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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 6 |
Related structures:
AlphaFold database: E9AMN3
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006163 | purine nucleotide metabolic process | 5 | 2 |
GO:0006164 | purine nucleotide biosynthetic process | 6 | 2 |
GO:0006171 | cAMP biosynthetic process | 8 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009058 | biosynthetic process | 2 | 2 |
GO:0009117 | nucleotide metabolic process | 5 | 2 |
GO:0009150 | purine ribonucleotide metabolic process | 6 | 2 |
GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 2 |
GO:0009165 | nucleotide biosynthetic process | 6 | 2 |
GO:0009187 | cyclic nucleotide metabolic process | 6 | 2 |
GO:0009190 | cyclic nucleotide biosynthetic process | 7 | 2 |
GO:0009259 | ribonucleotide metabolic process | 5 | 2 |
GO:0009260 | ribonucleotide biosynthetic process | 6 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0018130 | heterocycle biosynthetic process | 4 | 2 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0019693 | ribose phosphate metabolic process | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044249 | cellular biosynthetic process | 3 | 2 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0046058 | cAMP metabolic process | 7 | 2 |
GO:0046390 | ribose phosphate biosynthetic process | 5 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 2 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0072521 | purine-containing compound metabolic process | 4 | 2 |
GO:0072522 | purine-containing compound biosynthetic process | 5 | 2 |
GO:0090407 | organophosphate biosynthetic process | 4 | 2 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 2 |
GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 2 |
GO:1901576 | organic substance biosynthetic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 262 | 266 | PF00656 | 0.480 |
CLV_C14_Caspase3-7 | 491 | 495 | PF00656 | 0.543 |
CLV_C14_Caspase3-7 | 617 | 621 | PF00656 | 0.763 |
CLV_C14_Caspase3-7 | 639 | 643 | PF00656 | 0.805 |
CLV_C14_Caspase3-7 | 77 | 81 | PF00656 | 0.478 |
CLV_C14_Caspase3-7 | 858 | 862 | PF00656 | 0.794 |
CLV_C14_Caspase3-7 | 873 | 877 | PF00656 | 0.642 |
CLV_NRD_NRD_1 | 255 | 257 | PF00675 | 0.426 |
CLV_NRD_NRD_1 | 465 | 467 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 577 | 579 | PF00675 | 0.441 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 665 | 667 | PF00675 | 0.633 |
CLV_NRD_NRD_1 | 772 | 774 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 972 | 974 | PF00675 | 0.399 |
CLV_PCSK_FUR_1 | 770 | 774 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 19 | 21 | PF00082 | 0.528 |
CLV_PCSK_KEX2_1 | 23 | 25 | PF00082 | 0.458 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 577 | 579 | PF00082 | 0.441 |
CLV_PCSK_KEX2_1 | 662 | 664 | PF00082 | 0.599 |
CLV_PCSK_KEX2_1 | 772 | 774 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 972 | 974 | PF00082 | 0.399 |
CLV_PCSK_PC1ET2_1 | 19 | 21 | PF00082 | 0.528 |
