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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: A4H8L1
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 9 |
GO:0006793 | phosphorus metabolic process | 3 | 9 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016310 | phosphorylation | 5 | 9 |
GO:0019538 | protein metabolic process | 3 | 9 |
GO:0036211 | protein modification process | 4 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0043412 | macromolecule modification | 4 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 9 |
GO:0003824 | catalytic activity | 1 | 9 |
GO:0004672 | protein kinase activity | 3 | 9 |
GO:0005488 | binding | 1 | 9 |
GO:0005524 | ATP binding | 5 | 9 |
GO:0016301 | kinase activity | 4 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 9 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 9 |
GO:0017076 | purine nucleotide binding | 4 | 9 |
GO:0030554 | adenyl nucleotide binding | 5 | 9 |
GO:0032553 | ribonucleotide binding | 3 | 9 |
GO:0032555 | purine ribonucleotide binding | 4 | 9 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 9 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 9 |
GO:0036094 | small molecule binding | 2 | 9 |
GO:0043167 | ion binding | 2 | 9 |
GO:0043168 | anion binding | 3 | 9 |
GO:0097159 | organic cyclic compound binding | 2 | 9 |
GO:0097367 | carbohydrate derivative binding | 2 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
GO:1901265 | nucleoside phosphate binding | 3 | 9 |
GO:1901363 | heterocyclic compound binding | 2 | 9 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.664 |
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.562 |
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.561 |
CLV_NRD_NRD_1 | 217 | 219 | PF00675 | 0.577 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 217 | 219 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.623 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.358 |
CLV_PCSK_PC1ET2_1 | 664 | 666 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 211 | 215 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 227 | 231 | PF00082 | 0.612 |
CLV_PCSK_SKI1_1 | 399 | 403 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.461 |
DEG_SCF_FBW7_1 | 103 | 109 | PF00400 | 0.542 |
DOC_CDC14_PxL_1 | 59 | 67 | PF14671 | 0.539 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.544 |
DOC_CKS1_1 | 155 | 160 | PF01111 | 0.604 |
DOC_CYCLIN_yCln2_LP_2 | 140 | 143 | PF00134 | 0.484 |
DOC_MAPK_gen_1 | 196 | 204 | PF00069 | 0.582 |
DOC_MAPK_gen_1 | 217 | 224 | PF00069 | 0.485 |
DOC_MAPK_gen_1 | 274 | 284 | PF00069 | 0.559 |
DOC_MAPK_gen_1 | 393 | 402 | PF00069 | 0.240 |
DOC_PP1_RVXF_1 | 197 | 204 | PF00149 | 0.459 |
DOC_PP1_RVXF_1 | 266 | 272 | PF00149 | 0.550 |
DOC_PP1_RVXF_1 | 417 | 424 | PF00149 | 0.438 |
DOC_PP2B_LxvP_1 | 140 | 143 | PF13499 | 0.484 |
DOC_PP2B_LxvP_1 | 168 | 171 | PF13499 | 0.682 |
DOC_PP4_FxxP_1 | 124 | 127 | PF00568 | 0.524 |
DOC_PP4_FxxP_1 | 156 | 159 | PF00568 | 0.428 |
DOC_PP4_MxPP_1 | 21 | 24 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 534 | 538 | PF00917 | 0.438 |
DOC_USP7_UBL2_3 | 399 | 403 | PF12436 | 0.438 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.713 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.592 |
DOC_WW_Pin1_4 | 175 | 180 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.745 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.531 |
DOC_WW_Pin1_4 | 644 | 649 | PF00397 | 0.240 |
DOC_WW_Pin1_4 | 91 | 96 | PF00397 | 0.780 |
LIG_14-3-3_CanoR_1 | 132 | 140 | PF00244 | 0.711 |
