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 | 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: Q4Q0N5
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:0006284 | base-excision repair | 6 | 2 |
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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 10 |
GO:0003677 | DNA binding | 4 | 10 |
GO:0003824 | catalytic activity | 1 | 10 |
GO:0003906 | DNA-(apurinic or apyrimidinic site) endonuclease activity | 4 | 4 |
GO:0004518 | nuclease activity | 4 | 10 |
GO:0004519 | endonuclease activity | 5 | 10 |
GO:0004527 | exonuclease activity | 5 | 7 |
GO:0004529 | DNA exonuclease activity | 5 | 2 |
GO:0004536 | DNA nuclease activity | 4 | 2 |
GO:0005488 | binding | 1 | 10 |
GO:0008081 | phosphoric diester hydrolase activity | 5 | 2 |
GO:0008296 | 3'-5'-DNA exonuclease activity | 7 | 2 |
GO:0008309 | double-stranded DNA exodeoxyribonuclease activity | 7 | 2 |
GO:0008311 | double-stranded DNA 3'-5' DNA exonuclease activity | 8 | 2 |
GO:0008408 | 3'-5' exonuclease activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 10 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 10 |
GO:0016796 | exonuclease activity, active with either ribo- or deoxyribonucleic acids and producing 5'-phosphomonoesters | 6 | 2 |
GO:0016895 | DNA exonuclease activity, producing 5'-phosphomonoesters | 6 | 2 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 10 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 4 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 4 |
GO:1901363 | heterocyclic compound binding | 2 | 10 |
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 | 106 | 110 | PF00656 | 0.317 |
CLV_C14_Caspase3-7 | 440 | 444 | PF00656 | 0.390 |
CLV_C14_Caspase3-7 | 88 | 92 | PF00656 | 0.217 |
CLV_MEL_PAP_1 | 18 | 24 | PF00089 | 0.217 |
CLV_NRD_NRD_1 | 132 | 134 | PF00675 | 0.306 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.292 |
CLV_NRD_NRD_1 | 225 | 227 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 485 | 487 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.398 |
CLV_PCSK_FUR_1 | 483 | 487 | PF00082 | 0.308 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.355 |
CLV_PCSK_KEX2_1 | 485 | 487 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 685 | 687 | PF00082 | 0.753 |
CLV_PCSK_KEX2_1 | 73 | 75 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.398 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.355 |
CLV_PCSK_PC1ET2_1 | 685 | 687 | PF00082 | 0.753 |
CLV_PCSK_PC1ET2_1 | 73 | 75 | PF00082 | 0.282 |
CLV_PCSK_PC1ET2_1 | 80 | 82 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 134 | 138 | PF00082 | 0.292 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 312 | 316 | PF00082 | 0.411 |
DEG_APCC_DBOX_1 | 225 | 233 | PF00400 | 0.306 |
DEG_APCC_DBOX_1 | 311 | 319 | PF00400 | 0.355 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.304 |
DEG_SCF_TRCP1_1 | 282 | 287 | PF00400 | 0.217 |
DEG_SCF_TRCP1_1 | 689 | 695 | PF00400 | 0.518 |
DEG_SPOP_SBC_1 | 288 | 292 | PF00917 | 0.317 |
DEG_SPOP_SBC_1 | 401 | 405 | PF00917 | 0.317 |
DEG_SPOP_SBC_1 | 693 | 697 | PF00917 | 0.510 |
DOC_CKS1_1 | 594 | 599 | PF01111 | 0.347 |
DOC_CKS1_1 | 658 | 663 | PF01111 | 0.608 |
DOC_CYCLIN_yCln2_LP_2 | 321 | 324 | PF00134 | 0.355 |
DOC_MAPK_gen_1 | 65 | 71 | PF00069 | 0.217 |
