Protein kinase, serine/threonine- kinase
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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pescher et al. (upgregulation) | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Lahav et al. - mRNA
- Protein
|
Related structures:
AlphaFold database: A4HZM2
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 12 |
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:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016310 | phosphorylation | 5 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
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:0071704 | organic substance metabolic process | 2 | 12 |
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: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 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 514 | 518 | PF00656 | 0.674 |
CLV_C14_Caspase3-7 | 693 | 697 | PF00656 | 0.579 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.586 |
CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.550 |
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.442 |
CLV_NRD_NRD_1 | 332 | 334 | PF00675 | 0.565 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 352 | 354 | PF00675 | 0.268 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 439 | 441 | PF00675 | 0.473 |
CLV_NRD_NRD_1 | 492 | 494 | PF00675 | 0.618 |
CLV_NRD_NRD_1 | 512 | 514 | PF00675 | 0.342 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 588 | 590 | PF00675 | 0.775 |
CLV_NRD_NRD_1 | 658 | 660 | PF00675 | 0.496 |
CLV_NRD_NRD_1 | 677 | 679 | PF00675 | 0.381 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.616 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.566 |
CLV_PCSK_KEX2_1 | 340 | 342 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 354 | 356 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 399 | 401 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 512 | 514 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 657 | 659 | PF00082 | 0.441 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.396 |
CLV_PCSK_PC1ET2_1 | 354 | 356 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.276 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.163 |
CLV_PCSK_SKI1_1 | 127 | 131 | PF00082 | 0.263 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 354 | 358 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 493 | 497 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 680 | 684 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 699 | 703 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.357 |
DEG_APCC_DBOX_1 | 258 | 266 | PF00400 | 0.323 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.393 |
DEG_SCF_FBW7_1 | 480 | 487 | PF00400 | 0.723 |
DEG_SCF_FBW7_2 | 630 | 635 | PF00400 | 0.713 |
DEG_SPOP_SBC_1 | 484 | 488 | PF00917 | 0.703 |
DOC_CKS1_1 | 481 | 486 | PF01111 | 0.725 |
DOC_CYCLIN_yCln2_LP_2 | 612 | 615 | PF00134 | 0.530 |
DOC_MAPK_gen_1 | 127 | 136 | PF00069 | 0.261 |
DOC_MAPK_gen_1 | 273 | 282 | PF00069 | 0.592 |
DOC_MAPK_gen_1 | 340 | 350 | PF00069 | 0.522 |
DOC_MAPK_MEF2A_6 | 721 | 729 | PF00069 | 0.374 |
DOC_MAPK_MEF2A_6 | 73 | 80 | PF00069 | 0.279 |
DOC_PP2B_LxvP_1 | 569 | 572 | PF13499 | 0.680 |
DOC_PP2B_LxvP_1 | 602 | 605 | PF13499 | 0.496 |
DOC_PP2B_LxvP_1 | 612 | 615 | PF13499 | 0.562 |
DOC_PP4_FxxP_1 | 707 | 710 | PF00568 | 0.546 |
DOC_USP7_MATH_1 | 247 | 251 | PF00917 | 0.277 |
DOC_USP7_MATH_1 | 485 | 489 | PF00917 | 0.716 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.786 |
DOC_USP7_MATH_1 | 564 | 568 | PF00917 | 0.544 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.595 |
DOC_USP7_MATH_1 | 710 | 714 | PF00917 | 0.401 |
DOC_USP7_MATH_1 | 789 | 793 | PF00917 | 0.559 |
DOC_USP7_MATH_2 | 42 | 48 | PF00917 | 0.261 |
DOC_USP7_UBL2_3 | 373 | 377 | PF12436 | 0.624 |
DOC_USP7_UBL2_3 | 581 | 585 | PF12436 | 0.723 |
DOC_USP7_UBL2_3 | 675 | 679 | PF12436 | 0.577 |
DOC_USP7_UBL2_3 | 8 | 12 | PF12436 | 0.353 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 411 | 416 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 480 | 485 | PF00397 | 0.619 |
DOC_WW_Pin1_4 | 493 | 498 | PF00397 | 0.555 |
DOC_WW_Pin1_4 | 543 | 548 | PF00397 | 0.693 |
DOC_WW_Pin1_4 | 591 | 596 | PF00397 | 0.683 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 628 | 633 | PF00397 | 0.668 |
