Homologous to animal V-type proton pumps, vacuolar or lysosomal. For some reason, this family expanded in kinetoplastids. Localization: Endosomal (by homology) / Lysosomal (by homology)
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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000220 | vacuolar proton-transporting V-type ATPase, V0 domain | 5 | 22 |
GO:0016020 | membrane | 2 | 22 |
GO:0016469 | proton-transporting two-sector ATPase complex | 3 | 3 |
GO:0016471 | vacuolar proton-transporting V-type ATPase complex | 5 | 3 |
GO:0032991 | protein-containing complex | 1 | 22 |
GO:0033176 | proton-transporting V-type ATPase complex | 4 | 3 |
GO:0033177 | proton-transporting two-sector ATPase complex, proton-transporting domain | 3 | 22 |
GO:0033179 | proton-transporting V-type ATPase, V0 domain | 4 | 22 |
GO:0098796 | membrane protein complex | 2 | 22 |
GO:0110165 | cellular anatomical entity | 1 | 22 |
GO:0000323 | lytic vacuole | 6 | 1 |
GO:0005764 | lysosome | 7 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0020022 | acidocalcisome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: Q4Q5J0
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 3 |
GO:0006885 | regulation of pH | 8 | 3 |
GO:0007035 | vacuolar acidification | 10 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0019725 | cellular homeostasis | 2 | 3 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 3 |
GO:0030004 | obsolete cellular monovalent inorganic cation homeostasis | 6 | 3 |
GO:0030641 | regulation of cellular pH | 7 | 3 |
GO:0042592 | homeostatic process | 3 | 3 |
GO:0048878 | chemical homeostasis | 4 | 3 |
GO:0050801 | monoatomic ion homeostasis | 5 | 3 |
GO:0051452 | intracellular pH reduction | 9 | 3 |
GO:0051453 | regulation of intracellular pH | 8 | 3 |
GO:0055067 | obsolete monovalent inorganic cation homeostasis | 7 | 3 |
GO:0055080 | monoatomic cation homeostasis | 6 | 3 |
GO:0055082 | intracellular chemical homeostasis | 3 | 3 |
GO:0065007 | biological regulation | 1 | 3 |
GO:0065008 | regulation of biological quality | 2 | 3 |
GO:0098771 | inorganic ion homeostasis | 6 | 3 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 22 |
GO:0005488 | binding | 1 | 3 |
GO:0005515 | protein binding | 2 | 3 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 22 |
GO:0009678 | pyrophosphate hydrolysis-driven proton transmembrane transporter activity | 5 | 22 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 22 |
GO:0015078 | proton transmembrane transporter activity | 5 | 22 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 22 |
GO:0015399 | primary active transmembrane transporter activity | 4 | 22 |
GO:0019829 | ATPase-coupled monoatomic cation transmembrane transporter activity | 3 | 22 |
GO:0019899 | enzyme binding | 3 | 3 |
GO:0022804 | active transmembrane transporter activity | 3 | 22 |
GO:0022853 | active monoatomic ion transmembrane transporter activity | 4 | 22 |
GO:0022857 | transmembrane transporter activity | 2 | 22 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 22 |
GO:0042625 | ATPase-coupled ion transmembrane transporter activity | 3 | 22 |
GO:0042626 | ATPase-coupled transmembrane transporter activity | 2 | 22 |
GO:0044769 | ATPase activity, coupled to transmembrane movement of ions, rotational mechanism | 4 | 22 |
GO:0046961 | proton-transporting ATPase activity, rotational mechanism | 4 | 22 |
GO:0051117 | ATPase binding | 4 | 3 |
GO:0140657 | ATP-dependent activity | 1 | 22 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 696 | 700 | PF00656 | 0.368 |