DOC_MAPK_gen_1 | 711 | 720 | PF00069 | 0.615 |
DOC_MAPK_MEF2A_6 | 199 | 208 | PF00069 | 0.277 |
DOC_MAPK_MEF2A_6 | 394 | 402 | PF00069 | 0.402 |
DOC_MAPK_MEF2A_6 | 633 | 642 | PF00069 | 0.516 |
DOC_PP1_RVXF_1 | 132 | 139 | PF00149 | 0.306 |
DOC_PP1_RVXF_1 | 181 | 187 | PF00149 | 0.399 |
DOC_PP1_RVXF_1 | 579 | 586 | PF00149 | 0.416 |
DOC_PP2B_LxvP_1 | 321 | 324 | PF13499 | 0.355 |
DOC_PP2B_LxvP_1 | 398 | 401 | PF13499 | 0.391 |
DOC_PP2B_PxIxI_1 | 203 | 209 | PF00149 | 0.398 |
DOC_PP2B_PxIxI_1 | 452 | 458 | PF00149 | 0.292 |
DOC_PP4_FxxP_1 | 594 | 597 | PF00568 | 0.341 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.353 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.432 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.251 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.345 |
DOC_USP7_MATH_1 | 522 | 526 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 654 | 658 | PF00917 | 0.624 |
DOC_USP7_MATH_1 | 677 | 681 | PF00917 | 0.715 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 699 | 703 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.388 |
DOC_USP7_UBL2_3 | 199 | 203 | PF12436 | 0.285 |
DOC_USP7_UBL2_3 | 256 | 260 | PF12436 | 0.483 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.343 |
DOC_WW_Pin1_4 | 657 | 662 | PF00397 | 0.641 |
LIG_14-3-3_CanoR_1 | 133 | 139 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 155 | 165 | PF00244 | 0.306 |
LIG_14-3-3_CanoR_1 | 353 | 361 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 399 | 408 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 410 | 419 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 524 | 532 | PF00244 | 0.650 |
LIG_14-3-3_CanoR_1 | 66 | 72 | PF00244 | 0.340 |
LIG_APCC_ABBA_1 | 381 | 386 | PF00400 | 0.306 |
LIG_BIR_III_2 | 724 | 728 | PF00653 | 0.505 |
LIG_BRCT_BRCA1_1 | 141 | 145 | PF00533 | 0.323 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.306 |
LIG_CtBP_PxDLS_1 | 341 | 345 | PF00389 | 0.355 |
LIG_CtBP_PxDLS_1 | 53 | 57 | PF00389 | 0.383 |
LIG_deltaCOP1_diTrp_1 | 109 | 115 | PF00928 | 0.285 |
LIG_EVH1_1 | 563 | 567 | PF00568 | 0.521 |
LIG_EVH1_2 | 564 | 568 | PF00568 | 0.544 |
LIG_FHA_1 | 246 | 252 | PF00498 | 0.327 |
LIG_FHA_1 | 292 | 298 | PF00498 | 0.459 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.253 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.358 |
LIG_FHA_1 | 658 | 664 | PF00498 | 0.598 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.317 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.291 |
LIG_FHA_2 | 475 | 481 | PF00498 | 0.282 |
LIG_FHA_2 | 490 | 496 | PF00498 | 0.282 |
LIG_FHA_2 | 615 | 621 | PF00498 | 0.505 |
LIG_FHA_2 | 86 | 92 | PF00498 | 0.375 |
LIG_GBD_Chelix_1 | 262 | 270 | PF00786 | 0.317 |
LIG_LIR_Apic_2 | 591 | 597 | PF02991 | 0.340 |
LIG_LIR_Gen_1 | 109 | 117 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 162 | 172 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 370 | 381 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 495 | 504 | PF02991 | 0.282 |
LIG_LIR_Gen_1 | 539 | 550 | PF02991 | 0.477 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 20 | 25 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 495 | 499 | PF02991 | 0.282 |
LIG_LIR_Nem_3 | 539 | 545 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 582 | 588 | PF02991 | 0.412 |
