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)
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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A0A3S5H6C4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006163 | purine nucleotide metabolic process | 5 | 7 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 7 |
GO:0006171 | cAMP biosynthetic process | 8 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 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:0009058 | biosynthetic process | 2 | 7 |
GO:0009117 | nucleotide metabolic process | 5 | 7 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 7 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 7 |
GO:0009165 | nucleotide biosynthetic process | 6 | 7 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 7 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 7 |
GO:0009259 | ribonucleotide metabolic process | 5 | 7 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0018130 | heterocycle biosynthetic process | 4 | 7 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 7 |
GO:0019637 | organophosphate metabolic process | 3 | 7 |
GO:0019693 | ribose phosphate metabolic process | 4 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044249 | cellular biosynthetic process | 3 | 7 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 7 |
GO:0044281 | small molecule metabolic process | 2 | 7 |
GO:0046058 | cAMP metabolic process | 7 | 7 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 7 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0072521 | purine-containing compound metabolic process | 4 | 7 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 7 |
GO:0090407 | organophosphate biosynthetic process | 4 | 7 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 7 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 7 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 7 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 7 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 7 |
GO:1901576 | organic substance biosynthetic process | 3 | 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 647 | 651 | PF00656 | 0.510 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.569 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.255 |
CLV_NRD_NRD_1 | 562 | 564 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 598 | 600 | PF00675 | 0.516 |
CLV_NRD_NRD_1 | 786 | 788 | PF00675 | 0.593 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.255 |
CLV_PCSK_KEX2_1 | 249 | 251 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 562 | 564 | PF00082 | 0.455 |
CLV_PCSK_KEX2_1 | 598 | 600 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 249 | 251 | PF00082 | 0.664 |
CLV_PCSK_PC7_1 | 20 | 26 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 151 | 155 | PF00082 | 0.572 |
CLV_PCSK_SKI1_1 | 441 | 445 | PF00082 | 0.380 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.351 |
CLV_PCSK_SKI1_1 | 541 | 545 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 599 | 603 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 638 | 642 | PF00082 | 0.654 |
CLV_PCSK_SKI1_1 | 725 | 729 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 741 | 745 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 770 | 774 | PF00082 | 0.540 |
CLV_PCSK_SKI1_1 | 787 | 791 | PF00082 | 0.622 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.675 |
DEG_APCC_DBOX_1 | 724 | 732 | PF00400 | 0.420 |
DEG_SCF_FBW7_1 | 172 | 177 | PF00400 | 0.324 |
DEG_SPOP_SBC_1 | 407 | 411 | PF00917 | 0.556 |
DEG_SPOP_SBC_1 | 566 | 570 | PF00917 | 0.626 |
DOC_CYCLIN_yCln2_LP_2 | 727 | 733 | PF00134 | 0.370 |
DOC_CYCLIN_yCln2_LP_2 | 772 | 778 | PF00134 | 0.378 |
DOC_MAPK_DCC_7 | 13 | 21 | PF00069 | 0.588 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.624 |
DOC_MAPK_gen_1 | 24 | 32 | PF00069 | 0.462 |
DOC_MAPK_gen_1 | 516 | 523 | PF00069 | 0.543 |
DOC_MAPK_MEF2A_6 | 13 | 21 | PF00069 | 0.591 |
DOC_MAPK_MEF2A_6 | 734 | 742 | PF00069 | 0.440 |
DOC_MAPK_MEF2A_6 | 754 | 762 | PF00069 | 0.343 |
DOC_PP1_RVXF_1 | 739 | 745 | PF00149 | 0.374 |
DOC_PP1_RVXF_1 | 768 | 774 | PF00149 | 0.391 |
DOC_PP1_RVXF_1 | 815 | 822 | PF00149 | 0.333 |
DOC_PP2B_LxvP_1 | 104 | 107 | PF13499 | 0.327 |
DOC_PP2B_LxvP_1 | 776 | 779 | PF13499 | 0.385 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.312 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.316 |
DOC_PP4_FxxP_1 | 489 | 492 | PF00568 | 0.535 |
DOC_PP4_FxxP_1 | 792 | 795 | PF00568 | 0.342 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.324 |
DOC_USP7_MATH_1 | 242 | 246 | PF00917 | 0.303 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.604 |
DOC_USP7_MATH_1 | 566 | 570 | PF00917 | 0.772 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.811 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 663 | 667 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 695 | 699 | PF00917 | 0.536 |
DOC_USP7_MATH_2 | 573 | 579 | PF00917 | 0.663 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.368 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.380 |
DOC_WW_Pin1_4 | 291 | 296 | PF00397 | 0.462 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.404 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.337 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 641 | 646 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 832 | 837 | PF00397 | 0.534 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.499 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.466 |
LIG_14-3-3_CanoR_1 | 286 | 292 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 525 | 530 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 565 | 574 | PF00244 | 0.629 |
LIG_14-3-3_CanoR_1 | 786 | 795 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 815 | 820 | PF00244 | 0.364 |
LIG_14-3-3_CterR_2 | 847 | 850 | PF00244 | 0.429 |
LIG_Actin_WH2_2 | 498 | 513 | PF00022 | 0.625 |
LIG_APCC_ABBA_1 | 256 | 261 | PF00400 | 0.302 |
LIG_BRCT_BRCA1_1 | 695 | 699 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 714 | 718 | PF00533 | 0.431 |
LIG_BRCT_BRCA1_1 | 817 | 821 | PF00533 | 0.366 |
LIG_EH_1 | 238 | 242 | PF12763 | 0.404 |
LIG_EH1_1 | 92 | 100 | PF00400 | 0.264 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.365 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.391 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.430 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.611 |
LIG_FHA_1 | 408 | 414 | PF00498 | 0.544 |
LIG_FHA_1 | 542 | 548 | PF00498 | 0.745 |
LIG_FHA_1 | 556 | 562 | PF00498 | 0.782 |
LIG_FHA_1 | 581 | 587 | PF00498 | 0.667 |
LIG_FHA_1 | 706 | 712 | PF00498 | 0.502 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.363 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.429 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.319 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.387 |
LIG_FHA_2 | 210 | 216 | PF00498 | 0.367 |
LIG_FHA_2 | 425 | 431 | PF00498 | 0.612 |
LIG_FHA_2 | 494 | 500 | PF00498 | 0.605 |
LIG_FHA_2 | 591 | 597 | PF00498 | 0.726 |
LIG_FHA_2 | 671 | 677 | PF00498 | 0.563 |
LIG_LIR_Apic_2 | 790 | 795 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 118 | 127 | PF02991 | 0.369 |
LIG_LIR_Gen_1 | 173 | 183 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 283 | 291 | PF02991 | 0.375 |
LIG_LIR_Gen_1 | 745 | 753 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 283 | 287 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.315 |
LIG_LIR_Nem_3 | 745 | 749 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 752 | 758 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 767 | 772 | PF02991 | 0.366 |
LIG_MAD2 | 10 | 18 | PF02301 | 0.612 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.609 |
LIG_NRBOX | 324 | 330 | PF00104 | 0.291 |
LIG_NRBOX | 590 | 596 | PF00104 | 0.691 |
LIG_NRP_CendR_1 | 847 | 850 | PF00754 | 0.629 |
LIG_PCNA_PIPBox_1 | 796 | 805 | PF02747 | 0.392 |
LIG_Pex14_1 | 223 | 227 | PF04695 | 0.252 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.322 |
LIG_SH2_CRK | 746 | 750 | PF00017 | 0.400 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.310 |
LIG_SH2_CRK | 769 | 773 | PF00017 | 0.399 |
LIG_SH2_CRK | 842 | 846 | PF00017 | 0.422 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.340 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.593 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.403 |
LIG_SH2_PTP2 | 185 | 188 | PF00017 | 0.305 |
LIG_SH2_PTP2 | 26 | 29 | PF00017 | 0.360 |
LIG_SH2_SRC | 546 | 549 | PF00017 | 0.622 |
LIG_SH2_SRC | 755 | 758 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.593 |
LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.369 |
LIG_SH2_STAT3 | 400 | 403 | PF00017 | 0.611 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 412 | 415 | PF00017 | 0.562 |
LIG_SH2_STAT5 | 546 | 549 | PF00017 | 0.747 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 764 | 767 | PF00017 | 0.316 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.349 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.414 |
LIG_SH3_3 | 545 | 551 | PF00018 | 0.701 |
LIG_SH3_3 | 639 | 645 | PF00018 | 0.528 |
LIG_SH3_3 | 685 | 691 | PF00018 | 0.499 |
LIG_SH3_3 | 727 | 733 | PF00018 | 0.372 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.669 |
LIG_SH3_3 | 820 | 826 | PF00018 | 0.409 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.291 |
LIG_SUMO_SIM_par_1 | 316 | 323 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 77 | 82 | PF11976 | 0.360 |
LIG_TRAF2_1 | 427 | 430 | PF00917 | 0.603 |
LIG_TYR_ITIM | 753 | 758 | PF00017 | 0.369 |
LIG_UBA3_1 | 47 | 55 | PF00899 | 0.458 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.365 |
MOD_CDK_SPK_2 | 146 | 151 | PF00069 | 0.264 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.506 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.419 |
MOD_CK1_1 | 411 | 417 | PF00069 | 0.580 |
MOD_CK1_1 | 493 | 499 | PF00069 | 0.586 |
MOD_CK1_1 | 512 | 518 | PF00069 | 0.685 |
MOD_CK1_1 | 550 | 556 | PF00069 | 0.713 |
MOD_CK1_1 | 577 | 583 | PF00069 | 0.714 |
MOD_CK1_1 | 615 | 621 | PF00069 | 0.584 |
MOD_CK1_1 | 644 | 650 | PF00069 | 0.557 |
MOD_CK1_1 | 666 | 672 | PF00069 | 0.487 |
MOD_CK1_1 | 682 | 688 | PF00069 | 0.541 |
MOD_CK1_1 | 693 | 699 | PF00069 | 0.520 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.417 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.313 |
MOD_CK2_1 | 423 | 429 | PF00069 | 0.577 |
MOD_CK2_1 | 493 | 499 | PF00069 | 0.608 |
MOD_CK2_1 | 575 | 581 | PF00069 | 0.679 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.498 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.581 |
MOD_GlcNHglycan | 179 | 182 | PF01048 | 0.649 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.651 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.446 |
MOD_GlcNHglycan | 261 | 265 | PF01048 | 0.580 |
MOD_GlcNHglycan | 325 | 328 | PF01048 | 0.379 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.514 |
MOD_GlcNHglycan | 617 | 620 | PF01048 | 0.722 |
MOD_GlcNHglycan | 624 | 627 | PF01048 | 0.725 |
MOD_GlcNHglycan | 646 | 649 | PF01048 | 0.843 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.804 |
MOD_GlcNHglycan | 665 | 668 | PF01048 | 0.735 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.768 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.376 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.511 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.398 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.364 |
MOD_GSK3_1 | 319 | 326 | PF00069 | 0.369 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.590 |
MOD_GSK3_1 | 465 | 472 | PF00069 | 0.622 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.767 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.782 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.651 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.586 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.549 |
MOD_GSK3_1 | 690 | 697 | PF00069 | 0.504 |
MOD_GSK3_1 | 701 | 708 | PF00069 | 0.540 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.617 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.580 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.508 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.689 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.583 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.562 |
MOD_N-GLC_1 | 259 | 264 | PF02516 | 0.598 |
MOD_N-GLC_1 | 310 | 315 | PF02516 | 0.602 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.317 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.385 |
MOD_NEK2_1 | 269 | 274 | PF00069 | 0.421 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.240 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.324 |
MOD_NEK2_1 | 340 | 345 | PF00069 | 0.563 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.584 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.616 |
MOD_NEK2_1 | 469 | 474 | PF00069 | 0.670 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.707 |
MOD_NEK2_1 | 681 | 686 | PF00069 | 0.577 |
MOD_NEK2_1 | 765 | 770 | PF00069 | 0.387 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.341 |
MOD_NEK2_2 | 254 | 259 | PF00069 | 0.283 |
MOD_PIKK_1 | 276 | 282 | PF00454 | 0.459 |
MOD_PIKK_1 | 580 | 586 | PF00454 | 0.731 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.304 |
MOD_PKA_1 | 128 | 134 | PF00069 | 0.298 |
MOD_PKA_2 | 128 | 134 | PF00069 | 0.336 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.365 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.465 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.471 |
MOD_PKB_1 | 563 | 571 | PF00069 | 0.629 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.366 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.368 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.308 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.442 |
MOD_Plk_2-3 | 575 | 581 | PF00069 | 0.641 |
MOD_Plk_2-3 | 670 | 676 | PF00069 | 0.474 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.394 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.401 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.300 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.537 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.597 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.756 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.370 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.380 |
MOD_ProDKin_1 | 291 | 297 | PF00069 | 0.461 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.402 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.337 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.722 |
MOD_ProDKin_1 | 641 | 647 | PF00069 | 0.564 |
MOD_ProDKin_1 | 682 | 688 | PF00069 | 0.553 |
MOD_ProDKin_1 | 832 | 838 | PF00069 | 0.533 |
TRG_DiLeu_BaEn_1 | 447 | 452 | PF01217 | 0.620 |
TRG_DiLeu_BaEn_1 | 676 | 681 | PF01217 | 0.441 |
TRG_DiLeu_BaEn_1 | 757 | 762 | PF01217 | 0.378 |
TRG_DiLeu_BaEn_4 | 369 | 375 | PF01217 | 0.626 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.322 |
TRG_DiLeu_BaLyEn_6 | 446 | 451 | PF01217 | 0.624 |
TRG_DiLeu_BaLyEn_6 | 727 | 732 | PF01217 | 0.395 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 746 | 749 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 755 | 758 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 769 | 772 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 842 | 845 | PF00928 | 0.435 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.660 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.322 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.336 |
TRG_ER_diArg_1 | 24 | 26 | PF00400 | 0.557 |
TRG_ER_diArg_1 | 303 | 306 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 524 | 527 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 561 | 563 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 598 | 600 | PF00400 | 0.716 |
TRG_ER_diArg_1 | 785 | 787 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 725 | 729 | PF00026 | 0.707 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C6 | Leptomonas seymouri | 50% | 99% |
A0A3R7NB09 | Trypanosoma rangeli | 32% | 96% |
A0A3S7WQJ6 | Leishmania donovani | 50% | 92% |
A4H5K6 | Leishmania braziliensis | 41% | 98% |
A4H5K7 | Leishmania braziliensis | 69% | 100% |
A4HTU4 | Leishmania infantum | 50% | 100% |
A4HTU5 | Leishmania infantum | 99% | 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% |