CLV_NRD_NRD_1 | 292 | 294 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.448 |
CLV_NRD_NRD_1 | 671 | 673 | PF00675 | 0.241 |
CLV_NRD_NRD_1 | 679 | 681 | PF00675 | 0.251 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.444 |
CLV_PCSK_FUR_1 | 292 | 296 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 292 | 294 | PF00082 | 0.522 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.267 |
CLV_PCSK_KEX2_1 | 670 | 672 | PF00082 | 0.250 |
CLV_PCSK_KEX2_1 | 678 | 680 | PF00082 | 0.232 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 666 | 668 | PF00082 | 0.273 |
CLV_PCSK_PC7_1 | 667 | 673 | PF00082 | 0.309 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.458 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 347 | 351 | PF00082 | 0.440 |
CLV_PCSK_SKI1_1 | 459 | 463 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 56 | 60 | PF00082 | 0.542 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.267 |
DEG_APCC_DBOX_1 | 458 | 466 | PF00400 | 0.304 |
DEG_SCF_TRCP1_1 | 716 | 721 | PF00400 | 0.354 |
DOC_CKS1_1 | 156 | 161 | PF01111 | 0.238 |
DOC_CKS1_1 | 505 | 510 | PF01111 | 0.334 |
DOC_CYCLIN_RxL_1 | 64 | 78 | PF00134 | 0.321 |
DOC_CYCLIN_yClb1_LxF_4 | 532 | 537 | PF00134 | 0.266 |
DOC_MAPK_gen_1 | 205 | 215 | PF00069 | 0.279 |
DOC_MAPK_gen_1 | 249 | 257 | PF00069 | 0.296 |
DOC_MAPK_gen_1 | 292 | 300 | PF00069 | 0.286 |
DOC_MAPK_gen_1 | 306 | 314 | PF00069 | 0.266 |
DOC_MAPK_gen_1 | 515 | 524 | PF00069 | 0.154 |
DOC_MAPK_gen_1 | 542 | 551 | PF00069 | 0.246 |
DOC_MAPK_gen_1 | 683 | 692 | PF00069 | 0.518 |
DOC_MAPK_MEF2A_6 | 13 | 22 | PF00069 | 0.331 |
DOC_MAPK_MEF2A_6 | 249 | 257 | PF00069 | 0.293 |
DOC_MAPK_MEF2A_6 | 542 | 551 | PF00069 | 0.252 |
DOC_PP1_RVXF_1 | 532 | 538 | PF00149 | 0.279 |
DOC_PP1_RVXF_1 | 571 | 577 | PF00149 | 0.517 |
DOC_PP1_RVXF_1 | 68 | 75 | PF00149 | 0.317 |
DOC_PP1_RVXF_1 | 861 | 867 | PF00149 | 0.446 |
DOC_PP2B_LxvP_1 | 577 | 580 | PF13499 | 0.348 |
DOC_PP2B_LxvP_1 | 655 | 658 | PF13499 | 0.319 |
DOC_PP4_FxxP_1 | 54 | 57 | PF00568 | 0.266 |
DOC_PP4_FxxP_1 | 621 | 624 | PF00568 | 0.246 |
DOC_PP4_FxxP_1 | 745 | 748 | PF00568 | 0.354 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 174 | 178 | PF00917 | 0.306 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.311 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 748 | 752 | PF00917 | 0.381 |
DOC_USP7_UBL2_3 | 309 | 313 | PF12436 | 0.332 |
DOC_USP7_UBL2_3 | 569 | 573 | PF12436 | 0.532 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.332 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.261 |
DOC_WW_Pin1_4 | 504 | 509 | PF00397 | 0.247 |
LIG_14-3-3_CanoR_1 | 103 | 107 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 183 | 188 | PF00244 | 0.309 |
LIG_14-3-3_CanoR_1 | 306 | 312 | PF00244 | 0.294 |
LIG_14-3-3_CanoR_1 | 382 | 390 | PF00244 | 0.332 |
LIG_14-3-3_CanoR_1 | 683 | 692 | PF00244 | 0.438 |
LIG_APCC_ABBA_1 | 365 | 370 | PF00400 | 0.238 |
LIG_BRCT_BRCA1_1 | 177 | 181 | PF00533 | 0.290 |
LIG_BRCT_BRCA1_1 | 811 | 815 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 828 | 832 | PF00533 | 0.252 |
LIG_Clathr_ClatBox_1 | 849 | 853 | PF01394 | 0.297 |
LIG_CSL_BTD_1 | 336 | 339 | PF09270 | 0.252 |
LIG_CtBP_PxDLS_1 | 883 | 887 | PF00389 | 0.516 |
LIG_deltaCOP1_diTrp_1 | 568 | 578 | PF00928 | 0.487 |
LIG_EH1_1 | 770 | 778 | PF00400 | 0.532 |
LIG_eIF4E_1 | 149 | 155 | PF01652 | 0.238 |
LIG_eIF4E_1 | 572 | 578 | PF01652 | 0.438 |
