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: A4HH06
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 | 351 | 355 | PF00656 | 0.536 |
CLV_C14_Caspase3-7 | 358 | 362 | PF00656 | 0.468 |
CLV_NRD_NRD_1 | 138 | 140 | PF00675 | 0.512 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.181 |
CLV_NRD_NRD_1 | 305 | 307 | PF00675 | 0.171 |
CLV_PCSK_KEX2_1 | 246 | 248 | PF00082 | 0.275 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.181 |
CLV_PCSK_PC1ET2_1 | 246 | 248 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 213 | 217 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 306 | 310 | PF00082 | 0.161 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 522 | 526 | PF00082 | 0.211 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.323 |
DEG_ODPH_VHL_1 | 187 | 200 | PF01847 | 0.417 |
DEG_SPOP_SBC_1 | 497 | 501 | PF00917 | 0.290 |
DOC_CKS1_1 | 471 | 476 | PF01111 | 0.565 |
DOC_CYCLIN_RxL_1 | 172 | 182 | PF00134 | 0.245 |
DOC_CYCLIN_RxL_1 | 210 | 220 | PF00134 | 0.161 |
DOC_MAPK_DCC_7 | 186 | 196 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 246 | 254 | PF00069 | 0.522 |
DOC_MAPK_gen_1 | 520 | 527 | PF00069 | 0.447 |
DOC_MAPK_MEF2A_6 | 222 | 230 | PF00069 | 0.161 |
DOC_MAPK_MEF2A_6 | 39 | 48 | PF00069 | 0.506 |
DOC_MAPK_MEF2A_6 | 520 | 529 | PF00069 | 0.563 |
DOC_MAPK_NFAT4_5 | 522 | 530 | PF00069 | 0.561 |
DOC_MAPK_RevD_3 | 234 | 248 | PF00069 | 0.313 |
DOC_PP1_RVXF_1 | 518 | 524 | PF00149 | 0.433 |
DOC_PP4_FxxP_1 | 157 | 160 | PF00568 | 0.331 |
DOC_PP4_FxxP_1 | 457 | 460 | PF00568 | 0.245 |
DOC_USP7_MATH_1 | 110 | 114 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.331 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.473 |
DOC_USP7_MATH_1 | 363 | 367 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.338 |
DOC_USP7_MATH_1 | 497 | 501 | PF00917 | 0.290 |
DOC_USP7_UBL2_3 | 300 | 304 | PF12436 | 0.417 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.331 |
DOC_WW_Pin1_4 | 352 | 357 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 470 | 475 | PF00397 | 0.490 |
LIG_14-3-3_CanoR_1 | 139 | 144 | PF00244 | 0.161 |
LIG_14-3-3_CanoR_1 | 279 | 283 | PF00244 | 0.554 |
LIG_14-3-3_CanoR_1 | 364 | 372 | PF00244 | 0.448 |
LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.527 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.166 |
LIG_BRCT_BRCA1_1 | 543 | 547 | PF00533 | 0.385 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.517 |
LIG_FHA_1 | 313 | 319 | PF00498 | 0.493 |
LIG_FHA_1 | 427 | 433 | PF00498 | 0.313 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.311 |
LIG_FHA_1 | 482 | 488 | PF00498 | 0.329 |
LIG_FHA_1 | 491 | 497 | PF00498 | 0.347 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.357 |
LIG_FHA_1 | 534 | 540 | PF00498 | 0.338 |
LIG_GBD_Chelix_1 | 165 | 173 | PF00786 | 0.236 |
LIG_GBD_Chelix_1 | 482 | 490 | PF00786 | 0.245 |
LIG_HP1_1 | 83 | 87 | PF01393 | 0.239 |
LIG_LIR_Apic_2 | 155 | 160 | PF02991 | 0.331 |
LIG_LIR_Apic_2 | 456 | 460 | PF02991 | 0.245 |
LIG_LIR_Apic_2 | 492 | 497 | PF02991 | 0.346 |
LIG_LIR_Gen_1 | 203 | 212 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 82 | 91 | PF02991 | 0.245 |
LIG_LIR_Gen_1 | 97 | 106 | PF02991 | 0.389 |
