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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 7 |
GO:0110165 | cellular anatomical entity | 1 | 7 |
Related structures:
AlphaFold database: A4HTU6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006163 | purine nucleotide metabolic process | 5 | 3 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 3 |
GO:0006171 | cAMP biosynthetic process | 8 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 3 |
GO:0006793 | phosphorus metabolic process | 3 | 3 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009058 | biosynthetic process | 2 | 3 |
GO:0009117 | nucleotide metabolic process | 5 | 3 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 3 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 3 |
GO:0009165 | nucleotide biosynthetic process | 6 | 3 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 3 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 3 |
GO:0009259 | ribonucleotide metabolic process | 5 | 3 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0018130 | heterocycle biosynthetic process | 4 | 3 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 3 |
GO:0019637 | organophosphate metabolic process | 3 | 3 |
GO:0019693 | ribose phosphate metabolic process | 4 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0044249 | cellular biosynthetic process | 3 | 3 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 3 |
GO:0044281 | small molecule metabolic process | 2 | 3 |
GO:0046058 | cAMP metabolic process | 7 | 3 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 3 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0072521 | purine-containing compound metabolic process | 4 | 3 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 3 |
GO:0090407 | organophosphate biosynthetic process | 4 | 3 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 3 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 3 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 3 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 3 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 3 |
GO:1901576 | organic substance biosynthetic process | 3 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 546 | 550 | PF00656 | 0.539 |
CLV_C14_Caspase3-7 | 568 | 572 | PF00656 | 0.598 |
CLV_C14_Caspase3-7 | 6 | 10 | PF00656 | 0.398 |
CLV_C14_Caspase3-7 | 615 | 619 | PF00656 | 0.522 |
CLV_C14_Caspase3-7 | 795 | 799 | PF00656 | 0.577 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.456 |
CLV_NRD_NRD_1 | 394 | 396 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 506 | 508 | PF00675 | 0.613 |
CLV_NRD_NRD_1 | 592 | 594 | PF00675 | 0.823 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.815 |
CLV_NRD_NRD_1 | 642 | 644 | PF00675 | 0.822 |
CLV_NRD_NRD_1 | 707 | 709 | PF00675 | 0.836 |
CLV_NRD_NRD_1 | 923 | 925 | PF00675 | 0.591 |
CLV_PCSK_FUR_1 | 705 | 709 | PF00082 | 0.785 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.473 |
CLV_PCSK_KEX2_1 | 394 | 396 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 506 | 508 | PF00082 | 0.613 |
CLV_PCSK_KEX2_1 | 592 | 594 | PF00082 | 0.783 |
CLV_PCSK_KEX2_1 | 642 | 644 | PF00082 | 0.822 |
CLV_PCSK_KEX2_1 | 707 | 709 | PF00082 | 0.836 |
CLV_PCSK_KEX2_1 | 923 | 925 | PF00082 | 0.591 |
CLV_PCSK_PC1ET2_1 | 260 | 262 | PF00082 | 0.473 |
CLV_PCSK_SKI1_1 | 234 | 238 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 243 | 247 | PF00082 | 0.406 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.311 |
CLV_PCSK_SKI1_1 | 394 | 398 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 475 | 479 | PF00082 | 0.642 |
CLV_PCSK_SKI1_1 | 533 | 537 | PF00082 | 0.744 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.591 |
CLV_PCSK_SKI1_1 | 907 | 911 | PF00082 | 0.583 |
