Carries an ATP pyrophosphate-lyase domain on its cytoplasmic segment. Likely acts as a receptor for some unknown extracellular stimulus. Extremely expanded kinetoplastid protein family.. Expressed in the insect stage (promastigote) but not in the mammalian host stage of the parasite life cycle.. 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. | yes | yes: 10 |
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 | yes | yes: 8, no: 8 |
NetGPI | no | yes: 0, no: 16 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 8 |
GO:0110165 | cellular anatomical entity | 1 | 8 |
Related structures:
AlphaFold database: A4H8V6
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:0007165 | signal transduction | 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:0035556 | intracellular signal transduction | 3 | 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:0050789 | regulation of biological process | 2 | 2 |
GO:0050794 | regulation of cellular process | 3 | 2 |
GO:0052652 | cyclic purine nucleotide metabolic process | 6 | 2 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
GO:0065007 | biological regulation | 1 | 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 | 8 |
GO:0004016 | adenylate cyclase activity | 3 | 7 |
GO:0009975 | cyclase activity | 2 | 7 |
GO:0016829 | lyase activity | 2 | 8 |
GO:0016849 | phosphorus-oxygen lyase activity | 3 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 237 | 241 | PF00656 | 0.576 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.533 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 383 | 385 | PF00675 | 0.409 |
CLV_NRD_NRD_1 | 419 | 421 | PF00675 | 0.448 |
CLV_PCSK_FUR_1 | 195 | 199 | PF00082 | 0.497 |
CLV_PCSK_KEX2_1 | 12 | 14 | PF00082 | 0.705 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 383 | 385 | PF00082 | 0.409 |
CLV_PCSK_KEX2_1 | 419 | 421 | PF00082 | 0.409 |
CLV_PCSK_SKI1_1 | 118 | 122 | PF00082 | 0.501 |
CLV_PCSK_SKI1_1 | 198 | 202 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.228 |
CLV_PCSK_SKI1_1 | 274 | 278 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.513 |
CLV_PCSK_SKI1_1 | 383 | 387 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 559 | 563 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 645 | 649 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 97 | 101 | PF00082 | 0.560 |
DEG_SPOP_SBC_1 | 280 | 284 | PF00917 | 0.568 |
DOC_CDC14_PxL_1 | 121 | 129 | PF14671 | 0.568 |
DOC_CDC14_PxL_1 | 510 | 518 | PF14671 | 0.582 |
DOC_CKS1_1 | 446 | 451 | PF01111 | 0.389 |
DOC_CYCLIN_yCln2_LP_2 | 226 | 232 | PF00134 | 0.570 |
DOC_CYCLIN_yCln2_LP_2 | 410 | 416 | PF00134 | 0.538 |
DOC_MAPK_gen_1 | 195 | 204 | PF00069 | 0.393 |
DOC_MAPK_MEF2A_6 | 180 | 187 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 501 | 510 | PF00069 | 0.534 |
DOC_MAPK_RevD_3 | 183 | 198 | PF00069 | 0.494 |
DOC_PP1_RVXF_1 | 293 | 299 | PF00149 | 0.463 |
DOC_PP1_RVXF_1 | 680 | 686 | PF00149 | 0.550 |
DOC_PP2B_LxvP_1 | 226 | 229 | PF13499 | 0.567 |
DOC_PP4_FxxP_1 | 134 | 137 | PF00568 | 0.494 |
DOC_PP4_FxxP_1 | 155 | 158 | PF00568 | 0.524 |
DOC_PP4_FxxP_1 | 589 | 592 | PF00568 | 0.455 |
DOC_PP4_FxxP_1 | 603 | 606 | PF00568 | 0.573 |
DOC_PP4_FxxP_1 | 658 | 661 | PF00568 | 0.554 |
DOC_USP7_MATH_1 | 280 | 284 | PF00917 | 0.560 |
DOC_USP7_MATH_1 | 624 | 628 | PF00917 | 0.622 |
DOC_USP7_MATH_1 | 661 | 665 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 670 | 674 | PF00917 | 0.591 |
