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: 3 |
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: 23 |
NetGPI | no | yes: 0, no: 23 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 24 |
GO:0110165 | cellular anatomical entity | 1 | 24 |
Related structures:
AlphaFold database: E9ACJ5
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 24 |
GO:0006811 | monoatomic ion transport | 4 | 24 |
GO:0006817 | phosphate ion transport | 7 | 24 |
GO:0006820 | monoatomic anion transport | 5 | 24 |
GO:0009987 | cellular process | 1 | 4 |
GO:0015698 | inorganic anion transport | 6 | 24 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 4 |
GO:0035435 | phosphate ion transmembrane transport | 6 | 4 |
GO:0051179 | localization | 1 | 24 |
GO:0051234 | establishment of localization | 2 | 24 |
GO:0055085 | transmembrane transport | 2 | 4 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 4 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 4 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 4 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 24 |
GO:0005315 | inorganic phosphate transmembrane transporter activity | 4 | 24 |
GO:0015291 | secondary active transmembrane transporter activity | 4 | 24 |
GO:0015293 | symporter activity | 5 | 24 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 24 |
GO:0022804 | active transmembrane transporter activity | 3 | 24 |
GO:0022857 | transmembrane transporter activity | 2 | 24 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 351 | 355 | PF00656 | 0.535 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.511 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.228 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.239 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.180 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.169 |
CLV_NRD_NRD_1 | 530 | 532 | PF00675 | 0.235 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.274 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.208 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.180 |
CLV_PCSK_KEX2_1 | 530 | 532 | PF00082 | 0.300 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.336 |
CLV_PCSK_SKI1_1 | 140 | 144 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.169 |
CLV_PCSK_SKI1_1 | 329 | 333 | PF00082 | 0.347 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.316 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.329 |
DEG_ODPH_VHL_1 | 187 | 200 | PF01847 | 0.416 |
DEG_SPOP_SBC_1 | 508 | 512 | PF00917 | 0.288 |
DOC_CKS1_1 | 482 | 487 | PF01111 | 0.564 |
DOC_CYCLIN_RxL_1 | 172 | 182 | PF00134 | 0.243 |
DOC_CYCLIN_RxL_1 | 329 | 338 | PF00134 | 0.403 |
DOC_MAPK_DCC_7 | 186 | 196 | PF00069 | 0.416 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.520 |
DOC_MAPK_gen_1 | 530 | 538 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 39 | 48 | PF00069 | 0.504 |
DOC_MAPK_MEF2A_6 | 531 | 540 | PF00069 | 0.562 |
DOC_MAPK_RevD_3 | 232 | 248 | PF00069 | 0.326 |
DOC_MAPK_RevD_3 | 518 | 531 | PF00069 | 0.361 |
DOC_PP1_RVXF_1 | 213 | 219 | PF00149 | 0.297 |
DOC_PP1_RVXF_1 | 528 | 535 | PF00149 | 0.283 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.329 |
DOC_PP4_FxxP_1 | 468 | 471 | PF00568 | 0.243 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.329 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.300 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.457 |
DOC_USP7_MATH_1 | 364 | 368 | PF00917 | 0.533 |
DOC_USP7_MATH_1 | 413 | 417 | PF00917 | 0.319 |
DOC_USP7_MATH_1 | 418 | 422 | PF00917 | 0.337 |
DOC_USP7_MATH_1 | 508 | 512 | PF00917 | 0.288 |
DOC_USP7_MATH_1 | 568 | 572 | PF00917 | 0.531 |
DOC_USP7_MATH_2 | 317 | 323 | PF00917 | 0.403 |
DOC_USP7_UBL2_3 | 300 | 304 | PF12436 | 0.416 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.329 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.525 |
DOC_WW_Pin1_4 | 481 | 486 | PF00397 | 0.488 |
LIG_14-3-3_CanoR_1 | 213 | 219 | PF00244 | 0.304 |
