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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000439 | transcription factor TFIIH core complex | 4 | 12 |
GO:0005654 | nucleoplasm | 2 | 2 |
GO:0005667 | transcription regulator complex | 2 | 12 |
GO:0005675 | transcription factor TFIIH holo complex | 4 | 2 |
GO:0032806 | carboxy-terminal domain protein kinase complex | 3 | 2 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 2 |
GO:0090575 | RNA polymerase II transcription regulator complex | 3 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:1902494 | catalytic complex | 2 | 2 |
GO:1902554 | serine/threonine protein kinase complex | 6 | 2 |
GO:1902911 | protein kinase complex | 5 | 2 |
GO:1990234 | transferase complex | 3 | 2 |
Related structures:
AlphaFold database: Q4Q1Z6
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:0006289 | nucleotide-excision repair | 6 | 12 |
GO:0006355 | regulation of DNA-templated transcription | 6 | 2 |
GO:0006357 | regulation of transcription by RNA polymerase II | 7 | 2 |
GO:0006468 | protein phosphorylation | 5 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
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:0009889 | regulation of biosynthetic process | 4 | 2 |
GO:0009987 | cellular process | 1 | 12 |
GO:0010468 | regulation of gene expression | 5 | 2 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 2 |
GO:0016310 | phosphorylation | 5 | 2 |
GO:0019219 | regulation of nucleobase-containing compound metabolic process | 5 | 2 |
GO:0019222 | regulation of metabolic process | 3 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0031323 | regulation of cellular metabolic process | 4 | 2 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 2 |
GO:0033554 | cellular response to stress | 3 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 2 |
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:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 12 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 2 |
GO:0051252 | regulation of RNA metabolic process | 5 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 12 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0070816 | obsolete phosphorylation of RNA polymerase II C-terminal domain | 6 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0080090 | regulation of primary metabolic process | 4 | 2 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1903506 | regulation of nucleic acid-templated transcription | 7 | 2 |
GO:2001141 | regulation of RNA biosynthetic process | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0001671 | ATPase activator activity | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 2 |
GO:0003677 | DNA binding | 4 | 2 |
GO:0003690 | double-stranded DNA binding | 5 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0097159 | organic cyclic compound binding | 2 | 2 |
GO:0098772 | molecular function regulator activity | 1 | 12 |
GO:0140677 | molecular function activator activity | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 541 | 545 | PF00656 | 0.629 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.455 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.269 |
CLV_NRD_NRD_1 | 373 | 375 | PF00675 | 0.366 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.284 |
CLV_NRD_NRD_1 | 475 | 477 | PF00675 | 0.322 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 529 | 531 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.413 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.521 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 25 | 27 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.284 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.577 |
CLV_PCSK_KEX2_1 | 529 | 531 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.400 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.523 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 27 | 31 | PF00082 | 0.443 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.346 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 322 | 326 | PF00082 | 0.335 |
CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 568 | 572 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 587 | 591 | PF00082 | 0.319 |
DEG_APCC_DBOX_1 | 181 | 189 | PF00400 | 0.508 |
DOC_CKS1_1 | 202 | 207 | PF01111 | 0.381 |
DOC_CKS1_1 | 260 | 265 | PF01111 | 0.292 |
DOC_CYCLIN_RxL_1 | 177 | 186 | PF00134 | 0.451 |
DOC_CYCLIN_RxL_1 | 296 | 304 | PF00134 | 0.362 |
DOC_MAPK_FxFP_2 | 342 | 345 | PF00069 | 0.367 |
DOC_PP1_RVXF_1 | 24 | 31 | PF00149 | 0.446 |
DOC_PP1_RVXF_1 | 320 | 327 | PF00149 | 0.413 |
DOC_PP1_RVXF_1 | 565 | 572 | PF00149 | 0.418 |
DOC_PP2B_LxvP_1 | 549 | 552 | PF13499 | 0.488 |
DOC_PP2B_LxvP_1 | 620 | 623 | PF13499 | 0.442 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.476 |
