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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: Q4QHZ4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 6 |
GO:0006163 | purine nucleotide metabolic process | 5 | 6 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 6 |
GO:0006171 | cAMP biosynthetic process | 8 | 6 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 6 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 6 |
GO:0006793 | phosphorus metabolic process | 3 | 6 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 6 |
GO:0006807 | nitrogen compound metabolic process | 2 | 6 |
GO:0008152 | metabolic process | 1 | 6 |
GO:0009058 | biosynthetic process | 2 | 6 |
GO:0009117 | nucleotide metabolic process | 5 | 6 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 6 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 6 |
GO:0009165 | nucleotide biosynthetic process | 6 | 6 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 6 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 6 |
GO:0009259 | ribonucleotide metabolic process | 5 | 6 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0018130 | heterocycle biosynthetic process | 4 | 6 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 6 |
GO:0019637 | organophosphate metabolic process | 3 | 6 |
GO:0019693 | ribose phosphate metabolic process | 4 | 6 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 6 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 6 |
GO:0044238 | primary metabolic process | 2 | 6 |
GO:0044249 | cellular biosynthetic process | 3 | 6 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 6 |
GO:0044281 | small molecule metabolic process | 2 | 6 |
GO:0046058 | cAMP metabolic process | 7 | 6 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 6 |
GO:0046483 | heterocycle metabolic process | 3 | 6 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 6 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 6 |
GO:0071704 | organic substance metabolic process | 2 | 6 |
GO:0072521 | purine-containing compound metabolic process | 4 | 6 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 6 |
GO:0090407 | organophosphate biosynthetic process | 4 | 6 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 6 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 6 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 6 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 6 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 6 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 6 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 6 |
GO:1901576 | organic substance biosynthetic process | 3 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 607 | 611 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 693 | 697 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 747 | 751 | PF00656 | 0.434 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.383 |
CLV_NRD_NRD_1 | 265 | 267 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 730 | 732 | PF00675 | 0.675 |
CLV_NRD_NRD_1 | 849 | 851 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 878 | 880 | PF00675 | 0.604 |
CLV_PCSK_KEX2_1 | 194 | 196 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 265 | 267 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 730 | 732 | PF00082 | 0.681 |
CLV_PCSK_KEX2_1 | 849 | 851 | PF00082 | 0.604 |
CLV_PCSK_PC1ET2_1 | 194 | 196 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 499 | 503 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 526 | 530 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 788 | 792 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 804 | 808 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 833 | 837 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 850 | 854 | PF00082 | 0.631 |
CLV_PCSK_SKI1_1 | 879 | 883 | PF00082 | 0.529 |
DEG_APCC_DBOX_1 | 787 | 795 | PF00400 | 0.396 |
DEG_SPOP_SBC_1 | 484 | 488 | PF00917 | 0.367 |
DOC_CKS1_1 | 174 | 179 | PF01111 | 0.606 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 325 | 331 | PF00134 | 0.508 |
DOC_CYCLIN_yCln2_LP_2 | 790 | 796 | PF00134 | 0.387 |
DOC_CYCLIN_yCln2_LP_2 | 835 | 841 | PF00134 | 0.397 |
DOC_MAPK_gen_1 | 206 | 212 | PF00069 | 0.533 |
DOC_MAPK_gen_1 | 381 | 389 | PF00069 | 0.585 |
DOC_MAPK_MEF2A_6 | 797 | 805 | PF00069 | 0.438 |
