Uncharacterized Protein, Uncharacterized
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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | yes | yes: 6, no: 5 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005886 | plasma membrane | 3 | 8 |
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
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: A4IA41
Term | Name | Level | Count |
---|---|---|---|
GO:0010960 | magnesium ion homeostasis | 8 | 12 |
GO:0042592 | homeostatic process | 3 | 12 |
GO:0048878 | chemical homeostasis | 4 | 12 |
GO:0050801 | monoatomic ion homeostasis | 5 | 12 |
GO:0055065 | obsolete metal ion homeostasis | 7 | 12 |
GO:0055080 | monoatomic cation homeostasis | 6 | 12 |
GO:0065007 | biological regulation | 1 | 12 |
GO:0065008 | regulation of biological quality | 2 | 12 |
GO:0072507 | obsolete divalent inorganic cation homeostasis | 7 | 12 |
GO:0098771 | inorganic ion homeostasis | 6 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 73 | 77 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 347 | 349 | PF00675 | 0.479 |
CLV_NRD_NRD_1 | 443 | 445 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.506 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.605 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 347 | 349 | PF00082 | 0.493 |
CLV_PCSK_KEX2_1 | 432 | 434 | PF00082 | 0.610 |
CLV_PCSK_KEX2_1 | 443 | 445 | PF00082 | 0.517 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.550 |
CLV_PCSK_PC1ET2_1 | 432 | 434 | PF00082 | 0.624 |
CLV_PCSK_SKI1_1 | 240 | 244 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 325 | 329 | PF00082 | 0.485 |
CLV_PCSK_SKI1_1 | 337 | 341 | PF00082 | 0.462 |
CLV_Separin_Metazoa | 577 | 581 | PF03568 | 0.351 |
DEG_APCC_DBOX_1 | 11 | 19 | PF00400 | 0.593 |
DEG_APCC_DBOX_1 | 234 | 242 | PF00400 | 0.212 |
DEG_COP1_1 | 549 | 557 | PF00400 | 0.304 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.471 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.279 |
DOC_MAPK_gen_1 | 10 | 17 | PF00069 | 0.702 |
DOC_MAPK_gen_1 | 21 | 29 | PF00069 | 0.472 |
DOC_MAPK_MEF2A_6 | 10 | 17 | PF00069 | 0.537 |
DOC_MAPK_MEF2A_6 | 198 | 205 | PF00069 | 0.284 |
DOC_MAPK_MEF2A_6 | 315 | 323 | PF00069 | 0.264 |
DOC_MAPK_MEF2A_6 | 337 | 344 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 530 | 537 | PF00069 | 0.323 |
DOC_MAPK_NFAT4_5 | 10 | 18 | PF00069 | 0.532 |
DOC_MAPK_NFAT4_5 | 530 | 538 | PF00069 | 0.304 |
DOC_PP1_RVXF_1 | 237 | 244 | PF00149 | 0.212 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.580 |
DOC_PP2B_LxvP_1 | 552 | 555 | PF13499 | 0.319 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.226 |
DOC_USP7_MATH_1 | 490 | 494 | PF00917 | 0.446 |
DOC_USP7_MATH_1 | 547 | 551 | PF00917 | 0.338 |
DOC_USP7_UBL2_3 | 223 | 227 | PF12436 | 0.314 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.291 |
LIG_14-3-3_CanoR_1 | 10 | 16 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 22 | 28 | PF00244 | 0.572 |
LIG_14-3-3_CanoR_1 | 55 | 59 | PF00244 | 0.305 |
LIG_14-3-3_CanoR_1 | 601 | 606 | PF00244 | 0.430 |
LIG_APCC_ABBA_1 | 504 | 509 | PF00400 | 0.376 |
LIG_BIR_III_4 | 76 | 80 | PF00653 | 0.381 |
LIG_BRCT_BRCA1_1 | 405 | 409 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_1 | 512 | 516 | PF00533 | 0.266 |
LIG_BRCT_BRCA1_1 | 549 | 553 | PF00533 | 0.353 |
LIG_Clathr_ClatBox_1 | 104 | 108 | PF01394 | 0.514 |
LIG_Clathr_ClatBox_1 | 393 | 397 | PF01394 | 0.248 |
LIG_Clathr_ClatBox_1 | 83 | 87 | PF01394 | 0.330 |
LIG_EH1_1 | 387 | 395 | PF00400 | 0.256 |
LIG_eIF4E_1 | 388 | 394 | PF01652 | 0.254 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.422 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.265 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.480 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.328 |
LIG_FHA_1 | 334 | 340 | PF00498 | 0.277 |
LIG_FHA_1 | 354 | 360 | PF00498 | 0.165 |
