 | 501 | PF00017 | 0.595 |
LIG_SH2_STAT5 | 114 | 117 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.483 |
LIG_SH2_STAT5 | 483 | 486 | PF00017 | 0.467 |
LIG_SH3_1 | 114 | 120 | PF00018 | 0.471 |
LIG_SH3_3 | 114 | 120 | PF00018 | 0.471 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.483 |
LIG_SH3_3 | 419 | 425 | PF00018 | 0.465 |
LIG_SH3_3 | 499 | 505 | PF00018 | 0.548 |
LIG_SH3_3 | 537 | 543 | PF00018 | 0.656 |
LIG_SH3_3 | 549 | 555 | PF00018 | 0.567 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.747 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.483 |
LIG_SH3_3 | 761 | 767 | PF00018 | 0.688 |
LIG_SH3_4 | 298 | 305 | PF00018 | 0.402 |
LIG_SUMO_SIM_anti_2 | 475 | 481 | PF11976 | 0.521 |
LIG_SUMO_SIM_anti_2 | 583 | 588 | PF11976 | 0.551 |
LIG_SUMO_SIM_par_1 | 302 | 308 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 580 | 585 | PF11976 | 0.474 |
LIG_SUMO_SIM_par_1 | 666 | 677 | PF11976 | 0.646 |
LIG_TRAF2_1 | 778 | 781 | PF00917 | 0.542 |
LIG_TRFH_1 | 85 | 89 | PF08558 | 0.433 |
MOD_CDC14_SPxK_1 | 644 | 647 | PF00782 | 0.685 |
MOD_CDK_SPK_2 | 18 | 23 | PF00069 | 0.568 |
MOD_CDK_SPK_2 | 641 | 646 | PF00069 | 0.682 |
MOD_CDK_SPxK_1 | 641 | 647 | PF00069 | 0.683 |
MOD_CDK_SPxxK_3 | 641 | 648 | PF00069 | 0.685 |
MOD_CDK_SPxxK_3 | 698 | 705 | PF00069 | 0.688 |
MOD_CK1_1 | 442 | 448 | PF00069 | 0.432 |
MOD_CK1_1 | 616 | 622 | PF00069 | 0.632 |
MOD_CK1_1 | 625 | 631 | PF00069 | 0.565 |
MOD_CK1_1 | 634 | 640 | PF00069 | 0.642 |
MOD_CK1_1 | 743 | 749 | PF00069 | 0.684 |
MOD_CK1_1 | 770 | 776 | PF00069 | 0.557 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.587 |
MOD_CK2_1 | 734 | 740 | PF00069 | 0.736 |
MOD_CK2_1 | 770 | 776 | PF00069 | 0.600 |
MOD_CK2_1 | 85 | 91 | PF00069 | 0.314 |
MOD_Cter_Amidation | 695 | 698 | PF01082 | 0.674 |
MOD_DYRK1A_RPxSP_1 | 539 | 543 | PF00069 | 0.661 |
MOD_DYRK1A_RPxSP_1 | 698 | 702 | PF00069 | 0.676 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.336 |
MOD_GlcNHglycan | 278 | 282 | PF01048 | 0.331 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.527 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.408 |
MOD_GlcNHglycan | 308 | 312 | PF01048 | 0.398 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.405 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.299 |
MOD_GlcNHglycan | 378 | 383 | PF01048 | 0.557 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.399 |
MOD_GlcNHglycan | 570 | 573 | PF01048 | 0.757 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.563 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.558 |
MOD_GlcNHglycan | 707 | 710 | PF01048 | 0.640 |
MOD_GlcNHglycan | 734 | 737 | PF01048 | 0.630 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.331 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.520 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.336 |
MOD_GSK3_1 | 460 | 467 | PF00069 | 0.587 |
MOD_GSK3_1 | 550 | 557 | PF00069 | 0.654 |
MOD_GSK3_1 | 568 | 575 | PF00069 | 0.595 |
MOD_GSK3_1 | 609 | 616 | PF00069 | 0.793 |
MOD_GSK3_1 | 618 | 625 | PF00069 | 0.595 |
MOD_GSK3_1 | 627 | 634 | PF00069 | 0.521 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.665 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.745 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.698 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.433 |
