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: 0 |
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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 23 |
GO:0110165 | cellular anatomical entity | 1 | 23 |
GO:0000323 | lytic vacuole | 6 | 1 |
GO:0005764 | lysosome | 7 | 1 |
GO:0005773 | vacuole | 5 | 1 |
GO:0020022 | acidocalcisome | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H6H7
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 23 |
GO:0015203 | polyamine transmembrane transporter activity | 3 | 23 |
GO:0022857 | transmembrane transporter activity | 2 | 23 |
GO:0003824 | catalytic activity | 1 | 5 |
GO:0016787 | hydrolase activity | 2 | 5 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.200 |
CLV_NRD_NRD_1 | 455 | 457 | PF00675 | 0.505 |
CLV_PCSK_KEX2_1 | 301 | 303 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 455 | 457 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 429 | 433 | PF00082 | 0.396 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.253 |
DOC_CYCLIN_yCln2_LP_2 | 361 | 367 | PF00134 | 0.425 |
DOC_MAPK_gen_1 | 107 | 116 | PF00069 | 0.289 |
DOC_MAPK_MEF2A_6 | 343 | 351 | PF00069 | 0.318 |
DOC_MAPK_MEF2A_6 | 373 | 382 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 397 | 406 | PF00069 | 0.314 |
DOC_PP1_RVXF_1 | 427 | 434 | PF00149 | 0.530 |
DOC_PP1_RVXF_1 | 59 | 65 | PF00149 | 0.309 |
DOC_PP4_FxxP_1 | 365 | 368 | PF00568 | 0.436 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.284 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.328 |
DOC_USP7_MATH_1 | 438 | 442 | PF00917 | 0.694 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.429 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.383 |
LIG_14-3-3_CanoR_1 | 205 | 211 | PF00244 | 0.435 |
LIG_14-3-3_CanoR_1 | 429 | 434 | PF00244 | 0.633 |
LIG_Actin_WH2_2 | 243 | 258 | PF00022 | 0.251 |
LIG_APCC_ABBA_1 | 391 | 396 | PF00400 | 0.295 |
LIG_Clathr_ClatBox_1 | 122 | 126 | PF01394 | 0.152 |
LIG_Clathr_ClatBox_1 | 332 | 336 | PF01394 | 0.325 |
LIG_CtBP_PxDLS_1 | 232 | 236 | PF00389 | 0.200 |
LIG_deltaCOP1_diTrp_1 | 171 | 175 | PF00928 | 0.452 |
LIG_FHA_1 | 1 | 7 | PF00498 | 0.318 |
LIG_FHA_1 | 129 | 135 | PF00498 | 0.299 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.529 |
LIG_FHA_1 | 276 | 282 | PF00498 | 0.403 |
LIG_FHA_1 | 397 | 403 | PF00498 | 0.269 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.578 |
LIG_FHA_1 | 452 | 458 | PF00498 | 0.716 |
LIG_FHA_2 | 189 | 195 | PF00498 | 0.484 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.290 |
LIG_LIR_Gen_1 | 169 | 179 | PF02991 | 0.469 |
LIG_LIR_Gen_1 | 240 | 250 | PF02991 | 0.277 |
LIG_LIR_Gen_1 | 312 | 323 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 414 | 421 | PF02991 | 0.385 |
LIG_LIR_Gen_1 | 67 | 77 | PF02991 | 0.259 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 240 | 246 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.436 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.335 |
LIG_LIR_Nem_3 | 320 | 326 | PF02991 | 0.257 |
LIG_LIR_Nem_3 | 328 | 332 | PF02991 | 0.203 |
LIG_LIR_Nem_3 | 350 | 354 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 76 | 82 | PF02991 | 0.317 |
LIG_LIR_Nem_3 | 89 | 94 | PF02991 | 0.255 |
LIG_LYPXL_S_1 | 86 | 90 | PF13949 | 0.457 |
LIG_LYPXL_yS_3 | 87 | 90 | PF13949 | 0.241 |
LIG_NRBOX | 110 | 116 | PF00104 | 0.329 |
LIG_Pex14_1 | 238 | 242 | PF04695 | 0.237 |
LIG_Pex14_1 | 311 | 315 | PF04695 | 0.232 |
LIG_Pex14_2 | 143 | 147 | PF04695 | 0.260 |
LIG_Pex14_2 | 156 | 160 | PF04695 | 0.444 |
LIG_Pex14_2 | 365 | 369 | PF04695 | 0.469 |
LIG_PTB_Apo_2 | 81 | 88 | PF02174 | 0.229 |