LIG_14-3-3_CanoR_1 | 163 | 169 | PF00244 | 0.668 |
LIG_14-3-3_CanoR_1 | 227 | 237 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 277 | 282 | PF00244 | 0.526 |
LIG_14-3-3_CanoR_1 | 422 | 427 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 618 | 623 | PF00244 | 0.336 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.736 |
LIG_BIR_III_4 | 144 | 148 | PF00653 | 0.383 |
LIG_BRCT_BRCA1_1 | 120 | 124 | PF00533 | 0.662 |
LIG_BRCT_BRCA1_1 | 274 | 278 | PF00533 | 0.546 |
LIG_BRCT_BRCA1_1 | 403 | 407 | PF00533 | 0.438 |
LIG_BRCT_BRCA1_1 | 419 | 423 | PF00533 | 0.438 |
LIG_CaM_IQ_9 | 284 | 299 | PF13499 | 0.555 |
LIG_Clathr_ClatBox_1 | 518 | 522 | PF01394 | 0.269 |
LIG_CtBP_PxDLS_1 | 192 | 196 | PF00389 | 0.441 |
LIG_CtBP_PxDLS_1 | 67 | 71 | PF00389 | 0.549 |
LIG_DLG_GKlike_1 | 277 | 284 | PF00625 | 0.598 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.681 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.484 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.593 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.427 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.438 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.438 |
LIG_FHA_1 | 645 | 651 | PF00498 | 0.364 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.481 |
LIG_FHA_2 | 327 | 333 | PF00498 | 0.634 |
LIG_FHA_2 | 368 | 374 | PF00498 | 0.609 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.413 |
LIG_FHA_2 | 596 | 602 | PF00498 | 0.438 |
LIG_FHA_2 | 630 | 636 | PF00498 | 0.427 |
LIG_FHA_2 | 85 | 91 | PF00498 | 0.564 |
LIG_FXI_DFP_1 | 574 | 578 | PF00024 | 0.391 |
LIG_GBD_Chelix_1 | 432 | 440 | PF00786 | 0.391 |
LIG_GBD_Chelix_1 | 650 | 658 | PF00786 | 0.326 |
LIG_Integrin_RGD_1 | 467 | 469 | PF01839 | 0.454 |
LIG_LIR_Apic_2 | 121 | 127 | PF02991 | 0.531 |
LIG_LIR_Apic_2 | 153 | 159 | PF02991 | 0.631 |
LIG_LIR_Apic_2 | 181 | 187 | PF02991 | 0.653 |
LIG_LIR_Apic_2 | 541 | 547 | PF02991 | 0.357 |
LIG_LIR_Gen_1 | 134 | 145 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 280 | 287 | PF02991 | 0.597 |
LIG_LIR_Gen_1 | 420 | 430 | PF02991 | 0.430 |
LIG_LIR_Gen_1 | 434 | 442 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 134 | 140 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 275 | 281 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 324 | 328 | PF02991 | 0.641 |
LIG_LIR_Nem_3 | 381 | 387 | PF02991 | 0.645 |
LIG_LIR_Nem_3 | 420 | 426 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 434 | 438 | PF02991 | 0.277 |
LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 606 | 612 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 659 | 663 | PF02991 | 0.417 |
LIG_LYPXL_yS_3 | 429 | 432 | PF13949 | 0.240 |
LIG_MYND_1 | 106 | 110 | PF01753 | 0.536 |
LIG_MYND_1 | 63 | 67 | PF01753 | 0.538 |
LIG_NRBOX | 563 | 569 | PF00104 | 0.240 |
LIG_PDZ_Class_2 | 681 | 686 | PF00595 | 0.625 |
LIG_Pex14_2 | 471 | 475 | PF04695 | 0.438 |
LIG_PTB_Apo_2 | 503 | 510 | PF02174 | 0.438 |
LIG_REV1ctd_RIR_1 | 201 | 209 | PF16727 | 0.653 |
LIG_SH2_CRK | 165 | 169 | PF00017 | 0.574 |
LIG_SH2_CRK | 256 | 260 | PF00017 | 0.534 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.619 |
LIG_SH2_CRK | 660 | 664 | PF00017 | 0.438 |
LIG_SH2_PTP2 | 281 | 284 | PF00017 | 0.587 |
LIG_SH2_SRC | 128 | 131 | PF00017 | 0.536 |
LIG_SH2_SRC | 454 | 457 | PF00017 | 0.438 |
LIG_SH2_STAP1 | 137 | 141 | PF00017 | 0.516 |
LIG_SH2_STAP1 | 4 | 8 | PF00017 | 0.637 |
LIG_SH2_STAT3 | 682 | 685 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 128 | 131 | PF00017 | 0.720 |
LIG_SH2_STAT5 | 154 | 157 | PF00017 | 0.570 |
