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)
Acidocalcisome, V-type proton ATPase subunit a
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:0032991 | protein-containing complex | 1 | 22 |
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:0016469 | proton-transporting two-sector ATPase complex | 3 | 2 |
GO:0016471 | vacuolar proton-transporting V-type ATPase complex | 5 | 2 |
GO:0033176 | proton-transporting V-type ATPase complex | 4 | 2 |
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: A4I0M2
Term | Name | Level | Count |
---|---|---|---|
GO:0006873 | intracellular monoatomic ion homeostasis | 4 | 2 |
GO:0006885 | regulation of pH | 8 | 2 |
GO:0007035 | vacuolar acidification | 10 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019725 | cellular homeostasis | 2 | 2 |
GO:0030003 | intracellular monoatomic cation homeostasis | 5 | 2 |
GO:0030004 | obsolete cellular monovalent inorganic cation homeostasis | 6 | 2 |
GO:0030641 | regulation of cellular pH | 7 | 2 |
GO:0042592 | homeostatic process | 3 | 2 |
GO:0048878 | chemical homeostasis | 4 | 2 |
GO:0050801 | monoatomic ion homeostasis | 5 | 2 |
GO:0051452 | intracellular pH reduction | 9 | 2 |
GO:0051453 | regulation of intracellular pH | 8 | 2 |
GO:0055067 | obsolete monovalent inorganic cation homeostasis | 7 | 2 |
GO:0055080 | monoatomic cation homeostasis | 6 | 2 |
GO:0055082 | intracellular chemical homeostasis | 3 | 2 |
GO:0065007 | biological regulation | 1 | 2 |
GO:0065008 | regulation of biological quality | 2 | 2 |
GO:0098771 | inorganic ion homeostasis | 6 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 22 |
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: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:0140657 | ATP-dependent activity | 1 | 22 |
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0019899 | enzyme binding | 3 | 2 |
GO:0051117 | ATPase binding | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 140 | 144 | PF00656 | 0.293 |
CLV_C14_Caspase3-7 | 223 | 227 | PF00656 | 0.279 |
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.286 |
CLV_C14_Caspase3-7 | 461 | 465 | PF00656 | 0.339 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.231 |
CLV_NRD_NRD_1 | 271 | 273 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 61 | 63 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 67 | 69 | PF00675 | 0.460 |
CLV_PCSK_KEX2_1 | 271 | 273 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 421 | 425 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 563 | 567 | PF00082 | 0.536 |
DEG_APCC_DBOX_1 | 206 | 214 | PF00400 | 0.252 |
DEG_APCC_DBOX_1 | 256 | 264 | PF00400 | 0.260 |
DEG_APCC_DBOX_1 | 420 | 428 | PF00400 | 0.310 |
DOC_CDC14_PxL_1 | 200 | 208 | PF14671 | 0.290 |
DOC_CYCLIN_RxL_1 | 62 | 76 | PF00134 | 0.329 |
DOC_CYCLIN_yClb1_LxF_4 | 496 | 501 | PF00134 | 0.273 |
DOC_MAPK_gen_1 | 123 | 132 | PF00069 | 0.249 |
DOC_MAPK_gen_1 | 205 | 213 | PF00069 | 0.292 |
DOC_MAPK_gen_1 | 255 | 263 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 506 | 515 | PF00069 | 0.248 |