LIG_PTB_Phospho_1 | 81 | 87 | PF10480 | 0.241 |
LIG_REV1ctd_RIR_1 | 418 | 427 | PF16727 | 0.513 |
LIG_SH2_GRB2like | 157 | 160 | PF00017 | 0.448 |
LIG_SH2_PTP2 | 218 | 221 | PF00017 | 0.290 |
LIG_SH2_PTP2 | 79 | 82 | PF00017 | 0.200 |
LIG_SH2_SRC | 165 | 168 | PF00017 | 0.480 |
LIG_SH2_SRC | 218 | 221 | PF00017 | 0.290 |
LIG_SH2_STAP1 | 2 | 6 | PF00017 | 0.302 |
LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.430 |
LIG_SH2_STAT5 | 165 | 168 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.289 |
LIG_SH2_STAT5 | 218 | 221 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 417 | 420 | PF00017 | 0.352 |
LIG_SH2_STAT5 | 69 | 72 | PF00017 | 0.269 |
LIG_SH2_STAT5 | 79 | 82 | PF00017 | 0.228 |
LIG_SH2_STAT5 | 94 | 97 | PF00017 | 0.215 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.496 |
LIG_SUMO_SIM_anti_2 | 206 | 212 | PF11976 | 0.152 |
LIG_SUMO_SIM_anti_2 | 24 | 30 | PF11976 | 0.396 |
LIG_SUMO_SIM_anti_2 | 331 | 336 | PF11976 | 0.332 |
LIG_SUMO_SIM_anti_2 | 396 | 402 | PF11976 | 0.292 |
LIG_SUMO_SIM_par_1 | 131 | 139 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 21 | 27 | PF11976 | 0.318 |
LIG_SUMO_SIM_par_1 | 231 | 236 | PF11976 | 0.366 |
LIG_SUMO_SIM_par_1 | 331 | 336 | PF11976 | 0.305 |
LIG_SUMO_SIM_par_1 | 344 | 350 | PF11976 | 0.405 |
LIG_SUMO_SIM_par_1 | 386 | 392 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 39 | 45 | PF11976 | 0.372 |
LIG_SxIP_EBH_1 | 429 | 443 | PF03271 | 0.505 |
LIG_TYR_ITIM | 77 | 82 | PF00017 | 0.232 |
LIG_TYR_ITSM | 238 | 245 | PF00017 | 0.251 |
LIG_UBA3_1 | 390 | 397 | PF00899 | 0.238 |
LIG_UBA3_1 | 57 | 61 | PF00899 | 0.518 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.369 |
LIG_WRC_WIRS_1 | 245 | 250 | PF05994 | 0.143 |
LIG_WRC_WIRS_1 | 326 | 331 | PF05994 | 0.244 |
LIG_WRC_WIRS_1 | 348 | 353 | PF05994 | 0.379 |
LIG_WRC_WIRS_1 | 412 | 417 | PF05994 | 0.410 |
LIG_WRC_WIRS_1 | 430 | 435 | PF05994 | 0.549 |
MOD_CK1_1 | 177 | 183 | PF00069 | 0.450 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.417 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.250 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.251 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.495 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.202 |
MOD_CK1_1 | 443 | 449 | PF00069 | 0.722 |
MOD_CK2_1 | 181 | 187 | PF00069 | 0.443 |
MOD_CK2_1 | 188 | 194 | PF00069 | 0.412 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.571 |
MOD_GlcNHglycan | 183 | 186 | PF01048 | 0.280 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.288 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.226 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.286 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.326 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.185 |
MOD_GlcNHglycan | 6 | 9 | PF01048 | 0.446 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.297 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.453 |
MOD_GSK3_1 | 177 | 184 | PF00069 | 0.435 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.475 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.303 |
MOD_GSK3_1 | 256 | 263 | PF00069 | 0.308 |
MOD_GSK3_1 | 270 | 277 | PF00069 | 0.271 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.424 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.313 |
MOD_GSK3_1 | 407 | 414 | PF00069 | 0.330 |
MOD_GSK3_1 | 429 | 436 | PF00069 | 0.636 |
MOD_GSK3_1 | 45 | 52 | PF00069 | 0.359 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.782 |
MOD_GSK3_1 | 60 | 67 | PF00069 | 0.260 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.223 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.436 |
