Acyltransferase involved in GPI anchor remodelling (homologue of yeast GUP1)
Protein kinase, kinase Uncharacterized
Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 2 |
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: 25 |
NetGPI | no | yes: 0, no: 25 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 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: A0A3Q8IE25
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 26 |
GO:0006793 | phosphorus metabolic process | 3 | 26 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 26 |
GO:0006807 | nitrogen compound metabolic process | 2 | 26 |
GO:0008152 | metabolic process | 1 | 26 |
GO:0009987 | cellular process | 1 | 26 |
GO:0016310 | phosphorylation | 5 | 26 |
GO:0019538 | protein metabolic process | 3 | 26 |
GO:0036211 | protein modification process | 4 | 26 |
GO:0043170 | macromolecule metabolic process | 3 | 26 |
GO:0043412 | macromolecule modification | 4 | 26 |
GO:0044237 | cellular metabolic process | 2 | 26 |
GO:0044238 | primary metabolic process | 2 | 26 |
GO:0071704 | organic substance metabolic process | 2 | 26 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 26 |
GO:0007165 | signal transduction | 2 | 2 |
GO:0035556 | intracellular signal transduction | 3 | 2 |
GO:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0046777 | protein autophosphorylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 26 |
GO:0003824 | catalytic activity | 1 | 26 |
GO:0004672 | protein kinase activity | 3 | 26 |
GO:0005488 | binding | 1 | 26 |
GO:0005524 | ATP binding | 5 | 26 |
GO:0016301 | kinase activity | 4 | 26 |
GO:0016740 | transferase activity | 2 | 26 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 26 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 26 |
GO:0017076 | purine nucleotide binding | 4 | 26 |
GO:0030554 | adenyl nucleotide binding | 5 | 26 |
GO:0032553 | ribonucleotide binding | 3 | 26 |
GO:0032555 | purine ribonucleotide binding | 4 | 26 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 26 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 26 |
GO:0036094 | small molecule binding | 2 | 26 |
GO:0043167 | ion binding | 2 | 26 |
GO:0043168 | anion binding | 3 | 26 |
GO:0097159 | organic cyclic compound binding | 2 | 26 |
GO:0097367 | carbohydrate derivative binding | 2 | 26 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 26 |
GO:1901265 | nucleoside phosphate binding | 3 | 26 |
GO:1901363 | heterocyclic compound binding | 2 | 26 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 17 |
GO:0004707 | MAP kinase activity | 5 | 4 |
GO:0004683 | calmodulin-dependent protein kinase activity | 5 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
GO:0009931 | calcium-dependent protein serine/threonine kinase activity | 5 | 1 |
GO:0010857 | calcium-dependent protein kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 81 | 85 | PF00656 | 0.348 |
CLV_NRD_NRD_1 | 147 | 149 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 366 | 368 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.602 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 593 | 595 | PF00675 | 0.554 |
CLV_NRD_NRD_1 | 618 | 620 | PF00675 | 0.604 |
CLV_PCSK_FUR_1 | 591 | 595 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.300 |
CLV_PCSK_KEX2_1 | 326 | 328 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 437 | 439 | PF00082 | 0.583 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 593 | 595 | PF00082 | 0.540 |
CLV_PCSK_PC1ET2_1 | 132 | 134 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 326 | 328 | PF00082 | 0.522 |
CLV_PCSK_PC1ET2_1 | 437 | 439 | PF00082 | 0.628 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.307 |