DOC_PP1_RVXF_1 | 802 | 808 | PF00149 | 0.422 |
DOC_PP1_RVXF_1 | 831 | 837 | PF00149 | 0.374 |
DOC_PP2B_LxvP_1 | 72 | 75 | PF13499 | 0.421 |
DOC_PP2B_LxvP_1 | 839 | 842 | PF13499 | 0.407 |
DOC_PP4_FxxP_1 | 566 | 569 | PF00568 | 0.377 |
DOC_PP4_FxxP_1 | 855 | 858 | PF00568 | 0.384 |
DOC_USP7_MATH_1 | 14 | 18 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.526 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.371 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.583 |
DOC_USP7_MATH_1 | 676 | 680 | PF00917 | 0.567 |
DOC_USP7_MATH_1 | 689 | 693 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 725 | 729 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 906 | 910 | PF00917 | 0.454 |
DOC_USP7_MATH_2 | 60 | 66 | PF00917 | 0.460 |
DOC_WW_Pin1_4 | 173 | 178 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 235 | 240 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 387 | 392 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 5 | 10 | PF00397 | 0.456 |
DOC_WW_Pin1_4 | 618 | 623 | PF00397 | 0.441 |
DOC_WW_Pin1_4 | 679 | 684 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 698 | 703 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 769 | 774 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 77 | 82 | PF00397 | 0.469 |
DOC_WW_Pin1_4 | 900 | 905 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 15 | 19 | PF00244 | 0.505 |
LIG_14-3-3_CanoR_1 | 198 | 203 | PF00244 | 0.613 |
LIG_14-3-3_CanoR_1 | 265 | 272 | PF00244 | 0.663 |
LIG_14-3-3_CanoR_1 | 286 | 294 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 526 | 532 | PF00244 | 0.326 |
LIG_14-3-3_CanoR_1 | 593 | 599 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 617 | 622 | PF00244 | 0.573 |
LIG_14-3-3_CanoR_1 | 738 | 746 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 849 | 858 | PF00244 | 0.395 |
LIG_Actin_RPEL_3 | 376 | 395 | PF02755 | 0.539 |
LIG_Clathr_ClatBox_1 | 778 | 782 | PF01394 | 0.458 |
LIG_deltaCOP1_diTrp_1 | 297 | 302 | PF00928 | 0.515 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.389 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.274 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.591 |
LIG_FHA_1 | 308 | 314 | PF00498 | 0.533 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.647 |
LIG_FHA_1 | 365 | 371 | PF00498 | 0.567 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.539 |
LIG_FHA_1 | 458 | 464 | PF00498 | 0.375 |
LIG_FHA_1 | 485 | 491 | PF00498 | 0.347 |
LIG_FHA_1 | 595 | 601 | PF00498 | 0.463 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.443 |
LIG_FHA_1 | 785 | 791 | PF00498 | 0.393 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.411 |
LIG_FHA_1 | 811 | 817 | PF00498 | 0.388 |
LIG_FHA_1 | 880 | 886 | PF00498 | 0.331 |
LIG_FHA_2 | 363 | 369 | PF00498 | 0.552 |
LIG_FHA_2 | 502 | 508 | PF00498 | 0.423 |
LIG_FHA_2 | 571 | 577 | PF00498 | 0.367 |
LIG_FHA_2 | 8 | 14 | PF00498 | 0.510 |
LIG_Integrin_RGD_1 | 748 | 750 | PF01839 | 0.664 |
LIG_LIR_Apic_2 | 549 | 555 | PF02991 | 0.381 |
LIG_LIR_Apic_2 | 671 | 676 | PF02991 | 0.422 |
LIG_LIR_Apic_2 | 853 | 858 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 143 | 153 | PF02991 | 0.531 |
LIG_LIR_Gen_1 | 256 | 264 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 356 | 362 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.577 |
LIG_LIR_Gen_1 | 592 | 601 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 630 | 640 | PF02991 | 0.445 |
LIG_LIR_Gen_1 | 808 | 816 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.576 |
LIG_LIR_Nem_3 | 169 | 174 | PF02991 | 0.550 |
LIG_LIR_Nem_3 | 256 | 262 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 297 | 303 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 356 | 360 | PF02991 | 0.679 |
LIG_LIR_Nem_3 | 384 | 389 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 401 | 406 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 592 | 598 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 630 | 635 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 808 | 812 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 830 | 835 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 97 | 101 | PF02991 | 0.290 |
LIG_NRBOX | 630 | 636 | PF00104 | 0.379 |
LIG_PCNA_PIPBox_1 | 859 | 868 | PF02747 | 0.368 |
LIG_PDZ_Class_2 | 913 | 918 | PF00595 | 0.452 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.573 |