DOC_WW_Pin1_4 | 308 | 313 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.390 |
DOC_WW_Pin1_4 | 583 | 588 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 666 | 671 | PF00397 | 0.603 |
LIG_14-3-3_CanoR_1 | 166 | 175 | PF00244 | 0.357 |
LIG_14-3-3_CanoR_1 | 195 | 204 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 274 | 280 | PF00244 | 0.541 |
LIG_14-3-3_CanoR_1 | 281 | 288 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 522 | 527 | PF00244 | 0.531 |
LIG_Actin_WH2_2 | 179 | 194 | PF00022 | 0.460 |
LIG_Actin_WH2_2 | 562 | 577 | PF00022 | 0.477 |
LIG_AP2alpha_2 | 68 | 70 | PF02296 | 0.377 |
LIG_APCC_ABBA_1 | 131 | 136 | PF00400 | 0.532 |
LIG_APCC_ABBA_1 | 298 | 303 | PF00400 | 0.541 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.744 |
LIG_BRCT_BRCA1_1 | 475 | 479 | PF00533 | 0.343 |
LIG_BRCT_BRCA1_1 | 585 | 589 | PF00533 | 0.503 |
LIG_FHA_1 | 112 | 118 | PF00498 | 0.493 |
LIG_FHA_1 | 12 | 18 | PF00498 | 0.617 |
LIG_FHA_1 | 182 | 188 | PF00498 | 0.459 |
LIG_FHA_1 | 321 | 327 | PF00498 | 0.391 |
LIG_FHA_1 | 346 | 352 | PF00498 | 0.568 |
LIG_FHA_1 | 563 | 569 | PF00498 | 0.490 |
LIG_FHA_1 | 580 | 586 | PF00498 | 0.390 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.528 |
LIG_FHA_1 | 663 | 669 | PF00498 | 0.510 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.451 |
LIG_FHA_2 | 309 | 315 | PF00498 | 0.584 |
LIG_GBD_Chelix_1 | 269 | 277 | PF00786 | 0.486 |
LIG_Integrin_isoDGR_2 | 95 | 97 | PF01839 | 0.538 |
LIG_IRF3_LxIS_1 | 579 | 586 | PF10401 | 0.509 |
LIG_LIR_Apic_2 | 152 | 158 | PF02991 | 0.521 |
LIG_LIR_Apic_2 | 442 | 446 | PF02991 | 0.564 |
LIG_LIR_Apic_2 | 586 | 592 | PF02991 | 0.483 |
LIG_LIR_Apic_2 | 657 | 661 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 199 | 209 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 211 | 222 | PF02991 | 0.459 |
LIG_LIR_Gen_1 | 246 | 256 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 271 | 280 | PF02991 | 0.547 |
LIG_LIR_Gen_1 | 327 | 336 | PF02991 | 0.381 |
LIG_LIR_Gen_1 | 537 | 546 | PF02991 | 0.587 |
LIG_LIR_Gen_1 | 599 | 608 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 122 | 127 | PF02991 | 0.542 |
LIG_LIR_Nem_3 | 199 | 204 | PF02991 | 0.510 |
LIG_LIR_Nem_3 | 211 | 217 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 254 | 258 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 271 | 275 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 327 | 331 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 537 | 541 | PF02991 | 0.613 |
LIG_LIR_Nem_3 | 599 | 604 | PF02991 | 0.554 |
LIG_LIR_Nem_3 | 611 | 616 | PF02991 | 0.387 |
LIG_LYPXL_yS_3 | 124 | 127 | PF13949 | 0.443 |
LIG_LYPXL_yS_3 | 255 | 258 | PF13949 | 0.480 |
LIG_MYND_1 | 133 | 137 | PF01753 | 0.333 |
LIG_MYND_3 | 605 | 609 | PF01753 | 0.586 |
LIG_Pex14_1 | 477 | 481 | PF04695 | 0.378 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.536 |
LIG_Pex14_2 | 481 | 485 | PF04695 | 0.584 |
LIG_PTB_Apo_2 | 59 | 66 | PF02174 | 0.479 |
LIG_PTB_Phospho_1 | 59 | 65 | PF10480 | 0.477 |
LIG_Rb_pABgroove_1 | 421 | 429 | PF01858 | 0.359 |
LIG_RPA_C_Fungi | 613 | 625 | PF08784 | 0.392 |
LIG_SH2_CRK | 214 | 218 | PF00017 | 0.500 |
LIG_SH2_CRK | 232 | 236 | PF00017 | 0.581 |
LIG_SH2_CRK | 328 | 332 | PF00017 | 0.433 |
LIG_SH2_CRK | 443 | 447 | PF00017 | 0.568 |
LIG_SH2_GRB2like | 328 | 331 | PF00017 | 0.404 |
LIG_SH2_NCK_1 | 328 | 332 | PF00017 | 0.568 |
