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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A0A3Q8IEM0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006259 | DNA metabolic process | 4 | 12 |
GO:0006281 | DNA repair | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 12 |
GO:0006974 | DNA damage response | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 2 |
GO:0006301 | postreplication repair | 6 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009059 | macromolecule biosynthetic process | 4 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019985 | translesion synthesis | 7 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0042276 | error-prone translesion synthesis | 8 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0071897 | DNA biosynthetic process | 5 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
GO:0006260 | DNA replication | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003677 | DNA binding | 4 | 12 |
GO:0003684 | damaged DNA binding | 5 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016779 | nucleotidyltransferase activity | 4 | 12 |
GO:0034061 | DNA polymerase activity | 4 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043169 | cation binding | 3 | 1 |
GO:0046872 | metal ion binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 677 | 681 | PF00656 | 0.662 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.387 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 213 | 215 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 273 | 275 | PF00675 | 0.219 |
CLV_NRD_NRD_1 | 31 | 33 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 454 | 456 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 504 | 506 | PF00675 | 0.282 |
CLV_NRD_NRD_1 | 532 | 534 | PF00675 | 0.275 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 606 | 608 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 651 | 653 | PF00675 | 0.658 |
CLV_NRD_NRD_1 | 663 | 665 | PF00675 | 0.562 |
CLV_PCSK_KEX2_1 | 213 | 215 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 31 | 33 | PF00082 | 0.569 |
CLV_PCSK_KEX2_1 | 363 | 365 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 532 | 534 | PF00082 | 0.219 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 605 | 607 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 650 | 652 | PF00082 | 0.660 |
CLV_PCSK_KEX2_1 | 665 | 667 | PF00082 | 0.551 |
CLV_PCSK_PC1ET2_1 | 665 | 667 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 23 | 27 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 577 | 581 | PF00082 | 0.240 |
CLV_Separin_Metazoa | 574 | 578 | PF03568 | 0.440 |
DEG_APCC_DBOX_1 | 22 | 30 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 445 | 453 | PF00400 | 0.341 |
DEG_APCC_DBOX_1 | 519 | 527 | PF00400 | 0.447 |
DEG_APCC_DBOX_1 | 576 | 584 | PF00400 | 0.440 |
DEG_SCF_FBW7_1 | 54 | 61 | PF00400 | 0.564 |
DEG_SCF_FBW7_1 | 62 | 69 | PF00400 | 0.537 |
DEG_SPOP_SBC_1 | 478 | 482 | PF00917 | 0.544 |
DEG_SPOP_SBC_1 | 712 | 716 | PF00917 | 0.564 |
DOC_ANK_TNKS_1 | 665 | 672 | PF00023 | 0.554 |
DOC_CKS1_1 | 55 | 60 | PF01111 | 0.577 |
DOC_CKS1_1 | 63 | 68 | PF01111 | 0.560 |
DOC_MAPK_gen_1 | 184 | 193 | PF00069 | 0.404 |
DOC_MAPK_MEF2A_6 | 227 | 236 | PF00069 | 0.375 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.450 |
DOC_MIT_MIM_1 | 594 | 606 | PF04212 | 0.416 |
DOC_PP1_RVXF_1 | 139 | 146 | PF00149 | 0.514 |
DOC_PP2B_LxvP_1 | 583 | 586 | PF13499 | 0.455 |
DOC_PP4_FxxP_1 | 126 | 129 | PF00568 | 0.512 |
DOC_SPAK_OSR1_1 | 351 | 355 | PF12202 | 0.440 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.661 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 477 | 481 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.590 |
