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: E9AJT3
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 | 309 | 313 | PF00656 | 0.532 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.214 |
CLV_NRD_NRD_1 | 247 | 249 | PF00675 | 0.235 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.194 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.186 |
CLV_NRD_NRD_1 | 489 | 491 | PF00675 | 0.220 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.493 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.256 |
CLV_PCSK_KEX2_1 | 247 | 249 | PF00082 | 0.205 |
CLV_PCSK_KEX2_1 | 260 | 262 | PF00082 | 0.194 |
CLV_PCSK_KEX2_1 | 489 | 491 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.322 |
CLV_PCSK_SKI1_1 | 133 | 137 | PF00082 | 0.303 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.334 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.222 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.354 |
DEG_ODPH_VHL_1 | 145 | 157 | PF01847 | 0.408 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.271 |
DOC_CKS1_1 | 148 | 153 | PF01111 | 0.157 |
DOC_CKS1_1 | 441 | 446 | PF01111 | 0.555 |
DOC_CYCLIN_RxL_1 | 130 | 140 | PF00134 | 0.233 |
DOC_CYCLIN_RxL_1 | 287 | 296 | PF00134 | 0.397 |
DOC_MAPK_DCC_7 | 144 | 154 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 204 | 212 | PF00069 | 0.505 |
DOC_MAPK_gen_1 | 489 | 497 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 490 | 499 | PF00069 | 0.555 |
DOC_MAPK_NFAT4_5 | 492 | 500 | PF00069 | 0.550 |
DOC_MAPK_RevD_3 | 190 | 206 | PF00069 | 0.303 |
DOC_MAPK_RevD_3 | 477 | 490 | PF00069 | 0.337 |
DOC_PP1_RVXF_1 | 171 | 177 | PF00149 | 0.280 |
DOC_PP1_RVXF_1 | 487 | 494 | PF00149 | 0.261 |
DOC_PP4_FxxP_1 | 115 | 118 | PF00568 | 0.305 |
DOC_PP4_FxxP_1 | 427 | 430 | PF00568 | 0.233 |
DOC_USP7_MATH_1 | 102 | 106 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 377 | 381 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.271 |
DOC_USP7_MATH_1 | 527 | 531 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 68 | 72 | PF00917 | 0.305 |
DOC_USP7_MATH_2 | 275 | 281 | PF00917 | 0.397 |
DOC_USP7_UBL2_3 | 258 | 262 | PF12436 | 0.408 |
DOC_WW_Pin1_4 | 114 | 119 | PF00397 | 0.305 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.354 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.509 |
DOC_WW_Pin1_4 | 440 | 445 | PF00397 | 0.471 |
LIG_14-3-3_CanoR_1 | 173 | 183 | PF00244 | 0.298 |
LIG_14-3-3_CanoR_1 | 264 | 271 | PF00244 | 0.580 |
LIG_BRCT_BRCA1_1 | 513 | 517 | PF00533 | 0.362 |
LIG_CaM_NSCaTE_8 | 411 | 418 | PF13499 | 0.336 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.354 |
LIG_EH1_1 | 362 | 370 | PF00400 | 0.354 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.499 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.301 |
LIG_FHA_1 | 424 | 430 | PF00498 | 0.294 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.309 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.322 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.332 |
LIG_FHA_1 | 504 | 510 | PF00498 | 0.319 |
LIG_FHA_1 | 521 | 527 | PF00498 | 0.356 |
LIG_FHA_2 | 244 | 250 | PF00498 | 0.364 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.513 |
LIG_FHA_2 | 34 | 40 | PF00498 | 0.197 |
LIG_GBD_Chelix_1 | 452 | 460 | PF00786 | 0.233 |
LIG_LIR_Apic_2 | 113 | 118 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 426 | 430 | PF02991 | 0.233 |
LIG_LIR_Apic_2 | 462 | 467 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 156 | 167 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 182 | 190 | PF02991 | 0.157 |
