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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 9 |
GO:0110165 | cellular anatomical entity | 1 | 9 |
Related structures:
AlphaFold database: A4H5K7
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 | 162 | 166 | PF00656 | 0.394 |
CLV_C14_Caspase3-7 | 177 | 181 | PF00656 | 0.257 |
CLV_C14_Caspase3-7 | 385 | 389 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 468 | 472 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 597 | 601 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 651 | 655 | PF00656 | 0.489 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.541 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.490 |
CLV_NRD_NRD_1 | 434 | 436 | PF00675 | 0.328 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.472 |
CLV_NRD_NRD_1 | 602 | 604 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 638 | 640 | PF00675 | 0.621 |
CLV_NRD_NRD_1 | 789 | 791 | PF00675 | 0.629 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.541 |
CLV_PCSK_KEX2_1 | 434 | 436 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.472 |
CLV_PCSK_KEX2_1 | 602 | 604 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 638 | 640 | PF00082 | 0.621 |
CLV_PCSK_KEX2_1 | 789 | 791 | PF00082 | 0.629 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 206 | 210 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 442 | 446 | PF00082 | 0.377 |
CLV_PCSK_SKI1_1 | 450 | 454 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 574 | 578 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 603 | 607 | PF00082 | 0.312 |
CLV_PCSK_SKI1_1 | 628 | 632 | PF00082 | 0.647 |
CLV_PCSK_SKI1_1 | 728 | 732 | PF00082 | 0.671 |
CLV_PCSK_SKI1_1 | 744 | 748 | PF00082 | 0.492 |
CLV_PCSK_SKI1_1 | 773 | 777 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 790 | 794 | PF00082 | 0.583 |
CLV_Separin_Metazoa | 194 | 198 | PF03568 | 0.288 |
DEG_APCC_DBOX_1 | 12 | 20 | PF00400 | 0.687 |
DEG_APCC_DBOX_1 | 507 | 515 | PF00400 | 0.557 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.607 |
DEG_SCF_FBW7_1 | 172 | 177 | PF00400 | 0.377 |
DEG_SPOP_SBC_1 | 408 | 412 | PF00917 | 0.554 |
DOC_AGCK_PIF_1 | 222 | 227 | PF00069 | 0.224 |
DOC_CDC14_PxL_1 | 292 | 300 | PF14671 | 0.279 |
DOC_CDC14_PxL_1 | 98 | 106 | PF14671 | 0.359 |
DOC_CKS1_1 | 663 | 668 | PF01111 | 0.440 |
DOC_CKS1_1 | 692 | 697 | PF01111 | 0.400 |
DOC_CYCLIN_yCln2_LP_2 | 775 | 781 | PF00134 | 0.385 |
DOC_MAPK_DCC_7 | 628 | 637 | PF00069 | 0.424 |
DOC_MAPK_gen_1 | 286 | 294 | PF00069 | 0.326 |
DOC_MAPK_MEF2A_6 | 20 | 29 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 475 | 483 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 628 | 637 | PF00069 | 0.424 |
DOC_MAPK_MEF2A_6 | 757 | 765 | PF00069 | 0.270 |
DOC_PP1_RVXF_1 | 771 | 777 | PF00149 | 0.412 |
DOC_PP2B_LxvP_1 | 104 | 107 | PF13499 | 0.388 |
DOC_PP2B_LxvP_1 | 779 | 782 | PF13499 | 0.394 |
DOC_PP2B_PxIxI_1 | 632 | 638 | PF00149 | 0.422 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.414 |
DOC_PP4_FxxP_1 | 490 | 493 | PF00568 | 0.552 |
DOC_PP4_FxxP_1 | 663 | 666 | PF00568 | 0.437 |
DOC_PP4_FxxP_1 | 795 | 798 | PF00568 | 0.367 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.347 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.585 |
DOC_USP7_MATH_1 | 570 | 574 | PF00917 | 0.740 |
DOC_USP7_MATH_1 | 608 | 612 | PF00917 | 0.256 |
DOC_USP7_MATH_1 | 621 | 625 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 671 | 675 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 715 | 719 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 821 | 825 | PF00917 | 0.342 |
DOC_USP7_UBL2_3 | 351 | 355 | PF12436 | 0.498 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.413 |
DOC_WW_Pin1_4 | 311 | 316 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 662 | 667 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.467 |
