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: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: Q4Q5X3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006259 | DNA metabolic process | 4 | 2 |
GO:0006260 | DNA replication | 5 | 2 |
GO:0006281 | DNA repair | 5 | 2 |
GO:0006468 | protein phosphorylation | 5 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0006950 | response to stress | 2 | 2 |
GO:0006974 | DNA damage response | 4 | 2 |
GO:0007059 | chromosome segregation | 2 | 2 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018209 | peptidyl-serine modification | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0033554 | cellular response to stress | 3 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0050896 | response to stimulus | 1 | 2 |
GO:0051716 | cellular response to stimulus | 2 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004672 | protein kinase activity | 3 | 12 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 147 | 151 | PF00656 | 0.469 |
CLV_C14_Caspase3-7 | 21 | 25 | PF00656 | 0.579 |
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.532 |
CLV_C14_Caspase3-7 | 68 | 72 | PF00656 | 0.574 |
CLV_C14_Caspase3-7 | 96 | 100 | PF00656 | 0.705 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 169 | 171 | PF00675 | 0.522 |
CLV_NRD_NRD_1 | 185 | 187 | PF00675 | 0.510 |
CLV_NRD_NRD_1 | 211 | 213 | PF00675 | 0.371 |
CLV_NRD_NRD_1 | 335 | 337 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.262 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.656 |
CLV_PCSK_KEX2_1 | 169 | 171 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 211 | 213 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 254 | 256 | PF00082 | 0.342 |
CLV_PCSK_KEX2_1 | 335 | 337 | PF00082 | 0.335 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.239 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.493 |
CLV_PCSK_PC1ET2_1 | 17 | 19 | PF00082 | 0.579 |
CLV_PCSK_PC1ET2_1 | 254 | 256 | PF00082 | 0.409 |
CLV_PCSK_PC1ET2_1 | 452 | 454 | PF00082 | 0.269 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.310 |
CLV_PCSK_PC7_1 | 207 | 213 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 123 | 127 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 242 | 246 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 327 | 331 | PF00082 | 0.363 |
CLV_PCSK_SKI1_1 | 356 | 360 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 455 | 459 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 463 | 467 | PF00082 | 0.239 |
DEG_APCC_DBOX_1 | 355 | 363 | PF00400 | 0.273 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.715 |
DEG_SCF_FBW7_1 | 603 | 609 | PF00400 | 0.232 |
DEG_SPOP_SBC_1 | 85 | 89 | PF00917 | 0.743 |
DOC_ANK_TNKS_1 | 575 | 582 | PF00023 | 0.239 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.621 |
DOC_CKS1_1 | 603 | 608 | PF01111 | 0.232 |
DOC_CYCLIN_RxL_1 | 239 | 250 | PF00134 | 0.345 |
DOC_CYCLIN_yCln2_LP_2 | 479 | 485 | PF00134 | 0.382 |
DOC_CYCLIN_yCln2_LP_2 | 665 | 668 | PF00134 | 0.637 |
DOC_MAPK_gen_1 | 169 | 176 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 240 | 248 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 240 | 248 | PF00069 | 0.416 |
DOC_MAPK_MEF2A_6 | 430 | 438 | PF00069 | 0.382 |
DOC_PP1_RVXF_1 | 461 | 467 | PF00149 | 0.382 |
DOC_PP1_RVXF_1 | 596 | 603 | PF00149 | 0.273 |
DOC_PP2B_LxvP_1 | 346 | 349 | PF13499 | 0.430 |
DOC_PP2B_LxvP_1 | 665 | 668 | PF13499 | 0.647 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.653 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.508 |
DOC_USP7_MATH_1 | 606 | 610 | PF00917 | 0.264 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.666 |
DOC_USP7_MATH_1 | 93 | 97 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 328 | 332 | PF12436 | 0.373 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 478 | 483 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 549 | 554 | PF00397 | 0.239 |
DOC_WW_Pin1_4 | 602 | 607 | PF00397 | 0.232 |
DOC_WW_Pin1_4 | 660 | 665 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 670 | 675 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 86 | 91 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 240 | 245 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 302 | 309 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 474 | 480 | PF00244 | 0.382 |