LIG_LIR_Gen_1 | 39 | 49 | PF02991 | 0.232 |
LIG_LIR_Gen_1 | 55 | 65 | PF02991 | 0.365 |
LIG_LIR_LC3C_4 | 454 | 458 | PF02991 | 0.335 |
LIG_LIR_LC3C_4 | 506 | 509 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 100 | 104 | PF02991 | 0.258 |
LIG_LIR_Nem_3 | 105 | 110 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 182 | 186 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 360 | 366 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 39 | 45 | PF02991 | 0.253 |
LIG_LIR_Nem_3 | 485 | 491 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 55 | 61 | PF02991 | 0.352 |
LIG_MYND_1 | 147 | 151 | PF01753 | 0.408 |
LIG_NRP_CendR_1 | 528 | 531 | PF00754 | 0.567 |
LIG_Pex14_2 | 155 | 159 | PF04695 | 0.306 |
LIG_Pex14_2 | 162 | 166 | PF04695 | 0.307 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.397 |
LIG_SH2_CRK | 390 | 394 | PF00017 | 0.208 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.341 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.365 |
LIG_SH2_NCK_1 | 390 | 394 | PF00017 | 0.208 |
LIG_SH2_PTP2 | 42 | 45 | PF00017 | 0.157 |
LIG_SH2_SRC | 347 | 350 | PF00017 | 0.408 |
LIG_SH2_STAP1 | 390 | 394 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 129 | 132 | PF00017 | 0.468 |
LIG_SH2_STAT5 | 148 | 151 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 253 | 256 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.306 |
LIG_SH3_3 | 438 | 444 | PF00018 | 0.555 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.154 |
LIG_SUMO_SIM_anti_2 | 437 | 443 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 108 | 113 | PF11976 | 0.296 |
LIG_SUMO_SIM_par_1 | 150 | 156 | PF11976 | 0.336 |
LIG_SUMO_SIM_par_1 | 456 | 463 | PF11976 | 0.295 |
LIG_SUMO_SIM_par_1 | 477 | 482 | PF11976 | 0.321 |
LIG_SUMO_SIM_par_1 | 505 | 510 | PF11976 | 0.332 |
LIG_TRAF2_1 | 275 | 278 | PF00917 | 0.408 |
LIG_TYR_ITIM | 298 | 303 | PF00017 | 0.397 |
LIG_TYR_ITIM | 44 | 49 | PF00017 | 0.295 |
LIG_UBA3_1 | 199 | 204 | PF00899 | 0.295 |
LIG_UBA3_1 | 431 | 438 | PF00899 | 0.496 |
LIG_ULM_U2AF65_1 | 489 | 494 | PF00076 | 0.396 |
LIG_WRC_WIRS_1 | 241 | 246 | PF05994 | 0.408 |
LIG_WRC_WIRS_1 | 34 | 39 | PF05994 | 0.197 |
LIG_WRC_WIRS_1 | 424 | 429 | PF05994 | 0.366 |
MOD_CDK_SPxK_1 | 440 | 446 | PF00069 | 0.471 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.486 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.324 |
MOD_CK2_1 | 243 | 249 | PF00069 | 0.440 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.408 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.590 |
MOD_GlcNHglycan | 12 | 16 | PF01048 | 0.379 |
MOD_GlcNHglycan | 176 | 179 | PF01048 | 0.581 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.317 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.182 |
MOD_GlcNHglycan | 28 | 31 | PF01048 | 0.453 |
MOD_GlcNHglycan | 348 | 352 | PF01048 | 0.370 |
MOD_GlcNHglycan | 403 | 406 | PF01048 | 0.519 |
MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.318 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.316 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.177 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.321 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.513 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.464 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.248 |
MOD_GSK3_1 | 377 | 384 | PF00069 | 0.325 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.371 |