DOC_MAPK_MEF2A_6 | 11 | 20 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 255 | 263 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 506 | 515 | PF00069 | 0.260 |
DOC_MAPK_MEF2A_6 | 541 | 548 | PF00069 | 0.288 |
DOC_PP1_RVXF_1 | 496 | 502 | PF00149 | 0.287 |
DOC_PP1_RVXF_1 | 535 | 541 | PF00149 | 0.516 |
DOC_PP1_RVXF_1 | 66 | 73 | PF00149 | 0.322 |
DOC_PP1_RVXF_1 | 742 | 748 | PF00149 | 0.454 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.248 |
DOC_PP4_FxxP_1 | 585 | 588 | PF00568 | 0.254 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.287 |
DOC_USP7_MATH_2 | 2 | 8 | PF00917 | 0.395 |
DOC_WW_Pin1_4 | 332 | 337 | PF00397 | 0.320 |
DOC_WW_Pin1_4 | 479 | 484 | PF00397 | 0.284 |
LIG_14-3-3_CanoR_1 | 233 | 239 | PF00244 | 0.303 |
LIG_14-3-3_CanoR_1 | 272 | 281 | PF00244 | 0.306 |
LIG_Actin_WH2_2 | 19 | 35 | PF00022 | 0.356 |
LIG_APCC_ABBA_1 | 397 | 402 | PF00400 | 0.313 |
LIG_APCC_ABBA_1 | 620 | 625 | PF00400 | 0.310 |
LIG_BRCT_BRCA1_1 | 133 | 137 | PF00533 | 0.382 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.313 |
LIG_BRCT_BRCA1_1 | 692 | 696 | PF00533 | 0.313 |
LIG_BRCT_BRCA1_1 | 697 | 701 | PF00533 | 0.313 |
LIG_Clathr_ClatBox_1 | 702 | 706 | PF01394 | 0.424 |
LIG_Clathr_ClatBox_1 | 730 | 734 | PF01394 | 0.304 |
LIG_deltaCOP1_diTrp_1 | 694 | 701 | PF00928 | 0.297 |
LIG_EVH1_2 | 336 | 340 | PF00568 | 0.273 |
LIG_FHA_1 | 147 | 153 | PF00498 | 0.237 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.232 |
LIG_FHA_1 | 244 | 250 | PF00498 | 0.272 |
LIG_FHA_1 | 340 | 346 | PF00498 | 0.260 |
LIG_FHA_1 | 525 | 531 | PF00498 | 0.336 |
LIG_FHA_1 | 588 | 594 | PF00498 | 0.227 |
LIG_FHA_1 | 724 | 730 | PF00498 | 0.335 |
LIG_FHA_1 | 81 | 87 | PF00498 | 0.304 |
LIG_FHA_2 | 323 | 329 | PF00498 | 0.251 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.217 |
LIG_FHA_2 | 82 | 88 | PF00498 | 0.307 |
LIG_LIR_Apic_2 | 451 | 456 | PF02991 | 0.218 |
LIG_LIR_Apic_2 | 582 | 588 | PF02991 | 0.258 |
LIG_LIR_Gen_1 | 103 | 112 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 114 | 120 | PF02991 | 0.218 |
LIG_LIR_Gen_1 | 346 | 356 | PF02991 | 0.263 |
LIG_LIR_Gen_1 | 392 | 400 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 412 | 422 | PF02991 | 0.327 |
LIG_LIR_Gen_1 | 500 | 507 | PF02991 | 0.254 |
LIG_LIR_Gen_1 | 527 | 536 | PF02991 | 0.487 |
LIG_LIR_Gen_1 | 552 | 562 | PF02991 | 0.315 |
LIG_LIR_Gen_1 | 651 | 662 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 676 | 687 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 698 | 707 | PF02991 | 0.286 |
LIG_LIR_Nem_3 | 103 | 109 | PF02991 | 0.294 |
LIG_LIR_Nem_3 | 114 | 119 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.293 |
LIG_LIR_Nem_3 | 346 | 352 | PF02991 | 0.255 |
LIG_LIR_Nem_3 | 373 | 377 | PF02991 | 0.263 |
LIG_LIR_Nem_3 | 392 | 397 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 412 | 417 | PF02991 | 0.402 |
LIG_LIR_Nem_3 | 500 | 505 | PF02991 | 0.254 |
LIG_LIR_Nem_3 | 527 | 532 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 552 | 558 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 651 | 657 | PF02991 | 0.462 |
