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: Q4QH82
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 | 298 | 302 | PF00656 | 0.542 |
CLV_NRD_NRD_1 | 140 | 142 | PF00675 | 0.559 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 188 | 190 | PF00082 | 0.350 |
CLV_PCSK_KEX2_1 | 216 | 218 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 248 | 250 | PF00082 | 0.275 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.446 |
CLV_PCSK_PC1ET2_1 | 188 | 190 | PF00082 | 0.246 |
CLV_PCSK_PC1ET2_1 | 216 | 218 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 248 | 250 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.477 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.365 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.268 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.313 |
DEG_SPOP_SBC_1 | 112 | 116 | PF00917 | 0.303 |
DEG_SPOP_SBC_1 | 433 | 437 | PF00917 | 0.349 |
DOC_CKS1_1 | 407 | 412 | PF01111 | 0.568 |
DOC_MAPK_gen_1 | 188 | 196 | PF00069 | 0.550 |
DOC_MAPK_gen_1 | 324 | 334 | PF00069 | 0.446 |
DOC_MAPK_MEF2A_6 | 189 | 198 | PF00069 | 0.451 |
DOC_MAPK_MEF2A_6 | 370 | 378 | PF00069 | 0.352 |
DOC_MAPK_MEF2A_6 | 458 | 465 | PF00069 | 0.570 |
DOC_MAPK_NFAT4_5 | 458 | 466 | PF00069 | 0.564 |
DOC_PP1_RVXF_1 | 214 | 221 | PF00149 | 0.305 |
DOC_PP2B_LxvP_1 | 109 | 112 | PF13499 | 0.485 |
DOC_PP4_FxxP_1 | 159 | 162 | PF00568 | 0.334 |
DOC_SPAK_OSR1_1 | 177 | 181 | PF12202 | 0.518 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.334 |
DOC_USP7_MATH_1 | 299 | 303 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 433 | 437 | PF00917 | 0.349 |
DOC_USP7_UBL2_3 | 184 | 188 | PF12436 | 0.438 |
DOC_USP7_UBL2_3 | 212 | 216 | PF12436 | 0.268 |
DOC_USP7_UBL2_3 | 79 | 83 | PF12436 | 0.268 |
DOC_WW_Pin1_4 | 158 | 163 | PF00397 | 0.326 |
DOC_WW_Pin1_4 | 406 | 411 | PF00397 | 0.493 |
LIG_14-3-3_CanoR_1 | 110 | 119 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 189 | 195 | PF00244 | 0.507 |
LIG_14-3-3_CanoR_1 | 217 | 223 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.530 |
LIG_Actin_WH2_2 | 203 | 221 | PF00022 | 0.478 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.392 |
LIG_BRCT_BRCA1_1 | 239 | 243 | PF00533 | 0.363 |
LIG_BRCT_BRCA1_1 | 410 | 414 | PF00533 | 0.338 |
LIG_BRCT_BRCA1_1 | 479 | 483 | PF00533 | 0.388 |
LIG_CaM_NSCaTE_8 | 377 | 384 | PF13499 | 0.364 |
LIG_deltaCOP1_diTrp_1 | 322 | 329 | PF00928 | 0.468 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.305 |
LIG_FHA_1 | 163 | 169 | PF00498 | 0.414 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.520 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.465 |
LIG_FHA_1 | 363 | 369 | PF00498 | 0.317 |
LIG_FHA_1 | 390 | 396 | PF00498 | 0.323 |
LIG_FHA_1 | 435 | 441 | PF00498 | 0.356 |
LIG_FHA_1 | 44 | 50 | PF00498 | 0.419 |
LIG_FHA_1 | 470 | 476 | PF00498 | 0.341 |
LIG_FHA_1 | 66 | 72 | PF00498 | 0.278 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.489 |
LIG_GBD_Chelix_1 | 196 | 204 | PF00786 | 0.357 |
LIG_GBD_Chelix_1 | 474 | 482 | PF00786 | 0.334 |
LIG_IBAR_NPY_1 | 5 | 7 | PF08397 | 0.377 |
LIG_LIR_Apic_2 | 157 | 162 | PF02991 | 0.334 |
LIG_LIR_Apic_2 | 428 | 433 | PF02991 | 0.349 |
LIG_LIR_Gen_1 | 107 | 113 | PF02991 | 0.557 |
LIG_LIR_Gen_1 | 205 | 214 | PF02991 | 0.336 |
LIG_LIR_Gen_1 | 451 | 462 | PF02991 | 0.314 |
LIG_LIR_LC3C_4 | 419 | 424 | PF02991 | 0.360 |
LIG_LIR_LC3C_4 | 472 | 475 | PF02991 | 0.291 |
LIG_LIR_Nem_3 | 107 | 111 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 326 | 332 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 451 | 457 | PF02991 | 0.323 |
LIG_Pex14_2 | 203 | 207 | PF04695 | 0.335 |
LIG_SH2_CRK | 173 | 177 | PF00017 | 0.274 |
LIG_SH2_CRK | 192 | 196 | PF00017 | 0.308 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.391 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 321 | 325 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.445 |
LIG_SH2_STAT5 | 331 | 334 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 7 | 10 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.334 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.439 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.206 |
LIG_SH3_3 | 404 | 410 | PF00018 | 0.568 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.343 |
LIG_Sin3_3 | 420 | 427 | PF02671 | 0.439 |
LIG_SUMO_SIM_anti_2 | 403 | 409 | PF11976 | 0.568 |
LIG_SUMO_SIM_anti_2 | 46 | 53 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 41 | 46 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 443 | 448 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 47 | 53 | PF11976 | 0.323 |
LIG_SUMO_SIM_par_1 | 471 | 476 | PF11976 | 0.360 |
LIG_TRAF2_1 | 261 | 264 | PF00917 | 0.504 |
LIG_TYR_ITIM | 171 | 176 | PF00017 | 0.419 |
LIG_UBA3_1 | 460 | 464 | PF00899 | 0.327 |
LIG_ULM_U2AF65_1 | 216 | 221 | PF00076 | 0.290 |
LIG_WRC_WIRS_1 | 16 | 21 | PF05994 | 0.361 |