MOD_GSK3_1 | 468 | 475 | PF00069 | 0.304 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.340 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.337 |
MOD_N-GLC_2 | 320 | 322 | PF02516 | 0.202 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.516 |
MOD_NEK2_1 | 174 | 179 | PF00069 | 0.305 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.448 |
MOD_NEK2_1 | 456 | 461 | PF00069 | 0.322 |
MOD_NEK2_1 | 479 | 484 | PF00069 | 0.233 |
MOD_NEK2_1 | 48 | 53 | PF00069 | 0.280 |
MOD_NEK2_1 | 507 | 512 | PF00069 | 0.357 |
MOD_NEK2_1 | 60 | 65 | PF00069 | 0.201 |
MOD_PK_1 | 206 | 212 | PF00069 | 0.397 |
MOD_PK_1 | 237 | 243 | PF00069 | 0.397 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.354 |
MOD_PKA_1 | 97 | 103 | PF00069 | 0.227 |
MOD_PKA_2 | 172 | 178 | PF00069 | 0.197 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.567 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.375 |
MOD_Plk_1 | 137 | 143 | PF00069 | 0.408 |
MOD_Plk_2-3 | 306 | 312 | PF00069 | 0.516 |
MOD_Plk_4 | 110 | 116 | PF00069 | 0.292 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.168 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.324 |
MOD_ProDKin_1 | 114 | 120 | PF00069 | 0.305 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.354 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.509 |
MOD_ProDKin_1 | 440 | 446 | PF00069 | 0.471 |
MOD_SUMO_for_1 | 271 | 274 | PF00179 | 0.397 |
MOD_SUMO_rev_2 | 257 | 267 | PF00179 | 0.354 |
TRG_DiLeu_BaLyEn_6 | 115 | 120 | PF01217 | 0.295 |
TRG_DiLeu_BaLyEn_6 | 430 | 435 | PF01217 | 0.442 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.397 |
TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.208 |
TRG_ENDOCYTIC_2 | 42 | 45 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.302 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.417 |
TRG_ER_diArg_1 | 488 | 490 | PF00400 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 133 | 138 | PF00026 | 0.208 |
TRG_Pf-PMV_PEXEL_1 | 433 | 437 | PF00026 | 0.230 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S5 | Leptomonas seymouri | 48% | 100% |
A0A0S4JEW4 | Bodo saltans | 24% | 84% |
A0A1X0NXY5 | Trypanosomatidae | 47% | 100% |
A0A1X0P0T2 | Trypanosomatidae | 24% | 80% |
A0A3Q8I8Y3 | Leishmania donovani | 46% | 100% |
A0A3Q8IBK1 | Leishmania donovani | 44% | 98% |
A0A3R7K4N2 | Trypanosoma rangeli | 40% | 100% |
A0A3R7L5P3 | Trypanosoma rangeli | 24% | 88% |
A0A3S5H545 | Leishmania donovani | 90% | 93% |
A4H5Y5 | Leishmania braziliensis | 46% | 94% |
A4H6C2 | Leishmania braziliensis | 46% | 94% |
A4HBH2 | Leishmania braziliensis | 43% | 100% |
A4HH06 | Leishmania braziliensis | 76% | 100% |
A4HUP5 | Leishmania infantum | 46% | 100% |
A4HYJ6 | Leishmania infantum | 44% | 98% |
C9ZHT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 46% | 100% |
C9ZHU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 100% |
E9ACJ5 | Leishmania major | 89% | 100% |
E9AG39 | Leishmania infantum | 91% | 93% |
E9AN09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 44% | 100% |
E9ANE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |
E9AUE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 43% | 93% |
P15710 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 29% | 90% |
P38361 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 93% |
Q4QH82 | Leishmania major | 46% | 94% |
Q4QHL7 | Leishmania major | 46% | 94% |
Q63488 | Rattus norvegicus | 27% | 81% |
Q80UP8 | Mus musculus | 27% | 81% |
Q95L97 | Felis catus | 27% | 81% |
V5DS90 | Trypanosoma cruzi | 45% | 100% |