MOD_NEK2_1 | 175 | 180 | PF00069 | 0.443 |
MOD_NEK2_1 | 233 | 238 | PF00069 | 0.364 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.263 |
MOD_NEK2_1 | 275 | 280 | PF00069 | 0.421 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.315 |
MOD_NEK2_1 | 4 | 9 | PF00069 | 0.246 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.658 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.288 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.312 |
MOD_PIKK_1 | 233 | 239 | PF00454 | 0.208 |
MOD_PKA_1 | 455 | 461 | PF00069 | 0.555 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.650 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.177 |
MOD_Plk_1 | 12 | 18 | PF00069 | 0.201 |
MOD_Plk_1 | 170 | 176 | PF00069 | 0.427 |
MOD_Plk_1 | 199 | 205 | PF00069 | 0.360 |
MOD_Plk_1 | 233 | 239 | PF00069 | 0.257 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.201 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.299 |
MOD_Plk_4 | 171 | 177 | PF00069 | 0.370 |
MOD_Plk_4 | 188 | 194 | PF00069 | 0.479 |
MOD_Plk_4 | 199 | 205 | PF00069 | 0.433 |
MOD_Plk_4 | 206 | 212 | PF00069 | 0.242 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.274 |
MOD_Plk_4 | 260 | 266 | PF00069 | 0.296 |
MOD_Plk_4 | 277 | 283 | PF00069 | 0.461 |
MOD_Plk_4 | 314 | 320 | PF00069 | 0.258 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.294 |
MOD_Plk_4 | 386 | 392 | PF00069 | 0.273 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.240 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.297 |
MOD_Plk_4 | 429 | 435 | PF00069 | 0.637 |
MOD_Plk_4 | 73 | 79 | PF00069 | 0.263 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.263 |
MOD_SUMO_rev_2 | 441 | 451 | PF00179 | 0.549 |
TRG_DiLeu_BaEn_2 | 170 | 176 | PF01217 | 0.343 |
TRG_ENDOCYTIC_2 | 242 | 245 | PF00928 | 0.216 |
TRG_ENDOCYTIC_2 | 358 | 361 | PF00928 | 0.445 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.369 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.275 |
TRG_ENDOCYTIC_2 | 79 | 82 | PF00928 | 0.231 |
TRG_ENDOCYTIC_2 | 87 | 90 | PF00928 | 0.234 |
TRG_ER_diArg_1 | 455 | 457 | PF00400 | 0.686 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2T0 | Leptomonas seymouri | 68% | 81% |
A0A0N1PGN1 | Leptomonas seymouri | 34% | 89% |
A0A0S4IJF6 | Bodo saltans | 22% | 80% |
A0A0S4ISA5 | Bodo saltans | 22% | 81% |
A0A0S4JBT0 | Bodo saltans | 27% | 90% |
A0A1X0NNQ0 | Trypanosomatidae | 30% | 74% |
A0A1X0NV66 | Trypanosomatidae | 50% | 89% |
A0A1X0P501 | Trypanosomatidae | 35% | 86% |
A0A3R7M6P3 | Trypanosoma rangeli | 31% | 76% |
A0A3R7N0T9 | Trypanosoma rangeli | 52% | 92% |
A0A3S5IRV3 | Trypanosoma rangeli | 35% | 92% |
A0A3S7WRN2 | Leishmania donovani | 84% | 100% |
A0A3S7XA01 | Leishmania donovani | 34% | 90% |
A2X8M8 | Oryza sativa subsp. indica | 27% | 88% |
A4HNB0 | Leishmania braziliensis | 36% | 90% |
A4HUW5 | Leishmania infantum | 84% | 100% |
A4IBY1 | Leishmania infantum | 35% | 90% |
C9ZYM5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 95% |
D0A7J0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 92% |
E9AFR8 | Leishmania major | 35% | 100% |
E9ANJ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 100% |
E9B6X1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 90% |
Q4QH28 | Leishmania major | 82% | 100% |
Q6Z8D0 | Oryza sativa subsp. japonica | 27% | 88% |
Q9C6S4 | Arabidopsis thaliana | 27% | 97% |
Q9C6S5 | Arabidopsis thaliana | 29% | 94% |
Q9FFL1 | Arabidopsis thaliana | 28% | 95% |
Q9LH39 | Arabidopsis thaliana | 26% | 97% |
Q9LHN7 | Arabidopsis thaliana | 24% | 98% |
V5BCQ1 | Trypanosoma cruzi | 37% | 100% |
V5DDZ5 | Trypanosoma cruzi | 30% | 74% |