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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
GO:0030870 | Mre11 complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0035861 | site of double-strand break | 3 | 1 |
GO:0090734 | site of DNA damage | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: E9AZ91
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006302 | double-strand break repair | 6 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0000075 | cell cycle checkpoint signaling | 4 | 1 |
GO:0000077 | DNA damage checkpoint signaling | 5 | 1 |
GO:0000723 | telomere maintenance | 5 | 1 |
GO:0000724 | double-strand break repair via homologous recombination | 7 | 1 |
GO:0000725 | recombinational repair | 6 | 1 |
GO:0006303 | double-strand break repair via nonhomologous end joining | 7 | 1 |
GO:0006310 | DNA recombination | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0007093 | mitotic cell cycle checkpoint signaling | 4 | 1 |
GO:0007095 | mitotic G2 DNA damage checkpoint signaling | 6 | 1 |
GO:0007165 | signal transduction | 2 | 1 |
GO:0007346 | regulation of mitotic cell cycle | 5 | 1 |
GO:0010389 | regulation of G2/M transition of mitotic cell cycle | 7 | 1 |
GO:0010564 | regulation of cell cycle process | 5 | 1 |
GO:0010948 | negative regulation of cell cycle process | 6 | 1 |
GO:0010972 | negative regulation of G2/M transition of mitotic cell cycle | 8 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0022402 | cell cycle process | 2 | 1 |
GO:0022414 | reproductive process | 1 | 2 |
GO:0031570 | DNA integrity checkpoint signaling | 5 | 1 |
GO:0032200 | telomere organization | 6 | 1 |
GO:0035556 | intracellular signal transduction | 3 | 1 |
GO:0042138 | meiotic DNA double-strand break formation | 4 | 1 |
GO:0042770 | signal transduction in response to DNA damage | 4 | 1 |
GO:0044773 | mitotic DNA damage checkpoint signaling | 6 | 1 |
GO:0044774 | mitotic DNA integrity checkpoint signaling | 5 | 1 |
GO:0044818 | mitotic G2/M transition checkpoint | 5 | 1 |
GO:0045786 | negative regulation of cell cycle | 5 | 1 |
GO:0045930 | negative regulation of mitotic cell cycle | 6 | 1 |
GO:0048519 | negative regulation of biological process | 3 | 1 |
GO:0048523 | negative regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0051726 | regulation of cell cycle | 4 | 1 |
GO:0061982 | meiosis I cell cycle process | 3 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0097551 | mitochondrial double-strand break repair | 7 | 1 |
GO:0097552 | mitochondrial double-strand break repair via homologous recombination | 7 | 1 |
GO:1901987 | regulation of cell cycle phase transition | 6 | 1 |
GO:1901988 | negative regulation of cell cycle phase transition | 7 | 1 |
GO:1901990 | regulation of mitotic cell cycle phase transition | 6 | 1 |
GO:1901991 | negative regulation of mitotic cell cycle phase transition | 7 | 1 |
GO:1902749 | regulation of cell cycle G2/M phase transition | 7 | 1 |
GO:1902750 | negative regulation of cell cycle G2/M phase transition | 8 | 1 |
GO:1903046 | meiotic cell cycle process | 2 | 1 |
GO:1903047 | mitotic cell cycle process | 3 | 1 |
GO:0007049 | cell cycle | 2 | 1 |
GO:0051321 | meiotic cell cycle | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004518 | nuclease activity | 4 | 7 |
GO:0004519 | endonuclease activity | 5 | 7 |
GO:0004527 | exonuclease activity | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 7 |
GO:0030145 | manganese ion binding | 6 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043169 | cation binding | 3 | 7 |
GO:0046872 | metal ion binding | 4 | 7 |
GO:0046914 | transition metal ion binding | 5 | 7 |
GO:0000014 | single-stranded DNA endodeoxyribonuclease activity | 6 | 1 |
GO:0004520 | DNA endonuclease activity | 5 | 2 |
GO:0004536 | DNA nuclease activity | 4 | 2 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 2 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 2 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 1 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 1 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.475 |
CLV_C14_Caspase3-7 | 751 | 755 | PF00656 | 0.533 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.326 |
CLV_NRD_NRD_1 | 200 | 202 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 405 | 407 | PF00675 | 0.286 |
CLV_NRD_NRD_1 | 496 | 498 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 574 | 576 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 73 | 75 | PF00675 | 0.313 |
CLV_NRD_NRD_1 | 772 | 774 | PF00675 | 0.762 |
CLV_PCSK_FUR_1 | 640 | 644 | PF00082 | 0.651 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 303 | 305 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.286 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.474 |