LIG_EVH1_2 | 374 | 378 | PF00568 | 0.266 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.287 |
LIG_FHA_1 | 443 | 449 | PF00498 | 0.438 |
LIG_FHA_1 | 57 | 63 | PF00498 | 0.262 |
LIG_FHA_1 | 685 | 691 | PF00498 | 0.479 |
LIG_FHA_1 | 731 | 737 | PF00498 | 0.557 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.438 |
LIG_FHA_1 | 821 | 827 | PF00498 | 0.258 |
LIG_FHA_1 | 843 | 849 | PF00498 | 0.289 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.329 |
LIG_FHA_2 | 128 | 134 | PF00498 | 0.272 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.210 |
LIG_FHA_2 | 261 | 267 | PF00498 | 0.285 |
LIG_FHA_2 | 30 | 36 | PF00498 | 0.283 |
LIG_FHA_2 | 374 | 380 | PF00498 | 0.249 |
LIG_FHA_2 | 757 | 763 | PF00498 | 0.519 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.295 |
LIG_LIR_Apic_2 | 52 | 57 | PF02991 | 0.268 |
LIG_LIR_Apic_2 | 618 | 624 | PF02991 | 0.250 |
LIG_LIR_Gen_1 | 178 | 188 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 235 | 244 | PF02991 | 0.283 |
LIG_LIR_Gen_1 | 310 | 319 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 536 | 546 | PF02991 | 0.246 |
LIG_LIR_Gen_1 | 581 | 589 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 766 | 776 | PF02991 | 0.476 |
LIG_LIR_Gen_1 | 795 | 806 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 178 | 184 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 186 | 191 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 310 | 314 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 335 | 340 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 411 | 415 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 466 | 471 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 478 | 482 | PF02991 | 0.187 |
LIG_LIR_Nem_3 | 492 | 496 | PF02991 | 0.214 |
LIG_LIR_Nem_3 | 536 | 541 | PF02991 | 0.246 |
LIG_LIR_Nem_3 | 568 | 574 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 581 | 585 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 588 | 594 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 766 | 771 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 795 | 801 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 812 | 818 | PF02991 | 0.297 |
LIG_PCNA_PIPBox_1 | 852 | 861 | PF02747 | 0.446 |
LIG_Pex14_2 | 383 | 387 | PF04695 | 0.255 |
LIG_Pex14_2 | 412 | 416 | PF04695 | 0.246 |
LIG_Pex14_2 | 427 | 431 | PF04695 | 0.297 |
LIG_Pex14_2 | 54 | 58 | PF04695 | 0.283 |
LIG_Pex14_2 | 555 | 559 | PF04695 | 0.365 |
LIG_Pex14_2 | 578 | 582 | PF04695 | 0.378 |
LIG_Pex14_2 | 869 | 873 | PF04695 | 0.446 |
LIG_PTB_Apo_2 | 474 | 481 | PF02174 | 0.297 |
LIG_PTB_Apo_2 | 561 | 568 | PF02174 | 0.306 |
LIG_PTB_Apo_2 | 626 | 633 | PF02174 | 0.238 |
LIG_PTB_Apo_2 | 691 | 698 | PF02174 | 0.382 |
LIG_PTB_Apo_2 | 868 | 875 | PF02174 | 0.451 |
LIG_PTB_Phospho_1 | 561 | 567 | PF10480 | 0.306 |
LIG_PTB_Phospho_1 | 691 | 697 | PF10480 | 0.354 |
LIG_PTB_Phospho_1 | 868 | 874 | PF10480 | 0.451 |
LIG_REV1ctd_RIR_1 | 433 | 443 | PF16727 | 0.285 |
LIG_SH2_CRK | 152 | 156 | PF00017 | 0.238 |
LIG_SH2_CRK | 471 | 475 | PF00017 | 0.441 |
LIG_SH2_CRK | 538 | 542 | PF00017 | 0.246 |
LIG_SH2_CRK | 591 | 595 | PF00017 | 0.297 |
LIG_SH2_NCK_1 | 697 | 701 | PF00017 | 0.410 |
LIG_SH2_SRC | 169 | 172 | PF00017 | 0.349 |
LIG_SH2_SRC | 302 | 305 | PF00017 | 0.324 |
LIG_SH2_SRC | 780 | 783 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 567 | 571 | PF00017 | 0.532 |