DOC_USP7_UBL2_3 | 165 | 169 | PF12436 | 0.394 |
DOC_USP7_UBL2_3 | 560 | 564 | PF12436 | 0.440 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 38 | 43 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 62 | 67 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.645 |
DOC_WW_Pin1_4 | 716 | 721 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 110 | 119 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 23 | 29 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 32 | 42 | PF00244 | 0.689 |
LIG_14-3-3_CanoR_1 | 455 | 459 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 505 | 509 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 532 | 538 | PF00244 | 0.463 |
LIG_14-3-3_CanoR_1 | 640 | 649 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 76 | 83 | PF00244 | 0.535 |
LIG_Actin_WH2_2 | 519 | 534 | PF00022 | 0.498 |
LIG_APCC_ABBA_1 | 232 | 237 | PF00400 | 0.252 |
LIG_APCC_ABBA_1 | 566 | 571 | PF00400 | 0.455 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.610 |
LIG_BRCT_BRCA1_1 | 307 | 311 | PF00533 | 0.455 |
LIG_BRCT_BRCA1_1 | 634 | 638 | PF00533 | 0.484 |
LIG_Clathr_ClatBox_1 | 324 | 328 | PF01394 | 0.419 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.432 |
LIG_FHA_1 | 267 | 273 | PF00498 | 0.418 |
LIG_FHA_1 | 379 | 385 | PF00498 | 0.449 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.554 |
LIG_FHA_1 | 637 | 643 | PF00498 | 0.552 |
LIG_FHA_1 | 78 | 84 | PF00498 | 0.510 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.343 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.434 |
LIG_FHA_2 | 701 | 707 | PF00498 | 0.588 |
LIG_GSK3_LRP6_1 | 62 | 67 | PF00069 | 0.538 |
LIG_LIR_Apic_2 | 125 | 129 | PF02991 | 0.513 |
LIG_LIR_Apic_2 | 389 | 394 | PF02991 | 0.518 |
LIG_LIR_Gen_1 | 228 | 236 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 239 | 247 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 457 | 466 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 589 | 599 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 220 | 226 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 228 | 232 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 239 | 245 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 457 | 461 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 511 | 517 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 589 | 594 | PF02991 | 0.425 |
LIG_MLH1_MIPbox_1 | 634 | 638 | PF16413 | 0.484 |
LIG_NRBOX | 579 | 585 | PF00104 | 0.455 |
LIG_PCNA_PIPBox_1 | 331 | 340 | PF02747 | 0.455 |
LIG_PCNA_PIPBox_1 | 631 | 640 | PF02747 | 0.512 |
LIG_PCNA_yPIPBox_3 | 179 | 192 | PF02747 | 0.370 |
LIG_PCNA_yPIPBox_3 | 631 | 640 | PF02747 | 0.512 |
LIG_PTB_Apo_2 | 247 | 254 | PF02174 | 0.455 |
LIG_PTB_Phospho_1 | 247 | 253 | PF10480 | 0.455 |
LIG_Rb_pABgroove_1 | 466 | 474 | PF01858 | 0.384 |
LIG_REV1ctd_RIR_1 | 635 | 644 | PF16727 | 0.533 |
LIG_SH2_CRK | 391 | 395 | PF00017 | 0.387 |
LIG_SH2_CRK | 528 | 532 | PF00017 | 0.439 |
LIG_SH2_GRB2like | 174 | 177 | PF00017 | 0.353 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.462 |
LIG_SH2_SRC | 253 | 256 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 318 | 322 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 458 | 462 | PF00017 | 0.299 |
LIG_SH2_STAT3 | 276 | 279 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 233 | 236 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.449 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.488 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.442 |
LIG_SH2_STAT5 | 682 | 685 | PF00017 | 0.513 |
LIG_SH3_1 | 60 | 66 | PF00018 | 0.521 |
LIG_SH3_2 | 55 | 60 | PF14604 | 0.549 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.455 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.603 |