LIG_14-3-3_CanoR_1 | 129 | 134 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 190 | 199 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 450 | 456 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 662 | 666 | PF00244 | 0.479 |
LIG_14-3-3_CanoR_1 | 668 | 676 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 688 | 693 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 789 | 798 | PF00244 | 0.421 |
LIG_Actin_WH2_2 | 36 | 53 | PF00022 | 0.243 |
LIG_Actin_WH2_2 | 499 | 514 | PF00022 | 0.614 |
LIG_BIR_III_2 | 515 | 519 | PF00653 | 0.490 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.303 |
LIG_BRCT_BRCA1_1 | 659 | 663 | PF00533 | 0.484 |
LIG_BRCT_BRCA1_1 | 717 | 721 | PF00533 | 0.493 |
LIG_EH_1 | 238 | 242 | PF12763 | 0.392 |
LIG_EH1_1 | 31 | 39 | PF00400 | 0.226 |
LIG_FHA_1 | 158 | 164 | PF00498 | 0.294 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.415 |
LIG_FHA_1 | 224 | 230 | PF00498 | 0.308 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.414 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.350 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.297 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.606 |
LIG_FHA_1 | 409 | 415 | PF00498 | 0.534 |
LIG_FHA_1 | 546 | 552 | PF00498 | 0.684 |
LIG_FHA_1 | 627 | 633 | PF00498 | 0.603 |
LIG_FHA_1 | 709 | 715 | PF00498 | 0.563 |
LIG_FHA_1 | 725 | 731 | PF00498 | 0.371 |
LIG_FHA_1 | 734 | 740 | PF00498 | 0.374 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.426 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.376 |
LIG_FHA_2 | 266 | 272 | PF00498 | 0.387 |
LIG_FHA_2 | 288 | 294 | PF00498 | 0.404 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.584 |
LIG_FHA_2 | 595 | 601 | PF00498 | 0.577 |
LIG_IRF3_LxIS_1 | 81 | 87 | PF10401 | 0.250 |
LIG_LIR_Apic_2 | 473 | 479 | PF02991 | 0.555 |
LIG_LIR_Apic_2 | 660 | 666 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 793 | 798 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 226 | 235 | PF02991 | 0.231 |
LIG_LIR_Gen_1 | 251 | 260 | PF02991 | 0.271 |
LIG_LIR_Gen_1 | 649 | 654 | PF02991 | 0.421 |
LIG_LIR_Gen_1 | 748 | 756 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 221 | 225 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 226 | 230 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.528 |
LIG_LIR_Nem_3 | 251 | 256 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 283 | 288 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 527 | 531 | PF02991 | 0.700 |
LIG_LIR_Nem_3 | 548 | 553 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 649 | 653 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 748 | 752 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 755 | 761 | PF02991 | 0.356 |
LIG_LIR_Nem_3 | 770 | 775 | PF02991 | 0.387 |
LIG_NRBOX | 325 | 331 | PF00104 | 0.355 |
LIG_NRBOX | 594 | 600 | PF00104 | 0.586 |
LIG_PCNA_PIPBox_1 | 216 | 225 | PF02747 | 0.262 |
LIG_PCNA_PIPBox_1 | 799 | 808 | PF02747 | 0.394 |
LIG_PCNA_yPIPBox_3 | 592 | 603 | PF02747 | 0.502 |
LIG_Pex14_1 | 223 | 227 | PF04695 | 0.291 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.365 |
LIG_PTB_Apo_2 | 520 | 527 | PF02174 | 0.559 |
LIG_PTB_Phospho_1 | 520 | 526 | PF10480 | 0.555 |
LIG_SH2_CRK | 145 | 149 | PF00017 | 0.245 |
LIG_SH2_CRK | 749 | 753 | PF00017 | 0.399 |
LIG_SH2_CRK | 758 | 762 | PF00017 | 0.335 |
LIG_SH2_CRK | 772 | 776 | PF00017 | 0.415 |
LIG_SH2_NCK_1 | 214 | 218 | PF00017 | 0.374 |
LIG_SH2_NCK_1 | 66 | 70 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 185 | 188 | PF00017 | 0.375 |
LIG_SH2_PTP2 | 26 | 29 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 455 | 459 | PF00017 | 0.563 |
LIG_SH2_STAP1 | 57 | 61 | PF00017 | 0.375 |
LIG_SH2_STAT3 | 401 | 404 | PF00017 | 0.605 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.407 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 550 | 553 | PF00017 | 0.667 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.389 |
LIG_SH2_STAT5 | 698 | 701 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 767 | 770 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 814 | 817 | PF00017 | 0.338 |
LIG_SH2_STAT5 | 93 | 96 | PF00017 | 0.358 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.253 |
LIG_SH3_3 | 293 | 299 | PF00018 | 0.464 |
LIG_SH3_3 | 548 | 554 | PF00018 | 0.599 |
LIG_SH3_3 | 627 | 633 | PF00018 | 0.544 |
LIG_SUMO_SIM_anti_2 | 316 | 324 | PF11976 | 0.305 |
LIG_SUMO_SIM_anti_2 | 45 | 51 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 572 | 580 | PF11976 | 0.619 |
LIG_SUMO_SIM_par_1 | 159 | 165 | PF11976 | 0.293 |
LIG_SUMO_SIM_par_1 | 262 | 273 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 318 | 324 | PF11976 | 0.324 |
LIG_SUMO_SIM_par_1 | 683 | 689 | PF11976 | 0.423 |
LIG_SUMO_SIM_par_1 | 77 | 82 | PF11976 | 0.327 |
LIG_TRAF2_1 | 428 | 431 | PF00917 | 0.652 |
LIG_TYR_ITIM | 756 | 761 | PF00017 | 0.352 |
LIG_UBA3_1 | 47 | 55 | PF00899 | 0.466 |
LIG_WRC_WIRS_1 | 219 | 224 | PF05994 | 0.368 |
LIG_WRC_WIRS_1 | 647 | 652 | PF05994 | 0.421 |
LIG_WRC_WIRS_1 | 716 | 721 | PF05994 | 0.401 |
MOD_CDK_SPxK_1 | 662 | 668 | PF00069 | 0.440 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.543 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.573 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.669 |
MOD_CK1_1 | 569 | 575 | PF00069 | 0.714 |
MOD_CK1_1 | 642 | 648 | PF00069 | 0.514 |
MOD_CK1_1 | 664 | 670 | PF00069 | 0.648 |
MOD_CK1_1 | 674 | 680 | PF00069 | 0.522 |
MOD_CK1_1 | 686 | 692 | PF00069 | 0.526 |
MOD_CK1_1 | 707 | 713 | PF00069 | 0.410 |
MOD_CK1_1 | 96 | 102 | PF00069 | 0.359 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.447 |
MOD_CK2_1 | 265 | 271 | PF00069 | 0.391 |
MOD_CK2_1 | 424 | 430 | PF00069 | 0.642 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.548 |
MOD_CK2_1 | 831 | 837 | PF00069 | 0.520 |
MOD_Cter_Amidation | 564 | 567 | PF01082 | 0.423 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.601 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.447 |
MOD_GlcNHglycan | 245 | 248 | PF01048 | 0.548 |
MOD_GlcNHglycan | 262 | 266 | PF01048 | 0.636 |
MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.349 |
MOD_GlcNHglycan | 426 | 429 | PF01048 | 0.253 |
MOD_GlcNHglycan | 541 | 545 | PF01048 | 0.533 |
MOD_GlcNHglycan | 568 | 571 | PF01048 | 0.417 |
MOD_GlcNHglycan | 621 | 624 | PF01048 | 0.747 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.822 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.770 |
MOD_GlcNHglycan | 673 | 676 | PF01048 | 0.679 |
MOD_GSK3_1 | 119 | 126 | PF00069 | 0.334 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.378 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.283 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.481 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.327 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.584 |
MOD_GSK3_1 | 466 | 473 | PF00069 | 0.726 |
MOD_GSK3_1 | 526 | 533 | PF00069 | 0.770 |
MOD_GSK3_1 | 555 | 562 | PF00069 | 0.702 |
MOD_GSK3_1 | 566 | 573 | PF00069 | 0.659 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.735 |
MOD_GSK3_1 | 639 | 646 | PF00069 | 0.521 |
MOD_GSK3_1 | 653 | 660 | PF00069 | 0.523 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.577 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.539 |
MOD_GSK3_1 | 704 | 711 | PF00069 | 0.532 |
MOD_GSK3_1 | 822 | 829 | PF00069 | 0.487 |
MOD_LATS_1 | 828 | 834 | PF00433 | 0.388 |
MOD_N-GLC_1 | 102 | 107 | PF02516 | 0.620 |
MOD_N-GLC_1 | 129 | 134 | PF02516 | 0.508 |
MOD_N-GLC_1 | 209 | 214 | PF02516 | 0.580 |
MOD_N-GLC_1 | 230 | 235 | PF02516 | 0.543 |
MOD_N-GLC_1 | 260 | 265 | PF02516 | 0.591 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.499 |
MOD_N-GLC_1 | 626 | 631 | PF02516 | 0.637 |
MOD_N-GLC_1 | 704 | 709 | PF02516 | 0.645 |
MOD_NEK2_1 | 225 | 230 | PF00069 | 0.313 |
MOD_NEK2_1 | 241 | 246 | PF00069 | 0.322 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.427 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.315 |
MOD_NEK2_1 | 341 | 346 | PF00069 | 0.538 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.576 |
MOD_NEK2_1 | 424 | 429 | PF00069 | 0.568 |
MOD_NEK2_1 | 451 | 456 | PF00069 | 0.542 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.717 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.618 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.587 |
MOD_NEK2_1 | 768 | 773 | PF00069 | 0.392 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.397 |
MOD_NEK2_2 | 545 | 550 | PF00069 | 0.665 |
MOD_PIKK_1 | 4 | 10 | PF00454 | 0.674 |
MOD_PIKK_1 | 588 | 594 | PF00454 | 0.662 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.357 |
MOD_PIKK_1 | 93 | 99 | PF00454 | 0.314 |
MOD_PK_1 | 639 | 645 | PF00069 | 0.413 |
MOD_PK_1 | 757 | 763 | PF00069 | 0.274 |
MOD_PKA_1 | 566 | 572 | PF00069 | 0.618 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.402 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.448 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.618 |
MOD_PKA_2 | 637 | 643 | PF00069 | 0.435 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.512 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.357 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.472 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.305 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.232 |
MOD_Plk_1 | 626 | 632 | PF00069 | 0.437 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.428 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.419 |
MOD_Plk_4 | 174 | 180 | PF00069 | 0.351 |
MOD_Plk_4 | 218 | 224 | PF00069 | 0.370 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.249 |
MOD_Plk_4 | 332 | 338 | PF00069 | 0.377 |
MOD_Plk_4 | 409 | 415 | PF00069 | 0.532 |
MOD_Plk_4 | 43 | 49 | PF00069 | 0.393 |
MOD_Plk_4 | 491 | 497 | PF00069 | 0.578 |
MOD_Plk_4 | 545 | 551 | PF00069 | 0.695 |
MOD_Plk_4 | 837 | 843 | PF00069 | 0.388 |
MOD_Plk_4 | 96 | 102 | PF00069 | 0.379 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.402 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.414 |
MOD_ProDKin_1 | 311 | 317 | PF00069 | 0.500 |
MOD_ProDKin_1 | 662 | 668 | PF00069 | 0.529 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.468 |
TRG_DiLeu_BaEn_1 | 448 | 453 | PF01217 | 0.667 |
TRG_DiLeu_BaEn_4 | 370 | 376 | PF01217 | 0.582 |
TRG_DiLeu_BaLyEn_6 | 447 | 452 | PF01217 | 0.570 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.271 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 749 | 752 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 758 | 761 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 772 | 775 | PF00928 | 0.387 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 204 | 206 | PF00400 | 0.340 |
TRG_ER_diArg_1 | 304 | 307 | PF00400 | 0.430 |
TRG_ER_diArg_1 | 434 | 436 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 602 | 604 | PF00400 | 0.615 |
TRG_ER_diArg_1 | 637 | 639 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 788 | 790 | PF00400 | 0.424 |
TRG_Pf-PMV_PEXEL_1 | 728 | 732 | PF00026 | 0.725 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5C6 | Leptomonas seymouri | 49% | 98% |
A0A1X0NMS3 | Trypanosomatidae | 32% | 93% |
A0A3S5H6C4 | Leishmania donovani | 69% | 99% |
A4HTU4 | Leishmania infantum | 45% | 100% |
A4HTU5 | Leishmania infantum | 69% | 100% |
E9AMN1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 92% |
E9AMN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 99% |
Q4QHZ3 | Leishmania major | 68% | 100% |
Q4QHZ4 | Leishmania major | 45% | 100% |