MOD_N-GLC_1 | 650 | 655 | PF02516 | 0.626 |
MOD_N-GLC_1 | 677 | 682 | PF02516 | 0.677 |
MOD_NEK2_1 | 235 | 240 | PF00069 | 0.492 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.408 |
MOD_NEK2_1 | 613 | 618 | PF00069 | 0.609 |
MOD_NEK2_1 | 627 | 632 | PF00069 | 0.537 |
MOD_NEK2_2 | 631 | 636 | PF00069 | 0.653 |
MOD_PIKK_1 | 545 | 551 | PF00454 | 0.596 |
MOD_PIKK_1 | 613 | 619 | PF00454 | 0.642 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.331 |
MOD_PKA_2 | 22 | 28 | PF00069 | 0.477 |
MOD_PKA_2 | 460 | 466 | PF00069 | 0.554 |
MOD_PKA_2 | 728 | 734 | PF00069 | 0.668 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.262 |
MOD_PKB_1 | 648 | 656 | PF00069 | 0.671 |
MOD_Plk_1 | 582 | 588 | PF00069 | 0.496 |
MOD_Plk_2-3 | 677 | 683 | PF00069 | 0.682 |
MOD_Plk_2-3 | 776 | 782 | PF00069 | 0.621 |
MOD_Plk_4 | 300 | 306 | PF00069 | 0.396 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.421 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.308 |
MOD_ProDKin_1 | 18 | 24 | PF00069 | 0.521 |
MOD_ProDKin_1 | 482 | 488 | PF00069 | 0.433 |
MOD_ProDKin_1 | 539 | 545 | PF00069 | 0.751 |
MOD_ProDKin_1 | 57 | 63 | PF00069 | 0.331 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.683 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.637 |
MOD_ProDKin_1 | 713 | 719 | PF00069 | 0.680 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.318 |
MOD_SUMO_rev_2 | 381 | 390 | PF00179 | 0.611 |
MOD_SUMO_rev_2 | 692 | 699 | PF00179 | 0.706 |
TRG_DiLeu_BaEn_1 | 252 | 257 | PF01217 | 0.492 |
TRG_DiLeu_BaEn_1 | 472 | 477 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 521 | 526 | PF01217 | 0.419 |
TRG_DiLeu_BaLyEn_6 | 192 | 197 | PF01217 | 0.331 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 272 | 275 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 45 | 48 | PF00928 | 0.331 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.341 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 538 | 540 | PF00400 | 0.662 |
TRG_ER_diArg_1 | 589 | 592 | PF00400 | 0.497 |
TRG_ER_diArg_1 | 645 | 648 | PF00400 | 0.671 |
TRG_ER_diArg_1 | 82 | 84 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 92 | 94 | PF00400 | 0.365 |
TRG_NES_CRM1_1 | 31 | 42 | PF08389 | 0.320 |
TRG_NLS_MonoExtC_3 | 645 | 650 | PF00514 | 0.659 |
TRG_NLS_MonoExtN_4 | 645 | 651 | PF00514 | 0.663 |
TRG_Pf-PMV_PEXEL_1 | 169 | 173 | PF00026 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 195 | 199 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 415 | 420 | PF00026 | 0.482 |
TRG_Pf-PMV_PEXEL_1 | 618 | 622 | PF00026 | 0.563 |
TRG_Pf-PMV_PEXEL_1 | 721 | 725 | PF00026 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 94 | 98 | PF00026 | 0.433 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEU7 | Leptomonas seymouri | 53% | 99% |
A0A3S5H795 | Leishmania donovani | 86% | 100% |
A4HBQ9 | Leishmania braziliensis | 79% | 100% |
A4HZ61 | Leishmania infantum | 92% | 100% |
E8NHQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
E9AV29 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 100% |
Q04049 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 100% |