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: E9AUE3
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:0015698 | inorganic anion transport | 6 | 24 |
GO:0051179 | localization | 1 | 24 |
GO:0051234 | establishment of localization | 2 | 24 |
GO:0009987 | cellular process | 1 | 3 |
GO:0034220 | monoatomic ion transmembrane transport | 3 | 3 |
GO:0035435 | phosphate ion transmembrane transport | 6 | 3 |
GO:0055085 | transmembrane transport | 2 | 3 |
GO:0098656 | monoatomic anion transmembrane transport | 4 | 3 |
GO:0098660 | inorganic ion transmembrane transport | 4 | 3 |
GO:0098661 | inorganic anion transmembrane transport | 5 | 3 |
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 | 134 | 138 | PF00656 | 0.199 |
CLV_C14_Caspase3-7 | 343 | 347 | PF00656 | 0.542 |
CLV_C14_Caspase3-7 | 53 | 57 | PF00656 | 0.163 |
CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.225 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.329 |
CLV_NRD_NRD_1 | 548 | 550 | PF00675 | 0.620 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.269 |
CLV_PCSK_KEX2_1 | 322 | 324 | PF00082 | 0.186 |
CLV_PCSK_KEX2_1 | 548 | 550 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 566 | 568 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 245 | 247 | PF00082 | 0.321 |
CLV_PCSK_PC1ET2_1 | 566 | 568 | PF00082 | 0.511 |
CLV_PCSK_PC7_1 | 562 | 568 | PF00082 | 0.503 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 202 | 206 | PF00082 | 0.278 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.321 |
CLV_PCSK_SKI1_1 | 566 | 570 | PF00082 | 0.511 |
DEG_SCF_FBW7_1 | 299 | 305 | PF00400 | 0.360 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.303 |
DEG_SPOP_SBC_1 | 416 | 420 | PF00917 | 0.274 |
DEG_SPOP_SBC_1 | 481 | 485 | PF00917 | 0.349 |
DOC_CKS1_1 | 299 | 304 | PF01111 | 0.360 |
DOC_CKS1_1 | 455 | 460 | PF01111 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 189 | 195 | PF00134 | 0.218 |
DOC_MAPK_MEF2A_6 | 186 | 195 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 506 | 513 | PF00069 | 0.570 |
DOC_MAPK_NFAT4_5 | 186 | 194 | PF00069 | 0.399 |
DOC_MAPK_NFAT4_5 | 506 | 514 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 212 | 218 | PF00149 | 0.301 |
DOC_PP2B_LxvP_1 | 106 | 109 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 189 | 192 | PF13499 | 0.218 |
DOC_PP4_FxxP_1 | 156 | 159 | PF00568 | 0.334 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 302 | 306 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.434 |
DOC_USP7_MATH_1 | 406 | 410 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 481 | 485 | PF00917 | 0.349 |
DOC_USP7_MATH_1 | 525 | 529 | PF00917 | 0.369 |
DOC_USP7_UBL2_3 | 245 | 249 | PF12436 | 0.386 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 298 | 303 | PF00397 | 0.475 |
DOC_WW_Pin1_4 | 307 | 312 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 454 | 459 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 179 | 185 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 186 | 192 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 261 | 267 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 541 | 550 | PF00244 | 0.316 |
LIG_Actin_WH2_2 | 166 | 181 | PF00022 | 0.237 |
LIG_BRCT_BRCA1_1 | 236 | 240 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 458 | 462 | PF00533 | 0.338 |
LIG_BRCT_BRCA1_1 | 527 | 531 | PF00533 | 0.388 |
LIG_CaM_NSCaTE_8 | 425 | 432 | PF13499 | 0.364 |
LIG_FHA_1 | 105 | 111 | PF00498 | 0.455 |
LIG_FHA_1 | 160 | 166 | PF00498 | 0.430 |
LIG_FHA_1 | 188 | 194 | PF00498 | 0.526 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.340 |
LIG_FHA_1 | 411 | 417 | PF00498 | 0.317 |
LIG_FHA_1 | 422 | 428 | PF00498 | 0.384 |
LIG_FHA_1 | 438 | 444 | PF00498 | 0.323 |
LIG_FHA_1 | 483 | 489 | PF00498 | 0.355 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.341 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.278 |
LIG_FHA_2 | 369 | 375 | PF00498 | 0.465 |
LIG_HCF-1_HBM_1 | 80 | 83 | PF13415 | 0.294 |
LIG_LIR_Apic_2 | 154 | 159 | PF02991 | 0.334 |
LIG_LIR_Apic_2 | 476 | 481 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 104 | 110 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 384 | 394 | PF02991 | 0.163 |
LIG_LIR_Gen_1 | 80 | 90 | PF02991 | 0.252 |
LIG_LIR_LC3C_4 | 467 | 472 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 104 | 108 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 237 | 243 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 374 | 380 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.313 |
LIG_NRBOX | 444 | 450 | PF00104 | 0.494 |
LIG_Pex14_1 | 542 | 546 | PF04695 | 0.315 |
LIG_Pex14_2 | 200 | 204 | PF04695 | 0.335 |
LIG_REV1ctd_RIR_1 | 197 | 206 | PF16727 | 0.163 |
LIG_SH2_CRK | 377 | 381 | PF00017 | 0.494 |
LIG_SH2_CRK | 478 | 482 | PF00017 | 0.391 |
LIG_SH2_CRK | 87 | 91 | PF00017 | 0.368 |
LIG_SH2_NCK_1 | 316 | 320 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 369 | 373 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 387 | 391 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 278 | 281 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 379 | 382 | PF00017 | 0.334 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.390 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.460 |
LIG_SH3_3 | 452 | 458 | PF00018 | 0.568 |
LIG_Sin3_3 | 468 | 475 | PF02671 | 0.439 |
LIG_SUMO_SIM_anti_2 | 451 | 457 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 193 | 198 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 280 | 290 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 39 | 44 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 519 | 524 | PF11976 | 0.360 |