LIG_SH2_NCK_1 | 639 | 643 | PF00017 | 0.532 |
LIG_SH2_SRC | 328 | 331 | PF00017 | 0.575 |
LIG_SH2_STAP1 | 302 | 306 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 487 | 491 | PF00017 | 0.597 |
LIG_SH2_STAP1 | 564 | 568 | PF00017 | 0.497 |
LIG_SH2_STAP1 | 616 | 620 | PF00017 | 0.377 |
LIG_SH2_STAT3 | 344 | 347 | PF00017 | 0.380 |
LIG_SH2_STAT3 | 459 | 462 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 286 | 289 | PF00017 | 0.384 |
LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 493 | 496 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 564 | 567 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 601 | 604 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 613 | 616 | PF00017 | 0.342 |
LIG_SH3_1 | 443 | 449 | PF00018 | 0.372 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.401 |
LIG_SH3_3 | 443 | 449 | PF00018 | 0.550 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.459 |
LIG_SH3_3 | 581 | 587 | PF00018 | 0.493 |
LIG_SUMO_SIM_anti_2 | 181 | 188 | PF11976 | 0.401 |
LIG_SUMO_SIM_anti_2 | 565 | 570 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 181 | 188 | PF11976 | 0.343 |
LIG_SUMO_SIM_par_1 | 564 | 570 | PF11976 | 0.481 |
LIG_SUMO_SIM_par_1 | 581 | 586 | PF11976 | 0.434 |
LIG_TRFH_1 | 224 | 228 | PF08558 | 0.524 |
LIG_TRFH_1 | 65 | 69 | PF08558 | 0.511 |
LIG_TYR_ITIM | 326 | 331 | PF00017 | 0.526 |
LIG_UBA3_1 | 186 | 192 | PF00899 | 0.554 |
LIG_UBA3_1 | 468 | 474 | PF00899 | 0.354 |
LIG_WRC_WIRS_1 | 221 | 226 | PF05994 | 0.544 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.457 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.557 |
MOD_CK1_1 | 375 | 381 | PF00069 | 0.629 |
MOD_CK1_1 | 480 | 486 | PF00069 | 0.551 |
MOD_CK1_1 | 640 | 646 | PF00069 | 0.499 |
MOD_CK1_1 | 673 | 679 | PF00069 | 0.592 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.507 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.402 |
MOD_GlcNHglycan | 232 | 235 | PF01048 | 0.468 |
MOD_GlcNHglycan | 240 | 243 | PF01048 | 0.423 |
MOD_GlcNHglycan | 283 | 286 | PF01048 | 0.524 |
MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.553 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.628 |
MOD_GlcNHglycan | 38 | 41 | PF01048 | 0.622 |
MOD_GlcNHglycan | 482 | 485 | PF01048 | 0.564 |
MOD_GlcNHglycan | 503 | 506 | PF01048 | 0.413 |
MOD_GlcNHglycan | 532 | 536 | PF01048 | 0.642 |
MOD_GlcNHglycan | 628 | 631 | PF01048 | 0.466 |
MOD_GlcNHglycan | 640 | 643 | PF01048 | 0.521 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.493 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.470 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.516 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.688 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.420 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.453 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.519 |
MOD_GSK3_1 | 473 | 480 | PF00069 | 0.455 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.531 |
MOD_GSK3_1 | 579 | 586 | PF00069 | 0.511 |
MOD_GSK3_1 | 620 | 627 | PF00069 | 0.512 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.567 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.613 |
MOD_GSK3_1 | 86 | 93 | PF00069 | 0.453 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.469 |
MOD_N-GLC_1 | 508 | 513 | PF02516 | 0.519 |
MOD_N-GLC_1 | 546 | 551 | PF02516 | 0.530 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.507 |