LIG_SH2_STAT5 | 246 | 249 | PF00017 | 0.730 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.240 |
LIG_SH2_STAT5 | 646 | 649 | PF00017 | 0.448 |
LIG_SH2_STAT5 | 682 | 685 | PF00017 | 0.521 |
LIG_SH3_2 | 127 | 132 | PF14604 | 0.529 |
LIG_SH3_2 | 158 | 163 | PF14604 | 0.642 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.591 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.557 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.532 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.664 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.508 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.541 |
LIG_SH3_3 | 5 | 11 | PF00018 | 0.550 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.357 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.804 |
LIG_SUMO_SIM_par_1 | 653 | 659 | PF11976 | 0.438 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.536 |
LIG_TYR_ITIM | 433 | 438 | PF00017 | 0.381 |
LIG_TYR_ITIM | 658 | 663 | PF00017 | 0.438 |
LIG_TYR_ITSM | 252 | 259 | PF00017 | 0.406 |
LIG_WW_3 | 22 | 26 | PF00397 | 0.556 |
MOD_CDC14_SPxK_1 | 160 | 163 | PF00782 | 0.602 |
MOD_CDC14_SPxK_1 | 349 | 352 | PF00782 | 0.629 |
MOD_CDK_SPK_2 | 346 | 351 | PF00069 | 0.616 |
MOD_CDK_SPK_2 | 91 | 96 | PF00069 | 0.742 |
MOD_CDK_SPxK_1 | 157 | 163 | PF00069 | 0.593 |
MOD_CDK_SPxK_1 | 19 | 25 | PF00069 | 0.566 |
MOD_CDK_SPxK_1 | 346 | 352 | PF00069 | 0.617 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.699 |
MOD_CK1_1 | 231 | 237 | PF00069 | 0.526 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.466 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.484 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.510 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.651 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.438 |
MOD_CK1_1 | 607 | 613 | PF00069 | 0.490 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.331 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.316 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.560 |
MOD_CK2_1 | 175 | 181 | PF00069 | 0.734 |
MOD_CK2_1 | 318 | 324 | PF00069 | 0.656 |
MOD_CK2_1 | 326 | 332 | PF00069 | 0.633 |
MOD_CK2_1 | 367 | 373 | PF00069 | 0.605 |
MOD_CK2_1 | 392 | 398 | PF00069 | 0.574 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.667 |
MOD_CK2_1 | 629 | 635 | PF00069 | 0.427 |
MOD_Cter_Amidation | 197 | 200 | PF01082 | 0.491 |
MOD_DYRK1A_RPxSP_1 | 102 | 106 | PF00069 | 0.545 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.715 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.741 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.597 |
MOD_GlcNHglycan | 232 | 236 | PF01048 | 0.687 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.597 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.669 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.520 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.734 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.648 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.790 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.752 |
MOD_GlcNHglycan | 609 | 612 | PF01048 | 0.503 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.462 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.699 |
MOD_GSK3_1 | 244 | 251 | PF00069 | 0.648 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.379 |
MOD_GSK3_1 | 282 | 289 | PF00069 | 0.545 |
MOD_GSK3_1 | 326 | 333 | PF00069 | 0.686 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.509 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.337 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.438 |