LIG_MYND_1 | 466 | 470 | PF01753 | 0.398 |
LIG_NRBOX | 228 | 234 | PF00104 | 0.398 |
LIG_OCRL_FandH_1 | 21 | 33 | PF00620 | 0.330 |
LIG_PCNA_yPIPBox_3 | 362 | 376 | PF02747 | 0.342 |
LIG_PDZ_Class_3 | 730 | 735 | PF00595 | 0.613 |
LIG_Pex14_2 | 182 | 186 | PF04695 | 0.306 |
LIG_Pex14_2 | 2 | 6 | PF04695 | 0.321 |
LIG_PTB_Apo_2 | 557 | 564 | PF02174 | 0.500 |
LIG_PTB_Phospho_1 | 557 | 563 | PF10480 | 0.498 |
LIG_Rb_pABgroove_1 | 342 | 350 | PF01858 | 0.355 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.299 |
LIG_SH2_CRK | 636 | 640 | PF00017 | 0.401 |
LIG_SH2_NCK_1 | 337 | 341 | PF00017 | 0.398 |
LIG_SH2_PTP2 | 496 | 499 | PF00017 | 0.282 |
LIG_SH2_STAP1 | 356 | 360 | PF00017 | 0.398 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 356 | 359 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 471 | 474 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 476 | 479 | PF00017 | 0.246 |
LIG_SH2_STAT5 | 496 | 499 | PF00017 | 0.282 |
LIG_SH3_1 | 467 | 473 | PF00018 | 0.355 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.429 |
LIG_SH3_3 | 460 | 466 | PF00018 | 0.356 |
LIG_SH3_3 | 467 | 473 | PF00018 | 0.275 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.473 |
LIG_SH3_3 | 592 | 598 | PF00018 | 0.345 |
LIG_SH3_3 | 655 | 661 | PF00018 | 0.672 |
LIG_SUMO_SIM_anti_2 | 456 | 462 | PF11976 | 0.383 |
LIG_SUMO_SIM_par_1 | 204 | 210 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 294 | 302 | PF11976 | 0.358 |
LIG_SUMO_SIM_par_1 | 728 | 734 | PF11976 | 0.630 |
LIG_TRAF2_1 | 76 | 79 | PF00917 | 0.328 |
LIG_TRAF2_2 | 597 | 602 | PF00917 | 0.351 |
LIG_TYR_ITIM | 494 | 499 | PF00017 | 0.282 |
LIG_UBA3_1 | 36 | 43 | PF00899 | 0.398 |
LIG_UBA3_1 | 71 | 80 | PF00899 | 0.217 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.334 |
LIG_WRC_WIRS_1 | 235 | 240 | PF05994 | 0.397 |
LIG_WRC_WIRS_1 | 642 | 647 | PF05994 | 0.516 |
LIG_WW_3 | 322 | 326 | PF00397 | 0.355 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.333 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.342 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.358 |
MOD_CK1_1 | 298 | 304 | PF00069 | 0.439 |
MOD_CK1_1 | 327 | 333 | PF00069 | 0.425 |
MOD_CK1_1 | 385 | 391 | PF00069 | 0.437 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.634 |
MOD_CK1_1 | 657 | 663 | PF00069 | 0.620 |
MOD_CK1_1 | 697 | 703 | PF00069 | 0.721 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.414 |
MOD_CK2_1 | 614 | 620 | PF00069 | 0.507 |
MOD_CK2_1 | 709 | 715 | PF00069 | 0.646 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.306 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.272 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.388 |
MOD_GlcNHglycan | 291 | 294 | PF01048 | 0.398 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.418 |
MOD_GlcNHglycan | 386 | 390 | PF01048 | 0.423 |
MOD_GlcNHglycan | 404 | 407 | PF01048 | 0.403 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.430 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.411 |
MOD_GlcNHglycan | 526 | 529 | PF01048 | 0.650 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.751 |
MOD_GlcNHglycan | 699 | 702 | PF01048 | 0.676 |
MOD_GlcNHglycan | 96 | 99 | PF01048 | 0.434 |
MOD_GSK3_1 | 139 | 146 | PF00069 | 0.390 |
MOD_GSK3_1 | 234 | 241 | PF00069 | 0.227 |