LIG_14-3-3_CanoR_1 | 279 | 286 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.525 |
LIG_BRCT_BRCA1_1 | 554 | 558 | PF00533 | 0.384 |
LIG_CaM_NSCaTE_8 | 452 | 459 | PF13499 | 0.359 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.515 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.480 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.313 |
LIG_FHA_1 | 465 | 471 | PF00498 | 0.318 |
LIG_FHA_1 | 493 | 499 | PF00498 | 0.328 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.356 |
LIG_FHA_1 | 545 | 551 | PF00498 | 0.337 |
LIG_FHA_2 | 375 | 381 | PF00498 | 0.528 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.203 |
LIG_GBD_Chelix_1 | 194 | 202 | PF00786 | 0.352 |
LIG_GBD_Chelix_1 | 493 | 501 | PF00786 | 0.243 |
LIG_HP1_1 | 193 | 197 | PF01393 | 0.177 |
LIG_HP1_1 | 83 | 87 | PF01393 | 0.237 |
LIG_LIR_Apic_2 | 155 | 160 | PF02991 | 0.329 |
LIG_LIR_Apic_2 | 467 | 471 | PF02991 | 0.243 |
LIG_LIR_Apic_2 | 503 | 508 | PF02991 | 0.345 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 380 | 388 | PF02991 | 0.394 |
LIG_LIR_Gen_1 | 81 | 91 | PF02991 | 0.248 |
LIG_LIR_Gen_1 | 97 | 107 | PF02991 | 0.387 |
LIG_LIR_LC3C_4 | 495 | 499 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 147 | 152 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 380 | 386 | PF02991 | 0.529 |
LIG_LIR_Nem_3 | 401 | 407 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 526 | 532 | PF02991 | 0.319 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.375 |
LIG_MYND_1 | 189 | 193 | PF01753 | 0.416 |
LIG_NRP_CendR_1 | 569 | 572 | PF00754 | 0.568 |
LIG_Pex14_2 | 200 | 204 | PF04695 | 0.332 |
LIG_SH2_CRK | 342 | 346 | PF00017 | 0.403 |
LIG_SH2_CRK | 431 | 435 | PF00017 | 0.216 |
LIG_SH2_CRK | 505 | 509 | PF00017 | 0.387 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 431 | 435 | PF00017 | 0.216 |
LIG_SH2_SRC | 388 | 391 | PF00017 | 0.416 |
LIG_SH2_STAP1 | 431 | 435 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.436 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.538 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.330 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.408 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.564 |
LIG_Sin3_3 | 166 | 173 | PF02671 | 0.213 |
LIG_SUMO_SIM_anti_2 | 233 | 238 | PF11976 | 0.371 |
LIG_SUMO_SIM_anti_2 | 478 | 484 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 150 | 155 | PF11976 | 0.312 |
LIG_SUMO_SIM_par_1 | 497 | 504 | PF11976 | 0.319 |
LIG_SUMO_SIM_par_1 | 518 | 523 | PF11976 | 0.345 |
LIG_SUMO_SIM_par_1 | 546 | 551 | PF11976 | 0.356 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.416 |
LIG_TYR_ITIM | 340 | 345 | PF00017 | 0.403 |
LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.319 |
LIG_UBA3_1 | 472 | 479 | PF00899 | 0.512 |
LIG_WRC_WIRS_1 | 283 | 288 | PF05994 | 0.416 |
LIG_WRC_WIRS_1 | 465 | 470 | PF05994 | 0.387 |
LIG_WRC_WIRS_1 | 76 | 81 | PF05994 | 0.203 |
MOD_CDK_SPxK_1 | 481 | 487 | PF00069 | 0.488 |
MOD_CK1_1 | 217 | 223 | PF00069 | 0.194 |
MOD_CK1_1 | 282 | 288 | PF00069 | 0.503 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.578 |
MOD_CK1_1 | 500 | 506 | PF00069 | 0.345 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.524 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.207 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.416 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.592 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.533 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.327 |
MOD_GlcNHglycan | 389 | 393 | PF01048 | 0.374 |
MOD_GlcNHglycan | 444 | 447 | PF01048 | 0.533 |
MOD_GlcNHglycan | 54 | 58 | PF01048 | 0.400 |
MOD_GlcNHglycan | 554 | 557 | PF01048 | 0.342 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.470 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.340 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.528 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.547 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.443 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.527 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.243 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.315 |