MOD_N-GLC_1 | 579 | 584 | PF02516 | 0.362 |
MOD_NEK2_1 | 138 | 143 | PF00069 | 0.511 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.431 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.533 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.516 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.352 |
MOD_NEK2_1 | 317 | 322 | PF00069 | 0.471 |
MOD_NEK2_1 | 345 | 350 | PF00069 | 0.446 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.459 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.703 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.438 |
MOD_NEK2_2 | 168 | 173 | PF00069 | 0.542 |
MOD_NEK2_2 | 286 | 291 | PF00069 | 0.475 |
MOD_NEK2_2 | 7 | 12 | PF00069 | 0.747 |
MOD_PIKK_1 | 390 | 396 | PF00454 | 0.508 |
MOD_PIKK_1 | 546 | 552 | PF00454 | 0.558 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.690 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.547 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.528 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.386 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.464 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.478 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.499 |
MOD_Plk_1 | 351 | 357 | PF00069 | 0.580 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.553 |
MOD_Plk_1 | 645 | 651 | PF00069 | 0.583 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.530 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.473 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.532 |
MOD_Plk_4 | 351 | 357 | PF00069 | 0.550 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.429 |
MOD_Plk_4 | 590 | 596 | PF00069 | 0.422 |
MOD_ProDKin_1 | 308 | 314 | PF00069 | 0.567 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.387 |
MOD_ProDKin_1 | 583 | 589 | PF00069 | 0.487 |
MOD_ProDKin_1 | 666 | 672 | PF00069 | 0.603 |
MOD_SUMO_rev_2 | 103 | 108 | PF00179 | 0.536 |
MOD_SUMO_rev_2 | 354 | 363 | PF00179 | 0.582 |
MOD_SUMO_rev_2 | 68 | 78 | PF00179 | 0.489 |
TRG_DiLeu_BaLyEn_6 | 569 | 574 | PF01217 | 0.521 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.546 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 255 | 258 | PF00928 | 0.536 |
TRG_ENDOCYTIC_2 | 301 | 304 | PF00928 | 0.514 |
TRG_ENDOCYTIC_2 | 328 | 331 | PF00928 | 0.390 |
TRG_ENDOCYTIC_2 | 601 | 604 | PF00928 | 0.573 |
TRG_ENDOCYTIC_2 | 616 | 619 | PF00928 | 0.553 |
TRG_ER_diArg_1 | 194 | 197 | PF00400 | 0.483 |
TRG_ER_diArg_1 | 382 | 384 | PF00400 | 0.419 |
TRG_NES_CRM1_1 | 215 | 227 | PF08389 | 0.372 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0NPQ6 | Trypanosomatidae | 26% | 76% |
A0A1X0NPY2 | Trypanosomatidae | 28% | 95% |
A0A3R7KBB6 | Trypanosoma rangeli | 26% | 78% |
A0A3R7R8G4 | Trypanosoma rangeli | 26% | 67% |
A0A422MVE8 | Trypanosoma rangeli | 27% | 100% |
A0A422NJL1 | Trypanosoma rangeli | 26% | 89% |
A4HX88 | Leishmania infantum | 52% | 76% |
C9ZM85 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZN42 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
C9ZN86 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 91% |
C9ZQ91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 74% |
C9ZTS3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
C9ZUG1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E8NHJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 62% | 80% |
V5AW53 | Trypanosoma cruzi | 28% | 85% |