CLV_PCSK_PC1ET2_1 | 23 | 25 | PF00082 | 0.458 |
CLV_PCSK_PC1ET2_1 | 331 | 333 | PF00082 | 0.713 |
CLV_PCSK_PC1ET2_1 | 662 | 664 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 157 | 161 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 314 | 318 | PF00082 | 0.598 |
CLV_PCSK_SKI1_1 | 324 | 328 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 465 | 469 | PF00082 | 0.393 |
CLV_PCSK_SKI1_1 | 473 | 477 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 546 | 550 | PF00082 | 0.531 |
CLV_PCSK_SKI1_1 | 604 | 608 | PF00082 | 0.554 |
CLV_PCSK_SKI1_1 | 927 | 931 | PF00082 | 0.452 |
CLV_PCSK_SKI1_1 | 956 | 960 | PF00082 | 0.387 |
CLV_PCSK_SKI1_1 | 973 | 977 | PF00082 | 0.400 |
CLV_PCSK_SKI1_1 | 992 | 996 | PF00082 | 0.379 |
CLV_Separin_Metazoa | 462 | 466 | PF03568 | 0.634 |
DEG_APCC_DBOX_1 | 550 | 558 | PF00400 | 0.674 |
DEG_MDM2_SWIB_1 | 158 | 165 | PF02201 | 0.441 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.785 |
DEG_SIAH_1 | 676 | 684 | PF03145 | 0.786 |
DEG_SPOP_SBC_1 | 1037 | 1041 | PF00917 | 0.797 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.435 |
DEG_SPOP_SBC_1 | 865 | 869 | PF00917 | 0.684 |
DOC_CDC14_PxL_1 | 100 | 108 | PF14671 | 0.399 |
DOC_CKS1_1 | 45 | 50 | PF01111 | 0.428 |
DOC_CKS1_1 | 748 | 753 | PF01111 | 0.866 |
DOC_CYCLIN_RxL_1 | 462 | 471 | PF00134 | 0.589 |
DOC_CYCLIN_yCln2_LP_2 | 958 | 964 | PF00134 | 0.594 |
DOC_MAPK_gen_1 | 19 | 29 | PF00069 | 0.697 |
DOC_MAPK_gen_1 | 318 | 327 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 339 | 346 | PF00069 | 0.498 |
DOC_MAPK_gen_1 | 536 | 545 | PF00069 | 0.700 |
DOC_MAPK_MEF2A_6 | 932 | 939 | PF00069 | 0.715 |
DOC_PP1_RVXF_1 | 24 | 30 | PF00149 | 0.605 |
DOC_PP1_RVXF_1 | 318 | 324 | PF00149 | 0.499 |
DOC_PP1_RVXF_1 | 954 | 960 | PF00149 | 0.582 |
DOC_PP2B_PxIxI_1 | 822 | 828 | PF00149 | 0.627 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.732 |
DOC_PP4_FxxP_1 | 513 | 516 | PF00568 | 0.563 |
DOC_PP4_FxxP_1 | 814 | 817 | PF00568 | 0.636 |
DOC_PP4_FxxP_1 | 978 | 981 | PF00568 | 0.589 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.631 |
DOC_USP7_MATH_1 | 636 | 640 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 696 | 700 | PF00917 | 0.794 |
DOC_USP7_MATH_1 | 755 | 759 | PF00917 | 0.776 |
DOC_USP7_MATH_1 | 782 | 786 | PF00917 | 0.842 |
DOC_USP7_MATH_1 | 802 | 806 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 843 | 847 | PF00917 | 0.720 |
DOC_USP7_MATH_1 | 879 | 883 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 886 | 890 | PF00917 | 0.695 |
DOC_USP7_UBL2_3 | 19 | 23 | PF12436 | 0.717 |
DOC_USP7_UBL2_3 | 320 | 324 | PF12436 | 0.286 |
DOC_USP7_UBL2_3 | 374 | 378 | PF12436 | 0.693 |
DOC_WW_Pin1_4 | 1018 | 1023 | PF00397 | 0.684 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.415 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 197 | 202 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 334 | 339 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 683 | 688 | PF00397 | 0.840 |
DOC_WW_Pin1_4 | 741 | 746 | PF00397 | 0.754 |
DOC_WW_Pin1_4 | 747 | 752 | PF00397 | 0.808 |
DOC_WW_Pin1_4 | 839 | 844 | PF00397 | 0.841 |
LIG_14-3-3_CanoR_1 | 473 | 479 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 546 | 555 | PF00244 | 0.713 |
LIG_14-3-3_CanoR_1 | 604 | 610 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 709 | 715 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 915 | 925 | PF00244 | 0.707 |
LIG_14-3-3_CanoR_1 | 972 | 981 | PF00244 | 0.596 |
LIG_Actin_WH2_2 | 532 | 548 | PF00022 | 0.707 |
LIG_Actin_WH2_2 | 550 | 568 | PF00022 | 0.493 |
LIG_AP2alpha_2 | 182 | 184 | PF02296 | 0.453 |
LIG_BIR_III_2 | 876 | 880 | PF00653 | 0.627 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.606 |
LIG_BRCT_BRCA1_1 | 536 | 540 | PF00533 | 0.647 |
LIG_BRCT_BRCA1_1 | 620 | 624 | PF00533 | 0.761 |
LIG_EH1_1 | 248 | 256 | PF00400 | 0.529 |
LIG_eIF4E_1 | 123 | 129 | PF01652 | 0.482 |
LIG_FHA_1 | 1002 | 1008 | PF00498 | 0.619 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.423 |
LIG_FHA_1 | 231 | 237 | PF00498 | 0.382 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.426 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.422 |
LIG_FHA_1 | 335 | 341 | PF00498 | 0.449 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.578 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.547 |
LIG_FHA_1 | 45 | 51 | PF00498 | 0.426 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.786 |
LIG_FHA_1 | 748 | 754 | PF00498 | 0.864 |
LIG_FHA_1 | 813 | 819 | PF00498 | 0.733 |
LIG_FHA_1 | 839 | 845 | PF00498 | 0.792 |
LIG_FHA_1 | 993 | 999 | PF00498 | 0.696 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.316 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.477 |
LIG_FHA_2 | 449 | 455 | PF00498 | 0.663 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.707 |
LIG_FHA_2 | 55 | 61 | PF00498 | 0.320 |
LIG_FHA_2 | 75 | 81 | PF00498 | 0.389 |
LIG_FHA_2 | 856 | 862 | PF00498 | 0.792 |
LIG_FHA_2 | 918 | 924 | PF00498 | 0.638 |
LIG_LIR_Apic_2 | 195 | 201 | PF02991 | 0.379 |
LIG_LIR_Apic_2 | 453 | 459 | PF02991 | 0.694 |
LIG_LIR_Apic_2 | 811 | 817 | PF02991 | 0.637 |
LIG_LIR_Apic_2 | 976 | 981 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 124 | 129 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 181 | 192 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 537 | 548 | PF02991 | 0.647 |
LIG_LIR_Gen_1 | 938 | 949 | PF02991 | 0.597 |
LIG_LIR_LC3C_4 | 688 | 693 | PF02991 | 0.793 |
LIG_LIR_LC3C_4 | 815 | 820 | PF02991 | 0.781 |
LIG_LIR_Nem_3 | 124 | 128 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 239 | 244 | PF02991 | 0.373 |
LIG_LIR_Nem_3 | 537 | 543 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 938 | 944 | PF02991 | 0.606 |
LIG_LIR_Nem_3 | 953 | 958 | PF02991 | 0.576 |
LIG_LYPXL_yS_3 | 609 | 612 | PF13949 | 0.684 |
LIG_MYND_1 | 751 | 755 | PF01753 | 0.796 |
LIG_PCNA_PIPBox_1 | 982 | 991 | PF02747 | 0.568 |
LIG_Pex14_2 | 158 | 162 | PF04695 | 0.424 |
LIG_Pex14_2 | 244 | 248 | PF04695 | 0.506 |
LIG_Pex14_2 | 540 | 544 | PF04695 | 0.696 |
LIG_PTB_Apo_2 | 235 | 242 | PF02174 | 0.532 |
LIG_PTB_Apo_2 | 593 | 600 | PF02174 | 0.599 |
LIG_PTB_Phospho_1 | 593 | 599 | PF10480 | 0.597 |
LIG_SH2_CRK | 198 | 202 | PF00017 | 0.485 |
LIG_SH2_CRK | 456 | 460 | PF00017 | 0.701 |
LIG_SH2_CRK | 941 | 945 | PF00017 | 0.602 |
LIG_SH2_CRK | 955 | 959 | PF00017 | 0.575 |
LIG_SH2_CRK | 971 | 975 | PF00017 | 0.589 |
LIG_SH2_PTP2 | 361 | 364 | PF00017 | 0.343 |
LIG_SH2_SRC | 123 | 126 | PF00017 | 0.267 |
LIG_SH2_SRC | 361 | 364 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 125 | 129 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 274 | 278 | PF00017 | 0.446 |
LIG_SH2_STAP1 | 478 | 482 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 74 | 78 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 424 | 427 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 118 | 121 | PF00017 | 0.495 |
LIG_SH2_STAT5 | 271 | 274 | PF00017 | 0.580 |
LIG_SH2_STAT5 | 28 | 31 | PF00017 | 0.357 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.688 |
LIG_SH2_STAT5 | 95 | 98 | PF00017 | 0.366 |
LIG_SH2_STAT5 | 950 | 953 | PF00017 | 0.554 |
LIG_SH3_1 | 198 | 204 | PF00018 | 0.471 |
LIG_SH3_2 | 201 | 206 | PF14604 | 0.504 |
LIG_SH3_3 | 198 | 204 | PF00018 | 0.445 |
LIG_SH3_3 | 670 | 676 | PF00018 | 0.644 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.864 |
LIG_SH3_3 | 749 | 755 | PF00018 | 0.786 |
LIG_SH3_3 | 816 | 822 | PF00018 | 0.822 |
LIG_SUMO_SIM_anti_2 | 37 | 44 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 284 | 291 | PF11976 | 0.525 |
LIG_SUMO_SIM_par_1 | 342 | 348 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 37 | 44 | PF11976 | 0.380 |
LIG_SUMO_SIM_par_1 | 400 | 408 | PF11976 | 0.588 |
LIG_SUMO_SIM_par_1 | 517 | 522 | PF11976 | 0.547 |
LIG_TRAF2_1 | 451 | 454 | PF00917 | 0.665 |
LIG_TRAF2_1 | 744 | 747 | PF00917 | 0.666 |
LIG_TYR_ITIM | 939 | 944 | PF00017 | 0.571 |
LIG_WRC_WIRS_1 | 165 | 170 | PF05994 | 0.353 |
LIG_WW_2 | 751 | 754 | PF00397 | 0.654 |
LIG_WW_3 | 713 | 717 | PF00397 | 0.731 |
MOD_CDK_SPK_2 | 334 | 339 | PF00069 | 0.523 |
MOD_CDK_SPxK_1 | 683 | 689 | PF00069 | 0.636 |
MOD_CDK_SPxxK_3 | 106 | 113 | PF00069 | 0.520 |
MOD_CDK_SPxxK_3 | 334 | 341 | PF00069 | 0.517 |
MOD_CK1_1 | 130 | 136 | PF00069 | 0.441 |
MOD_CK1_1 | 237 | 243 | PF00069 | 0.323 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.551 |
MOD_CK1_1 | 561 | 567 | PF00069 | 0.644 |
MOD_CK1_1 | 629 | 635 | PF00069 | 0.797 |
MOD_CK1_1 | 699 | 705 | PF00069 | 0.840 |
MOD_CK1_1 | 725 | 731 | PF00069 | 0.849 |
MOD_CK1_1 | 732 | 738 | PF00069 | 0.806 |
MOD_CK1_1 | 758 | 764 | PF00069 | 0.651 |
MOD_CK1_1 | 838 | 844 | PF00069 | 0.830 |
MOD_CK1_1 | 845 | 851 | PF00069 | 0.757 |
MOD_CK1_1 | 889 | 895 | PF00069 | 0.670 |
MOD_CK1_1 | 919 | 925 | PF00069 | 0.702 |
MOD_CK1_1 | 940 | 946 | PF00069 | 0.569 |
MOD_CK2_1 | 164 | 170 | PF00069 | 0.480 |
MOD_CK2_1 | 208 | 214 | PF00069 | 0.507 |
MOD_CK2_1 | 447 | 453 | PF00069 | 0.656 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.374 |
MOD_CK2_1 | 561 | 567 | PF00069 | 0.644 |
MOD_CK2_1 | 736 | 742 | PF00069 | 0.796 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.515 |
MOD_GlcNHglycan | 1022 | 1025 | PF01048 | 0.607 |
MOD_GlcNHglycan | 627 | 631 | PF01048 | 0.540 |
MOD_GlcNHglycan | 638 | 641 | PF01048 | 0.502 |
MOD_GlcNHglycan | 650 | 653 | PF01048 | 0.592 |
MOD_GlcNHglycan | 657 | 660 | PF01048 | 0.517 |
MOD_GlcNHglycan | 697 | 701 | PF01048 | 0.626 |
MOD_GlcNHglycan | 724 | 727 | PF01048 | 0.607 |
MOD_GlcNHglycan | 732 | 735 | PF01048 | 0.541 |
MOD_GlcNHglycan | 786 | 789 | PF01048 | 0.644 |
MOD_GlcNHglycan | 798 | 801 | PF01048 | 0.486 |
MOD_GlcNHglycan | 804 | 807 | PF01048 | 0.430 |
MOD_GlcNHglycan | 837 | 840 | PF01048 | 0.519 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.666 |
MOD_GlcNHglycan | 888 | 891 | PF01048 | 0.522 |
MOD_GSK3_1 | 1018 | 1025 | PF00069 | 0.770 |
MOD_GSK3_1 | 1035 | 1042 | PF00069 | 0.617 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.487 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.522 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.281 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.405 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.512 |
MOD_GSK3_1 | 431 | 438 | PF00069 | 0.554 |
MOD_GSK3_1 | 557 | 564 | PF00069 | 0.635 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.684 |
MOD_GSK3_1 | 636 | 643 | PF00069 | 0.724 |
MOD_GSK3_1 | 644 | 651 | PF00069 | 0.677 |
MOD_GSK3_1 | 724 | 731 | PF00069 | 0.762 |
MOD_GSK3_1 | 732 | 739 | PF00069 | 0.748 |
MOD_GSK3_1 | 754 | 761 | PF00069 | 0.779 |
MOD_GSK3_1 | 782 | 789 | PF00069 | 0.840 |
MOD_GSK3_1 | 835 | 842 | PF00069 | 0.734 |
MOD_GSK3_1 | 851 | 858 | PF00069 | 0.780 |
MOD_LATS_1 | 1018 | 1024 | PF00433 | 0.758 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.726 |
MOD_N-GLC_1 | 170 | 175 | PF02516 | 0.671 |
MOD_N-GLC_1 | 228 | 233 | PF02516 | 0.618 |
MOD_N-GLC_1 | 237 | 242 | PF02516 | 0.369 |
MOD_N-GLC_1 | 278 | 283 | PF02516 | 0.475 |
MOD_N-GLC_1 | 561 | 566 | PF02516 | 0.441 |
MOD_N-GLC_1 | 640 | 645 | PF02516 | 0.614 |
MOD_N-GLC_1 | 796 | 801 | PF02516 | 0.485 |
MOD_N-GLC_1 | 906 | 911 | PF02516 | 0.575 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.497 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.340 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.536 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.485 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.549 |
MOD_NEK2_1 | 432 | 437 | PF00069 | 0.548 |
MOD_NEK2_1 | 447 | 452 | PF00069 | 0.537 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.519 |
MOD_NEK2_1 | 539 | 544 | PF00069 | 0.699 |
MOD_NEK2_1 | 594 | 599 | PF00069 | 0.645 |
MOD_NEK2_1 | 605 | 610 | PF00069 | 0.672 |
MOD_NEK2_1 | 619 | 624 | PF00069 | 0.745 |
MOD_NEK2_1 | 812 | 817 | PF00069 | 0.651 |
MOD_NEK2_1 | 864 | 869 | PF00069 | 0.786 |
MOD_NEK2_1 | 951 | 956 | PF00069 | 0.561 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.446 |
MOD_NEK2_2 | 134 | 139 | PF00069 | 0.486 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.362 |
MOD_NEK2_2 | 326 | 331 | PF00069 | 0.464 |
MOD_NEK2_2 | 74 | 79 | PF00069 | 0.477 |
MOD_NEK2_2 | 765 | 770 | PF00069 | 0.729 |
MOD_PIKK_1 | 1001 | 1007 | PF00454 | 0.627 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.618 |
MOD_PIKK_1 | 597 | 603 | PF00454 | 0.613 |
MOD_PIKK_1 | 880 | 886 | PF00454 | 0.631 |
MOD_PIKK_1 | 917 | 923 | PF00454 | 0.701 |
MOD_PKA_2 | 340 | 346 | PF00069 | 0.241 |
MOD_PKA_2 | 364 | 370 | PF00069 | 0.717 |
MOD_PKA_2 | 708 | 714 | PF00069 | 0.705 |
MOD_PKA_2 | 728 | 734 | PF00069 | 0.722 |
MOD_PKA_2 | 851 | 857 | PF00069 | 0.794 |
MOD_Plk_1 | 237 | 243 | PF00069 | 0.445 |
MOD_Plk_1 | 561 | 567 | PF00069 | 0.644 |
MOD_Plk_1 | 619 | 625 | PF00069 | 0.834 |
MOD_Plk_1 | 626 | 632 | PF00069 | 0.757 |
MOD_Plk_1 | 758 | 764 | PF00069 | 0.848 |
MOD_Plk_1 | 796 | 802 | PF00069 | 0.631 |
MOD_Plk_1 | 937 | 943 | PF00069 | 0.587 |
MOD_Plk_2-3 | 209 | 215 | PF00069 | 0.375 |
MOD_Plk_4 | 1003 | 1009 | PF00069 | 0.669 |
MOD_Plk_4 | 237 | 243 | PF00069 | 0.369 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.529 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.307 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.309 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.338 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.547 |
MOD_Plk_4 | 539 | 545 | PF00069 | 0.695 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.756 |
MOD_ProDKin_1 | 1018 | 1024 | PF00069 | 0.687 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.414 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.441 |
MOD_ProDKin_1 | 197 | 203 | PF00069 | 0.459 |
MOD_ProDKin_1 | 334 | 340 | PF00069 | 0.519 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.427 |
MOD_ProDKin_1 | 683 | 689 | PF00069 | 0.842 |
MOD_ProDKin_1 | 741 | 747 | PF00069 | 0.752 |
MOD_ProDKin_1 | 839 | 845 | PF00069 | 0.843 |
MOD_SUMO_rev_2 | 154 | 159 | PF00179 | 0.366 |
TRG_DiLeu_BaEn_1 | 1003 | 1008 | PF01217 | 0.666 |
TRG_DiLeu_BaEn_1 | 471 | 476 | PF01217 | 0.680 |
TRG_DiLeu_BaEn_2 | 153 | 159 | PF01217 | 0.445 |
TRG_DiLeu_BaEn_4 | 393 | 399 | PF01217 | 0.589 |
TRG_DiLeu_BaLyEn_6 | 463 | 468 | PF01217 | 0.607 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.553 |
TRG_DiLeu_BaLyEn_6 | 601 | 606 | PF01217 | 0.766 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.357 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.446 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.684 |
TRG_ENDOCYTIC_2 | 941 | 944 | PF00928 | 0.601 |
TRG_ENDOCYTIC_2 | 955 | 958 | PF00928 | 0.581 |
TRG_ENDOCYTIC_2 | 971 | 974 | PF00928 | 0.592 |
TRG_ER_diArg_1 | 338 | 341 | PF00400 | 0.452 |
TRG_ER_diArg_1 | 464 | 466 | PF00400 | 0.610 |
TRG_ER_diArg_1 | 576 | 578 | PF00400 | 0.634 |
TRG_ER_diArg_1 | 769 | 772 | PF00400 | 0.795 |
TRG_ER_diArg_1 | 971 | 973 | PF00400 | 0.597 |
TRG_NLS_MonoExtN_4 | 20 | 27 | PF00514 | 0.699 |
TRG_Pf-PMV_PEXEL_1 | 301 | 306 | PF00026 | 0.506 |
TRG_Pf-PMV_PEXEL_1 | 465 | 470 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQJ9 | Leishmania donovani | 87% | 98% |
A4H5K8 | Leishmania braziliensis | 67% | 97% |
A4HTU6 | Leishmania infantum | 86% | 100% |
Q4QHZ2 | Leishmania major | 85% | 100% |