LIG_LIR_Nem_3 | 676 | 682 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 693 | 699 | PF02991 | 0.304 |
LIG_LYPXL_S_1 | 467 | 471 | PF13949 | 0.539 |
LIG_MYND_1 | 456 | 460 | PF01753 | 0.260 |
LIG_NBox_RRM_1 | 717 | 727 | PF00076 | 0.204 |
LIG_NRP_CendR_1 | 773 | 775 | PF00754 | 0.347 |
LIG_PCNA_PIPBox_1 | 733 | 742 | PF02747 | 0.454 |
LIG_Pex14_1 | 697 | 701 | PF04695 | 0.297 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.248 |
LIG_Pex14_2 | 374 | 378 | PF04695 | 0.254 |
LIG_Pex14_2 | 414 | 418 | PF04695 | 0.430 |
LIG_Pex14_2 | 52 | 56 | PF04695 | 0.290 |
LIG_Pex14_2 | 750 | 754 | PF04695 | 0.454 |
LIG_PTB_Apo_2 | 436 | 443 | PF02174 | 0.304 |
LIG_PTB_Apo_2 | 525 | 532 | PF02174 | 0.313 |
LIG_PTB_Apo_2 | 749 | 756 | PF02174 | 0.458 |
LIG_PTB_Phospho_1 | 525 | 531 | PF10480 | 0.313 |
LIG_PTB_Phospho_1 | 749 | 755 | PF10480 | 0.458 |
LIG_SH2_CRK | 116 | 120 | PF00017 | 0.260 |
LIG_SH2_CRK | 193 | 197 | PF00017 | 0.264 |
LIG_SH2_CRK | 433 | 437 | PF00017 | 0.448 |
LIG_SH2_CRK | 502 | 506 | PF00017 | 0.254 |
LIG_SH2_CRK | 555 | 559 | PF00017 | 0.312 |
LIG_SH2_GRB2like | 531 | 534 | PF00017 | 0.512 |
LIG_SH2_SRC | 224 | 227 | PF00017 | 0.252 |
LIG_SH2_STAP1 | 106 | 110 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.245 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.273 |
LIG_SH2_STAT5 | 339 | 342 | PF00017 | 0.251 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 529 | 532 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 623 | 626 | PF00017 | 0.552 |
LIG_SH2_STAT5 | 668 | 671 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 679 | 682 | PF00017 | 0.452 |
LIG_SH3_1 | 453 | 459 | PF00018 | 0.260 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.240 |
LIG_SH3_3 | 466 | 472 | PF00018 | 0.285 |
LIG_SH3_3 | 477 | 483 | PF00018 | 0.281 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.223 |
LIG_SUMO_SIM_par_1 | 107 | 114 | PF11976 | 0.333 |
LIG_SUMO_SIM_par_1 | 12 | 19 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 143 | 149 | PF11976 | 0.330 |
LIG_SUMO_SIM_par_1 | 604 | 610 | PF11976 | 0.311 |
LIG_SUMO_SIM_par_1 | 701 | 706 | PF11976 | 0.421 |
LIG_TRFH_1 | 584 | 588 | PF08558 | 0.304 |
LIG_TYR_ITIM | 380 | 385 | PF00017 | 0.322 |
LIG_UBA3_1 | 617 | 626 | PF00899 | 0.299 |
LIG_WRC_WIRS_1 | 696 | 701 | PF05994 | 0.360 |
LIG_WW_1 | 336 | 339 | PF00397 | 0.332 |
MOD_CK1_1 | 290 | 296 | PF00069 | 0.318 |
MOD_CK1_1 | 348 | 354 | PF00069 | 0.381 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.368 |
MOD_CK1_1 | 490 | 496 | PF00069 | 0.127 |
MOD_CK1_1 | 690 | 696 | PF00069 | 0.313 |
MOD_CK2_1 | 322 | 328 | PF00069 | 0.297 |
MOD_CK2_1 | 490 | 496 | PF00069 | 0.332 |
MOD_CK2_1 | 563 | 569 | PF00069 | 0.290 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.321 |
MOD_CK2_1 | 93 | 99 | PF00069 | 0.418 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.365 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.319 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.316 |
MOD_GlcNHglycan | 318 | 321 | PF01048 | 0.331 |
MOD_GlcNHglycan | 450 | 453 | PF01048 | 0.312 |
MOD_GlcNHglycan | 48 | 52 | PF01048 | 0.332 |
