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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 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:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IDU8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 10 |
GO:0006259 | DNA metabolic process | 4 | 10 |
GO:0006281 | DNA repair | 5 | 10 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 10 |
GO:0006807 | nitrogen compound metabolic process | 2 | 10 |
GO:0006950 | response to stress | 2 | 10 |
GO:0006974 | DNA damage response | 4 | 10 |
GO:0008152 | metabolic process | 1 | 10 |
GO:0009987 | cellular process | 1 | 10 |
GO:0033554 | cellular response to stress | 3 | 10 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 10 |
GO:0043170 | macromolecule metabolic process | 3 | 10 |
GO:0044237 | cellular metabolic process | 2 | 10 |
GO:0044238 | primary metabolic process | 2 | 10 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 10 |
GO:0046483 | heterocycle metabolic process | 3 | 10 |
GO:0050896 | response to stimulus | 1 | 10 |
GO:0051716 | cellular response to stimulus | 2 | 10 |
GO:0071704 | organic substance metabolic process | 2 | 10 |
GO:0090304 | nucleic acid metabolic process | 4 | 10 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 10 |
GO:0006284 | base-excision repair | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004519 | endonuclease activity | 5 | 10 |
GO:0004527 | exonuclease activity | 5 | 7 |
GO:0005488 | binding | 1 | 10 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
GO:0003906 | DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 3 |
GO:0004529 | DNA exonuclease activity | 5 | 1 |
GO:0004536 | DNA nuclease activity | 4 | 1 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 1 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 1 |
GO:0008309 | double-stranded DNA exodeoxyribonuclease activity | 7 | 1 |
GO:0008311 | double-stranded DNA 3'-5' DNA exonuclease activity | 8 | 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 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
GO:0016829 | lyase activity | 2 | 2 |
GO:0016835 | carbon-oxygen lyase activity | 3 | 2 |
GO:0140078 | class I DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 103 | 107 | PF00656 | 0.245 |
CLV_C14_Caspase3-7 | 437 | 441 | PF00656 | 0.336 |
CLV_C14_Caspase3-7 | 705 | 709 | PF00656 | 0.599 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.298 |
CLV_NRD_NRD_1 | 194 | 196 | PF00675 | 0.308 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 482 | 484 | PF00675 | 0.333 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.391 |
CLV_PCSK_FUR_1 | 480 | 484 | PF00082 | 0.298 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 257 | 259 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.391 |
CLV_PCSK_KEX2_1 | 682 | 684 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.391 |
CLV_PCSK_PC1ET2_1 | 257 | 259 | PF00082 | 0.336 |
CLV_PCSK_PC1ET2_1 | 682 | 684 | PF00082 | 0.705 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.282 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.284 |
CLV_PCSK_SKI1_1 | 309 | 313 | PF00082 | 0.371 |
DEG_APCC_DBOX_1 | 222 | 230 | PF00400 | 0.298 |
DEG_APCC_DBOX_1 | 308 | 316 | PF00400 | 0.336 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.293 |
DEG_SPOP_SBC_1 | 285 | 289 | PF00917 | 0.302 |
DEG_SPOP_SBC_1 | 398 | 402 | PF00917 | 0.302 |
DOC_CKS1_1 | 591 | 596 | PF01111 | 0.327 |
DOC_CKS1_1 | 655 | 660 | PF01111 | 0.531 |
DOC_CYCLIN_yCln2_LP_2 | 318 | 321 | PF00134 | 0.336 |
DOC_MAPK_gen_1 | 649 | 655 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 196 | 205 | PF00069 | 0.268 |
DOC_MAPK_MEF2A_6 | 391 | 399 | PF00069 | 0.394 |
DOC_MAPK_MEF2A_6 | 630 | 639 | PF00069 | 0.506 |
DOC_PP1_RVXF_1 | 129 | 136 | PF00149 | 0.298 |
DOC_PP1_RVXF_1 | 178 | 184 | PF00149 | 0.407 |
DOC_PP1_RVXF_1 | 576 | 583 | PF00149 | 0.415 |
DOC_PP2B_LxvP_1 | 318 | 321 | PF13499 | 0.336 |
DOC_PP2B_LxvP_1 | 395 | 398 | PF13499 | 0.383 |
DOC_PP2B_PxIxI_1 | 200 | 206 | PF00149 | 0.391 |
DOC_PP2B_PxIxI_1 | 449 | 455 | PF00149 | 0.279 |
DOC_PP4_FxxP_1 | 591 | 594 | PF00568 | 0.320 |
DOC_USP7_MATH_1 | 285 | 289 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 352 | 356 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.302 |
DOC_USP7_MATH_1 | 519 | 523 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 529 | 533 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 651 | 655 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 690 | 694 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 696 | 700 | PF00917 | 0.632 |
DOC_USP7_UBL2_3 | 196 | 200 | PF12436 | 0.277 |
DOC_USP7_UBL2_3 | 253 | 257 | PF12436 | 0.481 |
DOC_WW_Pin1_4 | 333 | 338 | PF00397 | 0.223 |
DOC_WW_Pin1_4 | 358 | 363 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 409 | 414 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 446 | 451 | PF00397 | 0.480 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.321 |
