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: A0A3S7WQJ9
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 | 618 | 622 | PF00656 | 0.481 |
CLV_C14_Caspase3-7 | 640 | 644 | PF00656 | 0.531 |
CLV_C14_Caspase3-7 | 687 | 691 | PF00656 | 0.466 |
CLV_C14_Caspase3-7 | 78 | 82 | PF00656 | 0.318 |
CLV_C14_Caspase3-7 | 867 | 871 | PF00656 | 0.514 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.355 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.584 |
CLV_NRD_NRD_1 | 578 | 580 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 664 | 666 | PF00675 | 0.738 |
CLV_NRD_NRD_1 | 667 | 669 | PF00675 | 0.734 |
CLV_NRD_NRD_1 | 714 | 716 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 779 | 781 | PF00675 | 0.810 |
CLV_NRD_NRD_1 | 995 | 997 | PF00675 | 0.566 |
CLV_PCSK_FUR_1 | 777 | 781 | PF00082 | 0.726 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.359 |
CLV_PCSK_KEX2_1 | 332 | 334 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 466 | 468 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 578 | 580 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 664 | 666 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 714 | 716 | PF00082 | 0.744 |
CLV_PCSK_KEX2_1 | 779 | 781 | PF00082 | 0.810 |
CLV_PCSK_KEX2_1 | 995 | 997 | PF00082 | 0.566 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.385 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.359 |
CLV_PCSK_PC1ET2_1 | 332 | 334 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 1015 | 1019 | PF00082 | 0.545 |
CLV_PCSK_SKI1_1 | 2 | 6 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.343 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.382 |
CLV_PCSK_SKI1_1 | 315 | 319 | PF00082 | 0.323 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.239 |
CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.544 |
CLV_PCSK_SKI1_1 | 547 | 551 | PF00082 | 0.575 |
CLV_PCSK_SKI1_1 | 605 | 609 | PF00082 | 0.676 |
CLV_PCSK_SKI1_1 | 950 | 954 | PF00082 | 0.534 |
CLV_PCSK_SKI1_1 | 979 | 983 | PF00082 | 0.553 |
CLV_PCSK_SKI1_1 | 996 | 1000 | PF00082 | 0.569 |
CLV_Separin_Metazoa | 463 | 467 | PF03568 | 0.349 |
DEG_APCC_DBOX_1 | 551 | 559 | PF00400 | 0.334 |
DEG_Kelch_Keap1_1 | 210 | 215 | PF01344 | 0.381 |
DEG_MDM2_SWIB_1 | 159 | 166 | PF02201 | 0.363 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.662 |
DEG_SIAH_1 | 678 | 686 | PF03145 | 0.506 |
DEG_SPOP_SBC_1 | 1060 | 1064 | PF00917 | 0.487 |
DEG_SPOP_SBC_1 | 130 | 134 | PF00917 | 0.319 |
DEG_SPOP_SBC_1 | 432 | 436 | PF00917 | 0.319 |
DEG_SPOP_SBC_1 | 809 | 813 | PF00917 | 0.495 |
DOC_ANK_TNKS_1 | 489 | 496 | PF00023 | 0.335 |
DOC_CDC14_PxL_1 | 101 | 109 | PF14671 | 0.406 |
DOC_CKS1_1 | 46 | 51 | PF01111 | 0.426 |
DOC_CKS1_1 | 755 | 760 | PF01111 | 0.559 |
DOC_CYCLIN_RxL_1 | 463 | 472 | PF00134 | 0.341 |
DOC_CYCLIN_yCln2_LP_2 | 759 | 765 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 821 | 827 | PF00134 | 0.489 |
DOC_CYCLIN_yCln2_LP_2 | 981 | 987 | PF00134 | 0.361 |
DOC_MAPK_gen_1 | 20 | 30 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 319 | 328 | PF00069 | 0.560 |
DOC_MAPK_gen_1 | 340 | 347 | PF00069 | 0.548 |
DOC_MAPK_gen_1 | 537 | 546 | PF00069 | 0.391 |
DOC_MAPK_MEF2A_6 | 955 | 962 | PF00069 | 0.371 |
DOC_MAPK_RevD_3 | 765 | 780 | PF00069 | 0.461 |
DOC_PP1_RVXF_1 | 25 | 31 | PF00149 | 0.508 |
DOC_PP1_RVXF_1 | 319 | 325 | PF00149 | 0.591 |
DOC_PP1_RVXF_1 | 977 | 983 | PF00149 | 0.347 |
DOC_PP2B_LxvP_1 | 985 | 988 | PF13499 | 0.361 |
DOC_PP4_FxxP_1 | 1001 | 1004 | PF00568 | 0.358 |
DOC_PP4_FxxP_1 | 5 | 8 | PF00568 | 0.643 |
DOC_PP4_FxxP_1 | 514 | 517 | PF00568 | 0.317 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.386 |
DOC_USP7_MATH_1 | 673 | 677 | PF00917 | 0.489 |
DOC_USP7_MATH_1 | 698 | 702 | PF00917 | 0.505 |
DOC_USP7_MATH_1 | 765 | 769 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 791 | 795 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 809 | 813 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 913 | 917 | PF00917 | 0.476 |
DOC_USP7_UBL2_3 | 20 | 24 | PF12436 | 0.617 |
DOC_USP7_UBL2_3 | 302 | 306 | PF12436 | 0.546 |
DOC_USP7_UBL2_3 | 321 | 325 | PF12436 | 0.455 |
DOC_USP7_UBL2_3 | 375 | 379 | PF12436 | 0.390 |
DOC_WW_Pin1_4 | 107 | 112 | PF00397 | 0.417 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.362 |
DOC_WW_Pin1_4 | 335 | 340 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.363 |
DOC_WW_Pin1_4 | 685 | 690 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 748 | 753 | PF00397 | 0.558 |
DOC_WW_Pin1_4 | 754 | 759 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 761 | 766 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 848 | 853 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 904 | 909 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 547 | 556 | PF00244 | 0.354 |
LIG_14-3-3_CanoR_1 | 605 | 611 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 735 | 743 | PF00244 | 0.500 |
LIG_14-3-3_CanoR_1 | 912 | 922 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 938 | 948 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 995 | 1004 | PF00244 | 0.365 |
LIG_Actin_WH2_2 | 533 | 549 | PF00022 | 0.347 |
LIG_Actin_WH2_2 | 551 | 569 | PF00022 | 0.346 |
LIG_AP2alpha_2 | 183 | 185 | PF02296 | 0.365 |
LIG_BRCT_BRCA1_1 | 290 | 294 | PF00533 | 0.667 |
LIG_BRCT_BRCA1_1 | 300 | 304 | PF00533 | 0.575 |
LIG_BRCT_BRCA1_1 | 353 | 357 | PF00533 | 0.308 |
LIG_BRCT_BRCA1_1 | 537 | 541 | PF00533 | 0.361 |
LIG_BRCT_BRCA1_1 | 621 | 625 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 797 | 801 | PF00533 | 0.485 |
LIG_BRCT_BRCA1_2 | 300 | 306 | PF00533 | 0.542 |
LIG_EH1_1 | 249 | 257 | PF00400 | 0.383 |
LIG_eIF4E_1 | 124 | 130 | PF01652 | 0.375 |
LIG_FHA_1 | 1016 | 1022 | PF00498 | 0.387 |
LIG_FHA_1 | 1025 | 1031 | PF00498 | 0.353 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.357 |
LIG_FHA_1 | 274 | 280 | PF00498 | 0.564 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.548 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.540 |
LIG_FHA_1 | 336 | 342 | PF00498 | 0.548 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.295 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.335 |
LIG_FHA_1 | 433 | 439 | PF00498 | 0.306 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.366 |
LIG_FHA_1 | 678 | 684 | PF00498 | 0.477 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.572 |
LIG_FHA_1 | 771 | 777 | PF00498 | 0.421 |
LIG_FHA_1 | 809 | 815 | PF00498 | 0.494 |
LIG_FHA_1 | 820 | 826 | PF00498 | 0.475 |
LIG_FHA_1 | 848 | 854 | PF00498 | 0.516 |
LIG_FHA_2 | 311 | 317 | PF00498 | 0.518 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.353 |
LIG_FHA_2 | 549 | 555 | PF00498 | 0.400 |
LIG_FHA_2 | 599 | 605 | PF00498 | 0.438 |
LIG_FHA_2 | 611 | 617 | PF00498 | 0.445 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.318 |
LIG_FHA_2 | 865 | 871 | PF00498 | 0.515 |
LIG_FHA_2 | 941 | 947 | PF00498 | 0.365 |
LIG_LIR_Apic_2 | 196 | 202 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 454 | 460 | PF02991 | 0.384 |
LIG_LIR_Apic_2 | 999 | 1004 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 182 | 193 | PF02991 | 0.344 |
LIG_LIR_Gen_1 | 354 | 365 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 538 | 549 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 930 | 940 | PF02991 | 0.370 |