MOD_GSK3_1 | 51 | 58 | PF00069 | 0.711 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.415 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.391 |
MOD_GSK3_1 | 610 | 617 | PF00069 | 0.356 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.615 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.378 |
MOD_N-GLC_1 | 345 | 350 | PF02516 | 0.448 |
MOD_N-GLC_1 | 639 | 644 | PF02516 | 0.492 |
MOD_NEK2_1 | 230 | 235 | PF00069 | 0.702 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.696 |
MOD_NEK2_1 | 40 | 45 | PF00069 | 0.762 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.400 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.324 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.568 |
MOD_NEK2_2 | 417 | 422 | PF00069 | 0.364 |
MOD_NEK2_2 | 97 | 102 | PF00069 | 0.590 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.628 |
MOD_PIKK_1 | 582 | 588 | PF00454 | 0.438 |
MOD_PK_1 | 618 | 624 | PF00069 | 0.240 |
MOD_PKA_1 | 318 | 324 | PF00069 | 0.656 |
MOD_PKA_1 | 664 | 670 | PF00069 | 0.438 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.724 |
MOD_PKA_2 | 291 | 297 | PF00069 | 0.586 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.542 |
MOD_PKA_2 | 617 | 623 | PF00069 | 0.336 |
MOD_PKA_2 | 664 | 670 | PF00069 | 0.438 |
MOD_Plk_1 | 330 | 336 | PF00069 | 0.600 |
MOD_Plk_1 | 471 | 477 | PF00069 | 0.438 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.645 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.452 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.594 |
MOD_Plk_4 | 422 | 428 | PF00069 | 0.387 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.393 |
MOD_Plk_4 | 569 | 575 | PF00069 | 0.438 |
MOD_Plk_4 | 604 | 610 | PF00069 | 0.413 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.566 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.694 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.714 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.598 |
MOD_ProDKin_1 | 175 | 181 | PF00069 | 0.636 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.750 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.532 |
MOD_ProDKin_1 | 644 | 650 | PF00069 | 0.240 |
MOD_ProDKin_1 | 91 | 97 | PF00069 | 0.781 |
MOD_SUMO_for_1 | 306 | 309 | PF00179 | 0.582 |
MOD_SUMO_for_1 | 502 | 505 | PF00179 | 0.357 |
MOD_SUMO_for_1 | 550 | 553 | PF00179 | 0.438 |
MOD_SUMO_rev_2 | 404 | 414 | PF00179 | 0.492 |
TRG_DiLeu_BaEn_1 | 649 | 654 | PF01217 | 0.240 |
TRG_DiLeu_BaEn_4 | 60 | 66 | PF01217 | 0.540 |
TRG_ENDOCYTIC_2 | 137 | 140 | PF00928 | 0.525 |
TRG_ENDOCYTIC_2 | 165 | 168 | PF00928 | 0.569 |
TRG_ENDOCYTIC_2 | 256 | 259 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.587 |
TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.631 |
TRG_ENDOCYTIC_2 | 384 | 387 | PF00928 | 0.632 |
TRG_ENDOCYTIC_2 | 429 | 432 | PF00928 | 0.371 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.375 |
TRG_ENDOCYTIC_2 | 660 | 663 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 199 | 201 | PF00400 | 0.513 |
TRG_ER_diArg_1 | 217 | 220 | PF00400 | 0.554 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.628 |
TRG_ER_FFAT_2 | 606 | 613 | PF00635 | 0.240 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 385 | 389 | PF00026 | 0.534 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE38 | Leptomonas seymouri | 75% | 100% |
A0A0S4JLW5 | Bodo saltans | 35% | 90% |
A0A3S5H6X9 | Leishmania donovani | 75% | 100% |
A4HWY3 | Leishmania infantum | 76% | 100% |
C9ZW20 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 100% |
E9AQP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QET2 | Leishmania major | 76% | 100% |