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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4IE49
Term | Name | Level | Count |
---|---|---|---|
GO:0006468 | protein phosphorylation | 5 | 7 |
GO:0006793 | phosphorus metabolic process | 3 | 7 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0016310 | phosphorylation | 5 | 7 |
GO:0019538 | protein metabolic process | 3 | 7 |
GO:0036211 | protein modification process | 4 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0043412 | macromolecule modification | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:0018105 | peptidyl-serine phosphorylation | 6 | 1 |
GO:0018107 | peptidyl-threonine phosphorylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018209 | peptidyl-serine modification | 6 | 1 |
GO:0018210 | peptidyl-threonine modification | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 7 |
GO:0003824 | catalytic activity | 1 | 7 |
GO:0004672 | protein kinase activity | 3 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0005524 | ATP binding | 5 | 7 |
GO:0016301 | kinase activity | 4 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 7 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 7 |
GO:0030554 | adenyl nucleotide binding | 5 | 7 |
GO:0032553 | ribonucleotide binding | 3 | 7 |
GO:0032555 | purine ribonucleotide binding | 4 | 7 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 7 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 7 |
GO:0036094 | small molecule binding | 2 | 7 |
GO:0043167 | ion binding | 2 | 7 |
GO:0043168 | anion binding | 3 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:0097367 | carbohydrate derivative binding | 2 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
GO:1901265 | nucleoside phosphate binding | 3 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0004674 | protein serine/threonine kinase activity | 4 | 1 |
GO:0004713 | protein tyrosine kinase activity | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 219 | 223 | PF00656 | 0.557 |
CLV_C14_Caspase3-7 | 372 | 376 | PF00656 | 0.389 |
CLV_C14_Caspase3-7 | 503 | 507 | PF00656 | 0.397 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.436 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 438 | 440 | PF00675 | 0.369 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.411 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.411 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 438 | 440 | PF00082 | 0.369 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 390 | 394 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 64 | 68 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 735 | 739 | PF00082 | 0.571 |
CLV_Separin_Metazoa | 108 | 112 | PF03568 | 0.411 |
DEG_APCC_DBOX_1 | 63 | 71 | PF00400 | 0.411 |
DEG_APCC_KENBOX_2 | 76 | 80 | PF00400 | 0.513 |
DEG_Nend_Nbox_1 | 1 | 2 | PF02207 | 0.428 |
DEG_SCF_FBW7_2 | 495 | 502 | PF00400 | 0.436 |
DEG_SIAH_1 | 760 | 768 | PF03145 | 0.706 |
DEG_SPOP_SBC_1 | 579 | 583 | PF00917 | 0.689 |
DOC_CYCLIN_RxL_1 | 387 | 397 | PF00134 | 0.424 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 101 | 110 | PF00134 | 0.411 |
DOC_MAPK_gen_1 | 111 | 120 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 121 | 130 | PF00069 | 0.411 |
DOC_MAPK_HePTP_8 | 118 | 130 | PF00069 | 0.436 |
DOC_MAPK_MEF2A_6 | 121 | 130 | PF00069 | 0.436 |
DOC_PP2B_LxvP_1 | 594 | 597 | PF13499 | 0.781 |
DOC_PP4_FxxP_1 | 285 | 288 | PF00568 | 0.666 |
DOC_PP4_FxxP_1 | 426 | 429 | PF00568 | 0.513 |