LIG_LIR_LC3C_4 | 484 | 488 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 141 | 146 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 203 | 209 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 390 | 396 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.376 |
LIG_MYND_1 | 189 | 193 | PF01753 | 0.417 |
LIG_Pex14_2 | 197 | 201 | PF04695 | 0.331 |
LIG_Pex14_2 | 204 | 208 | PF04695 | 0.332 |
LIG_SH2_CRK | 420 | 424 | PF00017 | 0.217 |
LIG_SH2_CRK | 494 | 498 | PF00017 | 0.382 |
LIG_SH2_CRK | 88 | 92 | PF00017 | 0.365 |
LIG_SH2_NCK_1 | 420 | 424 | PF00017 | 0.217 |
LIG_SH2_SRC | 377 | 380 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 420 | 424 | PF00017 | 0.286 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 374 | 377 | PF00017 | 0.539 |
LIG_SH2_STAT5 | 5 | 8 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.282 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.331 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.410 |
LIG_SH3_3 | 468 | 474 | PF00018 | 0.565 |
LIG_SUMO_SIM_anti_2 | 467 | 473 | PF11976 | 0.565 |
LIG_SUMO_SIM_par_1 | 150 | 155 | PF11976 | 0.313 |
LIG_SUMO_SIM_par_1 | 45 | 51 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 486 | 493 | PF11976 | 0.320 |
LIG_SUMO_SIM_par_1 | 507 | 512 | PF11976 | 0.346 |
LIG_SUMO_SIM_par_1 | 535 | 540 | PF11976 | 0.357 |
LIG_TRAF2_1 | 260 | 263 | PF00917 | 0.495 |
LIG_TRAF2_1 | 317 | 320 | PF00917 | 0.417 |
LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.320 |
LIG_UBA3_1 | 461 | 468 | PF00899 | 0.513 |
LIG_UBA3_1 | 524 | 528 | PF00899 | 0.474 |
LIG_WRC_WIRS_1 | 283 | 288 | PF05994 | 0.417 |
LIG_WRC_WIRS_1 | 454 | 459 | PF05994 | 0.388 |
MOD_CDK_SPxK_1 | 470 | 476 | PF00069 | 0.490 |
MOD_CK1_1 | 335 | 341 | PF00069 | 0.467 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.580 |
MOD_CK1_1 | 489 | 495 | PF00069 | 0.333 |
MOD_CK2_1 | 48 | 54 | PF00069 | 0.342 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.209 |
MOD_Cter_Amidation | 137 | 140 | PF01082 | 0.417 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.594 |
MOD_GlcNHglycan | 162 | 165 | PF01048 | 0.442 |
MOD_GlcNHglycan | 219 | 222 | PF01048 | 0.576 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.301 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.329 |
MOD_GlcNHglycan | 378 | 382 | PF01048 | 0.376 |
MOD_GlcNHglycan | 543 | 546 | PF01048 | 0.343 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.471 |
MOD_GSK3_1 | 105 | 112 | PF00069 | 0.455 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.341 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.495 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.582 |
MOD_GSK3_1 | 31 | 38 | PF00069 | 0.445 |
MOD_GSK3_1 | 348 | 355 | PF00069 | 0.528 |
MOD_GSK3_1 | 397 | 404 | PF00069 | 0.245 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.317 |
MOD_GSK3_1 | 486 | 493 | PF00069 | 0.353 |
MOD_GSK3_1 | 498 | 505 | PF00069 | 0.326 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.362 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.346 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.365 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.216 |
MOD_NEK2_1 | 179 | 184 | PF00069 | 0.532 |
MOD_NEK2_1 | 216 | 221 | PF00069 | 0.322 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.491 |
MOD_NEK2_1 | 426 | 431 | PF00069 | 0.161 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.385 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.346 |