CLV_PCSK_SKI1_1 | 924 | 928 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 943 | 947 | PF00082 | 0.567 |
CLV_Separin_Metazoa | 391 | 395 | PF03568 | 0.418 |
DEG_APCC_DBOX_1 | 479 | 487 | PF00400 | 0.396 |
DEG_Kelch_Keap1_1 | 138 | 143 | PF01344 | 0.401 |
DEG_MDM2_SWIB_1 | 87 | 94 | PF02201 | 0.441 |
DEG_SIAH_1 | 606 | 614 | PF03145 | 0.574 |
DEG_SPOP_SBC_1 | 360 | 364 | PF00917 | 0.345 |
DEG_SPOP_SBC_1 | 58 | 62 | PF00917 | 0.391 |
DEG_SPOP_SBC_1 | 737 | 741 | PF00917 | 0.570 |
DEG_SPOP_SBC_1 | 988 | 992 | PF00917 | 0.530 |
DOC_ANK_TNKS_1 | 417 | 424 | PF00023 | 0.360 |
DOC_CDC14_PxL_1 | 29 | 37 | PF14671 | 0.428 |
DOC_CKS1_1 | 683 | 688 | PF01111 | 0.651 |
DOC_CYCLIN_RxL_1 | 391 | 400 | PF00134 | 0.372 |
DOC_CYCLIN_yCln2_LP_2 | 687 | 693 | PF00134 | 0.486 |
DOC_CYCLIN_yCln2_LP_2 | 749 | 755 | PF00134 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 909 | 915 | PF00134 | 0.392 |
DOC_MAPK_gen_1 | 247 | 256 | PF00069 | 0.628 |
DOC_MAPK_gen_1 | 268 | 275 | PF00069 | 0.618 |
DOC_MAPK_gen_1 | 465 | 474 | PF00069 | 0.483 |
DOC_MAPK_MEF2A_6 | 883 | 890 | PF00069 | 0.438 |
DOC_MAPK_RevD_3 | 693 | 708 | PF00069 | 0.480 |
DOC_PP1_RVXF_1 | 247 | 253 | PF00149 | 0.701 |
DOC_PP1_RVXF_1 | 905 | 911 | PF00149 | 0.376 |
DOC_PP2B_LxvP_1 | 913 | 916 | PF13499 | 0.390 |
DOC_PP4_FxxP_1 | 442 | 445 | PF00568 | 0.348 |
DOC_PP4_FxxP_1 | 929 | 932 | PF00568 | 0.385 |
DOC_USP7_MATH_1 | 255 | 259 | PF00917 | 0.592 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.412 |
DOC_USP7_MATH_1 | 601 | 605 | PF00917 | 0.543 |
DOC_USP7_MATH_1 | 626 | 630 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 719 | 723 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 737 | 741 | PF00917 | 0.616 |
DOC_USP7_MATH_1 | 841 | 845 | PF00917 | 0.551 |
DOC_USP7_UBL2_3 | 230 | 234 | PF12436 | 0.628 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.487 |
DOC_USP7_UBL2_3 | 303 | 307 | PF12436 | 0.479 |
DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.439 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.433 |
DOC_WW_Pin1_4 | 613 | 618 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 676 | 681 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 682 | 687 | PF00397 | 0.573 |
DOC_WW_Pin1_4 | 689 | 694 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 776 | 781 | PF00397 | 0.578 |
DOC_WW_Pin1_4 | 832 | 837 | PF00397 | 0.523 |
LIG_14-3-3_CanoR_1 | 475 | 484 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 663 | 671 | PF00244 | 0.547 |
LIG_14-3-3_CanoR_1 | 840 | 850 | PF00244 | 0.600 |
LIG_14-3-3_CanoR_1 | 866 | 876 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 923 | 932 | PF00244 | 0.391 |
LIG_Actin_WH2_2 | 461 | 477 | PF00022 | 0.417 |
LIG_Actin_WH2_2 | 479 | 497 | PF00022 | 0.417 |
LIG_AP2alpha_2 | 111 | 113 | PF02296 | 0.435 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.298 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.298 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.698 |
LIG_BRCT_BRCA1_1 | 228 | 232 | PF00533 | 0.602 |
LIG_BRCT_BRCA1_1 | 281 | 285 | PF00533 | 0.389 |
LIG_BRCT_BRCA1_1 | 465 | 469 | PF00533 | 0.430 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.536 |
LIG_BRCT_BRCA1_1 | 725 | 729 | PF00533 | 0.538 |
LIG_BRCT_BRCA1_2 | 228 | 234 | PF00533 | 0.626 |
LIG_EH1_1 | 177 | 185 | PF00400 | 0.512 |
LIG_eIF4E_1 | 52 | 58 | PF01652 | 0.469 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.372 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.647 |
LIG_FHA_1 | 212 | 218 | PF00498 | 0.622 |
LIG_FHA_1 | 240 | 246 | PF00498 | 0.605 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.627 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.314 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.358 |
LIG_FHA_1 | 361 | 367 | PF00498 | 0.335 |
LIG_FHA_1 | 606 | 612 | PF00498 | 0.547 |
LIG_FHA_1 | 683 | 689 | PF00498 | 0.627 |
LIG_FHA_1 | 699 | 705 | PF00498 | 0.409 |
LIG_FHA_1 | 737 | 743 | PF00498 | 0.571 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.520 |
LIG_FHA_1 | 776 | 782 | PF00498 | 0.582 |
LIG_FHA_1 | 944 | 950 | PF00498 | 0.441 |
LIG_FHA_1 | 953 | 959 | PF00498 | 0.397 |
LIG_FHA_2 | 239 | 245 | PF00498 | 0.620 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.445 |
LIG_FHA_2 | 4 | 10 | PF00498 | 0.384 |
LIG_FHA_2 | 477 | 483 | PF00498 | 0.488 |
LIG_FHA_2 | 527 | 533 | PF00498 | 0.478 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.489 |
LIG_FHA_2 | 793 | 799 | PF00498 | 0.578 |
LIG_FHA_2 | 869 | 875 | PF00498 | 0.433 |
LIG_LIR_Apic_2 | 124 | 130 | PF02991 | 0.406 |
LIG_LIR_Apic_2 | 382 | 388 | PF02991 | 0.477 |
LIG_LIR_Apic_2 | 927 | 932 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 110 | 121 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 282 | 293 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 466 | 477 | PF02991 | 0.472 |
LIG_LIR_Gen_1 | 858 | 868 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 889 | 900 | PF02991 | 0.372 |
LIG_LIR_LC3C_4 | 618 | 623 | PF02991 | 0.575 |
LIG_LIR_LC3C_4 | 750 | 755 | PF02991 | 0.570 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.415 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.355 |
LIG_LIR_Nem_3 | 197 | 203 | PF02991 | 0.580 |
LIG_LIR_Nem_3 | 282 | 288 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 858 | 863 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 889 | 895 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 904 | 909 | PF02991 | 0.369 |
LIG_MLH1_MIPbox_1 | 549 | 553 | PF16413 | 0.451 |
LIG_MYND_1 | 686 | 690 | PF01753 | 0.564 |
LIG_PCNA_PIPBox_1 | 933 | 942 | PF02747 | 0.361 |
LIG_Pex14_2 | 173 | 177 | PF04695 | 0.509 |
LIG_Pex14_2 | 232 | 236 | PF04695 | 0.603 |
LIG_Pex14_2 | 469 | 473 | PF04695 | 0.408 |
LIG_Pex14_2 | 87 | 91 | PF04695 | 0.462 |
LIG_PTB_Apo_2 | 164 | 171 | PF02174 | 0.524 |
LIG_REV1ctd_RIR_1 | 550 | 559 | PF16727 | 0.450 |
LIG_SH2_CRK | 127 | 131 | PF00017 | 0.461 |
LIG_SH2_CRK | 385 | 389 | PF00017 | 0.485 |
LIG_SH2_CRK | 892 | 896 | PF00017 | 0.371 |
LIG_SH2_CRK | 906 | 910 | PF00017 | 0.368 |
LIG_SH2_CRK | 922 | 926 | PF00017 | 0.382 |
LIG_SH2_PTP2 | 290 | 293 | PF00017 | 0.327 |
LIG_SH2_SRC | 290 | 293 | PF00017 | 0.388 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.630 |
LIG_SH2_STAP1 | 3 | 7 | PF00017 | 0.455 |
LIG_SH2_STAP1 | 407 | 411 | PF00017 | 0.319 |
LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.396 |
LIG_SH2_STAT3 | 353 | 356 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.555 |
LIG_SH2_STAT5 | 24 | 27 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 290 | 293 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 365 | 368 | PF00017 | 0.337 |
LIG_SH2_STAT5 | 47 | 50 | PF00017 | 0.413 |
LIG_SH2_STAT5 | 484 | 487 | PF00017 | 0.387 |
LIG_SH2_STAT5 | 515 | 518 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 901 | 904 | PF00017 | 0.344 |
LIG_SH3_1 | 127 | 133 | PF00018 | 0.444 |
LIG_SH3_2 | 130 | 135 | PF14604 | 0.470 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.418 |
LIG_SH3_3 | 677 | 683 | PF00018 | 0.572 |
LIG_SH3_3 | 687 | 693 | PF00018 | 0.579 |
LIG_SH3_3 | 751 | 757 | PF00018 | 0.551 |
LIG_SH3_4 | 230 | 237 | PF00018 | 0.617 |
LIG_SUMO_SIM_par_1 | 119 | 124 | PF11976 | 0.437 |
LIG_SUMO_SIM_par_1 | 213 | 220 | PF11976 | 0.625 |
LIG_SUMO_SIM_par_1 | 329 | 337 | PF11976 | 0.367 |
LIG_SUMO_SIM_par_1 | 446 | 451 | PF11976 | 0.330 |
LIG_TRAF2_1 | 380 | 383 | PF00917 | 0.447 |
LIG_TYR_ITIM | 890 | 895 | PF00017 | 0.360 |
LIG_UBA3_1 | 120 | 128 | PF00899 | 0.376 |
LIG_UBA3_1 | 25 | 30 | PF00899 | 0.343 |
LIG_WW_3 | 647 | 651 | PF00397 | 0.505 |
MOD_CDK_SPK_2 | 263 | 268 | PF00069 | 0.740 |
MOD_CDK_SPxxK_3 | 263 | 270 | PF00069 | 0.730 |
MOD_CDK_SPxxK_3 | 35 | 42 | PF00069 | 0.505 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.336 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.431 |
MOD_CK1_1 | 558 | 564 | PF00069 | 0.531 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.405 |
MOD_CK1_1 | 631 | 637 | PF00069 | 0.618 |
MOD_CK1_1 | 659 | 665 | PF00069 | 0.629 |
MOD_CK1_1 | 667 | 673 | PF00069 | 0.584 |
MOD_CK1_1 | 775 | 781 | PF00069 | 0.620 |
MOD_CK1_1 | 782 | 788 | PF00069 | 0.545 |
MOD_CK1_1 | 870 | 876 | PF00069 | 0.499 |
MOD_CK1_1 | 891 | 897 | PF00069 | 0.359 |
MOD_CK2_1 | 137 | 143 | PF00069 | 0.483 |
MOD_CK2_1 | 376 | 382 | PF00069 | 0.439 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.431 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.539 |
MOD_CK2_1 | 79 | 85 | PF00069 | 0.398 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.507 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.656 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.581 |
MOD_GlcNHglycan | 556 | 560 | PF01048 | 0.742 |
MOD_GlcNHglycan | 565 | 568 | PF01048 | 0.717 |
MOD_GlcNHglycan | 580 | 583 | PF01048 | 0.683 |
MOD_GlcNHglycan | 587 | 590 | PF01048 | 0.720 |
MOD_GlcNHglycan | 603 | 606 | PF01048 | 0.733 |
MOD_GlcNHglycan | 630 | 633 | PF01048 | 0.772 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.772 |
MOD_GlcNHglycan | 666 | 669 | PF01048 | 0.706 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.764 |
MOD_GlcNHglycan | 733 | 736 | PF01048 | 0.801 |
MOD_GlcNHglycan | 774 | 777 | PF01048 | 0.739 |
MOD_GlcNHglycan | 781 | 784 | PF01048 | 0.736 |
MOD_GlcNHglycan | 816 | 819 | PF01048 | 0.694 |
MOD_GlcNHglycan | 852 | 855 | PF01048 | 0.758 |
MOD_GlcNHglycan | 971 | 974 | PF01048 | 0.686 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.341 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.697 |
MOD_GSK3_1 | 360 | 367 | PF00069 | 0.342 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.421 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.524 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.576 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.573 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.432 |
MOD_GSK3_1 | 569 | 576 | PF00069 | 0.504 |
MOD_GSK3_1 | 59 | 66 | PF00069 | 0.419 |
MOD_GSK3_1 | 601 | 608 | PF00069 | 0.543 |
MOD_GSK3_1 | 626 | 633 | PF00069 | 0.581 |
MOD_GSK3_1 | 658 | 665 | PF00069 | 0.538 |
MOD_GSK3_1 | 689 | 696 | PF00069 | 0.515 |
MOD_GSK3_1 | 717 | 724 | PF00069 | 0.560 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.564 |
MOD_GSK3_1 | 772 | 779 | PF00069 | 0.540 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.588 |
MOD_GSK3_1 | 814 | 821 | PF00069 | 0.448 |
MOD_GSK3_1 | 969 | 976 | PF00069 | 0.450 |
MOD_N-GLC_1 | 157 | 162 | PF02516 | 0.646 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.411 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.523 |
MOD_N-GLC_1 | 35 | 40 | PF02516 | 0.639 |
MOD_N-GLC_1 | 490 | 495 | PF02516 | 0.629 |
MOD_N-GLC_1 | 569 | 574 | PF02516 | 0.814 |
MOD_N-GLC_1 | 578 | 583 | PF02516 | 0.760 |
MOD_N-GLC_1 | 858 | 863 | PF02516 | 0.755 |
MOD_N-GLC_1 | 94 | 99 | PF02516 | 0.730 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.471 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.672 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.433 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.337 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.319 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.410 |
MOD_NEK2_1 | 505 | 510 | PF00069 | 0.466 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.435 |
MOD_NEK2_1 | 534 | 539 | PF00069 | 0.462 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.521 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.410 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.372 |
MOD_NEK2_1 | 729 | 734 | PF00069 | 0.597 |
MOD_NEK2_1 | 747 | 752 | PF00069 | 0.532 |
MOD_NEK2_1 | 850 | 855 | PF00069 | 0.516 |
MOD_NEK2_1 | 902 | 907 | PF00069 | 0.351 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.532 |
MOD_NEK2_2 | 112 | 117 | PF00069 | 0.389 |
MOD_NEK2_2 | 255 | 260 | PF00069 | 0.679 |
MOD_NEK2_2 | 3 | 8 | PF00069 | 0.473 |
MOD_NEK2_2 | 63 | 68 | PF00069 | 0.477 |
MOD_NEK2_2 | 700 | 705 | PF00069 | 0.511 |
MOD_NEK2_2 | 738 | 743 | PF00069 | 0.471 |
MOD_PIKK_1 | 448 | 454 | PF00454 | 0.395 |
MOD_PIKK_1 | 868 | 874 | PF00454 | 0.497 |
MOD_PIKK_1 | 952 | 958 | PF00454 | 0.410 |
MOD_PKA_2 | 293 | 299 | PF00069 | 0.508 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.427 |
MOD_PKA_2 | 662 | 668 | PF00069 | 0.497 |
MOD_PKA_2 | 729 | 735 | PF00069 | 0.537 |
MOD_PKA_2 | 788 | 794 | PF00069 | 0.557 |
MOD_Plk_1 | 166 | 172 | PF00069 | 0.404 |
MOD_Plk_1 | 490 | 496 | PF00069 | 0.431 |
MOD_Plk_1 | 548 | 554 | PF00069 | 0.610 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.531 |
MOD_Plk_1 | 693 | 699 | PF00069 | 0.631 |
MOD_Plk_1 | 888 | 894 | PF00069 | 0.379 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.352 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.705 |
MOD_Plk_4 | 274 | 280 | PF00069 | 0.364 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.335 |
MOD_Plk_4 | 399 | 405 | PF00069 | 0.379 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.406 |
MOD_Plk_4 | 548 | 554 | PF00069 | 0.479 |
MOD_Plk_4 | 954 | 960 | PF00069 | 0.435 |
MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.438 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.733 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.441 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.429 |
MOD_ProDKin_1 | 613 | 619 | PF00069 | 0.581 |
MOD_ProDKin_1 | 676 | 682 | PF00069 | 0.578 |
MOD_ProDKin_1 | 689 | 695 | PF00069 | 0.561 |
MOD_ProDKin_1 | 776 | 782 | PF00069 | 0.579 |
MOD_ProDKin_1 | 832 | 838 | PF00069 | 0.523 |
MOD_SUMO_for_1 | 222 | 225 | PF00179 | 0.639 |
MOD_SUMO_rev_2 | 82 | 88 | PF00179 | 0.365 |
TRG_DiLeu_BaEn_1 | 400 | 405 | PF01217 | 0.461 |
TRG_DiLeu_BaEn_1 | 89 | 94 | PF01217 | 0.339 |
TRG_DiLeu_BaEn_1 | 954 | 959 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_2 | 82 | 88 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_4 | 322 | 328 | PF01217 | 0.374 |
TRG_DiLeu_BaLyEn_6 | 392 | 397 | PF01217 | 0.390 |
TRG_DiLeu_BaLyEn_6 | 530 | 535 | PF01217 | 0.555 |
TRG_DiLeu_BaLyEn_6 | 683 | 688 | PF01217 | 0.548 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.388 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 892 | 895 | PF00928 | 0.370 |
TRG_ENDOCYTIC_2 | 906 | 909 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 922 | 925 | PF00928 | 0.385 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.654 |
TRG_ER_diArg_1 | 393 | 395 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 505 | 507 | PF00400 | 0.406 |
TRG_ER_diArg_1 | 642 | 644 | PF00400 | 0.622 |
TRG_ER_diArg_1 | 704 | 707 | PF00400 | 0.581 |
TRG_ER_diArg_1 | 922 | 924 | PF00400 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 187 | 191 | PF00026 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 394 | 399 | PF00026 | 0.605 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKJ0 | Leptomonas seymouri | 48% | 86% |
A0A3S7WQJ9 | Leishmania donovani | 100% | 93% |
A4H5K8 | Leishmania braziliensis | 65% | 100% |
E9AMN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 86% | 100% |
Q4QHZ2 | Leishmania major | 90% | 100% |