DOC_PP4_FxxP_1 | 804 | 807 | PF00568 | 0.528 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 171 | 175 | PF00917 | 0.612 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.660 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 394 | 398 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.513 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 610 | 614 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 625 | 629 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 761 | 765 | PF00917 | 0.705 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.661 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 495 | 500 | PF00397 | 0.513 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 589 | 594 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.677 |
DOC_WW_Pin1_4 | 708 | 713 | PF00397 | 0.703 |
DOC_WW_Pin1_4 | 726 | 731 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 745 | 750 | PF00397 | 0.540 |
DOC_WW_Pin1_4 | 794 | 799 | PF00397 | 0.623 |
LIG_14-3-3_CanoR_1 | 129 | 137 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 15 | 21 | PF00244 | 0.482 |
LIG_14-3-3_CanoR_1 | 155 | 159 | PF00244 | 0.694 |
LIG_14-3-3_CanoR_1 | 216 | 225 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 309 | 313 | PF00244 | 0.615 |
LIG_14-3-3_CanoR_1 | 530 | 540 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 63 | 70 | PF00244 | 0.411 |
LIG_Actin_WH2_2 | 140 | 157 | PF00022 | 0.411 |
LIG_BIR_III_2 | 328 | 332 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 229 | 233 | PF00533 | 0.687 |
LIG_BRCT_BRCA1_1 | 728 | 732 | PF00533 | 0.692 |
LIG_CtBP_PxDLS_1 | 117 | 121 | PF00389 | 0.411 |
LIG_deltaCOP1_diTrp_1 | 375 | 384 | PF00928 | 0.411 |
LIG_eIF4E_1 | 332 | 338 | PF01652 | 0.459 |
LIG_EVH1_2 | 16 | 20 | PF00568 | 0.533 |
LIG_EVH1_2 | 647 | 651 | PF00568 | 0.602 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.672 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.830 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.460 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.411 |
LIG_FHA_1 | 479 | 485 | PF00498 | 0.436 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.418 |
LIG_FHA_1 | 579 | 585 | PF00498 | 0.717 |
LIG_FHA_1 | 636 | 642 | PF00498 | 0.725 |
LIG_FHA_1 | 666 | 672 | PF00498 | 0.764 |
LIG_FHA_1 | 673 | 679 | PF00498 | 0.662 |
LIG_FHA_1 | 681 | 687 | PF00498 | 0.533 |
LIG_FHA_2 | 299 | 305 | PF00498 | 0.698 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.411 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.389 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.380 |
LIG_IBAR_NPY_1 | 330 | 332 | PF08397 | 0.599 |
LIG_LIR_Apic_2 | 13 | 17 | PF02991 | 0.533 |
LIG_LIR_Apic_2 | 282 | 288 | PF02991 | 0.663 |
LIG_LIR_Apic_2 | 356 | 362 | PF02991 | 0.411 |
LIG_LIR_Apic_2 | 424 | 429 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 708 | 712 | PF02991 | 0.697 |
LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 33 | 39 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 339 | 343 | PF02991 | 0.381 |
LIG_LIR_Nem_3 | 348 | 354 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 652 | 657 | PF02991 | 0.779 |
LIG_LYPXL_yS_3 | 654 | 657 | PF13949 | 0.791 |
LIG_MYND_1 | 167 | 171 | PF01753 | 0.667 |
LIG_PTB_Apo_2 | 109 | 116 | PF02174 | 0.367 |
LIG_PTB_Apo_2 | 136 | 143 | PF02174 | 0.513 |
LIG_PTB_Phospho_1 | 136 | 142 | PF10480 | 0.513 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.529 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.411 |
LIG_SH2_CRK | 43 | 47 | PF00017 | 0.411 |
LIG_SH2_CRK | 709 | 713 | PF00017 | 0.711 |
LIG_SH2_STAP1 | 370 | 374 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 43 | 47 | PF00017 | 0.299 |
LIG_SH2_STAT3 | 253 | 256 | PF00017 | 0.826 |