LIG_Actin_WH2_2 | 306 | 321 | PF00022 | 0.423 |
LIG_APCC_ABBA_1 | 493 | 498 | PF00400 | 0.382 |
LIG_APCC_ABBAyCdc20_2 | 453 | 459 | PF00400 | 0.321 |
LIG_BIR_III_2 | 671 | 675 | PF00653 | 0.569 |
LIG_deltaCOP1_diTrp_1 | 370 | 375 | PF00928 | 0.239 |
LIG_deltaCOP1_diTrp_1 | 560 | 568 | PF00928 | 0.239 |
LIG_eIF4E_1 | 357 | 363 | PF01652 | 0.239 |
LIG_EVH1_2 | 543 | 547 | PF00568 | 0.239 |
LIG_FHA_1 | 137 | 143 | PF00498 | 0.563 |
LIG_FHA_1 | 241 | 247 | PF00498 | 0.447 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.483 |
LIG_FHA_1 | 398 | 404 | PF00498 | 0.315 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.691 |
LIG_FHA_1 | 550 | 556 | PF00498 | 0.239 |
LIG_FHA_1 | 603 | 609 | PF00498 | 0.268 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.676 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.484 |
LIG_FHA_2 | 319 | 325 | PF00498 | 0.522 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.468 |
LIG_FHA_2 | 499 | 505 | PF00498 | 0.382 |
LIG_Integrin_RGD_1 | 430 | 432 | PF01839 | 0.382 |
LIG_LIR_Apic_2 | 538 | 544 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 243 | 251 | PF02991 | 0.414 |
LIG_LIR_Gen_1 | 342 | 351 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 355 | 363 | PF02991 | 0.194 |
LIG_LIR_Gen_1 | 422 | 429 | PF02991 | 0.239 |
LIG_LIR_Gen_1 | 432 | 441 | PF02991 | 0.239 |
LIG_LIR_LC3C_4 | 52 | 56 | PF02991 | 0.637 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 342 | 348 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 369 | 375 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 422 | 428 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 432 | 438 | PF02991 | 0.239 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.276 |
LIG_NRBOX | 358 | 364 | PF00104 | 0.273 |
LIG_Pex14_2 | 368 | 372 | PF04695 | 0.239 |
LIG_Rb_pABgroove_1 | 419 | 427 | PF01858 | 0.239 |
LIG_SH2_CRK | 133 | 137 | PF00017 | 0.517 |
LIG_SH2_CRK | 569 | 573 | PF00017 | 0.239 |
LIG_SH2_GRB2like | 441 | 444 | PF00017 | 0.315 |
LIG_SH2_SRC | 541 | 544 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 382 | 385 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 402 | 405 | PF00017 | 0.109 |
LIG_SH2_STAT5 | 450 | 453 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 475 | 478 | PF00017 | 0.239 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.249 |
LIG_SH2_STAT5 | 638 | 641 | PF00017 | 0.341 |
LIG_SH3_2 | 13 | 18 | PF14604 | 0.503 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.616 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.494 |
LIG_SH3_3 | 600 | 606 | PF00018 | 0.239 |
LIG_SH3_3 | 661 | 667 | PF00018 | 0.630 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.637 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.519 |
LIG_SUMO_SIM_anti_2 | 409 | 414 | PF11976 | 0.273 |
LIG_SUMO_SIM_par_1 | 52 | 59 | PF11976 | 0.725 |
LIG_TRAF2_1 | 19 | 22 | PF00917 | 0.730 |
LIG_TRAF2_1 | 26 | 29 | PF00917 | 0.754 |
LIG_TRAF2_1 | 273 | 276 | PF00917 | 0.536 |
LIG_TRFH_1 | 486 | 490 | PF08558 | 0.239 |
LIG_TYR_ITIM | 567 | 572 | PF00017 | 0.239 |
LIG_UBA3_1 | 359 | 365 | PF00899 | 0.239 |
LIG_UBA3_1 | 502 | 506 | PF00899 | 0.382 |
LIG_UBA3_1 | 567 | 575 | PF00899 | 0.364 |
MOD_CDK_SPK_2 | 549 | 554 | PF00069 | 0.239 |
MOD_CDK_SPK_2 | 602 | 607 | PF00069 | 0.232 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.645 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.704 |
MOD_CK1_1 | 44 | 50 | PF00069 | 0.665 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.379 |
MOD_CK1_1 | 533 | 539 | PF00069 | 0.273 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.239 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.522 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.437 |
MOD_CK2_1 | 148 | 154 | PF00069 | 0.547 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.541 |
MOD_CK2_1 | 347 | 353 | PF00069 | 0.473 |
MOD_CK2_1 | 434 | 440 | PF00069 | 0.239 |
MOD_Cter_Amidation | 167 | 170 | PF01082 | 0.451 |
MOD_Cter_Amidation | 573 | 576 | PF01082 | 0.239 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.661 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.498 |
MOD_GlcNHglycan | 280 | 284 | PF01048 | 0.589 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.432 |
MOD_GlcNHglycan | 595 | 598 | PF01048 | 0.239 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.628 |
MOD_GlcNHglycan | 651 | 654 | PF01048 | 0.652 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.580 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.707 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.647 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.510 |
MOD_GSK3_1 | 144 | 151 | PF00069 | 0.546 |
MOD_GSK3_1 | 226 | 233 | PF00069 | 0.570 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.730 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.693 |
MOD_GSK3_1 | 521 | 528 | PF00069 | 0.250 |
MOD_GSK3_1 | 529 | 536 | PF00069 | 0.223 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.109 |
MOD_GSK3_1 | 602 | 609 | PF00069 | 0.267 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.471 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.739 |
MOD_N-GLC_1 | 31 | 36 | PF02516 | 0.704 |
MOD_N-GLC_1 | 37 | 42 | PF02516 | 0.700 |
MOD_N-GLC_2 | 102 | 104 | PF02516 | 0.701 |
MOD_NEK2_1 | 113 | 118 | PF00069 | 0.709 |
MOD_NEK2_1 | 221 | 226 | PF00069 | 0.425 |
MOD_NEK2_1 | 27 | 32 | PF00069 | 0.508 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.398 |
MOD_NEK2_1 | 434 | 439 | PF00069 | 0.248 |
MOD_NEK2_1 | 510 | 515 | PF00069 | 0.332 |
MOD_NEK2_1 | 547 | 552 | PF00069 | 0.250 |
MOD_NEK2_1 | 639 | 644 | PF00069 | 0.449 |
MOD_PIKK_1 | 249 | 255 | PF00454 | 0.501 |
MOD_PIKK_1 | 530 | 536 | PF00454 | 0.239 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.239 |
MOD_PIKK_1 | 631 | 637 | PF00454 | 0.254 |
MOD_PKA_2 | 148 | 154 | PF00069 | 0.547 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.479 |
MOD_PKA_2 | 553 | 559 | PF00069 | 0.239 |
MOD_PKA_2 | 640 | 646 | PF00069 | 0.469 |
MOD_PKB_1 | 18 | 26 | PF00069 | 0.649 |
MOD_PKB_1 | 277 | 285 | PF00069 | 0.593 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.583 |
MOD_Plk_2-3 | 498 | 504 | PF00069 | 0.382 |
MOD_Plk_2-3 | 525 | 531 | PF00069 | 0.239 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.441 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.541 |
MOD_Plk_4 | 446 | 452 | PF00069 | 0.346 |
MOD_Plk_4 | 498 | 504 | PF00069 | 0.301 |
MOD_Plk_4 | 535 | 541 | PF00069 | 0.239 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.677 |
MOD_ProDKin_1 | 478 | 484 | PF00069 | 0.382 |
MOD_ProDKin_1 | 549 | 555 | PF00069 | 0.239 |
MOD_ProDKin_1 | 602 | 608 | PF00069 | 0.232 |
MOD_ProDKin_1 | 660 | 666 | PF00069 | 0.709 |
MOD_ProDKin_1 | 670 | 676 | PF00069 | 0.714 |
MOD_ProDKin_1 | 86 | 92 | PF00069 | 0.701 |
MOD_SUMO_for_1 | 142 | 145 | PF00179 | 0.496 |
MOD_SUMO_rev_2 | 322 | 330 | PF00179 | 0.344 |
MOD_SUMO_rev_2 | 481 | 491 | PF00179 | 0.375 |
MOD_SUMO_rev_2 | 498 | 508 | PF00179 | 0.159 |
MOD_SUMO_rev_2 | 609 | 615 | PF00179 | 0.239 |
TRG_DiLeu_BaEn_2 | 325 | 331 | PF01217 | 0.357 |
TRG_DiLeu_BaEn_3 | 610 | 616 | PF01217 | 0.266 |
TRG_DiLeu_BaEn_4 | 256 | 262 | PF01217 | 0.429 |
TRG_DiLeu_BaLyEn_6 | 460 | 465 | PF01217 | 0.254 |
TRG_ENDOCYTIC_2 | 133 | 136 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.273 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 569 | 572 | PF00928 | 0.239 |
TRG_ER_diArg_1 | 123 | 125 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.499 |
TRG_ER_diArg_1 | 334 | 336 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.262 |
TRG_ER_diArg_1 | 73 | 76 | PF00400 | 0.631 |
TRG_Pf-PMV_PEXEL_1 | 212 | 216 | PF00026 | 0.509 |
TRG_Pf-PMV_PEXEL_1 | 585 | 589 | PF00026 | 0.289 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBJ1 | Leptomonas seymouri | 78% | 99% |
A0A1X0NJ50 | Trypanosomatidae | 59% | 100% |
A0A3S5IR34 | Trypanosoma rangeli | 56% | 100% |
A0A3S7X4W6 | Leishmania donovani | 97% | 100% |
A4HJS4 | Leishmania braziliensis | 92% | 100% |
A4I790 | Leishmania infantum | 97% | 100% |
C9ZMG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 100% |
C9ZWL6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B285 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O55047 | Mus musculus | 38% | 94% |
Q08CW1 | Xenopus tropicalis | 36% | 97% |
Q1ECX4 | Danio rerio | 36% | 97% |
Q39238 | Arabidopsis thaliana | 41% | 98% |
Q86UE8 | Homo sapiens | 37% | 88% |
Q8C0V0 | Mus musculus | 37% | 88% |
Q90ZY6 | Danio rerio | 38% | 89% |
Q9UKI8 | Homo sapiens | 37% | 88% |
V5B7L8 | Trypanosoma cruzi | 61% | 100% |