DOC_WW_Pin1_4 | 647 | 652 | PF00397 | 0.648 |
LIG_14-3-3_CanoR_1 | 154 | 158 | PF00244 | 0.261 |
LIG_14-3-3_CanoR_1 | 233 | 239 | PF00244 | 0.339 |
LIG_14-3-3_CanoR_1 | 246 | 255 | PF00244 | 0.204 |
LIG_14-3-3_CanoR_1 | 276 | 280 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 534 | 543 | PF00244 | 0.556 |
LIG_Actin_WH2_2 | 145 | 162 | PF00022 | 0.261 |
LIG_Actin_WH2_2 | 204 | 219 | PF00022 | 0.277 |
LIG_Actin_WH2_2 | 28 | 43 | PF00022 | 0.353 |
LIG_AP2alpha_1 | 682 | 686 | PF02296 | 0.615 |
LIG_APCC_ABBA_1 | 725 | 730 | PF00400 | 0.354 |
LIG_APCC_ABBAyCdc20_2 | 122 | 128 | PF00400 | 0.254 |
LIG_BRCT_BRCA1_1 | 504 | 508 | PF00533 | 0.639 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.277 |
LIG_FHA_1 | 154 | 160 | PF00498 | 0.291 |
LIG_FHA_1 | 62 | 68 | PF00498 | 0.261 |
LIG_FHA_1 | 704 | 710 | PF00498 | 0.447 |
LIG_FHA_1 | 713 | 719 | PF00498 | 0.407 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.581 |
LIG_FHA_2 | 535 | 541 | PF00498 | 0.743 |
LIG_FHA_2 | 650 | 656 | PF00498 | 0.584 |
LIG_LIR_Apic_2 | 166 | 172 | PF02991 | 0.261 |
LIG_LIR_Apic_2 | 706 | 710 | PF02991 | 0.536 |
LIG_LIR_Gen_1 | 2 | 10 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 660 | 670 | PF02991 | 0.402 |
LIG_LIR_Gen_1 | 75 | 83 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 2 | 7 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 660 | 666 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 87 | 92 | PF02991 | 0.261 |
LIG_LYPXL_S_1 | 219 | 223 | PF13949 | 0.277 |
LIG_LYPXL_yS_3 | 220 | 223 | PF13949 | 0.261 |
LIG_MAD2 | 214 | 222 | PF02301 | 0.261 |
LIG_PCNA_yPIPBox_3 | 209 | 220 | PF02747 | 0.282 |
LIG_PDZ_Class_2 | 795 | 800 | PF00595 | 0.634 |
LIG_Pex14_2 | 15 | 19 | PF04695 | 0.261 |
LIG_Pex14_2 | 682 | 686 | PF04695 | 0.615 |
LIG_SH2_CRK | 4 | 8 | PF00017 | 0.321 |
LIG_SH2_CRK | 89 | 93 | PF00017 | 0.261 |
LIG_SH2_GRB2like | 82 | 85 | PF00017 | 0.296 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.261 |
LIG_SH2_SRC | 82 | 85 | PF00017 | 0.261 |
LIG_SH2_STAP1 | 227 | 231 | PF00017 | 0.277 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.278 |
LIG_SH2_STAT5 | 4 | 7 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.625 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.261 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.296 |
LIG_SH3_3 | 472 | 478 | PF00018 | 0.662 |
LIG_SH3_3 | 530 | 536 | PF00018 | 0.548 |
LIG_SH3_3 | 557 | 563 | PF00018 | 0.678 |
LIG_SH3_3 | 608 | 614 | PF00018 | 0.736 |
LIG_SH3_4 | 581 | 588 | PF00018 | 0.657 |
LIG_SUMO_SIM_par_1 | 250 | 256 | PF11976 | 0.268 |
LIG_SUMO_SIM_par_1 | 278 | 284 | PF11976 | 0.590 |
LIG_TRAF2_1 | 281 | 284 | PF00917 | 0.526 |
LIG_TRAF2_1 | 349 | 352 | PF00917 | 0.522 |
LIG_TRAF2_1 | 496 | 499 | PF00917 | 0.565 |
LIG_TRAF2_1 | 576 | 579 | PF00917 | 0.639 |
LIG_UBA3_1 | 238 | 245 | PF00899 | 0.333 |
LIG_WW_3 | 479 | 483 | PF00397 | 0.729 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.261 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.291 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.586 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.752 |
MOD_CK1_1 | 556 | 562 | PF00069 | 0.783 |
MOD_CK1_1 | 791 | 797 | PF00069 | 0.613 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.578 |
MOD_CK2_1 | 427 | 433 | PF00069 | 0.563 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.591 |
MOD_CK2_1 | 534 | 540 | PF00069 | 0.745 |
MOD_CK2_1 | 647 | 653 | PF00069 | 0.578 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.570 |
MOD_GlcNHglycan | 16 | 19 | PF01048 | 0.261 |
MOD_GlcNHglycan | 428 | 432 | PF01048 | 0.521 |
MOD_GlcNHglycan | 46 | 49 | PF01048 | 0.261 |
MOD_GlcNHglycan | 468 | 473 | PF01048 | 0.701 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.689 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.706 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.447 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.556 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.545 |
MOD_GlcNHglycan | 760 | 763 | PF01048 | 0.543 |
MOD_GlcNHglycan | 791 | 794 | PF01048 | 0.659 |
MOD_GlcNHglycan | 795 | 798 | PF01048 | 0.673 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.261 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.282 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.735 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.723 |