MOD_GSK3_1 | 497 | 504 | PF00069 | 0.384 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.328 |
MOD_GSK3_1 | 544 | 551 | PF00069 | 0.361 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.345 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.363 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.215 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.530 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.297 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.465 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.490 |
MOD_NEK2_1 | 497 | 502 | PF00069 | 0.345 |
MOD_NEK2_1 | 520 | 525 | PF00069 | 0.243 |
MOD_NEK2_1 | 548 | 553 | PF00069 | 0.379 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.303 |
MOD_PK_1 | 248 | 254 | PF00069 | 0.403 |
MOD_PK_1 | 279 | 285 | PF00069 | 0.403 |
MOD_PKA_2 | 214 | 220 | PF00069 | 0.203 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.574 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.522 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.416 |
MOD_Plk_2-3 | 348 | 354 | PF00069 | 0.530 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.407 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.348 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.329 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.499 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.525 |
MOD_ProDKin_1 | 481 | 487 | PF00069 | 0.488 |
MOD_SUMO_for_1 | 313 | 316 | PF00179 | 0.403 |
MOD_SUMO_rev_2 | 376 | 383 | PF00179 | 0.369 |
TRG_AP2beta_CARGO_1 | 203 | 213 | PF09066 | 0.177 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 471 | 476 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 342 | 345 | PF00928 | 0.403 |
TRG_ENDOCYTIC_2 | 431 | 434 | PF00928 | 0.217 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.321 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.332 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.326 |
TRG_ER_diArg_1 | 213 | 216 | PF00400 | 0.169 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 529 | 531 | PF00400 | 0.511 |
TRG_NLS_Bipartite_1 | 289 | 307 | PF00514 | 0.369 |
TRG_NLS_MonoExtC_3 | 302 | 307 | PF00514 | 0.369 |
TRG_NLS_MonoExtN_4 | 300 | 307 | PF00514 | 0.369 |
TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.216 |
TRG_Pf-PMV_PEXEL_1 | 474 | 478 | PF00026 | 0.246 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S5 | Leptomonas seymouri | 49% | 100% |
A0A0S4JEW4 | Bodo saltans | 26% | 90% |
A0A1X0NXY5 | Trypanosomatidae | 47% | 100% |
A0A1X0P0T2 | Trypanosomatidae | 25% | 87% |
A0A3Q8I8Y3 | Leishmania donovani | 48% | 100% |
A0A3Q8IBK1 | Leishmania donovani | 46% | 100% |
A0A3R7K4N2 | Trypanosoma rangeli | 44% | 100% |
A0A3R7L5P3 | Trypanosoma rangeli | 25% | 95% |
A0A3S5H545 | Leishmania donovani | 96% | 100% |
A4H5Y5 | Leishmania braziliensis | 47% | 100% |
A4H6C2 | Leishmania braziliensis | 47% | 100% |
A4HBH2 | Leishmania braziliensis | 45% | 100% |
A4HH06 | Leishmania braziliensis | 80% | 100% |
A4HUP5 | Leishmania infantum | 48% | 100% |
A4HYJ6 | Leishmania infantum | 46% | 100% |
C9ZHT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
C9ZHU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
E9AG39 | Leishmania infantum | 96% | 100% |
E9AJT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
E9AN09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9ANE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 47% | 100% |
E9AUE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
P15710 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 97% |
P38361 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q08357 | Homo sapiens | 26% | 88% |
Q28E01 | Xenopus tropicalis | 28% | 88% |
Q4QH82 | Leishmania major | 49% | 100% |
Q4QHL7 | Leishmania major | 49% | 100% |
Q80UP8 | Mus musculus | 28% | 87% |
V5DS90 | Trypanosoma cruzi | 45% | 100% |