LIG_SH3_3 | 47 | 53 | PF00018 | 0.613 |
LIG_SH3_3 | 56 | 62 | PF00018 | 0.595 |
LIG_SH3_3 | 705 | 711 | PF00018 | 0.687 |
LIG_SH3_4 | 393 | 400 | PF00018 | 0.348 |
LIG_SUMO_SIM_par_1 | 293 | 300 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 692 | 700 | PF11976 | 0.602 |
LIG_TYR_ITIM | 526 | 531 | PF00017 | 0.275 |
LIG_UBA3_1 | 163 | 169 | PF00899 | 0.408 |
LIG_UBA3_1 | 449 | 456 | PF00899 | 0.438 |
LIG_WRC_WIRS_1 | 123 | 128 | PF05994 | 0.470 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.289 |
MOD_CDK_SPK_2 | 41 | 46 | PF00069 | 0.562 |
MOD_CDK_SPxK_1 | 54 | 60 | PF00069 | 0.529 |
MOD_CDK_SPxK_1 | 70 | 76 | PF00069 | 0.560 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.584 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.708 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.584 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.416 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.391 |
MOD_CK1_1 | 228 | 234 | PF00069 | 0.348 |
MOD_CK1_1 | 264 | 270 | PF00069 | 0.319 |
MOD_CK1_1 | 41 | 47 | PF00069 | 0.666 |
MOD_CK1_1 | 426 | 432 | PF00069 | 0.377 |
MOD_CK1_1 | 482 | 488 | PF00069 | 0.557 |
MOD_CK1_1 | 534 | 540 | PF00069 | 0.276 |
MOD_CK1_1 | 610 | 616 | PF00069 | 0.533 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.604 |
MOD_CK1_1 | 719 | 725 | PF00069 | 0.795 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.597 |
MOD_CK1_1 | 88 | 94 | PF00069 | 0.628 |
MOD_CK2_1 | 435 | 441 | PF00069 | 0.333 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.267 |
MOD_CK2_1 | 620 | 626 | PF00069 | 0.551 |
MOD_CK2_1 | 683 | 689 | PF00069 | 0.601 |
MOD_CK2_1 | 700 | 706 | PF00069 | 0.596 |
MOD_Cter_Amidation | 503 | 506 | PF01082 | 0.416 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.561 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.413 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.487 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.301 |
MOD_GlcNHglycan | 374 | 377 | PF01048 | 0.349 |
MOD_GlcNHglycan | 481 | 484 | PF01048 | 0.739 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.564 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.648 |
MOD_GlcNHglycan | 727 | 730 | PF01048 | 0.569 |
MOD_GlcNHglycan | 743 | 747 | PF01048 | 0.708 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.638 |
MOD_GlcNHglycan | 91 | 94 | PF01048 | 0.611 |
MOD_GlcNHglycan | 99 | 103 | PF01048 | 0.583 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.663 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.689 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.377 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.247 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.594 |
MOD_GSK3_1 | 478 | 485 | PF00069 | 0.611 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.677 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.600 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.606 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.517 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.631 |
MOD_GSK3_1 | 712 | 719 | PF00069 | 0.665 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.665 |
MOD_GSK3_1 | 98 | 105 | PF00069 | 0.549 |
MOD_LATS_1 | 558 | 564 | PF00433 | 0.297 |
MOD_N-GLC_1 | 134 | 139 | PF02516 | 0.525 |
MOD_N-GLC_1 | 169 | 174 | PF02516 | 0.371 |
MOD_N-GLC_1 | 722 | 727 | PF02516 | 0.499 |
MOD_N-GLC_1 | 89 | 94 | PF02516 | 0.596 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.432 |
MOD_NEK2_1 | 265 | 270 | PF00069 | 0.289 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.271 |
MOD_NEK2_1 | 35 | 40 | PF00069 | 0.562 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.290 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.354 |