DOC_WW_Pin1_4 | 654 | 659 | PF00397 | 0.522 |
LIG_14-3-3_CanoR_1 | 130 | 136 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 152 | 158 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 176 | 180 | PF00244 | 0.262 |
LIG_14-3-3_CanoR_1 | 314 | 319 | PF00244 | 0.496 |
LIG_14-3-3_CanoR_1 | 350 | 358 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 396 | 405 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 407 | 413 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 521 | 529 | PF00244 | 0.635 |
LIG_APCC_ABBA_1 | 378 | 383 | PF00400 | 0.298 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.315 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.298 |
LIG_CtBP_PxDLS_1 | 338 | 342 | PF00389 | 0.336 |
LIG_CtBP_PxDLS_1 | 53 | 57 | PF00389 | 0.374 |
LIG_deltaCOP1_diTrp_1 | 106 | 112 | PF00928 | 0.277 |
LIG_EVH1_1 | 560 | 564 | PF00568 | 0.498 |
LIG_EVH1_2 | 561 | 565 | PF00568 | 0.521 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.317 |
LIG_FHA_1 | 243 | 249 | PF00498 | 0.310 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.454 |
LIG_FHA_1 | 429 | 435 | PF00498 | 0.380 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.551 |
LIG_FHA_2 | 232 | 238 | PF00498 | 0.306 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.282 |
LIG_FHA_2 | 472 | 478 | PF00498 | 0.274 |
LIG_FHA_2 | 487 | 493 | PF00498 | 0.274 |
LIG_FHA_2 | 525 | 531 | PF00498 | 0.647 |
LIG_FHA_2 | 612 | 618 | PF00498 | 0.480 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.724 |
LIG_GBD_Chelix_1 | 259 | 267 | PF00786 | 0.302 |
LIG_LIR_Apic_2 | 333 | 337 | PF02991 | 0.317 |
LIG_LIR_Apic_2 | 588 | 594 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 106 | 114 | PF02991 | 0.298 |
LIG_LIR_Gen_1 | 159 | 169 | PF02991 | 0.264 |
LIG_LIR_Gen_1 | 234 | 243 | PF02991 | 0.280 |
LIG_LIR_Gen_1 | 367 | 378 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 492 | 501 | PF02991 | 0.274 |
LIG_LIR_Gen_1 | 536 | 547 | PF02991 | 0.404 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 159 | 164 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 234 | 238 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 579 | 585 | PF02991 | 0.459 |
LIG_MYND_1 | 463 | 467 | PF01753 | 0.391 |
LIG_NRBOX | 225 | 231 | PF00104 | 0.391 |
LIG_OCRL_FandH_1 | 21 | 33 | PF00620 | 0.313 |
LIG_PCNA_yPIPBox_3 | 359 | 373 | PF02747 | 0.333 |
LIG_PDZ_Class_3 | 727 | 732 | PF00595 | 0.567 |
LIG_Pex14_2 | 179 | 183 | PF04695 | 0.298 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.310 |
LIG_PTB_Apo_2 | 554 | 561 | PF02174 | 0.484 |
LIG_PTB_Phospho_1 | 554 | 560 | PF10480 | 0.483 |
LIG_Rb_pABgroove_1 | 339 | 347 | PF01858 | 0.336 |
LIG_SH2_CRK | 370 | 374 | PF00017 | 0.332 |
LIG_SH2_CRK | 633 | 637 | PF00017 | 0.400 |
LIG_SH2_NCK_1 | 334 | 338 | PF00017 | 0.391 |
LIG_SH2_NCK_1 | 370 | 374 | PF00017 | 0.223 |
LIG_SH2_NCK_1 | 442 | 446 | PF00017 | 0.223 |
LIG_SH2_PTP2 | 493 | 496 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 353 | 357 | PF00017 | 0.391 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 212 | 215 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.274 |
LIG_SH3_1 | 464 | 470 | PF00018 | 0.336 |
LIG_SH3_3 | 163 | 169 | PF00018 | 0.391 |
LIG_SH3_3 | 457 | 463 | PF00018 | 0.328 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.279 |
LIG_SH3_3 | 513 | 519 | PF00018 | 0.403 |
LIG_SH3_3 | 558 | 564 | PF00018 | 0.410 |
LIG_SH3_3 | 589 | 595 | PF00018 | 0.359 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.462 |
LIG_SH3_3 | 652 | 658 | PF00018 | 0.616 |
LIG_SUMO_SIM_anti_2 | 453 | 459 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 201 | 207 | PF11976 | 0.298 |
LIG_SUMO_SIM_par_1 | 291 | 299 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 651 | 657 | PF11976 | 0.651 |
LIG_SUMO_SIM_par_1 | 725 | 731 | PF11976 | 0.597 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.311 |
LIG_TRAF2_2 | 594 | 599 | PF00917 | 0.330 |
LIG_TYR_ITIM | 491 | 496 | PF00017 | 0.274 |
LIG_UBA3_1 | 36 | 43 | PF00899 | 0.391 |
LIG_WRC_WIRS_1 | 125 | 130 | PF05994 | 0.325 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.401 |
LIG_WRC_WIRS_1 | 639 | 644 | PF05994 | 0.485 |
LIG_WRC_WIRS_1 | 691 | 696 | PF05994 | 0.544 |
LIG_WW_3 | 319 | 323 | PF00397 | 0.336 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.337 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.333 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.333 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.410 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.375 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.426 |
MOD_CK1_1 | 303 | 309 | PF00069 | 0.466 |