CLV_PCSK_SKI1_1 | 247 | 251 | PF00082 | 0.329 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 33 | 37 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 409 | 413 | PF00082 | 0.589 |
CLV_PCSK_SKI1_1 | 646 | 650 | PF00082 | 0.491 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.345 |
DEG_APCC_DBOX_1 | 120 | 128 | PF00400 | 0.343 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.385 |
DEG_SPOP_SBC_1 | 388 | 392 | PF00917 | 0.551 |
DEG_SPOP_SBC_1 | 520 | 524 | PF00917 | 0.568 |
DOC_AGCK_PIF_2 | 77 | 82 | PF00069 | 0.255 |
DOC_CYCLIN_RxL_1 | 212 | 221 | PF00134 | 0.255 |
DOC_CYCLIN_yClb1_LxF_4 | 73 | 79 | PF00134 | 0.255 |
DOC_MAPK_gen_1 | 138 | 147 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 181 | 190 | PF00069 | 0.337 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 651 | 659 | PF00069 | 0.508 |
DOC_MAPK_HePTP_8 | 178 | 190 | PF00069 | 0.337 |
DOC_MAPK_JIP1_4 | 141 | 147 | PF00069 | 0.268 |
DOC_MAPK_MEF2A_6 | 181 | 190 | PF00069 | 0.337 |
DOC_MAPK_MEF2A_6 | 481 | 488 | PF00069 | 0.526 |
DOC_PP2B_LxvP_1 | 396 | 399 | PF13499 | 0.525 |
DOC_USP7_MATH_1 | 267 | 271 | PF00917 | 0.273 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.610 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.534 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 472 | 476 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.532 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.272 |
DOC_USP7_UBL2_3 | 34 | 38 | PF12436 | 0.273 |
DOC_WW_Pin1_4 | 101 | 106 | PF00397 | 0.295 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.300 |
DOC_WW_Pin1_4 | 338 | 343 | PF00397 | 0.770 |
DOC_WW_Pin1_4 | 389 | 394 | PF00397 | 0.601 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.609 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 507 | 512 | PF00397 | 0.824 |
DOC_WW_Pin1_4 | 521 | 526 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 606 | 611 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 639 | 644 | PF00397 | 0.551 |
LIG_14-3-3_CanoR_1 | 253 | 257 | PF00244 | 0.358 |
LIG_14-3-3_CanoR_1 | 291 | 298 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 354 | 361 | PF00244 | 0.548 |
LIG_14-3-3_CanoR_1 | 593 | 603 | PF00244 | 0.595 |
LIG_BIR_III_2 | 397 | 401 | PF00653 | 0.521 |
LIG_BRCT_BRCA1_1 | 365 | 369 | PF00533 | 0.546 |
LIG_eIF4E_1 | 183 | 189 | PF01652 | 0.255 |
LIG_eIF4E_1 | 82 | 88 | PF01652 | 0.302 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.337 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.396 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.245 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.288 |
LIG_FHA_1 | 428 | 434 | PF00498 | 0.581 |
LIG_FHA_1 | 611 | 617 | PF00498 | 0.578 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.695 |
LIG_FHA_2 | 372 | 378 | PF00498 | 0.508 |
LIG_FHA_2 | 39 | 45 | PF00498 | 0.334 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.535 |
LIG_IBAR_NPY_1 | 515 | 517 | PF08397 | 0.542 |
LIG_LIR_Apic_2 | 180 | 186 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 468 | 472 | PF02991 | 0.550 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.305 |
LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 161 | 165 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 255 | 259 | PF02991 | 0.327 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 75 | 80 | PF02991 | 0.318 |
LIG_LYPXL_yS_3 | 113 | 116 | PF13949 | 0.300 |
LIG_MYND_1 | 576 | 580 | PF01753 | 0.513 |
LIG_NRBOX | 644 | 650 | PF00104 | 0.541 |
LIG_PTB_Apo_2 | 586 | 593 | PF02174 | 0.546 |
LIG_PTB_Phospho_1 | 586 | 592 | PF10480 | 0.546 |
LIG_SH2_CRK | 254 | 258 | PF00017 | 0.248 |
LIG_SH2_CRK | 469 | 473 | PF00017 | 0.561 |