LIG_FHA_1 | 515 | 521 | PF00498 | 0.244 |
LIG_FHA_1 | 543 | 549 | PF00498 | 0.332 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.273 |
LIG_FHA_2 | 270 | 276 | PF00498 | 0.275 |
LIG_FHA_2 | 393 | 399 | PF00498 | 0.244 |
LIG_FHA_2 | 44 | 50 | PF00498 | 0.316 |
LIG_LIR_Gen_1 | 513 | 524 | PF02991 | 0.249 |
LIG_LIR_Gen_1 | 539 | 548 | PF02991 | 0.260 |
LIG_LIR_Gen_1 | 573 | 581 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 78 | 86 | PF02991 | 0.314 |
LIG_LIR_LC3C_4 | 517 | 520 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 385 | 390 | PF02991 | 0.296 |
LIG_LIR_Nem_3 | 406 | 412 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 513 | 519 | PF02991 | 0.248 |
LIG_LIR_Nem_3 | 539 | 543 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.335 |
LIG_NRBOX | 28 | 34 | PF00104 | 0.416 |
LIG_PCNA_yPIPBox_3 | 134 | 145 | PF02747 | 0.412 |
LIG_PDZ_Class_3 | 603 | 608 | PF00595 | 0.436 |
LIG_Pex14_2 | 206 | 210 | PF04695 | 0.250 |
LIG_Pex14_2 | 553 | 557 | PF04695 | 0.309 |
LIG_Pex14_2 | 93 | 97 | PF04695 | 0.265 |
LIG_SH2_STAP1 | 126 | 130 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 364 | 367 | PF00017 | 0.272 |
LIG_SH2_STAT5 | 575 | 578 | PF00017 | 0.361 |
LIG_SH3_3 | 210 | 216 | PF00018 | 0.309 |
LIG_SH3_3 | 273 | 279 | PF00018 | 0.271 |
LIG_SH3_3 | 484 | 490 | PF00018 | 0.305 |
LIG_SUMO_SIM_anti_2 | 101 | 106 | PF11976 | 0.118 |
LIG_SUMO_SIM_anti_2 | 111 | 118 | PF11976 | 0.412 |
LIG_SUMO_SIM_anti_2 | 258 | 263 | PF11976 | 0.285 |
LIG_SUMO_SIM_anti_2 | 26 | 31 | PF11976 | 0.562 |
LIG_SUMO_SIM_anti_2 | 336 | 342 | PF11976 | 0.272 |
LIG_SUMO_SIM_anti_2 | 370 | 377 | PF11976 | 0.265 |
LIG_SUMO_SIM_anti_2 | 82 | 88 | PF11976 | 0.245 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.412 |
LIG_SUMO_SIM_par_1 | 281 | 287 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 516 | 521 | PF11976 | 0.253 |
LIG_SUMO_SIM_par_1 | 82 | 88 | PF11976 | 0.316 |
LIG_SxIP_EBH_1 | 303 | 314 | PF03271 | 0.305 |
LIG_TYR_ITIM | 447 | 452 | PF00017 | 0.299 |
LIG_UBA3_1 | 358 | 363 | PF00899 | 0.265 |
LIG_WRC_WIRS_1 | 554 | 559 | PF05994 | 0.287 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.367 |
MOD_CK1_1 | 439 | 445 | PF00069 | 0.410 |
MOD_CK1_1 | 514 | 520 | PF00069 | 0.359 |
MOD_CK1_1 | 587 | 593 | PF00069 | 0.436 |
MOD_CK2_1 | 115 | 121 | PF00069 | 0.418 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.374 |
MOD_CK2_1 | 43 | 49 | PF00069 | 0.354 |
MOD_CK2_1 | 459 | 465 | PF00069 | 0.341 |
MOD_Cter_Amidation | 19 | 22 | PF01082 | 0.637 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.212 |
MOD_GlcNHglycan | 18 | 21 | PF01048 | 0.544 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.217 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.237 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.522 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.647 |
MOD_GlcNHglycan | 469 | 474 | PF01048 | 0.615 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.500 |
MOD_GlcNHglycan | 594 | 597 | PF01048 | 0.633 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.601 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.250 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.272 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.379 |
MOD_GSK3_1 | 510 | 517 | PF00069 | 0.287 |
MOD_GSK3_1 | 538 | 545 | PF00069 | 0.363 |
MOD_GSK3_1 | 587 | 594 | PF00069 | 0.450 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.356 |
MOD_N-GLC_1 | 425 | 430 | PF02516 | 0.689 |
MOD_NEK2_1 | 11 | 16 | PF00069 | 0.713 |
MOD_NEK2_1 | 140 | 145 | PF00069 | 0.250 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.250 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.601 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.525 |
MOD_NEK2_1 | 459 | 464 | PF00069 | 0.302 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.359 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.274 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.370 |