MOD_NEK2_1 | 543 | 548 | PF00069 | 0.264 |
MOD_NEK2_1 | 632 | 637 | PF00069 | 0.463 |
MOD_NEK2_1 | 642 | 647 | PF00069 | 0.463 |
MOD_NEK2_1 | 713 | 718 | PF00069 | 0.757 |
MOD_NEK2_2 | 119 | 124 | PF00069 | 0.476 |
MOD_NEK2_2 | 198 | 203 | PF00069 | 0.362 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.281 |
MOD_PIKK_1 | 697 | 703 | PF00454 | 0.557 |
MOD_PKA_2 | 109 | 115 | PF00069 | 0.546 |
MOD_PKA_2 | 426 | 432 | PF00069 | 0.357 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.360 |
MOD_PKA_2 | 504 | 510 | PF00069 | 0.243 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.276 |
MOD_PKA_2 | 75 | 81 | PF00069 | 0.661 |
MOD_PKB_1 | 605 | 613 | PF00069 | 0.458 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.373 |
MOD_Plk_1 | 198 | 204 | PF00069 | 0.365 |
MOD_Plk_1 | 510 | 516 | PF00069 | 0.289 |
MOD_Plk_4 | 122 | 128 | PF00069 | 0.551 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.373 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.322 |
MOD_Plk_4 | 24 | 30 | PF00069 | 0.595 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.247 |
MOD_Plk_4 | 426 | 432 | PF00069 | 0.373 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.645 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.243 |
MOD_ProDKin_1 | 38 | 44 | PF00069 | 0.610 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.613 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.491 |
MOD_ProDKin_1 | 62 | 68 | PF00069 | 0.579 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.647 |
MOD_ProDKin_1 | 716 | 722 | PF00069 | 0.654 |
MOD_SUMO_rev_2 | 146 | 150 | PF00179 | 0.369 |
MOD_SUMO_rev_2 | 172 | 181 | PF00179 | 0.429 |
MOD_SUMO_rev_2 | 704 | 711 | PF00179 | 0.572 |
TRG_DiLeu_BaEn_1 | 21 | 26 | PF01217 | 0.561 |
TRG_DiLeu_BaLyEn_6 | 187 | 192 | PF01217 | 0.279 |
TRG_DiLeu_BaLyEn_6 | 592 | 597 | PF01217 | 0.283 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 233 | 236 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 253 | 256 | PF00928 | 0.150 |
TRG_ENDOCYTIC_2 | 458 | 461 | PF00928 | 0.349 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.541 |
TRG_ENDOCYTIC_2 | 528 | 531 | PF00928 | 0.250 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.297 |
TRG_ER_diArg_1 | 363 | 365 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 446 | 449 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 531 | 533 | PF00400 | 0.247 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 604 | 607 | PF00400 | 0.276 |
TRG_ER_diArg_1 | 649 | 652 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 664 | 667 | PF00400 | 0.552 |
TRG_NES_CRM1_1 | 323 | 336 | PF08389 | 0.298 |
TRG_NES_CRM1_1 | 574 | 589 | PF08389 | 0.286 |
TRG_NLS_Bipartite_1 | 650 | 669 | PF00514 | 0.501 |
TRG_NLS_MonoCore_2 | 664 | 669 | PF00514 | 0.552 |
TRG_NLS_MonoExtC_3 | 663 | 668 | PF00514 | 0.578 |
TRG_NLS_MonoExtN_4 | 664 | 669 | PF00514 | 0.552 |
TRG_Pf-PMV_PEXEL_1 | 210 | 215 | PF00026 | 0.376 |
TRG_Pf-PMV_PEXEL_1 | 357 | 361 | PF00026 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 364 | 368 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 578 | 582 | PF00026 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 668 | 672 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7I6 | Leptomonas seymouri | 56% | 100% |
A0A0S4JDU0 | Bodo saltans | 38% | 85% |
A0A3S7X1J7 | Leishmania donovani | 36% | 100% |
A4HGJ3 | Leishmania braziliensis | 72% | 99% |
A4I3M0 | Leishmania infantum | 99% | 100% |
A4I3M1 | Leishmania infantum | 36% | 100% |
E9AZW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
E9AZW2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
P34409 | Caenorhabditis elegans | 31% | 100% |
Q4Q8C4 | Leishmania major | 36% | 100% |
Q4Q8C5 | Leishmania major | 89% | 100% |