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: A4HBH2
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 | 135 | 139 | PF00656 | 0.199 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.451 |
CLV_NRD_NRD_1 | 340 | 342 | PF00675 | 0.327 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.270 |
CLV_PCSK_SKI1_1 | 3 | 7 | PF00082 | 0.364 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.321 |
DEG_SPOP_SBC_1 | 110 | 114 | PF00917 | 0.303 |
DEG_SPOP_SBC_1 | 482 | 486 | PF00917 | 0.293 |
DOC_CKS1_1 | 264 | 269 | PF01111 | 0.364 |
DOC_CKS1_1 | 456 | 461 | PF01111 | 0.568 |
DOC_CYCLIN_yCln2_LP_2 | 190 | 196 | PF00134 | 0.218 |
DOC_MAPK_gen_1 | 248 | 258 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 187 | 196 | PF00069 | 0.460 |
DOC_MAPK_MEF2A_6 | 251 | 260 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 507 | 514 | PF00069 | 0.570 |
DOC_MAPK_NFAT4_5 | 187 | 195 | PF00069 | 0.399 |
DOC_MAPK_NFAT4_5 | 507 | 515 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 213 | 219 | PF00149 | 0.301 |
DOC_PP2B_LxvP_1 | 107 | 110 | PF13499 | 0.485 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.218 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.334 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.351 |
DOC_USP7_MATH_1 | 231 | 235 | PF00917 | 0.290 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 319 | 323 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.362 |
DOC_USP7_MATH_1 | 482 | 486 | PF00917 | 0.293 |
DOC_USP7_MATH_1 | 526 | 530 | PF00917 | 0.369 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.334 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.418 |
DOC_WW_Pin1_4 | 303 | 308 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 180 | 186 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 323 | 329 | PF00244 | 0.364 |
LIG_Actin_WH2_2 | 167 | 182 | PF00022 | 0.237 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.384 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.279 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.279 |
LIG_BRCT_BRCA1_1 | 158 | 162 | PF00533 | 0.189 |
LIG_BRCT_BRCA1_1 | 237 | 241 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 28 | 32 | PF00533 | 0.494 |
LIG_BRCT_BRCA1_1 | 459 | 463 | PF00533 | 0.339 |
LIG_BRCT_BRCA1_1 | 528 | 532 | PF00533 | 0.388 |
LIG_CaM_NSCaTE_8 | 426 | 433 | PF13499 | 0.364 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.455 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.430 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.526 |
LIG_FHA_1 | 197 | 203 | PF00498 | 0.340 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.491 |
LIG_FHA_1 | 349 | 355 | PF00498 | 0.456 |
LIG_FHA_1 | 412 | 418 | PF00498 | 0.317 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.324 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.355 |
LIG_FHA_1 | 64 | 70 | PF00498 | 0.278 |
LIG_FHA_2 | 370 | 376 | PF00498 | 0.465 |
LIG_HCF-1_HBM_1 | 81 | 84 | PF13415 | 0.294 |
LIG_LIR_Apic_2 | 155 | 160 | PF02991 | 0.334 |
LIG_LIR_Apic_2 | 477 | 482 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 105 | 111 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 521 | 532 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 81 | 91 | PF02991 | 0.252 |
LIG_LIR_LC3C_4 | 468 | 473 | PF02991 | 0.361 |
LIG_LIR_Nem_3 | 105 | 109 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 159 | 165 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 173 | 179 | PF02991 | 0.206 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 238 | 244 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 375 | 381 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 521 | 527 | PF02991 | 0.377 |
LIG_NRBOX | 445 | 451 | PF00104 | 0.494 |
LIG_Pex14_2 | 201 | 205 | PF04695 | 0.335 |
LIG_Pex14_2 | 520 | 524 | PF04695 | 0.170 |
LIG_SH2_CRK | 378 | 382 | PF00017 | 0.494 |
LIG_SH2_CRK | 479 | 483 | PF00017 | 0.391 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.368 |
LIG_SH2_STAT3 | 370 | 373 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 380 | 383 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.334 |
LIG_SH3_3 | 261 | 267 | PF00018 | 0.364 |
LIG_SH3_3 | 301 | 307 | PF00018 | 0.448 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.568 |
LIG_Sin3_3 | 469 | 476 | PF02671 | 0.439 |
LIG_SUMO_SIM_anti_2 | 44 | 51 | PF11976 | 0.436 |
LIG_SUMO_SIM_anti_2 | 452 | 458 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 194 | 199 | PF11976 | 0.371 |
LIG_SUMO_SIM_par_1 | 350 | 356 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 39 | 44 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.324 |
LIG_TYR_ITIM | 126 | 131 | PF00017 | 0.170 |
LIG_UBA3_1 | 509 | 513 | PF00899 | 0.477 |
LIG_WRC_WIRS_1 | 14 | 19 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 202 | 207 | PF05994 | 0.288 |
LIG_WRC_WIRS_1 | 439 | 444 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 472 | 477 | PF05994 | 0.363 |
MOD_CDK_SPxK_1 | 455 | 461 | PF00069 | 0.493 |
MOD_CK1_1 | 113 | 119 | PF00069 | 0.303 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.359 |
MOD_CK1_1 | 322 | 328 | PF00069 | 0.456 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.276 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.349 |
MOD_CK1_1 | 60 | 66 | PF00069 | 0.302 |
MOD_CK2_1 | 350 | 356 | PF00069 | 0.526 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.442 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.421 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.345 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.280 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.378 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.330 |
MOD_GlcNHglycan | 467 | 470 | PF01048 | 0.327 |
MOD_GlcNHglycan | 528 | 531 | PF01048 | 0.346 |
MOD_GlcNHglycan | 62 | 65 | PF01048 | 0.491 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.471 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.458 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.345 |
MOD_GSK3_1 | 231 | 238 | PF00069 | 0.290 |
MOD_GSK3_1 | 298 | 305 | PF00069 | 0.507 |
MOD_GSK3_1 | 356 | 363 | PF00069 | 0.582 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.247 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.471 |
MOD_GSK3_1 | 483 | 490 | PF00069 | 0.317 |
MOD_GSK3_1 | 518 | 525 | PF00069 | 0.365 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.297 |
MOD_N-GLC_1 | 348 | 353 | PF02516 | 0.190 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.309 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.494 |
MOD_NEK2_1 | 369 | 374 | PF00069 | 0.494 |
MOD_NEK2_1 | 41 | 46 | PF00069 | 0.360 |
MOD_NEK2_1 | 471 | 476 | PF00069 | 0.349 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.388 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.384 |
MOD_NEK2_2 | 350 | 355 | PF00069 | 0.364 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.205 |
MOD_PIKK_1 | 369 | 375 | PF00454 | 0.364 |
MOD_PIKK_1 | 41 | 47 | PF00454 | 0.439 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.364 |
MOD_Plk_1 | 348 | 354 | PF00069 | 0.481 |
MOD_Plk_2-3 | 132 | 138 | PF00069 | 0.190 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.354 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.361 |
MOD_Plk_4 | 152 | 158 | PF00069 | 0.320 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.307 |
MOD_Plk_4 | 407 | 413 | PF00069 | 0.199 |
MOD_Plk_4 | 418 | 424 | PF00069 | 0.182 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.334 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.418 |
MOD_ProDKin_1 | 303 | 309 | PF00069 | 0.471 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.493 |
TRG_DiLeu_BaLyEn_6 | 240 | 245 | PF01217 | 0.319 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.464 |
TRG_ENDOCYTIC_2 | 128 | 131 | PF00928 | 0.205 |
TRG_ENDOCYTIC_2 | 378 | 381 | PF00928 | 0.461 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.330 |
TRG_Pf-PMV_PEXEL_1 | 448 | 452 | PF00026 | 0.250 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S5 | Leptomonas seymouri | 70% | 100% |
A0A1X0NXY5 | Trypanosomatidae | 58% | 100% |
A0A3Q8I8Y3 | Leishmania donovani | 61% | 100% |
A0A3Q8IBK1 | Leishmania donovani | 80% | 100% |
A0A3R7K4N2 | Trypanosoma rangeli | 52% | 100% |
A0A3R7L5P3 | Trypanosoma rangeli | 26% | 90% |
A0A3S5H545 | Leishmania donovani | 46% | 95% |
A1A4I1 | Bos taurus | 28% | 84% |
A4H5Y5 | Leishmania braziliensis | 61% | 91% |
A4H6C2 | Leishmania braziliensis | 61% | 91% |
A4HH06 | Leishmania braziliensis | 45% | 97% |
A4HUP5 | Leishmania infantum | 61% | 100% |
A4HYJ6 | Leishmania infantum | 80% | 100% |
C9ZHT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
C9ZHU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 100% |
E9ACJ5 | Leishmania major | 45% | 100% |
E9AG39 | Leishmania infantum | 46% | 95% |
E9AJT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 100% |
E9AN09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 100% |
E9ANE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 60% | 100% |
E9AUE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 95% |
P0AFJ7 | Escherichia coli (strain K12) | 22% | 100% |
P0AFJ8 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 22% | 100% |
P0AFJ9 | Escherichia coli O157:H7 | 22% | 100% |
P15710 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 30% | 92% |
P38361 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 94% |
Q4QH82 | Leishmania major | 61% | 91% |
Q4QHL7 | Leishmania major | 61% | 91% |
Q6NV12 | Danio rerio | 29% | 83% |
V5DS90 | Trypanosoma cruzi | 55% | 100% |