MOD_NEK2_2 | 555 | 560 | PF00069 | 0.257 |
MOD_PKA_1 | 601 | 607 | PF00069 | 0.397 |
MOD_PKA_2 | 11 | 17 | PF00069 | 0.472 |
MOD_PKA_2 | 54 | 60 | PF00069 | 0.346 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.423 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.269 |
MOD_Plk_1 | 293 | 299 | PF00069 | 0.304 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.361 |
MOD_Plk_1 | 479 | 485 | PF00069 | 0.318 |
MOD_Plk_1 | 563 | 569 | PF00069 | 0.273 |
MOD_Plk_2-3 | 108 | 114 | PF00069 | 0.412 |
MOD_Plk_2-3 | 117 | 123 | PF00069 | 0.442 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.270 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.312 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.118 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.259 |
MOD_Plk_4 | 25 | 31 | PF00069 | 0.479 |
MOD_Plk_4 | 269 | 275 | PF00069 | 0.269 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.336 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.365 |
MOD_Plk_4 | 563 | 569 | PF00069 | 0.265 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.295 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.296 |
MOD_SUMO_rev_2 | 234 | 241 | PF00179 | 0.212 |
MOD_SUMO_rev_2 | 354 | 359 | PF00179 | 0.256 |
MOD_SUMO_rev_2 | 385 | 393 | PF00179 | 0.272 |
MOD_SUMO_rev_2 | 594 | 604 | PF00179 | 0.443 |
TRG_DiLeu_BaEn_1 | 237 | 242 | PF01217 | 0.212 |
TRG_DiLeu_BaEn_1 | 295 | 300 | PF01217 | 0.310 |
TRG_DiLeu_BaEn_1 | 389 | 394 | PF01217 | 0.257 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.285 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 575 | 578 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 443 | 445 | PF00400 | 0.317 |
TRG_ER_diArg_1 | 485 | 488 | PF00400 | 0.399 |
TRG_NES_CRM1_1 | 275 | 290 | PF08389 | 0.311 |
TRG_Pf-PMV_PEXEL_1 | 134 | 139 | PF00026 | 0.212 |
TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.555 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0B7P9G0 | Drosophila melanogaster | 33% | 73% |
A0A0N1PDI6 | Leptomonas seymouri | 84% | 100% |
A0A0S4JSF9 | Bodo saltans | 69% | 100% |
A0A131MCZ8 | Caenorhabditis elegans | 31% | 76% |
A0A1X0PAL3 | Trypanosomatidae | 75% | 100% |
A0A3Q8IC75 | Leishmania donovani | 24% | 100% |
A0A3Q8IL77 | Leishmania donovani | 100% | 100% |
A0A3Q8ITK0 | Leishmania donovani | 23% | 100% |
A0A3S7WUR9 | Leishmania donovani | 29% | 82% |
A0A422NS01 | Trypanosoma rangeli | 71% | 100% |
A0JPA0 | Xenopus tropicalis | 36% | 79% |
A3QM97 | Caenorhabditis elegans | 31% | 75% |
A4HAY2 | Leishmania braziliensis | 90% | 99% |
A4HIN7 | Leishmania braziliensis | 23% | 100% |
A4HKU5 | Leishmania braziliensis | 23% | 100% |
A4HXP0 | Leishmania infantum | 30% | 82% |
A4I5Y4 | Leishmania infantum | 24% | 100% |
A4I8C4 | Leishmania infantum | 22% | 100% |
C9ZM59 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 69% | 100% |
D0A017 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 30% | 82% |
E9ARF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 82% |
E9B177 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B383 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 22% | 100% |
E9B555 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
P0C588 | Rattus norvegicus | 35% | 79% |
Q32NY4 | Mus musculus | 28% | 85% |
Q3TWN3 | Mus musculus | 35% | 69% |
Q4Q2T0 | Leishmania major | 96% | 100% |
Q4Q4X2 | Leishmania major | 22% | 100% |
Q4Q6Y7 | Leishmania major | 24% | 100% |
Q4QE28 | Leishmania major | 29% | 82% |
Q4QE29 | Leishmania major | 31% | 100% |
Q5U2P1 | Rattus norvegicus | 35% | 69% |
Q69ZF7 | Mus musculus | 36% | 79% |
Q6P4Q7 | Homo sapiens | 36% | 78% |
Q8NE01 | Homo sapiens | 27% | 86% |
Q9GYL2 | Caenorhabditis elegans | 29% | 80% |
Q9H8M5 | Homo sapiens | 35% | 69% |
V5BKR5 | Trypanosoma cruzi | 73% | 100% |