LIG_SH2_STAT3 | 352 | 355 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.493 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 370 | 373 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 663 | 666 | PF00017 | 0.770 |
LIG_SH2_STAT5 | 709 | 712 | PF00017 | 0.814 |
LIG_SH2_STAT5 | 773 | 776 | PF00017 | 0.724 |
LIG_SH2_STAT5 | 799 | 802 | PF00017 | 0.744 |
LIG_SH3_3 | 388 | 394 | PF00018 | 0.411 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.411 |
LIG_SH3_3 | 599 | 605 | PF00018 | 0.674 |
LIG_SH3_3 | 755 | 761 | PF00018 | 0.709 |
LIG_SH3_3 | 810 | 816 | PF00018 | 0.654 |
LIG_SUMO_SIM_anti_2 | 509 | 517 | PF11976 | 0.397 |
LIG_SUMO_SIM_par_1 | 116 | 122 | PF11976 | 0.411 |
LIG_TRAF2_1 | 197 | 200 | PF00917 | 0.654 |
LIG_TRAF2_1 | 508 | 511 | PF00917 | 0.411 |
LIG_UBA3_1 | 383 | 390 | PF00899 | 0.411 |
LIG_UBA3_1 | 73 | 77 | PF00899 | 0.411 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.411 |
MOD_CDK_SPK_2 | 240 | 245 | PF00069 | 0.685 |
MOD_CDK_SPK_2 | 730 | 735 | PF00069 | 0.573 |
MOD_CK1_1 | 161 | 167 | PF00069 | 0.648 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.544 |
MOD_CK1_1 | 220 | 226 | PF00069 | 0.767 |
MOD_CK1_1 | 227 | 233 | PF00069 | 0.693 |
MOD_CK1_1 | 243 | 249 | PF00069 | 0.676 |
MOD_CK1_1 | 478 | 484 | PF00069 | 0.383 |
MOD_CK1_1 | 486 | 492 | PF00069 | 0.383 |
MOD_CK1_1 | 592 | 598 | PF00069 | 0.622 |
MOD_CK1_1 | 601 | 607 | PF00069 | 0.619 |
MOD_CK1_1 | 711 | 717 | PF00069 | 0.742 |
MOD_CK1_1 | 724 | 730 | PF00069 | 0.679 |
MOD_CK1_1 | 777 | 783 | PF00069 | 0.755 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.411 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.459 |
MOD_CK2_1 | 484 | 490 | PF00069 | 0.380 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.399 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.428 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.668 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.685 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.820 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.707 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.640 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.650 |
MOD_GlcNHglycan | 549 | 552 | PF01048 | 0.675 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.533 |
MOD_GlcNHglycan | 612 | 615 | PF01048 | 0.688 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.411 |
MOD_GlcNHglycan | 69 | 73 | PF01048 | 0.411 |
MOD_GlcNHglycan | 723 | 726 | PF01048 | 0.773 |
MOD_GlcNHglycan | 776 | 779 | PF01048 | 0.754 |
MOD_GlcNHglycan | 792 | 795 | PF01048 | 0.500 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.490 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.552 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.607 |
MOD_GSK3_1 | 216 | 223 | PF00069 | 0.638 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.704 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.730 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.739 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.389 |
MOD_GSK3_1 | 525 | 532 | PF00069 | 0.362 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.707 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.683 |
MOD_GSK3_1 | 635 | 642 | PF00069 | 0.771 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.701 |
MOD_GSK3_1 | 708 | 715 | PF00069 | 0.791 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.700 |
MOD_GSK3_1 | 786 | 793 | PF00069 | 0.787 |
MOD_N-GLC_1 | 175 | 180 | PF02516 | 0.713 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.708 |
MOD_N-GLC_1 | 216 | 221 | PF02516 | 0.522 |
MOD_N-GLC_1 | 298 | 303 | PF02516 | 0.724 |
MOD_N-GLC_1 | 543 | 548 | PF02516 | 0.603 |
MOD_N-GLC_1 | 665 | 670 | PF02516 | 0.678 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.629 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.513 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.395 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.678 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.687 |
MOD_NEK2_1 | 531 | 536 | PF00069 | 0.389 |
MOD_NEK2_1 | 578 | 583 | PF00069 | 0.643 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.727 |
MOD_NEK2_1 | 672 | 677 | PF00069 | 0.711 |
MOD_NEK2_1 | 697 | 702 | PF00069 | 0.788 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.683 |
MOD_NEK2_2 | 133 | 138 | PF00069 | 0.513 |
MOD_NEK2_2 | 658 | 663 | PF00069 | 0.669 |
MOD_PIKK_1 | 316 | 322 | PF00454 | 0.755 |
MOD_PIKK_1 | 410 | 416 | PF00454 | 0.389 |
MOD_PIKK_1 | 421 | 427 | PF00454 | 0.389 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.411 |
MOD_PIKK_1 | 640 | 646 | PF00454 | 0.744 |
MOD_PIKK_1 | 677 | 683 | PF00454 | 0.787 |
MOD_PIKK_1 | 714 | 720 | PF00454 | 0.739 |
MOD_PKA_2 | 154 | 160 | PF00069 | 0.591 |
MOD_PKA_2 | 179 | 185 | PF00069 | 0.606 |
MOD_PKA_2 | 215 | 221 | PF00069 | 0.565 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.763 |
MOD_PKA_2 | 275 | 281 | PF00069 | 0.546 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.753 |
MOD_PKA_2 | 529 | 535 | PF00069 | 0.411 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.513 |
MOD_Plk_1 | 216 | 222 | PF00069 | 0.617 |
MOD_Plk_1 | 320 | 326 | PF00069 | 0.740 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.411 |
MOD_Plk_1 | 634 | 640 | PF00069 | 0.725 |
MOD_Plk_1 | 68 | 74 | PF00069 | 0.411 |
MOD_Plk_1 | 79 | 85 | PF00069 | 0.411 |
MOD_Plk_2-3 | 506 | 512 | PF00069 | 0.411 |
MOD_Plk_4 | 220 | 226 | PF00069 | 0.690 |
MOD_Plk_4 | 347 | 353 | PF00069 | 0.411 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.411 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.299 |
MOD_Plk_4 | 625 | 631 | PF00069 | 0.776 |
MOD_Plk_4 | 658 | 664 | PF00069 | 0.786 |
MOD_Plk_4 | 769 | 775 | PF00069 | 0.665 |
MOD_Plk_4 | 809 | 815 | PF00069 | 0.665 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.650 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.664 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.685 |
MOD_ProDKin_1 | 495 | 501 | PF00069 | 0.513 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.684 |
MOD_ProDKin_1 | 589 | 595 | PF00069 | 0.683 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.676 |
MOD_ProDKin_1 | 708 | 714 | PF00069 | 0.703 |
MOD_ProDKin_1 | 726 | 732 | PF00069 | 0.697 |
MOD_ProDKin_1 | 745 | 751 | PF00069 | 0.541 |
MOD_ProDKin_1 | 794 | 800 | PF00069 | 0.623 |
MOD_SUMO_for_1 | 147 | 150 | PF00179 | 0.411 |
MOD_SUMO_rev_2 | 140 | 149 | PF00179 | 0.513 |
TRG_DiLeu_BaEn_1 | 490 | 495 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_1 | 510 | 515 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_1 | 69 | 74 | PF01217 | 0.411 |
TRG_DiLeu_BaEn_4 | 490 | 496 | PF01217 | 0.513 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 43 | 46 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 654 | 657 | PF00928 | 0.791 |
TRG_ER_diArg_1 | 110 | 113 | PF00400 | 0.411 |
TRG_ER_diArg_1 | 154 | 156 | PF00400 | 0.436 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.411 |
TRG_Pf-PMV_PEXEL_1 | 104 | 108 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PCR0 | Leptomonas seymouri | 57% | 100% |
A0A3S7XBF4 | Leishmania donovani | 100% | 100% |
A4HPU4 | Leishmania braziliensis | 78% | 100% |
E9ATK9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4Q0Y9 | Leishmania major | 94% | 100% |