CLV_PCSK_KEX2_1 | 520 | 522 | PF00082 | 0.470 |
CLV_PCSK_KEX2_1 | 574 | 576 | PF00082 | 0.590 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.653 |
CLV_PCSK_KEX2_1 | 691 | 693 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 772 | 774 | PF00082 | 0.762 |
CLV_PCSK_PC1ET2_1 | 520 | 522 | PF00082 | 0.470 |
CLV_PCSK_PC1ET2_1 | 691 | 693 | PF00082 | 0.650 |
CLV_PCSK_PC7_1 | 299 | 305 | PF00082 | 0.275 |
CLV_PCSK_SKI1_1 | 397 | 401 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 7 | 11 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 75 | 79 | PF00082 | 0.342 |
CLV_PCSK_SKI1_1 | 826 | 830 | PF00082 | 0.664 |
CLV_Separin_Metazoa | 35 | 39 | PF03568 | 0.312 |
CLV_Separin_Metazoa | 394 | 398 | PF03568 | 0.475 |
CLV_Separin_Metazoa | 581 | 585 | PF03568 | 0.589 |
DEG_SCF_TRCP1_1 | 596 | 601 | PF00400 | 0.611 |
DOC_CYCLIN_RxL_1 | 4 | 13 | PF00134 | 0.312 |
DOC_CYCLIN_yCln2_LP_2 | 395 | 401 | PF00134 | 0.529 |
DOC_MAPK_FxFP_2 | 192 | 195 | PF00069 | 0.291 |
DOC_MAPK_gen_1 | 162 | 170 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 183 | 192 | PF00069 | 0.313 |
DOC_MAPK_gen_1 | 201 | 209 | PF00069 | 0.312 |
DOC_MAPK_MEF2A_6 | 355 | 363 | PF00069 | 0.475 |
DOC_PP1_RVXF_1 | 186 | 193 | PF00149 | 0.291 |
DOC_PP1_SILK_1 | 504 | 509 | PF00149 | 0.585 |
DOC_PP2B_LxvP_1 | 246 | 249 | PF13499 | 0.397 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.510 |
DOC_PP2B_PxIxI_1 | 107 | 113 | PF00149 | 0.285 |
DOC_PP4_FxxP_1 | 105 | 108 | PF00568 | 0.312 |
DOC_PP4_FxxP_1 | 192 | 195 | PF00568 | 0.330 |
DOC_USP7_MATH_1 | 415 | 419 | PF00917 | 0.424 |
DOC_USP7_MATH_1 | 502 | 506 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 674 | 678 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 836 | 840 | PF00917 | 0.565 |
DOC_WW_Pin1_4 | 288 | 293 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 755 | 760 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 162 | 168 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 284 | 289 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 303 | 307 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 38 | 46 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 68 | 73 | PF00244 | 0.312 |
LIG_14-3-3_CanoR_1 | 692 | 701 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 826 | 831 | PF00244 | 0.604 |
LIG_Actin_WH2_2 | 147 | 164 | PF00022 | 0.388 |
LIG_Actin_WH2_2 | 382 | 399 | PF00022 | 0.475 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.525 |
LIG_EH1_1 | 43 | 51 | PF00400 | 0.312 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.312 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.291 |
LIG_FHA_1 | 303 | 309 | PF00498 | 0.537 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.475 |
LIG_FHA_1 | 528 | 534 | PF00498 | 0.409 |
LIG_FHA_1 | 723 | 729 | PF00498 | 0.813 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.414 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.319 |
LIG_FHA_2 | 29 | 35 | PF00498 | 0.312 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.312 |
LIG_Integrin_RGD_1 | 25 | 27 | PF01839 | 0.312 |
LIG_LIR_Apic_2 | 370 | 376 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 165 | 173 | PF02991 | 0.354 |
LIG_LIR_Gen_1 | 253 | 260 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 27 | 37 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 364 | 373 | PF02991 | 0.475 |
LIG_LIR_Gen_1 | 578 | 588 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 165 | 170 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 253 | 258 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 3 | 9 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 364 | 368 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.312 |
LIG_LYPXL_yS_3 | 356 | 359 | PF13949 | 0.475 |
LIG_NRBOX | 482 | 488 | PF00104 | 0.451 |
LIG_PALB2_WD40_1 | 199 | 207 | PF16756 | 0.312 |
LIG_PCNA_yPIPBox_3 | 216 | 229 | PF02747 | 0.291 |
LIG_Pex14_2 | 605 | 609 | PF04695 | 0.708 |
LIG_SH2_GRB2like | 141 | 144 | PF00017 | 0.312 |
LIG_SH2_STAP1 | 527 | 531 | PF00017 | 0.505 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 293 | 296 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.312 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.312 |
LIG_SH3_3 | 245 | 251 | PF00018 | 0.437 |
LIG_SH3_3 | 254 | 260 | PF00018 | 0.404 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.475 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.475 |
LIG_SH3_3 | 683 | 689 | PF00018 | 0.683 |
LIG_SH3_3 | 817 | 823 | PF00018 | 0.692 |
LIG_SUMO_SIM_anti_2 | 130 | 138 | PF11976 | 0.314 |
LIG_TRAF2_1 | 269 | 272 | PF00917 | 0.423 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.312 |
LIG_TRFH_1 | 288 | 292 | PF08558 | 0.475 |
LIG_TYR_ITIM | 354 | 359 | PF00017 | 0.488 |
LIG_UBA3_1 | 483 | 492 | PF00899 | 0.448 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.312 |
LIG_WRC_WIRS_1 | 321 | 326 | PF05994 | 0.475 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.470 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.312 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.478 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.446 |
MOD_CK1_1 | 848 | 854 | PF00069 | 0.578 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.315 |
MOD_CK2_1 | 146 | 152 | PF00069 | 0.300 |
MOD_CK2_1 | 266 | 272 | PF00069 | 0.418 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.312 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.529 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.475 |
MOD_CK2_1 | 552 | 558 | PF00069 | 0.609 |
MOD_CK2_1 | 596 | 602 | PF00069 | 0.671 |
MOD_Cter_Amidation | 199 | 202 | PF01082 | 0.285 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.552 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.302 |
MOD_GlcNHglycan | 417 | 420 | PF01048 | 0.272 |
MOD_GlcNHglycan | 462 | 466 | PF01048 | 0.275 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.727 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.686 |
MOD_GlcNHglycan | 778 | 781 | PF01048 | 0.595 |
MOD_GlcNHglycan | 787 | 790 | PF01048 | 0.521 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.606 |
MOD_GlcNHglycan | 817 | 820 | PF01048 | 0.539 |
MOD_GlcNHglycan | 832 | 835 | PF01048 | 0.773 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.391 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.425 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.511 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.499 |
MOD_GSK3_1 | 411 | 418 | PF00069 | 0.400 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.478 |
MOD_GSK3_1 | 560 | 567 | PF00069 | 0.549 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.630 |
MOD_GSK3_1 | 605 | 612 | PF00069 | 0.640 |
MOD_GSK3_1 | 783 | 790 | PF00069 | 0.505 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.615 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.371 |
MOD_N-GLC_1 | 502 | 507 | PF02516 | 0.588 |
MOD_N-GLC_2 | 453 | 455 | PF02516 | 0.329 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.416 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.312 |
MOD_NEK2_1 | 324 | 329 | PF00069 | 0.478 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.439 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.635 |
MOD_NEK2_1 | 787 | 792 | PF00069 | 0.507 |
MOD_PIKK_1 | 487 | 493 | PF00454 | 0.481 |
MOD_PIKK_1 | 851 | 857 | PF00454 | 0.570 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.388 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.439 |
MOD_PKA_2 | 302 | 308 | PF00069 | 0.503 |
MOD_PKA_2 | 594 | 600 | PF00069 | 0.543 |
MOD_Plk_1 | 2 | 8 | PF00069 | 0.394 |
MOD_Plk_1 | 26 | 32 | PF00069 | 0.312 |
MOD_Plk_1 | 502 | 508 | PF00069 | 0.587 |
MOD_Plk_1 | 721 | 727 | PF00069 | 0.654 |
MOD_Plk_1 | 734 | 740 | PF00069 | 0.514 |
MOD_Plk_2-3 | 314 | 320 | PF00069 | 0.475 |
MOD_Plk_2-3 | 331 | 337 | PF00069 | 0.475 |
MOD_Plk_2-3 | 659 | 665 | PF00069 | 0.679 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.312 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.409 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.476 |
MOD_Plk_4 | 453 | 459 | PF00069 | 0.475 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.486 |
MOD_Plk_4 | 502 | 508 | PF00069 | 0.551 |
MOD_Plk_4 | 564 | 570 | PF00069 | 0.509 |
MOD_Plk_4 | 674 | 680 | PF00069 | 0.585 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.312 |
MOD_Plk_4 | 807 | 813 | PF00069 | 0.603 |
MOD_ProDKin_1 | 288 | 294 | PF00069 | 0.492 |
MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.645 |
MOD_ProDKin_1 | 755 | 761 | PF00069 | 0.529 |
MOD_SUMO_for_1 | 401 | 404 | PF00179 | 0.529 |
MOD_SUMO_rev_2 | 54 | 62 | PF00179 | 0.312 |
TRG_DiLeu_BaEn_1 | 242 | 247 | PF01217 | 0.371 |
TRG_DiLeu_BaLyEn_6 | 354 | 359 | PF01217 | 0.529 |
TRG_ENDOCYTIC_2 | 278 | 281 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 356 | 359 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 385 | 388 | PF00928 | 0.475 |
TRG_ER_diArg_1 | 23 | 25 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 302 | 304 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.584 |
TRG_ER_diArg_1 | 495 | 497 | PF00400 | 0.482 |
TRG_ER_diArg_1 | 640 | 643 | PF00400 | 0.693 |
TRG_NES_CRM1_1 | 226 | 242 | PF08389 | 0.312 |
TRG_NES_CRM1_1 | 433 | 445 | PF08389 | 0.475 |
TRG_NLS_MonoExtN_4 | 688 | 695 | PF00514 | 0.707 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB75 | Leptomonas seymouri | 64% | 99% |
A0A3Q8IDJ4 | Leishmania donovani | 93% | 100% |
A4HFW3 | Leishmania braziliensis | 84% | 100% |
A4I2Z5 | Leishmania infantum | 93% | 100% |
E9ADG7 | Leishmania major | 92% | 100% |