LIG_LIR_Gen_1 | 961 | 972 | PF02991 | 0.337 |
LIG_LIR_LC3C_4 | 690 | 695 | PF02991 | 0.506 |
LIG_LIR_LC3C_4 | 822 | 827 | PF02991 | 0.506 |
LIG_LIR_Nem_3 | 161 | 166 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 182 | 188 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 240 | 245 | PF02991 | 0.310 |
LIG_LIR_Nem_3 | 269 | 275 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.308 |
LIG_LIR_Nem_3 | 538 | 544 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 930 | 935 | PF02991 | 0.385 |
LIG_LIR_Nem_3 | 961 | 967 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 976 | 981 | PF02991 | 0.371 |
LIG_MLH1_MIPbox_1 | 621 | 625 | PF16413 | 0.429 |
LIG_MYND_1 | 758 | 762 | PF01753 | 0.495 |
LIG_PCNA_PIPBox_1 | 1005 | 1014 | PF02747 | 0.335 |
LIG_Pex14_2 | 159 | 163 | PF04695 | 0.369 |
LIG_Pex14_2 | 245 | 249 | PF04695 | 0.333 |
LIG_Pex14_2 | 304 | 308 | PF04695 | 0.512 |
LIG_Pex14_2 | 541 | 545 | PF04695 | 0.336 |
LIG_PTB_Apo_2 | 236 | 243 | PF02174 | 0.383 |
LIG_REV1ctd_RIR_1 | 622 | 631 | PF16727 | 0.426 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.381 |
LIG_SH2_CRK | 457 | 461 | PF00017 | 0.392 |
LIG_SH2_CRK | 964 | 968 | PF00017 | 0.332 |
LIG_SH2_CRK | 978 | 982 | PF00017 | 0.361 |
LIG_SH2_CRK | 994 | 998 | PF00017 | 0.441 |
LIG_SH2_PTP2 | 362 | 365 | PF00017 | 0.270 |
LIG_SH2_SRC | 362 | 365 | PF00017 | 0.288 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.323 |
LIG_SH2_STAP1 | 275 | 279 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 479 | 483 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 75 | 79 | PF00017 | 0.368 |
LIG_SH2_STAT3 | 425 | 428 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 119 | 122 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 29 | 32 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 362 | 365 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 437 | 440 | PF00017 | 0.309 |
LIG_SH2_STAT5 | 556 | 559 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 587 | 590 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 600 | 603 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 96 | 99 | PF00017 | 0.374 |
LIG_SH2_STAT5 | 973 | 976 | PF00017 | 0.346 |
LIG_SH3_1 | 199 | 205 | PF00018 | 0.374 |
LIG_SH3_2 | 202 | 207 | PF14604 | 0.408 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.359 |
LIG_SH3_3 | 749 | 755 | PF00018 | 0.512 |
LIG_SH3_3 | 759 | 765 | PF00018 | 0.512 |
LIG_SH3_3 | 823 | 829 | PF00018 | 0.483 |
LIG_SH3_4 | 302 | 309 | PF00018 | 0.539 |
LIG_SUMO_SIM_anti_2 | 38 | 45 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 48 | 54 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 191 | 196 | PF11976 | 0.357 |
LIG_SUMO_SIM_par_1 | 285 | 292 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 38 | 45 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 401 | 409 | PF11976 | 0.341 |
LIG_SUMO_SIM_par_1 | 518 | 523 | PF11976 | 0.301 |
LIG_TRAF2_1 | 452 | 455 | PF00917 | 0.355 |
LIG_TYR_ITIM | 962 | 967 | PF00017 | 0.337 |
LIG_UBA3_1 | 192 | 200 | PF00899 | 0.316 |
LIG_UBA3_1 | 97 | 102 | PF00899 | 0.287 |
LIG_WW_3 | 719 | 723 | PF00397 | 0.460 |
MOD_CDK_SPK_2 | 335 | 340 | PF00069 | 0.614 |
MOD_CDK_SPxxK_3 | 107 | 114 | PF00069 | 0.411 |
MOD_CDK_SPxxK_3 | 335 | 342 | PF00069 | 0.608 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.333 |
MOD_CK1_1 | 436 | 442 | PF00069 | 0.308 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.367 |
MOD_CK1_1 | 630 | 636 | PF00069 | 0.489 |
MOD_CK1_1 | 703 | 709 | PF00069 | 0.539 |
MOD_CK1_1 | 731 | 737 | PF00069 | 0.614 |
MOD_CK1_1 | 739 | 745 | PF00069 | 0.524 |
MOD_CK1_1 | 847 | 853 | PF00069 | 0.539 |
MOD_CK1_1 | 854 | 860 | PF00069 | 0.496 |
MOD_CK1_1 | 942 | 948 | PF00069 | 0.479 |
MOD_CK1_1 | 963 | 969 | PF00069 | 0.335 |
MOD_CK2_1 | 151 | 157 | PF00069 | 0.343 |
MOD_CK2_1 | 165 | 171 | PF00069 | 0.344 |
MOD_CK2_1 | 209 | 215 | PF00069 | 0.429 |
MOD_CK2_1 | 448 | 454 | PF00069 | 0.346 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.367 |
MOD_CK2_1 | 742 | 748 | PF00069 | 0.484 |
MOD_GlcNHglycan | 1043 | 1046 | PF01048 | 0.617 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.419 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.595 |
MOD_GlcNHglycan | 628 | 632 | PF01048 | 0.683 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.690 |
MOD_GlcNHglycan | 652 | 655 | PF01048 | 0.723 |
MOD_GlcNHglycan | 659 | 662 | PF01048 | 0.675 |
MOD_GlcNHglycan | 675 | 678 | PF01048 | 0.670 |
MOD_GlcNHglycan | 702 | 705 | PF01048 | 0.706 |
MOD_GlcNHglycan | 730 | 733 | PF01048 | 0.712 |
MOD_GlcNHglycan | 738 | 741 | PF01048 | 0.673 |
MOD_GlcNHglycan | 793 | 796 | PF01048 | 0.691 |
MOD_GlcNHglycan | 805 | 808 | PF01048 | 0.747 |
MOD_GlcNHglycan | 846 | 849 | PF01048 | 0.827 |
MOD_GlcNHglycan | 853 | 856 | PF01048 | 0.750 |
MOD_GlcNHglycan | 87 | 90 | PF01048 | 0.508 |
MOD_GlcNHglycan | 888 | 891 | PF01048 | 0.641 |
MOD_GlcNHglycan | 924 | 927 | PF01048 | 0.699 |
MOD_GSK3_1 | 1041 | 1048 | PF00069 | 0.449 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.346 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.280 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.605 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.315 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.358 |
MOD_GSK3_1 | 594 | 601 | PF00069 | 0.449 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.503 |
MOD_GSK3_1 | 615 | 622 | PF00069 | 0.512 |
MOD_GSK3_1 | 630 | 637 | PF00069 | 0.419 |
MOD_GSK3_1 | 641 | 648 | PF00069 | 0.511 |
MOD_GSK3_1 | 673 | 680 | PF00069 | 0.483 |
MOD_GSK3_1 | 698 | 705 | PF00069 | 0.594 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.526 |
MOD_GSK3_1 | 761 | 768 | PF00069 | 0.487 |
MOD_GSK3_1 | 789 | 796 | PF00069 | 0.484 |
MOD_GSK3_1 | 830 | 837 | PF00069 | 0.516 |
MOD_GSK3_1 | 844 | 851 | PF00069 | 0.575 |
MOD_GSK3_1 | 860 | 867 | PF00069 | 0.598 |
MOD_GSK3_1 | 886 | 893 | PF00069 | 0.427 |
MOD_LATS_1 | 1041 | 1047 | PF00433 | 0.402 |
MOD_N-GLC_1 | 107 | 112 | PF02516 | 0.565 |
MOD_N-GLC_1 | 166 | 171 | PF02516 | 0.645 |
MOD_N-GLC_1 | 229 | 234 | PF02516 | 0.625 |
MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.293 |
MOD_N-GLC_1 | 279 | 284 | PF02516 | 0.408 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.565 |
MOD_N-GLC_1 | 641 | 646 | PF02516 | 0.772 |
MOD_N-GLC_1 | 650 | 655 | PF02516 | 0.697 |
MOD_N-GLC_1 | 930 | 935 | PF02516 | 0.672 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.363 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.337 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.300 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.431 |
MOD_NEK2_1 | 193 | 198 | PF00069 | 0.371 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.660 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.308 |
MOD_NEK2_1 | 448 | 453 | PF00069 | 0.289 |
MOD_NEK2_1 | 540 | 545 | PF00069 | 0.339 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.395 |
MOD_NEK2_1 | 595 | 600 | PF00069 | 0.402 |
MOD_NEK2_1 | 606 | 611 | PF00069 | 0.421 |
MOD_NEK2_1 | 620 | 625 | PF00069 | 0.471 |
MOD_NEK2_1 | 801 | 806 | PF00069 | 0.547 |
MOD_NEK2_1 | 819 | 824 | PF00069 | 0.463 |
MOD_NEK2_1 | 922 | 927 | PF00069 | 0.451 |
MOD_NEK2_1 | 974 | 979 | PF00069 | 0.325 |
MOD_NEK2_2 | 135 | 140 | PF00069 | 0.383 |
MOD_NEK2_2 | 184 | 189 | PF00069 | 0.349 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.561 |
MOD_NEK2_2 | 75 | 80 | PF00069 | 0.371 |
MOD_NEK2_2 | 772 | 777 | PF00069 | 0.484 |
MOD_NEK2_2 | 810 | 815 | PF00069 | 0.431 |
MOD_PIKK_1 | 1024 | 1030 | PF00454 | 0.378 |
MOD_PIKK_1 | 520 | 526 | PF00454 | 0.326 |
MOD_PIKK_1 | 940 | 946 | PF00454 | 0.408 |
MOD_PKA_2 | 365 | 371 | PF00069 | 0.407 |
MOD_PKA_2 | 577 | 583 | PF00069 | 0.354 |
MOD_PKA_2 | 734 | 740 | PF00069 | 0.467 |
MOD_PKA_2 | 801 | 807 | PF00069 | 0.488 |
MOD_PKA_2 | 860 | 866 | PF00069 | 0.486 |
MOD_Plk_1 | 238 | 244 | PF00069 | 0.334 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.367 |
MOD_Plk_1 | 620 | 626 | PF00069 | 0.525 |
MOD_Plk_1 | 627 | 633 | PF00069 | 0.479 |
MOD_Plk_1 | 765 | 771 | PF00069 | 0.548 |
MOD_Plk_1 | 960 | 966 | PF00069 | 0.356 |
MOD_Plk_4 | 1026 | 1032 | PF00069 | 0.391 |
MOD_Plk_4 | 238 | 244 | PF00069 | 0.310 |
MOD_Plk_4 | 283 | 289 | PF00069 | 0.590 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.307 |
MOD_Plk_4 | 35 | 41 | PF00069 | 0.278 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.273 |
MOD_Plk_4 | 433 | 439 | PF00069 | 0.306 |
MOD_Plk_4 | 471 | 477 | PF00069 | 0.322 |
MOD_Plk_4 | 540 | 546 | PF00069 | 0.335 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.445 |
MOD_ProDKin_1 | 107 | 113 | PF00069 | 0.416 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.359 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.363 |
MOD_ProDKin_1 | 335 | 341 | PF00069 | 0.650 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.367 |
MOD_ProDKin_1 | 685 | 691 | PF00069 | 0.511 |
MOD_ProDKin_1 | 748 | 754 | PF00069 | 0.559 |
MOD_ProDKin_1 | 761 | 767 | PF00069 | 0.472 |
MOD_ProDKin_1 | 848 | 854 | PF00069 | 0.511 |
MOD_ProDKin_1 | 904 | 910 | PF00069 | 0.484 |
MOD_SUMO_for_1 | 294 | 297 | PF00179 | 0.545 |
MOD_SUMO_rev_2 | 154 | 160 | PF00179 | 0.324 |
TRG_DiLeu_BaEn_1 | 1026 | 1031 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.301 |
TRG_DiLeu_BaEn_1 | 472 | 477 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_2 | 154 | 160 | PF01217 | 0.369 |
TRG_DiLeu_BaEn_4 | 394 | 400 | PF01217 | 0.344 |
TRG_DiLeu_BaLyEn_6 | 464 | 469 | PF01217 | 0.359 |
TRG_DiLeu_BaLyEn_6 | 602 | 607 | PF01217 | 0.486 |
TRG_DiLeu_BaLyEn_6 | 755 | 760 | PF01217 | 0.497 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.326 |
TRG_ENDOCYTIC_2 | 29 | 32 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.288 |
TRG_ENDOCYTIC_2 | 964 | 967 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 978 | 981 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 994 | 997 | PF00928 | 0.443 |
TRG_ER_diArg_1 | 339 | 342 | PF00400 | 0.569 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.363 |
TRG_ER_diArg_1 | 577 | 579 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 714 | 716 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 776 | 779 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 994 | 996 | PF00400 | 0.389 |
TRG_NLS_MonoExtN_4 | 21 | 28 | PF00514 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 259 | 263 | PF00026 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 466 | 471 | PF00026 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IKJ0 | Leptomonas seymouri | 49% | 93% |
A4H5K8 | Leishmania braziliensis | 66% | 96% |
A4HTU6 | Leishmania infantum | 100% | 100% |
E9AMN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 98% |
Q4QHZ2 | Leishmania major | 90% | 100% |