LIG_WRC_WIRS_1 | 204 | 209 | PF05994 | 0.288 |
LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.391 |
LIG_WRC_WIRS_1 | 423 | 428 | PF05994 | 0.363 |
MOD_CDK_SPxK_1 | 406 | 412 | PF00069 | 0.349 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.297 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.358 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.371 |
MOD_CK1_1 | 347 | 353 | PF00069 | 0.338 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.349 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.331 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.300 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.400 |
MOD_CK2_1 | 50 | 56 | PF00069 | 0.343 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.442 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.152 |
MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.468 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.311 |
MOD_GlcNHglycan | 418 | 421 | PF01048 | 0.310 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.285 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.346 |
MOD_GlcNHglycan | 488 | 491 | PF01048 | 0.478 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.323 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.320 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.332 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.325 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.397 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.326 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.322 |
MOD_GSK3_1 | 469 | 476 | PF00069 | 0.365 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.355 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.303 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.439 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.351 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.327 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.349 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.359 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.384 |
MOD_PIKK_1 | 270 | 276 | PF00454 | 0.287 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.284 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.439 |
MOD_PK_1 | 370 | 376 | PF00069 | 0.314 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.414 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.314 |
MOD_Plk_4 | 104 | 110 | PF00069 | 0.353 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.346 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.320 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.320 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.307 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.419 |
MOD_Plk_4 | 445 | 451 | PF00069 | 0.314 |
MOD_ProDKin_1 | 158 | 164 | PF00069 | 0.326 |
MOD_ProDKin_1 | 406 | 412 | PF00069 | 0.349 |
MOD_SUMO_rev_2 | 72 | 81 | PF00179 | 0.314 |
TRG_DiLeu_BaLyEn_6 | 242 | 247 | PF01217 | 0.319 |
TRG_ENDOCYTIC_2 | 173 | 176 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.302 |
TRG_ENDOCYTIC_2 | 7 | 10 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.330 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4S5 | Leptomonas seymouri | 68% | 94% |
A0A1X0NXY5 | Trypanosomatidae | 60% | 93% |
A0A3Q8I8Y3 | Leishmania donovani | 99% | 100% |
A0A3Q8IBK1 | Leishmania donovani | 62% | 91% |
A0A3R7K4N2 | Trypanosoma rangeli | 57% | 100% |
A0A3S5H545 | Leishmania donovani | 49% | 86% |
A4H5Y5 | Leishmania braziliensis | 92% | 100% |
A4H6C2 | Leishmania braziliensis | 91% | 100% |
A4HBH2 | Leishmania braziliensis | 61% | 91% |
A4HH06 | Leishmania braziliensis | 49% | 88% |
A4HUP5 | Leishmania infantum | 99% | 100% |
A4HYJ6 | Leishmania infantum | 62% | 91% |
C9ZHT9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 58% | 96% |
C9ZHU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 96% |
E9ACJ5 | Leishmania major | 49% | 100% |
E9AG39 | Leishmania infantum | 49% | 86% |
E9AJT3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 93% |
E9AN09 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9ANE4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
E9AUE3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 61% | 86% |
O84698 | Chlamydia trachomatis (strain D/UW-3/Cx) | 32% | 100% |
P0AFJ7 | Escherichia coli (strain K12) | 24% | 99% |
P0AFJ8 | Escherichia coli O6:H1 (strain CFT073 / ATCC 700928 / UPEC) | 24% | 99% |
P0AFJ9 | Escherichia coli O157:H7 | 24% | 99% |
P38361 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 86% |
Q4QHL7 | Leishmania major | 100% | 100% |
Q6PFM1 | Danio rerio | 31% | 74% |
Q8K903 | Buchnera aphidicola subsp. Schizaphis graminum (strain Sg) | 22% | 100% |
Q9PLN5 | Chlamydia muridarum (strain MoPn / Nigg) | 31% | 100% |
Q9Z7M4 | Chlamydia pneumoniae | 32% | 100% |
Q9ZJC8 | Helicobacter pylori (strain J99 / ATCC 700824) | 30% | 92% |
V5DS90 | Trypanosoma cruzi | 59% | 100% |