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: Q4QHZ3
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 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 643 | 647 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 663 | 667 | PF00656 | 0.464 |
CLV_NRD_NRD_1 | 128 | 130 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 594 | 596 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 782 | 784 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 128 | 130 | PF00082 | 0.570 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.525 |
CLV_PCSK_KEX2_1 | 250 | 252 | PF00082 | 0.667 |
CLV_PCSK_KEX2_1 | 594 | 596 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 782 | 784 | PF00082 | 0.621 |
CLV_PCSK_PC1ET2_1 | 250 | 252 | PF00082 | 0.667 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.520 |
CLV_PCSK_SKI1_1 | 423 | 427 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 537 | 541 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 595 | 599 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 721 | 725 | PF00082 | 0.679 |
CLV_PCSK_SKI1_1 | 737 | 741 | PF00082 | 0.521 |
CLV_PCSK_SKI1_1 | 766 | 770 | PF00082 | 0.569 |
CLV_PCSK_SKI1_1 | 783 | 787 | PF00082 | 0.581 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.767 |
DEG_APCC_DBOX_1 | 720 | 728 | PF00400 | 0.406 |
DEG_SCF_FBW7_1 | 172 | 177 | PF00400 | 0.353 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.597 |
DEG_SPOP_SBC_1 | 659 | 663 | PF00917 | 0.445 |
DEG_SPOP_SBC_1 | 691 | 695 | PF00917 | 0.421 |
DOC_CDC14_PxL_1 | 682 | 690 | PF14671 | 0.424 |
DOC_CDC14_PxL_1 | 98 | 106 | PF14671 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 723 | 729 | PF00134 | 0.354 |
DOC_CYCLIN_yCln2_LP_2 | 768 | 774 | PF00134 | 0.417 |
DOC_MAPK_DCC_7 | 13 | 21 | PF00069 | 0.590 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.701 |
DOC_MAPK_MEF2A_6 | 13 | 21 | PF00069 | 0.594 |
DOC_MAPK_MEF2A_6 | 730 | 738 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 750 | 758 | PF00069 | 0.286 |
DOC_PP1_RVXF_1 | 735 | 741 | PF00149 | 0.362 |
DOC_PP1_RVXF_1 | 75 | 82 | PF00149 | 0.253 |
DOC_PP1_RVXF_1 | 764 | 770 | PF00149 | 0.382 |
DOC_PP2B_LxvP_1 | 104 | 107 | PF13499 | 0.347 |
DOC_PP2B_LxvP_1 | 772 | 775 | PF13499 | 0.421 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.327 |
DOC_PP4_FxxP_1 | 490 | 493 | PF00568 | 0.550 |
DOC_PP4_FxxP_1 | 788 | 791 | PF00568 | 0.362 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 569 | 573 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.573 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.509 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.492 |
DOC_USP7_MATH_2 | 569 | 575 | PF00917 | 0.677 |
DOC_USP7_MATH_2 | 668 | 674 | PF00917 | 0.433 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.360 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 292 | 297 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.490 |
DOC_WW_Pin1_4 | 42 | 47 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 561 | 566 | PF00397 | 0.658 |
DOC_WW_Pin1_4 | 824 | 829 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 128 | 134 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 190 | 196 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 211 | 215 | PF00244 | 0.438 |
LIG_14-3-3_CanoR_1 | 287 | 293 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 450 | 456 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 526 | 531 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 660 | 668 | PF00244 | 0.470 |
LIG_14-3-3_CanoR_1 | 708 | 713 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 782 | 791 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 833 | 839 | PF00244 | 0.417 |
LIG_14-3-3_CterR_2 | 843 | 846 | PF00244 | 0.453 |
LIG_Actin_WH2_2 | 499 | 514 | PF00022 | 0.559 |
LIG_APCC_ABBA_1 | 257 | 262 | PF00400 | 0.318 |
LIG_BRCT_BRCA1_1 | 710 | 714 | PF00533 | 0.446 |
LIG_BRCT_BRCA1_1 | 813 | 817 | PF00533 | 0.381 |
LIG_EH_1 | 238 | 242 | PF12763 | 0.371 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.502 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.606 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.542 |
LIG_FHA_1 | 552 | 558 | PF00498 | 0.654 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.668 |
LIG_FHA_1 | 702 | 708 | PF00498 | 0.472 |
LIG_FHA_1 | 718 | 724 | PF00498 | 0.389 |
LIG_FHA_1 | 744 | 750 | PF00498 | 0.399 |
LIG_FHA_2 | 116 | 122 | PF00498 | 0.329 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.360 |
LIG_FHA_2 | 426 | 432 | PF00498 | 0.602 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.565 |
LIG_FHA_2 | 587 | 593 | PF00498 | 0.582 |
LIG_FHA_2 | 661 | 667 | PF00498 | 0.474 |
LIG_FHA_2 | 825 | 831 | PF00498 | 0.458 |