DOC_PP4_FxxP_1 | 196 | 199 | PF00568 | 0.601 |
DOC_PP4_FxxP_1 | 342 | 345 | PF00568 | 0.367 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 492 | 496 | PF00917 | 0.317 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.619 |
DOC_WW_Pin1_4 | 201 | 206 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 377 | 382 | PF00397 | 0.297 |
DOC_WW_Pin1_4 | 508 | 513 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 524 | 529 | PF00397 | 0.447 |
LIG_14-3-3_CanoR_1 | 134 | 143 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 166 | 170 | PF00244 | 0.509 |
LIG_14-3-3_CanoR_1 | 182 | 192 | PF00244 | 0.553 |
LIG_14-3-3_CanoR_1 | 218 | 227 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 27 | 37 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 359 | 367 | PF00244 | 0.280 |
LIG_14-3-3_CanoR_1 | 468 | 472 | PF00244 | 0.249 |
LIG_14-3-3_CanoR_1 | 476 | 485 | PF00244 | 0.292 |
LIG_14-3-3_CanoR_1 | 486 | 491 | PF00244 | 0.336 |
LIG_14-3-3_CanoR_1 | 579 | 589 | PF00244 | 0.489 |
LIG_Actin_WH2_2 | 213 | 230 | PF00022 | 0.427 |
LIG_APCC_ABBAyCdc20_2 | 26 | 32 | PF00400 | 0.444 |
LIG_BIR_III_4 | 178 | 182 | PF00653 | 0.325 |
LIG_BRCT_BRCA1_1 | 136 | 140 | PF00533 | 0.629 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.388 |
LIG_BRCT_BRCA1_1 | 222 | 226 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 379 | 383 | PF00533 | 0.320 |
LIG_BRCT_BRCA1_1 | 395 | 399 | PF00533 | 0.395 |
LIG_BRCT_BRCA1_1 | 518 | 522 | PF00533 | 0.702 |
LIG_CaM_IQ_9 | 105 | 121 | PF13499 | 0.521 |
LIG_CtBP_PxDLS_1 | 394 | 398 | PF00389 | 0.395 |
LIG_FHA_1 | 230 | 236 | PF00498 | 0.438 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.475 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.414 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.456 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.453 |
LIG_FHA_1 | 538 | 544 | PF00498 | 0.684 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.505 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.519 |
LIG_FHA_2 | 13 | 19 | PF00498 | 0.433 |
LIG_FHA_2 | 202 | 208 | PF00498 | 0.663 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.713 |
LIG_LIR_Apic_2 | 170 | 176 | PF02991 | 0.558 |
LIG_LIR_Gen_1 | 137 | 146 | PF02991 | 0.606 |
LIG_LIR_Gen_1 | 279 | 285 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 606 | 617 | PF02991 | 0.377 |
LIG_LIR_LC3C_4 | 547 | 551 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 279 | 283 | PF02991 | 0.457 |
LIG_LIR_Nem_3 | 429 | 435 | PF02991 | 0.269 |
LIG_LIR_Nem_3 | 606 | 612 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 614 | 620 | PF02991 | 0.351 |
LIG_LYPXL_S_1 | 366 | 370 | PF13949 | 0.284 |
LIG_LYPXL_yS_3 | 367 | 370 | PF13949 | 0.284 |
LIG_MAD2 | 27 | 35 | PF02301 | 0.440 |
LIG_NRBOX | 126 | 132 | PF00104 | 0.597 |
LIG_NRBOX | 324 | 330 | PF00104 | 0.284 |
LIG_PCNA_PIPBox_1 | 586 | 595 | PF02747 | 0.537 |
LIG_PCNA_yPIPBox_3 | 245 | 253 | PF02747 | 0.364 |
LIG_PCNA_yPIPBox_3 | 288 | 301 | PF02747 | 0.337 |
LIG_PCNA_yPIPBox_3 | 579 | 593 | PF02747 | 0.538 |
LIG_SH2_CRK | 609 | 613 | PF00017 | 0.404 |
LIG_SH2_GRB2like | 437 | 440 | PF00017 | 0.201 |
LIG_SH2_SRC | 101 | 104 | PF00017 | 0.499 |
LIG_SH2_STAP1 | 101 | 105 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 437 | 441 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 340 | 343 | PF00017 | 0.367 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 592 | 595 | PF00017 | 0.537 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.555 |
LIG_SH3_3 | 207 | 213 | PF00018 | 0.524 |
LIG_SH3_3 | 257 | 263 | PF00018 | 0.376 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.395 |
LIG_SH3_3 | 375 | 381 | PF00018 | 0.318 |
LIG_SUMO_SIM_anti_2 | 298 | 304 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 56 | 62 | PF11976 | 0.521 |
LIG_SUMO_SIM_par_1 | 128 | 135 | PF11976 | 0.608 |
LIG_SUMO_SIM_par_1 | 212 | 217 | PF11976 | 0.539 |
LIG_SUMO_SIM_par_1 | 298 | 304 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 327 | 333 | PF11976 | 0.337 |
LIG_SUMO_SIM_par_1 | 35 | 41 | PF11976 | 0.441 |
LIG_SUMO_SIM_par_1 | 392 | 398 | PF11976 | 0.395 |
LIG_SUMO_SIM_par_1 | 96 | 102 | PF11976 | 0.542 |
LIG_TRFH_1 | 209 | 213 | PF08558 | 0.571 |
LIG_TRFH_1 | 377 | 381 | PF08558 | 0.280 |
LIG_TYR_ITIM | 365 | 370 | PF00017 | 0.328 |
LIG_TYR_ITIM | 99 | 104 | PF00017 | 0.438 |
LIG_WW_3 | 267 | 271 | PF00397 | 0.269 |
MOD_CDC14_SPxK_1 | 527 | 530 | PF00782 | 0.543 |
MOD_CDK_SPK_2 | 524 | 529 | PF00069 | 0.546 |
MOD_CDK_SPxK_1 | 524 | 530 | PF00069 | 0.545 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.470 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.390 |
MOD_CK1_1 | 408 | 414 | PF00069 | 0.439 |
MOD_CK1_1 | 45 | 51 | PF00069 | 0.608 |