MOD_GlcNHglycan | 489 | 492 | PF01048 | 0.314 |
MOD_GlcNHglycan | 596 | 599 | PF01048 | 0.439 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.482 |
MOD_GlcNHglycan | 708 | 711 | PF01048 | 0.324 |
MOD_GlcNHglycan | 736 | 739 | PF01048 | 0.309 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.300 |
MOD_GSK3_1 | 220 | 227 | PF00069 | 0.326 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.333 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.275 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.318 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.351 |
MOD_GSK3_1 | 564 | 571 | PF00069 | 0.339 |
MOD_GSK3_1 | 573 | 580 | PF00069 | 0.274 |
MOD_GSK3_1 | 671 | 678 | PF00069 | 0.309 |
MOD_GSK3_1 | 683 | 690 | PF00069 | 0.294 |
MOD_N-GLC_1 | 123 | 128 | PF02516 | 0.292 |
MOD_N-GLC_1 | 249 | 254 | PF02516 | 0.253 |
MOD_N-GLC_1 | 532 | 537 | PF02516 | 0.301 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.457 |
MOD_NEK2_1 | 146 | 151 | PF00069 | 0.441 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.342 |
MOD_NEK2_1 | 249 | 254 | PF00069 | 0.301 |
MOD_NEK2_1 | 287 | 292 | PF00069 | 0.292 |
MOD_NEK2_1 | 501 | 506 | PF00069 | 0.315 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.309 |
MOD_NEK2_1 | 532 | 537 | PF00069 | 0.400 |
MOD_NEK2_1 | 549 | 554 | PF00069 | 0.271 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.283 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.305 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.333 |
MOD_NEK2_1 | 723 | 728 | PF00069 | 0.321 |
MOD_NEK2_1 | 767 | 772 | PF00069 | 0.527 |
MOD_PIKK_1 | 243 | 249 | PF00454 | 0.367 |
MOD_PIKK_1 | 687 | 693 | PF00454 | 0.327 |
MOD_PK_1 | 169 | 175 | PF00069 | 0.313 |
MOD_PKA_2 | 165 | 171 | PF00069 | 0.310 |
MOD_PKA_2 | 474 | 480 | PF00069 | 0.357 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.448 |
MOD_Plk_1 | 401 | 407 | PF00069 | 0.286 |
MOD_Plk_1 | 47 | 53 | PF00069 | 0.309 |
MOD_Plk_1 | 532 | 538 | PF00069 | 0.301 |
MOD_Plk_2-3 | 573 | 579 | PF00069 | 0.246 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.297 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.383 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.276 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.315 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.279 |
MOD_Plk_4 | 348 | 354 | PF00069 | 0.279 |
MOD_Plk_4 | 389 | 395 | PF00069 | 0.283 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.291 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.267 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.304 |
MOD_Plk_4 | 81 | 87 | PF00069 | 0.385 |
MOD_ProDKin_1 | 332 | 338 | PF00069 | 0.398 |
MOD_ProDKin_1 | 479 | 485 | PF00069 | 0.347 |
MOD_SUMO_for_1 | 478 | 481 | PF00179 | 0.253 |
MOD_SUMO_rev_2 | 490 | 499 | PF00179 | 0.303 |
MOD_SUMO_rev_2 | 625 | 633 | PF00179 | 0.313 |
MOD_SUMO_rev_2 | 64 | 70 | PF00179 | 0.283 |
MOD_SUMO_rev_2 | 93 | 102 | PF00179 | 0.313 |
TRG_DiLeu_BaLyEn_6 | 206 | 211 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 106 | 109 | PF00928 | 0.355 |