LIG_GBD_Chelix_1 | 29 | 37 | PF00786 | 0.256 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.525 |
LIG_LIR_Apic_2 | 786 | 791 | PF02991 | 0.416 |
LIG_LIR_Gen_1 | 118 | 127 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 173 | 183 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 284 | 292 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 5 | 16 | PF02991 | 0.580 |
LIG_LIR_Gen_1 | 741 | 749 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 837 | 844 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 118 | 123 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 173 | 178 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 284 | 288 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 5 | 11 | PF02991 | 0.581 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 741 | 745 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 748 | 754 | PF02991 | 0.390 |
LIG_LIR_Nem_3 | 837 | 841 | PF02991 | 0.417 |
LIG_MAD2 | 10 | 18 | PF02301 | 0.615 |
LIG_MYND_1 | 14 | 18 | PF01753 | 0.611 |
LIG_NRBOX | 325 | 331 | PF00104 | 0.309 |
LIG_NRBOX | 586 | 592 | PF00104 | 0.561 |
LIG_NRP_CendR_1 | 843 | 846 | PF00754 | 0.653 |
LIG_PCNA_PIPBox_1 | 792 | 801 | PF02747 | 0.385 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.340 |
LIG_SH2_CRK | 742 | 746 | PF00017 | 0.410 |
LIG_SH2_CRK | 76 | 80 | PF00017 | 0.313 |
LIG_SH2_CRK | 8 | 12 | PF00017 | 0.585 |
LIG_SH2_CRK | 838 | 842 | PF00017 | 0.454 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.361 |
LIG_SH2_PTP2 | 185 | 188 | PF00017 | 0.318 |
LIG_SH2_PTP2 | 26 | 29 | PF00017 | 0.340 |
LIG_SH2_SRC | 751 | 754 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.359 |
LIG_SH2_STAT3 | 401 | 404 | PF00017 | 0.606 |
LIG_SH2_STAT3 | 807 | 810 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.318 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.404 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.558 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.368 |
LIG_SH2_STAT5 | 760 | 763 | PF00017 | 0.335 |
LIG_SH2_STAT5 | 807 | 810 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.362 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.393 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.719 |
LIG_SH3_3 | 635 | 641 | PF00018 | 0.505 |
LIG_SH3_3 | 681 | 687 | PF00018 | 0.514 |
LIG_SH3_3 | 723 | 729 | PF00018 | 0.396 |
LIG_SH3_3 | 8 | 14 | PF00018 | 0.678 |
LIG_SH3_3 | 816 | 822 | PF00018 | 0.427 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.339 |
LIG_SUMO_SIM_par_1 | 317 | 324 | PF11976 | 0.317 |
LIG_SUMO_SIM_par_1 | 377 | 385 | PF11976 | 0.570 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.653 |
LIG_TYR_ITIM | 749 | 754 | PF00017 | 0.436 |
LIG_UBA3_1 | 47 | 55 | PF00899 | 0.440 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.417 |
MOD_CDK_SPK_2 | 824 | 829 | PF00069 | 0.528 |
MOD_CK1_1 | 213 | 219 | PF00069 | 0.502 |
MOD_CK1_1 | 245 | 251 | PF00069 | 0.418 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.478 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.455 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.403 |
MOD_CK1_1 | 546 | 552 | PF00069 | 0.638 |
MOD_CK1_1 | 611 | 617 | PF00069 | 0.615 |
MOD_CK1_1 | 662 | 668 | PF00069 | 0.668 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.630 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.620 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.483 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.482 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.438 |
MOD_CK2_1 | 571 | 577 | PF00069 | 0.615 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.638 |
MOD_CK2_1 | 824 | 830 | PF00069 | 0.674 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.426 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.562 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.515 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.256 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.481 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.427 |
MOD_GlcNHglycan | 537 | 540 | PF01048 | 0.543 |
MOD_GlcNHglycan | 573 | 576 | PF01048 | 0.558 |
MOD_GlcNHglycan | 613 | 616 | PF01048 | 0.667 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.685 |
MOD_GlcNHglycan | 642 | 645 | PF01048 | 0.664 |
MOD_GlcNHglycan | 648 | 651 | PF01048 | 0.732 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.687 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.488 |
MOD_GSK3_1 | 209 | 216 | PF00069 | 0.631 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.539 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.351 |
MOD_GSK3_1 | 320 | 327 | PF00069 | 0.380 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.431 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.544 |
MOD_GSK3_1 | 531 | 538 | PF00069 | 0.657 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.711 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.797 |
MOD_GSK3_1 | 586 | 593 | PF00069 | 0.402 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.721 |
MOD_GSK3_1 | 666 | 673 | PF00069 | 0.683 |
MOD_GSK3_1 | 686 | 693 | PF00069 | 0.627 |
MOD_GSK3_1 | 697 | 704 | PF00069 | 0.609 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.575 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.577 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.382 |
MOD_N-GLC_1 | 151 | 156 | PF02516 | 0.450 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.467 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.426 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.522 |
MOD_N-GLC_1 | 311 | 316 | PF02516 | 0.467 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.384 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.356 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.576 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.415 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.376 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.638 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.460 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.445 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.403 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.650 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.439 |
MOD_NEK2_1 | 677 | 682 | PF00069 | 0.584 |
MOD_NEK2_1 | 761 | 766 | PF00069 | 0.464 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.456 |
MOD_NEK2_2 | 255 | 260 | PF00069 | 0.349 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.404 |
MOD_PIKK_1 | 576 | 582 | PF00454 | 0.570 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.373 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.433 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.502 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.534 |
MOD_PKA_2 | 659 | 665 | PF00069 | 0.645 |
MOD_PKA_2 | 707 | 713 | PF00069 | 0.505 |
MOD_Plk_1 | 121 | 127 | PF00069 | 0.363 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.390 |
MOD_Plk_1 | 209 | 215 | PF00069 | 0.552 |
MOD_Plk_1 | 53 | 59 | PF00069 | 0.393 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.502 |
MOD_Plk_2-3 | 666 | 672 | PF00069 | 0.592 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.481 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.447 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.452 |
MOD_Plk_4 | 225 | 231 | PF00069 | 0.414 |
MOD_Plk_4 | 321 | 327 | PF00069 | 0.346 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.398 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.434 |
MOD_Plk_4 | 537 | 543 | PF00069 | 0.575 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.436 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.463 |
MOD_ProDKin_1 | 292 | 298 | PF00069 | 0.373 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.609 |
MOD_ProDKin_1 | 42 | 48 | PF00069 | 0.354 |
MOD_ProDKin_1 | 561 | 567 | PF00069 | 0.572 |
MOD_ProDKin_1 | 824 | 830 | PF00069 | 0.629 |
TRG_DiLeu_BaEn_1 | 448 | 453 | PF01217 | 0.599 |
TRG_DiLeu_BaEn_1 | 753 | 758 | PF01217 | 0.452 |
TRG_DiLeu_BaEn_4 | 370 | 376 | PF01217 | 0.516 |
TRG_DiLeu_BaLyEn_6 | 43 | 48 | PF01217 | 0.303 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.513 |
TRG_DiLeu_BaLyEn_6 | 723 | 728 | PF01217 | 0.505 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.471 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 742 | 745 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 751 | 754 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 76 | 79 | PF00928 | 0.372 |
TRG_ENDOCYTIC_2 | 8 | 11 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 838 | 841 | PF00928 | 0.583 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 127 | 129 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.522 |
TRG_ER_diArg_1 | 525 | 528 | PF00400 | 0.518 |
TRG_ER_diArg_1 | 594 | 596 | PF00400 | 0.498 |
TRG_ER_diArg_1 | 781 | 783 | PF00400 | 0.513 |
TRG_Pf-PMV_PEXEL_1 | 721 | 725 | PF00026 | 0.571 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C6 | Leptomonas seymouri | 50% | 98% |
A0A3S5H6C4 | Leishmania donovani | 89% | 100% |
A0A3S7WQJ6 | Leishmania donovani | 48% | 100% |
A4H5K7 | Leishmania braziliensis | 68% | 100% |
A4HTU4 | Leishmania infantum | 48% | 100% |
A4HTU5 | Leishmania infantum | 89% | 100% |
D0A9A6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 98% |
E9AMN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AMN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 99% |
Q4QHZ4 | Leishmania major | 49% | 92% |