MOD_CK1_1 | 511 | 517 | PF00069 | 0.686 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.669 |
MOD_CK1_1 | 539 | 545 | PF00069 | 0.378 |
MOD_CK1_1 | 66 | 72 | PF00069 | 0.647 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.484 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.432 |
MOD_CK2_1 | 132 | 138 | PF00069 | 0.472 |
MOD_CK2_1 | 201 | 207 | PF00069 | 0.468 |
MOD_Cter_Amidation | 110 | 113 | PF01082 | 0.515 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.382 |
MOD_GlcNHglycan | 391 | 394 | PF01048 | 0.349 |
MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.366 |
MOD_GlcNHglycan | 410 | 413 | PF01048 | 0.421 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.439 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.644 |
MOD_GlcNHglycan | 524 | 527 | PF01048 | 0.617 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.558 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.551 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.488 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.634 |
MOD_GSK3_1 | 311 | 318 | PF00069 | 0.466 |
MOD_GSK3_1 | 330 | 337 | PF00069 | 0.160 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.445 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.336 |
MOD_GSK3_1 | 506 | 513 | PF00069 | 0.623 |
MOD_GSK3_1 | 516 | 523 | PF00069 | 0.668 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.474 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.423 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.505 |
MOD_N-GLC_1 | 312 | 317 | PF02516 | 0.309 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.422 |
MOD_N-GLC_1 | 63 | 68 | PF02516 | 0.414 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.579 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.670 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.396 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.390 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.398 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.328 |
MOD_NEK2_1 | 335 | 340 | PF00069 | 0.214 |
MOD_NEK2_1 | 37 | 42 | PF00069 | 0.446 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.339 |
MOD_NEK2_1 | 403 | 408 | PF00069 | 0.285 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.424 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.763 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.629 |
MOD_PIKK_1 | 144 | 150 | PF00454 | 0.564 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.437 |
MOD_PIKK_1 | 183 | 189 | PF00454 | 0.402 |
MOD_PIKK_1 | 335 | 341 | PF00454 | 0.259 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.362 |
MOD_PKA_2 | 118 | 124 | PF00069 | 0.664 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.506 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.280 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.277 |
MOD_Plk_1 | 335 | 341 | PF00069 | 0.259 |
MOD_Plk_4 | 330 | 336 | PF00069 | 0.439 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.278 |
MOD_Plk_4 | 492 | 498 | PF00069 | 0.420 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.501 |
MOD_ProDKin_1 | 201 | 207 | PF00069 | 0.468 |
MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.313 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.413 |
MOD_ProDKin_1 | 377 | 383 | PF00069 | 0.297 |
MOD_ProDKin_1 | 508 | 514 | PF00069 | 0.622 |
MOD_ProDKin_1 | 524 | 530 | PF00069 | 0.447 |
MOD_SUMO_rev_2 | 371 | 377 | PF00179 | 0.292 |
TRG_DiLeu_BaEn_1 | 298 | 303 | PF01217 | 0.337 |
TRG_DiLeu_BaEn_1 | 92 | 97 | PF01217 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 320 | 325 | PF01217 | 0.395 |
TRG_DiLeu_BaLyEn_6 | 33 | 38 | PF01217 | 0.437 |
TRG_DiLeu_BaLyEn_6 | 365 | 370 | PF01217 | 0.290 |
TRG_DiLeu_BaLyEn_6 | 620 | 625 | PF01217 | 0.387 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.389 |
TRG_ENDOCYTIC_2 | 367 | 370 | PF00928 | 0.291 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 24 | 27 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.287 |
TRG_ER_diArg_1 | 497 | 499 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 528 | 530 | PF00400 | 0.591 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 134 | 138 | PF00026 | 0.462 |
TRG_Pf-PMV_PEXEL_1 | 182 | 187 | PF00026 | 0.510 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7V5 | Leptomonas seymouri | 65% | 100% |
A0A0S4JS94 | Bodo saltans | 28% | 100% |
A0A1X0P966 | Trypanosomatidae | 42% | 100% |
A0A3S5H816 | Leishmania donovani | 94% | 100% |
A0A422NK89 | Trypanosoma rangeli | 45% | 100% |
A4HNU0 | Leishmania braziliensis | 83% | 100% |
A4ICQ4 | Leishmania infantum | 93% | 100% |
D0A2Q5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9ASK0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5B9Y1 | Trypanosoma cruzi | 44% | 100% |