LIG_SH2_NCK_1 | 469 | 473 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.337 |
LIG_SH2_STAT3 | 119 | 122 | PF00017 | 0.265 |
LIG_SH2_STAT3 | 572 | 575 | PF00017 | 0.549 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.311 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.300 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.559 |
LIG_SH2_STAT5 | 40 | 43 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 572 | 575 | PF00017 | 0.549 |
LIG_SH3_1 | 494 | 500 | PF00018 | 0.510 |
LIG_SH3_3 | 106 | 112 | PF00018 | 0.262 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.340 |
LIG_SH3_3 | 282 | 288 | PF00018 | 0.431 |
LIG_SH3_3 | 377 | 383 | PF00018 | 0.540 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.255 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.626 |
LIG_SH3_3 | 489 | 495 | PF00018 | 0.529 |
LIG_SH3_3 | 505 | 511 | PF00018 | 0.513 |
LIG_SH3_3 | 570 | 576 | PF00018 | 0.753 |
LIG_SH3_5 | 173 | 177 | PF00018 | 0.255 |
LIG_SUMO_SIM_anti_2 | 319 | 325 | PF11976 | 0.426 |
LIG_SUMO_SIM_anti_2 | 50 | 55 | PF11976 | 0.236 |
LIG_SUMO_SIM_par_1 | 385 | 392 | PF11976 | 0.521 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.243 |
LIG_TRAF2_1 | 41 | 44 | PF00917 | 0.255 |
LIG_TRFH_1 | 496 | 500 | PF08558 | 0.495 |
LIG_TYR_ITIM | 111 | 116 | PF00017 | 0.278 |
LIG_UBA3_1 | 123 | 132 | PF00899 | 0.337 |
LIG_UBA3_1 | 371 | 376 | PF00899 | 0.508 |
LIG_UBA3_1 | 87 | 95 | PF00899 | 0.334 |
MOD_CDC14_SPxK_1 | 404 | 407 | PF00782 | 0.549 |
MOD_CDK_SPK_2 | 476 | 481 | PF00069 | 0.596 |
MOD_CDK_SPK_2 | 507 | 512 | PF00069 | 0.549 |
MOD_CDK_SPK_2 | 606 | 611 | PF00069 | 0.548 |
MOD_CDK_SPxK_1 | 401 | 407 | PF00069 | 0.554 |
MOD_CDK_SPxxK_3 | 639 | 646 | PF00069 | 0.532 |
MOD_CK1_1 | 103 | 109 | PF00069 | 0.239 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.302 |
MOD_CK1_1 | 362 | 368 | PF00069 | 0.783 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.594 |
MOD_CK1_1 | 428 | 434 | PF00069 | 0.666 |
MOD_CK1_1 | 440 | 446 | PF00069 | 0.696 |
MOD_CK1_1 | 547 | 553 | PF00069 | 0.566 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.588 |
MOD_CK1_1 | 571 | 577 | PF00069 | 0.601 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.548 |
MOD_CK2_1 | 149 | 155 | PF00069 | 0.279 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.300 |
MOD_CK2_1 | 38 | 44 | PF00069 | 0.280 |
MOD_CK2_1 | 564 | 570 | PF00069 | 0.541 |
MOD_Cter_Amidation | 435 | 438 | PF01082 | 0.574 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.226 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.304 |
MOD_GlcNHglycan | 261 | 264 | PF01048 | 0.362 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.465 |
MOD_GlcNHglycan | 474 | 477 | PF01048 | 0.541 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.651 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.631 |
MOD_GlcNHglycan | 560 | 563 | PF01048 | 0.629 |
MOD_GlcNHglycan | 598 | 601 | PF01048 | 0.610 |
MOD_GlcNHglycan | 634 | 638 | PF01048 | 0.573 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.464 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.345 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.295 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.598 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.638 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.801 |
MOD_GSK3_1 | 440 | 447 | PF00069 | 0.625 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.563 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.595 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.697 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.686 |
MOD_N-GLC_1 | 400 | 405 | PF02516 | 0.530 |