MOD_CK1_1 | 324 | 330 | PF00069 | 0.400 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.403 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.627 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.608 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.701 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.395 |
MOD_CK2_1 | 231 | 237 | PF00069 | 0.389 |
MOD_CK2_1 | 524 | 530 | PF00069 | 0.609 |
MOD_CK2_1 | 611 | 617 | PF00069 | 0.481 |
MOD_CK2_1 | 706 | 712 | PF00069 | 0.641 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.298 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.264 |
MOD_GlcNHglycan | 279 | 283 | PF01048 | 0.391 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.412 |
MOD_GlcNHglycan | 323 | 326 | PF01048 | 0.403 |
MOD_GlcNHglycan | 383 | 387 | PF01048 | 0.391 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.444 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.476 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.343 |
MOD_GlcNHglycan | 523 | 526 | PF01048 | 0.644 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.609 |
MOD_GlcNHglycan | 694 | 697 | PF01048 | 0.698 |
MOD_GlcNHglycan | 698 | 701 | PF01048 | 0.677 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.305 |
MOD_GSK3_1 | 136 | 143 | PF00069 | 0.366 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.413 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.324 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.389 |
MOD_GSK3_1 | 333 | 340 | PF00069 | 0.470 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.430 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.621 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.720 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.722 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.395 |
MOD_N-GLC_1 | 208 | 213 | PF02516 | 0.274 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.330 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.287 |
MOD_NEK2_1 | 208 | 213 | PF00069 | 0.280 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.336 |
MOD_NEK2_1 | 278 | 283 | PF00069 | 0.373 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.368 |
MOD_NEK2_1 | 428 | 433 | PF00069 | 0.316 |
MOD_NEK2_1 | 495 | 500 | PF00069 | 0.336 |
MOD_NEK2_1 | 565 | 570 | PF00069 | 0.438 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.525 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.703 |
MOD_NEK2_2 | 175 | 180 | PF00069 | 0.245 |
MOD_NEK2_2 | 217 | 222 | PF00069 | 0.333 |
MOD_NEK2_2 | 638 | 643 | PF00069 | 0.575 |
MOD_OFUCOSY | 469 | 475 | PF10250 | 0.335 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.370 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.329 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.308 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.360 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.282 |
MOD_PKA_2 | 18 | 24 | PF00069 | 0.328 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.455 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.657 |
MOD_Plk_1 | 208 | 214 | PF00069 | 0.274 |
MOD_Plk_1 | 303 | 309 | PF00069 | 0.268 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.223 |
MOD_Plk_2-3 | 708 | 714 | PF00069 | 0.509 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.314 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.280 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.327 |
MOD_Plk_4 | 428 | 434 | PF00069 | 0.333 |
MOD_Plk_4 | 638 | 644 | PF00069 | 0.489 |
MOD_ProDKin_1 | 333 | 339 | PF00069 | 0.223 |
MOD_ProDKin_1 | 358 | 364 | PF00069 | 0.485 |
MOD_ProDKin_1 | 409 | 415 | PF00069 | 0.388 |
MOD_ProDKin_1 | 446 | 452 | PF00069 | 0.480 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.391 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.325 |
MOD_ProDKin_1 | 654 | 660 | PF00069 | 0.525 |
MOD_SUMO_rev_2 | 35 | 45 | PF00179 | 0.274 |
MOD_SUMO_rev_2 | 622 | 632 | PF00179 | 0.519 |
MOD_SUMO_rev_2 | 663 | 671 | PF00179 | 0.598 |
TRG_AP2beta_CARGO_1 | 536 | 546 | PF09066 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 388 | 393 | PF01217 | 0.391 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.336 |
TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 493 | 496 | PF00928 | 0.274 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.275 |
TRG_ER_diArg_1 | 462 | 465 | PF00400 | 0.468 |
TRG_ER_diArg_1 | 480 | 483 | PF00400 | 0.231 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 342 | 346 | PF00026 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 482 | 487 | PF00026 | 0.336 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB73 | Leptomonas seymouri | 58% | 98% |
A0A1X0P3V4 | Trypanosomatidae | 37% | 100% |
A0A3R7M024 | Trypanosoma rangeli | 41% | 100% |
A0A3S7XBT9 | Leishmania donovani | 100% | 100% |
D0A8S3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AIY2 | Leishmania braziliensis | 79% | 100% |
E9ATW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q0N5 | Leishmania major | 93% | 100% |