MOD_NEK2_1 | 509 | 514 | PF00069 | 0.245 |
MOD_NEK2_1 | 90 | 95 | PF00069 | 0.304 |
MOD_PIKK_1 | 287 | 293 | PF00454 | 0.376 |
MOD_PIKK_1 | 60 | 66 | PF00454 | 0.368 |
MOD_PKA_1 | 139 | 145 | PF00069 | 0.244 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.161 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.575 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.573 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.438 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.417 |
MOD_Plk_2-3 | 348 | 354 | PF00069 | 0.532 |
MOD_Plk_4 | 278 | 284 | PF00069 | 0.361 |
MOD_Plk_4 | 39 | 45 | PF00069 | 0.409 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.215 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.349 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.331 |
MOD_ProDKin_1 | 352 | 358 | PF00069 | 0.526 |
MOD_ProDKin_1 | 470 | 476 | PF00069 | 0.490 |
MOD_SUMO_rev_2 | 326 | 335 | PF00179 | 0.423 |
TRG_DiLeu_BaLyEn_6 | 157 | 162 | PF01217 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 391 | 396 | PF01217 | 0.361 |
TRG_DiLeu_BaLyEn_6 | 460 | 465 | PF01217 | 0.461 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 420 | 423 | PF00928 | 0.219 |
TRG_ENDOCYTIC_2 | 5 | 8 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.334 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.327 |
TRG_ER_diArg_1 | 247 | 249 | PF00400 | 0.434 |
TRG_ER_diArg_1 | 520 | 523 | PF00400 | 0.514 |
TRG_Pf-PMV_PEXEL_1 | 175 | 180 | PF00026 | 0.217 |
TRG_Pf-PMV_PEXEL_1 | 463 | 467 | PF00026 | 0.247 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S5 | Leptomonas seymouri | 49% | 100% |
A0A0S4JEW4 | Bodo saltans | 25% | 88% |
A0A1X0NXY5 | Trypanosomatidae | 49% | 100% |
A0A1X0P0T2 | Trypanosomatidae | 25% | 85% |
A0A3Q8I8Y3 | Leishmania donovani | 49% | 100% |
A0A3Q8IBK1 | Leishmania donovani | 47% | 100% |
A0A3R7K4N2 | Trypanosoma rangeli | 46% | 100% |
A0A3R7L5P3 | Trypanosoma rangeli | 25% | 94% |
A0A3S5H545 | Leishmania donovani | 80% | 98% |
A1A4I1 | Bos taurus | 28% | 87% |
A4H5Y5 | Leishmania braziliensis | 47% | 89% |
A4H6C2 | Leishmania braziliensis | 47% | 89% |
A4HBH2 | Leishmania braziliensis | 45% | 97% |
A4HUP5 | Leishmania infantum | 49% | 100% |
A4HYJ6 | Leishmania infantum | 47% | 100% |
C9ZHT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
C9ZHU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9ACJ5 | Leishmania major | 80% | 100% |
E9AG39 | Leishmania infantum | 80% | 98% |
E9AJT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
E9AN09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
E9ANE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 48% | 100% |
E9AUE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 45% | 98% |
O97596 | Felis catus | 28% | 82% |
P15710 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 30% | 95% |
P38361 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 98% |
Q28E01 | Xenopus tropicalis | 28% | 86% |
Q4QH82 | Leishmania major | 49% | 89% |
Q4QHL7 | Leishmania major | 50% | 89% |
Q5BL44 | Xenopus tropicalis | 25% | 82% |
Q61609 | Mus musculus | 26% | 82% |
Q63488 | Rattus norvegicus | 28% | 86% |
Q80UP8 | Mus musculus | 28% | 86% |
Q8WUM9 | Homo sapiens | 27% | 83% |
Q95L97 | Felis catus | 28% | 86% |
Q9ES44 | Cricetulus griseus | 28% | 86% |
V5DS90 | Trypanosoma cruzi | 47% | 100% |