MOD_N-GLC_1 | 587 | 592 | PF02516 | 0.640 |
MOD_N-GLC_1 | 606 | 611 | PF02516 | 0.661 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.618 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.655 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.786 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.597 |
MOD_NEK2_1 | 587 | 592 | PF00069 | 0.609 |
MOD_PIKK_1 | 437 | 443 | PF00454 | 0.549 |
MOD_PIKK_1 | 571 | 577 | PF00454 | 0.558 |
MOD_PK_1 | 229 | 235 | PF00069 | 0.300 |
MOD_PKA_1 | 437 | 443 | PF00069 | 0.599 |
MOD_PKA_1 | 593 | 599 | PF00069 | 0.587 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.313 |
MOD_PKA_2 | 290 | 296 | PF00069 | 0.329 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.583 |
MOD_PKA_2 | 437 | 443 | PF00069 | 0.623 |
MOD_PKA_2 | 593 | 599 | PF00069 | 0.742 |
MOD_PKA_2 | 610 | 616 | PF00069 | 0.572 |
MOD_PKB_1 | 591 | 599 | PF00069 | 0.521 |
MOD_Plk_1 | 357 | 363 | PF00069 | 0.520 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.737 |
MOD_Plk_1 | 547 | 553 | PF00069 | 0.596 |
MOD_Plk_1 | 587 | 593 | PF00069 | 0.609 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.300 |
MOD_Plk_4 | 568 | 574 | PF00069 | 0.628 |
MOD_Plk_4 | 582 | 588 | PF00069 | 0.574 |
MOD_ProDKin_1 | 101 | 107 | PF00069 | 0.295 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.300 |
MOD_ProDKin_1 | 338 | 344 | PF00069 | 0.770 |
MOD_ProDKin_1 | 389 | 395 | PF00069 | 0.602 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.610 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.675 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.676 |
MOD_ProDKin_1 | 507 | 513 | PF00069 | 0.823 |
MOD_ProDKin_1 | 521 | 527 | PF00069 | 0.515 |
MOD_ProDKin_1 | 606 | 612 | PF00069 | 0.651 |
MOD_ProDKin_1 | 639 | 645 | PF00069 | 0.550 |
MOD_SUMO_for_1 | 140 | 143 | PF00179 | 0.308 |
MOD_SUMO_for_1 | 532 | 535 | PF00179 | 0.499 |
MOD_SUMO_rev_2 | 560 | 569 | PF00179 | 0.545 |
TRG_DiLeu_BaEn_4 | 43 | 49 | PF01217 | 0.255 |
TRG_DiLeu_BaLyEn_6 | 106 | 111 | PF01217 | 0.243 |
TRG_DiLeu_BaLyEn_6 | 599 | 604 | PF01217 | 0.536 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.291 |
TRG_ER_diArg_1 | 406 | 409 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 54 | 56 | PF00400 | 0.315 |
TRG_ER_diArg_1 | 592 | 594 | PF00400 | 0.527 |
TRG_NES_CRM1_1 | 296 | 309 | PF08389 | 0.243 |
TRG_NLS_MonoExtC_3 | 436 | 442 | PF00514 | 0.550 |
TRG_NLS_MonoExtN_4 | 247 | 254 | PF00514 | 0.243 |
TRG_NLS_MonoExtN_4 | 435 | 441 | PF00514 | 0.553 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4E3 | Leptomonas seymouri | 57% | 98% |
A0A0S4J4B3 | Bodo saltans | 25% | 100% |
A0A3Q8IND3 | Leishmania donovani | 26% | 100% |
A0A3Q8IVR8 | Leishmania donovani | 33% | 100% |
A0A3R7K5U6 | Trypanosoma rangeli | 54% | 100% |
A0A3S5H6C8 | Leishmania donovani | 25% | 100% |
A0A3S7WQK7 | Leishmania donovani | 25% | 100% |
A0A3S7X8Z8 | Leishmania donovani | 23% | 100% |
A4H4S9 | Leishmania braziliensis | 25% | 100% |
A4H5L7 | Leishmania braziliensis | 25% | 100% |
A4HFC9 | Leishmania braziliensis | 82% | 100% |
A4HFF3 | Leishmania braziliensis | 24% | 100% |
A4HNT2 | Leishmania braziliensis | 35% | 100% |
A4HTV4 | Leishmania infantum | 25% | 100% |
A4HTV5 | Leishmania infantum | 25% | 100% |
A4I2K6 | Leishmania infantum | 100% | 100% |
A4IB02 | Leishmania infantum | 23% | 100% |
A4ICP8 | Leishmania infantum | 26% | 100% |
A4ICR2 | Leishmania infantum | 33% | 100% |
E9ACY7 | Leishmania major | 98% | 100% |
E9AET0 | Leishmania major | 24% | 100% |
E9ASJ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 33% | 100% |
E9AYR2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
E9B5Y5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |