Appears to be an enzyme-linked receptor, putatively a receptor nucleotide cyclase (cAMP synthase).. Expanded on the Leishmaniid lineage. The first helical segment is very similar to a signal peptide.. Localization: Cell surface (by feature)
Uncharacterized Protein, 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: 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:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4HTU5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006163 | purine nucleotide metabolic process | 5 | 5 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 5 |
GO:0006171 | cAMP biosynthetic process | 8 | 5 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 5 |
GO:0006793 | phosphorus metabolic process | 3 | 5 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009058 | biosynthetic process | 2 | 5 |
GO:0009117 | nucleotide metabolic process | 5 | 5 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 5 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 5 |
GO:0009165 | nucleotide biosynthetic process | 6 | 5 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 5 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 5 |
GO:0009259 | ribonucleotide metabolic process | 5 | 5 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0018130 | heterocycle biosynthetic process | 4 | 5 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 5 |
GO:0019637 | organophosphate metabolic process | 3 | 5 |
GO:0019693 | ribose phosphate metabolic process | 4 | 5 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0044249 | cellular biosynthetic process | 3 | 5 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 5 |
GO:0044281 | small molecule metabolic process | 2 | 5 |
GO:0046058 | cAMP metabolic process | 7 | 5 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 5 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0072521 | purine-containing compound metabolic process | 4 | 5 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 5 |
GO:0090407 | organophosphate biosynthetic process | 4 | 5 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 5 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 5 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 5 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 5 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 5 |
GO:1901576 | organic substance biosynthetic process | 3 | 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.495 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.259 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.480 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.422 |
CLV_NRD_NRD_1 | 785 | 787 | PF00675 | 0.624 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.259 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.480 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.422 |
CLV_PCSK_KEX2_1 | 785 | 787 | PF00082 | 0.624 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.666 |
CLV_PCSK_PC7_1 | 20 | 26 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.670 |
CLV_PCSK_SKI1_1 | 724 | 728 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 740 | 744 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 769 | 773 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 786 | 790 | PF00082 | 0.580 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.677 |
DEG_APCC_DBOX_1 | 723 | 731 | PF00400 | 0.422 |
DEG_SCF_FBW7_1 | 172 | 177 | PF00400 | 0.372 |
DEG_SPOP_SBC_1 | 407 | 411 | PF00917 | 0.593 |
DEG_SPOP_SBC_1 | 566 | 570 | PF00917 | 0.643 |
DOC_CYCLIN_yCln2_LP_2 | 726 | 732 | PF00134 | 0.373 |
DOC_CYCLIN_yCln2_LP_2 | 771 | 777 | PF00134 | 0.419 |
DOC_MAPK_DCC_7 | 13 | 21 | PF00069 | 0.620 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.765 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.466 |
DOC_MAPK_gen_1 | 516 | 523 | PF00069 | 0.510 |
DOC_MAPK_MEF2A_6 | 13 | 21 | PF00069 | 0.625 |
DOC_MAPK_MEF2A_6 | 733 | 741 | PF00069 | 0.445 |
DOC_MAPK_MEF2A_6 | 753 | 761 | PF00069 | 0.260 |
DOC_PP1_RVXF_1 | 738 | 744 | PF00149 | 0.381 |
DOC_PP1_RVXF_1 | 767 | 773 | PF00149 | 0.386 |
DOC_PP1_RVXF_1 | 814 | 821 | PF00149 | 0.347 |
DOC_PP2B_LxvP_1 | 104 | 107 | PF13499 | 0.376 |
DOC_PP2B_LxvP_1 | 775 | 778 | PF13499 | 0.427 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.361 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.364 |
DOC_PP4_FxxP_1 | 489 | 492 | PF00568 | 0.538 |
DOC_PP4_FxxP_1 | 791 | 794 | PF00568 | 0.365 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.339 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 662 | 666 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 694 | 698 | PF00917 | 0.522 |
DOC_USP7_MATH_2 | 573 | 579 | PF00917 | 0.700 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.491 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.341 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.657 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 681 | 686 | PF00397 | 0.504 |
DOC_WW_Pin1_4 | 831 | 836 | PF00397 | 0.548 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.498 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.474 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 286 | 292 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 525 | 530 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.646 |
LIG_14-3-3_CanoR_1 | 785 | 794 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 814 | 819 | PF00244 | 0.335 |
LIG_14-3-3_CterR_2 | 846 | 849 | PF00244 | 0.452 |
LIG_APCC_ABBA_1 | 256 | 261 | PF00400 | 0.339 |
LIG_BRCT_BRCA1_1 | 694 | 698 | PF00533 | 0.426 |
LIG_BRCT_BRCA1_1 | 713 | 717 | PF00533 | 0.475 |
LIG_BRCT_BRCA1_1 | 816 | 820 | PF00533 | 0.394 |
LIG_EH_1 | 238 | 242 | PF12763 | 0.386 |
LIG_EH1_1 | 92 | 100 | PF00400 | 0.285 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.352 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.412 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.408 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.609 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.541 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.699 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.691 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.676 |
LIG_FHA_1 | 705 | 711 | PF00498 | 0.566 |
LIG_FHA_1 | 721 | 727 | PF00498 | 0.357 |
LIG_FHA_1 | 747 | 753 | PF00498 | 0.414 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.358 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.379 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.370 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.596 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.580 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.587 |
LIG_FHA_2 | 670 | 676 | PF00498 | 0.486 |
LIG_LIR_Apic_2 | 789 | 794 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 118 | 127 | PF02991 | 0.365 |
LIG_LIR_Gen_1 | 173 | 183 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 283 | 291 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 744 | 752 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.451 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 744 | 748 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 751 | 757 | PF02991 | 0.380 |
LIG_LIR_Nem_3 | 766 | 771 | PF02991 | 0.382 |
LIG_MAD2 | 10 | 18 | PF02301 | 0.648 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.648 |
LIG_NRBOX | 324 | 330 | PF00104 | 0.350 |
LIG_NRBOX | 590 | 596 | PF00104 | 0.594 |
LIG_NRP_CendR_1 | 846 | 849 | PF00754 | 0.652 |
LIG_PCNA_PIPBox_1 | 795 | 804 | PF02747 | 0.386 |
LIG_Pex14_1 | 223 | 227 | PF04695 | 0.289 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.364 |
LIG_SH2_CRK | 745 | 749 | PF00017 | 0.418 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.343 |
LIG_SH2_CRK | 768 | 772 | PF00017 | 0.444 |
LIG_SH2_CRK | 841 | 845 | PF00017 | 0.442 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.376 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.577 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 185 | 188 | PF00017 | 0.355 |
LIG_SH2_PTP2 | 26 | 29 | PF00017 | 0.364 |
LIG_SH2_SRC | 546 | 549 | PF00017 | 0.598 |
LIG_SH2_SRC | 754 | 757 | PF00017 | 0.428 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.577 |
LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.558 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.372 |
LIG_SH2_STAT3 | 400 | 403 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.345 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.556 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.696 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 763 | 766 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.354 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.405 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.669 |
LIG_SH3_3 | 639 | 645 | PF00018 | 0.523 |
LIG_SH3_3 | 684 | 690 | PF00018 | 0.498 |
LIG_SH3_3 | 726 | 732 | PF00018 | 0.416 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.720 |
LIG_SH3_3 | 819 | 825 | PF00018 | 0.439 |
LIG_SUMO_SIM_par_1 | 316 | 323 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 77 | 82 | PF11976 | 0.324 |
LIG_TRAF2_1 | 427 | 430 | PF00917 | 0.649 |
LIG_TYR_ITIM | 752 | 757 | PF00017 | 0.359 |
LIG_UBA3_1 | 47 | 55 | PF00899 | 0.468 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.371 |
MOD_CDK_SPK_2 | 146 | 151 | PF00069 | 0.283 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.507 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.409 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.574 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.555 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.589 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.717 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.680 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.653 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.539 |
MOD_CK1_1 | 665 | 671 | PF00069 | 0.573 |
MOD_CK1_1 | 681 | 687 | PF00069 | 0.526 |
MOD_CK1_1 | 692 | 698 | PF00069 | 0.470 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.410 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.338 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.592 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.579 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.720 |
MOD_CK2_1 | 669 | 675 | PF00069 | 0.527 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.588 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.647 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.634 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.444 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.634 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.447 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.469 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.750 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.738 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.827 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.793 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.685 |
MOD_GlcNHglycan | 680 | 683 | PF01048 | 0.784 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.414 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.499 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.424 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.327 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.404 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.556 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.651 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.699 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.824 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.515 |
MOD_GSK3_1 | 657 | 664 | PF00069 | 0.575 |
MOD_GSK3_1 | 665 | 672 | PF00069 | 0.547 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.554 |
MOD_GSK3_1 | 700 | 707 | PF00069 | 0.586 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.666 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.668 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.542 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.687 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.611 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.564 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.599 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.602 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.323 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.430 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.446 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.245 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.336 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.630 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.578 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.567 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.712 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.581 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.487 |
MOD_NEK2_1 | 764 | 769 | PF00069 | 0.386 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.408 |
MOD_NEK2_2 | 254 | 259 | PF00069 | 0.322 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.369 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.709 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.355 |
MOD_PKA_1 | 128 | 134 | PF00069 | 0.321 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.321 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.408 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.441 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.481 |
MOD_PKB_1 | 563 | 571 | PF00069 | 0.645 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.359 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.416 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.365 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.423 |
MOD_Plk_2-3 | 575 | 581 | PF00069 | 0.663 |
MOD_Plk_2-3 | 669 | 675 | PF00069 | 0.498 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.415 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.390 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.336 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.534 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.573 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.709 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.407 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.412 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.458 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.488 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.341 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.661 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.623 |
MOD_ProDKin_1 | 681 | 687 | PF00069 | 0.502 |
MOD_ProDKin_1 | 831 | 837 | PF00069 | 0.547 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.677 |
TRG_DiLeu_BaEn_1 | 675 | 680 | PF01217 | 0.454 |
TRG_DiLeu_BaEn_1 | 756 | 761 | PF01217 | 0.424 |
TRG_DiLeu_BaEn_4 | 369 | 375 | PF01217 | 0.624 |
TRG_DiLeu_BaLyEn_6 | 446 | 451 | PF01217 | 0.619 |
TRG_DiLeu_BaLyEn_6 | 726 | 731 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.364 |
TRG_ENDOCYTIC_2 | 745 | 748 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 754 | 757 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.348 |
TRG_ENDOCYTIC_2 | 768 | 771 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 841 | 844 | PF00928 | 0.461 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.696 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.358 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.687 |
TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.653 |
TRG_ER_diArg_1 | 598 | 600 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 784 | 786 | PF00400 | 0.423 |
TRG_Pf-PMV_PEXEL_1 | 724 | 728 | PF00026 | 0.715 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C6 | Leptomonas seymouri | 50% | 99% |
A0A3S5H6C4 | Leishmania donovani | 99% | 100% |
A0A3S7WQJ6 | Leishmania donovani | 50% | 92% |
A4H5K7 | Leishmania braziliensis | 69% | 100% |
A4HTU4 | Leishmania infantum | 51% | 100% |
D0A9A6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 99% |
E9AMN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9AMN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QHZ3 | Leishmania major | 89% | 99% |
Q4QHZ4 | Leishmania major | 48% | 100% |