MOD_GSK3_1 | 489 | 496 | PF00069 | 0.682 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.757 |
MOD_GSK3_1 | 591 | 598 | PF00069 | 0.701 |
MOD_GSK3_1 | 787 | 794 | PF00069 | 0.553 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.261 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.296 |
MOD_N-GLC_1 | 247 | 252 | PF02516 | 0.296 |
MOD_N-GLC_1 | 61 | 66 | PF02516 | 0.261 |
MOD_N-GLC_1 | 710 | 715 | PF02516 | 0.509 |
MOD_N-GLC_1 | 746 | 751 | PF02516 | 0.507 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.379 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.261 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.261 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.362 |
MOD_NEK2_1 | 226 | 231 | PF00069 | 0.329 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.285 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.422 |
MOD_NEK2_1 | 54 | 59 | PF00069 | 0.396 |
MOD_NEK2_2 | 450 | 455 | PF00069 | 0.574 |
MOD_PIKK_1 | 107 | 113 | PF00454 | 0.277 |
MOD_PIKK_1 | 128 | 134 | PF00454 | 0.267 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.344 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.296 |
MOD_PIKK_1 | 459 | 465 | PF00454 | 0.683 |
MOD_PIKK_1 | 502 | 508 | PF00454 | 0.613 |
MOD_PK_1 | 553 | 559 | PF00069 | 0.542 |
MOD_PKA_2 | 153 | 159 | PF00069 | 0.261 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.596 |
MOD_PKA_2 | 44 | 50 | PF00069 | 0.268 |
MOD_PKA_2 | 450 | 456 | PF00069 | 0.657 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.261 |
MOD_Plk_1 | 229 | 235 | PF00069 | 0.346 |
MOD_Plk_1 | 247 | 253 | PF00069 | 0.170 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.541 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.269 |
MOD_Plk_1 | 695 | 701 | PF00069 | 0.568 |
MOD_Plk_4 | 114 | 120 | PF00069 | 0.379 |
MOD_Plk_4 | 148 | 154 | PF00069 | 0.277 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.305 |
MOD_Plk_4 | 253 | 259 | PF00069 | 0.318 |
MOD_Plk_4 | 450 | 456 | PF00069 | 0.642 |
MOD_Plk_4 | 665 | 671 | PF00069 | 0.424 |
MOD_Plk_4 | 72 | 78 | PF00069 | 0.296 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.261 |
MOD_ProDKin_1 | 411 | 417 | PF00069 | 0.679 |
MOD_ProDKin_1 | 480 | 486 | PF00069 | 0.620 |
MOD_ProDKin_1 | 493 | 499 | PF00069 | 0.547 |
MOD_ProDKin_1 | 543 | 549 | PF00069 | 0.694 |
MOD_ProDKin_1 | 591 | 597 | PF00069 | 0.682 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.580 |
MOD_ProDKin_1 | 628 | 634 | PF00069 | 0.666 |
MOD_ProDKin_1 | 647 | 653 | PF00069 | 0.642 |
MOD_SUMO_rev_2 | 347 | 356 | PF00179 | 0.544 |
MOD_SUMO_rev_2 | 372 | 378 | PF00179 | 0.487 |
MOD_SUMO_rev_2 | 573 | 583 | PF00179 | 0.657 |
MOD_SUMO_rev_2 | 68 | 75 | PF00179 | 0.379 |
MOD_SUMO_rev_2 | 697 | 707 | PF00179 | 0.624 |
TRG_DiLeu_BaLyEn_6 | 230 | 235 | PF01217 | 0.396 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.261 |
TRG_ENDOCYTIC_2 | 435 | 438 | PF00928 | 0.481 |
TRG_ENDOCYTIC_2 | 663 | 666 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 89 | 92 | PF00928 | 0.292 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.382 |
TRG_ER_diArg_1 | 299 | 301 | PF00400 | 0.500 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.571 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 438 | 440 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 511 | 513 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 657 | 659 | PF00400 | 0.566 |
TRG_NES_CRM1_1 | 260 | 275 | PF08389 | 0.436 |
TRG_NES_CRM1_1 | 716 | 730 | PF08389 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 123 | 128 | PF00026 | 0.274 |
TRG_Pf-PMV_PEXEL_1 | 333 | 337 | PF00026 | 0.515 |
TRG_Pf-PMV_PEXEL_1 | 340 | 345 | PF00026 | 0.466 |
TRG_Pf-PMV_PEXEL_1 | 355 | 359 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 365 | 370 | PF00026 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W7 | Leptomonas seymouri | 65% | 100% |
A0A0S4JKY4 | Bodo saltans | 45% | 100% |
A0A1X0NHD4 | Trypanosomatidae | 48% | 100% |
A0A3Q8IBZ9 | Leishmania donovani | 100% | 100% |
A0A3R7M6Z7 | Trypanosoma rangeli | 47% | 100% |
A4HC09 | Leishmania braziliensis | 84% | 100% |
D0A118 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AVE6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
Q4QC33 | Leishmania major | 95% | 100% |
V5BLW4 | Trypanosoma cruzi | 49% | 100% |