LIG_UBA3_1 | 193 | 202 | PF00899 | 0.163 |
LIG_WRC_WIRS_1 | 14 | 19 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 387 | 392 | PF05994 | 0.323 |
LIG_WRC_WIRS_1 | 438 | 443 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 471 | 476 | PF05994 | 0.363 |
MOD_CDK_SPxK_1 | 454 | 460 | PF00069 | 0.493 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.303 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.487 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.470 |
MOD_CK1_1 | 334 | 340 | PF00069 | 0.461 |
MOD_CK1_1 | 395 | 401 | PF00069 | 0.276 |
MOD_CK1_1 | 473 | 479 | PF00069 | 0.349 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.160 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.442 |
MOD_CK2_1 | 368 | 374 | PF00069 | 0.421 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.345 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.322 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.205 |
MOD_GlcNHglycan | 462 | 465 | PF01048 | 0.330 |
MOD_GlcNHglycan | 466 | 469 | PF01048 | 0.327 |
MOD_GlcNHglycan | 475 | 478 | PF01048 | 0.293 |
MOD_GlcNHglycan | 527 | 530 | PF01048 | 0.346 |
MOD_GlcNHglycan | 553 | 556 | PF01048 | 0.526 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.471 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.458 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.204 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.344 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.512 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.390 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.247 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.283 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.471 |
MOD_GSK3_1 | 482 | 489 | PF00069 | 0.316 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.365 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.343 |
MOD_GSK3_1 | 537 | 544 | PF00069 | 0.275 |
MOD_GSK3_1 | 556 | 563 | PF00069 | 0.298 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.297 |
MOD_LATS_1 | 560 | 566 | PF00433 | 0.301 |
MOD_NEK2_1 | 18 | 23 | PF00069 | 0.333 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.494 |
MOD_NEK2_1 | 368 | 373 | PF00069 | 0.494 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.359 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.433 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.349 |
MOD_NEK2_1 | 521 | 526 | PF00069 | 0.384 |
MOD_NEK2_2 | 406 | 411 | PF00069 | 0.205 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.160 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.439 |
MOD_PKB_1 | 549 | 557 | PF00069 | 0.314 |
MOD_Plk_1 | 324 | 330 | PF00069 | 0.360 |
MOD_Plk_4 | 101 | 107 | PF00069 | 0.354 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.361 |
MOD_Plk_4 | 151 | 157 | PF00069 | 0.320 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.433 |
MOD_Plk_4 | 406 | 412 | PF00069 | 0.199 |
MOD_Plk_4 | 417 | 423 | PF00069 | 0.182 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.249 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.334 |
MOD_ProDKin_1 | 298 | 304 | PF00069 | 0.475 |
MOD_ProDKin_1 | 307 | 313 | PF00069 | 0.522 |
MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.471 |
MOD_ProDKin_1 | 454 | 460 | PF00069 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 156 | 161 | PF01217 | 0.323 |
TRG_DiLeu_BaLyEn_6 | 239 | 244 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 444 | 449 | PF01217 | 0.464 |
TRG_DiLeu_BaLyEn_6 | 564 | 569 | PF01217 | 0.305 |
TRG_ENDOCYTIC_2 | 377 | 380 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.310 |
TRG_ENDOCYTIC_2 | 83 | 86 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 246 | 248 | PF00400 | 0.429 |
TRG_ER_diArg_1 | 548 | 551 | PF00400 | 0.325 |
TRG_NLS_MonoExtC_3 | 244 | 249 | PF00514 | 0.433 |
TRG_NLS_MonoExtN_4 | 242 | 249 | PF00514 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 447 | 451 | PF00026 | 0.250 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S5 | Leptomonas seymouri | 68% | 100% |
A0A0S4JEW4 | Bodo saltans | 24% | 90% |
A0A1X0NXY5 | Trypanosomatidae | 57% | 100% |
A0A3Q8I8Y3 | Leishmania donovani | 61% | 100% |
A0A3Q8IBK1 | Leishmania donovani | 89% | 100% |
A0A3R7K4N2 | Trypanosoma rangeli | 52% | 100% |
A0A3S5H545 | Leishmania donovani | 47% | 100% |
A4H5Y5 | Leishmania braziliensis | 61% | 91% |
A4H6C2 | Leishmania braziliensis | 61% | 91% |
A4HBH2 | Leishmania braziliensis | 78% | 100% |
A4HH06 | Leishmania braziliensis | 45% | 100% |
A4HUP5 | Leishmania infantum | 61% | 100% |
A4HYJ6 | Leishmania infantum | 89% | 100% |
C9ZHT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
C9ZHU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
E9ACJ5 | Leishmania major | 46% | 100% |
E9AG39 | Leishmania infantum | 47% | 100% |
E9AJT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 91% |
E9ANE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 91% |
P0AFJ7 | Escherichia coli (strain K12) | 23% | 100% |
P0AFJ8 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 23% | 100% |
P0AFJ9 | Escherichia coli O157:H7 | 23% | 100% |
P15710 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 31% | 97% |
P38361 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
P43676 | Escherichia coli (strain K12) | 22% | 100% |
Q4QH82 | Leishmania major | 61% | 91% |
Q4QHL7 | Leishmania major | 61% | 91% |
Q5R9L5 | Pongo abelii | 26% | 84% |
Q8WUM9 | Homo sapiens | 26% | 84% |
V5DS90 | Trypanosoma cruzi | 55% | 100% |