LIG_SH2_STAP1 | 697 | 701 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 262 | 265 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 311 | 314 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 414 | 417 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 460 | 463 | PF00017 | 0.291 |
LIG_SH2_STAT5 | 491 | 494 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 659 | 662 | PF00017 | 0.545 |
LIG_SH2_STAT5 | 697 | 700 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 780 | 783 | PF00017 | 0.447 |
LIG_SH2_STAT5 | 787 | 790 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 798 | 801 | PF00017 | 0.433 |
LIG_SH3_3 | 153 | 159 | PF00018 | 0.365 |
LIG_SH3_3 | 502 | 508 | PF00018 | 0.278 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.278 |
LIG_SH3_3 | 624 | 630 | PF00018 | 0.236 |
LIG_SUMO_SIM_anti_2 | 593 | 598 | PF11976 | 0.348 |
LIG_SUMO_SIM_anti_2 | 612 | 618 | PF11976 | 0.120 |
LIG_SUMO_SIM_par_1 | 211 | 216 | PF11976 | 0.267 |
LIG_SUMO_SIM_par_1 | 460 | 466 | PF11976 | 0.285 |
LIG_SUMO_SIM_par_1 | 612 | 618 | PF11976 | 0.332 |
LIG_SUMO_SIM_par_1 | 687 | 693 | PF11976 | 0.528 |
LIG_SUMO_SIM_par_1 | 822 | 827 | PF11976 | 0.326 |
LIG_SUMO_SIM_par_1 | 882 | 887 | PF11976 | 0.396 |
LIG_TRAF2_1 | 751 | 754 | PF00917 | 0.507 |
LIG_TRAF2_1 | 98 | 101 | PF00917 | 0.332 |
LIG_TRFH_1 | 620 | 624 | PF08558 | 0.297 |
LIG_TYR_ITIM | 418 | 423 | PF00017 | 0.315 |
LIG_UBA3_1 | 187 | 194 | PF00899 | 0.404 |
LIG_UBA3_1 | 246 | 252 | PF00899 | 0.417 |
LIG_UBA3_1 | 430 | 439 | PF00899 | 0.313 |
LIG_UBA3_1 | 594 | 599 | PF00899 | 0.265 |
LIG_WRC_WIRS_1 | 586 | 591 | PF05994 | 0.279 |
LIG_WRC_WIRS_1 | 815 | 820 | PF05994 | 0.353 |
LIG_WW_3 | 515 | 519 | PF00397 | 0.168 |
MOD_CK1_1 | 165 | 171 | PF00069 | 0.320 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.369 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.311 |
MOD_CK1_1 | 360 | 366 | PF00069 | 0.357 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.331 |
MOD_CK1_1 | 688 | 694 | PF00069 | 0.356 |
MOD_CK1_1 | 695 | 701 | PF00069 | 0.358 |
MOD_CK1_1 | 756 | 762 | PF00069 | 0.426 |
MOD_CK1_1 | 790 | 796 | PF00069 | 0.455 |
MOD_CK1_1 | 809 | 815 | PF00069 | 0.294 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.311 |
MOD_CK2_1 | 127 | 133 | PF00069 | 0.253 |
MOD_CK2_1 | 260 | 266 | PF00069 | 0.359 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.397 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.342 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.285 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.314 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.265 |
MOD_CK2_1 | 748 | 754 | PF00069 | 0.448 |
MOD_CK2_1 | 756 | 762 | PF00069 | 0.421 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.363 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.309 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.301 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.327 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.305 |
MOD_GlcNHglycan | 704 | 708 | PF01048 | 0.389 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.400 |
MOD_GlcNHglycan | 720 | 723 | PF01048 | 0.423 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.465 |
MOD_GlcNHglycan | 829 | 832 | PF01048 | 0.319 |
MOD_GlcNHglycan | 855 | 858 | PF01048 | 0.302 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.368 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.429 |
MOD_GSK3_1 | 175 | 182 | PF00069 | 0.394 |
MOD_GSK3_1 | 272 | 279 | PF00069 | 0.323 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.318 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.294 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.334 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.266 |
MOD_GSK3_1 | 485 | 492 | PF00069 | 0.382 |
MOD_GSK3_1 | 499 | 506 | PF00069 | 0.359 |
MOD_GSK3_1 | 558 | 565 | PF00069 | 0.285 |
MOD_GSK3_1 | 600 | 607 | PF00069 | 0.330 |
MOD_GSK3_1 | 684 | 691 | PF00069 | 0.386 |
MOD_GSK3_1 | 714 | 721 | PF00069 | 0.427 |
MOD_GSK3_1 | 749 | 756 | PF00069 | 0.422 |
MOD_GSK3_1 | 788 | 795 | PF00069 | 0.301 |
MOD_GSK3_1 | 802 | 809 | PF00069 | 0.287 |
MOD_GSK3_1 | 816 | 823 | PF00069 | 0.351 |
MOD_GSK3_1 | 884 | 891 | PF00069 | 0.550 |
MOD_N-GLC_1 | 165 | 170 | PF02516 | 0.283 |
MOD_N-GLC_1 | 357 | 362 | PF02516 | 0.417 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.276 |
MOD_N-GLC_1 | 827 | 832 | PF02516 | 0.422 |
MOD_N-GLC_2 | 323 | 325 | PF02516 | 0.324 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.369 |
MOD_NEK2_1 | 162 | 167 | PF00069 | 0.373 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.438 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.342 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.345 |
MOD_NEK2_1 | 307 | 312 | PF00069 | 0.375 |
MOD_NEK2_1 | 327 | 332 | PF00069 | 0.275 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.342 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.329 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.346 |
MOD_NEK2_1 | 480 | 485 | PF00069 | 0.182 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.345 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.313 |
MOD_NEK2_1 | 558 | 563 | PF00069 | 0.361 |
MOD_NEK2_1 | 585 | 590 | PF00069 | 0.298 |
MOD_NEK2_1 | 685 | 690 | PF00069 | 0.354 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.326 |
MOD_NEK2_1 | 816 | 821 | PF00069 | 0.307 |
MOD_NEK2_1 | 884 | 889 | PF00069 | 0.524 |
MOD_OFUCOSY | 325 | 332 | PF10250 | 0.325 |
MOD_PIKK_1 | 806 | 812 | PF00454 | 0.307 |
MOD_PK_1 | 609 | 615 | PF00069 | 0.285 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.281 |
MOD_PKA_2 | 204 | 210 | PF00069 | 0.303 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.372 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.296 |
MOD_PKA_2 | 711 | 717 | PF00069 | 0.342 |
MOD_Plk_1 | 118 | 124 | PF00069 | 0.341 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.354 |
MOD_Plk_1 | 283 | 289 | PF00069 | 0.435 |
MOD_Plk_1 | 342 | 348 | PF00069 | 0.404 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.276 |
MOD_Plk_1 | 75 | 81 | PF00069 | 0.372 |
MOD_Plk_2-3 | 260 | 266 | PF00069 | 0.226 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.316 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.417 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.376 |
MOD_Plk_4 | 242 | 248 | PF00069 | 0.317 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.334 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.291 |
MOD_Plk_4 | 307 | 313 | PF00069 | 0.341 |
MOD_Plk_4 | 360 | 366 | PF00069 | 0.306 |
MOD_Plk_4 | 373 | 379 | PF00069 | 0.266 |
MOD_Plk_4 | 463 | 469 | PF00069 | 0.380 |
MOD_Plk_4 | 562 | 568 | PF00069 | 0.340 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.344 |
MOD_Plk_4 | 609 | 615 | PF00069 | 0.256 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.383 |
MOD_Plk_4 | 756 | 762 | PF00069 | 0.427 |
MOD_Plk_4 | 794 | 800 | PF00069 | 0.297 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.417 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.318 |
MOD_ProDKin_1 | 504 | 510 | PF00069 | 0.298 |
MOD_SUMO_for_1 | 312 | 315 | PF00179 | 0.417 |
MOD_SUMO_rev_2 | 186 | 196 | PF00179 | 0.246 |
MOD_SUMO_rev_2 | 497 | 502 | PF00179 | 0.246 |
MOD_SUMO_rev_2 | 530 | 535 | PF00179 | 0.298 |
TRG_DiLeu_BaEn_1 | 581 | 586 | PF01217 | 0.348 |
TRG_DiLeu_BaEn_2 | 217 | 223 | PF01217 | 0.285 |
TRG_DiLeu_BaEn_4 | 197 | 203 | PF01217 | 0.417 |
TRG_DiLeu_BaLyEn_6 | 150 | 155 | PF01217 | 0.246 |
TRG_ENDOCYTIC_2 | 152 | 155 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 311 | 314 | PF00928 | 0.317 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.239 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.295 |
TRG_ENDOCYTIC_2 | 460 | 463 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 471 | 474 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 538 | 541 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 591 | 594 | PF00928 | 0.297 |
TRG_ENDOCYTIC_2 | 659 | 662 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 798 | 801 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 292 | 295 | PF00400 | 0.353 |
TRG_ER_diArg_1 | 346 | 348 | PF00400 | 0.422 |
TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 670 | 672 | PF00400 | 0.278 |
TRG_ER_diArg_1 | 678 | 680 | PF00400 | 0.310 |
TRG_NES_CRM1_1 | 853 | 868 | PF08389 | 0.297 |
TRG_Pf-PMV_PEXEL_1 | 153 | 157 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 348 | 352 | PF00026 | 0.359 |
TRG_Pf-PMV_PEXEL_1 | 724 | 729 | PF00026 | 0.285 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P622 | Leptomonas seymouri | 41% | 100% |
A0A0N1PFQ1 | Leptomonas seymouri | 70% | 97% |
A0A0S4JG87 | Bodo saltans | 37% | 99% |
A0A0S4JMR5 | Bodo saltans | 43% | 100% |
A0A1X0NV83 | Trypanosomatidae | 50% | 100% |
A0A1X0NWN0 | Trypanosomatidae | 43% | 100% |
A0A3Q8IB62 | Leishmania donovani | 43% | 100% |
A0A3Q8IGN1 | Leishmania donovani | 95% | 100% |
A0A3R7KUW1 | Trypanosoma rangeli | 48% | 100% |
A0A422NJD7 | Trypanosoma rangeli | 42% | 100% |
A1A5G6 | Xenopus tropicalis | 33% | 100% |
A4HD35 | Leishmania braziliensis | 41% | 100% |
A4HK73 | Leishmania braziliensis | 85% | 100% |
A4I0M2 | Leishmania infantum | 42% | 100% |
A4I7Q8 | Leishmania infantum | 95% | 100% |
B2MZD0 | Caenorhabditis elegans | 30% | 74% |
C9ZNR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
E9AWI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
E9B2L6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
G5EEK9 | Caenorhabditis elegans | 31% | 100% |
G5EGP4 | Caenorhabditis elegans | 27% | 100% |
O13742 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
O97681 | Bos taurus | 31% | 100% |
P15920 | Mus musculus | 31% | 100% |
P25286 | Rattus norvegicus | 32% | 100% |
P30628 | Caenorhabditis elegans | 30% | 99% |
P32563 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P37296 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q01290 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 32% | 100% |
Q13488 | Homo sapiens | 31% | 100% |
Q29466 | Bos taurus | 33% | 100% |
Q4QAY7 | Leishmania major | 42% | 100% |
Q54E04 | Dictyostelium discoideum | 34% | 100% |
Q5R422 | Pongo abelii | 32% | 100% |
Q8AVM5 | Xenopus laevis | 33% | 100% |
Q8RWZ7 | Arabidopsis thaliana | 31% | 100% |
Q8W4S4 | Arabidopsis thaliana | 34% | 100% |
Q920R6 | Mus musculus | 32% | 100% |
Q93050 | Homo sapiens | 33% | 100% |
Q9HBG4 | Homo sapiens | 33% | 100% |
Q9I8D0 | Gallus gallus | 30% | 100% |
Q9SJT7 | Arabidopsis thaliana | 32% | 100% |
Q9Y487 | Homo sapiens | 31% | 100% |
Q9Z1G4 | Mus musculus | 32% | 100% |
V5BQN9 | Trypanosoma cruzi | 51% | 100% |
V5D763 | Trypanosoma cruzi | 42% | 100% |