TRG_ENDOCYTIC_2 | 116 | 119 | PF00928 | 0.262 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 382 | 385 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 422 | 425 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 433 | 436 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 438 | 441 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 468 | 471 | PF00928 | 0.429 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.304 |
TRG_ENDOCYTIC_2 | 529 | 532 | PF00928 | 0.360 |
TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 679 | 682 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.302 |
TRG_ER_diArg_1 | 254 | 257 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 270 | 272 | PF00400 | 0.316 |
TRG_ER_diArg_1 | 60 | 62 | PF00400 | 0.313 |
TRG_NES_CRM1_1 | 734 | 749 | PF08389 | 0.304 |
TRG_Pf-PMV_PEXEL_1 | 71 | 75 | PF00026 | 0.283 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P622 | Leptomonas seymouri | 89% | 100% |
A0A0N1PFQ1 | Leptomonas seymouri | 42% | 84% |
A0A0S4JG87 | Bodo saltans | 47% | 86% |
A0A0S4JMR5 | Bodo saltans | 62% | 100% |
A0A1X0NV83 | Trypanosomatidae | 42% | 92% |
A0A1X0NWN0 | Trypanosomatidae | 74% | 100% |
A0A3Q8IB62 | Leishmania donovani | 100% | 100% |
A0A3Q8IGN1 | Leishmania donovani | 43% | 87% |
A0A3R7KUW1 | Trypanosoma rangeli | 43% | 91% |
A0A422NJD7 | Trypanosoma rangeli | 72% | 100% |
A1A5G6 | Xenopus tropicalis | 39% | 93% |
A4HD35 | Leishmania braziliensis | 92% | 100% |
A4HK73 | Leishmania braziliensis | 43% | 100% |
A4I7Q8 | Leishmania infantum | 43% | 87% |
C9ZNR3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 64% | 99% |
E9AWI3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
E9B2L6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
G5EEK9 | Caenorhabditis elegans | 34% | 89% |
G5EGP4 | Caenorhabditis elegans | 33% | 90% |
O13742 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 93% |
O29106 | Archaeoglobus fulgidus (strain ATCC 49558 / DSM 4304 / JCM 9628 / NBRC 100126 / VC-16) | 20% | 100% |
O97681 | Bos taurus | 35% | 91% |
P15920 | Mus musculus | 35% | 91% |
P25286 | Rattus norvegicus | 39% | 92% |
P30628 | Caenorhabditis elegans | 36% | 86% |
P32563 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 92% |
P37296 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 37% | 87% |
Q01290 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 34% | 91% |
Q13488 | Homo sapiens | 34% | 93% |
Q29466 | Bos taurus | 40% | 92% |
Q4Q5J0 | Leishmania major | 42% | 100% |
Q4QAY7 | Leishmania major | 97% | 100% |
Q54E04 | Dictyostelium discoideum | 38% | 95% |
Q5R422 | Pongo abelii | 40% | 93% |
Q8AVM5 | Xenopus laevis | 40% | 93% |
Q8RWZ7 | Arabidopsis thaliana | 37% | 95% |
Q8W4S4 | Arabidopsis thaliana | 39% | 94% |
Q920R6 | Mus musculus | 37% | 93% |
Q93050 | Homo sapiens | 40% | 93% |
Q9HBG4 | Homo sapiens | 37% | 92% |
Q9I8D0 | Gallus gallus | 39% | 92% |
Q9SJT7 | Arabidopsis thaliana | 38% | 94% |
Q9Y487 | Homo sapiens | 35% | 91% |
Q9Z1G4 | Mus musculus | 39% | 92% |
V5BQN9 | Trypanosoma cruzi | 43% | 100% |
V5D763 | Trypanosoma cruzi | 72% | 100% |