LIG_SH2_CRK | 673 | 677 | PF00017 | 0.483 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.462 |
LIG_SH2_CRK | 809 | 813 | PF00017 | 0.395 |
LIG_SH2_CRK | 832 | 836 | PF00017 | 0.431 |
LIG_SH2_NCK_1 | 259 | 263 | PF00017 | 0.573 |
LIG_SH2_SRC | 259 | 262 | PF00017 | 0.545 |
LIG_SH2_SRC | 818 | 821 | PF00017 | 0.460 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 531 | 535 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 477 | 480 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 329 | 332 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 632 | 635 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 673 | 676 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 827 | 830 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 99 | 102 | PF00017 | 0.352 |
LIG_SH3_3 | 223 | 229 | PF00018 | 0.566 |
LIG_SH3_3 | 236 | 242 | PF00018 | 0.556 |
LIG_SH3_3 | 366 | 372 | PF00018 | 0.632 |
LIG_SH3_3 | 45 | 51 | PF00018 | 0.557 |
LIG_SH3_3 | 790 | 796 | PF00018 | 0.462 |
LIG_SUMO_SIM_anti_2 | 392 | 398 | PF11976 | 0.533 |
LIG_SUMO_SIM_anti_2 | 405 | 410 | PF11976 | 0.260 |
LIG_SUMO_SIM_anti_2 | 597 | 604 | PF11976 | 0.458 |
LIG_SUMO_SIM_anti_2 | 777 | 782 | PF11976 | 0.403 |
LIG_SUMO_SIM_par_1 | 453 | 461 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 777 | 782 | PF11976 | 0.460 |
LIG_TRAF2_1 | 10 | 13 | PF00917 | 0.513 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.505 |
LIG_TRAF2_1 | 504 | 507 | PF00917 | 0.479 |
LIG_WRC_WIRS_1 | 296 | 301 | PF05994 | 0.539 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.598 |
MOD_CK1_1 | 17 | 23 | PF00069 | 0.492 |
MOD_CK1_1 | 183 | 189 | PF00069 | 0.549 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.626 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.592 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.541 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.503 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.549 |
MOD_CK1_1 | 488 | 494 | PF00069 | 0.347 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.485 |
MOD_CK1_1 | 570 | 576 | PF00069 | 0.361 |
MOD_CK1_1 | 679 | 685 | PF00069 | 0.578 |
MOD_CK1_1 | 698 | 704 | PF00069 | 0.539 |
MOD_CK1_1 | 706 | 712 | PF00069 | 0.511 |
MOD_CK1_1 | 713 | 719 | PF00069 | 0.515 |
MOD_CK1_1 | 80 | 86 | PF00069 | 0.454 |
MOD_CK1_1 | 894 | 900 | PF00069 | 0.492 |
MOD_CK2_1 | 246 | 252 | PF00069 | 0.612 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.495 |
MOD_CK2_1 | 500 | 506 | PF00069 | 0.472 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.369 |
MOD_CK2_1 | 7 | 13 | PF00069 | 0.511 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.431 |
MOD_CK2_1 | 768 | 774 | PF00069 | 0.585 |
MOD_CK2_1 | 892 | 898 | PF00069 | 0.529 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.371 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.360 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.249 |
MOD_GlcNHglycan | 217 | 220 | PF01048 | 0.294 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.652 |
MOD_GlcNHglycan | 255 | 258 | PF01048 | 0.476 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.675 |
MOD_GlcNHglycan | 349 | 352 | PF01048 | 0.378 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.659 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.646 |
MOD_GlcNHglycan | 627 | 630 | PF01048 | 0.652 |
MOD_GlcNHglycan | 678 | 681 | PF01048 | 0.689 |
MOD_GlcNHglycan | 696 | 700 | PF01048 | 0.798 |
MOD_GlcNHglycan | 705 | 709 | PF01048 | 0.677 |
MOD_GlcNHglycan | 737 | 741 | PF01048 | 0.758 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.460 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.521 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.620 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.500 |
MOD_GSK3_1 | 246 | 253 | PF00069 | 0.613 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.580 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.687 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.592 |
MOD_GSK3_1 | 385 | 392 | PF00069 | 0.608 |
MOD_GSK3_1 | 398 | 405 | PF00069 | 0.348 |
MOD_GSK3_1 | 484 | 491 | PF00069 | 0.354 |
MOD_GSK3_1 | 542 | 549 | PF00069 | 0.543 |
MOD_GSK3_1 | 585 | 592 | PF00069 | 0.425 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.565 |
MOD_GSK3_1 | 703 | 710 | PF00069 | 0.528 |
MOD_GSK3_1 | 715 | 722 | PF00069 | 0.481 |
MOD_GSK3_1 | 744 | 751 | PF00069 | 0.531 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.433 |
MOD_GSK3_1 | 887 | 894 | PF00069 | 0.449 |
MOD_GSK3_1 | 896 | 903 | PF00069 | 0.474 |
MOD_N-GLC_1 | 178 | 183 | PF02516 | 0.571 |
MOD_N-GLC_1 | 286 | 291 | PF02516 | 0.427 |
MOD_N-GLC_1 | 307 | 312 | PF02516 | 0.337 |
MOD_N-GLC_1 | 617 | 622 | PF02516 | 0.633 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.504 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.568 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.481 |
MOD_NEK2_1 | 417 | 422 | PF00069 | 0.522 |
MOD_NEK2_1 | 485 | 490 | PF00069 | 0.349 |
MOD_NEK2_1 | 500 | 505 | PF00069 | 0.353 |
MOD_NEK2_1 | 527 | 532 | PF00069 | 0.319 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.517 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.443 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.434 |
MOD_NEK2_1 | 828 | 833 | PF00069 | 0.361 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.597 |
MOD_NEK2_1 | 891 | 896 | PF00069 | 0.523 |
MOD_NEK2_2 | 108 | 113 | PF00069 | 0.300 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.574 |
MOD_NEK2_2 | 627 | 632 | PF00069 | 0.413 |
MOD_PIKK_1 | 50 | 56 | PF00454 | 0.502 |
MOD_PIKK_1 | 7 | 13 | PF00454 | 0.511 |
MOD_PIKK_1 | 725 | 731 | PF00454 | 0.480 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.469 |
MOD_PIKK_1 | 873 | 879 | PF00454 | 0.383 |
MOD_PIKK_1 | 892 | 898 | PF00454 | 0.388 |
MOD_PKA_1 | 265 | 271 | PF00069 | 0.546 |
MOD_PKA_1 | 879 | 885 | PF00069 | 0.325 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.572 |
MOD_PKA_2 | 14 | 20 | PF00069 | 0.501 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.630 |
MOD_PKA_2 | 285 | 291 | PF00069 | 0.580 |
MOD_PKA_2 | 382 | 388 | PF00069 | 0.574 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.618 |
MOD_Plk_1 | 362 | 368 | PF00069 | 0.564 |
MOD_Plk_1 | 897 | 903 | PF00069 | 0.524 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.294 |
MOD_Plk_4 | 14 | 20 | PF00069 | 0.501 |
MOD_Plk_4 | 144 | 150 | PF00069 | 0.539 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.626 |
MOD_Plk_4 | 295 | 301 | PF00069 | 0.540 |
MOD_Plk_4 | 382 | 388 | PF00069 | 0.696 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.401 |
MOD_Plk_4 | 485 | 491 | PF00069 | 0.347 |
MOD_Plk_4 | 567 | 573 | PF00069 | 0.364 |
MOD_Plk_4 | 627 | 633 | PF00069 | 0.454 |
MOD_Plk_4 | 668 | 674 | PF00069 | 0.478 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.463 |
MOD_Plk_4 | 774 | 780 | PF00069 | 0.416 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.354 |
MOD_ProDKin_1 | 173 | 179 | PF00069 | 0.586 |
MOD_ProDKin_1 | 235 | 241 | PF00069 | 0.631 |
MOD_ProDKin_1 | 387 | 393 | PF00069 | 0.676 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.488 |
MOD_ProDKin_1 | 5 | 11 | PF00069 | 0.456 |
MOD_ProDKin_1 | 618 | 624 | PF00069 | 0.438 |
MOD_ProDKin_1 | 679 | 685 | PF00069 | 0.471 |
MOD_ProDKin_1 | 698 | 704 | PF00069 | 0.573 |
MOD_ProDKin_1 | 769 | 775 | PF00069 | 0.491 |
MOD_ProDKin_1 | 77 | 83 | PF00069 | 0.467 |
MOD_ProDKin_1 | 900 | 906 | PF00069 | 0.488 |
TRG_DiLeu_BaEn_1 | 524 | 529 | PF01217 | 0.498 |
TRG_DiLeu_BaEn_1 | 754 | 759 | PF01217 | 0.484 |
TRG_DiLeu_BaEn_1 | 774 | 779 | PF01217 | 0.389 |
TRG_DiLeu_BaEn_1 | 820 | 825 | PF01217 | 0.449 |
TRG_DiLeu_BaEn_4 | 446 | 452 | PF01217 | 0.389 |
TRG_DiLeu_BaLyEn_6 | 523 | 528 | PF01217 | 0.397 |
TRG_DiLeu_BaLyEn_6 | 790 | 795 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.579 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.415 |
TRG_ENDOCYTIC_2 | 809 | 812 | PF00928 | 0.385 |
TRG_ENDOCYTIC_2 | 832 | 835 | PF00928 | 0.397 |
TRG_ER_diArg_1 | 264 | 266 | PF00400 | 0.632 |
TRG_ER_diArg_1 | 380 | 383 | PF00400 | 0.657 |
TRG_ER_diArg_1 | 848 | 850 | PF00400 | 0.398 |
TRG_Pf-PMV_PEXEL_1 | 788 | 792 | PF00026 | 0.741 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C6 | Leptomonas seymouri | 41% | 100% |
A0A3S5H6C4 | Leishmania donovani | 48% | 100% |
A0A3S7WQJ6 | Leishmania donovani | 89% | 100% |
A4H5K6 | Leishmania braziliensis | 66% | 100% |
A4H5K7 | Leishmania braziliensis | 45% | 100% |
A4HTU4 | Leishmania infantum | 90% | 100% |
A4HTU5 | Leishmania infantum | 48% | 100% |
E9AMN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9AMN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
Q4QHZ3 | Leishmania major | 49% | 100% |