MOD_GSK3_1 | 280 | 287 | PF00069 | 0.415 |
MOD_GSK3_1 | 291 | 298 | PF00069 | 0.415 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.405 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.623 |
MOD_GSK3_1 | 693 | 700 | PF00069 | 0.729 |
MOD_N-GLC_1 | 211 | 216 | PF02516 | 0.283 |
MOD_N-GLC_1 | 303 | 308 | PF02516 | 0.317 |
MOD_N-GLC_1 | 697 | 702 | PF02516 | 0.533 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.307 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.322 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.301 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.379 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.384 |
MOD_NEK2_1 | 431 | 436 | PF00069 | 0.323 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.355 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.457 |
MOD_NEK2_1 | 694 | 699 | PF00069 | 0.739 |
MOD_NEK2_2 | 220 | 225 | PF00069 | 0.342 |
MOD_NEK2_2 | 641 | 646 | PF00069 | 0.565 |
MOD_OFUCOSY | 472 | 478 | PF10250 | 0.353 |
MOD_PIKK_1 | 12 | 18 | PF00454 | 0.378 |
MOD_PIKK_1 | 139 | 145 | PF00454 | 0.454 |
MOD_PK_1 | 21 | 27 | PF00069 | 0.217 |
MOD_PKA_1 | 198 | 204 | PF00069 | 0.369 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.447 |
MOD_PKA_2 | 523 | 529 | PF00069 | 0.659 |
MOD_PKB_1 | 19 | 27 | PF00069 | 0.217 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.310 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.282 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.295 |
MOD_Plk_4 | 431 | 437 | PF00069 | 0.342 |
MOD_Plk_4 | 641 | 647 | PF00069 | 0.473 |
MOD_Plk_4 | 67 | 73 | PF00069 | 0.324 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.487 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.392 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.403 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.346 |
MOD_ProDKin_1 | 657 | 663 | PF00069 | 0.645 |
MOD_SUMO_rev_2 | 35 | 45 | PF00179 | 0.282 |
MOD_SUMO_rev_2 | 630 | 635 | PF00179 | 0.414 |
MOD_SUMO_rev_2 | 666 | 674 | PF00179 | 0.639 |
TRG_AP2beta_CARGO_1 | 539 | 549 | PF09066 | 0.532 |
TRG_DiLeu_BaEn_1 | 276 | 281 | PF01217 | 0.286 |
TRG_DiLeu_BaLyEn_6 | 391 | 396 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 450 | 455 | PF01217 | 0.355 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 496 | 499 | PF00928 | 0.282 |
TRG_ER_diArg_1 | 224 | 226 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 428 | 431 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 465 | 468 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 483 | 486 | PF00400 | 0.343 |
TRG_ER_diArg_1 | 65 | 67 | PF00400 | 0.420 |
TRG_ER_diArg_1 | 81 | 83 | PF00400 | 0.398 |
TRG_NES_CRM1_1 | 599 | 611 | PF08389 | 0.276 |
TRG_Pf-PMV_PEXEL_1 | 345 | 349 | PF00026 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 485 | 490 | PF00026 | 0.355 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB73 | Leptomonas seymouri | 57% | 99% |
A0A1X0P3V4 | Trypanosomatidae | 36% | 100% |
A0A3R7M024 | Trypanosoma rangeli | 41% | 100% |
A0A3S7XBT9 | Leishmania donovani | 92% | 100% |
A4IDU8 | Leishmania infantum | 93% | 100% |
D0A8S3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 36% | 100% |
E9AIY2 | Leishmania braziliensis | 80% | 99% |
E9ATW1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |