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: Q4QHZ2
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 | 212 | 216 | PF00656 | 0.393 |
CLV_C14_Caspase3-7 | 640 | 644 | PF00656 | 0.575 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.432 |
CLV_C14_Caspase3-7 | 800 | 804 | PF00656 | 0.464 |
CLV_C14_Caspase3-7 | 868 | 872 | PF00656 | 0.543 |
CLV_NRD_NRD_1 | 1057 | 1059 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.666 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.733 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.834 |
CLV_NRD_NRD_1 | 714 | 716 | PF00675 | 0.786 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.774 |
CLV_NRD_NRD_1 | 815 | 817 | PF00675 | 0.670 |
CLV_NRD_NRD_1 | 966 | 968 | PF00675 | 0.666 |
CLV_PCSK_FUR_1 | 777 | 781 | PF00082 | 0.770 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.418 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.666 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.733 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.804 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 714 | 716 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 779 | 781 | PF00082 | 0.774 |
CLV_PCSK_KEX2_1 | 815 | 817 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 966 | 968 | PF00082 | 0.666 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.465 |
CLV_PCSK_PC1ET2_1 | 664 | 666 | PF00082 | 0.744 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.544 |
CLV_PCSK_PC7_1 | 65 | 71 | PF00082 | 0.546 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.482 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.252 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.678 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.682 |
CLV_PCSK_SKI1_1 | 921 | 925 | PF00082 | 0.632 |
CLV_PCSK_SKI1_1 | 950 | 954 | PF00082 | 0.650 |
CLV_PCSK_SKI1_1 | 967 | 971 | PF00082 | 0.505 |
CLV_PCSK_SKI1_1 | 986 | 990 | PF00082 | 0.468 |
CLV_Separin_Metazoa | 463 | 467 | PF03568 | 0.398 |
DEG_APCC_DBOX_1 | 551 | 559 | PF00400 | 0.445 |
DEG_MDM2_SWIB_1 | 159 | 166 | PF02201 | 0.427 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.752 |
DEG_SIAH_1 | 678 | 686 | PF03145 | 0.557 |
DEG_SPOP_SBC_1 | 1031 | 1035 | PF00917 | 0.571 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.400 |
DEG_SPOP_SBC_1 | 432 | 436 | PF00917 | 0.415 |
DOC_CDC14_PxL_1 | 101 | 109 | PF14671 | 0.469 |
DOC_CKS1_1 | 46 | 51 | PF01111 | 0.502 |
DOC_CKS1_1 | 755 | 760 | PF01111 | 0.614 |
DOC_CKS1_1 | 876 | 881 | PF01111 | 0.455 |
DOC_CYCLIN_RxL_1 | 463 | 472 | PF00134 | 0.455 |
DOC_CYCLIN_yCln2_LP_2 | 821 | 827 | PF00134 | 0.523 |
DOC_CYCLIN_yCln2_LP_2 | 952 | 958 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 20 | 30 | PF00069 | 0.654 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.597 |
DOC_MAPK_gen_1 | 340 | 347 | PF00069 | 0.590 |
DOC_MAPK_gen_1 | 537 | 546 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 815 | 821 | PF00069 | 0.468 |
DOC_MAPK_MEF2A_6 | 27 | 35 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 926 | 933 | PF00069 | 0.462 |
DOC_PP1_RVXF_1 | 25 | 31 | PF00149 | 0.566 |
DOC_PP1_RVXF_1 | 319 | 325 | PF00149 | 0.660 |
DOC_PP1_RVXF_1 | 948 | 954 | PF00149 | 0.444 |
DOC_PP2B_LxvP_1 | 956 | 959 | PF13499 | 0.442 |
DOC_PP4_FxxP_1 | 5 | 8 | PF00568 | 0.699 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.430 |
DOC_PP4_FxxP_1 | 972 | 975 | PF00568 | 0.454 |
DOC_USP7_MATH_1 | 1032 | 1036 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.579 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.450 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 696 | 700 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 867 | 871 | PF00917 | 0.465 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.673 |
DOC_USP7_UBL2_3 | 302 | 306 | PF12436 | 0.605 |
DOC_USP7_UBL2_3 | 321 | 325 | PF12436 | 0.486 |
DOC_USP7_UBL2_3 | 375 | 379 | PF12436 | 0.447 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.479 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.425 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.500 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 730 | 735 | PF00397 | 0.517 |
DOC_WW_Pin1_4 | 748 | 753 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.572 |
DOC_WW_Pin1_4 | 849 | 854 | PF00397 | 0.596 |
DOC_WW_Pin1_4 | 875 | 880 | PF00397 | 0.452 |
LIG_14-3-3_CanoR_1 | 1058 | 1064 | PF00244 | 0.485 |
LIG_14-3-3_CanoR_1 | 547 | 556 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 735 | 743 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 883 | 893 | PF00244 | 0.539 |
LIG_14-3-3_CanoR_1 | 909 | 919 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 966 | 975 | PF00244 | 0.462 |
LIG_Actin_WH2_2 | 533 | 549 | PF00022 | 0.457 |
LIG_Actin_WH2_2 | 551 | 569 | PF00022 | 0.285 |
LIG_AP2alpha_2 | 183 | 185 | PF02296 | 0.416 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.655 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.582 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.366 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.409 |
LIG_BRCT_BRCA1_1 | 616 | 620 | PF00533 | 0.525 |
LIG_BRCT_BRCA1_1 | 621 | 625 | PF00533 | 0.530 |
LIG_BRCT_BRCA1_1 | 797 | 801 | PF00533 | 0.526 |
LIG_BRCT_BRCA1_2 | 300 | 306 | PF00533 | 0.602 |
LIG_EH1_1 | 249 | 257 | PF00400 | 0.466 |
LIG_eIF4E_1 | 124 | 130 | PF01652 | 0.436 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.389 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.390 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.618 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.592 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.632 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.653 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.309 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.448 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.419 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.492 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.558 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.616 |
LIG_FHA_1 | 809 | 815 | PF00498 | 0.546 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.507 |
LIG_FHA_1 | 849 | 855 | PF00498 | 0.559 |
LIG_FHA_1 | 987 | 993 | PF00498 | 0.450 |
LIG_FHA_1 | 996 | 1002 | PF00498 | 0.398 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.634 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.414 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.457 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.490 |
LIG_FHA_2 | 686 | 692 | PF00498 | 0.469 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.362 |
LIG_FHA_2 | 866 | 872 | PF00498 | 0.543 |
LIG_FHA_2 | 912 | 918 | PF00498 | 0.397 |
LIG_FHA_2 | 920 | 926 | PF00498 | 0.329 |
LIG_GBD_Chelix_1 | 33 | 41 | PF00786 | 0.283 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 454 | 460 | PF02991 | 0.445 |
LIG_LIR_Apic_2 | 970 | 975 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 354 | 365 | PF02991 | 0.366 |
LIG_LIR_Gen_1 | 538 | 549 | PF02991 | 0.409 |
LIG_LIR_Gen_1 | 932 | 943 | PF02991 | 0.433 |
LIG_LIR_LC3C_4 | 690 | 695 | PF02991 | 0.556 |
LIG_LIR_LC3C_4 | 822 | 827 | PF02991 | 0.545 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.366 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 932 | 938 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 947 | 952 | PF02991 | 0.297 |
LIG_MYND_1 | 758 | 762 | PF01753 | 0.565 |
LIG_PCNA_PIPBox_1 | 976 | 985 | PF02747 | 0.435 |
LIG_Pex14_2 | 159 | 163 | PF04695 | 0.434 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.399 |
LIG_Pex14_2 | 304 | 308 | PF04695 | 0.591 |
LIG_Pex14_2 | 541 | 545 | PF04695 | 0.448 |
LIG_PTB_Apo_2 | 236 | 243 | PF02174 | 0.466 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.305 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.447 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.283 |
LIG_SH2_CRK | 457 | 461 | PF00017 | 0.452 |
LIG_SH2_CRK | 876 | 880 | PF00017 | 0.455 |
LIG_SH2_CRK | 935 | 939 | PF00017 | 0.428 |
LIG_SH2_CRK | 949 | 953 | PF00017 | 0.305 |
LIG_SH2_CRK | 965 | 969 | PF00017 | 0.303 |
LIG_SH2_NCK_1 | 876 | 880 | PF00017 | 0.455 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.399 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.435 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.602 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.422 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.431 |
LIG_SH2_STAT3 | 425 | 428 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.451 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.614 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.491 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 944 | 947 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.435 |
LIG_SH3_1 | 199 | 205 | PF00018 | 0.434 |
LIG_SH3_1 | 605 | 611 | PF00018 | 0.454 |
LIG_SH3_1 | 759 | 765 | PF00018 | 0.482 |
LIG_SH3_2 | 202 | 207 | PF14604 | 0.462 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.366 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.414 |
LIG_SH3_3 | 605 | 611 | PF00018 | 0.454 |
LIG_SH3_3 | 749 | 755 | PF00018 | 0.612 |
LIG_SH3_3 | 759 | 765 | PF00018 | 0.525 |
LIG_SH3_3 | 823 | 829 | PF00018 | 0.577 |
LIG_SH3_4 | 302 | 309 | PF00018 | 0.593 |
LIG_SUMO_SIM_anti_2 | 38 | 44 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 190 | 196 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 285 | 292 | PF11976 | 0.648 |
LIG_SUMO_SIM_par_1 | 401 | 409 | PF11976 | 0.453 |
LIG_SUMO_SIM_par_1 | 518 | 523 | PF11976 | 0.414 |
LIG_TRAF2_1 | 452 | 455 | PF00917 | 0.416 |
LIG_TYR_ITIM | 933 | 938 | PF00017 | 0.525 |
MOD_CDK_SPK_2 | 335 | 340 | PF00069 | 0.589 |
MOD_CDK_SPK_2 | 730 | 735 | PF00069 | 0.571 |
MOD_CDK_SPK_2 | 754 | 759 | PF00069 | 0.599 |
MOD_CDK_SPxxK_3 | 107 | 114 | PF00069 | 0.582 |
MOD_CDK_SPxxK_3 | 335 | 342 | PF00069 | 0.582 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.491 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.492 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.510 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.496 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.736 |
MOD_CK1_1 | 653 | 659 | PF00069 | 0.588 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.768 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.743 |
MOD_CK1_1 | 74 | 80 | PF00069 | 0.350 |
MOD_CK1_1 | 742 | 748 | PF00069 | 0.652 |
MOD_CK1_1 | 845 | 851 | PF00069 | 0.747 |
MOD_CK1_1 | 855 | 861 | PF00069 | 0.660 |
MOD_CK1_1 | 913 | 919 | PF00069 | 0.549 |
MOD_CK1_1 | 934 | 940 | PF00069 | 0.525 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.459 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.491 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.496 |
MOD_CK2_1 | 696 | 702 | PF00069 | 0.580 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.684 |
MOD_CK2_1 | 882 | 888 | PF00069 | 0.562 |
MOD_Cter_Amidation | 1056 | 1059 | PF01082 | 0.609 |
MOD_GlcNHglycan | 1014 | 1017 | PF01048 | 0.615 |
MOD_GlcNHglycan | 1034 | 1037 | PF01048 | 0.596 |
MOD_GlcNHglycan | 1060 | 1063 | PF01048 | 0.595 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.644 |
MOD_GlcNHglycan | 169 | 172 | PF01048 | 0.581 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.562 |
MOD_GlcNHglycan | 628 | 632 | PF01048 | 0.731 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.650 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.559 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.639 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.562 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.756 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.693 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.621 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.751 |
MOD_GlcNHglycan | 805 | 808 | PF01048 | 0.585 |
MOD_GlcNHglycan | 811 | 814 | PF01048 | 0.515 |
MOD_GlcNHglycan | 844 | 847 | PF01048 | 0.678 |
MOD_GlcNHglycan | 854 | 857 | PF01048 | 0.628 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.507 |
MOD_GlcNHglycan | 895 | 898 | PF01048 | 0.681 |
MOD_GSK3_1 | 1012 | 1019 | PF00069 | 0.626 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.546 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.607 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.305 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.466 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.568 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.518 |
MOD_GSK3_1 | 471 | 478 | PF00069 | 0.345 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.482 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.705 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.588 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.609 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.539 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.624 |
MOD_GSK3_1 | 649 | 656 | PF00069 | 0.574 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.729 |
MOD_GSK3_1 | 696 | 703 | PF00069 | 0.715 |
MOD_GSK3_1 | 71 | 78 | PF00069 | 0.362 |
MOD_GSK3_1 | 735 | 742 | PF00069 | 0.721 |
MOD_GSK3_1 | 791 | 798 | PF00069 | 0.748 |
MOD_GSK3_1 | 841 | 848 | PF00069 | 0.709 |
MOD_GSK3_1 | 852 | 859 | PF00069 | 0.643 |
MOD_GSK3_1 | 861 | 868 | PF00069 | 0.541 |
MOD_LATS_1 | 1012 | 1018 | PF00433 | 0.589 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.591 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.643 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.604 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.346 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.563 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.491 |
MOD_N-GLC_1 | 641 | 646 | PF02516 | 0.726 |
MOD_N-GLC_1 | 650 | 655 | PF02516 | 0.670 |
MOD_N-GLC_1 | 901 | 906 | PF02516 | 0.630 |
MOD_N-GLC_2 | 283 | 285 | PF02516 | 0.413 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.499 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.549 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.368 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.646 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.532 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.487 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.509 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.285 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.410 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.551 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.544 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.536 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.669 |
MOD_NEK2_1 | 801 | 806 | PF00069 | 0.679 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.540 |
MOD_NEK2_1 | 841 | 846 | PF00069 | 0.575 |
MOD_NEK2_1 | 874 | 879 | PF00069 | 0.652 |
MOD_NEK2_1 | 893 | 898 | PF00069 | 0.633 |
MOD_NEK2_1 | 919 | 924 | PF00069 | 0.337 |
MOD_NEK2_1 | 945 | 950 | PF00069 | 0.513 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.544 |
MOD_NEK2_2 | 184 | 189 | PF00069 | 0.482 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.514 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.525 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.456 |
MOD_PIKK_1 | 653 | 659 | PF00454 | 0.621 |
MOD_PIKK_1 | 911 | 917 | PF00454 | 0.545 |
MOD_PIKK_1 | 995 | 1001 | PF00454 | 0.594 |
MOD_PKA_1 | 1058 | 1064 | PF00069 | 0.600 |
MOD_PKA_2 | 1040 | 1046 | PF00069 | 0.612 |
MOD_PKA_2 | 1057 | 1063 | PF00069 | 0.528 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.578 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.554 |
MOD_PKA_2 | 801 | 807 | PF00069 | 0.656 |
MOD_PKA_2 | 861 | 867 | PF00069 | 0.693 |
MOD_PKA_2 | 882 | 888 | PF00069 | 0.562 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.466 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.496 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.745 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.661 |
MOD_Plk_1 | 765 | 771 | PF00069 | 0.761 |
MOD_Plk_1 | 931 | 937 | PF00069 | 0.548 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.466 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.570 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.458 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.506 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.434 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.545 |
MOD_Plk_4 | 997 | 1003 | PF00069 | 0.534 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.590 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.491 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.516 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.584 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.504 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.758 |
MOD_ProDKin_1 | 730 | 736 | PF00069 | 0.644 |
MOD_ProDKin_1 | 748 | 754 | PF00069 | 0.647 |
MOD_ProDKin_1 | 849 | 855 | PF00069 | 0.756 |
MOD_ProDKin_1 | 875 | 881 | PF00069 | 0.554 |
MOD_SUMO_for_1 | 294 | 297 | PF00179 | 0.509 |
TRG_DiLeu_BaEn_1 | 472 | 477 | PF01217 | 0.524 |
TRG_DiLeu_BaEn_1 | 997 | 1002 | PF01217 | 0.532 |
TRG_DiLeu_BaEn_2 | 154 | 160 | PF01217 | 0.513 |
TRG_DiLeu_BaEn_4 | 394 | 400 | PF01217 | 0.559 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.545 |
TRG_DiLeu_BaLyEn_6 | 602 | 607 | PF01217 | 0.666 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.399 |
TRG_ENDOCYTIC_2 | 935 | 938 | PF00928 | 0.517 |
TRG_ENDOCYTIC_2 | 949 | 952 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 965 | 968 | PF00928 | 0.350 |
TRG_ER_diArg_1 | 25 | 28 | PF00400 | 0.385 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.512 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.551 |
TRG_ER_diArg_1 | 577 | 579 | PF00400 | 0.647 |
TRG_ER_diArg_1 | 714 | 716 | PF00400 | 0.807 |
TRG_ER_diArg_1 | 777 | 780 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 814 | 816 | PF00400 | 0.576 |
TRG_ER_diArg_1 | 965 | 967 | PF00400 | 0.569 |
TRG_NLS_MonoExtN_4 | 21 | 28 | PF00514 | 0.556 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.461 |
TRG_Pf-PMV_PEXEL_1 | 466 | 471 | PF00026 | 0.568 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WQJ9 | Leishmania donovani | 90% | 100% |
A4H5K8 | Leishmania braziliensis | 65% | 100% |
A4HTU6 | Leishmania infantum | 90% | 100% |
E9AMN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |